High Dielectric Performances of Flexible and Transparent Cellulose Hybrid Films Controlled by Multidimensional Metal Nanostructures

Various wearable electronic devices have been developed for extensive outdoor activities. The key metrics for these wearable devices are high touch sensitivity and good mechanical and thermal stability of the flexible touchscreen panels (TSPs). Their dielectric constants (k) are important for high touch sensitivities. Thus, studies on flexible and transparent cover layers that have high k with outstanding mechanical and thermal reliabilities are essential. Herein, an unconventional approach for forming flexible and transparent cellulose nanofiber (CNF) films is reported. These films are used to embed ultralong metal nanofibers that serve as nanofillers to increase k significantly (above 9.2 with high transmittance of 90%). Also, by controlling the dimensions and aspect ratios of these fillers, the effects of their nanostructures and contents on the optical and dielectric properties of the films have been studied. The length of the nanofibers can be controlled using a stretching method to break the highly aligned, ultralong nanofibers. These nanofiber‐embedded, high‐k films are mechanically and thermally stable, and they have better Young's modulus and tensile strength with lower thermal expansion than commercial transparent plastics. The demonstration of highly sensitive TSPs using high‐k CNF film for smartphones suggests that this film has significant potential for next‐generation, portable electronic devices.     

Flexible Thermoelectric Materials and Generators: Challenges and Innovations

The urgent need for ecofriendly, stable, long‐lifetime power sources is driving the booming market for miniaturized and integrated electronics, including wearable and medical implantable devices. Flexible thermoelectric materials and devices are receiving increasing attention, due to their capability to convert heat into electricity directly by conformably attaching them onto heat sources. Polymer‐based flexible thermoelectric materials are particularly fascinating because of their intrinsic flexibility, affordability, and low toxicity. There are other promising alternatives including inorganic‐based flexible thermoelectrics that have high energy‐conversion efficiency, large power output, and stability at relatively high temperature. Herein, the state‐of‐the‐art in the development of flexible thermoelectric materials and devices is summarized, including exploring the fundamentals behind the performance of flexible thermoelectric materials and devices by relating materials chemistry and physics to properties. By taking insights from carrier and phonon transport, the limitations of high‐performance flexible thermoelectric materials and the underlying mechanisms associated with each optimization strategy are highlighted. Finally, the remaining challenges in flexible thermoelectric materials are discussed in conclusion, and suggestions and a framework to guide future development are provided, which may pave the way for a bright future for flexible thermoelectric devices in the energy market.     

Superelastic Multimaterial Electronic and Photonic Fibers and Devices via Thermal Drawing

Electronic and photonic fiber devices that can sustain large elastic deformation are becoming key components in a variety of fields ranging from healthcare to robotics and wearable devices. The fabrication of highly elastic and functional fibers remains however challenging, which is limiting their technological developments. Simple and scalable fiber‐processing techniques to continuously codraw different materials within a polymeric structure constitute an ideal platform to realize functional fibers and devices. Despite decades of research however, elastomeric materials with the proper rheological attributes for multimaterial fiber processing cannot be identified. Here, the thermal drawing of hundreds‐of‐meters long multimaterial optical and electronic fibers and devices that can sustain up to 500% elastic deformation is demonstrated. From a rheological and microstructure analysis, thermoplastic elastomers that can be thermally drawn at high viscosities (above 10³ Pa s), allowing the encapsulation of a variety of microstructured, soft, and rigid materials are identified. Using this scalable approach, fiber devices combining high performance, extreme elasticity, and unprecedented functionalities, allowing novel applications in smart textiles, robotics, or medical implants, are demonstrated.     

