A paradigm shift in CO tolerant catalyst design for fuel cells via introducing defect-controlled carbon molecular sieve layers
- Authors
- Min, Jiho; Kim, Sungmin; Jeffery, Arokia Anto; Shin, Hyeyoung; Kang, Yun Sik; Kim, Youngjin; Jang, Jeonghee; Lee, Seunghyun; Park, Seok-Hee; Park, Gu-Gon; Yoo, Sung Jong; Yim, Sung-Dae; Jung, Namgee
- Issue Date
- 2022-10
- Publisher
- Elsevier
- Citation
- Materials Today Energy, v.29
- Abstract
- The CO poisoning effect leads to serious performance degradation of polymer electrolyte membrane fuel cells using reformed H2 as fuel. To address this problem, PtRu-based catalysts have been extensively studied over decades. Nevertheless, the catalyst stability issue due to Ru dissolution has always risen to the surface. Here, we propose a solution to simultaneously achieve high CO tolerance and stability of PtRu catalysts via introducing a defect-controlled carbon molecular sieve layer. The ultrathin carbon shell with controlled pore structures allows for the selective permeation of H2, providing exceptionally high CO tolerance. The molecular sieve effect is demonstrated even by Ru-free Pt nanoparticles with carbon shells. The carbon shell-encapsulated PtRu nanoparticles also show remarkably improved stability due to the protective carbon layer. This atomic-scale molecular sieve effect is expected to bring about a radical change in the design of CO tolerant catalyst structures that have been entirely dependent on metal composition.(c) 2022 Elsevier Ltd. All rights reserved.
- Keywords
- HYDROGEN OXIDATION; METHANOL; GRAPHENE; ANODE; PTRU; RU; STABILITY; PLATINUM; OXIDE; ELECTROCATALYSIS; CO tolerant; Carbon shell; Molecular sieve effect; Durability; Hydrogen oxidation reaction; Polymer electrolyte membrane fuel cells
- ISSN
- 2468-6069
- URI
- https://pubs.kist.re.kr/handle/201004/114459
- DOI
- 10.1016/j.mtener.2022.101124
- Appears in Collections:
- KIST Article > 2022
- Files in This Item:
There are no files associated with this item.
- Export
- RIS (EndNote)
- XLS (Excel)
- XML
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.