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Quantum Confined High-Entropy Lanthanide Oxysulfide Colloidal Nanocrystals
[Image: see text] We have synthesized the first reported example of quantum confined high-entropy (HE) nanoparticles, using the lanthanide oxysulfide, Ln(2)SO(2), system as the host phase for an equimolar mixture of Pr, Nd, Gd, Dy, and Er. A uniform HE phase was achieved via the simultaneous thermol...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9614967/ https://www.ncbi.nlm.nih.gov/pubmed/36194549 http://dx.doi.org/10.1021/acs.nanolett.2c01596 |
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author | Ward-O’Brien, Brendan McNaughter, Paul D. Cai, Rongsheng Chattopadhyay, Amrita Flitcroft, Joseph M. Smith, Charles T. Binks, David J. Skelton, Jonathan M. Haigh, Sarah J. Lewis, David J. |
author_facet | Ward-O’Brien, Brendan McNaughter, Paul D. Cai, Rongsheng Chattopadhyay, Amrita Flitcroft, Joseph M. Smith, Charles T. Binks, David J. Skelton, Jonathan M. Haigh, Sarah J. Lewis, David J. |
author_sort | Ward-O’Brien, Brendan |
collection | PubMed |
description | [Image: see text] We have synthesized the first reported example of quantum confined high-entropy (HE) nanoparticles, using the lanthanide oxysulfide, Ln(2)SO(2), system as the host phase for an equimolar mixture of Pr, Nd, Gd, Dy, and Er. A uniform HE phase was achieved via the simultaneous thermolysis of a mixture of lanthanide dithiocarbamate precursors in solution. This was confirmed by powder X-ray diffraction and high-resolution scanning transmission electron microscopy, with energy dispersive X-ray spectroscopic mapping confirming the uniform distribution of the lanthanides throughout the particles. The nanoparticle dispersion displayed a significant blue shift in the absorption and photoluminescence spectra relative to our previously reported bulk sample with the same composition, with an absorption edge at 330 nm and a λ(max) at 410 nm compared to the absorption edge at 500 nm and a λ(max) at 450 nm in the bulk, which is indicative of quantum confinement. We support this postulate with experimental and theoretical analysis of the bandgap energy as a function of strain and surface effects (ligand binding) as well as calculation of the exciton Bohr radiii of the end member compounds. |
format | Online Article Text |
id | pubmed-9614967 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-96149672022-10-29 Quantum Confined High-Entropy Lanthanide Oxysulfide Colloidal Nanocrystals Ward-O’Brien, Brendan McNaughter, Paul D. Cai, Rongsheng Chattopadhyay, Amrita Flitcroft, Joseph M. Smith, Charles T. Binks, David J. Skelton, Jonathan M. Haigh, Sarah J. Lewis, David J. Nano Lett [Image: see text] We have synthesized the first reported example of quantum confined high-entropy (HE) nanoparticles, using the lanthanide oxysulfide, Ln(2)SO(2), system as the host phase for an equimolar mixture of Pr, Nd, Gd, Dy, and Er. A uniform HE phase was achieved via the simultaneous thermolysis of a mixture of lanthanide dithiocarbamate precursors in solution. This was confirmed by powder X-ray diffraction and high-resolution scanning transmission electron microscopy, with energy dispersive X-ray spectroscopic mapping confirming the uniform distribution of the lanthanides throughout the particles. The nanoparticle dispersion displayed a significant blue shift in the absorption and photoluminescence spectra relative to our previously reported bulk sample with the same composition, with an absorption edge at 330 nm and a λ(max) at 410 nm compared to the absorption edge at 500 nm and a λ(max) at 450 nm in the bulk, which is indicative of quantum confinement. We support this postulate with experimental and theoretical analysis of the bandgap energy as a function of strain and surface effects (ligand binding) as well as calculation of the exciton Bohr radiii of the end member compounds. American Chemical Society 2022-10-04 2022-10-26 /pmc/articles/PMC9614967/ /pubmed/36194549 http://dx.doi.org/10.1021/acs.nanolett.2c01596 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Ward-O’Brien, Brendan McNaughter, Paul D. Cai, Rongsheng Chattopadhyay, Amrita Flitcroft, Joseph M. Smith, Charles T. Binks, David J. Skelton, Jonathan M. Haigh, Sarah J. Lewis, David J. Quantum Confined High-Entropy Lanthanide Oxysulfide Colloidal Nanocrystals |
title | Quantum Confined High-Entropy Lanthanide Oxysulfide
Colloidal Nanocrystals |
title_full | Quantum Confined High-Entropy Lanthanide Oxysulfide
Colloidal Nanocrystals |
title_fullStr | Quantum Confined High-Entropy Lanthanide Oxysulfide
Colloidal Nanocrystals |
title_full_unstemmed | Quantum Confined High-Entropy Lanthanide Oxysulfide
Colloidal Nanocrystals |
title_short | Quantum Confined High-Entropy Lanthanide Oxysulfide
Colloidal Nanocrystals |
title_sort | quantum confined high-entropy lanthanide oxysulfide
colloidal nanocrystals |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9614967/ https://www.ncbi.nlm.nih.gov/pubmed/36194549 http://dx.doi.org/10.1021/acs.nanolett.2c01596 |
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