Epitaxial Lift‐Off of Centimeter‐Scaled Spinel Ferrite Oxide Thin Films for Flexible Electronics

Mechanical flexibility of electronic devices has attracted much attention from research due to the great demand in practical applications and rich commercial value. Integration of functional oxide materials in flexible polymer materials has proven an effective way to achieve flexibility of functional electronic devices. However, the chemical and mechanical incompatibilities at the interfaces of dissimilar materials make it still a big challenge to synthesize high‐quality single‐crystalline oxide thin film directly on flexible polymer substrates. This study reports an improved method that is employed to successfully transfer a centimeter‐scaled single‐crystalline LiFe₅O₈ thin film on polyimide substrate. Structural characterizations show that the transferred films have essentially no difference in comparison with the as‐grown films with respect to the microstructure. In particular, the transferred LiFe₅O₈ films exhibit excellent magnetic properties under various mechanical bending statuses and show excellent fatigue properties during the bending cycle tests. These results demonstrate that the improved transfer method provides an effective way to compose single‐crystalline functional oxide thin films onto flexible substrates for applications in flexible and wearable electronics.     

Preparation and characterization of the Ag2Se flexible films tuned by PVP for wearable thermoelectric generator

In recent years, the demand for wearable devices has promoted the research of flexible thermoelectric generators. Herein, this work reports a facile method to prepare the flexible Ag₂Se/polyvinyl pyrrolidone (PVP) composite films. The Ag₂Se nanorods are synthesized by the template method and then mixed with PVP solution to form the composite film optimized by the content of Ag₂Se. The maximum power factor of the film is 16.18?µW m^?1 K^?2 at 320?K, and the thermoelectric generator (TEG) has an output voltage and power of 5.49?mV and 55.57 nW at a temperature difference of 40?K, respectively. Moreover, the Ag₂Se/PVP film has good flexibility and can withstand multiple bending, the electrical conductivity reaching 89.8% and 76?% at 500 and 1000, respectively. PVP has an excellent protective capabilities effect so that the TE performance can remain stable in 40?days, and then the electrical conductivity only drops to 89?% of the initial value at 50?days. This work provides an effective method for preparing wearable thermoelectric devices, which can be extended to other composite materials.

     

Thermoelectric textile devices with thin films of nanocellulose and copper iodide

Owing to the rapid development of wearable electronics and smart textiles, demands for flexible and wearable thermoelectric (TE) devices, which can generate electricity in a ubiquitous, unintermittent and noiseless way for on-body applications are growing rapidly. Due to the inherent flexibility and wearability features, textile-based thermoelectric generators (TEGs) possess significant potential for biomedical and consumer health and safety applications. In this study, using commercial cotton fabric, we created efficient thermoelectric (TE) textile that, unlike analogs, is based on thin-film composite of biocompatible semiconductor copper iodide (CuI) and biodegradable polymer nanocellulose (NC_p) obtained by processing a widespread plant common reed. The CuI films with average thickness 10 µm were deposited via low-temperature aqueous cheap, facile, and scalable fabrication technique Successive Ionic Layer Adsorption and Reaction (SILAR). The NC_p sublayer made it possible to fabricate thin-film ohmic contacts through vacuum deposition of chromium on the nanostructured CuI film in the TE textile. The topping of CuI film with NC_p layer improved durability and wear resistance of the wearable thermoelectric module fabricated with this TE textile. The developed TE module has shown output power density 44 µW/cm² at temperature gradient 50 K that is among the best currently known results for solid miniature flexible and fabric-based TEGs.

     

Atomically Thin Mesoporous Co3O4 Layers Strongly Coupled with N‐rGO Nanosheets as High‐Performance Bifunctional Catalysts for 1D Knittable Zinc–Air Batteries

Under development for next‐generation wearable electronics are flexible, knittable, and wearable energy‐storage devices with high energy density that can be integrated into textiles. Herein, knittable fiber‐shaped zinc–air batteries with high volumetric energy density (36.1 mWh cm^?3) are fabricated via a facile and continuous method with low‐cost materials. Furthermore, a high‐yield method is developed to prepare the key component of the fiber‐shaped zinc–air battery, i.e., a bifunctional catalyst composed of atomically thin layer‐by‐layer mesoporous Co₃O₄/nitrogen‐doped reduced graphene oxide (N‐rGO) nanosheets. Benefiting from the high surface area, mesoporous structure, and strong synergetic effect between the Co₃O₄ and N‐rGO nanosheets, the bifunctional catalyst exhibits high activity and superior durability for oxygen reduction and evolution reactions. Compared to a fiber‐shaped zinc–air battery using state‐of‐the‐art Pt/C + RuO₂ catalysts, the battery based on these Co₃O₄/N‐rGO nanosheets demonstrates enhanced and stable electrochemical performance, even under severe deformation. Such batteries, for the first time, can be successfully knitted into clothes without short circuits under external forces and can power various electronic devices and even charge a cellphone.     

