光催化
锐钛矿
异质结
金红石
材料科学
分解水
化学工程
可见光谱
半导体
纳米技术
催化作用
石墨氮化碳
X射线光电子能谱
煅烧
比表面积
二氧化钛
甲基橙
光电子学
化学
有机化学
工程类
作者
Yuxuan Fang,Wenxin Huang,Siyuan Yang,Xunfu Zhou,Chunyu Ge,Qiongzhi Gao,Yueping Fang,Shengsen Zhang
标识
DOI:10.1016/j.ijhydene.2020.04.214
摘要
Rational design of high-efficiency heterostructure photocatalyst is an effective strategy to realize photocatalytic H2 evolution from pure water, but remains still a considerable challenge. Herein, an anatase/rutile TiO2/g-C3N4 (A/R/CN) multi-heterostructure photocatalyst was prepared by a facile thermoset hybrid method. The combination of two type-II semiconductor heterostructures (i.e., A/R and R/CN) significantly improve the separation and transfer efficiency of photogenerated carriers of anatase TiO2, rutile TiO2 and g-C3N4, and A/R/CN photocatalyst with high activity is obtained. The optimal A/R/CN photocatalyst exhibits significantly increased photocatalytic overall water splitting activity with a rate of H2 evolution of 374.2 μmol g−1h−1, which is about 8 and 4 times that of pure g-C3N4 and P25. Moreover, it is demonstrated to be stable and retained a high activity (ca. 91.2%) after the fourth recycling experiment. This work comes up with an innovative perspective on the construction of multi-heterostructure interfaces to improve the overall photocatalytic water splitting performance.
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