Suppressing the Exacerbated Hydrogen Evolution of Porous Zn Anode with an Artificial Solid-Electrolyte Interphase Layer.

Rechargeable Zn batteries are widely studied as aqueous, safe, and environmentally friendly alternatives to Li-ion batteries. The 3D porous Zn anode has been extensively reported for suppressing Zn dendrite growth and accelerating the electrode kinetics. However, we demonstrate herein that the undesirable hydrogen evolution reaction (HER) is also exacerbated for porous Zn electrode. Therefore, a polytetrafluoroethylene (PTFE) coating is further applied on the porous Zn serving as the artificial solid-electrolyte interphase (SEI), which is demonstrated to effectively inhibit the hydrogen evolution and maintain the Zn plating kinetics. By utilizing the synergistic effects of the porous morphology and artificial SEI layer, better performances are obtained over porous Zn or bare Zn foil, including dendrite-free Zn plating/stripping up to 2000 h at 2 mA cm-2 and extended cycling in the Zn||V2O5 cell. This work suggests two complementary strategies for achieving simultaneously dendrite-free and side-reaction-suppressed Zn batteries.

Enhanced Photoluminescence of Flexible InGaN/GaN Multiple Quantum Wells on Fabric by Piezo-Phototronic Effect.

Fabric-based wearable electronics are showing advantages in emerging applications in wearable devices, Internet of everything, and artificial intelligence. Compared to the one with organic materials, devices based on inorganic semiconductors (e.g., GaN) commonly show advantages of superior characteristics and high stability. Upon the transfer of GaN-based heterogeneous films from their rigid substrates onto flexible/fabric substrates, changes in strain would influence the device performance. Here, we demonstrate the transfer of InGaN/GaN multiple quantum well (MQW) films onto flexible/fabric substrates with an effective lift-off technique. The physical properties of the InGaN/GaN MQWs film are characterized by atomic force microscopy and high-resolution X-ray diffraction, indicating that the transferred film does not suffer from huge damage. Excellent flexible properties are observed in the film transferred on fabric, and the photoluminescence (PL) intensity is enhanced by the piezo-phototronic effect, which shows an increase of about 10% by applying an external strain with increasing the film curvature to 6.25 mm-1. Moreover, energy band diagrams of the GaN/InGaN/GaN heterojunction at different strains are illustrated to clarify the internal modulation mechanism by the piezo-phototronic effect. This work would facilitate the guidance of constructing high-performance devices on fabrics and also push forward the rapid development of flexible and wearable electronics.

Dynamically Crosslinked Dry Ion-Conducting Elastomers for Soft Iontronics.

Soft ionic conductors show great promise in multifunctional iontronic devices, but currently utilized gel materials suffer from liquid leakage or evaporation issues. Here, a dry ion-conducting elastomer with dynamic crosslinking structures is reported. The dynamic crosslinking structures endow it with combined advantageous properties simultaneously, including high ionic conductivity (2.04 × 10-4 S cm-1 at 25 °C), self-healing capability (96% healing efficiency), stretchability (563%), and transparency (78%). With this ionic conductor as the electrode, two soft iontronic devices (electroluminescent devices and triboelectric nanogenerator tactile sensors) are realized with entirely self-healing and stretchable capabilities. Due to the absence of liquid materials, the dry ion-conducting elastomer shows wide operational temperature range, and the iontronic devices achieve excellent stability. These findings provide a promising strategy to achieve highly conductive and multifunctional soft dry ionic conductors, and demonstrate their great potential in soft iontronics or electronics.

Wearable Antifreezing Fiber-Shaped Zn/PANI Batteries with Suppressed Zn Dendrites and Operation in Sweat Electrolytes.

