期刊
ACS CATALYSIS
卷 11, 期 2, 页码 932-947出版社
AMER CHEMICAL SOC
DOI: 10.1021/acscatal.0c03973
关键词
hydrogen oxidation reaction; carbide supports; alkaline electrolyte; DFT; anion-exchange membrane fuel cell
资金
- Nancy & Stephen Grand Technion Energy Program (GTEP)
- European Union's Horizon 2020 research and innovation program [721065]
- Ministry of Science, Technology & Space of Israel [3-12948]
- Israel Science Foundation (ISF) [1481/17]
- Russell Berrie Nanotechnology Institute, Technion
- Ministry of National Infrastructure, Energy and Water Resources of Israel [3-13671, 3-15204]
- Satell Family Foundation
- Maurice G. Gamze Endowed Fund (at the American Technion Society)
- Larry Pitt and Phillis Meloff, The Eileen and Jerry Lieberman UConn/Israel Global Partnership Fund
- Grand Technion Energy Program (GTEP)
- Planning & Budgeting Committee/ISRAEL Council for Higher Education (CHE)
- Fuel Choice Initiative (Prime Minister Office of ISRAEL) of the Israel National Research Center for Electrochemical Propulsion (INREP)
- FCT, through IDMEC, under LAETA, project [UIDB/50022/2020]
- high performance computing (HPC) resources at Beihang University
Transition metal carbides were used as supports for PtRu nanoparticles in catalyzing the sluggish hydrogen oxidation reaction in alkaline electrolyte, demonstrating enhanced catalytic activity. The study provides experimental and theoretical evidence of strong metal-support interaction and a potential pathway for the development of advanced catalysts.
Owing to the sluggish kinetics of the hydrogen oxidation reaction (HOR) in alkaline electrolyte, it is considered a limiting reaction for the development of anion-exchange membrane fuel cell (AEMFC) technology. Studies of alkaline HOR catalysis mainly focus on carbon-supported nanoparticles, which have weak metal-support interactions. In this contribution, we present a unique support based on transition metal carbides (TMCs = Mo2C, Mo2C-TaC, and Mo2C-W2C) for the HOR. PtRu nanoparticles are deposited onto the TMC supports and are characterized by a variety of analytical techniques. The major findings are (i) experimental and theoretical evidence for strong-metal support interaction by both X-ray absorption near-edge structure and density functional theory, (ii) the kinetic current density (j(k,s)) @25 mV of PtRu/Mo2C-TaC catalyst are 1.65 and 1.50 times higher than that of PtRu/Mo2C and PtRu/Mo2C-W2C, respectively, and (iii) enhanced tethering of PtRu nanoparticles on TMC supports. Furthermore, the AEMFC based on the PtRu/Mo2C-TaC anode exhibited a peak power density of 1.2 W cm(-2) @70 degrees C, opening the doors for the development of advanced catalysts based on engineering support materials.
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