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Phase change fibers (PCFs), incorporating with diverse phase change materials (PCMs) such as paraffin wax (PW), have been recognized as one of the effective strategies for fabricate smart thermoregulatory textiles. However, some fatal defects exist in traditional paraffin-cellulose-based PCFs, including the paraffin leakage and the low fiber strength. In this work, we herein propose a facile method to prepare uniform and stable paraffin emulsions stabilized by cellulose nanofibrils (CNFs), followed by a simple coaxial wet spinning to develop smart and robust cellulose-based PCFs for human body temperature management. Benefiting from the CNF-reinforced encapsulation, the stability of paraffin capsules and the compatibility of cellulose and paraffin are indeed promoted, thus allowing the cellulose-based PCF with excellent mechanical strength, leakage prevention, and thermal regulation. As a result, the as-prepared PCF, namely CNF 1 -PE/PW with optimal 1 wt% CNF 1 loading, features a high tensile stress of 10.95 MPa at a strain of 111.2 % and a phase-change enthalpy value of 140.24 J/g with a slight paraffin leakage rate of 0.9 %. Moreover, the corresponding wearable fabric exhibits an excellent thermal storage and release recyclability even after 50 cycles. Therefore, this study provides a new idea for the development of intelligent cellulose-based phase change fiber materials., Competing Interests: Declaration of competing interest All the authors state that we have non-competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

The transition metal nanocatalysts containing disordered active sites can potentially achieve efficient Sabatier reactions with high selectivity. However, it remains a challenge to maintain the stability of these active sites in such an exothermic reaction. Here, a thermal management approach is reported to address this challenge. Specifically, an efficient and stable catalytic system is developed by integrating urchin-like Ru nanoparticles with disordered active sites (d-RuNUs) and multi-walled carbon nanotubes (MWCNTs) as heat transfer framework, which achieves a CH 4 yield of 3.3 mol g -1 h -1 with nearly 100% selectivity in 12 h. The characterizations reveal that the thermal-induced crystallization seriously weakens the adsorption of CO 2 , leading to significant degradation of catalytic performance. The heat transfer simulation confirms that the MWCNTs with high thermal conductivity play a key role in rapidly redistributing the reaction heat, thereby preventing the crystallization of disordered structures. This work elucidates the deactivation mechanism of disordered active sites in exothermic reactions and opens the avenue for local thermal management of non-thermal equilibrium reactions., (© 2024 The Author(s). Advanced Science published by Wiley‐VCH GmbH.)

Effective heat redistribution in specific directions is vital for advanced thermal management, significantly enhancing device performance by optimizing spatial heat configurations. We have designed and fabricated a hierarchical fibrous membrane that enables precise heat directing. By integrating hierarchical structure design with the anisotropic thermal conductivity of two-dimensional (2D) materials, we developed a fibrous membrane for anisotropic heat transfer. Such a structure is fabricated by aligning a 1D structured fiber in the 2D plane to achieve anisotropy at each scale level. The fiber units, where 2D nanosheets circumferentially and axially aligned, achieved a high axial thermal conductivity of 16.8 W·m -1 ·K -1 and advanced heat directing ability, confirmed by characterizations and simulations. The assembled membrane demonstrated an exceptional tensile strength (365 MPa) and high thermal conductivity (10.5 W·m -1 ·K -1 ) along the fiber axis. Our membranes are seen as a refined model for thermal management materials, combining the benefits of heat spreaders and thermal interface materials, thus being proficient in directing heat along programmed pathways. A practical wireless charging cooling demonstration illustrated this. Our methodology also proved versatile with different 2D fillers and various geometries. This research presents a method to achieve precise heat directing at the material's level, facilitating the systematic design of thermal management in electronics.

Industrial implementation of highly thermally conductive polymeric composites has been hindered by several hurdles, such as the low intrinsic thermal conductivity (TC) of polymers, the use of expensive thermally conductive fillers, and difficulty in processing composites with high filler loading. In this study, we introduce a straightforward fabrication method for a high TC polymeric composite with a programmed internal structure of a highly interconnected thermal conduction highway (HITCH) by the simple addition of partially cured resin fragments into the conventional filler/resin combination. Critical variables, such as the concentration of the added resin fragments and the local concentration of hexagonal boron nitride (hBN) in the HITCH, as well as the packing density of the fragments, were systematically tuned to maximize the TC with the use of the least amount of the filler. Careful choice of the compositions enabled a significant TC enhancement of the composite by 2.6 times (6.5 W/mK) compared to the value of the conventional composite at the same overall concentration of hBN (∼2.5 W/mK). Finally, a composite with high TC (∼12 W/mK) and strong tensile strength (∼22.6 MPa), which is good enough for most practical thermal management applications, could be successfully fabricated with the use of the least amount of the filler (∼34 wt %). The comprehensive study of the HITCH composite here can be easily extended to other combinations with various fillers and matrices and may provide a library to researchers looking for advanced materials for future thermal management systems.

Materials with anisotropic emission characteristics have attracted considerable attention for thermal management. Although many dual-mode emitters have been developed for this purpose in the form of textiles, multilayer films, and photonic structures, multiple functionalities are essential for their versatile applications. Herein, a highly stretchable dual-mode emitter with programmable emissivity and air permeability is presented. The emitter comprises a planar Ge 2 Sb 2 Te 5 (GST) cavity on one side of a perforated elastomer substrate and an infrared-reflecting metal layer on the other side. With a laser-induced phase transition from amorphous to crystalline GST, the emitter exhibits a large emissivity difference of 0.52 between both sides. The dual-mode emitter remains highly stable without mechanical failure after repeated stretching cycles to a strain of 50%. This air-permeable and stretchable emitter can be attached to any curved surface, including the human body. The GST-side emissivity can be programmed into an arbitrary emissivity pattern using a spatially modulated laser beam, ultimately enabling the printing of mutually independent visible and thermal images in a single emitter. This study provides a promising structure for multispectral optical security as well as thermal management.

Phonons, the collective excitations responsible for heat transport in crystalline insulating solids, lack electric charge or magnetic moment, which complicates their active control via external fields. This presents a significant challenge in designing thermal equivalents of basic electronic circuit elements, such as transistors or diodes. Achieving these goals requires precise and reversible modification of thermal conductivity in materials. In this work, the continuous tuning of local thermal conductivity in charge-transfer SrFeO 3-x and La 0.6 Sr 0.4 CoO 3-x oxides using a voltage-biased Atomic Force Microscopy (AFM) tip at room temperature is demonstrated. This method allows the creation of micron-sized domains with well-defined thermal conductivity, achieving reductions of up to 50%, measured by spatially resolved Frequency Domain Thermoreflectance (FDTR). By optimizing the oxide's chemical composition, the thermal states remain stable under normal atmospheric conditions but can be reverted to their original values through thermal annealing in air. A comparison between Mott-Hubbard and charge-transfer oxides reveals the critical role of redox-active lattice oxygen in ensuring full reversibility of the process. This approach marks a significant step toward fabricating oxide-based tunable microthermal resistances and other elements for thermal circuits., (© 2024 The Author(s). Advanced Materials published by Wiley‐VCH GmbH.)

The rapid development of modern electronic devices increasingly requires thermal management materials with controllable electrical properties, ranging from conductive and dielectric to insulating, to meet the needs of diverse applications. However, highly thermally conductive materials usually have a high electrical conductivity. Intrinsically highly thermally conductive, but electrically insulating materials are still limited to a few kinds of materials. To overcome the electrical-thermal conductance trade-off, here, we report a facile Pechini-based method to prepare multiple core (metal)/shell (metal oxide) engineered fillers, such as aluminum-oxide-coated and beryllium-oxide-coated Ag microspheres. In contrast to the previous in situ growth method which mainly focused on small-sized spheres with specific coating materials, our method combined with ultrafast joule heating treatment is more versatile and robust for varied-sized, especially large-sized core-shell fillers. Through size compounding, the as-synthesized core-shell-filled epoxy composites exhibit high isotropic thermal conductivity (∼3.8 W m -1 K -1 ) while maintaining high electrical resistivity (∼10 12 Ω cm) and good flowability, showing better heat dissipation properties than commercial thermally conductive packaging materials. The successful preparation of these core-shell fillers endows thermally conductive composites with controlled electrical properties for emerging electronic package applications, as demonstrated in circuit board and battery thermal management.

