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A Novel Carbon-Assisted Chemical Vapor Deposition Growth of Large-Area Uniform Monolayer MoS(2) and WS(2)
Monolayer MoS(2) can be used for various applications such as flexible optoelectronics and electronics due to its exceptional optical and electronic properties. For these applications, large-area synthesis of high-quality monolayer MoS(2) is highly desirable. However, the conventional chemical vapor...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8468553/ https://www.ncbi.nlm.nih.gov/pubmed/34578743 http://dx.doi.org/10.3390/nano11092423 |
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author | Bae, Jeonghwan Yoo, Youngdong |
author_facet | Bae, Jeonghwan Yoo, Youngdong |
author_sort | Bae, Jeonghwan |
collection | PubMed |
description | Monolayer MoS(2) can be used for various applications such as flexible optoelectronics and electronics due to its exceptional optical and electronic properties. For these applications, large-area synthesis of high-quality monolayer MoS(2) is highly desirable. However, the conventional chemical vapor deposition (CVD) method using MoO(3) and S powder has shown limitations in synthesizing high-quality monolayer MoS(2) over a large area on a substrate. In this study, we present a novel carbon cloth-assisted CVD method for large-area uniform synthesis of high-quality monolayer MoS(2). While the conventional CVD method produces thick MoS(2) films in the center of the substrate and forms MoS(2) monolayers at the edge of the thick MoS(2) films, our carbon cloth-assisted CVD method uniformly grows high-quality monolayer MoS(2) in the center of the substrate. The as-synthesized monolayer MoS(2) was characterized in detail by Raman/photoluminescence spectroscopy, atomic force microscopy, and transmission electron microscopy. We reveal the growth process of monolayer MoS(2) initiated from MoS(2) seeds by synthesizing monolayer MoS(2) with varying reaction times. In addition, we show that the CVD method employing carbon powder also produces uniform monolayer MoS(2) without forming thick MoS(2) films in the center of the substrate. This confirms that the large-area growth of monolayer MoS(2) using the carbon cloth-assisted CVD method is mainly due to reducing properties of the carbon material, rather than the effect of covering the carbon cloth. Furthermore, we demonstrate that our carbon cloth-assisted CVD method is generally applicable to large-area uniform synthesis of other monolayer transition metal dichalcogenides, including monolayer WS(2). |
format | Online Article Text |
id | pubmed-8468553 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-84685532021-09-27 A Novel Carbon-Assisted Chemical Vapor Deposition Growth of Large-Area Uniform Monolayer MoS(2) and WS(2) Bae, Jeonghwan Yoo, Youngdong Nanomaterials (Basel) Article Monolayer MoS(2) can be used for various applications such as flexible optoelectronics and electronics due to its exceptional optical and electronic properties. For these applications, large-area synthesis of high-quality monolayer MoS(2) is highly desirable. However, the conventional chemical vapor deposition (CVD) method using MoO(3) and S powder has shown limitations in synthesizing high-quality monolayer MoS(2) over a large area on a substrate. In this study, we present a novel carbon cloth-assisted CVD method for large-area uniform synthesis of high-quality monolayer MoS(2). While the conventional CVD method produces thick MoS(2) films in the center of the substrate and forms MoS(2) monolayers at the edge of the thick MoS(2) films, our carbon cloth-assisted CVD method uniformly grows high-quality monolayer MoS(2) in the center of the substrate. The as-synthesized monolayer MoS(2) was characterized in detail by Raman/photoluminescence spectroscopy, atomic force microscopy, and transmission electron microscopy. We reveal the growth process of monolayer MoS(2) initiated from MoS(2) seeds by synthesizing monolayer MoS(2) with varying reaction times. In addition, we show that the CVD method employing carbon powder also produces uniform monolayer MoS(2) without forming thick MoS(2) films in the center of the substrate. This confirms that the large-area growth of monolayer MoS(2) using the carbon cloth-assisted CVD method is mainly due to reducing properties of the carbon material, rather than the effect of covering the carbon cloth. Furthermore, we demonstrate that our carbon cloth-assisted CVD method is generally applicable to large-area uniform synthesis of other monolayer transition metal dichalcogenides, including monolayer WS(2). MDPI 2021-09-17 /pmc/articles/PMC8468553/ /pubmed/34578743 http://dx.doi.org/10.3390/nano11092423 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Bae, Jeonghwan Yoo, Youngdong A Novel Carbon-Assisted Chemical Vapor Deposition Growth of Large-Area Uniform Monolayer MoS(2) and WS(2) |
title | A Novel Carbon-Assisted Chemical Vapor Deposition Growth of Large-Area Uniform Monolayer MoS(2) and WS(2) |
title_full | A Novel Carbon-Assisted Chemical Vapor Deposition Growth of Large-Area Uniform Monolayer MoS(2) and WS(2) |
title_fullStr | A Novel Carbon-Assisted Chemical Vapor Deposition Growth of Large-Area Uniform Monolayer MoS(2) and WS(2) |
title_full_unstemmed | A Novel Carbon-Assisted Chemical Vapor Deposition Growth of Large-Area Uniform Monolayer MoS(2) and WS(2) |
title_short | A Novel Carbon-Assisted Chemical Vapor Deposition Growth of Large-Area Uniform Monolayer MoS(2) and WS(2) |
title_sort | novel carbon-assisted chemical vapor deposition growth of large-area uniform monolayer mos(2) and ws(2) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8468553/ https://www.ncbi.nlm.nih.gov/pubmed/34578743 http://dx.doi.org/10.3390/nano11092423 |
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