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The accurate identification of drug-target affinity (DTA) is crucial for advancements in drug discovery and development. Many deep learning-based approaches have been devised to predict drug-target binding affinity accurately, exhibiting notable improvements in performance. However, the existing prediction methods often fall short of capturing the global features of proteins. In this study, we proposed a novel model called ETransDTA, specifically designed for predicting drug-target binding affinity. ETransDTA combines convolutional layers and transformer, allowing for the simultaneous extraction of both global and local features of target proteins. Additionally, we have integrated a new graph pooling mechanism into the topology adaptive graph convolutional network (TAGCN) to enhance its capacity for learning feature representations of chemical compounds. The proposed ETransDTA model has been evaluated using the Davis and Kinase Inhibitor BioActivity (KIBA) datasets, consistently outperforming other baseline methods. The evaluation results on the KIBA dataset reveal that our model achieves the lowest mean square error (MSE) of 0.125, representing a 0.6% reduction compared to the lowest-performing baseline method. Furthermore, the incorporation of queries, keys and values produced by the stacked convolutional neural network (CNN) enables our model to better integrate the local and global context of protein representation, leading to further improvements in the accuracy of DTA prediction. [ABSTRACT FROM AUTHOR]

In recent years, single‐atom catalysts (SACs) have become the most active part of the catalytic field due to their excellent catalytic activity. Among them, Ru SACs exhibit excellent performance in many catalytic applications due to their high atomic utilization efficiency, catalytic activity and selectivity, and relatively low cost. In order to understand the structure–performance relationship and potential catalytic mechanism of Ru SACs, this review summarizes the research progress of Ru SACs in the fields of electrocatalytic water splitting, fuel cells, nitrogen reduction, and nitrate reduction in recent years. The catalytic process of Ru single atom in different synthesis methods and modification strategies is summarized. Finally, some opportunities and challenges for the future development of Ru SACs are prospected. [ABSTRACT FROM AUTHOR]

[Display omitted] The flexible and self-healing supercapacitors (SCs) are considered to be promising smart energy storage devices. Nevertheless, the SCs integrated with flexibility, lightweight, pattern editability, self-healing capabilities and desirable electrochemical properties remain a challenge. Herein, an all-in-one self-healing SC fabricated with the free-standing hybrid film (TCMP) composed of the 2,2,6,6-tetramethylpiperidin-1-yloxy-oxidized cellulose nanofibers (TOCNs) carried carbon nanotubes (CNTs), manganese dioxide (MnO 2) and polyaniline (PANI) as the electrode, polyvinyl alcohol/sulfuric acid (PVA/H 2 SO 4) gel as the electrolyte and dynamically cross-linked cellulose nanofibers/PVA/sodium tetraborate decahydrate (CNF/PB) hydrogel as the self-healing electrode matrix is developed. The TCMP film electrodes are fabricated through a facile in-situ polymerization of MnO 2 and PANI in TOCNs-dispersed CNTs composite networks, exhibiting lightweight, high electrical conductivity, flexibility, pattern editability and excellent electrochemical properties. Benefited from the hierarchically porous structure and high mechanical properties of TOCNs, excellent electrical conductivity of CNTs and the desirable synergistic effect of pseudocapacitance induced by MnO 2 and PANI, the assembled SC with an interdigital structure demonstrated a high areal capacitance of 1108 mF cm−2 at 2 mA cm−2, large areal energy density of 153.7 μWh cm−2 at 1101.7 μW cm−2. A satisfactory bending cycle performance (capacitance retention up to 95 % after 200 bending deformations) and self-healing characteristics (∼90 % capacitance retention after 10 cut/repair cycles) are demonstrated for the TCMP-based symmetric SC, delivering a feasible strategy for electrochemical energy storage devices with excellent performance, designable patterns and desirable safe lifespan. [ABSTRACT FROM AUTHOR]

