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Phase change materials (PCMs) are pivotal in thermal energy management and conversion applications owing to their exceptional thermal energy storage and release characteristics. However, persistent challenges such as poor thermal conductivity and leakage issues have impeded their widespread adoption. While existing approaches mitigate these challenges by constructing and incorporating 3D thermal conductive networks, they are constrained by discontinuous preparation methods and mold size limitations. Herein, a scalable sol–gel permeation assembly strategy is proposed to prepare phase change layered film by in situ filling polyethylene glycol (PEG) in aramid nanofibers (ANF)/graphene nanoplates (GNP) network. Befitting from the laminated network encapsulation effect of ANF and GNP, the phase change film demonstrates leak‐free and stable phase transition behavior, even after undergoing 500 heating/cooling cycles. Moreover, the resulting PEG/ANF/GNP layered film exhibits an impressive in‐plane thermal conductivity of 23.7 W mK−1 at GNP loading of 28.1 vol.%, rendering it suitable for thermal management applications in electronic devices. The phase change layered film possesses exceptional photo‐thermal conversion properties, maintaining temperatures exceeding 90 °C under a light power density of 200 mW cm−2. Capitalizing on the thermally induced flexibility of the phase transition film and its temperature‐dependent stiffness, its utility extended to developing a light‐thermal driving gripper. [ABSTRACT FROM AUTHOR]

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]

Electronic skin is increasingly receiving tremendous attention for its potential applications in medical rehabilitation and human‐machine interaction. However, the trade‐off between detection range and sensitivity of e‐skin has not been well addressed, although various strategies have been proposed. Interlocked microridges between the epidermis and dermis can effectively transfer stress to mechanoreceptors, allowing human skin to exhibit excellent sensitivity even upon both subtle and large external stimuli. Herein, inspired by human skin, a novel bionic e‐skin is developed in which interlocked microridges are introduced between the sensitive layer and interdigitated electrode. Thanks to the interlocked microridges, excellent compression capability and remarkable change of contact area between sensitive layer and interdigitated electrode can be achieved and the e‐skin exhibits an ultrahigh sensitivity (≈1502.5 kPa−1), excellent durability (10 000 cycles), a short response time (10 ms) as well as a wide detection range (≈160 kPa). Moreover, due to the effective transmission of external stress from a sensitive layer to an interdigitated electrode, such bionic e‐skin has ability to detect a wide range of human vital signs and vibrations caused by sound waves. Such facile preparation of bionic interlocked microridges opens a new pathway to achieve high‐performance e‐skins and extend their application prospects in future wearable intelligent systems. [ABSTRACT FROM AUTHOR]

With the rapid development of intelligent wearable technology, multimodal tactile sensors capable of data acquisition, decoupling of intermixed signals, and information processing have attracted increasing attention. Herein, a decoupled temperature–pressure dual‐mode sensor is developed based on single‐walled carbon nanotubes (SWCNT) and poly(3,4‐ethylenedioxythiophene): poly(styrenesulfonate) (PEDOT:PSS) decorated porous melamine foam (MF), integrating with a deep learning algorithm to obtain a multimodal input terminal. Importantly, the synergistic effect of PEDOT:PSS and SWCNT facilitates the sensor with ideal decoupling capability and sensitivity toward both temperature (38.2 µV K−1) and pressure (10.8% kPa−1) based on the thermoelectric and piezoresistive effects, respectively. Besides, the low thermal conductivity and excellent compressibility of MF also endow it with the merits of a low‐temperature detection limit (0.03 K), fast pressure response (120 ms), and long‐term stability. Benefiting from the outstanding sensing characteristics, the assembled sensor array showcases good capacity for identifying spatial distribution of temperature and pressure signals. With the assistance of a deep learning algorithm, it displays high recognition accuracy of 99% and 98% corresponding to “touch” and “press” actions, respectively, and realizes the encrypted transmission of information and accurate identification of random input sequences, providing a promising strategy for the design of high‐accuracy multimodal sensing platform in human–machine interaction. [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]