Applications In Wearable Electronics Research Articles

Environmentally stable, Adhesive, Self-healing, Stretchable and Transparent Gelatin based Eutectogels for Self-Powered Humidity Sensors

Intrinsic environmental and stability limitations of hydrogels have inhibited their practical applications as a flexible wearable device due to water evaporation or freezing in complex environments such as low temperatures and arid environments. In this work, a multifunctional gelatin based ionic conductive eutectogel with double network structure is designed via ternary deep eutectic solvent (DES) (acrylic acid (AA), choline chloride (ChCl) and ethylene glycol (EG)). In this system, the introduction of ethylene glycol (EG) can be used to dissolve gelatin. The resulting DESG eutectogel exhibited excellent adhesion, mechanical robustness, anti-freeze, anti-drying, and self-healing. Interestingly, the DESG gels showed high humidity sensitivity in a wide humidity detection range (11 %–83 %), which can be assembled as a self-powdered humidity sensor to monitor human mouth and nose breathing. This work is expected to bring new prospect to construct high performance humidity sensors using gelatin based humidity-responsive materials for a wide range of potential applications in respiratory diagnostics, sleep monitoring, electronic skin and wearable electronics.

Improved thermoelectric properties of metal ion doped aniline tetramer/carbon nanotube composite films

Carbon nanotubes and their composites have attracted much attention in the field of thermoelectric conversion for potential application in wearable electronics owing to their good electrical conductivity and excellent mechanical properties. However, low Seebeck coefficient of carbon nanotubes limit the improvement of their thermoelectric properties. In this work, metal ions (Mn+ = Fe3+, Ni2+, Cu2+) are used to further improve the thermoelectric properties of aniline tetramer (ANIT)/single-walled carbon nanotubes (SWCNT) composites, and Mn+@ANIT/SWCNT films are prepared by physical mixing and vacuum filtration method. The metal ions and concentrations for improving Mn+@ANIT/SWCNT thermoelectric films are optimized, and the metal ions doping optimizes carrier concentration and promotes carrier transport of the composites appropriately, which increased the Seebeck coefficient. Amone the prepared Mn+@ANIT/SWCNT films, the Cu2+@ANIT/SWCNT demonstrates the highest PF value of 145.3 ± 3.9 μW m−1 K−2 at the molar ratio of Cu2+/ANIT to being 5:100 with the σ of 560.1 ± 22.1 S cm−1, and the S of 51.0 ± 1.3 μV K−1 at room temperature. Finally, five pairs of p-type Cu2+@ANIT/SWCNT films and n-type copper sheets are connected in series to assemble a self-powered thermoelectric device, which demonstrates an actual output power of about 426 nW under a temperature difference of 50 K. Therefore, this work offers a metal ions doping strategy to improve the SWCNT composites with enhanced thermoelectric properties.

Highly mechanically stable and intrinsically stretchable large-area organic photovoltaics using nanoporous bulk-heterojunction

It is important to develop bulk-heterojunction films that simultaneously exhibit good photovoltaic properties and mechanical robustness to realize intrinsically stretchable organic photovoltaics (IS-OPVs). We developed a strategy for preparing nanoporous bulk-heterojunction (np-BHJ) films at a large area by nonsolvent-induced phase separation assisted by thermoplastic polyurethane. The resulting np-BHJ can form much improved adhesive interfaces with a neighbored stretchable layer in OPV devices and effectively dissipate applied mechanical stress. IS-OPVs using the np-BHJ films showed efficiency of 12.0 %, which is comparable performance to 12.4 % of the controlled BHJ. The IS-OPV device using np-BHJ films much improved mechanical stability and maintained 89 % of its initial efficiency under applied strain of 40 %. The corresponding module showed only 10 % decrease in efficiency after 1,000 cycles in stretching tests at 10 % strain. Because of high scalability of the np-BHJ morphology, IS-OPV modules with efficiency of 7.06 % and active area of 10.17 cm2 and were successfully demonstrated. Photoplethysmography sensors prepared using the IS-OPV module showed strong potential for application in wearable electronics.