A thin, lightweight and flexible electromagnetic interference (EMI) shielding paper composite is an urgent need for modern military confrontations. Herein, a sandwich-structured EMI shielding paper composite with an easy pavement consisting of a filter paper layer, middle AgNWs/MXene layer, and polyvinyl butyral (PVB) layer was constructed by vacuum-assisted filtration, spraying and air-drying. The middle AgNWs/MXene compound endowed the filter paper with excellent electrical conductivity (166 S cm−1) and the fabricated filter paper–AgNWs/MXene–PVB composite exhibits superior EMI shielding (30 dB) with a 141 μm thickness. Remarkably, the specific EMI shielding effectiveness (SSE/t) of the filter paper–AgNWs/MXene–PVB composite reached 13,000 dB cm2 g−1 within the X-band frequency range. This value represents one of the highest reported for cellulose-based EMI shielding materials. Therefore, our sandwich-structured filter paper composite with superior EMI shielding performance can be used in the medical and military fields. [ABSTRACT FROM AUTHOR]

This study describes a method of synthesising pyridine, quinoline, and isoquinoline ketones using 2‐halogenated N‐heterocycles as the starting materials under mild reaction conditions. Considering the significance of pyridones in organic chemistry, developing novel, green synthetic strategies is highly desirable. The reaction employs H2O as the solvent and source of O, rendering it green, and it is simple to execute, with a broad substrate scope and an excellent functional group tolerance. [ABSTRACT FROM AUTHOR]

Recently, there has been a growing demand for ultra‐thin carbonized wood films (CWF) with high shielding efficiency (SE) to replace non‐renewable alternatives. Researchers aim to enhance electromagnetic (EM) wave absorption and improve electromagnetic interference (EMI) SE in CWF materials to reduce secondary pollution from reflected EM waves. In this work, the carbonized wood composite film (CWF/EP/Co) with a thickness of 120 µm through the process of hot‐pressing and carbonizing wood soaked in a mixed solution of water‐borne epoxy (EP) and Co/Zn‐MOF (ZIF‐67/8) is obtained. The CWF/EP/Co film exhibits excellent conductivity (105 S cm−1) and demonstrates an excellent EMI SE (73 dB) at a 200 µm thickness. Remarkably, the specific EMI shielding effectiveness (SSE/t) of CWF/EP/Co films reached 15833.3 dB·cm2·g−1 in the X‐band, making it the highest reported value among all wood‐derived EMI shielding materials. CWF/EP/Co films have a high absorption coefficient (A) of 0.4, indicating their effectiveness in absorbing EM waves. Furthermore, the EMI shielding effect of the large‐scale wallpaper (170 mm×170 mm) is confirmed by finite element analysis. Additionally, the CWF/EP/Co film exhibits good mechanical properties and effective Joule heating performance. This shielding film shows promise in applications such as buildings and smart homes, providing EMI shielding and warming effects. [ABSTRACT FROM AUTHOR]

[Display omitted] • Ultra-flexible bimetallic nanowire decorated foams via facile dip-coating method. • An ultra-low filler content of 0.22 vol% for high performances. • Effective microwave absorption of −69.61 dB with ultra-wide absorption bandwidth. • Integrated multi-functional applications in one. Nowadays, functional electronic devices with excellent flexibility and thermal management capability for effective electromagnetic wave absorption are urgently in demand. Herein, a novel and highly flexible silver nanowire (AgNW)/iron nanowire (FeNW) decorated melamine composite foam (AgFe-MF) was prepared via simple dip-coating process. Owing to optimal impedance matching, synergistic dielectric and magnetic losses as well as three-dimensional porous structure, the AgFe-MF with an ultra-low filler content (0.22 vol%) exhibited an outstanding minimum reflection loss of −69.61 dB, and the best effective absorption bandwidth (EAB) could reach up to 6.37 GHz. Importantly, the EAB of long-time working AgFe-MF was enhanced to 7.01 GHz after 1000 compress-release cycles under 40 % strain. Besides, it also featured considerate Joule heating capacity and achieved a saturation temperature of over 85.7 ℃ under 2.6 V voltage. The impressive thermal isolation and long-term stability ensured the safety used as portable heater. Therefore, this work will provide a vital slight for fabricating smart wearable electronic devices with integrated anti-electromagnetic radiation and personalized thermal management performances towards potential thermal and health threats. [ABSTRACT FROM AUTHOR]

