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A Cu–Pd single-atom alloy catalyst for highly efficient NO reduction
A series of Cu–Pd alloy nanoparticles supported on Al(2)O(3) were prepared and tested as catalysts for deNO(x) reactions. XRD, HAADF-STEM, XAFS, and FT-IR analyses revealed that a single-atom alloy structure was formed when the Cu/Pd ratio was 5, where Pd atoms were well isolated by Cu atoms. Compar...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006621/ https://www.ncbi.nlm.nih.gov/pubmed/32110288 http://dx.doi.org/10.1039/c9sc03172c |
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author | Xing, Feilong Jeon, Jaewan Toyao, Takashi Shimizu, Ken-ichi Furukawa, Shinya |
author_facet | Xing, Feilong Jeon, Jaewan Toyao, Takashi Shimizu, Ken-ichi Furukawa, Shinya |
author_sort | Xing, Feilong |
collection | PubMed |
description | A series of Cu–Pd alloy nanoparticles supported on Al(2)O(3) were prepared and tested as catalysts for deNO(x) reactions. XRD, HAADF-STEM, XAFS, and FT-IR analyses revealed that a single-atom alloy structure was formed when the Cu/Pd ratio was 5, where Pd atoms were well isolated by Cu atoms. Compared with Pd/Al(2)O(3), Cu(5)Pd/Al(2)O(3) exhibited outstanding catalytic activity and N(2) selectivity in the reduction of NO by CO: for the first time, the complete conversion of NO to N(2) was achieved even at 175 °C, with long-term stability for at least 30 h. High catalytic performance was also obtained in the presence of O(2) and C(3)H(6) (model exhaust gas), where a 90% decrease in Pd use was achieved with minimum evolution of N(2)O. Kinetic and DFT studies demonstrated that N–O bond breaking of the (NO)(2) dimer was the rate-determining step and was kinetically promoted by the isolated Pd. |
format | Online Article Text |
id | pubmed-7006621 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-70066212020-02-27 A Cu–Pd single-atom alloy catalyst for highly efficient NO reduction Xing, Feilong Jeon, Jaewan Toyao, Takashi Shimizu, Ken-ichi Furukawa, Shinya Chem Sci Chemistry A series of Cu–Pd alloy nanoparticles supported on Al(2)O(3) were prepared and tested as catalysts for deNO(x) reactions. XRD, HAADF-STEM, XAFS, and FT-IR analyses revealed that a single-atom alloy structure was formed when the Cu/Pd ratio was 5, where Pd atoms were well isolated by Cu atoms. Compared with Pd/Al(2)O(3), Cu(5)Pd/Al(2)O(3) exhibited outstanding catalytic activity and N(2) selectivity in the reduction of NO by CO: for the first time, the complete conversion of NO to N(2) was achieved even at 175 °C, with long-term stability for at least 30 h. High catalytic performance was also obtained in the presence of O(2) and C(3)H(6) (model exhaust gas), where a 90% decrease in Pd use was achieved with minimum evolution of N(2)O. Kinetic and DFT studies demonstrated that N–O bond breaking of the (NO)(2) dimer was the rate-determining step and was kinetically promoted by the isolated Pd. The Royal Society of Chemistry 2019-08-05 /pmc/articles/PMC7006621/ /pubmed/32110288 http://dx.doi.org/10.1039/c9sc03172c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Xing, Feilong Jeon, Jaewan Toyao, Takashi Shimizu, Ken-ichi Furukawa, Shinya A Cu–Pd single-atom alloy catalyst for highly efficient NO reduction |
title | A Cu–Pd single-atom alloy catalyst for highly efficient NO reduction |
title_full | A Cu–Pd single-atom alloy catalyst for highly efficient NO reduction |
title_fullStr | A Cu–Pd single-atom alloy catalyst for highly efficient NO reduction |
title_full_unstemmed | A Cu–Pd single-atom alloy catalyst for highly efficient NO reduction |
title_short | A Cu–Pd single-atom alloy catalyst for highly efficient NO reduction |
title_sort | cu–pd single-atom alloy catalyst for highly efficient no reduction |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006621/ https://www.ncbi.nlm.nih.gov/pubmed/32110288 http://dx.doi.org/10.1039/c9sc03172c |
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