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Tapering-free monocrystalline Ge nanowires synthesized via plasma-assisted VLS using in and Sn catalysts. / Tang, Jian; Wang, Jun; Maurice, Jean Luc; Chen, Wanghua; Foldyna, Martin; Yu, Linwei; Leshchenko, Egor D.; Dubrovskii, Vladimir G.; Cabarrocas, Pere Roca I.

In: Nanotechnology, Vol. 33, No. 40, 405602, 01.10.2022.

Research output: Contribution to journalArticlepeer-review

Harvard

Tang, J, Wang, J, Maurice, JL, Chen, W, Foldyna, M, Yu, L, Leshchenko, ED, Dubrovskii, VG & Cabarrocas, PRI 2022, 'Tapering-free monocrystalline Ge nanowires synthesized via plasma-assisted VLS using in and Sn catalysts', Nanotechnology, vol. 33, no. 40, 405602. https://doi.org/10.1088/1361-6528/ac57d4

APA

Tang, J., Wang, J., Maurice, J. L., Chen, W., Foldyna, M., Yu, L., Leshchenko, E. D., Dubrovskii, V. G., & Cabarrocas, P. R. I. (2022). Tapering-free monocrystalline Ge nanowires synthesized via plasma-assisted VLS using in and Sn catalysts. Nanotechnology, 33(40), [405602]. https://doi.org/10.1088/1361-6528/ac57d4

Vancouver

Tang J, Wang J, Maurice JL, Chen W, Foldyna M, Yu L et al. Tapering-free monocrystalline Ge nanowires synthesized via plasma-assisted VLS using in and Sn catalysts. Nanotechnology. 2022 Oct 1;33(40). 405602. https://doi.org/10.1088/1361-6528/ac57d4

Author

Tang, Jian ; Wang, Jun ; Maurice, Jean Luc ; Chen, Wanghua ; Foldyna, Martin ; Yu, Linwei ; Leshchenko, Egor D. ; Dubrovskii, Vladimir G. ; Cabarrocas, Pere Roca I. / Tapering-free monocrystalline Ge nanowires synthesized via plasma-assisted VLS using in and Sn catalysts. In: Nanotechnology. 2022 ; Vol. 33, No. 40.

BibTeX

@article{9eec0bd2b3a8433d8594cf3ea75b11bd,
title = "Tapering-free monocrystalline Ge nanowires synthesized via plasma-assisted VLS using in and Sn catalysts",
abstract = "In and Sn are the type of catalysts which do not introduce deep level electrical defects within the bandgap of germanium (Ge). However, Ge nanowires produced using these catalysts usually have a large diameter, a tapered morphology, and mixed crystalline and amorphous phases. In this study, we show that plasma-assisted vapor-liquid-solid (PA-VLS) method can be used to synthesize Ge nanowires. Moreover, at certain parameter domains, the sidewall deposition issues of this synthesis method can be avoided and long, thin tapering-free monocrystalline Ge nanowires can be obtained with In and Sn catalysts. We find two quite different parameter domains where Ge nanowire growth can occur via PA-VLS using In and Sn catalysts: (i) a low temperature-low pressure domain, below ∼235 °C at a GeH4 partial pressure of ∼6 mTorr, where supersaturation in the catalyst occurs thanks to the low solubility of Ge in the catalysts, and (ii) a high temperature-high pressure domain, at ∼400 °C and a GeH4 partial pressure above ∼20 mTorr, where supersaturation occurs thanks to the high GeH4 concentration. While growth at 235 °C results in tapered short wires, operating at 400 °C enables cylindrical nanowire growth. With the increase of growth temperature, the crystalline structure of the nanowires changes from multi-crystalline to mono-crystalline and their growth rate increases from ∼0.3 nm s-1 to 5 nm s-1. The cylindrical Ge nanowires grown at 400°C usually have a length of few microns and a radius of around 10 nm, which is well below the Bohr exciton radius in bulk Ge (24.3 nm). To explain the growth mechanism, a detailed growth model based on the key chemical reactions is provided. ",
keywords = "germanium nanowires, In, plasma-assisted VLS, Sn, tapering-free, ultra-thin",
author = "Jian Tang and Jun Wang and Maurice, {Jean Luc} and Wanghua Chen and Martin Foldyna and Linwei Yu and Leshchenko, {Egor D.} and Dubrovskii, {Vladimir G.} and Cabarrocas, {Pere Roca I.}",
note = "Publisher Copyright: {\textcopyright} 2022 IOP Publishing Ltd.",
year = "2022",
month = oct,
day = "1",
doi = "10.1088/1361-6528/ac57d4",
language = "English",
volume = "33",
journal = "Nanotechnology",
issn = "0957-4484",
publisher = "IOP Publishing Ltd.",
number = "40",

}

RIS

TY - JOUR

T1 - Tapering-free monocrystalline Ge nanowires synthesized via plasma-assisted VLS using in and Sn catalysts

AU - Tang, Jian

AU - Wang, Jun

AU - Maurice, Jean Luc

AU - Chen, Wanghua

AU - Foldyna, Martin

AU - Yu, Linwei

AU - Leshchenko, Egor D.

