Efficient and stable visible-light-driven Z-scheme overall water splitting using an oxysulfide H2 evolution photocatalyst

被引:23
|
作者
Lin, Lihua [1 ]
Ma, Yiwen [1 ]
Vequizo, Junie Jhon M. [1 ]
Nakabayashi, Mamiko [2 ]
Gu, Chen [1 ]
Tao, Xiaoping [1 ]
Yoshida, Hiroaki [3 ,4 ]
Pihosh, Yuriy [5 ]
Nishina, Yuta [6 ]
Yamakata, Akira [7 ]
Shibata, Naoya [2 ]
Hisatomi, Takashi [1 ]
Takata, Tsuyoshi [1 ]
Domen, Kazunari [1 ,5 ]
机构
[1] Shinshu Univ, Res Initiat Supramat, Interdisciplinary Cluster Cutting Edge Res, Nagano, Japan
[2] Univ Tokyo, Inst Engn Innovat, Bunkyo Ku, Tokyo, Japan
[3] Mitsubishi Chem Corp, Sci & Innovat Ctr, Aoba Ku, Yokohama, Kanagawa 2278502, Japan
[4] Japan Technol Res Assoc Artificial Photosynthet Ch, Tokyo, Japan
[5] Univ Tokyo, Off Univ Prof, Bunkyo Ku, Tokyo 1138656, Japan
[6] Okayama Univ, Grad Sch Nat Sci & Technol, Kita Ku, Okayama, Japan
[7] Okayama Univ, Fac Nat Sci & Technol, Kita Ku, Okayama, Japan
关键词
REDUCED GRAPHENE OXIDE; SOLAR HYDROGEN-PRODUCTION; ENERGY-CONVERSION; O-2; IRRADIATION; SM2TI2S2O5; REDUCTION; BIVO4; MEDIATOR; SYSTEMS;
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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页数:12
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