Ultrawide bandgap semiconductors such as AlGaN, AlN, diamond, and β-Ga 2 O 3 have significantly enhanced the functionality of electronic and optoelectronic devices, particularly in harsh environment conditions. However, some of these materials face challenges such as low thermal conductivity, limited P-type conductivity, and scalability issues, which can hinder device performance under extreme conditions like high temperature and irradiation. In this review paper, we explore the integration of various two-dimensional materials (2DMs) to address these challenges. These materials offer excellent properties such as high thermal conductivity, mechanical strength, and electrical properties. Notably, graphene, hexagonal boron nitride, transition metal dichalcogenides, 2D and quasi-2D Ga 2 O 3 , TeO 2 , and others are investigated for their potential in improving ultrawide bandgap semiconductor-based devices. We highlight the significant improvement observed in the device performance after the incorporation of 2D materials. By leveraging the properties of these materials, ultrawide bandgap semiconductor devices demonstrate enhanced functionality and resilience in harsh environmental conditions. This review provides valuable insights into the role of 2D materials in advancing the field of ultrawide bandgap semiconductors and highlights opportunities for further research and development in this area.

While providing electrical energy for human society, power equipment also consumes electricity and generate heat. Cooling equipment consumes a significant amount of electricity, further increasing energy consumption and load on the power grid. Therefore, there is an urgent need to develop low-energy and sustainable cooling technologies for power equipment. In this study, a hybrid passive cooling composite designed to enhance heat dissipation for heavy-load power equipment is introduced. Specifically, the composite material achieves outstanding radiative cooling performance with an average solar reflectance of up to 0.98, while its excellent atmospheric water harvesting performance ensures high evaporation cooling power without the need for manual water replenishment. As a result, the composite effectively lowers the temperature of outdoor heavy-load power equipment (e.g., transformers) by 25.3 °C. The excellent heat dissipation properties of the composite make it a powerful tool in safeguarding electrical systems., (© 2024 Wiley‐VCH GmbH.)

Textiles with thermal/moisture managing functions are of high interest. However, making the textile sensitive to the surrounding environment is still challenging. Herein, a multimodal smart fabric is developed by stitching together the Ag coated thermal-humidity sensitive thermoplastic polyurethane (Ag-THSPU) and the hybrid of polyvinylidene fluoride and polyurethane (PU-PVDF). The porous PU-PVDF layer is used for solar reflection, infrared emissivity, and water resistance. The Ag-THSPU layer is designed for regulating thermal reflection, sweat evaporation as well as convection. In cold and dry state, the Ag domains are densely packed covering the crystalline polyurethane matrix, featuring low water transmission (102.74 g m -2 ·24 h -1 ), high thermal reflection and 2.4 °C warmer than with cotton fabric. In the hot and humid state, the THSPU layer is swollen by sweat and expands in area, resulting in the formation of micro-hook faces where the Ag domains spread apart to promote sweat evaporation (2084.88 g/m -2 ·24 h -1 ), thermal radiation and convection, offering 2.5 °C cooler than with cotton fabric. The strategy reported here opens a new door for the development of adaptive textiles in demanding situations., (© 2024 Wiley‐VCH GmbH.)

The rational design of dielectric fluids for immersion cooling of batteries requires a molecular-level understanding of the heat flow across the battery casing/dielectric fluid interface. Here, we use nonequilibrium molecular dynamics (NEMD) simulations to quantify the interfacial thermal resistance (ITR) between hematite and poly-α-olefin (PAO), which are representative of the outer surface of the steel battery casing and a synthetic hydrocarbon dielectric fluid, respectively. After identifying the most suitable force fields to model the thermal properties of the individual components, we then compared different solid-liquid interaction potentials for the calculation of the ITR. These potentials resulted in a wide range of ITR values (4-21 K m 2 GW -1 ), with stronger solid-liquid interactions leading to lower ITR. The increase in ITR is correlated with an increase in density of the fluid layer closest to the surface. Since the ITR has not been experimentally measured for the hematite/PAO interface, we validate the solid-liquid interaction potential using the work of adhesion calculated using the dry-surface method. The work of adhesion calculations from the simulations were compared to those derived from experimental contact angle measurements for PAO on steel. We find that all of the solid-liquid potentials overestimate the experimental work of adhesion. The experiments and simulations can only be reconciled by further reducing the strength of the interfacial interactions. This suggests some screening of the solid-liquid interactions, which may be due to the presence of an interfacial water layer between PAO and steel in the contact angle experiments. Using the solid-liquid interaction potential that reproduces the experimental work of adhesion, we obtain a higher ITR (33 K m 2 GW -1 ), suggesting inefficient thermal transport. The results of this study demonstrate the potential for NEMD simulations to improve understanding of the nanoscale thermal transport across industrially important interfaces. This study represents an important step toward the rational design of more effective fluids for immersion cooling systems for electric vehicles and other applications where thermal management is of high importance.

Besides the fact that the Proton Exchange Membrane Fuel Cells (PEMFCs) have become the industrial norm of today, the thermal management in PEMFCs is still challenging. Therefore, the present study delves deep understanding of the issue of thermal management and summarizes the relevant research studies that evaluate the efficiency of serpentine flow fields (SFFs) to other flow configurations for thermal management in PEMFCs. The current research explores the variety of aspects of SFFs i.e., temperature uniformity, cooling efficiency, pressure drop, and overall thermal performance to guide future design optimizations and practical implementations of SFFs. The study in hand also discusses developments in SFFs such as., Multi-Pass Serpentine Flow Fields (MPSFFs) and new hybrid designs that include a combination of traditional serpentine and other flow patterns to decrease pressure drop and increase net performance. The findings of various studies show that serpentine flow fields outperform alternative designs in coolant distribution, heat transfer efficiency, and operating temperature stability. Based on the findings, the present study recommends future research options, highlighting the need to include economic and environmental concerns in flow field (FF) design, as well as investigating the use of developing materials and technologies to improve PEMFC performance., Competing Interests: The authors declare the following financial interests/personal relationships which may be considered as potential competing interests:Muhammad Ahmed reports financial support, article publishing charges, equipment, drugs, or supplies, and writing assistance were provided by the Student’s Innovation Center at the College of Energy Engineering, 10.13039/501100004835Zhejiang University, Zhejiang, China and Jianbing Leading Goose Project (Grant Number: 2023C01239) in Zhejiang Province, China. If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (© 2024 The Authors. Published by Elsevier Ltd.)

Managing high-flux waste heat with controllable device working temperature is becoming challenging and critical for the artificial intelligence, communications, electric vehicles, defense and aerospace sectors. Spray cooling, which combines forced convection with phase-change latent heat of working fluids, is promising for high flux heat dissipation. Most of the previous studies on spray cooling enhancement adopted high spray flow rates to strengthen forced convection for high critical heat flux (CHF), leading to a low heat transfer coefficient (HTC). Micro/nanostructured surfaces can enhance boiling, but bubbles inside the structures tend to form a vapor blanket, which can deteriorate heat transfer. This work demonstrates simultaneous enhancement of CHF and HTC in spray cooling by improving both evaporation and liquid film boiling on three-dimensional (3D) ordered hierarchical micro/nano-structured surface. The hierarchical micro/nano-structured surface is designed to coordinate the transport of spray droplets, capillary liquid films, and boiling bubbles to enhance spray cooling performance. Boiling inversion where superheat decreases with increasing heat flux is observed, leading to an ultra-high HTC due to the simultaneous promotion of bubble nucleation and evaporation. Unprecedented CHF is obtained by overcoming the liquid-vapor counterflow, i.e., synergistically facilitating bubble escape and liquid permeation. A record-breaking heat transfer performance of spray cooling is achieved with a maximum heat flux of 1273 W/cm 2 and an HTC of 443.7 kW/(m 2 K) over a 1 cm 2 heating area., (Copyright © 2024 Science China Press. Published by Elsevier B.V. All rights reserved.)

