Journal
JOURNAL OF ENERGY CHEMISTRY
Volume 52, Issue -, Pages 291-300Publisher
ELSEVIER
DOI: 10.1016/j.jechem.2020.04.066
Keywords
Bimetallic MOFs; Fe-N/S-C; Oxygen reduction reaction; Acidic media
Funding
- National Natural Science Foundation of China [21978331, 21975292, 21905311]
- National Key Research and Development Program of China [2016YFB0101200 (2016YFB0101204)]
- Guangdong Basic and Applied Basic Research Foundation [2020A1515010343]
- Guangzhou Science and Technology Project [201707010079]
- fundamental Research Funds for Central Universities [19lgpy136, 19lgpy116]
- Tip-top Scientific and Technical Innovative Youth Talents of Guangdong special support program [2016TQ03N322]
- China Postdoctoral Science Foundation [2019M653142]
- Sun Yat-sen University [76110-18841219]
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A facile method to prepare Fe-N/S-C hybrid electrocatalysts has been developed, showing significantly improved ORR performance with high stability and methanol tolerance. This work represents a breakthrough in the development of efficient non-precious-metal catalysts to address challenges faced by Pt-based electrocatalysts.
Heteroatoms doped Fe-N-C electrocatalysts have been widely acknowledged as one of the most promising candidates to replace Pt-based materials for electrocatalyzing oxygen reduction reaction (ORR). However, the complicated synthesis method and controversial catalytic mechanism represent a substantial impediment as of today. Herein, a very facile strategy to prepare Fe-N/S-C hybrid through pyrolyzing Zn and Fe bimetallic MOFs is rationally designed. The electrocatalytic ORR performance shows a volcano type curve with the increment of added Fe content. The half-wave potential (E-1/2) for ORR at optimized Fe-N/S-C-10% (10% = n (Fe)/(n (Fe) + n (Zn)), n (Fe) and n (Zn) represent the moles of Fe2+ and Zn2+ in the precursors, respectively) shifts significantly to the positive direction of 19.6 mV with respect to that of Pt/C in acidic media, as well as a high 4e selectivity and methanol tolerance. After 10,000 potential cycles, E-1/2 exhibits a small negative shift of similar to 27.5 mV at Fe-N/S-C-10% compared favorably with Pt/C (similar to 141.0 mV). This can be attributed to: (i) large specific surface area (849 m(2)/g) and hierarchically porous structure are favorable for the rapid mass transfer and active sites exposure; (ii) the embedded Fe containing nanoparticles in porous carbon are difficult to be moved and further agglomerated during the electrochemical accelerated aging test, further improving its stability; (iii) there exist small Fe containing nanoparticles, uniformly doped N and S, abundant Fe-N as efficiently active sites. This work represents a breakthrough in the development of high-efficient non-precious-metal catalysts (NPMCs) to address the current Pt-based electrocatalysts challenges. (c) 2020 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by ELSEVIER B.V. and Science Press. All rights reserved.
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