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Electromagnetic interference (EMI) shielding fabrics are crucial in addressing the increasingly serious electromagnetic pollution. To meet wearable requirements, stretchability and thermal comfortability are often desired, but which still are challenging. Herein, a stretchable EMI shielding fabric is fabricated via electrospinning coupled with biaxial pre‐stretching spraying, in which a block stacking wrinkled silver nanowire (AgNW)/Ti3C2Tx MXene network is coated on one side of electrospun thermoplastic polyurethane (TPU)/polydimethylsiloxane (PDMS) fabric. As expected, the wrinkled structure protects conductive network from fracture during stretching process, so as to realize the strain‐invariant electrical conductivity. Thus, the fabric exhibits a stretchable EMI shielding performance of over 40 dB when subjected to 10–50% uniaxial strains or 21–125% biaxial strains. More importantly, the white TPU/PDMS side and the black AgNW/MXene side enable the fabric passive radiative cooling and heating, respectively. The cooling side exhibits high mid‐infrared emissivity (97.5%) and solar reflectance (90%), thus reducing the skin temperature by ≈4.9 °C. The heating side with high solar absorptivity (86.6%) and photothermal effect increased the skin temperature by ≈5 °C. Therefore, the fabirc with stretchable EMI shielding and Janus‐type dual‐mode personal passive thermal management is promising in future wearable products. [ABSTRACT FROM AUTHOR]

The development of flexible and adaptable multifunctional sensing systems for human–machine interaction, especially for animal voice‐emotion identification, is highly desirable yet quite challenging. Herein, a multifunctional triboelectric nanogenerator (TENG) based on ordered hierarchical microhump arrays is proposed and fabricated by template‐assisted electrospinning with a facile, low‐cost, and expandable manufacturing process. Performances of a single‐electrode TENG based on the patterned nanofiber films with microhump arrays (NFM‐TENG) are studied in detail by varying mesh number of the template. Electric field structure of the collector is altered by pore sizes, wire diameters, and protrusions of the receiving templates subjected to different mesh numbers, generating different degrees of microhump arrays on the surface of the nanofiber film. NFM‐TENG demonstrates high sensitivity (15.94 mV Pa−1), fast response and recovery time (76 and 58 ms), a large power density of 122 mW m−2, and excellent ability of structural retention. Integrated with four functions of energy harvesting, pressure sensing, human physiological sensing, and animal voice‐emotion identification, NFM‐TENG achieves real‐time monitoring of human physiological, motion, handwriting, and animal voice‐emotion signals without an external power supply. This study shows significant application strategies for self‐powered human–machine interaction devices, novel animal voice‐emotion identification, biodiversity conservation, and so on. [ABSTRACT FROM AUTHOR]

Continuous miniaturization of semiconductor devices is the key to boosting modern electronics development. However, this downscaling strategy has been rarely utilized in photoelectronics and photovoltaics. Here, in this work, a full‐van der Waals (vdWs) 1D p‐Te/2D n‐Bi2O2Se heterodiode with a rationally designed nanoscale ultra‐photosensitive channel is reported. Enabled by the dangling bond‐free mixed‐dimensional vdWs integration, the Te/Bi2O2Se type‐II diodes show a high rectification ratio of 3.6 × 104. Operating with 100 mV reverse bias or in a self‐power mode, the photodiodes demonstrate excellent photodetection performances, including high responsivities of 130 A W−1 (100 mV bias) and 768.8 mA W−1 (self‐power mode), surpassing most of the reports of other heterostructures. More importantly, a superlinear photoelectric conversion phenomenon is uncovered in these nanoscale full‐vdWs photodiodes, in which a model based on the in‐gap trap‐assisted recombination is proposed for this superlinearity. All these results provide valuable insights in light–matter interactions for further performance enhancement of photoelectronic devices. [ABSTRACT FROM AUTHOR]

Compared with conventional liquid batteries, all‐solid‐state batteries (ASSBs) show great promise for enabling higher safety in electric vehicles without compromising operational durability and range. As a key component of ASSBs, solid‐state electrolytes (SSEs) need high ionic conductivity and favorable interfacial compatibility between electrodes and SSEs. In the recent decade, numerous efforts have been devoted to SSE advancement and fruitful achievements have been made, particularly regarding metal anode‐oriented SSEs with high energy density. This review focuses on the historical process of SSEs employed in ASSBs. The new understanding and origins for the enhanced ionic conductivity and mechanical properties of SSEs are first summarized. As to the cathode/SSE interface, its decomposition mechanism and modification strategies are analyzed. As to the interfacial issues of SSEs with anodes, the mechanisms of dendrite formation and penetration into the SSEs are discussed in detail. Additionally, assisted by a library of big data sources, contributions are systematically highlighted from different countries, institutions, and corresponding authors to significantly advance SSE progress, and certain insights are provided into the underlying relationships between various items in a collective manner. Finally, current challenges and potential strategies are identified for the future development of SSEs in ASSBs. [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]

Enhancing the piezoelectricity of polymers while maintaining all components organic is still challenging but significantly important for developing flexible wearable energy harvesters and self‐powered devices. Here, a novel and versatile strategy is introduced to construct mixed‐dimensional all‐organic polymer heterostructures (MPHs) for enhanced piezoelectricity. By combining all‐polymer 1D nanofibers (NFs) with 2D crystals through epitaxial crystallization‐driven assembly (ECA), MPHs are engineered to capitalize on the synergistic effects of both dimensional nanostructures. The intrinsic piezoelectric activity of 1D NFs is amplified by the growth of 2D crystals, enhancing force‐sensitivity and overall piezoelectricity. The mixed‐dimensional assembly not only enables controlled in‐situ growth of MPHs, but also simultaneously induces preferential formation of electroactive phases through solvent‐induced phase transition. By modulating the epitaxial growth of 2D crystals on 1D NFs, effective tuning of MPH growth amount and morphology is achieved, resulting in significant improvements in deformability, dipole polarization, and durability. MPHs exhibit remarkable piezoelectric improvements, achieving higher output under lower‐level forces with a record‐high sensitivity of ≈670 mV kPa−1. Their superior responsivity enables the development of self‐powered wireless wearable motion‐monitoring systems for real‐time physiological movement detection and analysis. This work inspires the development of all‐organic piezoelectric devices for innovative flexible energy‐harvesting and sensing applications. [ABSTRACT FROM AUTHOR]