Ultrasensitive and wide-range MXene/PDMS piezoresistive sensors inspired by rose petals

Flexible pressure sensors are crucial in a variety of applications, including artificial intelligence (AI), the Internet of Things (IoT), and electronic skin (e-Skin), due to their ability to convert mechanical stimuli into electrical signals. However, achieving both high sensitivity and a wide detection range simultaneously remains challenging, often limiting their practical applications. To address this, we designed a three-dimensional contact interface with Ti3C2 MXene/polydimethylsiloxane (MP) inspired by rose petals, which allows for significant strain and resistance changes across a broad range of stress levels. The innovative design significantly extends the pressure detection range (0.033–535 kPa), enhances pressure sensitivity (0.432 kPa−1), offers a fast response/recovery times (57/4 ms), and ensures exceptional long-term durability (up to 2950 cycles). The structured MP sensor demonstrates the capability to detect human physiological movements, distinguish various voices and map real-time pressure distributions. Notably, it achieves real-time tracking of handwriting processes with high recognition accuracy through a machine learning module. The work offers a new strategy and inspiration for designing and manufacturing innovative structured pressure sensors with reliable performance, paving the way for their application in next-generation wearable and portable electronics.

Flexible All-Inorganic Thermoelectric Yarns.

Achieving both formability and functionality in thermoelectric materials remains a significant challenge due to their inherent brittleness. Previous approaches, such as polymer infiltration, often compromise thermoelectric efficiency, underscoring the need for flexible, all-inorganic alternatives. This study demonstrates that the extreme brittleness of thermoelectric bismuth telluride (Bi2Te3) bulk compounds can be overcome by harnessing the nanoscale flexibility of Bi2Te3 nanoribbons and twisting them into a yarn structure. The resulting Bi2Te3 yarn, with a Seebeck coefficient of -126.6µVK-1, exhibits remarkable deformability, enduring extreme bending curvatures (down to 0.5mm-1) and tensile strains of ≈5% through over 1000 cycles without significant resistance change. This breakthrough allows the yarn to be seamlessly integrated into various applications-wound around metallic pipes, embedded within life jackets, or woven into garments-demonstrating unprecedented adaptability and durability. Moreover, a simple 4-pair thermoelectric generator comprising Bi2Te3 yarns and metallic wires generates a maximum output voltage of 67.4mV, substantiating the effectiveness of thermoelectric yarns in waste heat harvesting. These advances not only challenge the traditional limitations posed by the brittleness of thermoelectric materials but also open new avenues for their application in wearable and structural electronics.

Oxygen vacancies enhancing hierarchical NiCo2S4@MnO2 electrode for flexible asymmetric supercapacitors

The limited energy density of supercapacitors hampers their widespread application in electronic devices. Metal oxides, employed as electrode materials, suffer from low conductivity and stability, prompting extensive research in recent years to enhance their electrochemical properties. Among these efforts, the construction of core–shell heterostructures and the utilization of oxygen vacancy (VO) engineering have emerged as pivotal strategies for improving material stability and ion diffusion rates. Herein, core–shell composites comprising NiCo2S4 nanospheres and MnO2 nanosheets are grown in situ on carbon cloth (CC), forming nanoflower clusters while introducing VO defects through a chemical reduction method. Density functional theory (DFT) results proves that the existence of VO effectively enhances electronic and structural properties of MnO2, thereby enhancing capacitive properties. The electrochemical test results show that NiCo2S4@MnO2-V3 exhibits excellent 1376 F g−1 mass capacitance and 2.06 F cm−2 area capacitance at 1 A g−1. Moreover, NiCo2S4@MnO2-V3//activated carbon (AC) asymmetric supercapacitor (ASC) can achieve an energy density of 39.7 Wh kg−1 at a power density of 775 W kg−1, and maintains 15.5 Wh kg−1 even at 7749.77 W kg−1. Capacitance retention is 73.1 % after 10,000 cycles at 5 A g−1, and coulombic efficiency reaches 100 %, demonstrating satisfactory cycle stability. In addition, the device’s excellent flexibility offers broad application prospects in wearable electronic applications.

