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通过钼表面改性显著提高富锂锰基层状阴极材料的容量和循环稳定性

Significant Enhancement of the Capacity and Cycling Stability of Lithium-Rich Manganese-Based Layered Cathode Materials via Molybdenum Surface Modification.

作者信息

Shao Yijia, Lu Zhiyuan, Li Luoqian, Liu Yanni, Yang Lijun, Shu Ting, Li Xiuhua, Liao Shijun

机构信息

The Key Laboratory of Fuel Cell Technology of Guangdong Province, School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou 510641, China.

出版信息

Molecules. 2022 Mar 24;27(7):2100. doi: 10.3390/molecules27072100.

DOI:10.3390/molecules27072100
PMID:35408499
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9000274/
Abstract

Lithium-rich manganese-based layered cathode materials are considered to be one of the best options for next-generation lithium-ion batteries, owing to their ultra-high specific capacity (>250 mAh·g−1) and platform voltage. However, their poor cycling stability, caused by the release of lattice oxygen as well as the electrode/electrolyte side reactions accompanying complex phase transformation, makes it difficult to use this material in practical applications. In this work, we suggest a molybdenum surface modification strategy to improve the electrochemical performance of Li1.2Mn0.54Ni0.13Co0.13O2. The Mo-modified Li1.2Mn0.54Ni0.13Co0.13O2 material exhibits an enhanced discharge specific capacity of up to 290.5 mAh·g−1 (20 mA·g−1) and a capacity retention rate of 82% (300 cycles at 200 mA·g−1), compared with 261.2 mAh·g−1 and a 70% retention rate for the material without Mo modification. The significantly enhanced performance of the modified material can be ascribed to the formation of a Mo-compound-involved nanolayer on the surface of the materials, which effectively lessens the electrolyte corrosion of the cathode, as well as the activation of Mo6+ towards Ni2+/Ni4+ redox couples and the pre-activation of a Mo compound. This study offers a facile and effective strategy to address the poor cyclability of lithium-rich manganese-based layered cathode materials.

摘要

富锂锰基层状正极材料因其超高的比容量(>250 mAh·g−1)和平台电压,被认为是下一代锂离子电池的最佳选择之一。然而,由于晶格氧的释放以及伴随复杂相变的电极/电解质副反应,导致其循环稳定性较差,使得这种材料难以在实际应用中使用。在这项工作中,我们提出了一种钼表面改性策略,以改善Li1.2Mn0.54Ni0.13Co0.13O2的电化学性能。与未进行钼改性的材料相比,钼改性的Li1.2Mn0.54Ni0.13Co0.13O2材料在20 mA·g−1时表现出高达290.5 mAh·g−1的增强放电比容量,在200 mA·g−1下循环300次时容量保持率为82%,而未改性材料的比容量为261.2 mAh·g−1,容量保持率为70%。改性材料性能的显著提升可归因于在材料表面形成了含钼化合物的纳米层,这有效地减轻了阴极的电解质腐蚀,以及Mo6+对Ni2+/Ni4+氧化还原对的激活和钼化合物的预激活。本研究提供了一种简便有效的策略来解决富锂锰基层状正极材料循环性能差的问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35f4/9000274/50acd73fe68c/molecules-27-02100-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35f4/9000274/185953a1031b/molecules-27-02100-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35f4/9000274/81a323d49dfa/molecules-27-02100-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35f4/9000274/6ebf66cf28d6/molecules-27-02100-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35f4/9000274/8155e4cea7b7/molecules-27-02100-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35f4/9000274/537b5b375c93/molecules-27-02100-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35f4/9000274/bec1cdc9de90/molecules-27-02100-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35f4/9000274/50acd73fe68c/molecules-27-02100-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35f4/9000274/185953a1031b/molecules-27-02100-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35f4/9000274/81a323d49dfa/molecules-27-02100-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35f4/9000274/6ebf66cf28d6/molecules-27-02100-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35f4/9000274/8155e4cea7b7/molecules-27-02100-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35f4/9000274/537b5b375c93/molecules-27-02100-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35f4/9000274/bec1cdc9de90/molecules-27-02100-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35f4/9000274/50acd73fe68c/molecules-27-02100-g006.jpg

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