Gel Electrolyte Research Articles

Activating the Intrinsic Zincophilicity of PAM Hydrogel to Stabilize the Metal-Electrolyte Dynamic Interface for Stable and Long-Life Zinc Metal Batteries.

As a potential material to solve rampant dendrites and hydrogen evolution reaction (HER) problem of aqueous zinc metal batteries (AZMB), hydrogel electrolytes usually require additional additives or multi-molecular network strategies to solve existing problems of ionic conductivity, mechanical properties and interface stability. However, the intrinsic zincophilic properties of the gel itself are widely neglected leading to the addition of additional molecules and the complexity of the preparation process. In this work, we innovatively utilize the characteristics of acrylamide's high zincophilic group density, activating the intrinsic zincophilic properties of PAM gel through a simple concentration control strategy which reconstructs a novel zinc-electrolyte interface different from conventional PAM electrolyte. The activated novel gel electrolyte with intrinsic zincophilic properties has high ionic conductivity and effectively suppresses water activity, thereby inhibiting HER corrosion. Meanwhile, it induces uniform deposition of (002) crystal planes, leading to excellent deposition kinetics and long cycle life, thereby ensuring high interfacial stability. Compared with conventional PAM gel electrolytes, the activated zincophilic group-rich hydrogel maintained excellent cycling stability (1 mA/cm2, 1 mAh/cm2) over 2250 hours; The Zn//MnO₂ coin cell using novel zincophilic group -rich hydrogel still retains a high specific capacity of more than 170 mAh/g at 0.5 A/g after 1000 cycles.

Comparative investigations on polymer gel electrolytes comprising triflate salts of Li, Na, Mg in TEGDME solvent and PVdF-HFP/PVP blend matrix

Comparative investigations on polymer gel electrolytes comprising triflate salts of Li, Na, Mg in TEGDME solvent and PVdF-HFP/PVP blend matrix

Hydrated Calcium Vanadate Nanoribbons with a Stable Structure and Fast Ion Diffusion as a Cathode for Quasi-Solid-State Zinc-Ion Batteries.

We demonstrated the use of hydrated calcium vanadate (CaV6O16·3H2O, denoted as CaVO-2) as a cathode for aqueous zinc-ion batteries (AZIBs). Nanoribbons of hydrated calcium vanadate facilitated shortening of the Zn2+ transport distance and accelerated zinc-ion insertion. The introduction of interlayer structure water increased the interlayer spacing of calcium vanadate and as a "lubricant". Ca2+ insertion also expanded the interlayer spacing and further stabilized the interlayer structure of vanadium-based oxide. The density functional theory results showed that the introduction of Ca2+ and structured water could effectively improve the diffusion kinetics, resulting in the rapid transport of zinc ions. As a result, AZIBs based on the CaVO-2 cathode offered high specific capacity (329.6 mAh g-1 at 200 mA g-1) and fast charge/discharge capability (147 mAh g-1 at 10 A g-1). Impressively, quasi-solid-state zinc-ion batteries based on the CaVO-2 cathode and polyacrylamide-cellulose nanofiber hydrogel electrolytes maintained an outstanding specific capacity and long cycle life (162 mAh g-1 over 10 000 cycles at 5 A g-1). This study provided a reliable strategy for metal-ion insertion and the structural water introduction of oxides to produce a high-quality cathode for ZIBs. Meanwhile, it provides ideas for the combination of vanadium-based materials and gel electrolytes to construct solid-state zinc-ion batteries.