Recyclable and Stable Strain Sensors Based on Semi‐Wrapped Structure of Silver Nanowires in Polyvinyl Alcohol for Human Motion Monitoring

AbstractHighly sensitive strain sensors have been widely used in human motion monitoring, medical treatment, soft robots, and human–computer interaction, and the recycling of functional materials is in a huge demand for eco‐friendly and sustainable electronics. However, the manufacturing of recyclable strain sensors still remains challenging. Here, a semi‐wrapped structure based on silver nanowires and polyvinyl alcohol is proposed to realize a recyclable and stable strain sensor. It has shown excellent sensitivity, fast response, high stretchability and good environmental stability, and is successfully applied for human motion monitoring. In addition, a simple strategy is developed to effectively recycle silver nanowires in an eco‐friendly manner. The recyclable and stable strain sensor demonstrates potential applications in wearable and stretchable electronics, and the recycling strategy can be extended to other noble metal nanomaterials.

Sandwich-Structured Carbon Nanotube Composite Films for Multifunctional Sensing and Electrothermal Application.

Electro-conductive films with excellent flexibility and thermal behavior have great potential in the fields of wearable electronics, artificial muscle, and soft robotics. Herein, we report a super-elastic and electro-conductive composite film with a sandwich structure. The composite film was constructed by spraying Polyvinyl alcohol (PVA) polymers onto a buckled conductive carbon nanotube-polydimethylsiloxane (CNTs-PDMS) composite film. In this system, the PVA and PDMS provide water sensing and stretchability, while the coiled CNT film offers sufficient conductivity. Notably, the composite film possesses high stretchability (205%), exceptional compression sensing ability, humility sensing ability, and remarkable electrical stability under various deformations. The produced CNT composite film exhibited deformation (bending/twisting) and high electro-heating performance (108 °C) at a low driving voltage of 2 V. The developed CNT composite film, together with its exceptional sensing and electrothermal performance, provides the material with promising prospects for practical applications in wearable electronics.

Stretchable and Self-Powered Mechanoluminescent Triboelectric Nanogenerator Fibers toward Wearable Amphibious Electro-Optical Sensor Textiles.

Flexible electro-optical dual-mode sensor fibers with capability of the perceiving and converting mechanical stimuli into digital-visual signals show good prospects in smart human-machine interaction interfaces. However, heavy mass, low stretchability, and lack of non-contact sensing function seriously impede their practical application in wearable electronics. To address these challenges, a stretchable and self-powered mechanoluminescent triboelectric nanogenerator fiber (MLTENGF) based on lightweight carbon nanotube fiber is successfully constructed. Taking advantage of their mechanoluminescent-triboelectric synergistic effect, the well-designed MLTENGF delivers an excellent enhancement electrical signal of 200% and an evident optical signal whether on land or underwater. More encouragingly, the MLTENGF device possesses outstanding stability with almost unchanged sensitivity after stretching for 200%. Furthermore, an extraordinary non-contact sensing capability with a detection distance of up to 35cm is achieved for the MLTENGF. As application demonstrations, MLTENGFs can be used for home security monitoring, intelligent zither, traffic vehicle collision avoidance, and underwater communication. Thus, this work accelerates the development of wearable electro-optical textile electronics for smart human-machine interaction interfaces.

