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Catalytic approaches towards highly durable proton exchange membrane fuel cells with minimized Pt use

Proton exchange membrane fuel cells (PEMFCs) produce electricity from H(2) without carbon emission, and they are considered as environmentally benign energy conversion devices. Although PEMFCs are mature enough to find themselves in a few commercial automobiles such as Hyundai Nexo and Toyota Mirai,...

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Autores principales: Kim, Hee-Eun, Kwon, Jaehoon, Lee, Hyunjoo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9200127/
https://www.ncbi.nlm.nih.gov/pubmed/35774157
http://dx.doi.org/10.1039/d2sc00541g
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author Kim, Hee-Eun
Kwon, Jaehoon
Lee, Hyunjoo
author_facet Kim, Hee-Eun
Kwon, Jaehoon
Lee, Hyunjoo
author_sort Kim, Hee-Eun
collection PubMed
description Proton exchange membrane fuel cells (PEMFCs) produce electricity from H(2) without carbon emission, and they are considered as environmentally benign energy conversion devices. Although PEMFCs are mature enough to find themselves in a few commercial automobiles such as Hyundai Nexo and Toyota Mirai, their durability should be enhanced, especially under transient conditions, and Pt use should be reduced significantly to expand their market. Herein, we introduce examples of how catalysts can contribute to enhancing the durability of PEMFCs while minimizing Pt use. Numerous electrocatalysts have been reported claiming superior activity in a half-cell setup, but they often fail to show the same enhancement in a single cell setup due to various transfer problems, impurity poisoning, etc. This perspective focuses on catalysts tested in a membrane-electrode-assembly (MEA) setup. As examples to obtain durability under transient conditions, catalysts used in reversal-tolerant anodes (RTAs) and selective anodes are explained. RTAs can endure sudden H(2) starvation, and selective anodes can operate properly when O(2) is unexpectedly mixed with H(2) in the anode. As examples with high durability in long-term operation, Pt-based nanoparticle catalysts encapsulated with carbon shells are explained. Interestingly, PtCo nanoparticles supported on Co–N–C or PtFe nanoparticles encapsulated with a carbon shell presented a superior cell performance in spite of <1/10 Pt use in an MEA setup. Non-Pt group metal (PGM) catalysts used in an MEA setup are also briefly explained. With these highly durable catalysts which can respond properly under transient conditions with minimum Pt use, PEMFC technology can bring about a more sustainable society.
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spelling pubmed-92001272022-06-29 Catalytic approaches towards highly durable proton exchange membrane fuel cells with minimized Pt use Kim, Hee-Eun Kwon, Jaehoon Lee, Hyunjoo Chem Sci Chemistry Proton exchange membrane fuel cells (PEMFCs) produce electricity from H(2) without carbon emission, and they are considered as environmentally benign energy conversion devices. Although PEMFCs are mature enough to find themselves in a few commercial automobiles such as Hyundai Nexo and Toyota Mirai, their durability should be enhanced, especially under transient conditions, and Pt use should be reduced significantly to expand their market. Herein, we introduce examples of how catalysts can contribute to enhancing the durability of PEMFCs while minimizing Pt use. Numerous electrocatalysts have been reported claiming superior activity in a half-cell setup, but they often fail to show the same enhancement in a single cell setup due to various transfer problems, impurity poisoning, etc. This perspective focuses on catalysts tested in a membrane-electrode-assembly (MEA) setup. As examples to obtain durability under transient conditions, catalysts used in reversal-tolerant anodes (RTAs) and selective anodes are explained. RTAs can endure sudden H(2) starvation, and selective anodes can operate properly when O(2) is unexpectedly mixed with H(2) in the anode. As examples with high durability in long-term operation, Pt-based nanoparticle catalysts encapsulated with carbon shells are explained. Interestingly, PtCo nanoparticles supported on Co–N–C or PtFe nanoparticles encapsulated with a carbon shell presented a superior cell performance in spite of <1/10 Pt use in an MEA setup. Non-Pt group metal (PGM) catalysts used in an MEA setup are also briefly explained. With these highly durable catalysts which can respond properly under transient conditions with minimum Pt use, PEMFC technology can bring about a more sustainable society. The Royal Society of Chemistry 2022-05-04 /pmc/articles/PMC9200127/ /pubmed/35774157 http://dx.doi.org/10.1039/d2sc00541g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Kim, Hee-Eun
Kwon, Jaehoon
Lee, Hyunjoo
Catalytic approaches towards highly durable proton exchange membrane fuel cells with minimized Pt use
title Catalytic approaches towards highly durable proton exchange membrane fuel cells with minimized Pt use
title_full Catalytic approaches towards highly durable proton exchange membrane fuel cells with minimized Pt use
title_fullStr Catalytic approaches towards highly durable proton exchange membrane fuel cells with minimized Pt use
title_full_unstemmed Catalytic approaches towards highly durable proton exchange membrane fuel cells with minimized Pt use
title_short Catalytic approaches towards highly durable proton exchange membrane fuel cells with minimized Pt use
title_sort catalytic approaches towards highly durable proton exchange membrane fuel cells with minimized pt use
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9200127/
https://www.ncbi.nlm.nih.gov/pubmed/35774157
http://dx.doi.org/10.1039/d2sc00541g
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