Agricultural and industrial wastes applied on the high performance energy storage devices

Driven by population growth, the destruction of the environment and the energy demand continue to increase dramatically. This study uses garlic skin and carbon fiber from agricultural and industrial wastes to prepare energy storage devices. Carbon quantum dots (CQDs) were obtained from garlic skin using high-temperature pyrolysis. The specific capacitance of the gel electrolyte could be effectively increased with a small number of CQDs doping. A methylcellulose-based carbon fiber-electrode was prepared by grinding and depositing the industrial recycled carbon fiber onto a biodegradable methylcellulose substrate. The methylcellulose-based recycled carbon fiber-electrode has the highest specific capacitance, energy density, and power density, which are 155 F/g, 10 Wh/kg, and 4047 W/kg, respectively, at a scan rate of 0.02 V/s, and demonstrates excellent performance, such like high specific capacitance, low internal resistance as well as rapid charge and discharge characteristics, which may have potential to replace the expensive carbon nanotubes and graphenes. The electrodes were made from recycled carbon fiber, the gel electrolyte with garlic CQDs, and a separator assembled into a sandwich structure to form supercapacitors. The capacity retention rate of the supercapacitor still retained 96 % of its initial value after 2000 cycles of charge and discharge testing at a constant current of 0.20 mA. This demonstrates the supercapacitor prepared in this study with competitive power density, energy density, high rate capability, and excellent life cycle stability by combining the garlic skin and carbon fiber from agricultural and industrial wastes, highlighting the enormous potential of agricultural and industrial wastes for energy storage applications.

Flexible aqueous zinc-ion battery with low-temperature resistant leather gel electrolyte

Flexible zinc-ion batteries (FZIBs) have been acknowledged as a potential cornerstone for the future development of flexible energy storage, yet conventional FZIBs still encounter challenges, particularly concerning performance failure at low temperatures. To address these challenges, a novel anti-freezing leather gel electrolyte (AFLGE-30) is designed, incorporating ethanol as a hydrogen bonding acceptor. The AFLGE-30 demonstrates exceptional frost resistance while maintaining favorable flexibility even at −30°C; accordingly, the battery can achieve a high specific capacity of about 70 mAh/g. Cu//Zn battery exhibits remarkable stability at room temperature, retaining ∼96% efficiency after 120 plating/stripping cycles at 1 mA/cm2. Concurrently, the Zn//Zn symmetric batteries demonstrate a lifespan of 4100 h at room temperature, which is attributed to the enhancement of Zn2+ deposition kinetics, restraining the formation of zinc dendrites. Furthermore, FZIBs exhibit minimal capacity loss even after bending, impacting, or burning. This work provides a promising strategy for designing low-temperature-resistant FZIBs.

Mitigating Gas Evolution in Electron Beam-Induced Gel Polymer Electrolytes Through Bi-Functional Cross-Linkable Additives.

The current high-capacity lithium-ion batteries (LIBs), reliant on flammable liquid electrolytes (LEs) and nickel-rich cathodes, are plagued by safety hazards, especially the risk of hazardous gas release stemming from internal side reactions. To address these safety concerns, an electron beam (E-beam)-induced gel polymer electrolyte (E-Gel) is introduced, employing dipentaerythritol hexaacrylate (DPH) as a bi-functional cross-linkable additive (CIA). The dual roles of DPH are exploited through a strategically designed E-beam irradiation process. Applying E-beam irradiation on the pre-cycled cells allows DPH to function as an additive during the initial cycle, establishing a protective layer on the surface of the anode and cathode and as a cross-linker during the E-beam irradiation step, forming a polymer framework. The prepared E-Gel with CIA has superior interfacial compatibility, facilitating lithium-ion diffusion at the electrode/E-Gel interface. The electrochemical assessment of 1.2 Ah pouch cells demonstrates that E-Gel substantially reduces gas release by 2.5 times compared to commercial LEs during the initial formation stage and ensures superior reversible capacity retention even after prolonged cycling at 55°C. The research underscores the synergy of bifunctional CIA with E-beam technology, paving the way for large-scale production of safe, high-capacity, and commercially viable LIBs.