Gallium oxide (Ga 2 O 3 ) emerges as a promising ultrawide bandgap semiconductor, which is expected to surpass the performance of current wide bandgap materials, like GaN and SiC, in electronic devices. However, widespread application of Ga 2 O 3 is hindered by its extremely low thermal conductivity and lack of effective device-level thermal management strategies. In this work, Ga 2 O 3 metal-oxide-semiconductor field-effect transistors (MOSFETs) are fabricated by conducting co-integrated design of substrate engineering with layer transferring and device packaging. 3D Raman thermography is introduced as a novel method to analyze the temperature distribution within the device, which provides valuable insights into their thermal performances. A high-quality Ga 2 O 3 -SiC heterogeneous integrated material is successfully fabricated with an extremely low interface thermal resistance of 6.67 ± 2 m 2 ·K/GW. Compared to the homoepitaxial Ga 2 O 3 MOSFETs, the degradation of I on / I off in Ga 2 O 3 -SiC MOSFETs is decreased by 1.5 orders of magnitude, and that of R on is decreased by 31%, showing the great thermal stability of Ga 2 O 3 -SiC MOSFETs. With the additional device packaging, a significant one order-of-magnitude reduction in the thermal resistance of the Ga 2 MOSFETs. This work demonstrates an efficient strategy for device-level thermal management in next-generation Ga 3 -SiC MOSFET is achieved, reaching a record-low value of 4.45 K·mm/W in the reported Ga 2 O 3 MOSFETs. This work demonstrates an efficient strategy for device-level thermal management in next-generation Ga 2 O 3 power and RF applications.

Phase-change materials (PCMs) stand a pivotal advancement in thermal energy storage and management due to their reversible phase transitions to store and release an abundance of heat energy. However, conventional solid-liquid PCMs suffer from fluidity and leakage in their molten state, limiting their applications at advanced levels. Herein, a novel Zn 2+ -crosslinked polyethylene glycol-co-polyphosphazene copolymer (PCEPN-Zn) as a solid-solid PCM through dynamic metal-ligand coordination is first designed and synthesized. The as-synthesized PCEPN-Zn is further integrated with an MXene film to construct a double-layered phase-change composite through layer-by layer adhesion. Owing to the introduction of MXene film with low emissivity, good light absorptivity, and nonflammability, the resultant phase-change composite not only presents a high latent-heat capacity, good thermal stability, high thermal reliability, and excellent shape stability, but also exhibits a superior self-healing ability, good recyclability, high adhesivity, and good flame-retardant performance. It can be easily adhered to on most objects for various application scenarios. With a combination of the excellent functions derived from PCEPN-Zn and MXene film, the developed phase-change composite exhibits broad prospects for versatile applications in the thermal management of CPUs and Li-ion batteries, thermal infrared stealth of high-temperature objects, heat therapy in the clinic, and fire-safety for various scenarios., (© 2024 Wiley‐VCH GmbH.)

Aerogel fibers are an emerging class of ultralightweight materials, which, compared to conventional bulk monolithic and aerogel films, provide better flexibility and extensibility. Despite the recent advancements in this field, due to their highly porous structure, their mechanical properties can be deteriorated. Inspired by the textile industry, we report the development of aerogel fiber bundles with twisted structures as a promising strategy to enhance the mechanical performance and practicality of aerogel fibers. Polyimide (PI) aerogel fibers were prepared via the sol-gel confined transition method. The fibers showed a unique nanostructured assembly with high specific surface area, excellent optical transparency, outstanding flexibility at diverse extreme conditions, self-extinguishing behavior, and superior thermal insulation performance. Using PI aerogel fibers as the backbone, aerogel fiber bundles in various configurations were designed and fabricated. A systematic study was performed to analyze the effect of design parameters on the mechanical performance of the bundles. Results revealed an optimal twist level for bundles, leading to a peak in mechanical properties across various bundle configurations. The observed improvement in mechanical properties was attributed to increased fiber-to-fiber binding strength, enhanced friction, and interlocking mechanism of fibers, underscoring the potential of the optimized twist level for enhancing the performance of aerogel fiber bundles. Overall, the development of aerogel fiber bundles holds great promise in revolutionizing the production of high-performance ultralightweight materials for thermal management applications.

Photothermal therapy (PTT) encounters challenges of rapid thermal loss and potential tissue damage. In response, we propose a Heat-Boost and Lock implant coating strategy inspired by the thermal adaptation of biological membranes, enabling precise local photothermal utilization. This coating incorporates a poly(tannic acid) (pTA) bridging layer on implants, facilitating stable layer-by-layer integration of a black phosphorus (BP) photothermal layer and a top cell membrane Heat-Boost and Lock layer. The cell membrane layer significantly curtails photothermal loss (extending the heat retention by 17.62%) and stores energy within its phospholipid bilayer, boosting photothermal effects near implants (achieving a temperature increasement of 275%). Theoretical analysis indicates that these local heat preservation properties of the cell membrane arise from its low thermal conductivity and phase-change properties. In a Staphylococcus aureus -infected bone implant model, our coating demonstrates precise antibacterial action around implants (reach an antibacterial ratio of 99.52%). The synergetic locking function of cell membrane and pTA delays BP biodegradation, ensuring favorable photothermal stability and long-term osteo-inductive performance (increasing the bone volume fraction by 53.45%). Beyond providing an endogenic biointerface, this strategy extends the application of cell membrane in local thermal management, offering possibilities for effective and safe PTT modalities.

As a novel approach to pursue high-performance multifunctional materials, the structural design of cutting-edge two-dimensional (2D) materials has ignited substantial interests. Borophene, an emerging member in the realm of 2D materials, exhibits crucial attributes, including high theoretical carrier density, electrical conductivity, magnetism, and high aspect ratio, rendering it highly promising for diverse applications. Yet, the exploration of porous structural configurations of borophene remains untapped. Addressing this gap, our study focuses on the fabrication of a multifunctional borophene hybrid foam (CMB-foam). This hybridization leverages the exceptional multifunctionality of MXene alongside borophene within a three-dimensional porous framework, facilitating reflection and absorption of electromagnetic waves, thereby demonstrating remarkable electromagnetic interference (EMI) shielding capabilities. Moreover, this structural configuration exposes an enlarged surface area, thus shortening the transport pathway for electrolyte ions, leading to an excellent energy storage performance. Additionally, CMB-foam performs well in thermal management and thermal insulation. These findings underscore the potential of borophene-based materials in multifunctional applications and offer valuable insights into further performance explorations in this domain.

The rapid growth of flexible electronics has led to significant demand for relevant accessories, particularly highly efficient flexible heat dissipators. The fluidity of liquid metal (LM) makes it a candidate for realizing flexible thermal interface materials (TIMs). However, it is still challenging to combine LM with a conductive thermal network to achieve the synchronous improvement of thermal conductivity and flexibility. In this work, highly conductive flexible LM@GN/ANF films are made by coating LM nano-droplets with graphene nanosheets (GN) via sonication, and then they are combined with aramid nanofibers (ANF). The LM@GN/ANF film is found to have a thermal conductivity of 5.67 W m -1  K -1 and a 24.5% reduction in Young's modulus, making it suitable for various flexible electronic applications such as wearable devices and biosensors., (© 2024 Wiley‐VCH GmbH.)