Fiber-shaped Zn batteries are promising candidates for wearable electronics owing to their high energy and low cost, but further studies are still required to address the issues related to detrimental Zn dendrite growth and limited low-temperature performances. Here, we report an antifreeze, long-life, and dendrite-free fiber-shaped Zn battery using both nanoporous Zn and polyaniline (PANI) electrodeposited on carbon nanofibers (CFs) as the cathode and anode, respectively. The fiber-shaped Zn anode achieves stable plating/stripping for 1000 mAh cm-2 accumulative capacity with low polarization (30 mV) at a current density of 2 mA cm-2. The dendrite-free Zn electrodes also enable the stable cycling of the fiber battery with 75.1% capacity retention after 1000 cycles. With an antifreeze agent added in the gel electrolyte, the fiber battery maintains excellent performance at temperatures as low as -30 °C. Lastly, by utilizing the doping/dedoping mechanism of Cl- in the PANI electrode, we achieve, for the first time, a Zn battery using human sweat as a harmless electrolyte. Our work provides a long-life and antifreeze fiber-shaped battery that is highly promising for future wearable energy storage devices.

Textile Triboelectric Nanogenerators Simultaneously Harvesting Multiple "High-Entropy" Kinetic Energies.

Distributed renewable kinetic energies are ubiquitous but with irregular amplitudes and frequencies, which, as one category of "high-entropy" energies, are crucial for next-generation self-powered electronics. Herein, we present a flexible waterproof dual-mode textile triboelectric nanogenerator (TENG), which can simultaneously scavenge multiple "high-entropy" kinetic energies, including human motions, raindrops, and winds. A freestanding-mode textile TENG (F-TENG) and a contact-separation-mode textile TENG (CS-TENG) are integrated together. The structure parameters of the textile TENG are optimized to improve the output performances. The raindrop can generate a voltage of up to ∼4.3 V and a current of about ∼6 µA, while human motion can generate a voltage of over 120 V and a peak power density of ∼500 mW m-2. The scavenged electrical energies can be stored in capacitors for powering small electronics. Therefore, we demonstrated a facile preparation of a TENG-based energy textile that is highly promising for kinetic energy harvesting and self-powered electronics.

Stretchable Coplanar Self-Charging Power Textile with Resist-Dyeing Triboelectric Nanogenerators and Microsupercapacitors.

The integration between energy-harvesting and energy-storage devices into a self-charging power unit is an effective approach to address the energy bottleneck of wearable/portable/wireless smart devices. Herein, we demonstrate a stretchable coplanar self-charging power textile (SCPT) with triboelectric nanogenerators (TENGs) and microsupercapacitors (MSCs) both fabricated through a resist-dyeing-analogous method. The textile electrodes maintain excellent conductivity at 600% and 200% tensile strain along course and wale directions, respectively. The fabric in-plane MSC with reduced graphene oxides as active materials reaches a maximum areal capacitance of 50.6 mF cm-2 at 0.01 V s-1 and shows no significant degradation at 50% of tensile strain. The stretchable fabric-based TENG can output 49 V open-circuit voltage and 94.5 mW m-2 peak power density. Finally, a stretchable coplanar SCPT with one-batch resist-dyeing fabrication is demonstrated for powering small electronics intermittently without extra recharging. Our approach is also compatible with conventional textile processing and suggests great potential in electronic textiles and wearable electronics.

Shape-Adaptive, Self-Healable Triboelectric Nanogenerator with Enhanced Performances by Soft Solid-Solid Contact Electrification.

The viable application of soft electronics/robotics relies on the development of power devices which are desired to be flexible, deformable, or even self-healable. We report here a shape-adaptive, self-healable triboelectric nanogenerator (SS-TENG) for harvesting biomechanical energies. The use of a viscoelastic polymer, normally known as Silly Putty, as the electrification material and as the matrix of a carbon-nanotube-filled composite (CNT-putty) electrode endows the SS-TENG the capability of adapting to arbitrary irregular surfaces and instantaneous healing from mechanical damage (almost completely recovered in 3 min without extra stimuli). Furthermore, the output performances of the SS-TENG have also been significantly improved because (i) the ideal soft contact is achieved at the solid-solid interfaces for more effective contact electrification and (ii) the introduced cation dopants make the putty even more tribo-negative than polytetrafluoroethylene. The SS-TENG can be adhered to any curvy surface, tailored, and reshaped into arbitrary configurations and utilized as a power supply for small electronics, suggesting promising applications in soft electronics/robotics in the future.