Ultrafast reaction kinetic of polyaniline in flexible hydrogel electrodes facilitated by graphene ribbons

Abstract By loading energy storage active materials on hydrogel which is inherently flexible, the flexibility of electrode materials can be simply realized, thereby achieving the flexibility of energy storage devices. However, the polymer network that constructs the three-dimensional skeleton of the hydrogel is not conductive, which inhibits the redox ability of the active material. If a high speed conductive structure can be added to the colloidal phase, the performance of the flexible electrode material can be greatly improved. Here, we introduce redox graphene ribbons into the polyvinyl alcohol hydrogel loaded with polyaniline. The in situ three-dimensional conductive graphene network greatly enhanced the conductivity of the hydrogel electrode, thus increasing the specific capacitance to as high as 1117 F g−1 at 2 mg cm−2 mass loading, with a retention ratio of 66.96% from 0.5 A g−1 to 20 A g−1. These highlighted properties enable the PRP hydrogel as an electrode for flexible supercapacitors, which provides a promising possibility for the practical application of wearable electronics.

Flexible sandwich-structured silver nanowire/exfoliated graphite platelet/aramid nanofiber composite films with excellent EMI shielding, thermal conduction and Joule heating performances

Multifunctional flexible sandwich-structured EMI shielding silver nanowire/exfoliated graphite platelet/aramid nanofiber (AgNW/EGP/ANF) composite films with excellent thermal conduction and Joule heating abilities were successfully prepared by a layer-by-layer vacuum filtration technique. The construction of EGP/ANF layer on the two sides is crucial in achieving outstanding thermal conductivity (TC) and contributes partial EMI shielding effectiveness (SE) for the composite films. The introduction of an ultrathin, dense, and sintered AgNW/ANF layer endows the composite films with significant enhancements in electrical conductivity and EMI SE. As a result, the optimal 30 μm-thick composite films with an AgNW loading of 35 wt% exhibit excellent EMI SE values of 69.0 dB in the X-band and 78.4 dB in the Ka-band and a superior in-plane TC of 48.7 W m−1 K−1. Besides, the prepared composite films present an outstanding Joule heating performance. Briefly, the sandwich-structured composite films show huge potential in advanced portable and wearable electronic applications.

Flexible all-solid-state asymmetric supercapacitor based on Ti3C2Tx MXene/graphene/carbon nanotubes

As the emerging 2D materials, MXenes have been regarded as promising electrode materials in supercapacitor as power supply for wearable and portable electronic devices due to their metallic conductivity, hydrophilic feature, abundant functional groups, and large theoretical specific surface area etc. The capacity and rate capability of MXene-based electrodes is limited by the sheet restacking, hindering their further development. Herein, Ti3C2Tx MXene/graphene/carbon nanotubes (MXene/graphene/CNTs) flexible film was successfully fabricated by vacuum assisted filtration. Intercalation and confinement of graphene and carbon nanotubes between the Ti3C2Tx MXene nanosheets could increase the spacing and specific surface area, alleviate the stacking of MXene nanosheets, thus enhancing the electrochemical properties. The prepared MXene/graphene/CNTs film possesses increased specific surface area, average pore size, pore volume (112.259 m2g−1, 9.982 nm, 0.276 cm3g−1), compared to MXene (93.088 m2g−1, 3.786 nm, 0.088 cm3g−1). Consequently, MXene/graphene/CNTs delivers high area specific capacitance of 1862.5 mF cm−2 at 1 mA cm−2 and excellent rate capability (1525 mF cm−2, 81.88 % at 20 mA cm−2). Flexible asymmetric supercapacitor constructed with MXene/graphene/CNTs film and active carbon as positive and negative electrodes, and PVA/H2SO4 gel as solid electrolyte, achieves an energy density of 133.75 μWh cm−2 at the power density of 750 μW cm−2. In addition, there is still 94.9 % of the initial performance after cycling 8000 charge/discharge cycles at 10 mA cm−2, corresponding to a single-turn decay rate down to 0.00019 %. Besides, this flexible supercapacitor manifests outstanding electrochemical stability at different bending times. These advantages make the flexible supercapacitor device very promising for wearable electronics applications.

High-Performance Flexible Sensor with Sensitive Strain/Magnetic Dual-Mode Sensing Characteristics Based on Sodium Alginate and Carboxymethyl Cellulose.