A Cross-Linked Gel Polymer Electrolyte Composed of PEGDA and Acrylonitrile for High-Voltage Lithium Metal Batteries

A Cross-Linked Gel Polymer Electrolyte Composed of PEGDA and Acrylonitrile for High-Voltage Lithium Metal Batteries

The construction of a flexible solid-state asymmetric supercapacitor device using nickel-copper oxide nanoplates and carbon nanosphere serving as positive and negative electrode, respectively with excellent electrochemical capabilities

Here, nickel-copper oxide nanoplates (NCN) and carbon nanosphere (CNS) as positive and negative electrodes are synthesised via a hydrothermal protocol without adding any surfactant and binders. The NCN and CNS electrodes in KOH electrolyte exhibit superior specific capacitance of ∼ 2362.5 F g−1 and ∼ 246.11 F g−1 at 1 A g−1 respectively. The NCN and CNS retained 98.54 % and 97.88 % of the initial capacitance after 3000 galvanostatic charge–discharge (GCD) cycles, respectively. Additionally, an asymmetric supercapacitor (ASC) device NCN//CNS is constructed using NCN and CNS as positive and negative electrodes, utilizing poly(vinyl alcohol) PVA − KOH gel electrolyte separator. The ASC device demonstrates a maximum energy density of 50.4 Wh kg−1 (181.44 KJ kg−1) with a power density ∼ 750 W kg−1 at 1 A g−1, maintaining 90.4 % cyclic stability after 10,000 GCD cycles. The electrochemical outputs of the device present significant potential for the advancement of high-performance ASC devices in electronic applications.

Ionic liquid- filled polymer gel electrolyte with self-healing capability at room-temperature for lithium-ion batteries

Nowadays, varied application environments require lithium-ion batteries to have self-healing capabilities so that they can avoid the breakage caused by volume changes during using and reach better safety, reliability, and longer cycle life. Herein, an ionic liquid filled polymer gel electrolyte IL-PEO was proposed, prepared by a simple method and process, the gel electrolyte exhibits significantly enhanced mechanical strength and demonstrates good resistance to heat, high ionic conductivity (1.05 × 10−3 S cm−1, 30°C) and Li transference number. The research show that the addition of BMIM-TFSI promoted the construction of SEI layer and effectively inhibited the growth of lithium dendrites in the gel electrolyte. The LiFePO4 / Li cells with IL-PEO-10 exhibited excellent cycling performance (initial specific capacity of 161.3 mAh g−1 and 94 % capacity retention after 100 cycles) and good rate performance. Most importantly, IL-PEO is able to heal the damage in LiFePO4 / Li batteries at 25 °C and restore the performance, thus improves the stability and safety of the batteries.

Self‐powered sensor based on compressible ionic gel electrolyte for simultaneous determination of temperature and pressure

AbstractThe simultaneous detection of multiple stimuli, such as pressure and temperature, has long been a persistent challenge for developing electronic skin (e‐skin) to emulate the functionality of human skin. Meanwhile, the demand for integrated power supply units is an additional pressing concern to achieve its lightweightness and flexibility. Herein, we propose a self‐powered dual temperature–pressure (SPDM) sensor, which utilizes a compressible ionic gel electrolyte driven by the potential difference between MXene and Al electrodes. The SPDM sensor exhibits a rapid and timely response to changes in pressure‐induced deformation, while exhibiting a slow and hysteretic response to temperature variations. These distinct response characteristics enable the differentiation of current signals generated by different stimuli through machine learning, resulting in an impressive accuracy rate of 99.1%. Furthermore, the developed SPDM sensor exhibits a wide pressure detection range of 0–800 kPa and a broad temperature detection range of 5–75°C, encompassing the environmental conditions encountered in daily human life. The dual‐mode coupled strategy by machine learning provides an effective approach for temperature and pressure detection and discrimination, showcasing its potential applications in wearable electronics, intelligent robots, human–machine interactions, and so on.