[Display omitted] • A facile "chemical blowing" strategy is developed to expand the dense and micron-scale thickness walls into interconnected carbon nanosheets. • Zn(NO 3) 2 is proved to functioned as blowing agent, precursor of template, activator, and nitrogen dopant. • The optimized thick carbon monolith with high-mass loading (∼30 mg cm−2) delivers encouraging capacitive performance in low-temperature. Biomass-derived carbon materials are promising electrode materials for capacitive energy storage. Herein, inspired by the hierarchical structure of natural wood, carbon monoliths built up by interconnected porous carbon nanosheets with enriched vertical channels were obtained via zinc nitrate (Zn(NO 3) 2)-assisted synthesis and served as thick electrodes for capacitive energy storage. Zn(NO 3) 2 is proved to function as expansion agent, activator, dopant, and precursor of the template. The dense and micron-scale thickness walls of wood were expanded by Zn(NO 3) 2 into porous and interconnected nanosheets. The pore volume and specific surface area were increased by more than 430 %. The initial specific capacitance and rate performance of the optimized carbon monolith was approximately three times that of the pristine dense carbon framework. The assembled symmetric supercapacitor possessed a high initial specific capacitance of 4564 mF cm−2 (0–1.7 V) at −40 °C. Impressively, the robust device could be cycled more than 100,000 times with little capacitance attenuation. The assembled zinc-ion hybrid capacitor (0.2–2 V) delivered a large specific capacitance of 4500 mF cm−2 at −40 °C, approximately 74 % of its specific capacitance at 25 °C. Our research paves a new avenue to design thick carbon electrodes with high capacitive performance by multifunctional Zn(NO 3) 2 for low-temperature applications. [ABSTRACT FROM AUTHOR]

Inspired by creatures, abundant stimulus-responsive hydrogel actuators with diverse functionalities have been manufactured for applications in soft robotics. However, constructing a shape memory and self-sensing bilayer hydrogel actuator with high mechanical strength and strong interfacial bonding still remains a challenge. Herein, a novel bilayer hydrogel with a stimulus-responsive TEMPO-oxidized cellulose nanofibers/poly(N-isopropylacrylamide) (TOCN/PNIPAM) layer and a non-responsive TOCN/polyacrylamide (TOCN/PAM) layer is proposed as a thermosensitive actuator. TOCNs as a nano-reinforced phase provide a high mechanical strength and endow the hydrogel actuator with a strong interfacial bonding. Due to the incorporation of TOCNs, the TOCN/PNIPAM hydrogel exhibits a high compressive strength (~89.2 kPa), elongation at break (~170.7 %) and tensile strength (~24.0 kPa). The prepared PNIPAM/TOCN/PAM hydrogel actuator performs the roles of an encapsulation, jack, temperature-controlled fluid valve and temperature-control manipulator. The incorporation of Fe3+ further endows the bilayer hydrogel actuator with a synergistic performance of shape memory and temperature-driven, which can be used as a temperature-responsive switch to detect ambient temperature. The PNIPAM/TOCN/PAM-Fe3+ conductive hydrogel can be assembled into a flexible sensor and generate sensing signals when driven by temperature changes to achieve real-time feedback. This research may lead to new insights into the design and manufacturing of intelligent flexible soft robots. [Display omitted] [ABSTRACT FROM AUTHOR]

