光催化
材料科学
异质结
三元运算
载流子
量子点
煅烧
可见光谱
介孔材料
制氢
分解水
半导体
化学工程
纳米技术
光电子学
氢
化学
催化作用
有机化学
计算机科学
工程类
程序设计语言
作者
Zifei Hu,Dan Shi,Guohong Wang,Tengyuan Gao,Juan Wang,Lianying Lu,Jun Li
标识
DOI:10.1016/j.apsusc.2022.154167
摘要
In recent years, coupling TiO2 with other narrow bandgap semiconductors to improve photocatalytic hydrogen generation rate has attracted widespread attention. Herein, carbon dots (C dots) decorated g-C3N4/TiO2 all-solid-state Z-scheme heterojunction photocatalysts with hierarchical macro/mesoporous structure have been fabricated via a facile solvothermal and calcination method. The dosage of C dots greatly influences the microstructure and the visible-light photocatalytic H2 evolution rate (HER). Under the optimal condition, the ternary composites consisting of C dots, g-C3N4 and TiO2 exhibited the highest HER of 580 μmol g−1 h−1, exceed the pure TiO2, pure g-C3N4 and the binary g-C3N4/TiO2 hybrid photocatalyst by a fact of 6.6 times, 2.1 times and 1.6 times, respectively. The excellent photocatalytic performance for hydrogen evolution is ascribed to the stronger light absorption, higher specific surface area and faster charge transportation. An all-solid-state Z-scheme heterojunction mechanism was proposed in which C dots serve as a mediator to improve the separation and transportation of photo-excited charge carriers.
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