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Developing thin-film sheets made of oxide-based solid electrolytes is essential for fabricating surface-mounted ultracompact multilayer oxide solid-state batteries. To this end, solid-electrolyte slurry must be optimized for excellent dispersibility. Although oxide-based solid electrolytes for multilayer structures require sintering, high processing temperatures cause problems such as Li-ion volatilization and reactions with graphite anodes. Thus, low-temperature sinterable oxide-based solid-electrolyte materials should be devised. We successfully developed the conditions for producing thin films from 21 μm thick solid-electrolyte sheets of LiO-BO-AlO, one of the most promising candidates for multilayer solid-state batteries. A comprehensive analysis of the fabricated thin films included X-ray diffraction (XRD) to confirm their amorphous structure, scanning electron microscopy (SEM) for particle morphology, and contact angle measurements to verify surface hydrophilicity. Evaluation of a 32-layer bulk sample of solid-electrolyte sheets revealed an ionic conductivity of 2.33 × 10 S/cm and charge transfer resistance of 100.1 kΩ at a sintering temperature of 430 °C. Based on these results, cathode and anode active materials will be applied to develop high-energy-density multilayer ceramic batteries with hundreds of layers in future work.
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http://dx.doi.org/10.3390/mi16010039 | DOI Listing |
Small Methods
September 2025
Hebei Key Laboratory of Optic-Electronic Information and Materials, National & Local Joint Engineering Laboratory of New Energy Photoelectric Devices, College of Physics, Science and Technology, Hebei University, Baoding, 071002, China.
As a new generation of high-energy-density energy storage system, solid-state aluminum-ion batteries have attracted much attention. Nowadays polyethylene oxide (PEO)-based electrolytes have been initially applied to Lithium-ion batteries due to their flexible processing and good interfacial compatibility, their application in aluminum-ion batteries still faces problems. To overcome the limitations in aluminum-ion batteries-specifically, strong Al coordination suppressing ion dissociation, high room-temperature crystallinity, and inadequate mechanical strength-this study develops a blended polymer electrolyte (BPE) of polypropylene carbonate (PPC) and PEO.
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September 2025
Institute of Chemistry, Academia Sinica, Taipei, 115201, Taiwan.
Achieving high capacitance while maintaining rapid charge transport and structural stability remains a major challenge in the design of battery-type supercapacitor electrodes. Herein, a molecularly engineered strategy is presented for constructing hierarchical hybrid electrodes by integrating petal-like NiCu-LDH nanosheets onto 3D HBC-x (x = H, F, OMe)-functionalized CNT paper via a one-step hydrothermal process. The incorporation of HBC effectively mitigates CNT agglomeration and constructs an interconnected conductive framework that enhances charge transport, shortens ion diffusion paths, and reduces internal resistance.
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September 2025
School of Materials Science and Engineering, East China Jiaotong University, Nanchang, 330013, China.
Covalent organic frameworks (COFs) exhibit outstanding structural tunability, clearly defined ion pathways, and remarkable thermal/chemical stabilities, rendering them highly promising candidates for applications in solid-state electrolytes. However, it remains a challenge to develop a versatile method to incorporate both ionic groups and electron-withdrawing units into a single framework for effectively improving the lithium-ion conductivity. Herein, a series of novel [3+3] defective COFs is successfully synthesized featuring active amine/aldehyde anchoring sites for subsequent post-modification, and regulates the ion conductivity through elaborately tuning the anionic/cationic groups and weak/strong electron-withdrawing units.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou, 325035, China.
Sulfide solid electrolytes (SEs) exhibit excellent ionic conductivity and good mechanical properties, but their poor air stability and solid-solid contact performance seriously hinder the wide application of sulfide all-solid-state batteries (ASSBs). Herein, this paper reviews the history and the major breakthroughs in the development of sulfide SEs. The theories of hard-soft-acid-base theory and glass structure theory, as well as several strategies to improve the chemical stability of sulfide SEs, are discussed emphatically.
View Article and Find Full Text PDFInorg Chem
September 2025
Department of Applied Chemistry, Graduate School of Engineering, Osaka Metropolitan University, 1-1 Gakuen-cho, Naka-ku, Sakai, Osaka 599-853, Japan.
Amorphous molybdenum polysulfides (a-MoS) have attracted considerable attention because of their unique physical and chemical properties, which enable their use in a wide range of applications including energy-storage materials. Among various synthesis methods, thermal decomposition provides an effective route for synthesizing a-MoS. In particular, amorphous molybdenum trisulfide (a-MoS) prepared via thermal decomposition has emerged as a promising active material for energy-storage applications owing to its unique structural and electrochemical characteristics.
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