Cargando…
Impact of the Experimental Parameters on Catalytic Activity When Preparing Polymer Protected Bimetallic Nanoparticle Catalysts on Activated Carbon
[Image: see text] Sol immobilization is used to produce bimetallic catalysts with higher activity to monometallic counterparts for a wide range of environmental and commercial catalytic transformations. Analysis of complementary surface characterization (XPS, Boehm’s titration, and zeta potential me...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9016708/ https://www.ncbi.nlm.nih.gov/pubmed/35465244 http://dx.doi.org/10.1021/acscatal.1c05904 |
_version_ | 1784688585533816832 |
---|---|
author | Paris, Charlie B. Howe, Alexander G. Lewis, Richard James Hewes, Daniel Morgan, David J. He, Qian Edwards, Jennifer K. |
author_facet | Paris, Charlie B. Howe, Alexander G. Lewis, Richard James Hewes, Daniel Morgan, David J. He, Qian Edwards, Jennifer K. |
author_sort | Paris, Charlie B. |
collection | PubMed |
description | [Image: see text] Sol immobilization is used to produce bimetallic catalysts with higher activity to monometallic counterparts for a wide range of environmental and commercial catalytic transformations. Analysis of complementary surface characterization (XPS, Boehm’s titration, and zeta potential measurements) was used to elucidate alterations in the surface functionality of two activated carbon supports during acid exposure. When considered in parallel to the experimentally determined electrostatic and conformational changes of the polymer surrounding the nanoparticles, an electrostatic model is proposed describing polymer protected nanoparticle deposition with several polymer–carbon support examples described. Consideration of the electrostatic interactions ensures full deposition of the polymer protected nanoparticles and at the same time influences the structure of the bimetallic nanoparticle immobilized on the support. The normalized activity of AuPd catalysts prepared with 133 ppm H(2)SO(4) has a much higher activity for the direct synthesis of hydrogen peroxide compared to catalysts prepared in the absence of acid. Detailed characterization by XPS indicates that the surface becomes enriched in Au in the Au–Pd samples prepared with acid, suggesting an improved dispersion of smaller bimetallic nanoparticles, rich in Au, that are known to be highly active for the direct synthesis reaction. Subsequent microscopy measurements confirmed this hypothesis, with the acid addition catalysts having a mean particle size ∼2 nm smaller than the zero acid counterparts. The addition of acid did not result in a morphology change, and random alloyed bimetallic AuPd nanoparticles were observed in catalysts prepared by sol immobilization in the presence and absence of acid. This work shows that the deposition of polymer protected AuPd nanoparticles onto activated carbon is heavily influenced by the acid addition step in the sol immobilization process. The physicochemical properties of both the polymer and the activated carbon support should be considered when designing a bimetallic nanoparticle catalyst by sol immobilization to ensure the optimum performance of the final catalyst. |
format | Online Article Text |
id | pubmed-9016708 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-90167082022-04-20 Impact of the Experimental Parameters on Catalytic Activity When Preparing Polymer Protected Bimetallic Nanoparticle Catalysts on Activated Carbon Paris, Charlie B. Howe, Alexander G. Lewis, Richard James Hewes, Daniel Morgan, David J. He, Qian Edwards, Jennifer K. ACS Catal [Image: see text] Sol immobilization is used to produce bimetallic catalysts with higher activity to monometallic counterparts for a wide range of environmental and commercial catalytic transformations. Analysis of complementary surface characterization (XPS, Boehm’s titration, and zeta potential measurements) was used to elucidate alterations in the surface functionality of two activated carbon supports during acid exposure. When considered in parallel to the experimentally determined electrostatic and conformational changes of the polymer surrounding the nanoparticles, an electrostatic model is proposed describing