Flexible sensors can measure various stimuli owing to their exceptional flexibility, stretchability, and electrical properties. However, the integration of multiple stimuli into a single sensor for measurement is challenging. To address this issue, the sensor developed in this study utilizes the natural biopolymers sodium alginate and carboxymethyl cellulose to construct a dual interpenetrating network, This results in a flexible porous sponge that exhibits a dual-modal response to strain and magnetic stimulation. The dual-mode flexible sensor achieved a maximum tensile strength of 429 kPa and elongation at break of 24.7%. It also exhibited rapid response times and reliable stability under both strain and magnetic stimuli. The porous foam sensor is intended for use as a wearable electronic device for monitoring joint movements of the body. It provides a swift and stable sensing response to mechanical stimuli arising from joint activities, such as stretching, compression, and bending. Furthermore, the sensor generates opposing response signals to strain and magnetic stimulation, enabling real-time decoupling of different stimuli. This study employed a simple and environmentally friendly manufacturing method for the dual-modal flexible sensor. Because of its remarkable performance, it has significant potential for application in smart wearable electronics and artificial electroskins.

Improved-quality graphene films via the synergism of large nanosheet aligning and nanotube bridging for flexible supercapacitors

Scalable production of reduced graphene oxide (rGO) films with high mechanical-electrical properties is desirable as these films are candidates for wearable electronics devices and energy storage applications. Removing structural incompleteness such as wrinkles or voids in the graphene films, which are generated from the assembly process, would greatly optimize their mechanical properties. However, the densely stacked graphene sheets in the films degrade their ionic kinetics and thus limit their development. Here, a horizontal-longitudinal-structure modulating strategy is demonstrated to produce enhanced mechanical, conductive, and capacitive graphene films. Typically, two-dimensional large graphene sheets (LGS) induce regular stacking of graphene oxide (GO) during the assembly process to reduce wrinkles, while one-dimensional single-walled carbon nanotubes (SWCNT) bridge with graphene sheets to strengthen the multidirectional intercalation and reduce GO layer restacking. The simultaneous incorporation of LGS and SWCNT synergistically creates a fine microstructure by improving the alignment of graphene sheets, increasing continuous conductive pathways to facilitate electron transport, and enlarging interlayer spacing to promote electrolyte ion diffusion. As a result, the obtained graphene films are flat and exhibit signally reinforced mechanical properties, electrical conductivity (38727 S m-1), as well as specific capacitance (232 F g-1) as supercapacitor electrodes compared to those of original rGO films. Moreover, owing to the comprehensive improved properties, a flexible gel supercapacitor assembled by the graphene film-based electrodes shows high energy density, good flexibility, and excellent cycling stability (93.8% capacitance retention after 10 000 cycles). This work provides a general strategy to manufacture robust graphene structural materials for energy storage applications in flexible and wearable electronics.

Gelatin/sodium alginate-based strongly adhesive, environmentally resistant, highly stable hydrogel for 3D printing to prepare multifunctional sensors and flexible supercapacitors

The increasing demand for environmentally friendly performance materials in the field of wearable electronics has brought renewable and low-cost hydrogels based on natural polymers into the research spotlight. As a biodegradable natural polymer, sodium alginate (SA) shows great promise for applications in wearable electronics. Here, we report a hydrogel with printability, adhesion, and is highly stable based on gelatin (Gel) and SA. SA improves the viscosity of the hydrogel, which can bond iron products weighing up to 20 kg due to metal coordination with the material, and the hydrogel binder is recyclable and reusable. The presence of glycerin allowed the hydrogel sensor device to maintain sensitivity after exposure to air at 25 °C for up to 35 days, and printed hydrogel samples retained their compressive resilience after exposure to air (25 °C, 55 % RH) for 30 days. Hydrogel-based supercapacitors show good stability after 58 h of charge/discharge cycling. This paper provides research ideas for the preparation of hydrogels with strong adhesion properties, as well as hydrogel 3D printing technology for the preparation of flexible sensor devices and flexible energy storage devices.

