Research output: Contribution to journal › Article › peer-review
Record pure zincblende phase in GaAs nanowires down to 5 nm in radius. / Gil, Evelyne; Dubrovskii, Vladimir G.; Avit, Geoffrey; André, Yamina; Leroux, Christine; Lekhal, Kaddour; Grecenkov, Jurij; Trassoudaine, Agnès; Castelluci, Dominique; Monier, Guillaume; Ramdani, Reda M.; Robert-Goumet, Christine; Bideux, Luc; Harmand, Jean Christophe; Glas, Frank.
In: Nano Letters, Vol. 14, No. 7, 09.07.2014, p. 3938-3944.Research output: Contribution to journal › Article › peer-review
}
TY - JOUR
T1 - Record pure zincblende phase in GaAs nanowires down to 5 nm in radius
AU - Gil, Evelyne
AU - Dubrovskii, Vladimir G.
AU - Avit, Geoffrey
AU - André, Yamina
AU - Leroux, Christine
AU - Lekhal, Kaddour
AU - Grecenkov, Jurij
AU - Trassoudaine, Agnès
AU - Castelluci, Dominique
AU - Monier, Guillaume
AU - Ramdani, Reda M.
AU - Robert-Goumet, Christine
AU - Bideux, Luc
AU - Harmand, Jean Christophe
AU - Glas, Frank
PY - 2014/7/9
Y1 - 2014/7/9
N2 - We report the Au catalyst-assisted synthesis of 20 μm long GaAs nanowires by the vapor-liquid-solid hydride vapor phase epitaxy (HVPE) exhibiting a polytypism-free zincblende phase for record radii lower than 15 nm down to 5 nm. HVPE makes use of GaCl gaseous growth precursors at high mass input of which fast dechlorination at the usual process temperature of 715 °C results in high planar growth rate (standard 30-40 μm/h). When it comes to the vapor-liquid-solid growth of nanowires, fast solidification at a rate higher than 100 μm/h is observed. Nanowire growth by HVPE only proceeds by introduction of precursors in the catalyst droplets from the vapor phase. This promotes almost pure axial growth leading to nanowires with a constant cylinder shape over unusual length. The question of the cubic zincblende structure observed in HVPE-grown GaAs nanowires regardless of their radius is at the heart of the paper. We demonstrate that the vapor-liquid-solid growth in our conditions takes place at high liquid chemical potential that originates from very high influxes of both As and Ga. This yields a Ga concentration systematically higher than 0.62 in the Au-Ga-As droplets. The high Ga concentration decreases the surface energy of the droplets, which disables nucleation at the triple phase line thus preventing the formation of wurtzite structure whatever the nanowire radius is.
AB - We report the Au catalyst-assisted synthesis of 20 μm long GaAs nanowires by the vapor-liquid-solid hydride vapor phase epitaxy (HVPE) exhibiting a polytypism-free zincblende phase for record radii lower than 15 nm down to 5 nm. HVPE makes use of GaCl gaseous growth precursors at high mass input of which fast dechlorination at the usual process temperature of 715 °C results in high planar growth rate (standard 30-40 μm/h). When it comes to the vapor-liquid-solid growth of nanowires, fast solidification at a rate higher than 100 μm/h is observed. Nanowire growth by HVPE only proceeds by introduction of precursors in the catalyst droplets from the vapor phase. This promotes almost pure axial growth leading to nanowires with a constant cylinder shape over unusual length. The question of the cubic zincblende structure observed in HVPE-grown GaAs nanowires regardless of their radius is at the heart of the paper. We demonstrate that the vapor-liquid-solid growth in our conditions takes place at high liquid chemical potential that originates from very high influxes of both As and Ga. This yields a Ga concentration systematically higher than 0.62 in the Au-Ga-As droplets. The high Ga concentration decreases the surface energy of the droplets, which disables nucleation at the triple phase line thus preventing the formation of wurtzite structure whatever the nanowire radius is.
KW - chemical potential
KW - crystal structure
KW - GaAs
KW - HVPE
KW - Nanowire
KW - VLS
UR - http://www.scopus.com/inward/record.url?scp=84904015856&partnerID=8YFLogxK
U2 - 10.1021/nl501239h
DO - 10.1021/nl501239h
M3 - Article
VL - 14
SP - 3938
EP - 3944
JO - Nano Letters
JF - Nano Letters
SN - 1530-6984
IS - 7
ER -
ID: 7321476