Flexible thermoelectric materials and devices: From materials to applications

With the ever-growing development of multifunctional and miniature electronics, the exploring of high-power microwatt-milliwatt self-charging technology is highly essential. Flexible thermoelectric materials and devices, utilizing small temperature difference to generate electricity, exhibit great potentials to provide the continuous power supply for wearable and implantable electronics. In this review, we summarize the recent progress of flexible thermoelectric materials, including conducting polymers, organic/inorganic hybrid composites, and fully inorganic materials. The strategies and approaches for enhancing the thermoelectric properties of different flexible materials are detailed overviewed. Besides, we highlight the advanced strategies for the design of mechanical robust flexible thermoelectric devices. In the end, we point out the challenges and outlook for the future development of flexible thermoelectric materials and devices.     

Bamboo‐Like Nitrogen‐Doped Carbon Nanotube Forests as Durable Metal‐Free Catalysts for Self‐Powered Flexible Li–CO2 Batteries

The Li–CO₂ battery is a promising energy storage device for wearable electronics due to its long discharge plateau, high energy density, and environmental friendliness. However, its utilization is largely hindered by poor cyclability and mechanical rigidity due to the lack of a flexible and durable catalyst electrode. Herein, flexible fiber‐shaped Li–CO₂ batteries with ultralong cycle‐life, high rate capability, and large specific capacity are fabricated, employing bamboo‐like N‐doped carbon nanotube fiber (B‐NCNT) as flexible, durable metal‐free catalysts for both CO₂ reduction and evolution reactions. Benefiting from high N‐doping with abundant pyridinic groups, rich defects, and active sites of the periodic bamboo‐like nodes, the fabricated Li–CO₂ battery shows outstanding electrochemical performance with high full‐discharge capacity of 23 328 mAh g^?1, high rate capability with a low potential gap up to 1.96 V at a current density of 1000 mA g^?1, stability over 360 cycles, and good flexibility. Meanwhile, the bifunctional B‐NCNT is used as the counter electrode for a fiber‐shaped dye‐sensitized solar cell to fabricate a self‐powered fiber‐shaped Li–CO₂ battery with overall photochemical–electric energy conversion efficiency of up to 4.6%. Along with a stable voltage output, this design demonstrates great adaptability and application potentiality in wearable electronics with a breath monitor as an example.     

聚3, 4-乙烯二氧噻吩: 聚苯乙烯磺酸盐基柔性复合热电材料研究进展

热电材料可以实现热能与电能的直接转化,是一种安全环保的新型能源材料。近年来,随着可穿戴电子设备的发展,柔性热电材料成为研究人员关注的焦点。传统无机热电材料具有优异的热电性能,但由于自身固有的脆性,限制了在柔性领域的发展。聚3, 4-乙烯二氧噻吩: 聚苯乙烯磺酸盐(PEDOT: PSS)具有高电导率、低热导率和良好的柔性,在柔性热电领域具有巨大的潜力。当选择合适的无机填料与PEDOT: PSS进行复合,可以得到优异的热电性能和良好的力学性能。本文综述了PEDOT: PSS基纳米复合薄膜的最新进展,并详细介绍了提高PEDOT: PSS基纳米复合薄膜热电性能的有效方法。最后,本文总结了实现高性能PEDOT: PSS基柔性热电材料的途径及面对的挑战。      

“Salting out” in Hofmeister Effect Enhancing Mechanical and Electrochemical Performance of Amide-based Hydrogel Electrolytes for Flexible Zinc-Ion Battery

