MgAl Saponite as a Transition-Metal-Free Anode Material for Lithium-Ion Batteries

Transition-metal compounds (oxides, sulfides, hydroxides, etc.) as lithium-ion battery (LIB) anodes usually show extraordinary capacity larger than the theoretical value due to the transformation of LiOH into Li2O/LiH. However, there has rarely been a report relaying the transformation of LiOH into...

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Published inACS applied materials & interfaces Vol. 14; no. 49; pp. 54812 - 54821
Main Authors Zhang, Jian, Li, Tianlin, Yuan, Qingyan, Wu, Yunjia, Dou, Yibo, Han, Jingbin
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 14.12.2022
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Summary:Transition-metal compounds (oxides, sulfides, hydroxides, etc.) as lithium-ion battery (LIB) anodes usually show extraordinary capacity larger than the theoretical value due to the transformation of LiOH into Li2O/LiH. However, there has rarely been a report relaying the transformation of LiOH into Li2O/LiH as the main reaction for LIBs, due to the strong alkalinity of LiOH leading to battery deterioration. In this work, layered silicate MgAl saponite (MA-SAP) is applied as a −OH donor to generate LiOH as the anode material of LIBs for the first time. The MA-SAP maintains a layered structure during the (dis)­charging process and has zero-strain characteristic on the (001) crystal plane. In the discharging process, Mg, Al, and Si in the saponite sheets become electron-rich, while the active hydroxyl groups escape from the sheets and combine with lithium ions to form LiOH in the “caves” on sheets, and the LiOH continues to decompose into Li2O and LiH. Consequently, the MA-SAP delivers a maximum capacity of 536 mA h·g–1 at 200 mA·g–1 with a good high-current discharging ability of 155 mA h·g–1 after 1000 cycles under 1 A·g–1. Considering its extremely low cost and completely nontoxic characteristics, MA-SAP has great application prospects in energy storage. In addition, this work has an enlightening effect on the development of new anodes based on extraordinary mechanisms.
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ISSN:1944-8244
1944-8252
DOI:10.1021/acsami.2c17932