With the development of technology, multifunctional multiband emitters have been paid much attention due to their wide range of applications, such as LIDAR detection, spectroscopic sensing, and infrared thermal management. However, the development of such emitters is impeded by incompatible structural requirements of different electromagnetic wavebands. Here, we demonstrate coupled modulation between near-infrared (NIR) laser-wavelength and long-wavelength-infrared by constructing a multifunctional emitter (MFE) with a structure of Al/HfO 2 /VO 2 , utilizing the phase transition of VO 2 . The MFE displays excellent thermal modulation capability within the 8-14 μm range, achieving a thermal insulation effect (ε 8-14 μm = 0.18) at low temperatures, and heat dissipation effect (ε 8-14 μm = 0.64) at high temperatures. The MFE's radiation power regulation capability is 145.06 W m -2 between a temperature of 0 to 60 °C. Moreover, the MFE possesses a large reflectivity modulation value of 0.78 at NIR laser-wavelength (1.06 μm) with a short phase transition time of 1003 ms under 3 W cm -2 laser irradiation. This study provides a guideline for the coordinated control of electromagnetic waves and intelligent collaborative thermal management through simple structural design, thus, having broad implications in energy saving and thermal information processing.

Passive radiative cooling (PRC) can spontaneously dissipate heat to outer space through atmospheric transparent windows, providing a promising path to meet sustainable development goals. However, achieving simultaneously high transparency, color-customizable, and thermal management of PRC anti ultraviolet (anti-UV) films remains a challenge. Herein, a simple strategy is proposed to utilize liquid crystalline polymer, with high mid-infrared emissive, forming customizable structural color film by molecular self-assembly and polymerization-induced pitch gradient, which guarantees the balance of transparency in visible spectrum and sunlight reflection, rendering anti-UV colored window for thermal management. By performing tests, temperature fall of 5.4 and 7.9 °C are demonstrated at noon with solar intensity of 717 W m -2 and night, respectively. Vivid red-, green-, blue-structured colors, and colorless films are designed and implemented to suppress the solar input and control the effective visible light transmissivity considering the efficiency function of human vision. In addition, temperature rise of 11.1 °C is achieved by applying an alternating current field on the PRC film. This study provides a new perspective on the thermal management and aesthetic functionalities of smart windows and wearables., (© 2024 Wiley‐VCH GmbH.)

The demand for flexible composite films with electromagnetic interference (EMI) shielding capabilities is rapidly increasing. Balancing high EMI performance with flexibility and portability has become a critical research focus in practical applications. In this study, an optimized strategy for aramid nanofibers (ANF) films was developed using spin-coating and sol-gel techniques. The resulting film features a smooth surface and excellent mechanical properties. ANF, initially an insulator, was transformed into a conductor through the in-situ polymerization of ion-doped polypyrrole (PPy). Leveraging a multilayer structural strategy, we prepared a symmetric composite film, ANF@PPy-(TA-MXene)-AgNWs-(TA-MXene)-ANF@PPy (PMA), using vacuum-assisted filtration and lamination hot pressing. This film, composed of ANF@PPy (PA) as the matrix, tannic acid (TA) modified MXene, and silver nanowires (AgNWs) as fillers, exhibited multiple shielding mechanisms as electromagnetic wave (EMW) passed through its various layers. This multilayer configuration provides significant flexibility in EMW shielding. Moreover, TA-modified MXene expands the lamellar spacing, enhancing the scattering efficiency of EMWs within the film, and serves as a medium connecting the upper and lower layers. This results in the efficient integration of the multilayer structure, synergistically improving both EMI shielding performance and mechanical properties. When the ratio of PA/MXene/AgNWs was 1:3:1, the film demonstrated optimal properties, including an EMI shielding effectiveness of 70.2 dB, thermal conductivity of 4.62 W/(m•K), and tensile strength of 50.2 MPa. Due to the exceptional EMI shielding and thermal properties of the PMA composite film, it holds great potential for applications in artificial intelligence, wearable heaters, and military equipment., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier Inc.)

The rapid evolution of power electronics has triggered an intensified focus on thermal management within electronics circuits, stemming from the critical necessity to mitigate thermal-related failure rates. Thermal management in power electronics circuits relies heavily on efficient heat transfer to prevent overheating of components and ensure their reliable operation, optimal performance, and safety. To facilitate the effective heat transfer, a thermal interface material (TIM) is utilized between switching components such as MOSFETs and heat sinks to improve surface contact, which increases heat transfer. In this research work, a novel thermal interface material (TIM) based on Tungsten-Gallium is introduced and evaluated to enhance thermal properties such as thermal conductivity and viscosity of Gallium-based TIM material with the addition of Tungsten microparticles. The study involves the examination of three distinct TIM samples with varying Tungsten content. Their surface morphology, composition, and topography were analyzed through techniques such as Scanning Electron Microscopy (SEM) and Atomic Force Microscopy (AFM) within the context of a DC-DC boost converter. The results indicate that the addition of Tungsten significantly enhances TIM's viscosity and fluidity, even at high temperatures reaching up to 308 °C, which is crucial for power electronics circuits. In addition, thermal constant analyzer, and DC-DC converter circuit such as boost converter circuit were utilized for thermal and electrical characterization, respectively. These characterization results demonstrate that 10%/wt. addition of Tungsten can increase the thermal conductivity of Gallium from 13.1 to 22.82 W/m.K at room temperature, which represents an overall 74.2% increase in thermal conductivity. Furthermore, when the proposed TIM sample 2 was used in a boost converter circuit, the switching frequency of MOSFET IRF3808 was increased up to 20 kHz while the conduction losses were also lowest compared to other TIM samples., (© 2024. The Author(s).)

Multiform NiO nanowalls with a high specific surface area were constructed in situ on carbon foam (CF) to construct NiO@CF/OD composite phase change materials (CPCMs). The synthesis mechanism, microstructures, thermal management capability, and photothermal conversion of NiO@CF/OD CPCMs were systematically studied. Additionally, the collaborative enhancement effects of CF and multiform NiO nanowalls on the thermal properties of OD PCMs were also investigated. NiO@CF not only maintains the porous 3D network structure of CF, but also effectively prevents the aggregation of NiO nanosheets. The chemical structures of NiO@CF/OD CPCMs were analyzed using XRD and FTIR spectroscopy. When combined with CF and NiO nanosheets, OD has high compatibility with NiO@CF. The thermal conductivity of NiO@CF/OD-L CPCMs was 1.12 W/m·K, which is 366.7% higher than that of OD. The improvement in thermal conductivity of CPCMs was theoretically analyzed according to the Debye model. NiO@CF/OD-L CPCMs have a photothermal conversion efficiency up to 77.6%. This article provided a theoretical basis for the optimal design and performance prediction of thermal storage materials and systems.

Direct synthesis of graphene on nonmetallic substrates via chemical vapor deposition (CVD) has become a frontier research realm targeting transfer-free applications of CVD graphene. However, the stable mass production of graphene with a favorable growth rate and quality remains a grand challenge. Herein, graphene glass fiber fabric (GGFF) was successfully developed through the controllable growth of graphene on non-catalytic glass fiber fabric, employing a synergistic binary-precursor CVD strategy to alleviate the dilemma between growth rate and quality. The binary precursors consisted of acetylene and acetone, where acetylene with high decomposition efficiency fed rapid graphene growth while oxygen-containing acetone was adopted for improving the layer uniformity and quality. Notably, the bifurcating introducing-confluent premixing (BI-CP) system was self-built for the controllable introduction of gas and liquid precursors, enabling the stable production of GGFF. GGFF features solar absorption and infrared emission properties, based on which the self-adaptive dual-mode thermal management film was developed. This film can automatically switch between heating and cooling modes by spontaneously perceiving the temperature, achieving excellent thermal management performances with heating and cooling power of ∼501.2 and ∼108.6 W m -2 , respectively. These findings unlock a new strategy for the large-scale batch production of graphene materials and inspire advanced possibilities for further applications., (Copyright © 2024 Science China Press. Published by Elsevier B.V. All rights reserved.)