As a convenient photothermal material, polydopamine (PDA) has been widely utilized in wood-based evaporators. However, the loading conditions of polydopamine on biomass bulk materials have not been systematically studied. In this paper, the suitable reaction conditions of polydopamine were studied with rattan as the substrate, and a reference for the improvement of the loading conditions was proposed. The polydopamine-loaded rattan-based evaporator (PDA-R) prepared on this basis exhibits excellent working stability due to the unique large-scale hierarchical porous structure of rattan. In addition to excellent salt resistance and cycle performance (evaporation rate decays by 5.1% after 30 cycles), the larger-aperture channel (200–450 μm) also brings better adaptability to salinity changes than polydopamine-loaded basswood-based evaporator (PDA-BW) (the attenuation coefficient of PDA-R is 6.2%, while the attenuation coefficient of PDA-BW is 16.3%). All of these indicate the broad prospects of polydopamine-loaded rattan-based evaporator as a multi-effect treatment scheme of brine. [Display omitted] • Loading conditions of polydopamine on biomass block material is systematic studied. • PDA-R has excellent salt resistance and cycling performance in high salinity brines. • PDA-R has great adaptability to salinity changes. • The effect of uniformly dense pore size of the substrate on salinity adaptability of evaporator is explored. [ABSTRACT FROM AUTHOR]

Amidst the burgeoning interest in multifunctional superhydrophobic wood-based composites (SWBCs) for their varied applications and the need for improved environmental resilience, recent efforts focus on enhancing their utility by integrating features such as mechanical and chemical stability, self-healing capabilities, flame resistance, and antimicrobial properties. Research indicates that various external conditions can influence the wettability and additional characteristics of SWBCs. This comprehensive review outlines three critical factors affecting SWBCs' performance: synthesis methods, wood taxonomy, and chemical agents. It further provides a detailed overview of SWBCs' specific attributes, including essential qualities for diverse applications and the limitations posed by different contexts. Additionally, it elaborates on performance evaluation techniques, offering a foundational framework for SWBCs' practical application. This work aims to serve as an important resource for future research and development in SWBC engineering. [Display omitted] • Preparation mechanism of superhydrophobic wood-based composites. • Factors affecting superhydrophobic wood-based composites. • Methods for evaluating superhydrophobic wood-based composites properties. • Challenges and directions for future development to achieve industrialization are presented. [ABSTRACT FROM AUTHOR]

Developing high-performance microwave absorption (MA) materials becomes an urgent concern in the field of electromagnetic protection. Constructing porous framework is an efficient approach to MA owing to the abilities of adjusting impedance matching and providing more reflection and scattering paths for electromagnetic waves. Herein, a cellulose nanofibril (CNF)/honeycomb-like carbon-shell encapsulated FeCoNi@C/carbon nanotube (CNT) composite aerogel was fabricated via a facile freeze-drying method. The super-lightweight composites showed a distinctive gradient structure for reflection and scattering inside aerogel pores, micrometer small pores, and nano-fillers on the pore walls. The composite aerogel showed an ideal minimum reflection loss (RL min) of −43.6 dB and remarkable adjustable effective absorption bandwidth (EAB) of 12.18 GHz due to good impedance matching, unique gradient porous structure, and synergies of multiple loss mechanisms. Therefore, this work will provide a viable strategy to improve the MA capability of absorbers by taking full advantage of constructing gradient reflection and scattering porous structure. [Display omitted] [ABSTRACT FROM AUTHOR]

[Display omitted] • Two basic design strategies for 3D COFs: high valency and functionalization. • 3D COFs: building blocks, topology, linkage, and PSM strategy. • Applications in adsorption and separation, catalysis, stimulus response, conduction and energy storage. • The challenges and opportunities are proposed for future research. Covalent organic frameworks (COFs) are a class of porous crystalline organic materials. The dynamic chemistry of covalent bonding and the applications of COFs have made great progress already. Three-dimensional (3D) COFs have attracted much attention in recent years because of their more diverse spatial structures and interconnected pore properties. High valency and functionalization are two key strategies of 3D COFs design, including the development of building blocks, topology, linkage and post synthetic modification strategy. As a result, the diversity of COF spatial structures is significantly extending and various applications in energy, environment, biology and chemical catalysis are developing. In this review, we summarized the recent articles about 3D COFs in the field of framework design, function development and applications, and put forward the critical strategies and comment, the future perspectives of the field are also prospected. [ABSTRACT FROM AUTHOR]