Recent Advances in Electrochromic Devices: From Multicolor to Flexible Applications

With increasing demand for energy saving and environmental sustainability, electrochromic devices (ECDs) are considered as emerging display devices with low energy consumption. While various reflective‐type displays produce images with low energy, achieving full color displays often involves much device complexity and nonflexibility. Multicolor ECDs aim to realize full color reflective‐type displays, surpassing the current monochromic type or limited coloration capabilities in a 1D color space. Enhancing device flexibility is also highly desirable for use of ECDs in wearable and flexible electronics for health monitoring and advanced textiles with easy visualization. In this review, recent advances in multicolor and flexible ECDs are examined. Several primary strategies to achieve multicolor ECD are described, including material modifications, color overlay, and dye‐mediated colorations. In addition, recent developments in flexible ECDs are explored, emphasizing novel materials and fabrication processes that improve mechanical durability and reliability under deformation. It is expected that this review will provide a comprehensive understanding of multicolor and flexible ECDs for applications in smart windows, displays, and wearable electronics.

Controllable synthesis of TiO2/graphene composites for human voice recognition in strain sensor.

Low-dimensional materials have demonstrated strong potential for use in diverse flexible strain sensors for wearable electronic device applications. However, the limited contact area in the sensing layer, caused by the low specific surface area of typical nanomaterials, hinders the pursuit of high-performance strain-sensor applications. Herein, we report an efficient method for synthesizing TiO2-based nanocomposite materials by directly using industrial raw materials with ultrahigh specific surface areas that can be used for strain sensors. A kinetic study of the self-seeded thermal hydrolysis sulfate process was conducted for the controllable synthesis of pure TiO2 and related TiO2/graphene composites. The hydrolysis readily modified the crystal form and morphology of the prepared TiO2 nanoparticles, and the prepared composite samples possessed a uniform nanoporous structure. Experiments demonstrated that the TiO2/graphene composite can be used in strain sensors with a maximum Gauge factor of 252. In addition, the TiO2/graphene composite-based strain sensor showed high stability by continuously operating over 1,000 loading cycles and aging tests over three months. It also shows that the fabricated strain sensors have the potential for human voice recognition by characterizing letters, words, and musical tones.

High-performance and flexible sodium ion-based electrochemical devices toward self-powered wearable volatile organic compounds sensing system

Self-powered wearable electronic systems are considered the ideal solution to realize ubiquitous Internet-of-Things (IoT), personalized healthcare, and point-to-care diagnosis. Here, we demonstrate the integration of a high-performance and ultra-stable sodium ion-based micro-supercapacitor (MSC) and a high-sensitive sensor for self-powered wearable Volatile Organic Compounds (VOC) sensing systems. It is found that a sodium-based solid electrolyte exhibited high ionic conductivity, reaching 2.4 mS cm−1 at 70 °C. Further, the inclusion of TiO2 NPs additive in the solid electrolyte can reduce the crystallinity and expand the electrode/electrolyte interface, which increases about 2.25 times in the capacitance of sodium ion-based MSC. PDMS-encapsulated MSC showed ultra-stability of capacitance retention (approximately 98.8 %) after 50,000 cycles while also achieving a high flexibility of 1000 cycles with a minimal capacitance change. As a proof-of-concept of a self-powered wearable sensor, it is demonstrated that an integrated polymer electrolyte-based VOC sensor powered by a charged-MSC can continuously operate for more than 4000 s (over 1.1 h) in the ethanol/nitrogen gas chamber. Therefore, we believe that our integration of sodium ion-based electrochemical storage and VOC sensor capabilities will pave a way to revolutionize the approach of wearable electronic applications toward self-powered systems.

