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• W3149721331 endingPage "6899" @default.
• W3149721331 startingPage "6886" @default.
• W3149721331 abstract "Carbon supported and nitrogen coordinated single Mn site (Mn–N–C) catalysts are the most desirable platinum group metal (PGM)-free cathode catalysts for proton-exchange membrane fuel cells (PEMFCs) due to their insignificant Fenton reactions (vs. Fe), earth abundances (vs. Co), and encouraging activity and stability. However, current Mn–N–C catalysts suffer from high overpotential due to low intrinsic activity and less dense MnN4 sites. Herein, we present a sulfur-doped Mn–N–C catalyst (Mn–N–C–S) synthesized through an effective adsorption-pyrolysis process. Using electron microscopy and X-ray absorption spectroscopy (XAS) techniques, we verify the uniform dispersion of MnN4 sites and confirm the effect of S doping on the Mn–N coordination. The Mn–N–C–S catalyst exhibits a favorable oxygen reduction reaction (ORR) activity in acidic media relative to the S-free Mn–N–C catalyst. The corresponding membrane electrode assembly (MEA) generates enhanced performance with a peak power density of 500 mW cm–2 under a realistic H2/air environment. The constant voltage tests of fuel cells confirm the much-enhanced stability of the Mn–N–C–S catalyst compared to the Fe–N–C and Fe–N–C–S catalysts. The electron microscopy and Fourier transform XAS analyses provide insights into catalyst degradation associated with Mn oxidation and agglomeration. The theoretical calculation elucidates that the promoted ORR activity is mainly attributed to the spatial effect stemmed from the repulsive interaction between the ORR intermediates and adjacent S dopants." @default.
• W3149721331 created "2021-04-13" @default.
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• W3149721331 date "2021-03-31" @default.
• W3149721331 modified "2023-10-16" @default.
• W3149721331 title "Promoting Atomically Dispersed MnN₄ Sites <i>via</i> Sulfur Doping for Oxygen Reduction: Unveiling Intrinsic Activity and Degradation in Fuel Cells" @default.
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• W3149721331 doi "https://doi.org/10.1021/acsnano.0c10637" @default.
• W3149721331 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/33787214" @default.
• W3149721331 hasPublicationYear "2021" @default.
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