电极
材料科学
光电子学
锂(药物)
极化(电化学)
显微镜
纳米技术
离子
化学
光学
物理
医学
内分泌学
物理化学
有机化学
作者
Raj Pandya,Angus Mathieson,Buddha Deka Boruah,Hilton B. de Aguiar,Michaël De Volder
出处
期刊:Nano Letters
[American Chemical Society]
日期:2023-08-08
卷期号:23 (16): 7288-7296
被引量:15
标识
DOI:10.1021/acs.nanolett.3c01148
摘要
Photobatteries, batteries with a light-sensitive electrode, have recently been proposed as a way of simultaneously capturing and storing solar energy in a single device. Despite reports of photocharging with multiple different electrode materials, the overall mechanism of operation remains poorly understood. Here, we use operando optical reflection microscopy to investigate light-induced charging in LixV2O5 electrodes. We image the electrode, at the single-particle level, under three conditions: (a) with a closed circuit and light but no electronic power source (photocharging), (b) during galvanostatic cycling with light (photoenhanced), and (c) with heat but no light (thermal). We demonstrate that light can indeed drive lithiation changes in LixV2O5 while maintaining charge neutrality, possibly via a combination of faradaic and nonfaradaic effects taking place in individual particles. Our results provide an addition to the photobattery mechanistic model highlighting that both intercalation-based charging and lithium concentration polarization effects contribute to the increased photocharging capacity.
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