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Wearable technology is experiencing remarkable progress, prompting the need for sustainable power sources like triboelectric nanogenerators (TENGs). However, integrating TENGs into fabrics and insufficient power outputs that allows for comfortable wear without obstructing user's movements presents a significant challenge. In this study, a novel kind of diamond‐structured fabric‐based triboelectric nanogenerators (DSF‐TENGs) is introduced utilizing an easy, economical, and scalable weaving method without any chemical modification. Owing to its 3D diamond pattern, surface interactions are enhanced for greater charge generation together with strengthened mechanical engagement for more effective charge transfer. The DSF‐TENG, with its unique self‐resilient structure, achieves impressive electric performance, including output voltage of ≈763 V, short‐circuit current of ≈20.4 µA, and power density of 2862.78 mW m−2, which is multiple times higher than most existing fabric‐based TENGs. It also offers excellent air permeability of 560 mm s−1, consistent electricity generation and sensing even after ten washing cycles, and incredible durability, withstanding over 30 000 cycles. Furthermore, DSF‐TENG is included in an insole that is capable of sensing gait patterns, walking speed, and fall detections of patients with Parkinson's disease. The remarkable power generation capabilities of DSF‐TENG indicate a strong potential for future developments in wearable electronics and healthcare applications. [ABSTRACT FROM AUTHOR]

Harnessing energy from underwater bubbles has garnered significant attention, particularly for powering off‐grid circuitry. However, the efficiency of bubble‐driven liquid‐solid interface charge transfer remains low. This research unveils a phenomenon: accelerated bubble slippage enhances liquid‐solid interfacial charge transfer. Building upon this discovery, a pulse bubble‐based power generation technique is proposed, achieving an energy density of 24.2 mJ L−1 generated by pulsed bubbles. The crux of pulse bubble power generation lies in the precise control of impact velocity. By meticulously regulating the impact kinetic energy of bubbles, the accumulated potential energy of multiple small bubbles is converted into instantaneous pulse kinetic energy. A typical pulse bubble is controlled within a 72 ms timeframe, unleashing a surge of energy that can directly illuminate 400 light‐emitting diodes. This approach represents a groundbreaking advancement in underwater energy harvesting technology, dramatically expanding its potential applications. [ABSTRACT FROM AUTHOR]

Piezoelectric nanogenerators (PENGs), the current pathway to sustainable energy harvesting, are mostly comprised of bulk oxide ceramics which are toxic, rigid, and costly to synthesize. A suitable alternative to them is flexible polar polymers like polyvinylidene fluoride (PVDF), but stabilizing its polar phase is also a daunting task. all these aforementioned issues by employing a biocompatible have been solved, above‐room‐temperature (Tc > 390 K) ferroelectric discrete molecular complex [Cu(L‐His)(bpy)]ClO4.1.5H2O (Cu‐FE) which is not only suitable for piezoelectric energy harvesting due to its large values of piezoelectric co‐efficient (d33 = 17 pm V−1) but also is capable of imparting polar β‐phase in PVDF via hydrogen bonding interactions under mild condition (60 °C). Among the PENG devices prepared with the composite films of PVDF and various weight % (w/V) compositions of Cu‐FE, the highest output voltage of 8 V (peak to peak) has been obtained, a power density of 4 µW cm−2, and an output current of 3 µA from the 1 wt.% composite film. The fabricated PENG device also exhibits swift capacitor charging in 40 s, and acts as an excellent pressure sensor, with exceptional sensitivity to low pressures (7 kPa), giving an output of 0.4 V. [ABSTRACT FROM AUTHOR]

Flexible piezoelectric energy harvesters (FPEHs) have wide applications in mechanical energy harvesting, portable device driving, and piezoelectric sensors. However, the poor output performance of piezoelectric energy harvesters and the intrinsic shortcoming of piezoelectric sensors that can only detect dynamic pressure limit their further applications. BaTiO3 (BT) and PVDF are deposited on the glass fiber electronic cloth (GFEC) by impregnation and spin‐coating methods, respectively, to form BT‐GFEC/PVDF piezoelectric composite films. A mixed solution of mechanoluminescence (ML) particles ZnS:Cu and PDMS are used as the encapsulation layer to construct a high‐performance ML‐FPEH with self‐powered electrical and optical dual‐mode response characteristics. Due to the interconnection structure of the piezoelectric films, the prepared ML‐FPEH illustrates a high effective energy harvesting performance (≈58 V, ≈43.56 µW cm−2). It can also effectively harvest mechanical energy from human activities. More importantly, ML‐FPEH can sense stress distribution of hand‐writing via ML to achieve stress visualization, making up for the shortcomings of piezoelectric sensors. This work provides a new strategy for endowing FPEH with dual‐mode sensing and energy harvesting. [ABSTRACT FROM AUTHOR]

To alleviate resource shortage and environmental pollution, solar energy can be converted into thermal energy stored in phase change materials and in turn generate electrical energy. To enhance the solar energy utilization efficiency of solar‐thermal‐electrical conversion devices and prevent the heat loss to the environment at night, an intelligent solar‐responsive phase‐change system is innovatively designed consisting of a graphene aerogel film/paraffin wax stamen with an ultra‐high thermal conductivity of 46.7 W m−1 K−1, and thermally preserving aerogel film/liquid crystal elastomer bilayer petals that can bend solar‐responsively by the synergistic effect of solar‐thermal energy conversion and heat‐induced contraction. The solar‐responsive phase‐change system achieves daytime blooming for solar‐thermal conversion with simultaneous energy storage and nighttime closing for minimizing heat loss to the environment, exhibiting a high solar‐thermal conversion and energy storage efficiency of 89.4% and delaying its temperature drop by the thermal preservation effect of the petals. The assembled solar‐responsive solar‐thermal‐electric generator can reach an output voltage of 1033.8 mV at a light intensity of 500 mW cm−2 and continue to generate electrical energy during nighttime, holding tremendous promise in efficient solar energy conversion, storage, and utilization. [ABSTRACT FROM AUTHOR]

A novel approach is proposed for combining phosphor materials with triboelectric nanogenerators (TENGs) for mechanical energy harvesting and illumination applications. For this purpose, strongly reddish‐orange‐emitting Ba0.5Sr0.5Nb2O6:0.25 mol Eu3+ (BSNb:0.25Eu) phosphor materials are synthesized. The photoluminescence properties of the synthesized BSNb:0.25Eu are analyzed. The synthesized BSNb:0.25Eu is utilized as a dielectric filler inside a polydimethylsiloxane polymeric film due to its high dielectric properties to improve the overall dielectric properties of the composite film (CF). TENG devices are fabricated using phosphor‐loaded CFs as the tribonegative layer, transparent polyvinyl alcohol as the tribopositive layer, and aluminum as the conductive electrode. All the TENGs operate in a contact‐separation mode, and the highest electrical output is attained by optimizing the phosphor filler concentration in the CF. The optimized TENG exhibits excellent stability in long‐term operational tests, under varying harsh ambient temperatures. Indium tin oxide sputtered on both triboelectric films as an electrode and combined with a transparent hard substrate to obtain a fully transparent TENG. A self‐illuminating TENG (SI‐TENG) is fabricated by integrating near‐ultraviolet light‐emitting diodes between two identical TENGs. The SI‐TENG can harvest the mechanical energy available in the surrounding environment and illuminate it as a light source. Additionally, the proposed phosphor‐loaded polymer films can be employed for optical thermometry and mechanical energy harvesting via SI‐TENG on a large scale. [ABSTRACT FROM AUTHOR]