[Display omitted] Self-supporting tree skeleton and densely stackable phenolic resin are cleverly coupled together by a "rebar-concrete" structure. The thick electrode as a master of space utilization has extremely high areal and volumetric energy density. This work confirms the effective coupling of the self-supporting skeleton and powder materials, providing novel ideas for the preparation of thick electrodes with high mass loading. • A "rebar-concrete" structure is proposed to facilitate the high space utilization of thick electrodes. • The areal capacitance of the thick electrode reaches an astonishing 11F cm−2. • The assembled SSC device delivers competitive areal energy density of 0.63 mWh cm−2. The thick electrode design with high packing density of active materials can increase the capacity in a limited space. However, the key challenge is still to develop a system with high space utilization and ensure electron/ion transport in thick electrode. This work proposes an interesting "rebar-concrete" structure, which successfully prepared wood/phenolic resin-derived thick electrode with high space utilization by in-situ polymerization of phenolic resin (concrete) in the wood (rebar) channel. The electrode exhibits an excellent three-dimensional interconnected hierarchical pore structure due to the uniform activation of in-situ anchored KOH particles. The mass loading (35 mg cm−2) and areal capacitance (11F cm−2) of the obtained composite electrode are increased to 446 % and 1257 % of the original balsa wood, respectively. The assembled symmetric supercapacitor (SSC) exhibits a high energy density of 0.63 mWh cm−2 (3.91 mWh cm−3) and an excellent cycle stability (95 % retention after 50 000 cycles), showing good practicability in lighting LEDs or driving a fan. This strategy achieves effective coupling of self-supporting skeleton and powder materials, providing more insights and possibilities for the preparation of high energy density thick electrodes. [ABSTRACT FROM AUTHOR]

Nowadays, electromagnetic pollution caused by the development of communication technology and electronic equipment has become an urgent problem to be solved. It is an effective solution to design high-performance electromagnetic wave absorption (EWA) materials with wide-band and powerful absorption characteristics for electromagnetic protection. In this work, a multi-scale MXene/carbon nanotube@Fe 3 O 4 composite material with a heterogeneous structure was synthesized by a solvothermal method, and the high/low-frequency EWA operating bands were adjusted by component regulation. The composite material performed excellent EWA performances based on the synergistic effect of polarization loss, conductive and magnetic loss, and three-dimensional heterointerfaces. Its minimum reflection loss reached − 59.95 dB with an effective absorption bandwidth of 4.7 GHz (13.3–18 GHz), which basically covered the Ku band. Therefore, this feasible scheme is expected to provide an effective strategy for controlling military and civil electromagnetic pollution. [Display omitted] • A facile preparation method of MXene-based multiscale composites was proposed. • Military/civil EWA operating frequency bands were adjusted by component regulation. • A superior RL min value of − 59.95 dB was obtained based on complex loss mechanisms. [ABSTRACT FROM AUTHOR]

The Review summarized and analyzed the modification strategies and application directions of ZIF-67 in photocatalysis. [Display omitted] • An introduction to the structure and properties of ZIF-67 is provided. • The synthetic pathways of ZIF-67 and its derivatives are summarized. • The regulation mechanism and improvement strategy of photocatalytic performance are discussed. • Pioneering and interdisciplinary application in the field of photocatalysis based on ZIF-67. • Application prospects and challenges of ZIF-67 in photocatalysis. Cobalt-based zeolitic imidazolate frameworks (Co-ZIF) have attracted intensive interest in multivariate applications because of their high specific surface area and presence of great active sites. At present, most of the reviews on ZIF-67 focus on electrocatalysis and degradation. This review mainly discusses the application of ZIF-67 and its derivatives in photocatalysis to fill the gap in this field. The structural properties of ZIF-67 and the preparation methods of ZIF-67-derived materials are firstly introduced. Subsequently, we summarize the strategies to improve the photocatalytic performance of ZIF-67, such as ion doping, construction of heterojunctions, and solution etching. Thirdly, the recent applications of ZIF-67 and its derivatives in photocatalysis, such as CO 2 reduction, H 2 production, degradation, and antibacterial are discussed. Finally, the Review summarizes the current development status of ZIF-67 in photocatalysis and provides an outlook on its future development trend and development constraints. [ABSTRACT FROM AUTHOR]

