3D Printing of Hydrogels for Stretchable Ionotronic Devices

In the booming development of flexible electronics represented by electronic skins, soft robots, and human–machine interfaces, 3D printing of hydrogels, an approach used by the biofabrication community, is drawing attention from researchers working on hydrogel-based stretchable ionotronic devices. Such devices can greatly benefit from the excellent patterning capability of 3D printing in three dimensions, as well as the free design complexity and easy upscale potential. Compared to the advanced stage of 3D bioprinting, 3D printing of hydrogel ionotronic devices is in its infancy due to the difficulty in balancing printability, ionic conductivity, shape fidelity, stretchability, and other functionalities. In this review, a guideline is provided on how to utilize the power of 3D printing in building high-performance hydrogel-based stretchable ionotronic devices mainly from a materials’ point of view, highlighting the systematic approach to balancing the printability, printing quality, and performance of printed devices. Various 3D printing methods for hydrogels are introduced, and then the ink design principles, balancing printing quality, printed functions, such as elastic conductivity, self-healing ability, and device (e.g., flexible sensors, shape-morphing actuators, soft robots, electroluminescent devices, and electrochemical biosensors) performances are discussed. In conclusion, perspectives on the future directions of this exciting field are presented.     

A Flexible Multifunctional Triboelectric Nanogenerator Based on MXene/PVA Hydrogel

Triboelectric nanogenerators (TENGs) represent an emerging technology in energy harvesting, medical treatment, and information technology. Flexible, portable, and self-powered electronic devices based on TENGs are much desired, whereas the complex preparation processes and high cost of traditional flexible electrodes hinder their practical applications. Here, an MXene/polyvinyl alcohol (PVA) hydrogel TENG (MH-TENG) is presented with simple fabrication, high output performance, and versatile applications. The doping of MXene nanosheets promotes the crosslinking of the PVA hydrogel and improves the stretchability of the composite hydrogel. The MXene nanosheets also form microchannels on surfaces, which not only enhances the conductivity of the hydrogel by improving the transport of ions but also generates an extra triboelectric output via a streaming vibration potential mechanism. The measured open-circuit voltage of the MH-TENG reaches up to 230 V even in a single-electrode mode. The MH-TENG can be stretched up to 200% of the original length and demonstrates a monotonical increasing relationship between the stretchable length and the short-circuit voltage. By utilizing the MH-TENG's outstanding stretchable property and ultrahigh sensitivity to mechanical stimuli, applications in wearable movement monitoring, high-precision written stroke recognition, and low-frequency mechanical energy harvesting are demonstrated.     

激光通信APT系统中快速反射镜研究

快速反射镜(FSM) 凭借其高精度、高带宽、高分辨率等优点,已经成为激光通信中捕获、瞄准和跟踪(APT)系统的关键组成部分。本文介绍了国内外研究机构所研制多种类型FSM。首先介绍国内外FSM的发展历程和研究重点,然后,对FSM的支撑类型、驱动类型和各种位置检测元件的选择及设计进行了讨论,得到不同的支撑结构、驱动类型和位置检测元件对FSM各性能指标的影响趋势。最后,通过对各种类型FSM进行归纳总结,提出了激光通信APT系统中FSM向大行程、高精度和高带宽等方向的发展趋势。     

一种基于柔性基底的薄膜体声波谐振器

为了能有效解决柔性基底体声波谐振器热稳定性不足及功率容量不足等问题,该文提出了一种新型的基于柔性基底的薄膜体声波谐振器。该谐振器的硅衬底上开设有一定数量的垂直上凸型结构,该结构既能有效抑制寄生模量,又能减小器件最高稳态温度和最大热应力。通过有限元分析软件Comsol Multiphics对谐振器进行仿真,结果表明,器件每增加一个上凸型结构,其最高稳态温度下降了4 ℃,最大热应力下降了1×104 GPa。与以往的柔性基底薄膜体声波谐振器相比,它具有更好的热传导能力和热应力稳定性。     

Ultrahigh‐Strength Ultrahigh Molecular Weight Polyethylene (UHMWPE)‐Based Fiber Electrode for High Performance Flexible Supercapacitors

Flexible fiber‐based supercapacitor (FSC) with excellent electrochemical performance and high tensile strength and modulus is strongly desired for some special circumstances, such as load‐bearing, abrasion resistant, and anticutting fabrics. Here, a series of ultrahigh‐strength fiber electrodes are prepared for flexible FSCs based on ultrahigh molecular weight polyethylene fibers, on which the polydopamine, Ag, and poly (3,4‐ethylene dioxythiophene): poly(styrenesulfonate) are deposited in sequence. The modified fiber‐based electrode exhibits superhigh strength up to 3.72 GPa, which is the highest among fiber‐based electrodes reported to date. In addition, FSCs fabricated with the optimized fiber electrode shows a specific areal capacity as high as 563 mF cm^?2 at 0.17 mA cm^?2, which corresponds to a high areal energy density of ≈50.1 µWh cm^?2 at a power density of ≈124 µW cm^?2. The specific areal capacity only decrease 8% after 1000 times bending test, indicating the outstanding bending performance of this composite fiber electrode. Furthermore, several FSCs can be connected in series or in parallel to get higher working voltage or higher capacity respectively, which demonstrates its potential for broad applications in flexible devices.     