Developing polymer‐based piezoelectric materials with multistimulus responsiveness is highly desirable for advancing multi‐source energy harvesting in wearable electronics. Inspired by the multifunctionality of muscle fibers, a nanostructure interface engineering strategy to create piezoelectric polymeric nanoheterostructures (PNHs) with remarkable responsiveness to both mechanical and nonmechanical contactless stimuli is introduced. Through precise interfacing of polymer nanofibers with nanoparticles via multiscale‐regulated interface electrostatic and chemical interactions, the study achieves a controlled assembly of stabilized and hierarchically organized nanoheterostructures featuring unique interface‐confined configurations. These configurations induce in situ stabilized dipole orientation and significant geometric stress nano‐confinement at interfaces, crucial for amplifying electricity generation. Compared to conventional polymer nanocomposites, engineered PNHs exhibit dramatically enhanced piezoelectricity, boasting a higher sensitivity of 1065 mV kPa−1 and piezoelectric coefficient of 76.2 pC N−1. Furthermore, PNHs demonstrate superior thermo‐actuated electricity generation under temperature fluctuations through cooperative spontaneous polarizations of constituent nanostructures, yielding a higher pyroelectric coefficient of 3.13 µC m2K−1. Additionally, the design enables photothermally‐activated switchable electricity generation and light‐energy harvesting, achieving a photo‐electric conversion efficiency tenfold higher than nanocomposites. This effective and versatile approach inspires the development of multi‐responsive nanogenerators for multi‐energy harvesting and self‐powered multistimulus‐sensing applications. [ABSTRACT FROM AUTHOR]

Functional triboelectric insoles hold promise for advancing self‐powered wearable technologies. However, their durability is compromised by continuous compressive forces and friction, leading to surface abrasion and material fracturing. To address these challenges, an innovative fabric‐reinforced structure combined with a dual‐L backrest design is developed that enhances anti‐fracture capabilities and electric outputs while enabling AI‐empowered motion monitoring. Polydimethylsiloxane (PDMS) is used as the negative triboelectric material with a dual‐L backrest design, while insulated copper wire (icuW) serves as the positive triboelectric material with an annular structure design. These components are intricately nested to enable a multilayered friction pairing. The fabric‐reinforced structure demonstrates excellent compressive rebound resilience, withstanding forces of at least 1000 N. The functional insole, featuring a fabric‐reinforced dual‐L backrest structure (FRdL‐insole), efficiently harvests biomechanical energy with a peak power of 8214 µW and maintains highly consistent performance after 10 washing cycles and 60 000 durability tests. It can power portable electronic devices such as digital watches, calculators, hygrometers, and LEDs. Enhanced with machine learning algorithms, the FRdL‐insole processes sensor signals to monitor human movements, accurately identifying seven distinct motions. This positions the insole as a smart, real‐time, self‐powered tool for activity recognition, showcasing its potential in intelligent wearable technology. [ABSTRACT FROM AUTHOR]

Significant efforts are devoted to optimizing the efficiency of triboelectric energy harvesting systems, particularly through the design of an advanced power management system (PMS) for Triboelectric Nanoenerators (TENGs). A critical aspect of PMS is the design and control of switches. However, existing switches face significant limitations. For spark switches, precise control cannot be achieved, and electronic switches can only operate at voltages below several hundred volts which is limited by the risk of electrical breakdown. To address these limitations, a hybrid electronic‐spark switch power management system (HESS) is proposed. HESS changes the connection of capacitors from parallel to series by deploying a maximum voltage tracking switch components at the peak voltage point, resulting in a much‐elevated voltage level to activate the spark switch. This approach achieves precise control of the spark switch for the first time and significantly reduces the operating voltage of electronic switches. Through simulation and experimental verification, HESS achieves the control at a voltage level of 1.8 kV for spark switch, with an electrical component breakdown voltage of only 450 V. The power density of the HESS is 29.8 mW Hz−1 m−2, which is a new record for electronic switches. [ABSTRACT FROM AUTHOR]

Bacterial cellulose is a biodegradable and ecologically safe material that has the potential to convert mechanical vibrations into electrical energy. This review introduces green energy harvesting, a novel concept that harnesses natural processes to provide sustainable energy. A thorough overview of bacterial cellulose, covering its distinctive features, its biological origin, and its energy conversion process, is fully presented. The different materials and methods used to design and fabricate bacterial cellulose‐based energy harvesters are explored. Moreover, the various applications and benefits of these devices in the context of renewable energy are examined. The current challenges and limitations of this emerging field are identified and the possible avenues for future research are suggested. The significance of adopting eco‐friendly approaches in achieving a balance between human needs and environmental preservation is highlighted. By providing a comprehensive and critical assessment of bacterial cellulose as a green energy harvester, this review aims to motivate researchers, engineers, and policymakers to tap into the rhythmic potential of this natural material in building a more sustainable and resilient future. [ABSTRACT FROM AUTHOR]

Understanding the structure and function of bioelectric materials is challenging due to the complex nature of biomaterials and a lack of appropriate tools. The precisely defined structures and genetic tunability of viruses provide an excellent model system to investigate bioelectrical behavior in biomaterials. This study presents the molecular mechanisms of piezoelectricity in the M13 bacteriophage (phage) under various mechanical stresses for bio‐piezoelectric generation. A computational approach is used to calculate the piezoelectric tensors of the M13 phage and quantify its direction‐dependent dipole moments. By computationally designing negatively charged residues on the phage surface, the surface charge density is enhanced to 16.7 µC cm−2. Using genetic engineering, phages are experimentally designed with different charges and tail structures to create model phage nanostructures, including individual phages, vertically standing phage films, and horizontally aligned phage films. Their vertical, horizontal, and shear‐mode piezoelectric properties are then measured using scanning probe microscopy techniques. The resulting phage‐based piezoelectric energy generators exhibit an effective piezoelectric coefficient of 15.4 pm V−1 and a power density of 4.2 µW cm−2. This phage‐based bioengineering approach provides a versatile platform for investigating fundamental mechanisms of bioelectricity and designing bioelectric materials for applications in energy harvesting, biomemory, and biosensors. [ABSTRACT FROM AUTHOR]

The practical application of solar energy harvesting urgently calls for the facile preparation of high‐performance ultrablack surfaces with broadband and omnidirectional light absorption performance; however, some roadblocks still need to meet these requirements simultaneously. Herein, cone‐array ultrablack (CAUB) surfaces are prepared by combining feasible template replication and blade coating techniques. The elaborate micro‐sized cone structure and high absorptive materials (polydimethylsiloxane@carbon black, PDMS@CB) offer the CAUB extremely high, broadband, and omnidirectional light absorption over the solar spectrum with an average absorbance of 99.35%. Under one sun irradiation, the CAUB can efficiently absorb solar energy, reaching a surface temperature as high as 75 °C. A solar‐thermal‐electric generator (STEG) made from the CAUB film demonstrates real‐time solar‐heat‐electric conversion, achieving a high output power density of 330 µW cm−2. The CAUB film possesses excellent water repellency, flexibility, chemical solvent resistance, and potential for large‐scale production, satisfying the application requirements of solar energy harvesting and utilization. [ABSTRACT FROM AUTHOR]