Structure and material designs of stretchable electrochromic devices

AbstractElectrochromic materials are a significant class of optoelectronic functional materials that can change colour by adjusting the voltage periodically. In recent years, there has been rapid development in electrochromic technology. However, current research predominantly focuses on traditional rigid electrochromic devices (ECDs), typically using conductive glass substrates such as indium tin oxide. These rigid colour‐changing devices face significant challenges, including large thickness, low mechanical strength, and high cost, which hinder the advancement and commercialisation of electrochromic technology. With the rise of wearable devices and electronic skins, among other future technologies, flexible ECDs have garnered much attention due to their foldability, wearability, and even embeddability. They have emerged as a research hotspot in the field of electrochromism. As a further development direction of flexible ECDs, achieving stretchability poses higher difficulties as it requires maintaining high performance under large strains and even distortions. This article provides an overview of the latest advances in stretchable electrochromic devices (SECDs) from the perspectives of structural and material design. Regarding structural design, the ‘island‐bridge’ structure, the ‘longitudinal wave’ structure, and core‐shell structures are discussed. In terms of material design, the design schemes of substrate, conductive layer, electrochromic layer and electrolyte layer are mainly introduced, with particular emphasis on the introduction of gel electrolyte. Finally, the challenges and difficulties faced by the development of SECDs are briefly analysed.

Ternary Solid Polymer Electrolytes at the Electrochemical Interface: A Computational Study.

Polymer-based solid-like gel electrolytes have emerged as a promising alternative to improve battery performance. However, there is a scarcity of studies on the behavior of these media at the electrochemical interface. In this work, we report classical MD simulations of ternary polymer electrolytes composed of poly(ethylene oxide), a lithium salt [lithium bis(trifluoromethanesulfonyl)imide], and different ionic liquids [1-butyl-1-methylpyrrolidinium bis(trifluoromethanesulfonyl)imide and 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide] confined between two charged and uncharged graphene-like surfaces. The molecular solvation of Li+ ions and their diffusion as well as the polymer conformational picture were characterized in terms of the radial distribution functions, coordination numbers, number density profiles, orientations, displacement variance, polymer radius of gyration, and polymer end-to-end distance. Our results show that the layering behavior of the ternary electrolyte in the interfacial region leads to a decrease of Li+ mobility in the direction perpendicular to the electrodes and high energy barriers that hinder lithium cations from coming into direct contact with the graphene-like surface. The nature of the ionic liquid and its concentration were found to influence the structural and dynamic properties at the electrode/electrolyte interface, the electrolyte with low amounts of the pyrrolidinium-based ionic liquid being that with the best performance since it favors the migration of Li+ cations toward the negative electrode when compared to the imidazolium-based one.

Thermogalvanic hydrogel-based e-skin for self-powered on-body dual-modal temperature and strain sensing

Sensing of both temperature and strain is crucial for various diagnostic and therapeutic purposes. Here, we present a novel hydrogel-based electronic skin (e-skin) capable of dual-mode sensing of temperature and strain. The thermocouple ion selected for this study is the iodine/triiodide (I−/I3−) redox couple, which is a common component in everyday disinfectants. By leveraging the thermoelectric conversion in conjunction with the inherent piezoresistive effect of a gel electrolyte, self-powered sensing is achieved by utilizing the temperature difference between the human body and the external environment. The composite hydrogels synthesized from polyvinyl alcohol (PVA) monomers using a simple freeze‒thaw method exhibit remarkable flexibility, extensibility, and adaptability to human tissue. The incorporation of zwitterions further augments the resistance of the hydrogel to dehydration and low temperatures, allowing maintenance of more than 90% of its weight after 48 h in the air. Given its robust thermal current response, the hydrogel was encapsulated and then integrated onto various areas of the human body, including the cheeks, fingers, and elbows. Furthermore, the detection of the head-down state and the monitoring of foot movements demonstrate the promising application of the hydrogel in supervising the neck posture of sedentary office workers and the activity status. The successful demonstration of self-powered on-body temperature and strain sensing opens up new possibilities for wearable intelligent electronics and robotics.