Manipulation of infrared emissivity, which is closely related to surface structure and optical parameters of materials, is a crucial approach for realizing dynamic thermal management. In this study, we design a metamaterial consisting of an array of aluminum disks embedded on a surface of a stretchable elastomeric substrate. Mechanical stretching-induced deformation allows dynamic modification of the surface structure and equivalent optical parameters, thus enabling dynamic control of the emissivity. By utilizing the elastomer polydimethylsiloxane (PDMS) as the substrate, the microstructure interdisk gap can be altered by stretching the PDMS. Through theoretical calculations, the plausibility of this approach is explained by the excitation of plasmon resonance and the variation in the exposed area of highly absorbent PDMS, and the optimal structures for tuning the infrared emissivity are revealed to be 6 μm in diameter and 100 nm in height. Based on this design, we prepare samples with periods of 7 and 7.9 μm and experimentally demonstrate that a change in the period can cause a change in the emissivity and thus tunability in thermal control performance. The temperature difference between the two samples reaches 44.1 °C at a heating power of 0.28 W/cm 2 for both samples. Furthermore, we construct a stretching platform that enables in situ mechanical stretching to realize dynamic changes in emissivity. The integral infrared emissivity of the sample increases from 0.32 to 0.5 at a biaxial tensile strain of 13%, achieving a 56% modulation rate of the integral infrared emissivity. The material is expected to enable dynamic thermal management.

The manipulation of interactions between light and matter plays a crucial role in the evolution of organisms and a better life for humans. As a result of natural selection, precise light-regulatory systems of biology have been engineered that provide many powerful and promising bioinspired strategies. As the "king of disguise", cephalopods, which can perfectly control the propagation of light and thus achieve excellent surrounding-matching via their delicate skin structure, have made themselves an exciting source of inspiration for developing optical and thermal regulation nanomaterials. This review presents cutting-edge advancements in cephalopod-inspired optical and thermal regulation nanomaterials, highlighting the key milestones and breakthroughs achieved thus far. We begin with the underlying mechanisms of the adaptive color-changing ability of cephalopods, as well as their special hierarchical skin structure. Then, different types of bioinspired nanomaterials and devices are comprehensively summarized. Furthermore, some advanced and emerging applications of these nanomaterials and devices, including camouflage, thermal management, pixelation, medical health, sensing and wireless communication, are addressed. Finally, some remaining but significant challenges and potential directions for future work are discussed. We anticipate that this comprehensive review will promote the further development of cephalopod-inspired nanomaterials for optical and thermal regulation and trigger ideas for bioinspired design of nanomaterials in multidisciplinary applications.

Water scarcity is a serious threat to the survival and development of mankind. Interfacial solar steam generation (ISSG) can alleviate the global freshwater shortage by converting sustainable solar power into thermal energy for desalination. ISSG possesses many advantages such as high photothermal efficiency, robust durability, and environmental friendliness. However, conventional evaporators suffered from huge heat losses in the evaporation process due to the lack of efficient thermal management. Herein, hydrophilic Tencel yarn is applied to fabricate a three-dimensional double-layer fabric evaporator (DLE) with efficient multi-stage thermal management. DLE enables multiple solar absorptions, promotes cold evaporation, and optimizes thermal management. The airflow was utilized after structure engineering for enhanced energy evaporation efficiency. The evaporation rate can reach 2.86 kg·m -2 ·h -1 under 1 sun (1 kW·m -2 ), and 6.26 kg·m -2 ·h -1 at a wind speed of 3 m·s -1 . After a long duration of outdoor operation, the average daily evaporation rate remains stable at over 8.9 kg·m -2 , and the removal rate of metal ions in seawater reaches 99%. Overall, DLE with efficient and durable three-dimensional multi-stage thermal management exhibits excellent practicality for solar desalination.

This study presents a comprehensive investigation into a 3D simulation of magnetorheological (MR) conical bearings, focusing on considering viscous dissipation using the conjugated heat transfer approach. The behavior of MR fluids is expressed through the utilization of the Bingham-Papanastasiou constitutive equation. Notably, this study considers variations in viscosity and yield stress as functions of both magnetic field intensity and temperature. The study utilizes a multidisciplinary approach, encompassing fluid dynamics, magnetism, and heat transfer, to model and analyze the behavior of MR fluids within conical bearing geometries. The governing equations containing Cauchy momentum, energy, and Maxwell equations are solved using the finite element method. This research delves into the impacts of viscous dissipation on the functional and characteristic attributes of conical bearings. The energy equations in solid and fluid domains and extended considerations to the plug region within viscous dissipation are specifically addressed. Extensive validation is performed through a comparative analysis involving experimental, numerical, and analytical studies to ensure the validity of results. The results reveal the substantial impact of temperature on both the characteristics and functionality of magnetorheological conical bearings., (© 2024. The Author(s).)

The development of electronic skin (e-skin) emulating the human skin's three essential functions (perception, protection, and thermoregulation) has great potential for human-machine interfaces and intelligent robotics. However, existing studies mainly focus on perception. This study presents a novel, eco-friendly, mechanically robust e-skin replicating human skin's three essential functions. The e-skin is composed of Ti 3 C 2 T x MXene, polypyrrole, and bacterial cellulose nanofibers, where the MXene nanoflakes form the matrix, the bacterial cellulose nanofibers act as the filler, and the polypyrrole serves as a conductive "cross-linker". This design allows customization of the electrical conductivity, microarchitecture, and mechanical properties, integrating sensing (perception), EMI shielding (protection), and thermal management (thermoregulation). The optimal e-skin can effectively sense various motions (including minuscule artery pulses), achieve an EMI shielding efficiency of 63.32 dB at 78 μm thickness, and regulate temperature up to 129 °C in 30 s at 2.4 V, demonstrating its potential for smart robotics in complex scenarios.

Phase change materials (PCMs) are crucial for sustainable thermal management in energy-efficient construction and cold chain logistics, as they can store and release renewable thermal energy. However, traditional PCMs suffer from leakage and a loss of formability above their phase change temperatures, limiting their shape stability and versatility. Inspired by the muscle structure, formable PCMs with a hierarchical structure and solvent-responsive supramolecular networks based on polyvinyl alcohol (PVA)/wood composites are developed. The material, in its hydrated state, demonstrates low stiffness and pliability due to the weak hydrogen bonding between aligned wood fibers and PVA molecules. Through treatment of poly(ethylene glycol) (PEG) into the PVA/wood PEG gel (PEG/PVA/W) with strengthened hydrogen bonds, the resulting wood-based PCMs in the hard and melting states elevate the tensile stress from 10.14 to 80.86 MPa and the stiffness from 420 MPa to 4.8 GPa, making it 530 times stiffer than the PEG/PVA counterpart. Capable of morphing in response to solvent changes, these formable PCMs enable intricate designs for thermal management. Furthermore, supported by a comprehensive life cycle assessment, these shape-adaptable, recyclable, and biodegradable PCMs with lower environmental footprint present a sustainable alternative to conventional plastics and thermal management materials., (© 2024 Wiley‐VCH GmbH.)