Reverse electrodialysis (RED) technology, relying on ion‐selective permeability membranes (ISPM), offers a direct means of harnessing osmotic energy from the salinity difference between seawater and freshwater. Critical technical challenges include limitations in ISPM's immobile charge carriers, transmembrane ionic internal resistance, and durability in water. Drawing inspiration from the subunit structure of the epithelial sodium channel (ENaC), an ISPM assembled using a supramolecular engineering strategy is introduced. This innovative approach enables the synergistic action of multiple molecular building blocks to mimic the distribution of ENaC subunit structures, strategically planning the placement of immobile charge carriers on nanofluidic channels. The design incorporates nano‐confined oxygen‐rich functionalized MXene (O‐MXene) and high‐strength polymer backbone aramid fibers to construct 3D nanofluidic channels with a high surface charge density. Enhanced by a bonding network of sodium carboxymethylcellulose, the ISPM achieved an exceptional output power density of 21.7 W m−2 and 46.0% energy conversion efficiency in a RED half‐cell system using natural seawater and river water, surpassing current technologies. This research not only advances RED technology but also provides biomimetic customization concepts for ISPM design across various applications, including flow batteries, fuel cells, and related fields. [ABSTRACT FROM AUTHOR]

Piezoionics, a new frontier that employs mobile ions as energy and charge carriers, plays an important role in new energy and intelligent electronics. However, a significant challenge consists in balancing the structural design of metal ions coordination hydrogel (HG‐MI) piezoionics for current conduction, voltage generation, and especially mechanical adaptability. Herein, inspired by the spider webs' unique structure, a strategy by realizing the full potential of metal‐ligand ions ([(OH)Cl2]3−) to facilitate the keggin‐type structure AlOHAlOH generation together with activate functional carboxyls is introduced. Impressively, the whole property of the product HG‐AlPAC, especially the mechanical performance is improved. For example, the toughness of HG‐AlPAC is 2.75 MJ m−3, more than twofold that of traditional HG‐AlAS/AC/AN samples. Due to the stable fixation of ─Al─OH─ thus promoting Cl− separation upon external force, HG‐AlPAC achieves a piezoionic coefficient of 0.89 mV KPa−1 and energy conversion efficiency of 1.29%, promising for mechanical‐electrical conversion and sensing. Combined with the good mechanical performance with the excellent piezoionic properties, underscores its potential as a tactile nerve system of analgesia patients to prevent them from being injured. This work intends to provide a stride toward mechanically robust self‐powered piezoionic sensors and offer insights into ionotropic materials for energy harvesting, human‐machine interaction, and biointerface. [ABSTRACT FROM AUTHOR]

Organic solar cells (OSCs) have emerged as promising candidates for renewable energy harvesting due to their lightweight, flexible, and low‐cost fabrication potential. The efficiency of OSCs is largely determined by the choice of solvents, which significantly affect the film morphology of the active layers, the intermixed donor‐acceptor domains, and overall device performance. Beginning with an introduction to the importance of solvent selection, the screening and classification of solvents, emphasizing their characteristics and classification based on sustainability, solubility, and other additional considerations are explored. Various non‐halogenated solvents, highlighting commonly used aromatic solvents, biomass‐derived solvents, and water/alcohol‐based solvents are explored. The state‐of‐the‐art donor and acceptor materials, focusing on efficient donor materials such as PM6 and D18, and high‐performing Y‐series acceptors are also presented. Strategies for developing high‐performance OSCs processed using non‐halogenated solvents are examined, including solvent engineering with additive and additive‐free approaches, ternary strategies, and layer‐by‐layer techniques. The fabrication of large‐area devices using non‐halogenated solvents is addressed, focusing on blade‐coating, slot‐coating, and other processing techniques. Finally, this review outlines future research directions in the non‐halogenated solvent processing of OSCs, emphasizing the need for continuous innovation to overcome existing limitations and propel OSC technology toward commercial viability. [ABSTRACT FROM AUTHOR]

Woody biomass is an abundant renewable resource. In this study, aerogels for versatile triboelectric devices are fabricated from poplar biomass via a dissolution‐and‐regeneration method with concentrated lithium bromide solution as the solvent. To improve the aerogels' structural homogeneity, two treatments—ball‐milling the raw poplar woody biomass before its dissolution, and, separately, ultrasonication following its dissolution—were applied. These treatments altered the porous structures and mechanical properties of the resulting aerogels, leading to a marked increase in their triboelectric performance. Removing the majority of the lignin from the aerogels was also explored, and resulted in triboelectric output ≈5 times greater than that of pristine woody biomass aerogel (i.e., without ball milling, ultrasonication, or lignin reduction). The underlying mechanisms of such increases were found to be both chemical and physical. Next, triboelectric devices were fabricated using the optimal (i.e., low‐lignin) aerogel for energy harvesting and biomechanical monitoring. These devices were able to: 1) respond sensitively to force, likely due to the aerogel's porous structures; 2) capture mechanical energy, charge capacitors, and power small portable electronics; and 3) monitor biomechanical movements including respiration, joint motions, and gait‐pattern changes. [ABSTRACT FROM AUTHOR]

The electrical double layer (EDL) between solids and liquids serves as the primary interface for ionic‐electronic coupling and is pivotal in nanoscale phenomena, governing electric field effects, ion transport, surface interactions, etc. Dynamically regulating the EDL through mechanical or electrostatic methods can influence charge carrier behavior, thereby impacting energy scavenging and storage processes. This regulation enabled efficient energy scavenging by governing ionic migration and optimizing charge carrier concentration at the interface, presenting a novel avenue to achieve efficient energy and information flow. Here, various scavenging energy and information devices through dynamically regulating the EDL are systematically reviewed. They are classified into three groups by regulating the distribution and movement of charge carriers throughout the entire EDL, diffuse layer, and Debye length range. The review provided a comprehensive overview of the operating principles, influencing factors, output characteristics, and typical applications, along with a discussion on future challenges. This holistic examination offers researchers valuable insights for evaluating their applicability in various scenarios. [ABSTRACT FROM AUTHOR]

Water constitutes a huge circulation network in solid, liquid and gaseous forms that contains inestimable recyclable energy. Obtaining energy from gaseous moisture is challenging but of great significance to promote the energy upgrading. The emergence of moisture‐driven actuator (MDA) provides an effective way in converting moisture energy to mechanical energy. The MDA can combine with water molecules through hygroscopicity and swell to produce macroscopic deformation. Due to the wide distribution of humidity and the wireless driving mode, MDA shows great application potential in the fields of environmental monitoring, remote control and energy harvesting. This paper comprehensively reviews the research progress of MDA from aspects of hydrophilic materials, structures, preparing methods, multi‐response integration and applications, aiming at providing guidance for the design, preparation and application of MDA. Besides, the challenges faced by MDA are analyzed and corresponding solutions are proposed, which points out the next stage developing direction of MDA. [ABSTRACT FROM AUTHOR]

Rapid advancements in nano‐exfoliation and dissolution strategies have effectively disassembled hierarchical biomass materials into nanosheets, nanofibers, and even atomic‐scale molecular chains, making them highly applicable in osmotic energy harvesting. However, sub‐nanosheets, situated between molecular chains and nanofibers, remain unexplored due to the demanding nature of their preparation methods. Herein, a pseudosolvent‐driven programmable ion intercalation‐exfoliation strategy is developed that triggers exfoliation along the lowest energy crystal plane (010), as simulations confirm. This method allows for the controlled exfoliation of chitin assemblies ranging from nanofibers to sub‐nanometer sheets and molecular chains. Specifically, compared to nanofibrils, sub‐nanometer sheet interfacial assembly exhibits higher surface charge density and interplanar spacing, leading to a 2.3‐fold increase in ion transport flux while maintaining high‐performance selective ion behavior, as confirmed by both experiments and molecular scale simulations, respectively. These enhancements result in superior ionic conductivity and power conversion performance (8.45 W m−2) under a 50‐fold salinity gradient, surpassing commercial standards (5.0 W m−2) and other all‐biomass membrane systems (Max. 2.87 W m−2). This work provides insights into the controlled exfoliation of biomass at the sub‐nanometer scale and enhancing osmotic energy harvesting. [ABSTRACT FROM AUTHOR]

