Abstract
The electrocatalytic oxygen reduction reaction (ORR) in acidic media is quite strenuous. Although platinum (Pt)-based materials are considered state-of-the-art ORR catalysts, their high cost and poor durability greatly impede their extensive application in polymer electrolyte membrane fuel cells and direct methanol fuel cells. Here, we report a bimetallic M–Nx–C-class electrocatalyst comprising Co- and Fe-coordinated graphitic carbon nitride ((Co,Fe)–CN) and reduced graphene oxide (RGO) as an effective substitute for expensive Pt-based catalysts for the ORR in acidic media. The fabricated (Co,Fe)–CN/RGO catalyst exhibits a high surface area, high porosity, fast charge-transfer kinetics at the (Co,Fe)–CN/RGO 2D/2D interface, and abundant Co–Nx–C and Fe–Nx–C active sites. Because of these favorable properties, the optimized (Co,Fe)–CN/RGO catalyst displayed extraordinary electrocatalytic ORR activity, with an onset potential of 875 mV, which is only 41 mV more negative than that of a commercial Pt/C, and follows an efficient four-electron reaction pathway in acidic media. Notably, the fabricated catalyst demonstrated excellent methanol tolerance and long-term stability compared with the reference Pt/C. Therefore, this work provides a rational design approach to fabricating graphitic-C3N4-based nonprecious bimetallic electrocatalysts with M–Nx–C active sites for enhanced ORR activity in fuel-cell applications.
Original language | English |
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Article number | 147367 |
Journal | Applied Surface Science |
Volume | 531 |
DOIs | |
State | Published - 30 Nov 2020 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2020 Elsevier B.V.
Funding
This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government (MSIT) (No. NRF-2018R1A5A1025137 ).
Funders | Funder number |
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National Research Foundation of Korea | |
Ministry of Science and ICT, South Korea | NRF-2018R1A5A1025137 |
Keywords
- Bimetallic
- Electrocatalysis
- Nonprecious catalyst
- Oxygen reduction reaction
- g-CN