Cargando…
Atomic Layer Deposition of Large-Area Polycrystalline Transition Metal Dichalcogenides from 100 °C through Control of Plasma Chemistry
[Image: see text] Two-dimensional transition metal dichalcogenides, such as MoS(2), are intensely studied for applications in electronics. However, the difficulty of depositing large-area films of sufficient quality under application-relevant conditions remains a major challenge. Herein, we demonstr...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9404538/ https://www.ncbi.nlm.nih.gov/pubmed/36032554 http://dx.doi.org/10.1021/acs.chemmater.2c01154 |
_version_ | 1784773663251234816 |
---|---|
author | Mattinen, Miika Gity, Farzan Coleman, Emma Vonk, Joris F. A. Verheijen, Marcel A. Duffy, Ray Kessels, Wilhelmus M. M. Bol, Ageeth A. |
author_facet | Mattinen, Miika Gity, Farzan Coleman, Emma Vonk, Joris F. A. Verheijen, Marcel A. Duffy, Ray Kessels, Wilhelmus M. M. Bol, Ageeth A. |
author_sort | Mattinen, Miika |
collection | PubMed |
description | [Image: see text] Two-dimensional transition metal dichalcogenides, such as MoS(2), are intensely studied for applications in electronics. However, the difficulty of depositing large-area films of sufficient quality under application-relevant conditions remains a major challenge. Herein, we demonstrate deposition of polycrystalline, wafer-scale MoS(2), TiS(2), and WS(2) films of controlled thickness at record-low temperatures down to 100 °C using plasma-enhanced atomic layer deposition. We show that preventing excess sulfur incorporation from H(2)S-based plasma is the key to deposition of crystalline films, which can be achieved by adding H(2) to the plasma feed gas. Film composition, crystallinity, growth, morphology, and electrical properties of MoS(x) films prepared within a broad range of deposition conditions have been systematically characterized. Film characteristics are correlated with results of field-effect transistors based on MoS(2) films deposited at 100 °C. The capability to deposit MoS(2) on poly(ethylene terephthalate) substrates showcases the potential of our process for flexible devices. Furthermore, the composition control achieved by tailoring plasma chemistry is relevant for all low-temperature plasma-enhanced deposition processes of metal chalcogenides. |
format | Online Article Text |
id | pubmed-9404538 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-94045382022-08-26 Atomic Layer Deposition of Large-Area Polycrystalline Transition Metal Dichalcogenides from 100 °C through Control of Plasma Chemistry Mattinen, Miika Gity, Farzan Coleman, Emma Vonk, Joris F. A. Verheijen, Marcel A. Duffy, Ray Kessels, Wilhelmus M. M. Bol, Ageeth A. Chem Mater [Image: see text] Two-dimensional transition metal dichalcogenides, such as MoS(2), are intensely studied for applications in electronics. However, the difficulty of depositing large-area films of sufficient quality under application-relevant conditions remains a major challenge. Herein, we demonstrate deposition of polycrystalline, wafer-scale MoS(2), TiS(2), and WS(2) films of controlled thickness at record-low temperatures down to 100 °C using plasma-enhanced atomic layer deposition. We show that preventing excess sulfur incorporation from H(2)S-based plasma is the key to deposition of crystalline films, which can be achieved by adding H(2) to the plasma feed gas. Film composition, crystallinity, growth, morphology, and electrical properties of MoS(x) films prepared within a broad range of deposition conditions have been systematically characterized. Film characteristics are correlated with results of field-effect transistors based on MoS(2) films deposited at 100 °C. The capability to deposit MoS(2) on poly(ethylene terephthalate) substrates showcases the potential of our process for flexible devices. Furthermore, the composition control achieved by tailoring plasma chemistry is relevant for all low-temperature plasma-enhanced deposition processes of metal chalcogenides. American Chemical Society 2022-08-05 2022-08-23 /pmc/articles/PMC9404538/ /pubmed/36032554 http://dx.doi.org/10.1021/acs.chemmater.2c01154 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 | Mattinen, Miika Gity, Farzan Coleman, Emma Vonk, Joris F. A. Verheijen, Marcel A. Duffy, Ray Kessels, Wilhelmus M. M. Bol, Ageeth A. Atomic Layer Deposition of Large-Area Polycrystalline Transition Metal Dichalcogenides from 100 °C through Control of Plasma Chemistry |
title | Atomic Layer
Deposition of Large-Area Polycrystalline
Transition Metal Dichalcogenides from 100 °C through Control
of Plasma Chemistry |
title_full | Atomic Layer
Deposition of Large-Area Polycrystalline
Transition Metal Dichalcogenides from 100 °C through Control
of Plasma Chemistry |
title_fullStr | Atomic Layer
Deposition of Large-Area Polycrystalline
Transition Metal Dichalcogenides from 100 °C through Control
of Plasma Chemistry |
title_full_unstemmed | Atomic Layer
Deposition of Large-Area Polycrystalline
Transition Metal Dichalcogenides from 100 °C through Control
of Plasma Chemistry |
title_short | Atomic Layer
Deposition of Large-Area Polycrystalline
Transition Metal Dichalcogenides from 100 °C through Control
of Plasma Chemistry |
title_sort | atomic layer
deposition of large-area polycrystalline
transition metal dichalcogenides from 100 °c through control
of plasma chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9404538/ https://www.ncbi.nlm.nih.gov/pubmed/36032554 http://dx.doi.org/10.1021/acs.chemmater.2c01154 |
work_keys_str_mv | AT mattinenmiika atomiclayerdepositionoflargeareapolycrystallinetransitionmetaldichalcogenidesfrom100cthroughcontrolofplasmachemistry AT gityfarzan atomiclayerdepositionoflargeareapolycrystallinetransitionmetaldichalcogenidesfrom100cthroughcontrolofplasmachemistry AT colemanemma atomiclayerdepositionoflargeareapolycrystallinetransitionmetaldichalcogenidesfrom100cthroughcontrolofplasmachemistry AT vonkjorisfa atomiclayerdepositionoflargeareapolycrystallinetransitionmetaldichalcogenidesfrom100cthroughcontrolofplasmachemistry AT verheijenmarcela atomiclayerdepositionoflargeareapolycrystallinetransitionmetaldichalcogenidesfrom100cthroughcontrolofplasmachemistry AT duffyray atomiclayerdepositionoflargeareapolycrystallinetransitionmetaldichalcogenidesfrom100cthroughcontrolofplasmachemistry AT kesselswilhelmusmm atomiclayerdepositionoflargeareapolycrystallinetransitionmetaldichalcogenidesfrom100cthroughcontrolofplasmachemistry AT bolageetha atomiclayerdepositionoflargeareapolycrystallinetransitionmetaldichalcogenidesfrom100cthroughcontrolofplasmachemistry |