Hydrogen-Mediated Thin Pt Layer Formation on Ni3N Nanoparticles for the Oxygen Reduction Reaction

Authors
Jeong, Hui-YunKim, Dong-GunAkpe, Shedrack G.Paidi, Vinod K.Park, Hyun S.Lee, Soo-HyoungLee, Kug-SeungHam, Hyung ChulKim, PilYoo, Sung Jong
Issue Date
2021-06-02
Publisher
American Chemical Society
Citation
ACS Applied Materials & Interfaces, v.13, no.21, pp.24624 - 24633
Abstract
A simple wet-chemical route for the preparation of core-shell-structured catalysts was developed to achieve high oxygen reduction reaction (ORR) activity with a low Pt loading amount. Nickel nitride (Ni3N) nanoparticles were used as earth-abundant metal-based cores to support thin Pt layers. To realize the site-selective formation of Pt layers on the Ni3N core, hydrogen molecules (H-2) were used as a mild reducing agent. As H-2 oxidation is catalyzed by the surface of Ni3N, the redox reaction between H-2 and Pt(IV) in solution was facilitated on the Ni3N surface, which resulted in the selective deposition of Pt on Ni3N. The controlled Pt formation led to a subnanometer (0.5-1 nm)thick Pt shell on the Ni3N core. By adopting the core-shell structure, higher ORR activity than the commercial Pt/C was achieved. Electrochemical measurements showed that the thin Pt layer on Ni3N nanoparticle exhibits 5 times higher mass activity and specific activity than that of commercial Pt/C. Furthermore, it is expected that the proposed simple wet-chemical method can be utilized to prepare various transition-metal-based core-shell nanocatalysts for a wide range of energy conversion reactions.
Keywords
X-RAY-ABSORPTION; CORE-SHELL CATALYST; SURFACE SEGREGATION; RECENT ADVANCEMENTS; HIGH-PERFORMANCE; IN-SITU; PLATINUM; ELECTROCATALYSTS; ALLOY; STABILITY; X-RAY-ABSORPTION; CORE-SHELL CATALYST; SURFACE SEGREGATION; RECENT ADVANCEMENTS; HIGH-PERFORMANCE; IN-SITU; PLATINUM; ELECTROCATALYSTS; ALLOY; STABILITY; fuel cell; oxygen reduction reaction; electrocatalyst; core-shell structure; platinum
ISSN
1944-8244
URI
https://pubs.kist.re.kr/handle/201004/116872
DOI
10.1021/acsami.1c01544
Appears in Collections:
KIST Article > 2021
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