材料科学
掺杂剂
阴极
兴奋剂
氧化物
化学物理
外延
价(化学)
密度泛函理论
扩散
热稳定性
热的
相(物质)
晶格常数
格子(音乐)
电极
Crystal(编程语言)
单晶
纳米技术
凝聚态物理
晶体结构
工作(物理)
光电子学
晶体生长
表面扩散
结晶学
化学工程
结构稳定性
电子结构
作者
Feng Li,Xin Zhang,Kaixin Zhang,Maosheng Gong,Zezhou Lin,Peiyu Hou,Jingyuan Liu,Heng-Jing Liu,Hongzhou Zhang,Xijin Xu,Haitao Huang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-12-18
卷期号:20 (1): 864-878
被引量:2
标识
DOI:10.1021/acsnano.5c15947
摘要
The synergistic effects of a single-crystal structure and high-entropy doping are expected to enhance the structural and thermal stability of high-capacity Ni-rich cathodes. Nonetheless, the pinning effect caused by heavy-mass dopants and surface phase segregation induced by the thermodynamic immiscibility of dissimilar elements hinder atomic diffusion and crystal fusion, making it extremely difficult to synthesize single crystals with high-entropy doping. In this study, density functional theory calculations confirm that effective diffusion is achievable within a grain-boundary-free single-crystal matrix at elevated temperatures, even for heavy-mass dopants with high valence states. A lattice-matched epitaxial growth approach is proposed to enable the synthesis of single-crystal Ni-rich oxides with high-entropy doping. The synergistic effects of high-entropy doping and single crystals within a Ni-rich cathode exhibit significantly reduced changes in the lattice volume and Ni-O/TM coordination distance and the absence of intragranular cracks upon Li+ de/intercalation, presenting highly improved cyclic and thermal stabilities compared with the high-entropy-doped polycrystal counterpart and single-crystal counterpart without high-entropy doping. This integration not only addresses the inherent limitations of Ni-rich compositions but can also be expanded to the design of other electrode materials, where entropy-driven stabilization and single crystals can work together to enhance cathode performance.
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