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在具有增强循环稳定性的单晶镍衬底上进行锂异质外延沉积。

Li Heteroepitaxial Deposition on Single Crystalline Ni Substrates With Enhanced Cycling Stability.

作者信息

Zheng Zhiqiang, Qiu Tian, Fu Zhanghua, Chen Chuang, Li Huancai, Hu Cheng

机构信息

Shenzhen Research Institute of Shandong University, Shenzhen, Guangdong, 518057, China.

Key Laboratory for Liquid-Solid Structural Evolution and Processing of Materials (Ministry of Education), School of Materials Science and Engineering, Shandong University, Jinan, Shandong, 250061, P.R. China.

出版信息

Chemistry. 2025 Jul 17;31(40):e202500954. doi: 10.1002/chem.202500954. Epub 2025 Jun 25.

Abstract

Lithium (Li) metal is recognized as a highly promising anode material for next-generation high-energy-density batteries. Nonetheless, dendrite growth and low coulombic efficiency (CE) significantly impede the practical application of Li metal anodes. The deposition morphology and chemical stability of Li are intricately linked to its crystallographic orientation. This study presents a substrate engineering approach that employs single-crystalline nickel (Ni) to facilitate epitaxial Li deposition due to their excellent lattice matching. The findings reveal that the Ni(110) substrate exhibits a more pronounced heteroepitaxial effect than Ni(111). A robust {110}-textured Li deposition was prepared on Ni(110) with a uniform planar morphology due to the lower Li self-diffusion barrier on the Li(110) plane. The {110}-textured Li epitaxial deposition improves the cycling stability in Ni-Li cells and full cells. Notably, the Li||LiFePO full cell utilizing the {110}-textured Li anode exhibits a high capacity retention of 109.6 mAh cm over 350 cycles at 1 C under a low negative-to-positive capacity ratio of 1.26. This investigation highlights the crucial role of substrate-induced heteroepitaxy in improving Li plating/stripping dynamics and provides insights for the development of stable Li metal anodes by crystallographic orientation modification.

摘要

锂(Li)金属被认为是下一代高能量密度电池极具前景的负极材料。尽管如此,枝晶生长和低库仑效率(CE)严重阻碍了锂金属负极的实际应用。锂的沉积形态和化学稳定性与其晶体取向密切相关。本研究提出了一种衬底工程方法,该方法采用单晶镍(Ni)来促进外延锂沉积,因为它们具有出色的晶格匹配。研究结果表明,Ni(110)衬底比Ni(111)表现出更显著的异质外延效应。由于Li(110)平面上较低的锂自扩散势垒,在Ni(110)上制备了具有均匀平面形态的坚固的{110}织构锂沉积。{110}织构锂外延沉积提高了镍-锂电池和全电池的循环稳定性。值得注意的是,使用{110}织构锂负极的Li||LiFePO全电池在1 C下,在1.26的低负正容量比下,经过350次循环后,具有109.6 mAh cm的高容量保持率。这项研究强调了衬底诱导异质外延在改善锂电镀/剥离动力学方面的关键作用,并为通过晶体取向改性开发稳定的锂金属负极提供了见解。

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