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Synthesis and Stabilization of Support-Free Mesoporous Gold Nanoparticles

Porous gold nanoparticles (PGNs) are usually prepared in an immobilized form on a solid substrate, which is not practical in many applications. In this work, a simple method is reported for the preparation and stabilization of mesoporous gold particles of a few hundred nanometers in size in aqueous...

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Autores principales: Juhász, Laura, Moldován, Krisztián, Herman, Petra, Erdélyi, Zoltán, Fábián, István, Kalmár, József, Cserháti, Csaba
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7353302/
https://www.ncbi.nlm.nih.gov/pubmed/32503247
http://dx.doi.org/10.3390/nano10061107
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author Juhász, Laura
Moldován, Krisztián
Herman, Petra
Erdélyi, Zoltán
Fábián, István
Kalmár, József
Cserháti, Csaba
author_facet Juhász, Laura
Moldován, Krisztián
Herman, Petra
Erdélyi, Zoltán
Fábián, István
Kalmár, József
Cserháti, Csaba
author_sort Juhász, Laura
collection PubMed
description Porous gold nanoparticles (PGNs) are usually prepared in an immobilized form on a solid substrate, which is not practical in many applications. In this work, a simple method is reported for the preparation and stabilization of mesoporous gold particles of a few hundred nanometers in size in aqueous suspension. Nanoparticles of Ag-Au alloy were fabricated on CaF [Formula: see text] and Si/SiO [Formula: see text] substrates by the solid-state dewetting method. Silver was selectively dissolved (dealloyed), and the resulting porous gold nanoparticles were chemically removed from the substrate either in a concerted step with dealloying, or in a subsequent step. Nitric acid was used for the one-step dealloying and detachment of the particles from CaF [Formula: see text] substrate. The consecutive use of HNO [Formula: see text] and HF resulted in the dealloying and the subsequent detachment of the particles from Si/SiO [Formula: see text] substrate. The PGNs were recovered from the aqueous suspensions by centrifugation. The Au content of the suspensions was monitored by using elemental analysis (ICP-OES), and recovery was optimized. The morphology and the optical characteristics of the support-free PGNs were analyzed by scanning electron microscopy (SEM), dynamic light scattering spectroscopy (DLS), and near-infrared spectrophotometry (NIR). The obtained PGNs are spherical disk-shaped with a mean particle size of 765 ± 149 nm. The suspended, support-free PGNs display an ideally narrow dipole plasmon peak at around 1450 nm in the NIR spectral region. Thus, the new colloidal PGNs are ideal candidates for biomedical applications, for instance photothermal therapy.
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spelling pubmed-73533022020-07-15 Synthesis and Stabilization of Support-Free Mesoporous Gold Nanoparticles Juhász, Laura Moldován, Krisztián Herman, Petra Erdélyi, Zoltán Fábián, István Kalmár, József Cserháti, Csaba Nanomaterials (Basel) Article Porous gold nanoparticles (PGNs) are usually prepared in an immobilized form on a solid substrate, which is not practical in many applications. In this work, a simple method is reported for the preparation and stabilization of mesoporous gold particles of a few hundred nanometers in size in aqueous suspension. Nanoparticles of Ag-Au alloy were fabricated on CaF [Formula: see text] and Si/SiO [Formula: see text] substrates by the solid-state dewetting method. Silver was selectively dissolved (dealloyed), and the resulting porous gold nanoparticles were chemically removed from the substrate either in a concerted step with dealloying, or in a subsequent step. Nitric acid was used for the one-step dealloying and detachment of the particles from CaF [Formula: see text] substrate. The consecutive use of HNO [Formula: see text] and HF resulted in the dealloying and the subsequent detachment of the particles from Si/SiO [Formula: see text] substrate. The PGNs were recovered from the aqueous suspensions by centrifugation. The Au content of the suspensions was monitored by using elemental analysis (ICP-OES), and recovery was optimized. The morphology and the optical characteristics of the support-free PGNs were analyzed by scanning electron microscopy (SEM), dynamic light scattering spectroscopy (DLS), and near-infrared spectrophotometry (NIR). The obtained PGNs are spherical disk-shaped with a mean particle size of 765 ± 149 nm. The suspended, support-free PGNs display an ideally narrow dipole plasmon peak at around 1450 nm in the NIR spectral region. Thus, the new colloidal PGNs are ideal candidates for biomedical applications, for instance photothermal therapy. MDPI 2020-06-03 /pmc/articles/PMC7353302/ /pubmed/32503247 http://dx.doi.org/10.3390/nano10061107 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Juhász, Laura
Moldován, Krisztián
Herman, Petra
Erdélyi, Zoltán
Fábián, István
Kalmár, József
Cserháti, Csaba
Synthesis and Stabilization of Support-Free Mesoporous Gold Nanoparticles
title Synthesis and Stabilization of Support-Free Mesoporous Gold Nanoparticles
title_full Synthesis and Stabilization of Support-Free Mesoporous Gold Nanoparticles
title_fullStr Synthesis and Stabilization of Support-Free Mesoporous Gold Nanoparticles
title_full_unstemmed Synthesis and Stabilization of Support-Free Mesoporous Gold Nanoparticles
title_short Synthesis and Stabilization of Support-Free Mesoporous Gold Nanoparticles
title_sort synthesis and stabilization of support-free mesoporous gold nanoparticles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7353302/
https://www.ncbi.nlm.nih.gov/pubmed/32503247
http://dx.doi.org/10.3390/nano10061107
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