Published April 11, 2018 | Version Supplemental Material
Journal Article Open

Ga-doped Pt-Ni Octahedral Nanoparticles as a Highly Active and Durable Electrocatalyst for Oxygen Reduction Reaction

  • 1. ROR icon Korea Advanced Institute of Science and Technology
  • 2. ROR icon California Institute of Technology
  • 3. ROR icon Pohang University of Science and Technology

Abstract

Bimetallic PtNi nanoparticles have been considered as a promising electrocatalyst for oxygen reduction reaction (ORR) in polymer electrolyte membrane fuel cells (PEMFCs) owing to their high catalytic activity. However, under typical fuel cell operating conditions, Ni atoms easily dissolve into the electrolyte, resulting in degradation of the catalyst and the membrane-electrode assembly (MEA). Here, we report gallium-doped PtNi octahedral nanoparticles on a carbon support (Ga-PtNi/C). The Ga-PtNi/C shows high ORR activity, marking an 11.7-fold improvement in the mass activity (1.24 A mgPt-1) and a 17.3-fold improvement in the specific activity (2.53 mA cm-2) compare to the commercial Pt/C (0.106 A mgPt-1 and 0.146 mA cm-2). Density functional theory calculations demonstrate that addition of Ga to octahedral PtNi can cause an increase in the oxygen intermediate binding energy, leading to the enhanced catalytic activity toward ORR. In a voltage-cycling test, the Ga-PtNi/C exhibits superior stability to PtNi/C and the commercial Pt/C, maintaining the initial Ni concentration and octahedral shape of the nanoparticles. Single cell using the Ga-PtNi/C exhibits higher initial performance and durability than those using the PtNi/C and the commercial Pt/C. The majority of the Ga-PtNi nanoparticles well maintain the octahedral shape without agglomeration after the single cell durability test (30,000 cycles). This work demonstrates that the octahedral Ga-PtNi/C can be utilized as a highly active and durable ORR catalyst in practical fuel cell applications.

Additional Information

© 2018 American Chemical Society. Received: January 3, 2018; Revised: March 5, 2018; Published: March 26, 2018. This work was supported by Korea Institute of Energy Technology Evaluation and Planning (KETEP) under contract No. 20143030031340 and Korea Institute of Science and Technology (KIST) under contract No. 2017081254 and the Agency for Defense Development in South Korea (ADD). The authors declare no competing financial interest.

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Identifiers

Eprint ID
85449
DOI
10.1021/acs.nanolett.8b00028
Resolver ID
CaltechAUTHORS:20180327-090854954

Related works

Funding

Korea Institute of Energy Technology Evaluation and Planning (KETEP)
20143030031340
Korea Institute of Science and Technology (KIST)
2017081254
Agency for Defense Development (South Korea)

Dates

Created
2018-03-27
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Updated
2021-11-15
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