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Cited 11 time in webofscience Cited 11 time in scopus
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Mitigating Pt Loss in Polymer Electrolyte Membrane Fuel Cell Cathode Catalysts Using Graphene Nanoplatelet Pickering Emulsion Processing SCIE SCOPUS

Title
Mitigating Pt Loss in Polymer Electrolyte Membrane Fuel Cell Cathode Catalysts Using Graphene Nanoplatelet Pickering Emulsion Processing
Authors
Park, Kyu‐YoungSweers, Matthew E.Berner, UlrichHirth, ErhardDowning, Julia R.Hui, JananMailoa, JonathanJohnston, ChristinaKim, SooSeitz, Linsey C.Hersam, Mark C.
Date Issued
2022-10
Publisher
John Wiley & Sons Ltd.
Abstract
Carbon-supported Pt nanoparticles are the leading catalysts for the cathode oxygen reduction reaction (ORR) in polymer electrolyte membrane fuel cells. However, these ORR catalysts suffer from poor electrochemical durability, particularly the loss of electrochemical surface area (ECSA) due to Pt nanoparticle dissolution and agglomeration. Here, Pt loss is mitigated through a Pickering emulsion-processing strategy that employs graphene nanoplatelet dispersions stabilized by the polymer ethyl cellulose. The resulting graphene-Pt/Vulcan carbon (Pt/C) catalysts exhibit superior durability and ECSA retention throughout an accelerated stress test compared with a commercial Pt/C standard catalyst, both in a diagnostic-rotating disc electrode setup and in a membrane electrode assembly full cell. These graphene-Pt/C catalysts also improve durability at high-voltage conditions, providing further evidence of their exceptional electrochemical stability. Consistent with density functional theory calculations, postelectrochemical characterization reveals that Pt nanoparticles localize at graphene defects both on the basal plane and especially at the edges of the graphene nanoplatelets. Since this Pt nanoparticle localization suppresses Pt nanoparticle dissolution and agglomeration without hindering accessibility of the reactant species to the catalyst surface, the ORR performance under both idealized and practical experimental conditions shows significantly improved durability while maintaining high electrochemical activity.
URI
https://oasis.postech.ac.kr/handle/2014.oak/114573
DOI
10.1002/adfm.202205216
ISSN
1616-301X
Article Type
Article
Citation
Advanced Functional Materials, vol. 32, no. 43, page. 2205216, 2022-10
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