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Ion transport property and water structure of electrolytes are two of the most important issues for aqueous batteries, especially when operated at extreme temperatures. To this end, a sepiolite-based clay electrolyte (SCYE) with nanoconfined channels as single-ion conductor is proposed. The inner Zn and anions solvation shells exhibit fascinating hydration-shell reconfiguration behavior compared to the conventional Zn(ClO) aqueous electrolytes. The bond-orientational order of the Zn and anions is broken and highly developed, respectively, thus improving the Zn transference number to 0.97. Moreover, free water molecules are dramatically reduced in the SCYE, contributing to improved anti-freezing ability and thermal stability. The single-ion transport property of the SCYE endows the PANI||Zn full cells with excellent rate performances, with an ≈84% capacity retention from 1 to 20 A g. Besides, full cells with the SCYE achieve 17,000 cycles under -40 °C with a specific capacity of 130 mAh g at 1 A g and considerable performances even at -60 °C, while they can operate over 3000 cycles at 60 °C with 87% capacity retention. This attracting effect can be expanded to several other clay materials, all presenting improved ion transport capability, which paves a road for future aqueous batteries across extreme temperatures.
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http://dx.doi.org/10.1002/adma.202510668 | DOI Listing |
Angew Chem Int Ed Engl
September 2025
State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry, Jilin University, Changchun, 130012, P.R. China.
Neutral aqueous Zn-air batteries (ZABs), while promising for extended lifespans and recyclability compared to alkaline systems, are hindered by sluggish kinetics that limit energy efficiency and power output. Here, we report an effective approach to construct a photo-assisted near-neutral ZAB based on a photo-responsive titanium silicalite-1 zeolite (TS-1). The incorporation of Ru active centers into the 3D porous architecture of TS@C (Ru@TS@C), which exhibits remarkably enhanced electronic conduction, creates interconnected conductive pathways.
View Article and Find Full Text PDFAdv Mater
September 2025
Department of Materials Science & Engineering, College of Design and Engineering, National University of Singapore, 9 Engineering Drive 1, Singapore, 117575, Singapore.
To advance the commercial utilization of aqueous electrochemical devices for grid-scale energy storage, it is crucial to address the current limitations related to energy density and cycle stability. Indeed, the lack of high-performance cathodes is still an obstructive issue, not to mention the limited capacities related to the monotonic cation intercalation/deintercalation mechanism. Fortunately, conversion chemistries with redox reactions bring a new dimension, where materials with multiple valence states facilitate multi-electron redox reactions, offering the potential for high-energy-density storage.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Laboratory of Advanced Materials, Aqueous Battery Center, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Shanghai Wusong Laboratory of Materials Science, College of Smart Materials and Future Energy, Fudan University, Shanghai 200433, China.
Potassium-ion batteries (PIBs) have emerged as an appealing, sustainable and cost-effective candidate for grid-scale energy storage due to abundant K resources and reversible K de/intercalation in graphite anodes (KC, 279 mAh g). However, their practical operation suffers from sluggish kinetics and severe capacity deterioration in traditional carbonate electrolytes. Herein, ethoxy (pentafluoro) cyclotriphosphazene (PFPN) and methyl (2,2,2-trifluoroethyl) carbonate (FEMC) are introduced as cosolvents to rejuvenate conventionally low-concentration (1 M) 1,2-dimethoxyethane (DME)-based electrolytes.
View Article and Find Full Text PDFACS Sustain Chem Eng
September 2025
Electrochemical Innovation Lab, Department of Chemical Engineering, University College London, Torrington Place, London WC1E 7JE, U.K.
Traditionally, binders such as poly-(vinylidene fluoride) (PVDF) have been used within lithium-sulfur (Li-S) batteries, but these present environmental and recyclability challenges and have little to no impact on the processes that drive degradation in the cell's chemistry. Ideally, a Li-S battery binder would contribute to the mitigation of the polysulfide shuttle effect and negate the impacts of positive electrode volume expansion while being compatible with aqueous ink preparation and low-energy, low-toxicity recycling processes. In this work, we demonstrate that fibroin, an economical and sustainable biological polymer with an abundance of functional groups, can effectively trap polysulfides while still offering the durability, cyclability, and ease of use offered by the current state-of-the-art binder (PVDF).
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
Department of Materials Science and Engineering, University of Washington, Seattle, WA 98195, USA. Electronic address:
Pre-intercalation has emerged as a highly effective strategy to enhance structural integrity and ion transport kinetics in cathodes for aqueous Zn-ion batteries. Here, we report a zinc-ion pre-intercalated hydrate vanadium oxide cathode, in which the initial insertion of Zn induces a significant expansion of the interplanar spacing, followed by contraction at higher Zn concentrations owing to strong electrostatic interactions with the VO framework. Such competing expansion and contraction of interplanar spacing enhances the overall electrochemical properties.
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