Neutral‐color semitransparent organic photovoltaics (ST‐OPVs) offer potential opportunities to improve solar energy harvesting in integrated buildings. Here, high‐performance multifunctional neutral‐color ST‐OPVs are successfully fabricated by integrating a Ag/TeO2/Ag/TeO2‐based Fabry–Perot resonant optical coating (FPOC). Two coupled resonators of FPOCs are successfully fabricated to manipulate two adjacent transmission peaks in the visible region (380–780 nm) and high reflection from 1200 to 2500 nm, revealing its excellent color rendering index (CRI) tunability and thermal insulation. The 75 nm FPOC‐integrated ST‐OPV exhibits a CRI of 97.31, a high average visible transmittance of 43.15%, and a light utilization efficiency of 3.90% with superior thermal insulation properties, where the highest total and near‐infrared solar‐energy‐rejected dual functional efficiencies are 2.92% and 3.47%, respectively. The record CRI value of 99.23 is achieved for the 65 nm FPOC‐integrated ST‐OPVs. Attributed to the angular tolerance of FPOC, the neutral‐color ST‐OPVs exhibit good angular insensitivity up to ±60°. The results demonstrate the flexibility and multifunctionality of visible dual‐band‐pass Ag/TeO2/Ag/TeO2‐based FPOC for constructing neutral‐color, heat‐insulated, and angular‐insensitive ST‐OPVs, opening up a new avenue for the realization of smart power windows. [ABSTRACT FROM AUTHOR]

Currently, enhancing the output power of rotational‐mode triboelectric nanogenerators (TENGs) using various complicated systems is a contentious issue; however, this is a challenging process owing to the inherent characteristics of TENGs, namely, low output currents as opposed to high voltages. Thus, this study proposes a simple and innovative strategy for ultra‐high output peak power generation of TENGs called a self‐boosted rotational electrostatic‐discharge TENG (SRE‐TENG). The SRE‐TENG mechanism is unique as it is based on charge control and boosted discharge design, thereby achieving a remarkable peak power of 1103.8 W, peak power density of 140.6 Kw m−2, low optimum resistance of 100 Ω, and broad peak power generation range of 10 Ω to 1 GΩ. Diligent measurements and analyses of the peak and root‐mean‐square voltage and current outputs of the SRE‐TENG are conducted for various design variables and circuit configurations. The proposed SRE‐TENG mechanism is validated using experimental and multiphysics simulation results. The high‐output performance of the SRE‐TENG is demonstrated via the lighting of 3,000 LEDs and a 60‐W lamp array, continuous driving of a commercial sensor array, and hydrogen/oxygen generation via water electrolysis. [ABSTRACT FROM AUTHOR]

Triboelectric nanogenerator (TENG) for mechanical energy harvesting has been regarded as one of the most prospective energy technologies for the new era. However, inevitable material wear during triboelectrification results in output reduction and even failure of the TENG. In this work, a submillimeter‐scale superlubric TENG (SS‐TENG) is reported that enables ultra‐low friction coefficient (µ) and stable power generation. By using the micro/nano‐processing technology, the interdigital electrodes are embedded into the dielectric layer as a flat surface, on which the highly‐hydrogenated diamond‐like carbon (PLC) is deposited as the triboelectric layer to effectively reduce the friction coefficient. The frictional properties are systematically investigated at different parameters, in which a submillimeter‐scale (130 µm) superlubricity state (µ = 0.0084) is achieved at 4 N, 2 Hz and nitrogen atmosphere. Meanwhile, the SS‐TENG has a maximum power density of 3 mW m−2, which can remain stable at the superlubric condition. This work has first realized the freestanding‐mode superlubric TENG in submillimeter scale and provided a viable strategy for the development of long‐lifetime TENG, which may have great applications in frictional energy recovery from mechanical components, human joint motion, and the natural environment. [ABSTRACT FROM AUTHOR]

The triboelectric nanogenerator (TENG) is a promising technology for self‐powered sensors and vibration‐driven energy harvesting, with its development especially influenced by the characteristics of tribomaterials. However, developing tribopositive materials with a strong cationic effect and high electron‐donating capability remains challenging. In this study, a novel polyethylene oxide@poly(diallyldimethylammonium chloride) (PEO@Poly‐DADMAC) composite nanofiber mat (NFM) is successfully fabricated using the electrospinning technique. It functions as a highly tribopositive material, particularly enhancing the performance of nanofiber‐based TENGs (NF‐TENGs). Through investigation of its physical and triboelectric properties, the study revealed that incorporating cationic Poly‐DADMAC with PEO effectively boosts NF‐TENG output by increasing the dielectric constant (twofold), electron‐donating affinities, and surface charge trapping capability. The fabricated NF‐TENG shows excellent output performance generating 980 V, a maximum power density of 5.6 Wm−2, and an ultrahigh sensitivity of 8.923 V kPa−1 which endows composite reliability for power supply and sensing capability. More importantly, the PEO@Poly‐DADMAC‐based self‐powered motion sensor with an NF‐TENG array is successfully demonstrated in multifunctional applications such as athlete activity tracking, and wireless gaming interface control. This study not only offers new insights into optimizing performance and selecting alternative tribomaterials but also provides valuable guidance for developing high‐output TENGs and highly sensitive self‐powered sensors. [ABSTRACT FROM AUTHOR]

Triboelectric nanogenerators have recently gained enormous attention as a low‐cost method for converting abundant mechanical energy into electricity. Here, a continuous direct current (DC) output from a triboelectric nanogenerator (TENG) is achieved using two dimensional (2D)‐WS2/Si heterojunctions, without any need for a rectifier circuit element. At the interface of the p–Si and n–WS2 heterojunction, the "Tribo‐photovoltaic effect" is observed, responsible for the generation of direct tribo‐outputs. The demonstrated multifunctional DC‐TENG with remarkable performance can concurrently convert mechanical and photonic energy into an electrical one. In comparison to dark conditions, the device's output performance is enhanced under UV illumination (365 nm, 1022 µW cm−2), and the exhibited output voltage (10.75 V) and current (466 nA) are higher by a factor of 3.9 and 2.4, with excellent power harvesting ability and outstanding robustness. This versatile DC‐TENG is demonstrated to be an attractive platform for high‐performance vision sensors and UV detection, which has significant implications for the rapid development of self‐powered portable sensing and IoT devices based on Si CMOS technology. [ABSTRACT FROM AUTHOR]

In this work, a green protocol for the synthesis of new para‐Azaquinodimethane (pAQM) small molecules, functionalized with anisole (An) or bithiophene (TT) moieties on the central unit and with different alkoxy groups as lateral substituents is developed and reported. The alkoxy lateral substituents are found to strongly impact the solubility and processability of the chromophores. On the other hand, the steady–state and time‐resolved spectroscopic results show completely different spectral and photophysical features for the An‐ and TT‐ derivatives. Only for the TT‐compounds, the nanosecond and femtosecond transient absorption experiments reveal low efficiency of triplet production in solution as well as ultrafast (≈1 ps) and efficient (≈200%) singlet fission (SF) in thin film. The yellow An‐containing molecules are instead used to sensitize the purple SF‐active TT‐compounds via quantitative FRET in mixed thin films, which interestingly exhibit panchromatic absorption extending in the entire visible spectral range. With this study, the synergy between FRET and SF is exploited at the intermolecular level in the solid‐state for the first time by considering unconventional and stable SF chromophores, opening intriguing new possibilities for solar energy harvesting. [ABSTRACT FROM AUTHOR]

