Investigation into the Surface Chemistry of Li4Ti5O12 Nanoparticles for Lithium Ion Batteries
Elucidating surface chemistry of Li4Ti5O12 anode material plays a critical role in solving gas evolution in Li4Ti5O12-based lithium ion batteries. Herein, we propose a CO2 cycloaddition reaction to study the surface chemistry of Li4Ti5O12 nanoparticles. Through the reaction, bare Li4Ti5O12 nanoparti...
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Veröffentlicht in: | ACS applied materials & interfaces 2016-10, Vol.8 (39), p.26008-26012 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | Elucidating surface chemistry of Li4Ti5O12 anode material plays a critical role in solving gas evolution in Li4Ti5O12-based lithium ion batteries. Herein, we propose a CO2 cycloaddition reaction to study the surface chemistry of Li4Ti5O12 nanoparticles. Through the reaction, bare Li4Ti5O12 nanoparticles were demonstrated to have extensive Lewis-acid sites, that is, dangling Ti bonds or hydroxyl groups. Lewis-acid site is considered to be able to initiate the decomposition of electrolyte solvents and may also serve as one of the main reasons for gas evolution. TiN x coating layer is used to cover up the Lewis-acid site and is able to decrease yield of the cycloaddition reaction to some extent. These findings may provide a simple yet very effective way to evaluate surface chemistry and gas evolution in other lithium ion batteries, not limited to Li4Ti5O12-based batteries. |
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ISSN: | 1944-8244 1944-8252 |
DOI: | 10.1021/acsami.6b07902 |