Resist-Dyed Textile Alkaline Zn Microbatteries with Significantly Suppressed Zn Dendrite Growth.

The progress of electronic textiles relies on the development of sustainable power sources without much sacrifice of convenience and comfort of fabrics. Herein, we present a rechargeable textile alkaline Zn microbattery (micro-AZB) fabricated by a process analogous to traditional resist-dyeing techniques. Conductive patterned electrodes are realized first by resist-aided electroless/electrodeposition of Ni/Cu films. The resulting coplanar micro-AZB in a single textile, with an electroplated Zn anode and a Ni0.7Co0.3OOH cathode, achieves high energy density (256.2 Wh kg-1), high power density (10.3 kW kg-1), and stable cycling performances (82.7% for 1500 cycles). The solid-state micro-AZB also shows excellent mechanical reliability (bending, twisting, tailoring, etc.). The improved reversibility and cyclability of textile Zn electrodes over conventional Zn foils are found to be due to the significantly inhibited Zn dendrite growth and suppressed undesirable side reactions. This work provides a new approach for energy-storage textile with high rechargeability, high safety, and aesthetic design versatility.

Triboelectric-Nanogenerator-Based Soft Energy-Harvesting Skin Enabled by Toughly Bonded Elastomer/Hydrogel Hybrids.

A major challenge accompanying the booming next-generation soft electronics is providing correspondingly soft and sustainable power sources for driving such devices. Here, we report stretchable triboelectric nanogenerators (TENG) with dual working modes based on the soft hydrogel-elastomer hybrid as energy skins for harvesting biomechanical energies. The tough interfacial bonding between the hydrophilic hydrogel and hydrophobic elastomer, achieved by the interface modification, ensures the stable mechanical and electrical performances of the TENGs. Furthermore, the dehydration of this toughly bonded hydrogel-elastomer hybrid is significantly inhibited (the average dehydration decreases by over 73%). With PDMS as the electrification layer and hydrogel as the electrode, a stretchable, transparent (90% transmittance), and ultrathin (380 µm) single-electrode TENG was fabricated to conformally attach on human skin and deform as the body moves. The two-electrode mode TENG is capable of harvesting energy from arbitrary human motions (press, stretch, bend, and twist) to drive the self-powered electronics. This work provides a feasible technology to design soft power sources, which could potentially solve the energy issues of soft electronics.

Hierarchically porous carbon/red phosphorus composite for high-capacity sodium-ion battery anode.

Red phosphorus has received remarkable attention as a promising anode material for sodium ion batteries (NIBs) due to its high theoretical capacity. However, its practical application has been impeded by its intrinsic low electronic conductivity and large volume variations during sodiation/desodiation process. Here, we design a composite to confine nanosized red phosphorus into the hierarchically porous carbon (HPC) walls by a vaporization-condensation strategy. The mass loading of P in the HPC/P composite is optimized to deliver a reversible specific capacity of 2,202 mAh/gp based on the mass of red P (836 mAh/gcomposite based on the total composite mass), a high capacity retention over 77% after 100 cycles, and excellent rate performance of 929 mAh/gp at 2 C. The hierarchical porous carbon serves as the conductive networks, downsize the red phosphorus to nanoscale, and provide free space to accommodate the large volume expansions. The suppressed mechanical failure of the red phosphorus also enhances the stability of solid-electrolyte interface (SEI) layer, which is confirmed by the microscopy and impedance spectroscopy after the cycling tests. Our studies provide a feasible approach for potentially viable high-capacity NIB anode.