光电阴极
材料科学
光激发
光电子学
带隙
光电效应
电子转移
共价键
电池(电)
电子
电子亲和性(数据页)
电压
能量转换效率
阴极
阳极
光化学
光敏剂
电子迁移率
电极
纳米技术
电子能带结构
可见光谱
阴极射线
太阳能转换
作者
Haohao Tang,Yu Xie,Weiyue Wang,Liguo Zhang,T.H Zhang,Wenchen Wang,Qiancheng Zhu
摘要
ABSTRACT A photocathode is critical for realizing bifunctionality of solar energy harvesting and storage within a single device, but it still faces challenges such as low photoelectric conversion efficiency (PCE) and poor light stability. Herein, a covalent organic framework (COF) named BQQPH was proposed as a photocathode material. It exhibits a reversible Zn 2 + /H + co‐intercalation accompanied by a 12‐electron transfer process, where C═O groups bond with H + , and C═N groups bond with Zn 2 + . Photoexcitation induces substantial electron accumulation at the C═O and C═N active sites, which serve as electron traps to enhance the coordination affinity of Zn 2 + and H + . Thus, the photocathode achieves a high discharge capacity of 411 mA h g − 1 at 1 A g − 1 , with 99% capacity retention (170 mAh g − 1 ) even after 6000 cycles at 30 A g − 1 and the corresponding PCE reaches 8.5%. Additionally, BQQPH exhibits a bandgap of 1.8 eV, the corresponding band structure can achieve photo self‐charging in thermodynamics. Without any external power supply, the battery achieves a high photo self‐charging voltage of 1.2 V and a discharge capacity of 248 mA h g − 1 . This study offers insights into the design of organic photocathodes for photo‐rechargeable batteries.
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