TY - JOUR
T1 - Surface Modifications of (ZnSe)0.5(CuGa2.5Se4.25)0.5to Promote Photocatalytic Z-Scheme Overall Water Splitting
AU - Chen, Shanshan
AU - Vequizo, Junie Jhon M.
AU - Pan, Zhenhua
AU - Hisatomi, Takashi
AU - Nakabayashi, Mamiko
AU - Lin, Lihua
AU - Wang, Zheng
AU - Kato, Kosaku
AU - Yamakata, Akira
AU - Shibata, Naoya
AU - Takata, Tsuyoshi
AU - Yamada, Taro
AU - Domen, Kazunari
N1 - Funding Information:
This work was financially supported by the Artificial Photosynthesis Project of the New Energy and Industrial Technology Development Organization (NEDO). Part of this work was conducted at the Advanced Characterization Nanotechnology Platform of the University of Tokyo, supported by the “Nanotechnology Platform” of the Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan (Grant JPMXP09-A-20-UT-0004). The authors thank Ms. Keiko Kato of the University of Tokyo for her assistance in ICP-AES characterization.
Publisher Copyright:
© 2021 American Chemical Society. All rights reserved.
PY - 2021/7/21
Y1 - 2021/7/21
N2 - Charge separation is crucial for an efficient artificial photosynthetic process, especially for narrow-bandgap metal sulfides/selenides. The present study demonstrates the application of a p-n junction to particulate metal selenides to enhance photocatalytic Z-scheme overall water splitting (OWS). The constructed p-n junction of CdS-(ZnSe)0.5(CuGa2.5Se4.25)0.5 significantly boosted charge separation. A thin TiO2 coating layer also was introduced to inhibit photocorrosion of CdS and suppress the backward reaction of water formation from hydrogen and oxygen. By employing Pt-loaded TiO2/CdS-(ZnSe)0.5(CuGa2.5Se4.25)0.5 as a hydrogen evolution photocatalyst (HEP), we assembled a Z-scheme OWS system, together with BiVO4:Mo and Au as an oxygen evolution photocatalyst and electron mediator, respectively. An apparent quantum yield of 1.5% at 420 nm was achieved, which is by far the highest among reported particulate photocatalytic Z-scheme OWS systems with metal sulfides/selenides as HEPs. The present work demonstrates that a well-tailored p-n junction structure is effective for promoting charge separation in photocatalysis and opens new pathways for the development of efficient artificial photosynthesis systems involving narrow bandgap photocatalysts.
AB - Charge separation is crucial for an efficient artificial photosynthetic process, especially for narrow-bandgap metal sulfides/selenides. The present study demonstrates the application of a p-n junction to particulate metal selenides to enhance photocatalytic Z-scheme overall water splitting (OWS). The constructed p-n junction of CdS-(ZnSe)0.5(CuGa2.5Se4.25)0.5 significantly boosted charge separation. A thin TiO2 coating layer also was introduced to inhibit photocorrosion of CdS and suppress the backward reaction of water formation from hydrogen and oxygen. By employing Pt-loaded TiO2/CdS-(ZnSe)0.5(CuGa2.5Se4.25)0.5 as a hydrogen evolution photocatalyst (HEP), we assembled a Z-scheme OWS system, together with BiVO4:Mo and Au as an oxygen evolution photocatalyst and electron mediator, respectively. An apparent quantum yield of 1.5% at 420 nm was achieved, which is by far the highest among reported particulate photocatalytic Z-scheme OWS systems with metal sulfides/selenides as HEPs. The present work demonstrates that a well-tailored p-n junction structure is effective for promoting charge separation in photocatalysis and opens new pathways for the development of efficient artificial photosynthesis systems involving narrow bandgap photocatalysts.
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U2 - 10.1021/jacs.1c03555
DO - 10.1021/jacs.1c03555
M3 - Article
C2 - 34235922
AN - SCOPUS:85111105223
SN - 0002-7863
VL - 143
SP - 10633
EP - 10641
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 28
ER -