With the development of flexible and wearable electronic devices, it is a new challenge for polymer hydrogel electrolytes to combine high mechanical flexibility and electrochemical performance into one membrane. In general, the high content of water in hydrogel electrolyte membranes always leads to poor mechanical strength, and limits their applications in flexible energy storage devices. In this work, based on the “salting out” phenomenon in Hofmeister effect, a kind of gelatin-based hydrogel electrolyte membrane is fabricated with high mechanical strength and ionic conductivity by soaking pre-gelated gelatin hydrogel in 2 m ZnSO₄ aqueous. Among various gelatin-based electrolyte membranes, the gelatin-ZnSO₄ electrolyte membrane delivers the “salting out” property of Hofmeister effect, which improves both the mechanical strength and electrochemical performance of gelatin-based electrolyte membranes. The breaking strength reaches 1.5 MPa. When applied to supercapacitors and zinc-ion batteries, it can sustain over 7500 and 9300 cycles for repeated charging and discharging processes. This study provides a very simple and universal method to prepare polymer hydrogel electrolytes with high strength, toughness, and stability, and its applications in flexible energy storage devices provide a new idea for the construction of secure and stable flexible and wearable electronic devices.     

Advanced Carbon for Flexible and Wearable Electronics

Flexible and wearable electronics are attracting wide attention due to their potential applications in wearable human health monitoring and care systems. Carbon materials have combined superiorities such as good electrical conductivity, intrinsic and structural flexibility, light weight, high chemical and thermal stability, ease of chemical functionalization, as well as potential mass production, enabling them to be promising candidate materials for flexible and wearable electronics. Consequently, great efforts are devoted to the controlled fabrication of carbon materials with rationally designed structures for applications in next‐generation electronics. Herein, the latest advances in the rational design and controlled fabrication of carbon materials toward applications in flexible and wearable electronics are reviewed. Various carbon materials (carbon nanotubes, graphene, natural‐biomaterial‐derived carbon, etc.) with controlled micro/nanostructures and designed macroscopic morphologies for high‐performance flexible electronics are introduced. The fabrication strategies, working mechanism, performance, and applications of carbon‐based flexible devices are reviewed and discussed, including strain/pressure sensors, temperature/humidity sensors, electrochemical sensors, flexible conductive electrodes/wires, and flexible power devices. Furthermore, the integration of multiple devices toward multifunctional wearable systems is briefly reviewed. Finally, the existing challenges and future opportunities in this field are summarized.     

Constructing Carbon Nanotube Hybrid Fiber Electrodes with Unique Hierarchical Microcrack Structure for High-Voltage,Ultrahigh-Rate,and Ultralong-Life Flexible Aqueous Zinc Batteries

Flexible aqueous zinc batteries are promising candidates as safe power sources for fast-growing portable and wearable electronics. However, the low working voltage, poor rate capability, and cycling stability have greatly restricted their development and applications. Here, a new family of flexible bimetallic phosphide/carbon nanotube hybrid fiber electrodes with unique macroscopic microcrack structure and microscopic porous nanoflower structure is reported. The hierarchical microcrack structure not only facilitates the penetration of electrolyte for effective exposure of active sites, but also can serve as buffers to relieve the stress concentrations of the fiber electrode under deformations, enabling impressive electrochemical performance and mechanical flexibility. Particularly, the fabricated flexible aqueous zinc batteries demonstrate high working voltage plateau and specific capacity (≈1.7 V, 258.9 mAh g⁻¹ at 2 A g⁻¹), ultrahigh rate capability (135.8 mAh g⁻¹ at 50 A g⁻¹, fully charged in only 9.8 s) and impressive power density of 79 000 W kg⁻¹. Moreover, the flexible batteries show ultralong cycling life with 74.6% capacity retention after 20 000 cycles. The fiber batteries are also highly flexible and can be easily knitted into soft electronic textiles to power a smartphone, which are particularly promising for the next-generation of flexible and wearable electronics.     

