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Enhancement of Catalytic Activity and Durability of Pt Nanoparticle through Strong Chemical Interaction with Electrically Conductive Support of Magnéli Phase Titanium Oxide

In this study, we address the catalytic performance of variously sized Pt nanoparticles (NPs) (from 1.7 to 2.9 nm) supported on magnéli phase titanium oxide (MPTO, Ti(4)O(7)) along with commercial solid type carbon (VXC-72R) for oxygen reduction reaction (ORR). Key idea is to utilize a robust and el...

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Autores principales: Dogan, Didem C., Choi, Jiye, Seo, Min Ho, Lee, Eunjik, Jung, Namgee, Yim, Sung-Dae, Yang, Tae-Hyun, Park, Gu-Gon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8063942/
https://www.ncbi.nlm.nih.gov/pubmed/33804971
http://dx.doi.org/10.3390/nano11040829
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author Dogan, Didem C.
Choi, Jiye
Seo, Min Ho
Lee, Eunjik
Jung, Namgee
Yim, Sung-Dae
Yang, Tae-Hyun
Park, Gu-Gon
author_facet Dogan, Didem C.
Choi, Jiye
Seo, Min Ho
Lee, Eunjik
Jung, Namgee
Yim, Sung-Dae
Yang, Tae-Hyun
Park, Gu-Gon
author_sort Dogan, Didem C.
collection PubMed
description In this study, we address the catalytic performance of variously sized Pt nanoparticles (NPs) (from 1.7 to 2.9 nm) supported on magnéli phase titanium oxide (MPTO, Ti(4)O(7)) along with commercial solid type carbon (VXC-72R) for oxygen reduction reaction (ORR). Key idea is to utilize a robust and electrically conductive MPTO as a support material so that we employed it to improve the catalytic activity and durability through the strong metal-support interaction (SMSI). Furthermore, we increase the specific surface area of MPTO up to 61.6 m(2) g(−1) to enhance the SMSI effect between Pt NP and MPTO. After the deposition of a range of Pt NPs on the support materials, we investigate the ORR activity and durability using a rotating disk electrode (RDE) technique in acid media. As a result of accelerated stress test (AST) for 30k cycles, regardless of the Pt particle size, we confirmed that Pt/MPTO samples show a lower electrochemical surface area (ECSA) loss (<20%) than that of Pt/C (~40%). That is explained by the increased dissolution potential and binding energy of Pt on MPTO against to carbon, which is supported by the density functional theory (DFT) calculations. Based on these results, we found that conductive metal oxides could be an alternative as a support material for the long-term fuel cell operation.
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spelling pubmed-80639422021-04-24 Enhancement of Catalytic Activity and Durability of Pt Nanoparticle through Strong Chemical Interaction with Electrically Conductive Support of Magnéli Phase Titanium Oxide Dogan, Didem C. Choi, Jiye Seo, Min Ho Lee, Eunjik Jung, Namgee Yim, Sung-Dae Yang, Tae-Hyun Park, Gu-Gon Nanomaterials (Basel) Article In this study, we address the catalytic performance of variously sized Pt nanoparticles (NPs) (from 1.7 to 2.9 nm) supported on magnéli phase titanium oxide (MPTO, Ti(4)O(7)) along with commercial solid type carbon (VXC-72R) for oxygen reduction reaction (ORR). Key idea is to utilize a robust and electrically conductive MPTO as a support material so that we employed it to improve the catalytic activity and durability through the strong metal-support interaction (SMSI). Furthermore, we increase the specific surface area of MPTO up to 61.6 m(2) g(−1) to enhance the SMSI effect between Pt NP and MPTO. After the deposition of a range of Pt NPs on the support materials, we investigate the ORR activity and durability using a rotating disk electrode (RDE) technique in acid media. As a result of accelerated stress test (AST) for 30k cycles, regardless of the Pt particle size, we confirmed that Pt/MPTO samples show a lower electrochemical surface area (ECSA) loss (<20%) than that of Pt/C (~40%). That is explained by the increased dissolution potential and binding energy of Pt on MPTO against to carbon, which is supported by the density functional theory (DFT) calculations. Based on these results, we found that conductive metal oxides could be an alternative as a support material for the long-term fuel cell operation. MDPI 2021-03-24 /pmc/articles/PMC8063942/ /pubmed/33804971 http://dx.doi.org/10.3390/nano11040829 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Article
Dogan, Didem C.
Choi, Jiye
Seo, Min Ho
Lee, Eunjik
Jung, Namgee
Yim, Sung-Dae
Yang, Tae-Hyun
Park, Gu-Gon
Enhancement of Catalytic Activity and Durability of Pt Nanoparticle through Strong Chemical Interaction with Electrically Conductive Support of Magnéli Phase Titanium Oxide
title Enhancement of Catalytic Activity and Durability of Pt Nanoparticle through Strong Chemical Interaction with Electrically Conductive Support of Magnéli Phase Titanium Oxide
title_full Enhancement of Catalytic Activity and Durability of Pt Nanoparticle through Strong Chemical Interaction with Electrically Conductive Support of Magnéli Phase Titanium Oxide
title_fullStr Enhancement of Catalytic Activity and Durability of Pt Nanoparticle through Strong Chemical Interaction with Electrically Conductive Support of Magnéli Phase Titanium Oxide
title_full_unstemmed Enhancement of Catalytic Activity and Durability of Pt Nanoparticle through Strong Chemical Interaction with Electrically Conductive Support of Magnéli Phase Titanium Oxide
title_short Enhancement of Catalytic Activity and Durability of Pt Nanoparticle through Strong Chemical Interaction with Electrically Conductive Support of Magnéli Phase Titanium Oxide
title_sort enhancement of catalytic activity and durability of pt nanoparticle through strong chemical interaction with electrically conductive support of magnéli phase titanium oxide
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8063942/
https://www.ncbi.nlm.nih.gov/pubmed/33804971
http://dx.doi.org/10.3390/nano11040829
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