AU - Dubrovskii, Vladimir G.

AU - Cabarrocas, Pere Roca I.

N1 - Publisher Copyright: © 2022 IOP Publishing Ltd.

PY - 2022/10/1

Y1 - 2022/10/1

N2 - In and Sn are the type of catalysts which do not introduce deep level electrical defects within the bandgap of germanium (Ge). However, Ge nanowires produced using these catalysts usually have a large diameter, a tapered morphology, and mixed crystalline and amorphous phases. In this study, we show that plasma-assisted vapor-liquid-solid (PA-VLS) method can be used to synthesize Ge nanowires. Moreover, at certain parameter domains, the sidewall deposition issues of this synthesis method can be avoided and long, thin tapering-free monocrystalline Ge nanowires can be obtained with In and Sn catalysts. We find two quite different parameter domains where Ge nanowire growth can occur via PA-VLS using In and Sn catalysts: (i) a low temperature-low pressure domain, below ∼235 °C at a GeH4 partial pressure of ∼6 mTorr, where supersaturation in the catalyst occurs thanks to the low solubility of Ge in the catalysts, and (ii) a high temperature-high pressure domain, at ∼400 °C and a GeH4 partial pressure above ∼20 mTorr, where supersaturation occurs thanks to the high GeH4 concentration. While growth at 235 °C results in tapered short wires, operating at 400 °C enables cylindrical nanowire growth. With the increase of growth temperature, the crystalline structure of the nanowires changes from multi-crystalline to mono-crystalline and their growth rate increases from ∼0.3 nm s-1 to 5 nm s-1. The cylindrical Ge nanowires grown at 400°C usually have a length of few microns and a radius of around 10 nm, which is well below the Bohr exciton radius in bulk Ge (24.3 nm). To explain the growth mechanism, a detailed growth model based on the key chemical reactions is provided.

AB - In and Sn are the type of catalysts which do not introduce deep level electrical defects within the bandgap of germanium (Ge). However, Ge nanowires produced using these catalysts usually have a large diameter, a tapered morphology, and mixed crystalline and amorphous phases. In this study, we show that plasma-assisted vapor-liquid-solid (PA-VLS) method can be used to synthesize Ge nanowires. Moreover, at certain parameter domains, the sidewall deposition issues of this synthesis method can be avoided and long, thin tapering-free monocrystalline Ge nanowires can be obtained with In and Sn catalysts. We find two quite different parameter domains where Ge nanowire growth can occur via PA-VLS using In and Sn catalysts: (i) a low temperature-low pressure domain, below ∼235 °C at a GeH4 partial pressure of ∼6 mTorr, where supersaturation in the catalyst occurs thanks to the low solubility of Ge in the catalysts, and (ii) a high temperature-high pressure domain, at ∼400 °C and a GeH4 partial pressure above ∼20 mTorr, where supersaturation occurs thanks to the high GeH4 concentration. While growth at 235 °C results in tapered short wires, operating at 400 °C enables cylindrical nanowire growth. With the increase of growth temperature, the crystalline structure of the nanowires changes from multi-crystalline to mono-crystalline and their growth rate increases from ∼0.3 nm s-1 to 5 nm s-1. The cylindrical Ge nanowires grown at 400°C usually have a length of few microns and a radius of around 10 nm, which is well below the Bohr exciton radius in bulk Ge (24.3 nm). To explain the growth mechanism, a detailed growth model based on the key chemical reactions is provided.

KW - germanium nanowires

KW - In

KW - plasma-assisted VLS

KW - Sn

KW - tapering-free

KW - ultra-thin

UR - http://www.scopus.com/inward/record.url?scp=85134632273&partnerID=8YFLogxK

U2 - 10.1088/1361-6528/ac57d4

DO - 10.1088/1361-6528/ac57d4

M3 - Article

C2 - 35196259

AN - SCOPUS:85134632273

VL - 33

JO - Nanotechnology

JF - Nanotechnology

SN - 0957-4484

IS - 40

M1 - 405602

ER -

ID: 100331527