A facile way to optimize thermoelectric properties of SnSe thin films via sonication-assisted liquid-phase exfoliation

In our work, SnSe nanosheets and nanostructured thin films were successfully synthesized via sonication-assisted exfoliation and coating process. The SnSe nanosheets respond to a uniform lateral size, with two to three single layers by 2.82 nm and 280 nm² of average thickness and average area, respectively. The results were confirmed by Scanning Electron Microscope, Transmission Electron Microscope, and Atomic Force Microscope. X-ray diffraction and Raman spectra indicate that the SnSe nanosheets have high crystalline quality along a-axis. The SnSe nanostructured thin films were prepared in various thicknesses from 350 to 650 nm. The highest power factor value is achieved at 450 nm in 375–600 K temperature range. A simple method of fabrication and controllable thermoelectric properties of SnSe nanostructured thin films as well as other two-dimensional (2D) materials are introduced.

     

Synthesis of P‐Doped and NiCo‐Hybridized Graphene‐Based Fibers for Flexible Asymmetrical Solid‐State Micro‐Energy Storage Device

Fiber supercapacitors (FSCs) are promising energy storage devices in portable and wearable smart electronics. Currently, a major challenge for FSCs is simultaneously achieving high volumetric energy and power densities. Herein, the microscale fiber electrode is designed by using carbon fibers as substrates and capillary channels as microreactors to space‐confined hydrothermal assembling. As P‐doped graphene oxide/carbon fiber (PGO/CF) and NiCo₂O₄‐based graphene oxide/carbon fiber (NCGO/CF) electrodes are successfully prepared, their unique hybrid structures exhibit a satisfactory electrochemical performance. An all‐solid‐state PGO/CF//NCGO/CF flexible asymmetric fiber supercapacitor (AFSC) based on the PGO/CF as the negative electrode, NCGO/CF hybrid electrode as the positive electrode, and poly(vinyl alcohol)/potassium hydroxide as the electrolyte is successfully assembled. The AFSC device delivers a higher volumetric energy density of 36.77 mW h cm^?3 at a power density of 142.5 mW cm^?3. In addition, a double reference electrode system is adopted to analyze and reduce the IR drop, as well as effectively matching negative and positive electrodes, which is conducive for the optimization and improvement of energy density. For the AFSC device, its better flexibility and electrochemical properties create a promising potential for high‐performance micro‐supercapacitors. Furthermore, the introduction of the double reference electrode system provides an interesting method for the study on the electrochemical performances of two‐electrode systems.     

Thin Film Tin Selenide (SnSe) Thermoelectric Generators Exhibiting Ultralow Thermal Conductivity

Tin selenide (SnSe) has attracted much attention in the field of thermoelectrics since the discovery of the record figure of merit (ZT) of 2.6 ± 0.3 along the b‐axis of the material. The record ZT is attributed to an ultralow thermal conductivity that arises from anharmonicity in bonding. While it is known that nanostructuring offers the prospect of enhanced thermoelectric performance, there have been minimal studies in the literature to date of the thermoelectric performance of thin films of SnSe. In this work, preferentially orientated porous networks of thin film SnSe nanosheets are fabricated using a simple thermal evaporation method, which exhibits an unprecedentedly low thermal conductivity of 0.08 W m^?1 K^?1 between 375 and 450 K. In addition, the first known example of a working SnSe thermoelectric generator is presented and characterized.     

Computing Fibers: A Novel Fiber for Intelligent Fabrics?

This communication describes a possible path for transition from a wearable computer to a fiber computer in which digital processing power is integrated directly into textiles via circuits on individual fibers. Three different classes of computing fiber substrate (active, passive, and intermediate) are discussed and some technologies for their manufacture are reviewed. It is shown here that with two of these techniques it is possible to develop new substrates for the semiconductor industry. Using an silicon‐on‐insulator (SOI) process, polycrystalline silicon fibers with a length of 42 mm have been successfully produced at NMRC in Ireland. These fibers are 35 μm wide and 1 μm thick. Silicon carbide (SiC) and silicon dioxide (SiO₂) endless fibers (subsequently cut in to 20 cm lengths) have also been produced by extrusion. After sintering, this method yielded polycrystalline SiC fibers and pure amorphous SiO₂ glass fibers. For many future applications, fiber computing appears to be a possible key to success. The computing power offered by such fibers may be combined with additional in‐ and output functions by weaving fiber‐based sensors and piezoelectric materials into textiles.     