Printing technologies have the potential to reduce the manufacturing costs of many electronic devices significantly. Here, a scalable manufacturing route for high‐performance fully printed thermoelectric generators (TEGs) as a cost‐effective solution for energy harvesting is demonstrated. This work presents a facile one‐pot synthesis method to develop a high‐performance Ag2Se‐based n‐type paste, which is used to fabricate a fully printed origami TEG by employing the Ag2Se‐based material for the n‐type legs and a previously reported Bi‐Sb‐Te‐based paste for the p‐type legs. The n‐type film exhibits a power factor of 13.5 µW cm−1 K−2 and a maximum figure‐of‐merit (ZT) of ≈ 0.92. Furthermore, printable carbon paste is introduced as an effective interface between the thermoelectric and electrode materials, which reduces the contact resistances in the thermoelectric device. The origami folded TEG exhibits an open‐circuit voltage (VOC) of 284 mV, a power output of 370.88 µW, and an exceptionally high power density (pmax) of 10.72 Wm−2 at a temperature difference (∆T) of 80.7 K, considering that the TEG fabrication does not involve any pressure treatment and vacuum sintering. These results underscore the scalability of the presented manufacturing process and the capability of printed origami TEGs for powering the Internet of Things (IoT) with low‐grade waste heat. [ABSTRACT FROM AUTHOR]

As continuous wearable physiological monitoring systems become more ubiquitous in healthcare, there is an increasing need for power sources that can sustainably power wireless sensors and electronics for long durations. Wearable energy harvesting with thermoelectric generators (TEGs), in which body heat is converted to electrical energy, presents a promising way to prolong wireless operation and address battery life concerns. In this work, high performance TEGs are introduced that combine 3D printed elastomers with liquid metal epoxy polymer composites and thermoelectric semiconductors to achieve elastic compliance and mechanical compatibility with the body. The thermoelectric properties are characterized in both energy harvesting (Seebeck) and active heating/cooling (Peltier) modes, and examine the performance of wearable energy harvesting under various conditions such as sitting, walking, and running. When worn on a user's forearm while walking outside, the TEG arrays are able to power circuitry to collect photoplethysmography (PPG) waveform data with a photonic sensor and wirelessly transmit the data to an external PC using an on‐board Bluetooth Low Energy (BLE) radio. This represents a significant step forward on the path to sustainable body‐worn smart electronics. [ABSTRACT FROM AUTHOR]

Triboelectric Nanogenerators (TENGs) represent a novel energy harvesting technology that combines contact electrification (CE) and electrostatic induction, rendering them a promising solution for self‐powering micro smart devices and addressing the energy crisis. At present, the efficiency and longevity of TENGs have been substantially improved through various methods. These advancements have overcome the limitations caused by interface friction, expanding the scalability and practical applications of TENGs. Specifically, it has been demonstrated that interface tribological optimization can simultaneously enhance electrical output performance and durability. This review will initially discuss the fundamental mechanism of TENGs and its profound connection with tribology. Subsequently, the optimization of interface tribology, encompassing structure design, surface modification, and lubricant utilization, will be comprehensively reviewed. Finally, the current challenges and future prospects will be summarized. [ABSTRACT FROM AUTHOR]

Manipulating elastic waves of all polarizations is highly challenging due to the complex behavior of elastic waves. To achieve simultaneous broadband vibration attenuation and energy harvesting across all polarizations of elastic waves at low‐frequency ranges, a chiral mechanical metamaterial‐based energy harvester is proposed in this study. The systematic development of a complete bandgap and defect structure is achieved through theoretical eigenfrequency analysis and numerical simulations. The defect structure is incorporated to induce defect modes for all wave polarizations within the complete bandgap region, ensuring their compatibility with the overall shape of the structure. The proposed chiral mechanical metamaterial with defect (CMMD) demonstrated significant performance improvements, achieving electrical output power enhancements that are 20.5 times for flexural waves and 511.4 times for longitudinal‐torsional waves compared to the defectless chiral mechanical metamaterial. This study accentuates the thoughtful design and multifaceted utility of chiral mechanical metamaterials, paving the way for their application not only in energy harvesting but also in wave attenuation for various polarizations. [ABSTRACT FROM AUTHOR]

The gradient concentration in nature has garnered significant attention as a promising source for energy harvesting. Researchers have explored various methods to harness electricity from gradient‐concentration‐induced flows, including evaporation‐driven nanogenerators and humidity‐gradient‐based power generators. However, their low current and power density are the main obstacles toward practical applications. Herein, a Bilayer Hydrogel Electricity Generator (BHEG) is presented to enable efficient energy harvesting through the synergy between ion gradient concentration and galvanic effects. A BHEG unit employing identical materials for both electrodes demonstrates an open‐circuit voltage of 0.7 V and a short‐circuit current of 4.34 mA—surpassing the currently reported average by over 73 times—and achieves a maximum power density of 72.2 mW m−2. Moreover, another BHEG unit using Zn─C electrode materials exhibit an open‐circuit voltage of 1.86 V and a short‐circuit current of 92 mA. Furthermore, the versatility of the BHEG extends beyond power generation, effectively providing passive thermal management for electronics, resulting in a maximum temperature reduction of ≈20 °C. Consequently, the study contributes insights into the design and fabrication of efficient hydrogel‐based power generators, providing a promising avenue for leveraging natural‐flow‐induced energy for various applications. [ABSTRACT FROM AUTHOR]

The dynamic electromechanical coupling behavior of composite materials is highly dependent on external excitation frequency. While degradable biomolecular materials typically exhibit lower piezoelectric coefficients compared to ceramics, neglecting their frequency‐dependent performance in the design of piezoelectric devices further leads to less efficient utilization of their piezoelectric properties. This oversight greatly hinders the practical application of these materials. To address this, a novel fractional derivation (FD) theory‐assisted model is introduced to reversely design the glycine‐polyvinyl alcohol (PVA) thin films for versatile enhanced bio‐applications. An electromechanical coupling model incorporating FD theory is developed to learn the relationships between FD parameters, film dimensions, and dynamic electromechanical properties. This model accurately predicts the electromechanical performance of the films across a wide frequency range, validated by both finite element simulations and experimental results. This therefore allows to establish key design principles for piezoelectric thin film in bioenergy harvesting and sensing, by tailoring thin film parameters to enhance the piezoelectric performance at specific stimuli frequencies. Demonstrations of glycine‐PVA film devices guided by this model reveal excellent performance in ultrasonic energy harvesting and carotid artery bio‐signal sensing. This study provides a robust theoretical framework for designing and optimizing biodegradable piezoelectric materials for various practical applications. [ABSTRACT FROM AUTHOR]

Microelastic topological metamaterials (METMs) are of great use in the robust conveying and harvesting of high‐frequency ultrasonic energies. However, current METMs only hold topological edge states of a single flexural mode, restricting their capacity to convey ultrasonic energies of other polarized elastic waves. Moreover, the potential of METMs for ultrasonic energy harvesting remains unexplored. To address these challenges, an all‐polarized elastic topological metamaterial (AETM) is developed, capable of simultaneous conveying and harvesting of ultrasonic energies from elastic waves of all polarizations. This AETM supports broadband topological edge states for both out‐of‐plane and in‐plane modes, enabling the robust conveying of ultrasonic energies from all‐polarized elastic waves. Subsequently, by integrating the AETM with a piezoelectric energy harvester, efficient harvesting of ultrasonic energies conveyed by the AETM is achieved. Notably, the developed AETM with structural simplicity can be easily integrated into micro‐electromechanical systems (MEMSs) for on‐chip ultrasonic wave communication and energy harvesting. This work advances the development of topological metamaterials that can concurrently convey and harvest ultrasonic energies from all‐polarized elastic waves, offering significant potential for various MEMS applications. [ABSTRACT FROM AUTHOR]

