Journal
JOURNAL OF MATERIALS CHEMISTRY A
Volume 10, Issue 10, Pages 5361-5372Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ta07264a
Keywords
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Funding
- National Research Foundation of Korea [NRF2018 M1A2A2063174]
- GIST Research Institute (GRI) - GIST [GK14650]
- National Research Foundation of Korea [PAL-2022] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
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FeCuxNC catalysts with ordered mesoporous grain-shaped particles were prepared and characterized, showing controlled electronic state of active sites and enhanced oxygen reduction reaction performance compared to Pt/C in alkaline conditions.
Non-precious metal catalysts for oxygen reduction reaction (ORR) are promising alternatives to Pt/C in fuel cells, thus, demand for advanced catalysts is arising. Herein, we prepared and characterized mesoporous Fe and Cu anchored in N-, S-, and P-doped carbon (FeCuxNC) catalysts, revealing the presence of ordered mesoporous grain-shaped particles and demonstrating that the electronic state of the active sites (Fe-N-x) is controlled by their environments, which can affect ORR kinetics. Half-cell measurements revealed that FeCuxNC promoted ORRs more effectively (0.92 V at 3 mA cm(-2)) than Pt/C (0.87 V at 3 mA cm(-2)) in alkaline conditions, while a current density of 490 mA cm(-2) was achieved at 0.6 V in a single-cell level. Multi-heteroatom doping modulated the energy of OOH* and OH- adsorption on the active sites, and the lowest overpotential (according to density functional theory calculations) was obtained for the Fe-Cu-N-3-C-P-S model.
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