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Promoting heterogeneous catalysis beyond catalyst design
Despite the indisputable success of conventional approaches to manipulate the performance of heterogeneous catalysts by tuning the composition and structure of active sites, future research on catalysis engineering will likely go beyond the catalyst itself. Recently, several auxiliary promotion meth...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7058091/ https://www.ncbi.nlm.nih.gov/pubmed/32180922 http://dx.doi.org/10.1039/c9sc05947d |
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author | Hülsey, Max J. Lim, Chia Wei Yan, Ning |
author_facet | Hülsey, Max J. Lim, Chia Wei Yan, Ning |
author_sort | Hülsey, Max J. |
collection | PubMed |
description | Despite the indisputable success of conventional approaches to manipulate the performance of heterogeneous catalysts by tuning the composition and structure of active sites, future research on catalysis engineering will likely go beyond the catalyst itself. Recently, several auxiliary promotion methods, either promoting the activity of reagents or enabling optimized adsorbate–catalyst interactions, have been proven as viable strategies to enhance catalytic reactions. Those auxiliary promotion methods range from electric/magnetic fields and electric potentials to mechanic stress, significantly altering the properties of reagent molecules and/or the surface characteristics of nanostructured catalysts. Apart from static enhancement effects, they in principle also allow for spatially and temporally variable modifications of catalyst surfaces. While some of those methods have been demonstrated, some are only theoretically predicted, opening exciting avenues for future experimental advances. Besides fundamental descriptions and comparisons of each activation method, in this perspective we plan to provide examples for the applications of those techniques for a variety of catalytic reactions as diverse as N(2) and CO(2) hydrogenation as well as electrochemical water splitting. Finally, we provide a unifying view and guidelines for future research into the use of promotion methods, generating deeper understanding of the complex dynamics on the nanoparticle surface under auxiliary promotion and the expansion of auxiliary techniques to different sustainability-related reactions. |
format | Online Article Text |
id | pubmed-7058091 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-70580912020-03-16 Promoting heterogeneous catalysis beyond catalyst design Hülsey, Max J. Lim, Chia Wei Yan, Ning Chem Sci Chemistry Despite the indisputable success of conventional approaches to manipulate the performance of heterogeneous catalysts by tuning the composition and structure of active sites, future research on catalysis engineering will likely go beyond the catalyst itself. Recently, several auxiliary promotion methods, either promoting the activity of reagents or enabling optimized adsorbate–catalyst interactions, have been proven as viable strategies to enhance catalytic reactions. Those auxiliary promotion methods range from electric/magnetic fields and electric potentials to mechanic stress, significantly altering the properties of reagent molecules and/or the surface characteristics of nanostructured catalysts. Apart from static enhancement effects, they in principle also allow for spatially and temporally variable modifications of catalyst surfaces. While some of those methods have been demonstrated, some are only theoretically predicted, opening exciting avenues for future experimental advances. Besides fundamental descriptions and comparisons of each activation method, in this perspective we plan to provide examples for the applications of those techniques for a variety of catalytic reactions as diverse as N(2) and CO(2) hydrogenation as well as electrochemical water splitting. Finally, we provide a unifying view and guidelines for future research into the use of promotion methods, generating deeper understanding of the complex dynamics on the nanoparticle surface under auxiliary promotion and the expansion of auxiliary techniques to different sustainability-related reactions. Royal Society of Chemistry 2020-01-14 /pmc/articles/PMC7058091/ /pubmed/32180922 http://dx.doi.org/10.1039/c9sc05947d Text en This journal is © The Royal Society of Chemistry 2020 https://creativecommons.org/licenses/by-nc/3.0/This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0) |
spellingShingle | Chemistry Hülsey, Max J. Lim, Chia Wei Yan, Ning Promoting heterogeneous catalysis beyond catalyst design |
title | Promoting heterogeneous catalysis beyond catalyst design |
title_full | Promoting heterogeneous catalysis beyond catalyst design |
title_fullStr | Promoting heterogeneous catalysis beyond catalyst design |
title_full_unstemmed | Promoting heterogeneous catalysis beyond catalyst design |
title_short | Promoting heterogeneous catalysis beyond catalyst design |
title_sort | promoting heterogeneous catalysis beyond catalyst design |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7058091/ https://www.ncbi.nlm.nih.gov/pubmed/32180922 http://dx.doi.org/10.1039/c9sc05947d |
work_keys_str_mv | AT hulseymaxj promotingheterogeneouscatalysisbeyondcatalystdesign AT limchiawei promotingheterogeneouscatalysisbeyondcatalystdesign AT yanning promotingheterogeneouscatalysisbeyondcatalystdesign |