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构建具有易脱溶剂化界面的水合CaVO阴极用于高性能水系锌离子电池。

Architecting a Hydrated CaVO Cathode with a Facile Desolvation Interface for Superior-Performance Aqueous Zinc Ion Batteries.

作者信息

Sun Qiangchao, Cheng Hongwei, Sun Congli, Liu Yanbo, Nie Wei, Zhao Kangning, Lu Xionggang, Zhou Jiang

机构信息

State Key Laboratory of Advanced Special Steel & Shanghai Key Laboratory of Advanced Ferrometallurgy & School of Materials Science and Engineering, Shanghai University, Shanghai 200,444, P. R. China.

State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, International School of Materials Science and Engineering, Wuhan University of Technology, Wuhan 430,070, P. R. China.

出版信息

ACS Appl Mater Interfaces. 2021 Dec 22;13(50):60035-60045. doi: 10.1021/acsami.1c19760. Epub 2021 Dec 13.

Abstract

Vanadium-based materials are promising cathode candidates for low-cost and high-safety aqueous zinc-ion batteries (AZIBs). However, they suffer from inferior rate capability and undesirable capacity fading due to their intrinsic poor conductivity and structural instability. Herein, we synthesize hydrated CaVO·0.75HO (CaVOH) nanoribbons with incorporations of the carbon nanotubes a one-step hydrothermal method, achieving an integrated architecture hybrid cathode (C/CaVOH) design. Benefitting from the robust structure and low desolvation interface, the prefabricated C/CaVOH cathodes deliver a high capacity of 384.2 mA h g at 0.5 A g with only 5.6% capacity decay over 300 cycles, enable an ultralong cycling life of 10,000 cycles at 20.0 A g with 80.2% capacity retention, and exhibit an impressive rate capability (165 mA h g at 40.0 A g) with a high mass loading of ∼4 mg cm. Moreover, through the theoretical calculations and a series of characterizations, we demonstrate the Zn/H co-intercalation storage mechanism, the key role of the gallery water, and the function of the induced C-O groups in promoting kinetics of the C/CaVOH electrode. This work highlights the strategy of implanted high conductivity materials to engineer vanadium-based or other cathodes for high-performance AZIBs.

摘要

钒基材料是低成本、高安全性水系锌离子电池(AZIBs)颇具潜力的阴极候选材料。然而,由于其固有的低导电性和结构不稳定性,它们的倍率性能较差且容量衰减不理想。在此,我们通过一步水热法合成了掺入碳纳米管的水合CaVO·0.75H₂O(CaVOH)纳米带,实现了一种集成结构的混合阴极(C/CaVOH)设计。受益于其坚固的结构和低去溶剂化界面,预制的C/CaVOH阴极在0.5 A g下具有384.2 mA h g的高容量,在300次循环中容量衰减仅5.6%,在20.0 A g下可实现10000次循环的超长循环寿命,容量保持率为80.2%,并且在约4 mg cm的高质量负载下表现出令人印象深刻的倍率性能(在40.0 A g下为165 mA h g)。此外,通过理论计算和一系列表征,我们证明了Zn/H共嵌入存储机制、层间水的关键作用以及诱导产生的C-O基团在促进C/CaVOH电极动力学方面的作用。这项工作突出了植入高导电性材料以设计用于高性能AZIBs的钒基或其他阴极的策略。

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