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揭示单晶富镍阴极的结构演变与可逆相变之间的相关性。

Revealing the Correlation between Structural Evolution and Reversible Phase Transition of Single-Crystalline Ni-Rich Cathode.

作者信息

Huang Yingde, Li Peiyao, Wei Hanxin, Luo Yu-Hong, Chen Min, Liu ShuLin, Yin Wen, Zhang Xia-Hui, Zheng Jun-Chao

机构信息

School of Metallurgy and Environment, Central South University, Changsha, Hunan 410083, China.

National Engineering Laboratory for High Efficiency Recovery of Refractory Nonferrous Metals, Central South University, Changsha 410083, China.

出版信息

ACS Nano. 2025 Jul 8;19(26):23719-23731. doi: 10.1021/acsnano.5c03464. Epub 2025 Jun 25.

Abstract

Single-crystal nickel-rich cathodes are widely used in electric vehicles. However, the irreversible phase transition of H2-H3 during cycling leads to severe lattice distortion and disruption of the crystal structure, which seriously hinders their practical application. Herein, we formed an atomic rearrangement structure with a superlattice phenomenon on the surface of the material by lattice engineering to achieve the reversible phase transition of H2-H3 and obtained structurally stable cathode materials. Benefiting from the synergistic effect of anionic and cationic codoping, the orderly occupation of transition metal ions with lithium ions stabilizes the long-range layered plate and realizes the reversible phase transition of H2-H3 in the highly charged state. Interestingly, the atomic rearrangement of the surface structure enhanced the mechanical modulus and suppressed particle cracks caused by compressive stress concentration. In addition, the stable electrode-electrolyte interface shielded the interfacial side reactions and mitigated the escape of lattice oxygen and the leaching of transition metals. As a result, the designed Zr/F-NCM||graphite pouch battery maintained 92.4% capacity after 1000 cycles, which provides a prospective guideline for improving the durability of layered oxide cathode materials.

摘要

单晶富镍阴极广泛应用于电动汽车中。然而,循环过程中H2-H3的不可逆相变会导致严重的晶格畸变和晶体结构破坏,这严重阻碍了它们的实际应用。在此,我们通过晶格工程在材料表面形成了具有超晶格现象的原子重排结构,以实现H2-H3的可逆相变,并获得结构稳定的阴极材料。受益于阴离子和阳离子共掺杂的协同效应,过渡金属离子与锂离子的有序占位稳定了长程层状板,并在高充电状态下实现了H2-H3的可逆相变。有趣的是,表面结构的原子重排提高了机械模量,并抑制了由压缩应力集中引起的颗粒裂纹。此外,稳定的电极-电解质界面屏蔽了界面副反应,减轻了晶格氧的逸出和过渡金属的浸出。结果,设计的Zr/F-NCM||石墨软包电池在1000次循环后保持了92..4%的容量,这为提高层状氧化物阴极材料的耐久性提供了前瞻性指导。

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