With the rapid development of the Internet of Things, nanogenerator as a green energy collection technology has attracted great attention in various fields. Specifically, the natural renewable nanocellulose as a raw material can significantly improve the environmental friendliness of the nanocellulose-based nanogenerators, which also makes the nanocellulose based nanogenerators expected to further develop in areas such as wearable devices and sensor networks. This paper mainly reports the application of nanocellulose in nanogenerator, focusing on the sensor. The types, sources and preparation methods of nanocellulose are briefly introduced. At the same time, the special structure of nanocellulose highlights the advantages of nanocellulose in nanogenerators. Then, the application of nanocellulose-based nanogenerators in sensors is introduced. Finally, the future development prospects and shortcomings of this nanogenerator are discussed. [ABSTRACT FROM AUTHOR]

Herein, we used a one-pot method to fabricate a novel MOF-on-MOF adsorbent, namely MOF(Zr)-on-MOF(Ce). The adsorbent demonstrated a high maximum fluoride-ions capture capacity of 164.47 mg g−1. The morphology, elemental distribution, pore size distribution, and thermal stability were studied using SEM-EDS, XRD, BET, and TGA. The influence of the temperature, solution pH, fluoride concentration, and coexisting ions was explored using intermittent experiments. The results suggested that MOF(Zr)-on-MOF(Ce) had a fast capture rate for fluoride. MOF(Zr)-on-MOF(Ce) maintained an excellent fluoride removal performance over a wide pH range with an initial fluoride concentration of 20 mg L−1. The optimal effect was obtained at a pH of 4, but a high removal efficiency of 94% was maintained even at a pH of 9. Interference experiments showed that only the PO 4 3– had an adverse inhibition influence. The field experiments demonstrated that MOF(Zr)-on-MOF(Ce) can keep the safety threshold levels of fluoride in drinking water. The Langmuir and pseudo-second order kinetic models were well fitted for the defluoridation process, demonstrating that the adsorption of fluoride ions on MOF(Zr)-on-MOF(Ce) was dominated by monolayer chemisorption. With the further characterization and kinetic thermodynamic studies indicates that the removal mechanism involves ion exchange, electrostatic interactions and complexation effect. [Display omitted] • A novel MOF(Zr)-on-MOF(Ce) adsorbent were fabricated via one-pot methods for defluorination. • The maximum adsorption capacity of MOF(Zr)-on-MOF(Ce) was 164.47 mg g–1 for F ions. • The adsorbent had an excellent defluoridation performance with a wide pH range. • The mechanisms are ion-exchange, electrostatic interaction and complexation effect. [ABSTRACT FROM AUTHOR]

Nanocellulose, as a nanoscale polymer material, has garnered significant attention worldwide due to its numerous advantages including excellent biocompatibility, thermal stability, non-toxicity, large specific surface area, and good hydrophilicity. Various methods can be employed for the preparation of nanocellulose. Traditional approaches such as mechanical, chemical, and biological methods possess their own distinct characteristics and limitations. However, with the growing deterioration of our living environment, several green and environmentally friendly preparation techniques have emerged. These novel approaches adopt eco-friendly technologies or employ green reagents to achieve environmental sustainability. Simultaneously, there is a current research focus on optimizing traditional nanocellulose preparation methods while addressing their inherent drawbacks. The combination of mechanical and chemical methods compensates for the limitations associated with using either method alone. Nanocellulose is widely used in wound dressings owing to its exceptional properties, which can accelerate the wound healing process and reduce patient discomfort. In this paper, the principle, advantages and disadvantages of each preparation method of nanocellulose and the research findings in recent years are introduced Moreover, this review provides an overview of the utilization of nanocellulose in wound dressing applications. Finally, the prospective trends in its development alongside corresponding preparation techniques are discussed. [ABSTRACT FROM AUTHOR]

