Tofu-derived heteroatom-doped carbon for oxygen reduction reaction in an anion exchange membrane-fuel cell
- Authors
 - Im, Kyungmin; Choi, Kyu Hwan; Park, Bum Jun; Yoo, Sung Jong; Kim, Jinsoo
 
- Issue Date
 - 2022-08
 
- Publisher
 - Pergamon Press Ltd.
 
- Citation
 - Energy Conversion and Management, v.265
 
- Abstract
 - The oxygen reduction reaction at the cathode of an anion exchange membrane-fuel cell progresses very slowly. Therefore, only platinum-based catalysts with adequate adsorption/desorption binding energy for oxygen are used in practical applications. Because noble metal-based electrocatalysts are very expensive, research is underway to reduce the amount of noble metals used or to replace platinum-based catalysts. Further, to reduce the production cost of fuel cells, a simple fabrication process enabling mass productivity and replacement of noble metals must be developed. Transition metal catalysts with metal-nitrogen-doped carbon have been investigated as an alternative to the noble metal catalysts for oxygen reduction reaction at the cathode of a fuel cell. In this study, to generate metal-nitrogen-carbon sites, protein precipitation was performed by chelating metal cations with the functional groups of proteins. This approach employed a traditional method that uses tofu (made from soy milk) to intake proteins. To separate the proteins dissolved in soy milk in the solid state, a coagulant containing transition metals was added. Tofu containing bimetallic zinc and cobalt ions was prepared and carbonized to synthesize nitrogen- and phosphorus-doped carbon structures and single-atomic cobalt active sites. The prepared tofu-derived catalyst exhibited excellent electrocatalytic performance with a half-wave potential of 0.86 V, an onset potential of 0.981 V, and high durability.
 
- Keywords
 - FREE CATALYSTS; Oxygen reduction reaction; Tofu; Heteroatom-doped carbon; Electrocatalyst; Fuel cell
 
- ISSN
 - 0196-8904
 
- URI
 - https://pubs.kist.re.kr/handle/201004/114829
 
- DOI
 - 10.1016/j.enconman.2022.115754
 
- Appears in Collections:
 - KIST Article > 2022
 
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