光电阴极
悬空债券
氢氟酸
制氢
制作
氢
氧化物
硅
材料科学
降级(电信)
光电子学
电子
纳米技术
化学
化学工程
化学物理
无机化学
计算机科学
物理
有机化学
冶金
量子力学
替代医学
病理
医学
工程类
电信
作者
Lang Hu,Xiaohao Jiang,Jiamin Wang,H. Wang,Ya Zhang,Xiaodong Yi,Jie Han
出处
期刊:Nano Letters
[American Chemical Society]
日期:2025-03-31
卷期号:25 (15): 6051-6058
被引量:2
标识
DOI:10.1021/acs.nanolett.4c06302
摘要
Silicon (Si)-based photocathodes are generally considered as ideal materials for photoelectrochemical (PEC) hydrogen production. The fabrication of Si-based photocathodes usually requires hydrofluoric acid (HF) treatment to remove the oxide layer first, and H-dangling bonds can be formed inevitably on the surface of Si at the same time. However, the impacts of Si-H bonds in the PEC reaction are usually ignored. Here we report that the enriched H-dangling bonds at the solid-liquid interface play multiple roles in PEC hydrogen production, which can both efficiently collect photogenerated electrons from Si and accelerate the kinetics of the hydrogen evolution reaction at the interface. Furthermore, the coupling mechanism of H2 production triggered by H-dangling bonds significantly improves the efficiency of the PEC process. This work demonstrates that the HF-treated Si photocathode can be directly used for efficient hydrogen production, which will undoubtedly force a new phase in the study of Si-based photocathodes.
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