质子
锌
离子
传输(计算)
光电子学
材料科学
化学
光化学
计算机科学
物理
有机化学
冶金
并行计算
量子力学
作者
Wenwen Zha,Qiushi Ruan,Long Ma,Meng Liu,Huiwen Lin,Litao Sun,ZhengMing Sun,Li Tao
出处
期刊:Angewandte Chemie
[Wiley]
日期:2024-02-09
卷期号:63 (15): e202400621-e202400621
被引量:57
标识
DOI:10.1002/anie.202400621
摘要
Abstract Photo‐assisted ion batteries utilize light to boost capacity but face cycling instability due to complex charge/ion transfer under illumination. This study identified photo‐induced proton transfer (photo‐induced PT) as a significant process in photo‐(dis)charging of widely‐used V 2 O 5 ‐based zinc‐ion batteries, contributing to enhanced capacity under illumination but jeopardizing photo‐stability. Photo‐induced PT occurs at 100 ps after photo‐excitation, inducing rapid proton extraction into V 2 O 5 photoelectrode. This process creates a proton‐deficient microenvironment on surface, leading to repetitive cathode dissolution and anode corrosion in each cycle. Enabling the intercalated protons from photo‐induced PT to be reversibly employed in charge‐discharge processes via the anode‐alloying strategy achieves high photo‐stability for the battery. Consequently, a ~54 % capacity enhancement was achieved in a V 2 O 5 ‐based zinc‐ion battery under illumination, with ~90 % capacity retention after 4000 cycles. This extends the photo‐stability record by 10 times. This study offers promising advancements in energy storage by addressing instability issues in photo‐assisted ion batteries.
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