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Hydroxyl-rich macromolecules enable the bio-inspired synthesis of single crystal nanocomposites
Acidic macromolecules are traditionally considered key to calcium carbonate biomineralisation and have long been first choice in the bio-inspired synthesis of crystalline materials. Here, we challenge this view and demonstrate that low-charge macromolecules can vastly outperform their acidic counter...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6908585/ https://www.ncbi.nlm.nih.gov/pubmed/31831739 http://dx.doi.org/10.1038/s41467-019-13422-9 |
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author | Kim, Yi-Yeoun Darkins, Robert Broad, Alexander Kulak, Alexander N. Holden, Mark A. Nahi, Ouassef Armes, Steven P. Tang, Chiu C. Thompson, Rebecca F. Marin, Frederic Duffy, Dorothy M. Meldrum, Fiona C. |
author_facet | Kim, Yi-Yeoun Darkins, Robert Broad, Alexander Kulak, Alexander N. Holden, Mark A. Nahi, Ouassef Armes, Steven P. Tang, Chiu C. Thompson, Rebecca F. Marin, Frederic Duffy, Dorothy M. Meldrum, Fiona C. |
author_sort | Kim, Yi-Yeoun |
collection | PubMed |
description | Acidic macromolecules are traditionally considered key to calcium carbonate biomineralisation and have long been first choice in the bio-inspired synthesis of crystalline materials. Here, we challenge this view and demonstrate that low-charge macromolecules can vastly outperform their acidic counterparts in the synthesis of nanocomposites. Using gold nanoparticles functionalised with low charge, hydroxyl-rich proteins and homopolymers as growth additives, we show that extremely high concentrations of nanoparticles can be incorporated within calcite single crystals, while maintaining the continuity of the lattice and the original rhombohedral morphologies of the crystals. The nanoparticles are perfectly dispersed within the host crystal and at high concentrations are so closely apposed that they exhibit plasmon coupling and induce an unexpected contraction of the crystal lattice. The versatility of this strategy is then demonstrated by extension to alternative host crystals. This simple and scalable occlusion approach opens the door to a novel class of single crystal nanocomposites. |
format | Online Article Text |
id | pubmed-6908585 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69085852019-12-16 Hydroxyl-rich macromolecules enable the bio-inspired synthesis of single crystal nanocomposites Kim, Yi-Yeoun Darkins, Robert Broad, Alexander Kulak, Alexander N. Holden, Mark A. Nahi, Ouassef Armes, Steven P. Tang, Chiu C. Thompson, Rebecca F. Marin, Frederic Duffy, Dorothy M. Meldrum, Fiona C. Nat Commun Article Acidic macromolecules are traditionally considered key to calcium carbonate biomineralisation and have long been first choice in the bio-inspired synthesis of crystalline materials. Here, we challenge this view and demonstrate that low-charge macromolecules can vastly outperform their acidic counterparts in the synthesis of nanocomposites. Using gold nanoparticles functionalised with low charge, hydroxyl-rich proteins and homopolymers as growth additives, we show that extremely high concentrations of nanoparticles can be incorporated within calcite single crystals, while maintaining the continuity of the lattice and the original rhombohedral morphologies of the crystals. The nanoparticles are perfectly dispersed within the host crystal and at high concentrations are so closely apposed that they exhibit plasmon coupling and induce an unexpected contraction of the crystal lattice. The versatility of this strategy is then demonstrated by extension to alternative host crystals. This simple and scalable occlusion approach opens the door to a novel class of single crystal nanocomposites. Nature Publishing Group UK 2019-12-12 /pmc/articles/PMC6908585/ /pubmed/31831739 http://dx.doi.org/10.1038/s41467-019-13422-9 Text en © The Author(s) 2019 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 Kim, Yi-Yeoun Darkins, Robert Broad, Alexander Kulak, Alexander N. Holden, Mark A. Nahi, Ouassef Armes, Steven P. Tang, Chiu C. Thompson, Rebecca F. Marin, Frederic Duffy, Dorothy M. Meldrum, Fiona C. Hydroxyl-rich macromolecules enable the bio-inspired synthesis of single crystal nanocomposites |
title | Hydroxyl-rich macromolecules enable the bio-inspired synthesis of single crystal nanocomposites |
title_full | Hydroxyl-rich macromolecules enable the bio-inspired synthesis of single crystal nanocomposites |
title_fullStr | Hydroxyl-rich macromolecules enable the bio-inspired synthesis of single crystal nanocomposites |
title_full_unstemmed | Hydroxyl-rich macromolecules enable the bio-inspired synthesis of single crystal nanocomposites |
title_short | Hydroxyl-rich macromolecules enable the bio-inspired synthesis of single crystal nanocomposites |
title_sort | hydroxyl-rich macromolecules enable the bio-inspired synthesis of single crystal nanocomposites |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6908585/ https://www.ncbi.nlm.nih.gov/pubmed/31831739 http://dx.doi.org/10.1038/s41467-019-13422-9 |
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