Abstract

Solar-driven water splitting over semiconductor photocatalysts is a promising approach for converting solar energy into renewable and storable chemical energy. CdS, an efficient photocatalyst for hydrogen evolution, suffers from high recombination of photogenerated electron-hole pairs and high photocorrosion in aqueous media, which limit its practical applications. Doping and the formation of heterojunctions are two efficient methods to improve the photocatalytic activities of photocatalysts. Herein, we rationally designed and fabricated P-doped 0D/2D ZnxCd1-xS/g-C3N4 nanocomposites by in-situ immobilizing ZnxCd1-xS onto the surface of g-C3N4 nanosheets in a hydrothermal environment, followed by a phosphorization process. The as-prepared P-doped ZnxCd1-xS/g-C3N4 nanocomposites were systematically characterized by analyzing the phase structure, chemical components, electronic and optical properties and separation of charge carriers. More importantly, these P-doped ZnxCd1-xS/g-C3N4 heterostructures have been proven to be highly efficient visible light responsive photocatalysts for hydrogen evolution, and meanwhile exhibit excellent photo-stability during recycling runs. The sufficient evidence exhibit that the significantly improved photocatalytic performance is mainly attributed to the prolonged lifetime of charge carriers and the improved separation efficiency of photogenerated electron-hole pairs.

Details

Title
0D/2D P-doped ZnxCd1-xS/g-C3N4 Heterojunctions towards Highly Efficient Photocatalytic Hydrogen Evolution
Author
Yin, Hongfei; Liu, Xiaoheng
Pages
32-40
Section
Articles
Publication year
2019
Publication date
Jul 24, 2019
Publisher
Taiwan Association of Engineering and Technology Innovation
ISSN
24137146
e-ISSN
2518833X
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2271074912
Copyright
© 2019. This work is published under https://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.