Reversible K-ion intercalation in CrSe2 cathodes for potassium-ion batteries: combined operando PXRD and DFT studies†

IF 9.5 2区 材料科学 Q1 CHEMISTRY, PHYSICAL Journal of Materials Chemistry A Pub Date : 2024-10-23 DOI:10.1039/D4TA05114A
Weihao Li, Johannes Döhn, Jinyu Chen, Manuel Dillenz, Mohsen Sotoudeh, David M. Pickup, Shunrui Luo, Ryan Parmenter, Jordi Arbiol, Maria Alfredsson, Alan V. Chadwick, Axel Groß, Maider Zarrabeitia and Alexey Y. Ganin
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Abstract

In the pursuit of more affordable battery technologies, potassium-ion batteries (KIBs) have emerged as a promising alternative to lithium-ion systems, owing to the abundance and wide distribution of potassium resources. While chalcogenides are uncommon as intercalation cathodes in KIBs, this study's electrochemical tests on CrSe2 revealed a reversible K+ intercalation/deintercalation process. The CrSe2 cathode achieved a KIB battery capacity of 125 mA h g−1 at a 0.1C rate within a practical 1–3.5 V vs. K+/K operation range, nearly matching the theoretical capacity of 127.7 mA h g−1. Notably, the battery retained 85% of its initial capacity at a high 1C rate, suggesting that CrSe2 is competitive for high-power applications with many current state-of-the-art cathodes. In-operando PXRD studies uncovered the nature of the intercalation behavior, revealing an initial biphasic region followed by a solid-solution formation during the potassium intercalation process. DFT calculations helped with the possible assignment of intermediate phase structures across the entire CrSe2–K1.0CrSe2 composition range, providing insights into the experimentally observed phase transformations. The results of this work underscore CrSe2's potential as a high-performance cathode material for KIBs, offering valuable insights into the intercalation mechanisms of layered transition metal chalcogenides and paving the way for future advancements in optimizing KIB cathodes.

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用于钾离子电池的 CrSe2 阴极中的可逆钾离子互掺:Operando PXRD 和 DFT 联合研究
为了追求更经济实惠的电池技术,钾离子电池(KIBs)因钾资源丰富且分布广泛而成为锂离子系统的一种有前途的替代品。在 KIB 中,铬化砷化物作为插层阴极并不常见,而本研究对 CrSe2 进行的电化学测试却揭示了一种可逆的 K+ 离子插层/脱插层过程。在 1-3.5 V vs K+/K 的实际操作范围内,CrSe2 阴极在 0.1C 速率下实现了 125 mAh/g 的 KIB 电池容量,几乎与 127.7 mAh/g 的理论容量相当。值得注意的是,该电池在 1C 的高倍率下仍能保持 85% 的初始容量,这表明 CrSe2 在高功率应用中与许多当前最先进的阴极相比具有竞争力。在操作过程中进行的 PXRD 研究揭示了插层行为的本质,发现在钾插层过程中,最初的双相区域随后形成固溶体。DFT 计算有助于确定整个 CrSe2 - K1.0CrSe2 成分范围内的中间相结构,为实验观察到的相变提供了见解。这项工作的结果强调了 CrSe2 作为 KIB 的高性能阴极材料的潜力,为层状过渡金属钙钛矿的插层机制提供了宝贵的见解,并为未来优化 KIB 阴极的进步铺平了道路。
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来源期刊
Journal of Materials Chemistry A
Journal of Materials Chemistry A CHEMISTRY, PHYSICAL-ENERGY & FUELS
CiteScore
19.50
自引率
5.00%
发文量
1892
审稿时长
1.5 months
期刊介绍: The Journal of Materials Chemistry A, B & C covers a wide range of high-quality studies in the field of materials chemistry, with each section focusing on specific applications of the materials studied. Journal of Materials Chemistry A emphasizes applications in energy and sustainability, including topics such as artificial photosynthesis, batteries, and fuel cells. Journal of Materials Chemistry B focuses on applications in biology and medicine, while Journal of Materials Chemistry C covers applications in optical, magnetic, and electronic devices. Example topic areas within the scope of Journal of Materials Chemistry A include catalysis, green/sustainable materials, sensors, and water treatment, among others.
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