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Fabrication and photoluminescent properties of Tb(3+) doped carbon nanodots
Carbon nanodots (CNDs) doped with Tb ions were synthesized using different synthetic routes: hydrothermal treatment of a solution containing carbon source (sodium dextran sulfate) and TbCl(3); mixing of CNDs and TbCl(3) solutions; freezing-induced loading of Tb and carbon-containing source into pore...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6214974/ https://www.ncbi.nlm.nih.gov/pubmed/30390023 http://dx.doi.org/10.1038/s41598-018-34683-2 |
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author | Vostrikova, Anna M. Kokorina, Alina A. Demina, Polina A. German, Sergei V. Novoselova, Marina V. Tarakina, Nadezda V. Sukhorukov, Gleb B. Goryacheva, Irina Y. |
author_facet | Vostrikova, Anna M. Kokorina, Alina A. Demina, Polina A. German, Sergei V. Novoselova, Marina V. Tarakina, Nadezda V. Sukhorukov, Gleb B. Goryacheva, Irina Y. |
author_sort | Vostrikova, Anna M. |
collection | PubMed |
description | Carbon nanodots (CNDs) doped with Tb ions were synthesized using different synthetic routes: hydrothermal treatment of a solution containing carbon source (sodium dextran sulfate) and TbCl(3); mixing of CNDs and TbCl(3) solutions; freezing-induced loading of Tb and carbon-containing source into pores of CaCO(3) microparticles followed by hydrothermal treatment. Binding of Tb ions to CNDs (Tb-CND coupling) was confirmed using size-exclusion chromatography and manifested itself through a decrease of the Tb photoluminescence lifetime signal. The shortest Tb photoluminescence lifetime was observed for samples obtained by hydrothermal synthesis of CaCO(3) microparticles where Tb and carbon source were loaded into pores via the freezing-induced process. The same system displays an increase of Tb photoluminescence via energy transfer with excitation at 320–340 nm. Based on the obtained results, freezing-induced loading of cations into CNDs using porous CaCO(3) microparticles as reactors is proposed to be a versatile route for the introduction of active components into CNDs. The obtained CNDs with long-lived emission may be used for time-resolved imaging and visualization in living biological samples where time-resolved and long-lived luminescence microscopy is required. |
format | Online Article Text |
id | pubmed-6214974 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62149742018-11-06 Fabrication and photoluminescent properties of Tb(3+) doped carbon nanodots Vostrikova, Anna M. Kokorina, Alina A. Demina, Polina A. German, Sergei V. Novoselova, Marina V. Tarakina, Nadezda V. Sukhorukov, Gleb B. Goryacheva, Irina Y. Sci Rep Article Carbon nanodots (CNDs) doped with Tb ions were synthesized using different synthetic routes: hydrothermal treatment of a solution containing carbon source (sodium dextran sulfate) and TbCl(3); mixing of CNDs and TbCl(3) solutions; freezing-induced loading of Tb and carbon-containing source into pores of CaCO(3) microparticles followed by hydrothermal treatment. Binding of Tb ions to CNDs (Tb-CND coupling) was confirmed using size-exclusion chromatography and manifested itself through a decrease of the Tb photoluminescence lifetime signal. The shortest Tb photoluminescence lifetime was observed for samples obtained by hydrothermal synthesis of CaCO(3) microparticles where Tb and carbon source were loaded into pores via the freezing-induced process. The same system displays an increase of Tb photoluminescence via energy transfer with excitation at 320–340 nm. Based on the obtained results, freezing-induced loading of cations into CNDs using porous CaCO(3) microparticles as reactors is proposed to be a versatile route for the introduction of active components into CNDs. The obtained CNDs with long-lived emission may be used for time-resolved imaging and visualization in living biological samples where time-resolved and long-lived luminescence microscopy is required. Nature Publishing Group UK 2018-11-02 /pmc/articles/PMC6214974/ /pubmed/30390023 http://dx.doi.org/10.1038/s41598-018-34683-2 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 Vostrikova, Anna M. Kokorina, Alina A. Demina, Polina A. German, Sergei V. Novoselova, Marina V. Tarakina, Nadezda V. Sukhorukov, Gleb B. Goryacheva, Irina Y. Fabrication and photoluminescent properties of Tb(3+) doped carbon nanodots |
title | Fabrication and photoluminescent properties of Tb(3+) doped carbon nanodots |
title_full | Fabrication and photoluminescent properties of Tb(3+) doped carbon nanodots |
title_fullStr | Fabrication and photoluminescent properties of Tb(3+) doped carbon nanodots |
title_full_unstemmed | Fabrication and photoluminescent properties of Tb(3+) doped carbon nanodots |
title_short | Fabrication and photoluminescent properties of Tb(3+) doped carbon nanodots |
title_sort | fabrication and photoluminescent properties of tb(3+) doped carbon nanodots |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6214974/ https://www.ncbi.nlm.nih.gov/pubmed/30390023 http://dx.doi.org/10.1038/s41598-018-34683-2 |
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