脱质子化
级联
插层(化学)
离子
化学物理
电子
分子
电池(电)
工作(物理)
质子
光化学
化学
材料科学
电解质
分子动力学
纳米技术
辐照
光电子学
模型系统
离子运输机
Boosting(机器学习)
极化(电化学)
小分子
作者
Wenwen Zha,Qiushi Ruan,Mengyun Yang,Jiaqiang Huang,Litao Sun,ZhengMing Sun,Li Tao
标识
DOI:10.1002/anie.202522461
摘要
Abstract While photo‐assisted ion batteries represent a promising energy storage frontier—with light irradiation significantly improving performance—their development remains hindered by a fundamental knowledge gap, as existing theories struggle to fully account for improved light‐driven ion intercalation. This work discovers the photoinduced proton‐zinc ion intercalation cascade mechanism, establishing a theoretical framework that explains the synergistic proton‐cation interplay and its role in capacity enhancement under illumination. Through light‐induced charge transfer, photogenerated electrons drive proton intercalation, which induces the deprotonation of Zn 2+ ‐coordinated water molecules due to the limited availability of free protons in the electrolyte. This deprotonation is energetically favored because of the lower deprotonation barrier of Zn 2+ ‐coordinated water compared to uncoordinated water, thereby accelerating zinc‐ion desolvation and promoting Zn 2+ intercalation. Consequently, the synergistic H + /Zn 2+ co‐intercalation enables an exceptional areal capacity of 12.86 mA h cm −2 under illumination in a photo‐assisted zinc‐ion battery with a high mass‐loading of 30 mg cm −2 . This work elucidates a proton‐cation cascade mechanism that governs light‐driven intercalation dynamics, providing the missing link between photo‐excitation and enhanced battery performance.
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