A thermostable ionic liquid-methacrylate-based polymer electrolyte for energy storage application

In recent years, gel polymer electrolytes (GPEs) incorporating ionic liquids (ILs) have been explored extensively for lithium-ion batteries due to their favourable thermal stability and high ionic conductivity. Gel polymer electrolytes can also improve the safety of lithium-ion batteries by eliminating the flammable organic solvents which are often used in traditional electrolyte systems. Herein, we report an efficient synthesis of a thermostable ionic liquid-methacrylate-based polymer gel electrolyte via a photo-initiated phase separation (PIPS) process in an inert environment. Anionic liquid phase of 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (EMIMTFSI), coupled with a low molecular weight polyethylene glycol dimethyl ether (PEGDME), was combined with a solid phase of bisphenol A ethoxylate dimethacrylate (BEMA) at varying solid to liquid ratios to produce a thermally stable gel electrolyte. The highest ionic conductivity of 1.9 × 10−3 S cm−1 (at 30 °C) was achieved for the electrolyte with a solid-to-liquid ratio of 1:3 by weight. The Lithium metal cells utilizing these electrolytes and LiFePO4 as cathode active material exhibited the initial discharge capacity of 144 mAh g−1 with capacity retention of 85 % over 100 cycles in ambient temperature. The thermal stability of the cells was significantly improved upon increasing the EMIMTFSI content. This study illustrates the potential application of the IL-methacrylate gel polymer electrolyte system in enhancing the safety of Li-ion batteries through careful tuning of the composition. Their versatile properties also make them suitable for quasi-solid-state batteries with high energy density and safety.

Dynamic Covalent Amphiphilic Polymer Conetworks Based on End-Linked Pluronic F108: Preparation, Characterization, and Evaluation as Matrices for Gel Polymer Electrolytes.

We present the development of a platform of well-defined, dynamic covalent amphiphilic polymer conetworks (APCN) based on an α,ω-dibenzaldehyde end-functionalized linear amphiphilic poly(ethylene glycol)-b-poly(propylene glycol)-b-poly(ethylene glycol) (PEG-b-PPG-b-PEG, Pluronic) copolymer end-linked with a triacylhydrazide oligo(ethylene glycol) triarmed star cross-linker. The developed APCNs were characterized in terms of their rheological (increase in the storage modulus by a factor of 2 with increase in temperature from 10 to 50 °C), self-healing, self-assembling, and mechanical properties and evaluated as a matrix for gel polymer electrolytes (GPEs) in both the stretched and unstretched states. Our results show that water-loaded APCNs almost completely self-mend, self-organize at room temperature into a body-centered cubic structure with long-range order exhibiting an aggregation number of around 80, and display an exceptional room temperature stretchability of ∼2400%. Furthermore, ionic liquid-loaded APCNs could serve as gel polymer electrolytes (GPEs), displaying a substantial ion conductivity in the unstretched state, which was gradually reduced upon elongation up to a strain of 4, above which it gradually increased. Finally, it was found that recycled (dissolved and re-formed) ionic liquid-loaded APCNs could be reused as GPEs preserving 50-70% of their original ion conductivity.

Ti3C2Tx Filled in EMIMBF4 Semi-Solid Polymer Electrolytes for the Zinc-Metal Battery.