Nano‐RuO2‐Decorated Holey Graphene Composite Fibers for Micro‐Supercapacitors with Ultrahigh Energy Density

Compactness and versatility of fiber‐based micro‐supercapacitors (FMSCs) make them promising for emerging wearable electronic devices as energy storage solutions. But, increasing the energy storage capacity of microscale fiber electrodes, while retaining their high power density, remains a significant challenge. Here, this issue is addressed by incorporating ultrahigh mass loading of ruthenium oxide (RuO₂) nanoparticles (up to 42.5 wt%) uniformly on nanocarbon‐based microfibers composed largely of holey reduced graphene oxide (HrGO) with a lower amount of single‐walled carbon nanotubes as nanospacers. This facile approach involes (1) space‐confined hydrothermal assembly of highly porous but 3D interconnected carbon structure, (2) impregnating wet carbon structures with aqueous Ru³⁺ ions, and (3) anchoring RuO₂ nanoparticles on HrGO surfaces. Solid‐state FMSCs assembled using those fibers demonstrate a specific volumetric capacitance of 199 F cm^?3 at 2 mV s^?1. Fabricated FMSCs also deliver an ultrahigh energy density of 27.3 mWh cm^?3, the highest among those reported for FMSCs to date. Furthermore, integrating 20 pieces of FMSCs with two commercial flexible solar cells as a self‐powering energy system, a light‐emitting diode panel can be lit up stably. The current work highlights the excellent potential of nano‐RuO₂‐decorated HrGO composite fibers for constructing micro‐supercapacitors with high energy density for wearable electronic devices.     

High‐Performance Piezoelectric Nanogenerators with Imprinted P(VDF‐TrFE)/BaTiO3 Nanocomposite Micropillars for Self‐Powered Flexible Sensors

Piezoelectric nanogenerators with large output, high sensitivity, and good flexibility have attracted extensive interest in wearable electronics and personal healthcare. In this paper, the authors propose a high‐performance flexible piezoelectric nanogenerator based on piezoelectrically enhanced nanocomposite micropillar array of polyvinylidene fluoride‐trifluoroethylene (P(VDF‐TrFE))/barium titanate (BaTiO₃) for energy harvesting and highly sensitive self‐powered sensing. By a reliable and scalable nanoimprinting process, the piezoelectrically enhanced vertically aligned P(VDF‐TrFE)/BaTiO₃ nanocomposite micropillar arrays are fabricated. The piezoelectric device exhibits enhanced voltage of 13.2 V and a current density of 0.33 µA cm^?2, which an enhancement by a factor of 7.3 relatives to the pristine P(VDF‐TrFE) bulk film. The mechanisms of high performance are mainly attributed to the enhanced piezoelectricity of the P(VDF‐TrFE)/BaTiO₃ nanocomposite materials and the improved mechanical flexibility of the micropillar array. Under mechanical impact, stable electricity is stably generated from the nanogenerator and used to drive various electronic devices to work continuously, implying its significance in the field of consumer electronic devices. Furthermore, it can be applied as self‐powered flexible sensor work in a noncontact mode for detecting air pressure and wearable sensors for detecting some human vital signs including different modes of breath and heartbeat pulse, which shows its potential applications in flexible electronics and medical sciences.     

Recent Advances in 1D Stretchable Electrodes and Devices for Textile and Wearable Electronics: Materials,Fabrications, and Applications

Research on wearable electronic devices that can be directly integrated into daily textiles or clothes has been explosively grown holding great potential for various practical wearable applications. These wearable electronic devices strongly demand 1D electronic devices that are light–weight, weavable, highly flexible, stretchable, and adaptable to comport to frequent deformations during usage in daily life. To this end, the development of 1D electrodes with high stretchability and electrical performance is fundamentally essential. Herein, the recent process of 1D stretchable electrodes for wearable and textile electronics is described, focusing on representative conductive materials, fabrication techniques for 1D stretchable electrodes with high performance, and designs and applications of various 1D stretchable electronic devices. To conclude, discussions are presented regarding limitations and perspectives of current materials and devices in terms of performance and scientific understanding that should be considered for further advances.