Sliding mode triboelectric nanogenerators (S‐TENG) have been validated as a simple and efficient mechanical energy harvesting technology in low frequency for constructing self‐powered systems. However, the charge invalid transfer in the S‐TENG leads to its output energy loss, which has not been addressed by researchers in this field. Herein, a novel transverse‐asymmetric electrode structure sliding TENG (TAE‐TENG) is proposed, where the specific asymmetric bottom electrode configuration distinguishes it from the previously reported S‐TENGs. This design can be equivalent to a hybrid model, consisting of two units, a sliding mode TENG with blank area and a freestanding mode TENG with a shielding electrode, which effectively eliminates the charge transfer loss and enhances the output performance. The insight mechanism of charge transfer in each operation process is analyzed. The TAE‐TENG achieves 1.42 µC output charge, 1.97‐fold as that of the conventional S‐TENG (0.72 µC) with equivalent dimensions, and also exhibits more sustained and higher current waveforms. The output charge, root‐mean‐square (RMS) current, and average power of the rotation‐TAE‐TENG at 60 rpm are 3.05 µC, 97.50 µA and 44.02 mW, respectively. This work provides a physical mechanism of charge transfer in sliding TENG and an effective method to improve its output energy. [ABSTRACT FROM AUTHOR]

Droplet‐based electricity generators (DEGs) have emerged as innovative devices capable of transducing the kinetic energy of falling water droplets into electrical power, thereby presenting a promising solution for ambient energy harvesting. For effective application, DEGs must exhibit transparency and flexibility to facilitate aesthetic integration and optical/mechanical adaptability for utilization on natural objects and wearable devices. In this study, a hydrogel‐based DEG (Hy‐DEG) designed is proposed to be seamlessly integrated into everyday environments without compromising design or functionality. With the intrinsic characteristics of hydrogel, the Hy‐DEG exhibits superior optical transmittance (≈99%) and stretchability (≈70% of its original length), generating the electrical output performance of ≈45 V of voltage, 15 µA of current, and 42 µW of maximum peak power, with single droplet impact. This capability of the Hy‐DEG can operate electronic devices for environmental monitoring while maintaining seamless integration with commonly encountered surfaces. In this context, this study elucidates the characteristics of hydrogel bestowing novel functionalities upon the DEG, expanding the potential for energy harvesting in residential and commercial contexts. The implications of this research extend beyond conventional energy generation, fostering the development of self‐powered, transparent, and flexible devices. [ABSTRACT FROM AUTHOR]

The utilization of salt concentration gradients as a renewable energy source represents a pivotal solution to the energy crisis. However, it is a persistent challenge to fabricate high‐performance ion permeable membranes with excellent ion permselectivity. In this work, hydrogen‐bonded organic framework (HOF) is in situ growth on anodic aluminum oxide (AAO) via chemical‐binding and solution‐processing strategy. The hydrogen bonding and π–π interactions forming the porous structure and the internal unprotonated carboxyl groups endow the HOF with superior cation selectivity and ion permeability. Furthermore, benefiting from the remarkable asymmetry of the prepared nanofluidic membrane arising from structure and charge of AAO and HOF, the HOF/AAO presents outstanding ion current rectification (ICR) characteristic, which can eliminate the ion concentration polarization (ICP) and power loss. Therefore, an impressive output power density with 500‐fold NaCl gradient is achieved as 75.2 W m−2 using the as‐prepared HOF/AAO, which is superior to most of reported membranes (7.0–40.0 W m−2). To show the critical role of HOF, 2D and 3D MOF with the same monomers are also synthesized, achieving decreased power densities of 36.2 and 58.3 W m−2 respectively. The present work provides a novel strategy to develop high‐performance nanofluidic ICR membranes for osmotic energy harvesting. [ABSTRACT FROM AUTHOR]

Harvesting low‐grade waste heat into electrical energy is recognized as a promising solution for sustainable energy supply. In parallel, thermotropic smart windows have emerged as an efficient way to reduce building energy consumption. It is posit that thermotropic smart windows with inherent thermoelectric property may offer unique advantages for practical applications. Herein, the preparation and characterization of a series of ionic hydrogels that exhibit temperature‐sensitive phase transition behavior is reported, which are suitable for both thermotropic smart windows and thermoelectric generators. Notably, the lower critical solution temperature (LCST) of this ionic hydrogels can be feasibly modulated, and the thermoteopic phase transition also induces a sharp increase in their Seebeck coefficient, reaching up to 39.03 mV K−1 with a power factor (PFi) value up to 0.838 mW m−1 K−2. A prototype dual functional thermotropic smart window that simultaneously works as an ionic thermoelectric generator is further demonstrated, achieving both efficient phase transition driven by solar heat at ≈26 °C and an energy density up to 250 mJ m−2. This study offers new opportunity for the development of smart materials that can bridge the gap between thermal comfort and energy sustainability for energy harvesting and smart building applicat. [ABSTRACT FROM AUTHOR]

Liquid metal (LM) micro‐nano droplets show the superiority in reducing the high surface tension applicable in conductive inks for flexible electronics. However, the dynamic surface makes LM droplets susceptible to be oxidized, facing challenges in storage and applications. Herein, a bifunctional groups cross‐linking strategy is adopted to encapsulate LM droplets into a robust shell. During sonicating LM in carboxymethyl chitosan (CMCS) solution with bifunctional groups (i.e., carboxyl and amino groups), a robust interface shell is constructed by anchoring effect, thereby providing high chemical stability (>7d). When directionally freezing‐drying LM dispersions, aerogel with Janus architecture is produced driven by the gravity of LM droplets. Due to the unique heterogeneous structure, the resultant aerogel exhibits a selective multifunctional response toward directional bending. In addition, owing to the gradient distribution of CMCS within aerogel, moisture electricity generator can be built with a high output voltage of 460 mV. Thus, this bifunctional groups cross‐linking strategy not only improves the chemical stability of LM micro‐nano droplets, but also renders a new method for producing multifunctional aerogel with energy harvesting and selective directional recognition, and applicable in smart sensors and power supplying devices. [ABSTRACT FROM AUTHOR]

The rapid development of the Internet of Things has led to numerous functional electronic devices, making it a significant challenge to provide power for these distributed devices. Triboelectric self‐power technology is ideal for smart devices due to its material diversity and high energy efficiency. However, traditional triboelectric materials have weak electrostatic induction due to their low dielectric constant. Additionally, the thermionic emission effect reduces their electric output in high temperatures, limiting their applications. This study designes a thermally robust aramid triboelectric material with a high dielectric constant through heat‐induced cross‐linking heterogeneous interface engineering. This novel material not only achieves high triboelectric output but also maintains high performance across a wide temperature range. The heat‐induced cross‐linking process enhances the interaction between aramid nanofibers and Al2O3 nanosheets, significantly improving the electrical performance, and flame retardance of the material, and the relative dielectric constant increases 16‐fold. The triboelectric nanogenerator constructed with this material achieves a power density of 3.97 W m−2, and maintains high triboelectric output at 260 °C. Finally, a self‐powered detection system collects high‐temperature gas energy and drives sensors is designed. This research presents a novel strategy for high‐performance triboelectric materials, showing significant potential for self‐powered devices. [ABSTRACT FROM AUTHOR]

