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A critical role of hydrogen sulfide evolution during MOCVD of single phase thin film tin sulfide using ditertiarybutylsulfide as a less toxic precursor
MRS Advances, Volume: 3, Issue: 32, Pages: 1849 - 1853
Swansea University Authors: Andrew Clayton , Cecile Charbonneau , Stuart Irvine
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DOI (Published version): 10.1557/adv.2018.239
Abstract
Thin film tin sulphide (SnS) was deposited on to molybdenum (Mo) substrates using metal organic chemical vapor deposition at 470°C using tetraethyltin and ditertiarybutylsulfide as precursors. In situ mass spectroscopy was used to study the exhaust gas species downstream of the reaction zone. The pr...
Published in: | MRS Advances |
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ISSN: | 2059-8521 |
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2018
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URI: | https://cronfa.swan.ac.uk/Record/cronfa40702 |
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2019-07-12T15:28:17.6871210 v2 40702 2018-06-13 A critical role of hydrogen sulfide evolution during MOCVD of single phase thin film tin sulfide using ditertiarybutylsulfide as a less toxic precursor cdef4ab8032ae2213a97638baac8176f 0000-0002-1540-0440 Andrew Clayton Andrew Clayton true false 4dc059714847cb22ed922ab058950560 0000-0001-9887-2007 Cecile Charbonneau Cecile Charbonneau true false 1ddb966eccef99aa96e87f1ea4917f1f 0000-0002-1652-4496 Stuart Irvine Stuart Irvine true false 2018-06-13 MTLS Thin film tin sulphide (SnS) was deposited on to molybdenum (Mo) substrates using metal organic chemical vapor deposition at 470°C using tetraethyltin and ditertiarybutylsulfide as precursors. In situ mass spectroscopy was used to study the exhaust gas species downstream of the reaction zone. The precursor vapor carrier gas was either nitrogen or hydrogen, thin film SnS only forming when the latter was used. Mass spectroscopy determined that hydrogen sulfide was being produced and playing a critical role in the vapor phase reaction process and adsorption of tin and sulfur on to the Mo surface. As-grown grain sizes were determined by scanning electron microscopy and were observed to be large averaging around 2 microns across. X-ray diffraction showed the films to be single phase SnS without any parasitic Sn2S3 or SnS2 phases, with a small amount of MoS2 also being detected. Journal Article MRS Advances 3 32 1849 1853 2059-8521 31 12 2018 2018-12-31 10.1557/adv.2018.239 COLLEGE NANME Materials Science and Engineering COLLEGE CODE MTLS Swansea University 2019-07-12T15:28:17.6871210 2018-06-13T13:18:47.8252155 Faculty of Science and Engineering School of Engineering and Applied Sciences - Materials Science and Engineering Andrew Clayton 0000-0002-1540-0440 1 Cecile Charbonneau 0000-0001-9887-2007 2 Peter J. Siderfin 3 Stuart Irvine 0000-0002-1652-4496 4 0040702-15062018111411.pdf clayton2018(2).pdf 2018-06-15T11:14:11.4770000 Output 607343 application/pdf Accepted Manuscript true 2019-02-26T00:00:00.0000000 true eng |
title |
A critical role of hydrogen sulfide evolution during MOCVD of single phase thin film tin sulfide using ditertiarybutylsulfide as a less toxic precursor |
spellingShingle |
A critical role of hydrogen sulfide evolution during MOCVD of single phase thin film tin sulfide using ditertiarybutylsulfide as a less toxic precursor Andrew Clayton Cecile Charbonneau Stuart Irvine |
title_short |
A critical role of hydrogen sulfide evolution during MOCVD of single phase thin film tin sulfide using ditertiarybutylsulfide as a less toxic precursor |
title_full |
A critical role of hydrogen sulfide evolution during MOCVD of single phase thin film tin sulfide using ditertiarybutylsulfide as a less toxic precursor |
title_fullStr |
A critical role of hydrogen sulfide evolution during MOCVD of single phase thin film tin sulfide using ditertiarybutylsulfide as a less toxic precursor |
title_full_unstemmed |
A critical role of hydrogen sulfide evolution during MOCVD of single phase thin film tin sulfide using ditertiarybutylsulfide as a less toxic precursor |
title_sort |
A critical role of hydrogen sulfide evolution during MOCVD of single phase thin film tin sulfide using ditertiarybutylsulfide as a less toxic precursor |
author_id_str_mv |
cdef4ab8032ae2213a97638baac8176f 4dc059714847cb22ed922ab058950560 1ddb966eccef99aa96e87f1ea4917f1f |
author_id_fullname_str_mv |
cdef4ab8032ae2213a97638baac8176f_***_Andrew Clayton 4dc059714847cb22ed922ab058950560_***_Cecile Charbonneau 1ddb966eccef99aa96e87f1ea4917f1f_***_Stuart Irvine |
author |
Andrew Clayton Cecile Charbonneau Stuart Irvine |
author2 |
Andrew Clayton Cecile Charbonneau Peter J. Siderfin Stuart Irvine |
format |
Journal article |
container_title |
MRS Advances |
container_volume |
3 |
container_issue |
32 |
container_start_page |
1849 |
publishDate |
2018 |
institution |
Swansea University |
issn |
2059-8521 |
doi_str_mv |
10.1557/adv.2018.239 |
college_str |
Faculty of Science and Engineering |
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facultyofscienceandengineering |
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Faculty of Science and Engineering |
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Faculty of Science and Engineering |
department_str |
School of Engineering and Applied Sciences - Materials Science and Engineering{{{_:::_}}}Faculty of Science and Engineering{{{_:::_}}}School of Engineering and Applied Sciences - Materials Science and Engineering |
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description |
Thin film tin sulphide (SnS) was deposited on to molybdenum (Mo) substrates using metal organic chemical vapor deposition at 470°C using tetraethyltin and ditertiarybutylsulfide as precursors. In situ mass spectroscopy was used to study the exhaust gas species downstream of the reaction zone. The precursor vapor carrier gas was either nitrogen or hydrogen, thin film SnS only forming when the latter was used. Mass spectroscopy determined that hydrogen sulfide was being produced and playing a critical role in the vapor phase reaction process and adsorption of tin and sulfur on to the Mo surface. As-grown grain sizes were determined by scanning electron microscopy and were observed to be large averaging around 2 microns across. X-ray diffraction showed the films to be single phase SnS without any parasitic Sn2S3 or SnS2 phases, with a small amount of MoS2 also being detected. |
published_date |
2018-12-31T03:51:48Z |
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1763752551384088576 |
score |
11.035634 |