TY - JOUR
T1 - Creation of active water-splitting photocatalysts by controlling cocatalysts using atomically precise metal nanoclusters
AU - Kawawaki, Tokuhisa
AU - Kataoka, Yuki
AU - Ozaki, Shuhei
AU - Kawachi, Masanobu
AU - Hirata, Momoko
AU - Negishi, Yuichi
N1 - Funding Information:
The authors wish to thank all the co-authors listed in the references. This work was supported by the Japan Society for the Promotion of Science (JSPS) KAKENHI (grant number 20H02698 and 20H02552), Scientific Research on Innovative Areas ‘‘Coordination Asymmetry’’ (grant number 17H05385 and 19H04595), and Scientific Research on Innovative Areas ‘‘Innovations for Light-Energy Conversion’’ (grant number 18H05178 and 20H05115). Funding from the Asahi Glass Foundation, TEPCO Memorial Foundation Research Grant (Basic Research), and Kato Foundation for Promotion of Science (grant number KJ-2904) is gratefully acknowledged.
PY - 2021/1/14
Y1 - 2021/1/14
N2 - With global warming and the depletion of fossil resources, our fossil-fuel-dependent society is expected to shift to one that instead uses hydrogen (H2) as clean and renewable energy. Water-splitting photocatalysts can produce H2 from water using sunlight, which are almost infinite on the earth. However, further improvements are indispensable to enable their practical application. To improve the efficiency of the photocatalytic water-splitting reaction, in addition to improving the semiconductor photocatalyst, it is extremely effective to improve the cocatalysts (loaded metal nanoclusters, NCs) that enable the reaction to proceed on the photocatalysts. We have thus attempted to strictly control metal NCs on photocatalysts by introducing the precise-control techniques of metal NCs established in the metal NC field into research on water-splitting photocatalysts. Specifically, the cocatalysts on the photocatalysts were controlled by adsorbing atomically precise metal NCs on the photocatalysts and then removing the protective ligands by calcination. This work has led to several findings on the electronic/geometrical structures of the loaded metal NCs, the correlation between the types of loaded metal NCs and the water-splitting activity, and the methods for producing high water-splitting activity. We expect that the obtained knowledge will lead to clear design guidelines for the creation of practical water-splitting photocatalysts and thereby contribute to the construction of a hydrogen-energy society.
AB - With global warming and the depletion of fossil resources, our fossil-fuel-dependent society is expected to shift to one that instead uses hydrogen (H2) as clean and renewable energy. Water-splitting photocatalysts can produce H2 from water using sunlight, which are almost infinite on the earth. However, further improvements are indispensable to enable their practical application. To improve the efficiency of the photocatalytic water-splitting reaction, in addition to improving the semiconductor photocatalyst, it is extremely effective to improve the cocatalysts (loaded metal nanoclusters, NCs) that enable the reaction to proceed on the photocatalysts. We have thus attempted to strictly control metal NCs on photocatalysts by introducing the precise-control techniques of metal NCs established in the metal NC field into research on water-splitting photocatalysts. Specifically, the cocatalysts on the photocatalysts were controlled by adsorbing atomically precise metal NCs on the photocatalysts and then removing the protective ligands by calcination. This work has led to several findings on the electronic/geometrical structures of the loaded metal NCs, the correlation between the types of loaded metal NCs and the water-splitting activity, and the methods for producing high water-splitting activity. We expect that the obtained knowledge will lead to clear design guidelines for the creation of practical water-splitting photocatalysts and thereby contribute to the construction of a hydrogen-energy society.
UR - http://www.scopus.com/inward/record.url?scp=85099723738&partnerID=8YFLogxK
U2 - 10.1039/d0cc06809h
DO - 10.1039/d0cc06809h
M3 - Article
C2 - 33350403
AN - SCOPUS:85099723738
VL - 57
SP - 417
EP - 440
JO - Chemical Communications
JF - Chemical Communications
SN - 1359-7345
IS - 4
ER -