Carbon Nitride Loaded with an Ultrafine, Monodisperse, Metallic Platinum‐Cluster Cocatalyst for the Photocatalytic Hydrogen‐Evolution Reaction

Author:

Yazaki Daichi1,Kawawaki Tokuhisa12ORCID,Hirayama Daisuke1,Kawachi Masanobu1,Kato Kosaku3ORCID,Oguchi Sota1,Yamaguchi Yuichi12ORCID,Kikkawa Soichi4ORCID,Ueki Yoshiya1,Hossain Sakiat2ORCID,Osborn D. J.5,Ozaki Fumihiko6,Tanaka Shunsuke6ORCID,Yoshinobu Jun6ORCID,Metha Gregory F.5ORCID,Yamazoe Seiji4ORCID,Kudo Akihiko12ORCID,Yamakata Akira3ORCID,Negishi Yuichi12ORCID

Affiliation:

1. Department of Applied Chemistry Faculty of Science Tokyo University of Science 1–3 Kagurazaka, Shinjuku‐ku Tokyo 162‐8601 Japan

2. Research Institute for Science & Technology Tokyo University of Science 2641 Yamazaki, Noda Chiba 278‐8510 Japan

3. Graduate School of Natural Science and Technology Okayama University 3‐1‐1 Tsushimanaka, Kita‐ku Okayama 700‐8530 Japan

4. Department of Chemistry Graduate School of Science Tokyo Metropolitan University 1‐1 Minami‐Osawa, Hachioji‐shi Tokyo 192−0397 Japan

5. Department of Chemistry University of Adelaide Adelaide South Australia 5005 Australia

6. The Institute for Solid State Physics The University of Tokyo 5‐1‐5, Kashiwanoha, Kashiwa Chiba 277‐8581 Japan

Abstract

AbstractFor the realization of a next‐generation energy society, further improvement in the activity of water‐splitting photocatalysts is essential. Platinum (Pt) is predicted to be the most effective cocatalyst for hydrogen evolution from water. However, when the number of active sites is increased by decreasing the particle size, the Pt cocatalyst is easily oxidized and thereby loses its activity. In this study, a method to load ultrafine, monodisperse, metallic Pt nanoclusters (NCs) on graphitic carbon nitride is developed, which is a promising visible‐light‐driven photocatalyst. In this photocatalyst, a part of the surface of the Pt NCs is protected by sulfur atoms, preventing oxidation. Consequently, the hydrogen‐evolution activity per loading weight of Pt cocatalyst is significantly improved, 53 times, compared with that of a Pt‐cocatalyst loaded photocatalyst by the conventional method. The developed method is also effective to enhance the overall water‐splitting activity of other advanced photocatalysts such as SrTiO3 and BaLa4Ti4O15.

Funder

Japan Society for the Promotion of Science

Yazaki Memorial Foundation for Science and Technology

Ministry of Education, Culture, Sports, Science and Technology

Publisher

Wiley

Subject

Biomaterials,Biotechnology,General Materials Science,General Chemistry

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