光催化
异质结
材料科学
X射线光电子能谱
分解水
纳米管
共沉淀
化学工程
析氧
氧化还原
载流子
纳米技术
催化作用
电化学
碳纳米管
光电子学
化学
电极
物理化学
有机化学
工程类
冶金
作者
Dong‐Sheng Li,Yong Liu,Difa Xu,Qinqin Liu,Hua Tang
标识
DOI:10.1016/j.ceramint.2021.09.308
摘要
Heterojunction engineering is considered as a hopeful approach to ameliorate the separation of photogenerated carriers of photocatalysts, realizing efficient water-splitting performance. In this study, an organic-inorganic S-scheme of a one-dimensional g-C3N4 nanotube (TCN)/Ag3PO4 photocatalytic system with high photocatalytic water oxidation activity was designed by coupling g-C3N4 nanotubes over Ag3PO4 particles through a chemical coprecipitation method. The TCN/Ag3PO4 heterojunction demonstrated excellent photocatalytic O2 production with an O2 evolution rate of up to 370.2 μmol·L−1·h−1. X-ray photoelectron spectroscopy analysis showed that electron migration between TCN and Ag3PO4 led to the formation of an internal electric field pointing from TCN to Ag3PO4, which drove the S-scheme charge transfer mode between TCN and Ag3PO4. Accordingly, the TCN/Ag3PO4 heterojunction possessed fast charge separation and high redox ability, leading to high photoactivity and photostability. This research provides a new strategy for fabricating highly efficient inorganic-organic S-scheme photocatalysts for O2 production.
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