Triboelectric nanogenerators (TENGs) hold immense potential as sustainable energy sources, with waste materials serving as promising materials for their fabrication. Nearly 270 million tons of waste is produced yearly, most of which remains unrecycled. TENGs can utilize this wide range of waste to convert mechanical energy to electrical energy while providing a solution for the global issue of plastic waste. On the other hand, the enormous demand for wearable electronics and the Internet of Things (IoT) trigger the development of self‐reliant energy sources. Currently, TENGs are one of the preferred choices as they are easy to design and generate high output. In this regard, TENGs are promising for utilizing waste materials, particularly for self‐powered or energy‐autonomous applications. This review focuses on utilizing waste materials from diverse sources, including biowaste, household waste, medical, laboratory, pharmaceutical, textile, electronic waste (e‐waste), and automotive waste for TENG development. Different waste materials are detailed for their potential as materials for TENGs, their availability, and recycling methods. The review also highlights the applications of TENGs fabricated from waste materials. Finally, the challenges, limitations, and future perspectives of using waste materials for TENG fabrication are discussed to motivate further advances. [ABSTRACT FROM AUTHOR]

Renewable osmotic energy between seawater and river water shows great potential in meeting global energy demand. Reverse electrodialysis (RED) technique using ion‐selective membrane is particularly outstanding for its easy operation. Preparing low‐cost and large‐area ion‐selective membranes with excellent ion transport characteristics is particularly important to promote commercial applications. Herein, large‐area ion‐selective membrane is prepared by scraping slurry of flocculated GO (graphene oxide)/PAAS (sodium polyacrylate) solution and then coated with PVA (polyvinyl alcohol)/SA (sodium alginate) gel layer. The PVA/SA molecules can penetrate into the membrane through the unique micro/meso‐pores, which together increase the ion selectivity, membrane permeability, and stability. This ion‐selective membrane can achieve a power density of 8.65 W m−2 under a 50‐fold salinity gradient (NaCl) simulating the sea/river junction environment (with the testing area of 0.0314 mm2). This work significantly promotes the application of GO in large‐area preparation of low‐cost ion‐selective membrane. [ABSTRACT FROM AUTHOR]

As large‐area and optically transparent photon harvesting devices, luminescent solar concentrators (LSCs) are promising candidates for building‐integrated photovoltaics owing to their high transmittance and resistance to shadowing effects existing in solar cells. Up to now, there are still many challenges in the practical application of LSCs: 1) Reabsorption loss is inevitable during photoluminescence transmission due to indirect illumination of solar cells in LSC system. 2) Satisfactory energy harvesting cannot be achieved in rainy conditions due to the substantial attenuation of the incident light intensity. 3) Evaporation residue on the surface of LSCs leads to device performance degradation. Pioneering researches and feasible strategies for reabsorption loss suppression, energy harvesting in rainy days as well as self‐cleaning property are still lacking demonstration. In this work, reabsorption loss is suppressed based on advanced structural LSCs with universally applicable optical spacer layer. Then the integrated LSCs with droplet‐based electricity generator (DEG) are proposed for the first time. Such DEG‐LSCs not only realize synergistic harvesting of solar and raindrop energy, but also possess self‐cleaning properties. Finally, a self‐powered temperature and humidity sensing system is designed and demonstrated to provide feasible ideas for the practical application of DEG‐LSCs in self‐powered intelligent buildings. [ABSTRACT FROM AUTHOR]

Silk nanofibers (SNFs) from abundant sources are low‐cost and environmentally friendly. Combined with other functional materials, SNFs can help create bioelectronics with excellent biocompatibility without environmental concerns. However, it is still challenging to construct an SNF‐based composite with high conductivity, flexibility, and mechanical strength for all SNF‐based electronics. Herein, this work reports the design and fabrication of Ti3C2Tx‐silver@silk nanofibers (Ti3C2Tx‐Ag@SNF) composites with multi‐dimensional heterogeneous conductive networks using combined in situ growth and vacuum filtration methods. The ultrahigh electrical conductivity of Ti3C2Tx‐Ag@SNF composites (142959 S m−1) provides the kirigami‐patterned soft heaters with a rapid heating rate of 87 °C s−1. The multi‐dimensional heterogeneous network further allows the creation of electromagnetic interference shielding devices with an exceptionally high specific shielding effectiveness of 10,088 dB cm−1. Besides working as a triboelectric layer to harvest the mechanical energy and recognize the hand gesture, the Ti3C2Tx‐Ag@SNF composites can also be combined with an ionic layer to result in a capacitive pressure sensor with a high sensitivity of 410 kPa−1 in a large range due to electronic‐double layer effect. The applications of the Ti3C2Tx‐Ag@SNF composites in recognizing human gestures and human‐machine interfaces to wirelessly control a trolley demonstrate the future development of all SNF‐based electronics. [ABSTRACT FROM AUTHOR]

Hybrid nanogenerators are advanced mechanical energy harvesters capable of simultaneously scavenging multiple types of energy. Additionally, thermochromic materials provide a practical and visually assessable method for real‐time temperature monitoring. In this report, a novel energy harvester and sensing patch (EHSP) is introduced, that utilizes combined piezoelectric and triboelectric effects to harvest mechanical energy efficiently. To optimize the EHSP, various energy harvester configurations are fabricated and tested, and the dielectric properties of triboelectric films are systematically investigated. These improvements are implemented to augment the overall energy harvesting capability. The thermochromic properties of the EHSP are also explored to enhance both the electrical performance and thermal responsiveness. The EHSP demonstrates the ability to generate maximum voltage and current outputs of 350 V and 20.4 µA, respectively. Moreover, it can detect temperature changes within seconds, making it suitable for both energy harvesting and sensing applications. The EHSP is tested in practical scenarios, proving its efficiency as an energy harvester and sensor for everyday human activities. Furthermore, its integration with multiple hybrid nanogenerators showcases its potential for industrial and wearable sensing applications. [ABSTRACT FROM AUTHOR]

Herein, we present a novel method for fabricating a triboelectric nanogenerator using Polyacrylonitrile (PAN) on both sides as triboelectric pairs, incorporating metal‐organic frameworks (MOFs) such as ZIF‐8, ZIF‐67, MIL‐100, and HKUST‐1 during the electrospinning process. The triboelectric properties of the MOF‐incorporated fibers are thus tailored and positioned within the triboelectric series for the first time. The resulting triboelectric polarity of the composite fiber is linked to the optical bandgap energy of the PAN and the MOF/PAN composite, facilitating electron transfer between materials of different work functions and leading to enhanced output in the developed triboelectric devices. Fascinatingly, the appropriate choice of MOF filler also displayed the potential for reversing the triboelectric polarity of PAN nanofiber. Consequently, incorporating ZIF‐8 and MIL‐100 into PAN nanofibers led notably to contrasting trends in triboelectric polarity, with the pair generating an open‐circuit output voltage of 100 V, short‐circuit current of 1.35 μA, and a power density of 18.4 mW/m2 respectively. The fabricated device demonstrated effectiveness for mechanical energy harvesting applications and also as a self‐powered humidity sensor, displaying rapid response to changes in ambient humidity levels with a maximum sensitivity of 2.14 V/%RH, for relative humidity range between 50 and 90% during the humidifying cycle. [ABSTRACT FROM AUTHOR]

