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Compensation Effect Exhibited by Gold Bimetallic Nanoparticles during CO Oxidation

[Image: see text] While CO oxidation catalyzed by gold nanoparticles has been practiced academically for several decades, there are still important discoveries to be made. One area of current interest is to pair Au with another alloying metal and observe the catalytic consequences of the presence of...

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Autores principales: Brindle, Joe, Nigra, Michael M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8459437/
https://www.ncbi.nlm.nih.gov/pubmed/34568704
http://dx.doi.org/10.1021/acsomega.1c04236
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author Brindle, Joe
Nigra, Michael M.
author_facet Brindle, Joe
Nigra, Michael M.
author_sort Brindle, Joe
collection PubMed
description [Image: see text] While CO oxidation catalyzed by gold nanoparticles has been practiced academically for several decades, there are still important discoveries to be made. One area of current interest is to pair Au with another alloying metal and observe the catalytic consequences of the presence of the other metal. In this work, TiO(2)-supported bimetallic Au nanoparticles are alloyed with Cu, Co, Ni, Pd, and Ru and used as catalysts for CO oxidation. Two synthetic methods for the alloys are presented: a strong electrostatic adsorption (SEA) method and a sterically demanding ligand synthesis (SDLS) method which uses triphenylphosphine (TPP) as the ligand. The catalytic performance of the materials synthesized with the SEA and SDLS methods is compared in CO oxidation. The results indicate that the materials tested present an enthalpy–entropy compensation effect. Interestingly, both the enthalpy of activation, ΔH(‡), and the entropy of activation, ΔS(‡), generally decrease with particle size. AuCo and AuRu materials exhibit a decrease in the overall activity as compared to Au and the other Au alloys when synthesized via SEA. Au face-centered-cubic alloys AuCu, AuNi, and AuPd prepared via SEA show an improvement in activity compared to monometallic Au in our reaction conditions. In situ diffuse reflectance infrared Fourier transform spectroscopy presents two distinct regions for Au bimetallics where AuCo and AuRu show peak positions in the region of 2070–2050 cm(–1), indicating a weaker interaction for AuCo and AuRu with CO when compared to that of the other alloys. For the SDLS method samples, the hypothesis is that TPP would enhance the CO oxidation rate by enhancing the charge transfer to the metallic surface. The results indicate that SDLS samples have lower CO oxidation rates and if any charge transfer occurs, it is masked by the lateral interactions of the CO π bonds and the phenyl groups of TPP.
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spelling pubmed-84594372021-09-24 Compensation Effect Exhibited by Gold Bimetallic Nanoparticles during CO Oxidation Brindle, Joe Nigra, Michael M. ACS Omega [Image: see text] While CO oxidation catalyzed by gold nanoparticles has been practiced academically for several decades, there are still important discoveries to be made. One area of current interest is to pair Au with another alloying metal and observe the catalytic consequences of the presence of the other metal. In this work, TiO(2)-supported bimetallic Au nanoparticles are alloyed with Cu, Co, Ni, Pd, and Ru and used as catalysts for CO oxidation. Two synthetic methods for the alloys are presented: a strong electrostatic adsorption (SEA) method and a sterically demanding ligand synthesis (SDLS) method which uses triphenylphosphine (TPP) as the ligand. The catalytic performance of the materials synthesized with the SEA and SDLS methods is compared in CO oxidation. The results indicate that the materials tested present an enthalpy–entropy compensation effect. Interestingly, both the enthalpy of activation, ΔH(‡), and the entropy of activation, ΔS(‡), generally decrease with particle size. AuCo and AuRu materials exhibit a decrease in the overall activity as compared to Au and the other Au alloys when synthesized via SEA. Au face-centered-cubic alloys AuCu, AuNi, and AuPd prepared via SEA show an improvement in activity compared to monometallic Au in our reaction conditions. In situ diffuse reflectance infrared Fourier transform spectroscopy presents two distinct regions for Au bimetallics where AuCo and AuRu show peak positions in the region of 2070–2050 cm(–1), indicating a weaker interaction for AuCo and AuRu with CO when compared to that of the other alloys. For the SDLS method samples, the hypothesis is that TPP would enhance the CO oxidation rate by enhancing the charge transfer to the metallic surface. The results indicate that SDLS samples have lower CO oxidation rates and if any charge transfer occurs, it is masked by the lateral interactions of the CO π bonds and the phenyl groups of TPP. American Chemical Society 2021-09-09 /pmc/articles/PMC8459437/ /pubmed/34568704 http://dx.doi.org/10.1021/acsomega.1c04236 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Brindle, Joe
Nigra, Michael M.
Compensation Effect Exhibited by Gold Bimetallic Nanoparticles during CO Oxidation
title Compensation Effect Exhibited by Gold Bimetallic Nanoparticles during CO Oxidation
title_full Compensation Effect Exhibited by Gold Bimetallic Nanoparticles during CO Oxidation
title_fullStr Compensation Effect Exhibited by Gold Bimetallic Nanoparticles during CO Oxidation
title_full_unstemmed Compensation Effect Exhibited by Gold Bimetallic Nanoparticles during CO Oxidation
title_short Compensation Effect Exhibited by Gold Bimetallic Nanoparticles during CO Oxidation
title_sort compensation effect exhibited by gold bimetallic nanoparticles during co oxidation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8459437/
https://www.ncbi.nlm.nih.gov/pubmed/34568704
http://dx.doi.org/10.1021/acsomega.1c04236
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