Zinc-ion batteries (ZIBs) are promising candidates for safe energy storage applications. However, undesirable parasitic reactions such as dendrite growth, gas evaluation, anode corrosion, and structural damage to the cathode under an acidic microenvironment severely affected cell performance. To resolve these issues, an MXene entrapped in an ionic liquid semi-solid gel polymer electrolyte (GPE) composite was explored. The molecular-level mixing of poly(vinylidene fluoride-co-hexafluoropropylene) (PVHF), zinc trifluoromethanesulfonate (Zn(OTF)2), 1-ethyl-3-methylimidazolium tetrafluoroborate (EMIBF4) ionic liquid, and Ti3C2Tx MXene provided a controlled Zn2+ shuttle toward the anode/cathode. Ti3C2Tx/EMIBF4/Zn(OTF)2/PVHF exhibited a breaking strength of 0.36 MPa with an associated extension of 23%. The Zn//Ti3C2Tx/EMIBF4/Zn(OTF)2/PVHF//Zn symmetric cell with continuous zinc plating/stripping exhibited excellent Zn2+ ion mobility toward the anode and cathode without undesired reactions. This was confirmed by post-mortem analysis after a symmetric cell compatibility test. The as-prepared GPE with a Na3V2(PO4)3 (NVP) cathode exhibited a high chemical diffusion coefficient of 1.14 × 10-7. It also showed an outstanding reversible capacity of 89 mAh g-1 at C/10 with an average discharge plateau voltage of 1.45 V, cycle durability, and controlled self-discharge. These results suggested that the Zn2+ ions in the Ti3C2Tx/EMIBF4/Zn(OTF)2/PVHF composite are reversibly labile in the anode and cathode directions.

In-situ growth of 3D amorphous Ni-Co-Mn phosphate on 2D Ti3C2Tx nanocomposite for commercial-level hybrid energy storage application

To overcome the limited electronic conductivity and capacity of single and binary transition metal phosphates (TMPs), highly electrochemical active materials and rational structural design of ternary TMPs composite are urgently required. In this study, we successfully synthesized an amorphous 3D Ni-Co-Mn phosphate@2D Ti3C2Tx (MXene) nanocomposite (NCMP series) through the electrodeposition method. The amorphous Ni-Co-Mn phosphate effectively restricts the self-accumulation of MXene nanosheets, resulting in the development of a porous nanostructure. This structure exposes more active sites, expands the ion transport path, and enhances the conductivity of the Ni-Co-Mn phosphate@Ti3C2Tx material. Owing to the synergistic effect offered by Ni-Co-Mn phosphate and MXene nanocomposite, the anchored Ni-Co-Mn phosphate@Ti3C2Tx (NCMP-5) electrode delivers an elevated capacity of 342 mAh/g (1230 C/g) at 5.0 A/g, surpassing the pristine Ni-Co-Mn phosphate (NCMP-4, 260 mAh/g) and MXene (33.3 mAh/g). Moreover, a hybrid solid-state supercapacitor (HSSC) device is assembled with NCMP-5 as a cathode and reduced graphene oxide (rGO) as an anode within a polymer gel (PVA-KOH) electrolyte. Notably, the fabricated HSSC device displays a supreme specific capacity of 27.5 mAh/g (99 C/g) and a high (volumetric) energy density of 22 Wh/kg (3.6 Wh/cm3) at a power density of 0.80 kW/kg (0.13 kW/cm3) for 1.0 A/g. Moreover, the HSSC device retains 95.4 % of its initial capacity even after 10,000 cycles. Importantly, the operational potential window of two serially connected HSSC devices approaches +3.2 V, enabling different colored commercial light-emitting diodes (LEDs) to be efficiently illuminated. Eventually, the remarkable supercapacitive characteristics of the 3D@2D amorphous Ni-Co-Mn phosphate@MXene nanocomposite make it an attractive choice for advanced electroactive materials in upcoming hybrid energy storage technologies.

Highly efficient suppression of zincate ion crossover in zinc–air batteries using selective membrane PVA-KOH/ZIF-8 gel polymer electrolytes

