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Hydrogen-Mediated Thin Pt Layer Formation on Ni3N Nanoparticles for the Oxygen Reduction Reaction.
Jeong, Hui-Yun; Kim, Dong-Gun; Akpe, Shedrack G; Paidi, Vinod K; Park, Hyun S; Lee, Soo-Hyoung; Lee, Kug-Seung; Ham, Hyung Chul; Kim, Pil; Yoo, Sung Jong.
Afiliação
  • Jeong HY; Center for Hydrogen Fuel Cell Research, Korea Institute of Science and Technology (KIST), Seoul 02792, Republic of Korea.
  • Kim DG; School of Chemical Engineering, Chonbuk National University, Jeonju 54896, Republic of Korea.
  • Akpe SG; Department of Chemistry and Chemical Engineering, Education and Research Center for Smart Energy and Materials, Inha University, Incheon 22212, Republic of Korea.
  • Paidi VK; Pohang Accelerator Laboratory (PAL), Pohang University of Science and Technology (POSTECH), Pohang 37673, Republic of Korea.
  • Park HS; Center for Hydrogen Fuel Cell Research, Korea Institute of Science and Technology (KIST), Seoul 02792, Republic of Korea.
  • Lee SH; School of Chemical Engineering, Chonbuk National University, Jeonju 54896, Republic of Korea.
  • Lee KS; Pohang Accelerator Laboratory (PAL), Pohang University of Science and Technology (POSTECH), Pohang 37673, Republic of Korea.
  • Ham HC; Department of Chemistry and Chemical Engineering, Education and Research Center for Smart Energy and Materials, Inha University, Incheon 22212, Republic of Korea.
  • Kim P; School of Chemical Engineering, Chonbuk National University, Jeonju 54896, Republic of Korea.
  • Yoo SJ; Center for Hydrogen Fuel Cell Research, Korea Institute of Science and Technology (KIST), Seoul 02792, Republic of Korea.
ACS Appl Mater Interfaces ; 13(21): 24624-24633, 2021 Jun 02.
Article em En | MEDLINE | ID: mdl-34003000
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 (H2) were used as a mild reducing agent. As H2 oxidation is catalyzed by the surface of Ni3N, the redox reaction between H2 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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: ACS Appl Mater Interfaces Assunto da revista: BIOTECNOLOGIA / ENGENHARIA BIOMEDICA Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: ACS Appl Mater Interfaces Assunto da revista: BIOTECNOLOGIA / ENGENHARIA BIOMEDICA Ano de publicação: 2021 Tipo de documento: Article