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In Situ Shell‐Isolated Nanoparticle‐Enhanced Raman Spectroscopy of Nickel‐Catalyzed Hydrogenation Reactions

Synthesis methods to prepare lower transition metal catalysts and specifically Ni for Shell‐Isolated Nanoparticle‐Enhanced Raman Spectroscopy (SHINERS) are explored. Impregnation, colloidal deposition, and spark ablation have been investigated as suitable synthesis routes to prepare SHINERS‐active N...

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Autores principales: Wondergem, Caterina S., Kromwijk, Josepha J. G., Slagter, Mark, Vrijburg, Wilbert L., Hensen, Emiel J. M., Monai, Matteo, Vogt, Charlotte, Weckhuysen, Bert M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7187311/
https://www.ncbi.nlm.nih.gov/pubmed/31981395
http://dx.doi.org/10.1002/cphc.201901162
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author Wondergem, Caterina S.
Kromwijk, Josepha J. G.
Slagter, Mark
Vrijburg, Wilbert L.
Hensen, Emiel J. M.
Monai, Matteo
Vogt, Charlotte
Weckhuysen, Bert M.
author_facet Wondergem, Caterina S.
Kromwijk, Josepha J. G.
Slagter, Mark
Vrijburg, Wilbert L.
Hensen, Emiel J. M.
Monai, Matteo
Vogt, Charlotte
Weckhuysen, Bert M.
author_sort Wondergem, Caterina S.
collection PubMed
description Synthesis methods to prepare lower transition metal catalysts and specifically Ni for Shell‐Isolated Nanoparticle‐Enhanced Raman Spectroscopy (SHINERS) are explored. Impregnation, colloidal deposition, and spark ablation have been investigated as suitable synthesis routes to prepare SHINERS‐active Ni/Au@SiO(2) catalyst/Shell‐Isolated Nanoparticles (SHINs). Ni precursors are confirmed to be notoriously difficult to reduce and the temperatures required are generally harsh enough to destroy SHINs, rendering SHINERS experiments on Ni infeasible using this approach. For colloidally synthesized Ni nanoparticles deposited on Au@SiO(2) SHINs, stabilizing ligands first need to be removed before application is possible in catalysis. The required procedure results in transformation of the metallic Ni core to a fully oxidized metal nanoparticle, again too challenging to reduce at temperatures still compatible with SHINs. Finally, by use of spark ablation we were able to prepare metallic Ni catalysts directly on Au@SiO(2) SHINs deposited on a Si wafer. These Ni/Au@SiO(2) catalyst/SHINs were subsequently successfully probed with several molecules (i. e. CO and acetylene) of interest for heterogeneous catalysis, and we show that they could be used to study the in situ hydrogenation of acetylene. We observe the interaction of acetylene with the Ni surface. This study further illustrates the true potential of SHINERS by opening the door to studying industrially relevant reactions under in situ or operando reaction conditions.
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spelling pubmed-71873112020-04-28 In Situ Shell‐Isolated Nanoparticle‐Enhanced Raman Spectroscopy of Nickel‐Catalyzed Hydrogenation Reactions Wondergem, Caterina S. Kromwijk, Josepha J. G. Slagter, Mark Vrijburg, Wilbert L. Hensen, Emiel J. M. Monai, Matteo Vogt, Charlotte Weckhuysen, Bert M. Chemphyschem Articles Synthesis methods to prepare lower transition metal catalysts and specifically Ni for Shell‐Isolated Nanoparticle‐Enhanced Raman Spectroscopy (SHINERS) are explored. Impregnation, colloidal deposition, and spark ablation have been investigated as suitable synthesis routes to prepare SHINERS‐active Ni/Au@SiO(2) catalyst/Shell‐Isolated Nanoparticles (SHINs). Ni precursors are confirmed to be notoriously difficult to reduce and the temperatures required are generally harsh enough to destroy SHINs, rendering SHINERS experiments on Ni infeasible using this approach. For colloidally synthesized Ni nanoparticles deposited on Au@SiO(2) SHINs, stabilizing ligands first need to be removed before application is possible in catalysis. The required procedure results in transformation of the metallic Ni core to a fully oxidized metal nanoparticle, again too challenging to reduce at temperatures still compatible with SHINs. Finally, by use of spark ablation we were able to prepare metallic Ni catalysts directly on Au@SiO(2) SHINs deposited on a Si wafer. These Ni/Au@SiO(2) catalyst/SHINs were subsequently successfully probed with several molecules (i. e. CO and acetylene) of interest for heterogeneous catalysis, and we show that they could be used to study the in situ hydrogenation of acetylene. We observe the interaction of acetylene with the Ni surface. This study further illustrates the true potential of SHINERS by opening the door to studying industrially relevant reactions under in situ or operando reaction conditions. John Wiley and Sons Inc. 2020-02-04 2020-04-02 /pmc/articles/PMC7187311/ /pubmed/31981395 http://dx.doi.org/10.1002/cphc.201901162 Text en © 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Wondergem, Caterina S.
Kromwijk, Josepha J. G.
Slagter, Mark
Vrijburg, Wilbert L.
Hensen, Emiel J. M.
Monai, Matteo
Vogt, Charlotte
Weckhuysen, Bert M.
In Situ Shell‐Isolated Nanoparticle‐Enhanced Raman Spectroscopy of Nickel‐Catalyzed Hydrogenation Reactions
title In Situ Shell‐Isolated Nanoparticle‐Enhanced Raman Spectroscopy of Nickel‐Catalyzed Hydrogenation Reactions
title_full In Situ Shell‐Isolated Nanoparticle‐Enhanced Raman Spectroscopy of Nickel‐Catalyzed Hydrogenation Reactions
title_fullStr In Situ Shell‐Isolated Nanoparticle‐Enhanced Raman Spectroscopy of Nickel‐Catalyzed Hydrogenation Reactions
title_full_unstemmed In Situ Shell‐Isolated Nanoparticle‐Enhanced Raman Spectroscopy of Nickel‐Catalyzed Hydrogenation Reactions
title_short In Situ Shell‐Isolated Nanoparticle‐Enhanced Raman Spectroscopy of Nickel‐Catalyzed Hydrogenation Reactions
title_sort in situ shell‐isolated nanoparticle‐enhanced raman spectroscopy of nickel‐catalyzed hydrogenation reactions
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7187311/
https://www.ncbi.nlm.nih.gov/pubmed/31981395
http://dx.doi.org/10.1002/cphc.201901162
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