Direct growth of nanocrystalline hexagonal boron nitride films on dielectric substrates
Atomically thin hexagonal-boron nitride (h-BN) films are primarily synthesized through chemical vapor deposition (CVD) on various catalytic transition metal substrates. In this work, a single-step metal-catalyst-free approach to obtain few- to multi-layer nanocrystalline h-BN (NCBN) directly on amor...
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sg-ntu-dr.10356-1072112020-09-26T22:19:51Z Direct growth of nanocrystalline hexagonal boron nitride films on dielectric substrates Tay, Roland Yingjie Tsang, Siu Hon Loeblein, Manuela Chow, Wai Leong Loh, Guan Chee Toh, Joo Wah Ang, Soon Loong Teo, Edwin Hang Tong School of Electrical and Electronic Engineering School of Materials Science & Engineering Temasek Laboratories DRNTU::Engineering::Materials::Microelectronics and semiconductor materials::Thin films Atomically thin hexagonal-boron nitride (h-BN) films are primarily synthesized through chemical vapor deposition (CVD) on various catalytic transition metal substrates. In this work, a single-step metal-catalyst-free approach to obtain few- to multi-layer nanocrystalline h-BN (NCBN) directly on amorphous SiO2/Si and quartz substrates is demonstrated. The as-grown thin films are continuous and smooth with no observable pinholes or wrinkles across the entire deposited substrate as inspected using optical and atomic force microscopy. The starting layers of NCBN orient itself parallel to the substrate, initiating the growth of the textured thin film. Formation of NCBN is due to the random and uncontrolled nucleation of h-BN on the dielectric substrate surface with no epitaxial relation, unlike on metal surfaces. The crystallite size is ∼25 nm as determined by Raman spectroscopy. Transmission electron microscopy shows that the NCBN formed sheets of multi-stacked layers with controllable thickness from ∼2 to 25 nm. The absence of transfer process in this technique avoids any additional degradation, such as wrinkles, tears or folding and residues on the film which are detrimental to device performance. This work provides a wider perspective of CVD-grown h-BN and presents a viable route towards large-scale manufacturing of h-BN substrates and for coating applications. Published version 2015-04-06T07:10:03Z 2019-12-06T22:26:47Z 2015-04-06T07:10:03Z 2019-12-06T22:26:47Z 2015 2015 Journal Article Tay, R. Y., Tsang, S. H., Loeblein, M., Chow, W. L., Loh, G. C., Toh, J. W., et al. (2015). Direct growth of nanocrystalline hexagonal boron nitride films on dielectric substrates. Applied physics letters, 106(10), 101901-. https://hdl.handle.net/10356/107211 http://hdl.handle.net/10220/25319 10.1063/1.4914474 en Applied physics letters © 2015 AIP Publishing LLC. This paper was published in Applied Physics Letters and is made available as an electronic reprint (preprint) with permission of AIP Publishing LLC. The paper can be found at the following official DOI: [http://dx.doi.org/10.1063/1.4914474]. One print or electronic copy may be made for personal use only. Systematic or multiple reproduction, distribution to multiple locations via electronic or other means, duplication of any material in this paper for a fee or for commercial purposes, or modification of the content of the paper is prohibited and is subject to penalties under law. 6 p. application/pdf |
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DRNTU::Engineering::Materials::Microelectronics and semiconductor materials::Thin films Tay, Roland Yingjie Tsang, Siu Hon Loeblein, Manuela Chow, Wai Leong Loh, Guan Chee Toh, Joo Wah Ang, Soon Loong Teo, Edwin Hang Tong Direct growth of nanocrystalline hexagonal boron nitride films on dielectric substrates |
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Atomically thin hexagonal-boron nitride (h-BN) films are primarily synthesized through chemical vapor deposition (CVD) on various catalytic transition metal substrates. In this work, a single-step metal-catalyst-free approach to obtain few- to multi-layer nanocrystalline h-BN (NCBN) directly on amorphous SiO2/Si and quartz substrates is demonstrated. The as-grown thin films are continuous and smooth with no observable pinholes or wrinkles across the entire deposited substrate as inspected using optical and atomic force microscopy. The starting layers of NCBN orient itself parallel to the substrate, initiating the growth of the textured thin film. Formation of NCBN is due to the random and uncontrolled nucleation of h-BN on the dielectric substrate surface with no epitaxial relation, unlike on metal surfaces. The crystallite size is ∼25 nm as determined by Raman spectroscopy. Transmission electron microscopy shows that the NCBN formed sheets of multi-stacked layers with controllable thickness from ∼2 to 25 nm. The absence of transfer process in this technique avoids any additional degradation, such as wrinkles, tears or folding and residues on the film which are detrimental to device performance. This work provides a wider perspective of CVD-grown h-BN and presents a viable route towards large-scale manufacturing of h-BN substrates and for coating applications. |
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School of Electrical and Electronic Engineering |
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School of Electrical and Electronic Engineering Tay, Roland Yingjie Tsang, Siu Hon Loeblein, Manuela Chow, Wai Leong Loh, Guan Chee Toh, Joo Wah Ang, Soon Loong Teo, Edwin Hang Tong |
format |
Article |
author |
Tay, Roland Yingjie Tsang, Siu Hon Loeblein, Manuela Chow, Wai Leong Loh, Guan Chee Toh, Joo Wah Ang, Soon Loong Teo, Edwin Hang Tong |
author_sort |
Tay, Roland Yingjie |
title |
Direct growth of nanocrystalline hexagonal boron nitride films on dielectric substrates |
title_short |
Direct growth of nanocrystalline hexagonal boron nitride films on dielectric substrates |
title_full |
Direct growth of nanocrystalline hexagonal boron nitride films on dielectric substrates |
title_fullStr |
Direct growth of nanocrystalline hexagonal boron nitride films on dielectric substrates |
title_full_unstemmed |
Direct growth of nanocrystalline hexagonal boron nitride films on dielectric substrates |
title_sort |
direct growth of nanocrystalline hexagonal boron nitride films on dielectric substrates |
publishDate |
2015 |
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https://hdl.handle.net/10356/107211 http://hdl.handle.net/10220/25319 |
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1681059651585572864 |