Drawing inspiration from nature has served as a crucial driving force behind human progress, enabling groundbreaking advancements and cross‐disciplinary integration through the emulation of biological superhydrophobic phenomena. Bioinspired superhydrophobic triboelectric materials stand out among advanced triboelectric materials due to their unique hydrophobic properties, exceptional moisture resistance, and remarkable electrical performance. However, the inherent complexity of natural phenomena and the need for refinement in bioinspired design pose significant challenges in the development of bioinspired superhydrophobic triboelectric materials. This comprehensive review delves into bioinspired superhydrophobic triboelectric materials from the perspectives of theoretical underpinnings, fabrication strategies, and cutting‐edge applications. Rooted in the interaction mechanisms between water molecules and triboelectric materials, the importance of enhanced hydrophobic properties is elucidated. A systematic overview of bioinspired superhydrophobic triboelectric materials’ construction strategies is presented, offering fresh perspectives and insights into the development and application of high‐performance triboelectric nanogenerators (TENGs). Finally, the current challenges and untapped opportunities in bioinspired superhydrophobic triboelectric materials are summarized to fully unlock their potential for applications in TENGs. [ABSTRACT FROM AUTHOR]

Thermal rectification devices, which facilitate preferential heat flow in a singular direction, stands as pivotal tools in the realization of solid‐state thermal circuits. 1D atomic chains, exhibit heightened thermal rectification efficiency owing to their exceptional directional heat conduction properties. These will find widespread utility in many applications, encompassing areas such as cooling, energy harvesting, and thermal isolation systems. However, unlike quasi‐1D materials, the intrinsic anisotropic heat transport in true‐1D atomic chains is yet to be systematically studied. Herein, the origins of the anisotropic heat transfer in three representative 1D structures (TaSe3 and BaTiS3 marked as quasi‐1D, MoI3 labeled as true‐1D) is first investigated by integrating a first‐principles density functional theory‐based framework of two‐channel heat conduction model. In contrast to quasi‐1D, MoI3 exhibits a giant anisotropy of lattice thermal conductivity (κL) in chain‐ and cross chain‐directions with a high ratio up to ≈20, which far exceeds the previous report for HfTe5 and ZrTe5. Such unique heat transfer reveals comprehensively by charge‐sharing and transferred charges, p‐‐d orbital hybridization and Young's modulus changes, induces an exceptionally large anisotropy. This study presents a high‐performance implementation of thermal rectification designed to regulate directional heat current, demonstrating its potential applicability in solid‐state thermal circuits. [ABSTRACT FROM AUTHOR]

The seamless integration of advanced triboelectric nanogenerators with fiber material has propelled the rapid advancement of intelligent wearable electronics. The overheating and mechanical abrasion associated with prolonged operation poses a significant challenge for conventional fiber‐based triboelectric materials. Aramid fibers, characterized by high thermal stability, ultra‐high mechanical strength, and excellent insulating properties, can effectively compensate for the limitations of triboelectric materials. However, the intrinsic advantages of aramid fiber triboelectric materials and their general structural design strategies have not yet to be comprehensively elucidated. In this review, the synthesis methods and development history of aramid fiber triboelectric materials in recent years are summarized. Importantly, the unique advantages and development potential of aramid fibers as triboelectric materials are systematically discussed, particularly regarding high‐temperature resistance, high strength, and electrical insulation. Furthermore, the latest advancements in the structural design and performance modulation of aramid fiber triboelectric materials are presented. The aramid fiber‐based self‐powered wearable electronics in high‐temperature warning, impact monitoring, and human energy harvesting are summarized. Finally, the challenges and opportunities facing the future development of aramid fiber‐based triboelectric nanogenerators are discussed. [ABSTRACT FROM AUTHOR]

Sustained thermoelectric efforts have concentrated on the enhancement of conversion efficiency of power generators, while simultaneously achieving high output power continues to lag. Specifically, the highest output power density of emerging Mg‐based modules reported so far is only half of that of commercial Bi2Te3‐based, mainly due to the low power factor of MgAgSb. Herein, homogenously distributed MgCuSb in situ nanoprecipitates in the MgAgSb matrix effectively optimized carrier concentration due to the effect of carrier injection from the metal–semiconductor Ohmic contact. As a result, a record‐high average power factor of 27.2 µW cm−1 K−2 is obtained in MgCu0.1Ag0.87Sb0.99 composite within the temperature range of 300–550 K, which is much higher than ever reported values of MgAgSb system. Benefiting from the combination of the optimized average power factor of p‐leg and low interface resistivity, a fabricated eight‐pair MgCu0.1Ag0.87Sb0.99/Mg3.2Bi1.5Sb0.5 module demonstrates an unprecedently high output power density of 2.9 W cm−2 under a temperature difference of 300 K, outperforming all low‐temperature advanced thermoelectric modules. Meanwhile, a competitive conversion efficiency of 7.65% is obtained simultaneously. The work significantly advances high‐power thermoelectric applications of Mg‐based modules in the field of low‐temperature sustainable energy harvesting. [ABSTRACT FROM AUTHOR]

With the rise of demand for smart wearable and flexible electronic devices in the modern world, high‐performance hybrid mechanical energy harvesters (HMEHs), which can easily convert biomechanical energy into electricity for powering a variety of portable electronic gadgets and operating smart sensors, have gained extensive interest. Herein, propose piezo/ferroelectric and dielectric niobium (Nb)‐doped bismuth titanate (Bi4Ti3‐xNbxO12, NBTO) plates, are proposed and synthesized by a molten‐salt synthesis technique, and they are further embedded into the poly(vinylidene fluoride‐co‐hexafluoropropylene) (NBTO/PVDF‐HFP) flexible composite film (CF) to construct a flexible HMEH. The prepared NBTO/PVDF‐HFP CFs reveal good piezo/ferroelectricity, β‐phase fraction, and dielectric properties, which can improve the electrical output performance of the HMEH. The 2 wt.% NBTO/PVDF‐HFP CF‐based HMEH exhibits high and stable electrical performance of ≈175 V, ≈5.8 µA, ≈76 µC m−2, and ≈2.02 W m−2, respectively. Furthermore, the durability and mechanical robustness analysis of the HMEH is conducted for several days. The real‐time applications of the HMEH are demonstrated by harvesting the biomechanical energy obtained from daily human activities and powering various portable electronics. Also, the HMEH integrated with an Arduino microcontroller unit is employed as a smart sensor switch for implementing smart home/building stair‐sensing applications and sending emergency e‐mail alerts. [ABSTRACT FROM AUTHOR]

Developing mechanical energy harvesters for electrical stimulation (ES) needed to augment cell behavior is a burgeoning area of interest. Mechanical energy harvesters that can generate electrical energy in electrolyte‐containing aqueous environments offer a unique solution for delivering ES to cells. In this work, a fully integrated ES assembly (FESA) is introduced that comprises coiled polydopamine (PDA) containing carbon nanotube yarn (CNT) harvesters, serving as ES generators, and poly(3,4‐ethylenedioxythiophene) coated carbon nanotube (PEDOT/CNT) sheets employed as a conductive scaffold. The PDA containing CNT (PDA/CNT) yarn, a novel twistron electrode, achieves an enhanced electrical power at a lower matching impedance than coiled CNT yarn to efficiently transfer ES to the conductive scaffold. The PEDOT used for the scaffold provides a suitable surface for cell adhesion and low resistance for effective ES transmission. In addition, the upscaled array of coiled PDA/CNT yarns provides an ES current density range up to 75.4 µA cm−2, which is much higher than for ES systems using different mechanical energy harvesters. This FESA is designed to provide an optimal level of ES for the proliferation and differentiation of chondrocytes. The findings illuminate the potential of chemically modified twistron energy harvesters as an innovative and effective strategy to promote biological response. [ABSTRACT FROM AUTHOR]