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通过原位透射电子显微镜揭示用于钾离子电池的BiVO阳极的不对称相变

Revealing Asymmetric Phase Transformation of the BiVO Anodes for Potassium-Ion Batteries by In Situ Transmission Electron Microscopy.

作者信息

An Quan, Zhang Wenqi, Ma Zelin, Guo Shiying, Wang Ying, Yao Yiqing, Dong Lixin, Xia Weiwei, Cai Ran, Wang Hongqiang

机构信息

School of Materials Science and Engineering, Northwestern Polytechnical University, Xi'an 710000, Shaanxi, China.

Department of Biomedical Engineering, City University of Hong Kong, Hong Kong 999077, China.

出版信息

ACS Appl Mater Interfaces. 2024 Oct 5. doi: 10.1021/acsami.4c12707.

Abstract

Potassium-ion batteries (PIBs) have emerged as a promising alternative to lithium-ion batteries (LIBs), thanks to the cost-effectiveness of potassium resources and a favorable redox potential of approximately -2.936 V. The monoclinic BiVO, known for its layered structure, shows noteworthy electrochemical properties when utilized as an anode material for both LIBs and sodium-ion batteries. However, the fundamental electrochemical reaction mechanisms of the BiVO anode during the potassium insertion/extraction processes remain unclear. Here, we constructed a BiVO anode PIB inside the transmission electron microscope (TEM) to explore the real-time potassiation/depotassiation behaviors of BiVO during electrochemical cycling. Utilizing the state-of-art in situ TEM technique, the BiVO nanorods are found to undergo an asymmetric phase transformation for the first time, where the pristine BiVO material is transformed into an amorphous KBiVO phase after the first cycle. More interestingly, the anode materials near and far from the potassium source exhibit opposite volume-changing trends under the same voltage potential. Also, this phenomenon should be attributed to the mass flow of the unstable K-Bi alloy under the electric field. Our findings provide significant insights into the electrochemical mechanism of BiVO nanorods during the potassiation/depotassiation process, with the hope of assistance in designing anodes for high-performance PIBs.

摘要

钾离子电池(PIBs)已成为锂离子电池(LIBs)的一种有前景的替代方案,这得益于钾资源的成本效益以及约 -2.936 V 的有利氧化还原电位。以其层状结构而闻名的单斜相 BiVO,在用作 LIBs 和钠离子电池的负极材料时表现出值得注意的电化学性能。然而,BiVO 负极在钾嵌入/脱出过程中的基本电化学反应机制仍不清楚。在此,我们在透射电子显微镜(TEM)内构建了一个 BiVO 负极 PIB,以探索 BiVO 在电化学循环过程中的实时钾化/去钾化行为。利用最先进的原位 TEM 技术,首次发现 BiVO 纳米棒经历不对称相变,其中原始 BiVO 材料在第一个循环后转变为非晶态 KBiVO 相。更有趣的是,在相同电压电位下,靠近和远离钾源的负极材料呈现出相反的体积变化趋势。此外,这种现象应归因于不稳定的 K-Bi 合金在电场下的质量流动。我们的研究结果为 BiVO 纳米棒在钾化/去钾化过程中的电化学机制提供了重要见解,有望有助于设计高性能 PIBs 的负极。

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