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Direct synthesis of nanostructured silver antimony sulfide powders from metal xanthate precursors
Silver(I) ethylxanthate [AgS(2)COEt] (1) and antimony(III) ethylxanthate [Sb(S(2)COEt)(3)] (2) have been synthesised, characterised and used as precursors for the preparation of AgSbS(2) powders and thin films using a solvent-free melt method and spin coating technique, respectively. The as-synthesi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7862388/ https://www.ncbi.nlm.nih.gov/pubmed/33542323 http://dx.doi.org/10.1038/s41598-021-82446-3 |
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author | Alharbi, Yasser T. Alam, Firoz Salhi, Abdelmajid Missous, Mohamed Lewis, David J. |
author_facet | Alharbi, Yasser T. Alam, Firoz Salhi, Abdelmajid Missous, Mohamed Lewis, David J. |
author_sort | Alharbi, Yasser T. |
collection | PubMed |
description | Silver(I) ethylxanthate [AgS(2)COEt] (1) and antimony(III) ethylxanthate [Sb(S(2)COEt)(3)] (2) have been synthesised, characterised and used as precursors for the preparation of AgSbS(2) powders and thin films using a solvent-free melt method and spin coating technique, respectively. The as-synthesized AgSbS(2) powders were characterized by powder X-ray diffraction (XRD), Raman spectroscopy, scanning electron microscopy (SEM) and energy dispersive X-ray (EDX) spectroscopy. The crystalline AgSbS(2) powder was investigated using XRD, which shows that AgSbS(2) has cuboargyrite as the dominant phase, which was also confirmed by Raman spectroscopy. SEM was also used to study the morphology of the resulting material which is potentially nanostructured. EDX spectra gives a clear indication of the presence of silver (Ag), antimony (Sb) and sulfur (S) in material, suggesting that decomposition is clean and produces high quality AgSbS(2) crystalline powder, which is consistent with the XRD and Raman data. Electronic properties of AgSbS(2) thin films deposited by spin coating show a p-type conductivity with measured carrier mobility of 81 cm(2) V(−1) s(−1) and carrier concentration of 1.9 × 10(15) cm(−3). The findings of this study reveal a new bottom-up route to these compounds, which have potential application as absorber layers in solar cells. |
format | Online Article Text |
id | pubmed-7862388 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78623882021-02-05 Direct synthesis of nanostructured silver antimony sulfide powders from metal xanthate precursors Alharbi, Yasser T. Alam, Firoz Salhi, Abdelmajid Missous, Mohamed Lewis, David J. Sci Rep Article Silver(I) ethylxanthate [AgS(2)COEt] (1) and antimony(III) ethylxanthate [Sb(S(2)COEt)(3)] (2) have been synthesised, characterised and used as precursors for the preparation of AgSbS(2) powders and thin films using a solvent-free melt method and spin coating technique, respectively. The as-synthesized AgSbS(2) powders were characterized by powder X-ray diffraction (XRD), Raman spectroscopy, scanning electron microscopy (SEM) and energy dispersive X-ray (EDX) spectroscopy. The crystalline AgSbS(2) powder was investigated using XRD, which shows that AgSbS(2) has cuboargyrite as the dominant phase, which was also confirmed by Raman spectroscopy. SEM was also used to study the morphology of the resulting material which is potentially nanostructured. EDX spectra gives a clear indication of the presence of silver (Ag), antimony (Sb) and sulfur (S) in material, suggesting that decomposition is clean and produces high quality AgSbS(2) crystalline powder, which is consistent with the XRD and Raman data. Electronic properties of AgSbS(2) thin films deposited by spin coating show a p-type conductivity with measured carrier mobility of 81 cm(2) V(−1) s(−1) and carrier concentration of 1.9 × 10(15) cm(−3). The findings of this study reveal a new bottom-up route to these compounds, which have potential application as absorber layers in solar cells. Nature Publishing Group UK 2021-02-04 /pmc/articles/PMC7862388/ /pubmed/33542323 http://dx.doi.org/10.1038/s41598-021-82446-3 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Alharbi, Yasser T. Alam, Firoz Salhi, Abdelmajid Missous, Mohamed Lewis, David J. Direct synthesis of nanostructured silver antimony sulfide powders from metal xanthate precursors |
title | Direct synthesis of nanostructured silver antimony sulfide powders from metal xanthate precursors |
title_full | Direct synthesis of nanostructured silver antimony sulfide powders from metal xanthate precursors |
title_fullStr | Direct synthesis of nanostructured silver antimony sulfide powders from metal xanthate precursors |
title_full_unstemmed | Direct synthesis of nanostructured silver antimony sulfide powders from metal xanthate precursors |
title_short | Direct synthesis of nanostructured silver antimony sulfide powders from metal xanthate precursors |
title_sort | direct synthesis of nanostructured silver antimony sulfide powders from metal xanthate precursors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7862388/ https://www.ncbi.nlm.nih.gov/pubmed/33542323 http://dx.doi.org/10.1038/s41598-021-82446-3 |
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