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Oxygen Vacancies Boosted Hydronium Intercalation: A Paradigm Shift in Aluminum-Based Batteries.

Chengxiang HuangZhou JiangFuxi LiuWenwen LiQing LiangZhenzhen ZhaoXin GeKexin SongLirong ZhengXinyan ZhouSifan QiaoWei ZhangWeitao Zheng
Published in: Angewandte Chemie (International ed. in English) (2024)
In aqueous aluminum-ion batteries (AAIBs), the insertion/extraction chemistry of Al 3+ often leads to poor kinetics, whereas the rapid diffusion kinetics of hydronium ions (H 3 O + ) may offer the solution. However, the presence of considerable Al 3+ in the electrolyte hinders the insertion reaction of H 3 O + . Herein, we report how oxygen-deficient α-MoO 3 nanosheets unlock selective H 3 O + insertion in a mild aluminum-ion electrolyte. The abundant oxygen defects impede the insertion of Al 3+ due to excessively strong adsorption, while allowing H 3 O + to be inserted/diffused through the Grotthuss proton conduction mechanism. This research advances our understanding of the mechanism behind selective H 3 O + insertion in mild electrolytes.
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