polymer protected nanoparticle deposition with several polymer–carbon support examples described. Consideration of the electrostatic interactions ensures full deposition of the polymer protected nanoparticles and at the same time influences the structure of the bimetallic nanoparticle immobilized on the support. The normalized activity of AuPd catalysts prepared with 133 ppm H(2)SO(4) has a much higher activity for the direct synthesis of hydrogen peroxide compared to catalysts prepared in the absence of acid. Detailed characterization by XPS indicates that the surface becomes enriched in Au in the Au–Pd samples prepared with acid, suggesting an improved dispersion of smaller bimetallic nanoparticles, rich in Au, that are known to be highly active for the direct synthesis reaction. Subsequent microscopy measurements confirmed this hypothesis, with the acid addition catalysts having a mean particle size ∼2 nm smaller than the zero acid counterparts. The addition of acid did not result in a morphology change, and random alloyed bimetallic AuPd nanoparticles were observed in catalysts prepared by sol immobilization in the presence and absence of acid. This work shows that the deposition of polymer protected AuPd nanoparticles onto activated carbon is heavily influenced by the acid addition step in the sol immobilization process. The physicochemical properties of both the polymer and the activated carbon support should be considered when designing a bimetallic nanoparticle catalyst by sol immobilization to ensure the optimum performance of the final catalyst. American Chemical Society 2022-03-30 2022-04-15 /pmc/articles/PMC9016708/ /pubmed/35465244 http://dx.doi.org/10.1021/acscatal.1c05904 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Paris, Charlie B. Howe, Alexander G. Lewis, Richard James Hewes, Daniel Morgan, David J. He, Qian Edwards, Jennifer K. Impact of the Experimental Parameters on Catalytic Activity When Preparing Polymer Protected Bimetallic Nanoparticle Catalysts on Activated Carbon |
title | Impact of the Experimental Parameters on Catalytic
Activity When Preparing Polymer Protected Bimetallic Nanoparticle
Catalysts on Activated Carbon |
title_full | Impact of the Experimental Parameters on Catalytic
Activity When Preparing Polymer Protected Bimetallic Nanoparticle
Catalysts on Activated Carbon |
title_fullStr | Impact of the Experimental Parameters on Catalytic
Activity When Preparing Polymer Protected Bimetallic Nanoparticle
Catalysts on Activated Carbon |
title_full_unstemmed | Impact of the Experimental Parameters on Catalytic
Activity When Preparing Polymer Protected Bimetallic Nanoparticle
Catalysts on Activated Carbon |
title_short | Impact of the Experimental Parameters on Catalytic
Activity When Preparing Polymer Protected Bimetallic Nanoparticle
Catalysts on Activated Carbon |
title_sort | impact of the experimental parameters on catalytic
activity when preparing polymer protected bimetallic nanoparticle
catalysts on activated carbon |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9016708/ https://www.ncbi.nlm.nih.gov/pubmed/35465244 http://dx.doi.org/10.1021/acscatal.1c05904 |
work_keys_str_mv | AT parischarlieb impactoftheexperimentalparametersoncatalyticactivitywhenpreparingpolymerprotectedbimetallicnanoparticlecatalystsonactivatedcarbon AT howealexanderg impactoftheexperimentalparametersoncatalyticactivitywhenpreparingpolymerprotectedbimetallicnanoparticlecatalystsonactivatedcarbon AT lewisrichardjames impactoftheexperimentalparametersoncatalyticactivitywhenpreparingpolymerprotectedbimetallicnanoparticlecatalystsonactivatedcarbon AT hewesdaniel impactoftheexperimentalparametersoncatalyticactivitywhenpreparingpolymerprotectedbimetallicnanoparticlecatalystsonactivatedcarbon AT morgandavidj impactoftheexperimentalparametersoncatalyticactivitywhenpreparingpolymerprotectedbimetallicnanoparticlecatalystsonactivatedcarbon AT heqian impactoftheexperimentalparametersoncatalyticactivitywhenpreparingpolymerprotectedbimetallicnanoparticlecatalystsonactivatedcarbon AT edwardsjenniferk impactoftheexperimentalparametersoncatalyticactivitywhenpreparingpolymerprotectedbimetallicnanoparticlecatalystsonactivatedcarbon |