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Facile synthesis of anatase/rutile TiO2/g-C3N4 multi-heterostructure for efficient photocatalytic overall water splitting.

Authors :
Fang, Yuxuan
Huang, Wenxin
Yang, Siyuan
Zhou, Xunfu
Ge, Chunyu
Gao, Qiongzhi
Fang, Yueping
Zhang, Shengsen
Source :
International Journal of Hydrogen Energy. Jul2020, Vol. 45 Issue 35, p17378-17387. 10p.
Publication Year :
2020

Abstract

Rational design of high-efficiency heterostructure photocatalyst is an effective strategy to realize photocatalytic H 2 evolution from pure water, but remains still a considerable challenge. Herein, an anatase/rutile TiO 2 /g-C 3 N 4 (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 TiO 2 , rutile TiO 2 and g-C 3 N 4 , 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 H 2 evolution of 374.2 μmol g−1h−1, which is about 8 and 4 times that of pure g-C 3 N 4 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. Image 1 • Anatase/rutile TiO 2 /g-C 3 N 4 (A/R/CN) multi-heterostructure was prepared. • The heterostructure can effectively separate and transfer photogenerated carriers. • The A/R/CN hybrids exhibite efficient photocatalytic overall water splitting. • The A/R/CN shows excellent stability and reusability. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03603199
Volume :
45
Issue :
35
Database :
Academic Search Index
Journal :
International Journal of Hydrogen Energy
Publication Type :
Academic Journal
Accession number :
144304849
Full Text :
https://doi.org/10.1016/j.ijhydene.2020.04.214