Pang Yanfei, Wang Yingshuai, Jiang Chunyu, Ding Xiangyu, Xin Yuhang, Zhou Qingbo, Chen Baorui, Liu Hongfeng, Singh Preetam, Wang Qianchen, Gao Hongcai
School of Materials Science and Engineering, Beijing Institute of Technology, Beijing, 100081, P.R. China.
Department of Ceramic Engineering, Indian Institute of Technology (BHU), Varanasi, 221005, India.
ChemSusChem. 2024 Dec 6;17(23):e202400768. doi: 10.1002/cssc.202400768. Epub 2024 Aug 7.
Layered transition metal oxides are widely considered as ideal cathode materials for SIBs. However, the existing P2 and O3 structures possess specific issues, which limit their practical applications. To address these issues, this work designed a novel intergrowth layered oxide cathode with P2 and O3 phases by implementing Cu and Ti into the structure with the formation of high-entropy cathode materials with superior performance for SIBs. The electrochemical test results show that the optimized high-entropy cathode with the P2/O3 intergrowth structure possesses a high initial discharge capacity of 157.85 mAh g at 0.1 C, an excellent rate performance of 84.41 mAh g at 10 C, and long-term stability with capacity retention of 83.25 % after 500 cycles at 5 C. Furthermore, the analysis results of ex situ XRD and in situ XRD indicate that the adverse phase transition of P2-O2 under high voltage is effectively suppressed. This work indicates that the integration of high-entropy strategy with the two-phase intergrowth structure can effectively stabilize the layered structure, suppress the slipping of transition metal layers, and improve electrochemical performance, which provides a new approach for designing high-performance and practical layered transition metal oxide cathode materials for advanced SIBs.
层状过渡金属氧化物被广泛认为是用于钠离子电池(SIBs)的理想正极材料。然而,现有的P2和O3结构存在特定问题,这限制了它们的实际应用。为了解决这些问题,本工作通过在结构中引入铜和钛,设计了一种具有P2和O3相的新型共生层状氧化物正极,形成了具有优异钠离子电池性能的高熵正极材料。电化学测试结果表明,优化后的具有P2/O3共生结构的高熵正极在0.1C下具有157.85 mAh g的高初始放电容量,在10C下具有84.41 mAh g的优异倍率性能,并且在5C下经过500次循环后具有83.25%的容量保持率的长期稳定性。此外,非原位XRD和原位XRD的分析结果表明,高压下P2-O2的不利相变得到有效抑制。本工作表明,高熵策略与两相共生结构的结合可以有效地稳定层状结构,抑制过渡金属层的滑移,并提高电化学性能,这为设计用于先进钠离子电池的高性能和实用的层状过渡金属氧化物正极材料提供了一种新方法。