Metal Single‐Atom Cocatalyst on Carbon Nitride for the Photocatalytic Hydrogen Evolution Reaction: Effects of Metal Species

Author:

Akinaga Yuki1,Kawawaki Tokuhisa12ORCID,Kameko Hinano1,Yamazaki Yuki1,Yamazaki Kenji3ORCID,Nakayasu Yuhi4,Kato Kosaku4,Tanaka Yuto5,Hanindriyo Adie Tri5ORCID,Takagi Makito5ORCID,Shimazaki Tomomi5ORCID,Tachikawa Masanori5,Yamakata Akira4,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. Division of Applied Physics Faculty of Engineering Hokkaido University 060‐8628 Sapporo Japan

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

5. Quantum Chemistry Division Yokohama City University 22‐2 Seto Kanazawa‐ku Yokohama 236‐0027 Japan

Abstract

AbstractSingle‐atom (SA) catalysts exhibit high activity in various reactions because there are no inactive internal atoms. Accordingly, SA cocatalysts are also an active research fields regarding photocatalytic hydrogen (H2) evolution which can be generated by abundant water and sunlight. Herein, it is investigated whether 10 transition metal elements can work as an SA on graphitic carbon nitride (g‐C3N4; i.e., gCN), a promising visible‐light‐driven photocatalyst. A method is established to prepare SA‐loaded gCN at high loadings (weight of ≈3 wt.% for Cu, Ni, Pd, Pt, Rh, and Ru) by modulating the photoreduction power. Regarding Au and Ag, SAs are formed with difficulty without aggregation because of the low binding energy between gCN and the SA. An evaluation of the photocatalytic H2‐evolution activity of the prepared metal SA‐loaded gCN reveals that Pd, Pt, and Rh SA‐loaded gCN exhibits relatively high H2‐evolution efficiency per SA. Transient absorption spectroscopy and electrochemical measurements reveal the following: i) Pd SA‐loaded gCN exhibits a particularly suitable electronic structure for proton adsorption and ii) therefore they exhibit the highest H2‐evolution efficiency per SA than other metal SA‐loaded gCN. Finally, the 8.6 times higher H2‐evolution rate per active site of Pd SA is achieved than that of Pd‐nanoparticles cocatalyst.

Funder

Japan Society for the Promotion of Science

Yazaki Memorial Foundation for Science and Technology

Kumagai Foundation for Science and Technology

Takahashi Industrial and Economic Research Foundation

Japan Science Society

Ogasawara Foundation for the Promotion of Science and Engineering

Publisher

Wiley

Subject

Electrochemistry,Condensed Matter Physics,Biomaterials,Electronic, Optical and Magnetic Materials

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