Enhancing Performance Stability of Electrochemically Active Polymers by Vapor‐Deposited Organic Networks

Performance stability of electrochemically active polymers (EAPs) remains one of the greatest and long‐standing challenges with regard to EAP‐based technologies for a myriad of energy, biomedical, and environmental applications. The performance instability of EAPs originates from their structural alteration under repeated charge–discharge cycling and/or flexing. In this work, a conceptually new “soft confinement” strategy to enhance EAP performance stability, including cyclic and mechanical, by using rationally designed, vapor‐deposited organic networks is presented. These chemically cross‐linked networks, when in contact with an electrolyte solution, turn into ultrathin, elastic hydrogel coatings that encapsulate conformally the EAP micro‐/nanostructures. Such hydrogel coatings allow easy passage of ions that intercalate with EAPs, while simultaneously mitigating the structural pulverization of the EAPs and/or their detachment from substrates. Fundamentally distinct from extensively studied “scaffolding” or “synthetic” approaches to stabilizing EAPs, this soft confinement strategy relies on a postmodification step completely decoupled from the EAP synthesis/fabrication, and enjoys the unique advantage of substrate‐independency. Hence, this strategy is broadly applicable to various types of EAPs. The proposed stability enhancement strategy is demonstrated to be effective for a range of EAP systems with differing chemical and morphological characteristics under various testing conditions (repeated charging/discharging, bending, and twisting).     

Multilayer‐Folded Graphene Ribbon Film with Ultrahigh Areal Capacitance and High Rate Performance for Compressible Supercapacitors

Limited by 2D geometric morphology and low bulk packing density, developing graphene‐based flexible/compressible supercapacitors with high specific capacitances (gravimetric/volumetric/areal), especially at high rates, is an outstanding challenge. Here, a strategy for the synthesis of free‐standing graphene ribbon films (GRFs) for high‐performance flexible and compressible supercapacitors through blade‐coating of interconnected graphene oxide ribbons and a subsequent thermal treatment process is reported. With an ultrahigh mass loading of 21 mg cm^?2, large ion‐accessible surface area, efficient electron and ion transport pathways as well as high packing density, the compressed multilayer‐folded GRF films (F‐GRF) exhibit ultrahigh areal capacitance of 6.7 F cm^?2 at 5 mA cm^?2, high gravimetric/volumetric capacitances (318 F g^?1, 293 F cm^?3), and high rate performance (3.9 F cm^?2 at 105 mA cm^?2), as well as excellent cycling stability (109% of capacitance retention after 40 000 cycles). Furthermore, the assembled F‐GRF symmetric supercapacitor with compressible and flexible characteristics, can deliver an ultrahigh areal energy density of 0.52 mWh cm^?2 in aqueous electrolyte, almost two times higher than the values obtained from symmetric supercapacitors with comparable dimensions.     

Flexible Artificial Synaptic Devices Based on Collagen from Fish Protein with Spike‐Timing‐Dependent Plasticity

Neuromorphic and cognitive computing with a capability of analyzing complicated information is explored as a new paradigm of intelligent systems. An implementation of a renewable material as an essential building block of an artificial synaptic device is suggested and a flexible and transparent synaptic device based on collagen extracted from fish skin is demonstrated. This device exhibits essential synaptic behaviors including analog memory characteristics, excitatory postsynaptic current, and paired‐pulse facilitation as short‐term plasticity. The brain‐inspired electronic synapse undergoes incremental potentiation and depression when flat or bent. The device emulates spike‐timing‐dependent plasticity when stimulated by engineered pre‐ and post‐neuron spikes with the appropriate time difference between the imposed pulses. The proposed synaptic device has the advantage of being biocompatible owing to use of Mg electrodes and collagen as a naturally abundant protein. This device has a potential to be used in flexible and implantable neuromorphic systems in the future.     

High‐Performance Near‐Infrared Photodetector Based on Ultrathin Bi2O2Se Nanosheets

As an emerging 2D layered material, Bi₂O₂Se has shown great potential for applications in thermoelectric and electronics, due to its high carrier mobility, near‐ideal subthreshold swing, and high air‐stability. Although Bi₂O₂Se has a suitable band gap for infrared (IR) applications, its photoresponse properties have not been investigated. Here, high‐quality ultrathin Bi₂O₂Se sheets are synthesized via a low‐pressure chemical vapor deposition method. The thickness of 90% Bi₂O₂Se sheets is below 10 nm and lateral sizes mainly distribute in the range of 7–11 µm. In addition, it is found that triangular sheets largely lack “O” content, even only 0.2 for Bi₂O_0.2Se. The near‐IR photodetection performance of Bi₂O₂Se nanosheets is systematically studied by variable temperature measurements. The response time, responsivity, and detectivity can approach up to 2.8 ms, 6.5 A W^?1, and 8.3 × 10¹¹ Jones, respectively. Additionally, the critical performance parameters, including responsivity, rising time, and decay time, remain at almost the same level when the temperature is changed from 80 to 300 K. These phenomena are likely due to the fact that as‐grown ultrathin Bi₂O₂Se sheets have no surface trap states and shallow defect energy levels. The findings indicate ultrathin Bi₂O₂Se sheets have great potentials for future applications in ultrafast, flexible near‐IR optoelectronic devices.