Promoting Oxygen Reduction Reaction by Excitation of Localized Surface Plasmon of Shape‐ and Facet‐Controlled Octahedral Au@Pt Core‐Shell Nanocrystals

Author:

Kameyama Tatsuya1ORCID,Sato Kentaro1,Yamamoto Takahisa2ORCID,Tamura Mamoru34ORCID,Iida Takuya35ORCID,Shoji Tatsuya6ORCID,Tsuboi Yasuyuki7ORCID,Torimoto Tsukasa1ORCID

Affiliation:

1. Department of Materials Chemistry Graduate School of Engineering Nagoya University Furo-cho, Chikusa-ku Nagoya 464-8603 Japan

2. Department of Materials Design Innovation Engineering Graduate School of Engineering Nagoya University Furo-cho, Chikusa-ku Nagoya 464-8603 Japan

3. Research Institute for Light-induced Acceleration System (RILACS) Osaka Metropolitan University 1-2 Gakuencho, Naka-ku Sakai Osaka 599-8570 Japan

4. Department of Material Engineering Science Graduate School of Engineering Science Osaka University 1-3 Machikaneyama-cho Toyonaka Osaka 560-8531 Japan

5. Department of Physics Graduate School of Science Osaka Metropolitan University 1-2 Gakuencho, Naka-ku Sakai Osaka 599-8570 Japan

6. Department of Science Faculty of Science Kanagawa University 3-27-1 Rokkakubashi, Kanagawa-ku Yokohama Kanagawa 221-8686 Japan

7. Department of Chemistry Graduate School of Science Osaka Metropolitan University 3-3-138 Sugimoto, Sumiyoshi-ku Osaka 558-8585 Japan

Abstract

AbstractMuch attention has been paid to the development of high‐performance electrocatalytic reactions by exploiting the plasmonic properties of noble metal nanoparticles. In this study, ultrathin Pt layers with different coverage ratios were prepared on plasmonic octahedral Au nanoparticles (NPs) by underpotential deposition (UPD) of Cu followed by redox replacement with Pt. The effect of the Cu UPD cycle on the deposited Cu and redox‐substituted Pt layers on octahedral Au NPs was investigated to evaluate the electrocatalytic activity of Pt‐decorated octahedral NPs for the oxygen reduction reaction (ORR). By varying the number of cycles of Cu UPD and Pt replacement, the coverage by the Pt layer on the Au NPs could be easily controlled. The resulting Pt‐coated octahedral Au NPs exhibited three times higher specific activity for ORR than commercial Pt/C nanocatalysts due to the deposited Pt layer reflecting the {111} plane of the core. The ORR activity of Pt‐coated octahedral Au NPs could be enhanced by photoexcitation with monochromatic LED irradiation, and the increase in enhancement factor was even greater when irradiated with a wavelength that could efficiently excite the localized surface plasmon resonance (LSPR) of the NPs. Analysis shows that this improvement is due to improved diffusion of oxygen to the electrode.

Funder

JST-Mirai Program

Publisher

Wiley

Subject

Electrochemistry,Catalysis

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