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An in-situ small angle x ray scattering analysis of nanopore formation during thermally induced chemical dealloying of brass thin foils

The development of non-noble nano-porous metal materials is hindered by surface oxidation reactions and from the difficulty to generate long range order pore arrays. Dealloying is a promising route to generate such materials by selective chemical etching of metal alloy materials. This process can ge...

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Autores principales: Lin, Bao, Döbeli, Max, Mudie, Stephen, Hawley, Adrian, Hodgson, Peter, Kong, Lingxue, Spolenak, Ralph, Dumée, Ludovic F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6193925/
https://www.ncbi.nlm.nih.gov/pubmed/30337676
http://dx.doi.org/10.1038/s41598-018-33787-z
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author Lin, Bao
Döbeli, Max
Mudie, Stephen
Hawley, Adrian
Hodgson, Peter
Kong, Lingxue
Spolenak, Ralph
Dumée, Ludovic F.
author_facet Lin, Bao
Döbeli, Max
Mudie, Stephen
Hawley, Adrian
Hodgson, Peter
Kong, Lingxue
Spolenak, Ralph
Dumée, Ludovic F.
author_sort Lin, Bao
collection PubMed
description The development of non-noble nano-porous metal materials is hindered by surface oxidation reactions and from the difficulty to generate long range order pore arrays. Dealloying is a promising route to generate such materials by selective chemical etching of metal alloy materials. This process can generate nano-metal materials with superior plasmonic, catalytic and adsorptive surface properties. Here, the impact of properties of the etching solution on the dealloying process to generate nano-pores across thin film alloys was investigated by in-situ SAXS dealloying experiments. Single phase CuZn alloys were used as model materials to evaluate the influence of the solution temperature on the pore formation kinetics. This novel analysis allowed to visualize the change in surface properties of the materials over time, including their surface area as well as their pore and ligament sizes. The dealloying kinetics at the very early stage of the process were found to be critical to both stable pore formation and stabilization. SAXS in-situ data were correlated to the morphological properties of the materials obtained from ex-situ samples by Rutherford back scattering and scanning electron microscopy.
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spelling pubmed-61939252018-10-23 An in-situ small angle x ray scattering analysis of nanopore formation during thermally induced chemical dealloying of brass thin foils Lin, Bao Döbeli, Max Mudie, Stephen Hawley, Adrian Hodgson, Peter Kong, Lingxue Spolenak, Ralph Dumée, Ludovic F. Sci Rep Article The development of non-noble nano-porous metal materials is hindered by surface oxidation reactions and from the difficulty to generate long range order pore arrays. Dealloying is a promising route to generate such materials by selective chemical etching of metal alloy materials. This process can generate nano-metal materials with superior plasmonic, catalytic and adsorptive surface properties. Here, the impact of properties of the etching solution on the dealloying process to generate nano-pores across thin film alloys was investigated by in-situ SAXS dealloying experiments. Single phase CuZn alloys were used as model materials to evaluate the influence of the solution temperature on the pore formation kinetics. This novel analysis allowed to visualize the change in surface properties of the materials over time, including their surface area as well as their pore and ligament sizes. The dealloying kinetics at the very early stage of the process were found to be critical to both stable pore formation and stabilization. SAXS in-situ data were correlated to the morphological properties of the materials obtained from ex-situ samples by Rutherford back scattering and scanning electron microscopy. Nature Publishing Group UK 2018-10-18 /pmc/articles/PMC6193925/ /pubmed/30337676 http://dx.doi.org/10.1038/s41598-018-33787-z Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lin, Bao
Döbeli, Max
Mudie, Stephen
Hawley, Adrian
Hodgson, Peter
Kong, Lingxue
Spolenak, Ralph
Dumée, Ludovic F.
An in-situ small angle x ray scattering analysis of nanopore formation during thermally induced chemical dealloying of brass thin foils
title An in-situ small angle x ray scattering analysis of nanopore formation during thermally induced chemical dealloying of brass thin foils
title_full An in-situ small angle x ray scattering analysis of nanopore formation during thermally induced chemical dealloying of brass thin foils
title_fullStr An in-situ small angle x ray scattering analysis of nanopore formation during thermally induced chemical dealloying of brass thin foils
title_full_unstemmed An in-situ small angle x ray scattering analysis of nanopore formation during thermally induced chemical dealloying of brass thin foils
title_short An in-situ small angle x ray scattering analysis of nanopore formation during thermally induced chemical dealloying of brass thin foils
title_sort in-situ small angle x ray scattering analysis of nanopore formation during thermally induced chemical dealloying of brass thin foils
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6193925/
https://www.ncbi.nlm.nih.gov/pubmed/30337676
http://dx.doi.org/10.1038/s41598-018-33787-z
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