Rechargeable zinc–air batteries have attracted considerable attention in the industries due to their high energy density, affordability, and safety. However, these batteries still have limitations in their lifetime because of the issue of zincate ion (Zn(OH)42−) crossover. To suppress this issue, a new PVA-KOH-based gel polymer electrolyte membrane incorporating zeolitic imidazolate framework-8 (ZIF-8) nanoparticles was developed as a selective membrane. The influence of different-sized ZIF-8 nanoparticles synthesized with three different zinc salts on thermal, physical, and electrochemical properties was investigated. The PVA-KOH/ZIF-8 membrane significantly reduced the diffusion coefficient of zincate ions to 3.27 × 10−6, 2.01 × 10−6, and 1.99 × 10−6 cm2 min−1 by the incorporation of ZIF-8, synthesized with Zn(NO3)2, Zn(OAc)2, and ZnSO4, respectively. Because of the pore apertures of ZIF-8 that are equivalent to Zn(OH)42−, the PVA-KOH/ZIF-8 selective membrane could block Zn(OH)42−and allowed OH− to pass through the membrane. Moreover, a large external hydrophilic surface was achieved by the influence of smaller-sized particles, which improved the retention of electrolytes. As a result, the ionic conductivity of the PVA-KOH/ZIF-8 membrane increased up to 164.27 mS cm−1 when added 10 wt% ZIF-8, synthesized by ZnSO4. Furthermore, this membrane showed the highest value of battery life cycle of 89 cycles at a current density 10 mA cm−2 and the discharge capacity of 396 mAh g−1. These results indicated that the development of a PVA-KOH/ZIF-8 membrane has a high potential and suitability for use as a new class of separators in rechargeable zinc–air batteries.

Novel sulfonated polyaniline/graphene oxide electrode with high cycling stability for all-solid-state flexible supercapacitors

Polyaniline (PANi) has high theoretical specific capacitance by storing energy through redox reactions and thus is widely used in supercapacitors. However, the skeleton of PANi expands and contracts during the process of ion inhalation and exfoliation, which leads to a decrease in electrochemical performance. To solve this problem, we graft the sulfonic acid group onto the PANi backbone via a borate ester bond, which serves as a proton reservoir to provide protons for PANi to undergo redox reactions and provide pseudocapacitance. SPANi is then polymerized in situ on graphene oxide (GO), and its comprehensive performance of the electrode is further enhanced by designing ordered structures and synergistic interactions. The SPANi5/GO5 composite that are created in-situ have a fantastic specific capacitance of 460.56 F g−1 at 1 A g−1 and maintained 85.19% of the primary capacitance after 10,000 cycles. The device is assembled with PAAM/H2SO4/GO as the gel electrolyte, which achieves a specific capacitance of 137.75 F g−1, and the capacitance is retains at 90.74% after 10,000 cycles. The supercapacitor exhibits a large energy density of 13.76 Wh kg−1 when the power density is 200.27 W kg−1. The present study presents a novel and efficient approach for the fabrication of high-performance supercapacitor electrodes.

High-performance fibre battery with polymer gel electrolyte.

Replacement of liquid electrolytes with polymer gel electrolytes is recognized as a general and effective way of solving safety problems and achieving high flexibility in wearable batteries1-6. However, the poor interface between polymer gel electrolyte and electrode, caused by insufficient wetting, produces much poorer electrochemical properties, especially during the deformation of the battery7-9. Here we report a strategy for designing channel structures in electrodes to incorporate polymer gel electrolytes and to form intimate and stable interfaces for high-performance wearable batteries. As a demonstration, multiple electrode fibres were rotated together to form aligned channels, whilethe surface of each electrode fibre was designed with networked channels. The monomer solution was effectively infiltrated first along the aligned channels and then into the networked channels. The monomers were then polymerized to produce a gel electrolyte and form intimate and stable interfaces with the electrodes. The resulting fibre lithium-ion battery (FLB) showed high electrochemical performances (for example, an energy density of about 128 Wh kg-1). This strategy also enabled the production of FLBs with a high rate of 3,600 m h-1 per winding unit. The continuous FLBs were woven into a 50 cm × 30 cm textile to provide an output capacity of 2,975 mAh. The FLB textiles worked safely under extreme conditions, such as temperatures of -40 °C and 80 °C and a vacuum of -0.08 MPa. The FLBs show promise for applications in firefighting and space exploration.