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Efficient and stable visible-light-driven Z-scheme overall water splitting using an oxysulfide H2 evolution photocatalyst (vol 15, 397, 2024)
被引:62
|作者:
Lin, Lihua
Ma, Yiwen
Vequizo, Junie Jhon M.
Nakabayashi, Mamiko
Gu, Chen
Tao, Xiaoping
Yoshida, Hiroaki
Pihosh, Yuriy
Nishina, Yuta
Yamakata, Akira
Shibata, Naoya
Hisatomi, Takashi
Takata, Tsuyoshi
Domen, Kazunari
机构:
[1] Research Initiative for Supra-Materials, Interdisciplinary Cluster for Cutting Edge Research, Shinshu University, Nagano
[2] Institute for Engineering Innovation, The University of Tokyo, Tokyo, Bunkyo-ku
[3] Science and Innovation Center, Mitsubishi Chemical Corporation, Aoba-ku, Kanagawa, Yokohama-shi
[4] Japan Technological Research Association of Artificial Photosynthetic Chemical Process (ARPChem), Tokyo
[5] Office of University Professors, The University of Tokyo, Tokyo, Bunkyo-ku
[6] Graduate School of Natural Science and Technology, Okayama University, Okayama, Kita-ku
[7] Faculty of Natural Science and Technology, Okayama University, Okayama, Kita-ku
关键词:
D O I:
10.1038/s41467-024-44706-4
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
So-called Z-scheme systems permit overall water splitting using narrow-bandgap photocatalysts. To boost the performance of such systems, it is necessary to enhance the intrinsic activities of the hydrogen evolution photocatalyst and oxygen evolution photocatalyst, promote electron transfer from the oxygen evolution photocatalyst to the hydrogen evolution photocatalyst, and suppress back reactions. The present work develop a high-performance oxysulfide photocatalyst, Sm2Ti2O5S2, as an hydrogen evolution photocatalyst for use in a Z-scheme overall water splitting system in combination with BiVO4 as the oxygen evolution photocatalyst and reduced graphene oxide as the solid-state electron mediator. After surface modifications of the photocatalysts to promote charge separation and redox reactions, this system is able to split water into hydrogen and oxygen for more than 100 hours with a solar-to-hydrogen energy conversion efficiency of 0.22%. In contrast to many existing photocatalytic systems, the water splitting activity of the present system is only minimally reduced by increasing the background pressure to 90 kPa. These results suggest characteristics suitable for applications under practical operating conditions.
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