This study introduces the synthesis and detailed characterization of a novel thermochromic material capable of reversible alterations in its thermotropic transmittance. Through an emulsion polymerization process, this newly developed material is composed of 75-85% octadecyl acrylate and 0-7% allyl methacrylate, demonstrating a pronounced discoloration effect across a narrow yet critical temperature range of 24.5-39 °C. The synthesized powder underwent a battery of tests, including differential scanning calorimetry and thermogravimetric analysis, as well as scanning electron microscopy. These comprehensive evaluations confirmed the material's exceptional thermal stability, uniform particle size distribution, and strong anchoring properties. Building upon these findings, we advanced the development of thermochromic polyvinyl butyral films and laminated glass products. By utilizing a coextrusion technique, we integrated these films into laminated glass, setting a new benchmark against existing glass technologies. Remarkably, the incorporation of thermochromic PVB films into laminated glass led to a significant reduction in solar irradiance of 20-30%, outperforming traditional double silver low-emissivity glass. This achievement demonstrates the exceptional shading and thermal insulation properties of the material. The research presented herein not only pioneers a valuable methodology for the engineering of smart materials with tunable thermotropic transmittance but also holds the key to unlocking enhanced energy efficiency across a spectrum of applications. The potential impact of this innovation on the realm of sustainable building materials is profound, promising significant strides toward energy conservation and environmental stewardship.

To address the escalating power consumption of processors in data centers and the growing emphasis on environmental sustainability, the prospective shift from traditional air-cooling to immersion liquid cooling necessitates multiple functional integrations in polymer-based thermal conductive materials. Here, drawing inspiration from mussels, we showed a copolymer, poly(dimethylsiloxane-co-dopamine methacrylate) (PDMS-DMA), with a variety of reversible molecular interactions and simply combined with liquid metal (EGaIn) can yield a flexible, waterproof, and electrically insulating thermal conductive composite. The obtained PDMS-DMA/EGaIn composites demonstrate a harmonious blend of attributes, including a low modulus (75.8 kPa), high thermal conductivity of 6.9 W m -1 K -1 , and rapid room-temperature self-healing capabilities, capable of complete repair within 20 min, even under water. Based on its electrically insulating and water resistance properties, PDMS-DMA/EGaIn emerges as a promising candidate for efficient and stable heat transfer in both air and underwater thermal management. Consequently, this water-resistant polymer-based composite holds significance for application in thermal protective layers for future immersion liquid cooling systems.

Energy and environmental issues have increasingly garnered significant attention for sustainable development. Flexible and shape-stable phase change materials display great potential in regulation of environmental temperature for energy saving and human comfort. Here, inspired by the water absorption behavior of salt-tolerant animals and plants in salinity environment and the Hofmeister theory, highly stable phase change salogels (PCSGs) are fabricated through in situ polymerization of hydrophilic monomers in molten salt hydrates, which can serve multiple functions including thermal management patches, smart windows, and ice blocking coatings. The gelation principles of the polymer in high ion concentration solution are explored through the density functional theory simulation and verified the feasibility of four types of salt hydrates. The high concentration chaotropic ions strongly interacted with polymer chains and promoted the gelation at low polymer concentrations which derive highly-stable and ultra-moisturizing PCSGs with high latent heat (> 200 J g -1 ). The synergistic adhesion and transparency switching abilities accompanied with phase transition enable their smart thermal management. The study resolves the melting leakage and thermal cycling stability of salt hydrates, and open an avenue to fabricate flexible PCM of low cost, high latent heat, and long-term durability for energy-saving, ice-blocking, and thermal management., (© 2024 The Author(s). Advanced Science published by Wiley‐VCH GmbH.)

The escalating global population has led to a surge in waste textiles, posing a significant challenge in landfill management worldwide. In this work, ionic liquid 1-butyl-3-methylimidazole acetate ([Bmim]OAc) and DMF (N, n-dimethylformamide) were used as solvents to dissolve waste denim fabric, then vanadium dioxide (VO 2 ) nanoparticles were introduced into the spinning solution, and cellulose fibers were regenerated by dry-wet spinning process, to promote the recycling of waste cotton fabric. Finally, regenerated cellulose fibers with high added value were prepared by dry-wet spinning. Through this innovative strategy, on the one hand, because VO 2 can form a large number of hydrogen bonds between the regenerated cellulose molecules, and realize the cross-networking structure of the molecular chains inside the fiber, the mechanical properties of the regenerated cellulose fibers are enhanced. On the other hand, due to the thermal phase transformation characteristics of VO 2 , it also endows the regenerated cellulose fiber unique intelligent temperature control function. Compared with the pristine regenerated fiber, the tensile stress of the regenerated fiber after adding VO 2 nanoparticles (F-VO 2 ) increased by 25.6 %, reaching 158.68 MPa. In addition, the F-VO 2 fibric provides excellent intelligent temperature control, reducing temperatures by up to 6.7 °C., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Cellulose papers (CPs) possess a pore structure, rendering them ideal precursors for carbon scaffolds because of their renewability. However, achieving a tradeoff between high electromagnetic shielding effectiveness and low reflection coefficient poses a tremendous challenge for CP-based carbon scaffolds. To meet the challenge, leveraging the synergistic effect of gravity and evaporation dynamics, laminar CP-based carbon scaffolds with a bidirectional gradient distribution of Fe 3 O 4 nanoparticles were fabricated via immersion, drying, and carbonization processes. The resulting carbon scaffold, owing to the bidirectional gradient structure of magnetic nanoparticles and unique laminar arrangement, exhibited excellent in-plane electrical conductivity (96.3 S/m), superior electromagnetic shielding efficiency (1805.9 dB/cm 2  g), low reflection coefficients (0.23), and a high green index (g s , 3.38), suggesting its green shielding capabilities. Furthermore, the laminar structure conferred upon the resultant carbon scaffold a surprisingly anisotropic thermal conductivity, with an in-plane thermal conductivity of 1.73 W/m K compared to a through-plane value of only 0.07 W/m K, confirming the integration of thermal insulation and thermal management functionalities. These green electromagnetic interference shielding materials, coupled with thermal insulation and thermal management properties, hold promising prospects for applications in sensitive devices., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

A flexible phase-change film with thermal management and microwave absorption capabilities was developed for use in wearable devices. The film was created using a solution casting method based on a porous carbon-loaded eicosane (LP33/EI) material. LP33 served as the porous encapsulation medium, while Eicosane (EI) acted as the phase change component. The flexible substrate was a blend of polyvinyl alcohol (PVA) and bacterial cellulose nanocellulose (BC). The ultrathin film had a thickness of 0.262 mm, and LP33/EI-4 exhibited exceptional mechanical strength of 188 MPa. Testing revealed that the phase transition process had melting and crystallization enthalpies of 134.71 J/g and 126.11 J/g, respectively. The encapsulation structure effectively prevented any leakage during the phase transition process. Under simulated solar irradiation of 200 mW/cm 2 , LP33/EI-4 achieved a photothermal conversion efficiency (η) of 89.46 %. Additionally, the porous LP33 structure and high dielectric loss contributed to remarkable microwave absorption capabilities of -42 dB in the X-band and - 52 dB in the Ku-band. Overall, LP33/EI films demonstrated exceptional performance in thermal management, energy storage, and microwave absorption, making them an ideal choice for a variety of applications in wearable devices., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

3D printing polymer or metal can achieve complicated structures while lacking multifunctional performance. Combined printing of polymer and metal is desirable and challenging due to their insurmountable mismatch in melting-point temperatures. Here, a novel volume-metallization 3D-printed polymer composite (VMPC) with bicontinuous phases for enabling coupled structure and function, which are prepared by infilling low-melting-point metal (LM) to controllable porous configuration is reported. Based on vacuum-assisted low-pressure conditions, LM is guided by atmospheric pressure action and overcomes surface tension to spread along the printed polymer pore channel, enabling the complete filling saturation of porous structures for enhanced tensile strength (up to 35.41 MPa), thermal (up to 25.29 Wm -1 K -1 ) and electrical (>10 6  S m -1 ) conductivities. The designed 3D-printed microstructure-oriented can achieve synergistic anisotropy in mechanics (1.67), thermal (27.2), and electrical (>10 12 ) conductivities. VMPC multifunction is demonstrated, including customized 3D electronics with elevated strength, electromagnetic wave-guided transport and signal amplification, heat dissipation device for chip temperature control, and storage components for thermoelectric generator energy conversion with light-heat-electricity., (© 2024 Wiley‐VCH GmbH.)

