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Self-assembled heterojunction of metal sulfides for improved photocatalysis

Authors :
Seung Yong Lee
Heechae Choi
So Hye Cho
Qiaohong Zhu
Jinlong Zhang
Sovann Khan
Seungchul Kim
Donghun Kim
Source :
Chemical Engineering Journal. 395:125092
Publication Year :
2020
Publisher :
Elsevier BV, 2020.

Abstract

Due to its high redox potential, zinc sulfide (ZnS) is considered an excellent semiconductor photocatalyst. However, the rapid recombination rate of the photogenerated electron-hole pairs limits the efficiency of ZnS for photocatalytic reactions. Herein, we suggest a design rule of heterojunction structure of ZnS for improvement of its photocatalytic performance. Two specific properties are specially emphasized: phase immiscibility and the different growth rates of the component materials. The phase immiscibility not only guarantees a well-separated interface, it also enables the technical convenience of one-pot synthesis. The different growth rates help form wide heterojunctions that foster the efficient consumption of materials. We found that the ZnS/NixSy composite not only meets the aforementioned requirements but also has proper band alignment. Ready-to-use heterojunction photocatalysts (ZnS/NixSy) were obtained via one-pot synthesis, thanks to the different growth rates and the immiscibility of the two sulfides. Combining ZnS with NixSy resulted in substantially improved photocatalytic activity in regard to dye decomposition and H2 production via water splitting. Both band position measurements and DFT simulations indicated that NixSy is a co-catalyst for ZnS, allowing sufficient band offset for electron-hole separation. Abundant and mass-producible, the ZnS/NixSy composite can effectively substitute for noble metal photocatalysis when it comes to organic pollutant degradation and water splitting.

Details

ISSN :
13858947
Volume :
395
Database :
OpenAIRE
Journal :
Chemical Engineering Journal
Accession number :
edsair.doi...........9a69c47e9e65f074b71fbda0a6de0ae0
Full Text :
https://doi.org/10.1016/j.cej.2020.125092