• A green and common method was proposed to prepare biomimetic actuators. • The PNPB actuator showed excellent multi-stimulus response and synergistic effect. • Anisotropic natural bamboo endowed the PNPB actuator programmable performance. • The PNPB actuator had application potential in complex environment. Hydrogel actuators with controllable deformation and excellent biocompatibility are widely used in soft robot, valve, drug delivery and lenses. However, the stimulation response performance of existing hydrogel actuators mostly focuses on a single active layer, which greatly affects its driving performance and service life. In this work, we integrate temperature-responsive hydrogel (Poly (N-isopropyl acrylamide), PNIPAM) and pH-responsive hydrogel (polyacrylic acid, PAAc) into one system to fabricate a dual active layer composite hydrogel actuator with high performance. Based on the PAAc hydrogels achieving contract or expand at different pH values, the obtained actuator exhibits admirable bidirectional bending characteristics. In addition, the anisotropic bamboo sheet endows the hydrogel actuator with programmable 3 D complex deformation. Benefitting from the synergy and different responsiveness between the two active layers, the hydrogel actuator not only has multiple response performance, but also greatly improves its deformation degree and response speed. More importantly, these promising properties of the actuator have broad application prospects in the development of pattern design and intelligent switch. This work proposes a promising strategy for the structural design of hydrogel actuators with excellent performance, and encourages more exploration of the application range of the actuator. [ABSTRACT FROM AUTHOR]

The absorption performance of broadband electromagnetic waves is of utmost importance in safeguarding diverse electronic equipment against electromagnetic wave pollution, necessitating materials with low density, thin thickness, and cost-effectiveness to be employed. This study presents the successful synthesis of biomass-derived carbon (BC) composites via the hydrothermal method, utilizing moss coated with flower-like CuS. The CuS was uniformly dispersed on BC matrix, contribute to dipole polarization relaxation. The formation of heterogeneous interfaces between CuS and the BC phase resulted in significant polarization loss. Additionally, the wrinkled BC and flower like CuS constructed by nanosheets boosted scattering of electromagnetic wave due to its large specific surface area, which can provide additional channels for charge transfer and avail dissipation of electromagnetic wave energy. With an efficient absorption bandwidth (EAB) that encompasses the whole X band, the electromagnetic waves absorption (EMA) performance of CuS/BC composites was able to reach a minimum reflection loss of − 28.8 dB. • A simple preparation method of biomass-derived carbon (BC) composites was proposed. • The wrinkled BC and flower like CuS boosted scattering of electromagnetic wave. • The CuS/BC composites reached a superior minimum reflection loss of − 28.8 dB. [ABSTRACT FROM AUTHOR]

Three-dimensional (3D) heterogeneous flower-like spherical MoS 2 /CNTs composites with worm-like interfaces were successfully fabricated by a simplified solvothermal reaction to achieve superb electromagnetic wave absorption (EWA) properties. The microstructure characteristics, morphology features, EWA performance and associated mechanism of as-prepared specimen were systematically analyzed. The incorporation of MoS 2 resulted in the establishment of a 3D conductive network and a substantial augmentation of the heterogeneous interfaces between MoS 2 and carbon nanotubes (CNTs), thereby inducing an amplified conductance loss and polarization loss, respectively. Moreover, the fabrication of 3D architecture not only enhances the structural robustness of the composites, but also broadens the avenue for electromagnetic wave (EW) reflection and scattering, thus augmenting the absorption of EW energy. As a result of the synergistic effect of augmented attenuation capability as well as optimized impedance matching, the EWA performance of materials was outstanding, with a minimum reflection loss (RL min) of −52.1 dB and an effective absorption bandwidth (EAB) of 1.93 GHz achieved at a thin thickness of 2.46 mm in the X band. This research will serve as a meaningful point of reference for exploring 3D flower-like spherical structure of EW absorber. [Display omitted] • 3D heterogeneous flower-like spherical MoS 2 /CNTs composites were prepared. • MoS 2 /CNTs composites have worm-like interfaces. • Superior EMA performance was achieved with minimum reflection loss was −52.1 dB. • The impedance matching and polarization loss was enhanced with MoS 2. • The electromagnetic wave absorption mechanism was proposed. [ABSTRACT FROM AUTHOR]