Magnetically responsive soft smart materials have garnered significant academic attention due to their flexibility, remote controllability, and reconfigurability. However, traditional soft materials used in the construction of these magnetically responsive systems typically exhibit low density and poor thermal and electrical conductivities. These limitations result in suboptimal performance in applications such as medical radiography, high-performance electronic devices, and thermal management. To address these challenges, magnetically responsive gallium-based liquid metals have emerged as promising alternatives. In this review, we summarize the methodologies for achieving magnetically responsive liquid metals, including the integration of magnetic agents into the liquid metal matrix and the utilization of induced Lorentz forces. We then provide a comprehensive discussion of the key physicochemical properties of these materials and the factors influencing them. Additionally, we explore the advanced and potential applications of magnetically responsive liquid metals. Finally, we discuss the current challenges in this field and present an outlook on future developments and research directions.

The development of efficient and high-performance electric vehicle (EV) batteries relies on improving various components, such as the anode and cathode electrodes, separators, and electrolytes. This review paper offers an elaborate overview of different materials for these components, emphasizing their respective contributions to the improvement of EV battery performance. Carbon-based materials, metal composites, and polymer nanocomposites are explored for the anode, offering high energy density and capacity. However, they are noted to be susceptible to Li plating. Unique structures, such as Titanium niobium oxide (TiNb 2 O 7 ), offer high theoretical capacity, quick Li + intercalation, and an extended lifecycle. Meanwhile, molybdenum disulfide (MoS 2 ), with 2D and 3D structures, exhibits high reversible specific capacity, outstanding rate performance, and cyclic stability, showing promising properties as anode material. For cathodes, lithium-iron phosphate (LFP), lithium-cobalt oxide (LCO), lithium-nickel-cobalt-aluminum oxide (NCA), lithium-nickel-manganese-cobalt oxide (NMC), and cobalt-free lithium-nickel-manganese oxide (NMO) are considered, offering specific energy and capacity advantages. For instance, LFP cathode electrodes show good thermal stability, good electrochemical performance, and long lifespan, while NMC exhibits high specific energy, relatively high capacity, and cost savings. NCA has a high specific energy, decent specific power, large capacity, and a long lifecycle. NMO shows excellent rate capability, cyclic stability, and cost-effectiveness but with limited cycle performance. Separator innovations, including polyolefin materials, nanofiber separators, graphene-based composites, and ceramic-polymer composites, are analyzed for use as separators, considering mechanical strength, porosity, wettability with the electrolyte, electrolytic absorption, cycling efficiency, and ionic conductivity. The electrolyte comprises lithium salts such as lithium tetrafluoroborate (LiBF 4 ), lithium hexafluorophosphate (LiPF 6 ), and other salts dissolved in carbonate solvents. This improves energy density, capacity, and cycling stability and provides high ion mobility and resistance to decomposition. By examining the existing literature, this review also explores research on the solid electrolyte interface (SEI) and lithium plating, providing valuable insights into understanding and mitigating these critical issues. Despite the progress, limitations such as practical implementation challenges, potential cost implications, and the need for further research on scale-up feasibility and long-term durability are acknowledged. These efforts to enhance the electrochemical characteristics of key battery parameters-positive and negative electrodes, separators, and electrolytes-aim to improve capacity, specific energy density, and overall energy density. These continuous endeavours strive for faster charging of EV batteries and longer travel ranges, contributing to the ongoing evolution of EV energy storage systems. Thus, this review paper not only explores remarkable strides in EV battery technology but also underscores the imperative of addressing challenges and propelling future research for sustainable and high-performance electric vehicle energy storage systems., Competing Interests: The authors declare that they have no known competing financial interests or personal relationships that could have influenced the work reported in this paper., (© 2024 The Authors.)

Flexible electronics toward high integration, miniaturization, and multifunctionality, leading to a dramatic increase in power density. However, the low thermal conductivity of flexible substrates impedes efficient heat dissipation and device performance improvement. In this work, we propose a template-assisted chemical conversion strategy for obtaining boron nitride nanotube (BNNT) films with high thermal conductivity and great flexibility. Aligned carbon nanotube (CNT) films have been adopted as templates; a low-temperature chemical conversion followed by a high-temperature annealing has been carried out to produce a highly ordered BNNT film. Benefiting from the high orientation order, the BNNT film exhibits an exceptional thermal conductivity of 45.5 W m -1 K -1 and presents excellent heat dissipation capability, much superior to the commonly used polyimide film. Furthermore, the BNNT film demonstrated excellent flexibility and high insulation resistance. The test of integration with film resistors demonstrated its potential as a thermally conductive substrate for electronics cooling. This work provides a solution for the effective thermal management of flexible electronics.

The development of multifunctional MXene-based fabrics for smart textiles and portable devices has garnered significant attention. However, very limited studies have focused on their structure design and associated mechanical properties. Here, the supertough MXene fiber felts composed of MXene/sodium alginate (SA) fibers were fabricated. The fracture strength and bending stiffness of felts can be up to 97.8 MPa and 1.04 N mm 2 , respectively. Besides, the fracture toughness of felts was evaluated using the classic Griffith theory, yielding to a critical stress intensity factor of 1.79 M P a m . In addition, this kind of felt presents outstanding electrothermal conversion performance (up to 119 °C at a voltage of 2.5 V), high cryogenic and high-temperature tolerance of photothermal conversion performance (-196 to 160 °C), and excellent electromagnetic interference (EMI) shielding effectiveness (54.4 dB in the X-band). This work provides new structural design concepts for high-performance MXene-based textiles, broadening their future applications.

Proper temperature regulation of photovoltaic (PV) modules increases their performance. Among various cooling techniques, phase change materials (PCMs) represent an effective thermal management route, thanks to their large latent heat at constant temperatures. Radiative cooling (RC) is also recently explored as a passive option for PV temperature regulation. In this paper, a heat sink (HS), phase change materials, and radiative cooling are integrated with photovoltaic modules to achieve low and uniform temperature distribution along the PV module and improved performance. Eight different combinations are considered for the proposed system, including HS, PCM, and RC, and their various combinations. The PCM is selected according to the environmental conditions of the selected location. A comprehensive 2-D model is developed and analyzed in COMSOL-Multiphysics software by solving the governing equations using the finite element method. The performance analysis is carried out for the climatic conditions of the Atacama Desert, having high solar radiation and ambient temperature. The effects of PCM height, ambient temperature, wind velocity, and solar radiation on the performance of the proposed system are studied. The performance of eight different configurations is also compared. The maximum reductions in PV temperature, maximum PV power, and a minimum drop in PV conversion efficiency are observed to be 22  o C, 152 W, and 14% using a combined heat sink and radiative cooling systems, among all other configurations. The findings of this study can be used to select the best PV cooling method among different configurations., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

The continued miniaturization of chips demands highly thermally conductive materials and effective thermal management strategies. Particularly, the high-field transport of the devices built with 2D materials is limited by self-heating. Here a systematic control of heat flow in single-side fluorinated graphene (FG) with varying degrees of fluorination is reported, revealing a superior room-temperature thermal conductivity as high as 128 W m -1 K -1 . Monolayer graphene/FG lateral heterostructures with seamless junctions are approached for device fabrication. Efficient in-plane heat removal paths from graphene channel to side FG are created, contributing significant reduction of the channel peak temperature and improvement in the current-carrying capability and power density. Molecular dynamics simulations indicate that the interfacial thermal conductance of the heterostructure is facilitated by the high degree of overlap in the phonon vibrational spectra. The findings offer novel design insights for efficient heat dissipation in micro- and nanoelectronic devices., (© 2024 The Authors. Advanced Science published by Wiley‐VCH GmbH.)

