Low-loading platinum-cobalt electrocatalyst supported on hollow carbon for enhanced oxygen reduction reaction

Authors
Lee, YoungbinLee, Jeong HeeLee, DongwookOh, SionPark, JongwookIm, KyungminYoo, Sung JongKim, Jinsoo
Issue Date
2024-11
Publisher
Elsevier BV
Citation
Chemical Engineering Journal, v.500
Abstract
The oxygen reduction reaction (ORR) at the cathode of proton exchange membrane fuel cells is very slow. Therefore, platinum (Pt)-based catalysts are only used in practical applications. However, due to the high cost of Pt-based noble electrocatalysts, research is underway to reduce the use of noble metals or replace Pt-based noble catalysts. To reduce the total production cost of catalysts in fuel cells, a simple mass production process is required and the use of noble metals should be reduced. Metal?organic framework (MOF)-derived non-noble metal electrocatalysts have been extensively investigated as ORR catalysts due to their large surface area and open pore structure. However, MOF-based non-noble metal catalysts exhibit low catalytic activity and stability compared to commercial Pt-based catalysts. To address this problem, a small amount of precious metal is added to MOFs to enhance the performance of MOF-based electrocatalysts. In this study, we synthesized an ultra-low-loading Pt electrocatalyst (2.2- wt% Pt) supported on MOF-derived hollow Co, nitrogen-doped carbon (h-Co-NC). h-Co-NC was prepared by carbonizing the MOF@MOF core?shell structure. After carbonization, Pt was loaded using the polyol method, and a hollow and single-atomic Pt/h-Co-NC electrocatalyst was successfully synthesized by annealing. The synthesized hollow Pt/h-Co-NC electrocatalyst exhibited superior ORR performance and stability compared with non-hollow Pt/Co-NC.
Keywords
TEMPERATURE FUEL-CELLS; PARTICLE-SIZE; CATALYSTS; PERFORMANCE; EVOLUTION; SHELL; Platinum; Ultra-low loading; Hollow structure; Oxygen reduction reaction; PEMFC
ISSN
1385-8947
URI
https://pubs.kist.re.kr/handle/201004/151144
DOI
10.1016/j.cej.2024.157072
Appears in Collections:
KIST Article > 2024
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