Affiliation:
1. Shanghai Key Lab of Chemical Assessment and Sustainability, School of Chemical Science and Engineering, Tongji University, Shanghai 200092, China
Abstract
Halide perovskites have been emerging as promising photocatalytic materials for H
2
evolution from water due to their outstanding photoelectric properties. However, the lack of proper surface reactive sites greatly hinders the photocatalytic potential of these fascinating compounds. Here, Mo
2
C nanoparticles have been anchored onto methylammonium lead iodide (MAPbI
3
) as a nonnoble metal cocatalyst to promote H
2
evolution reactions. The Mo
2
C nanoparticles have opposite zeta potential with MAPbI
3
thereby electrostatically assembled onto the MAPbI
3
surface, i.e., Mo
2
C@MAPbI
3
. Our results show that the anchored Mo
2
C nanoparticles have a strong interplay with MAPbI
3
substrate so that photogenerated electrons of MAPbI
3
can be rapidly separated and transferred into Mo
2
C for further H
2
evolution reactions. Under optimal conditions, Mo
2
C@MAPbI
3
delivers exceptionally high photocatalytic performance for visible light-driven H
2
evolution that clearly outperforms pristine MAPbI
3
and Pt-deposited MAPbI
3
. An apparent quantum efficiency as high as 12.65% at
600
±
40
nm
has been attained for H
2
evolution, surpassing most of the MAPbI
3
-based photocatalyst reported. These results signify the usefulness and applicability of Mo
2
C as a new nonnoble metal-based cocatalyst in solar water splitting.
Funder
Fundamental Research Funds for the Central Universities
Science and Technology Commission of Shanghai Municipality
Natural Science Foundation of Shanghai
National Natural Science Foundation of China
Publisher
American Association for the Advancement of Science (AAAS)
Subject
General Earth and Planetary Sciences,General Environmental Science
Cited by
14 articles.
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