Advanced thermal interface materials with high thermal conductivity are crucial for addressing the heat dissipation issue in high-power, highly integrated electronic devices. One great potential way in this field is to take advantage of cooling copper foil (Cu) materials based on graphene (G). However, the current manufacturing of these cooling copper foil materials is accompanied by high cost, process complexity, and environmental problems, which limit their development and application. In this work, a simple, low-cost, environmentally friendly graphene-copper foil composite film (rGO/G-Cu) with high thermal conductivity was successfully prepared using graphene oxide directly as a dispersant and binder of graphene coating. The microstructure characterization, thermal conductivity and thermal management performance tests were carried out on the composite films. The results demonstrate that compared to pure copper foil (342.47 W·m -1 ·K -1 ) and 10% PVA/G-Cu (367.98 W·m -1 ·K -1 ) with polyvinyl alcohol as a binder, 10% rGO/G-Cu exhibits better thermal conductivity (414.56 W·m -1 ·K -1 ). The introduction of two-dimensional graphene oxide effectively enhances the adhesion between the coating and the copper foil while greatly improving its thermal conductivity. Furthermore, experimental results indicate that rGO/G-Cu exhibits excellent heat transfer performance and flexibility. This work is highly relevant to the development of economical and environmentally friendly materials with high thermal conductivity to meet the increasing demand for heat dissipation.

Inorganic hydrated salt phase change materials (PCMs) hold promise for improving the energy conversion efficiency of thermal systems and facilitating the exploration of renewable thermal energy. Hydrated salts, however, often suffer from low thermal conductivity, supercooling, phase separation, leakage and poor solar absorptance. In recent years, compounding hydrated salts with functional carbon materials has emerged as a promising way to overcome these shortcomings and meet the application demands. This work reviews the recent progress in preparing carbon-enhanced hydrated salt phase change composites for thermal management applications. The intrinsic properties of hydrated salts and their shortcomings are firstly introduced. Then, the advantages of various carbon materials and general approaches for preparing carbon-enhanced hydrated salt PCM composites are briefly described. By introducing representative PCM composites loaded with carbon nanotubes, carbon fibers, graphene oxide, graphene, expanded graphite, biochar, activated carbon and multifunctional carbon, the ways that one-dimensional, two-dimensional, three-dimensional and hybrid carbon materials enhance the comprehensive thermophysical properties of hydrated salts and affect their phase change behavior is systematically discussed. Through analyzing the enhancement effects of different carbon fillers, the rationale for achieving the optimal performance of the PCM composites, including both thermal conductivity and phase change stability, is summarized. Regarding the applications of carbon-enhanced hydrate salt composites, their use for the thermal management of electronic devices, buildings and the human body is highlighted. Finally, research challenges for further improving the overall thermophysical properties of carbon-enhanced hydrated salt PCMs and pushing towards practical applications and potential research directions are discussed. It is expected that this timely review could provide valuable guidelines for the further development of carbon-enhanced hydrated salt composites and stimulate concerted research efforts from diverse communities to promote the widespread applications of high-performance PCM composites.

Phase change materials (PCMs) are used to cool high-power-density electronic devices because of their high latent heat and chemical stability. However, their low thermal conductivity limits the application of PCMs. To solve this problem, a double-porosity porous aluminum skeleton/paraffin phase change materials (DPAS/PCM) was prepared via additive manufacturing and the water-bath method. The thermal performance of the DPAS/PCM heat sink (HS) was experimentally investigated to examine the effects of the positive- and reverse-gradient porosity structures of the DPAS/PCM. The results show that a positive-gradient porosity arrangement is more conducive to achieving a low-temperature cooling target for LED operation. In particular, the temperature control time for the positive gradient porosity structure increased by 4.6-13.7% compared with the reverse gradient porosity structure. Additionally, the thermal performances of uniform porous aluminum skeleton/paraffin (UAS) and DPAS/PCMs were investigated. The temperature control effect of the DPAS/PCM was better than that of the UAS/PCM HS at high critical temperatures. Compared with the UAS/PCM HS, the temperature control time of the DPAS/PCM HS is increased by 7.8-12.5%. The results of this work show that the prepared DPAS/PCM is a high-potential hybrid system for thermal management of high-power electronic devices.

Transparent aerogels are ideal candidates for thermally insulating windows, solar thermal receivers, electronics, etc. However, they are usually prepared via energy-consuming supercritical drying and show brittleness and low tensile strength, significantly restricting their practical applications. It remains a great challenge to prepare transparent aerogels with high tensile strength and toughness. Herein, biomimetic transparent tough cellulose nanofiber-based nanocomposite aerogels with a layered nanofibrous structure are achieved by vacuum-assisted self-assembly combined with ambient pressure drying. The nacre-like layered homogeneous nanoporous structures can reduce light scattering and effectively transfer stress and prevent stress concentration under external forces. The aerogels exhibit an attractive combination of excellent transparency and hydrophobicity, high compressive and tensile strengths, high toughness, excellent machinability, thermal superinsulation, and wide working temperature range (-196 to 230 °C). It is demonstrated that they can be used for superinsulating windows of buildings and high-efficient thermal management for electronics and human bodies. In addition, a prototype of transparent flexible aerogel-based triboelectric nanogenerator is developed. This work provides a promising pathway toward transparent tough porous materials for energy saving/harvesting, thermal management, electronics, sensors, etc., (© 2023 Wiley‐VCH GmbH.)

Gallium-based (Ga-based) liquid metals have attracted considerable interest due to their low melting points, enabling them to feature both liquid properties and metallic properties at room temperature. In light of this, Ga-based liquid metals also possess excellent deformability, high electrical and thermal conductivity, superior metal affinity, and unique self-limited surface oxide, making them popular functional materials in energy storage. This provides a possibility to construct high-performance rechargeable batteries that are deformable, free of dendrite growth, and so on. This review primarily starts with the property of Ga-based liquid metal, and then focuses on the potential applications in rechargeable batteries by exploiting these advantages, aiming to construct the correlation between properties and structures. The glorious applications contain interface protection, self-healing electrode construction, thermal management, and flexible batteries. Finally, the opportunities and obstacles for the applications of liquid metal in batteries are presented., (© 2024 Wiley‐VCH GmbH.)

Whereas thermal comfort and healthcare management during long-term wear are essentially required for wearable system, simultaneously achieving them remains challenge. Herein, a highly comfortable and breathable smart textile for personal healthcare and thermal management is developed, via assembling stimuli-responsive core-sheath dual network that silver nanowires(AgNWs) core interlocked graphene sheath induced by MXene. Small MXene nanosheets with abundant groups is proposed as a novel "dispersant" to graphene according to "like dissolves like" theory, while simultaneously acting as "cross-linker" between AgNWs and graphene networks by filling the voids between them. The core-sheath heterogeneous interlocked conductive fiber induced by MXene "cross-linking" exhibits a reliable response to various mechanical/electrical/light stimuli, even under large mechanical deformations(100%). The core-sheath conductive fiber-enabled smart textile can adapt to movements of human body seamlessly, and convert these mechanical deformations into character signals for accurate healthcare monitoring with rapid response(440 ms). Moreover, smart textile with excellent Joule heating and photothermal effect exhibits instant thermal energy harvesting/storage during the stimuli-response process, which can be developed as self-powered thermal management and dynamic camouflage when integrated with phase change and thermochromic layer. The smart fibers/textiles with core-sheath heterogeneous interlocked structures hold great promise in personalized healthcare and thermal management., (© 2023 Wiley‐VCH GmbH.)