Tremendous Stiffness‐Changing Polymer Networks Enabled by Touch‐Induced Crystallization

AbstractStiffness‐changing polymers are critically needed for intelligent and adaptive applications in soft robotics and wearable electronics; however, they suffer from the requirement of persistent external stimulation. Herein, a stiffness‐changing polymer network impregnated with a supercooled ionic liquid is introduced, which undergoes touch‐induced crystallization from a soft ionogel to a stiff plastic. The network exhibits a remarkable tunability in stiffness change, with the highest value exceeding 190 000 times between the soft and stiff states (3.5 kPa vs 691.1 MPa). This tremendous transition is achieved through the first‐order liquid–solid phase transition of the supercooled ionic liquid, which is highly reversible and isochoric via a heating‐cooling process. Unlike traditional stimuli, only a single touch is needed without sustained stimulation to trigger the stiffening from soft to stiff states. Importantly, the touch‐responsive polymer network can be extended to various types of ionic liquids and monomers, indicating excellent strategic versatility. Moreover, this unique ionogel exhibits switchable adhesiveness and ionic conductivity, effectively demonstrating smart adhesives and ionic switches with enhancements of more than 66 and 5800 times, respectively. This work provides a facile and versatile strategy for designing stable stiffness‐changing polymers, unlocking significant potential applications for next‐generation smart devices.

Chitin and Cellulose as Constituents of Efficient, Sustainable, and Flexible Zinc-Ion Hybrid Supercapacitors

A zinc-ion hybrid supercapacitor (ZIHS) is a prospective energy storage device featuring cost-effectiveness, operational safety, environmental friendliness, high-power performance, and satisfied energy density.1 The sustainability of this ZIHS technology is even improved by introducing biopolymer constituents into the cell construction.2 Herein, efficient, sustainable, and flexible ZIHSs employing polysaccharide (chitin- or cellulose-based) components are developed.3 Using green ionic liquid solvents, biopolymer-bound, activated carbon-based cathode materials and hydrogel biopolymer electrolytes containing conductive zinc salts are obtained. According to systematical characterization results, the prepared materials possess favorable functional properties. Biopolymer binders provide homogeneity and integrity within the electrode network and high adhesion to the surface of the current collector. Depending on the type of zinc salt, hydrogel biopolymer electrolytes display high ionic conductivity (up to 46 mS cm−1), expanded electrochemical stability window (up to ca. 2.8 V), and zinc dendrites growth suppression. Biopolymer components assembled with zinc foil electrodes operate efficiently in both coin and pouch ZIHS cell configurations, providing satisfactory energy (45–50 Wh kg−1) and high power (10–20 kW kg−1) density combined with excellent cycle stability. Moreover, these ZIHS pouch-type devices exhibit superior durability and flexibility, withstanding mechanical stress up to 150° bending states with at least 90% of capacitance retention. It suggests a prospect for their application in wearable electronics.4 References(1) Wang, Y.; Sun, S.; Wu, X.; Liang, H.; Zhang, W. Status and Opportunities of Zinc Ion Hybrid Capacitors: Focus on Carbon Materials, Current Collectors, and Separators. Nano-Micro Lett. 2023, 15 (1), 78.(2) Kasprzak, D.; Mayorga-Martinez, C. C.; Pumera, M. Sustainable and Flexible Energy Storage Devices : A Review. Energy & Fuels 2023, 37, 74–97.(3) Kasprzak, D.; Liu, J. Chitin and Cellulose as Constituents of Efficient, Sustainable, and Flexible Zinc-Ion Hybrid Supercapacitors. Sustain. Mater. Technol. 2023, 38, e00726.(4) Dubal, D. P.; Chodankar, N. R.; Kim, D. H.; Gomez-Romero, P. Towards Flexible Solid-State Supercapacitors for Smart and Wearable Electronics. Chem. Soc. Rev. 2018, 47 (6), 2065–2129. Figure 1. Graphical abstract of the research on biopolymer-based Zn-ion hybrid supercapacitors. Figure 1