TY - JOUR
T1 - Antimony-Rich GaAsxSb1−x Nanowires Passivated by Organic Sulfides for High-Performance Transistors and Near-Infrared Photodetectors
AU - Wang, Wei
AU - Yip, Sen Po
AU - Meng, You
AU - Wang, Weijun
AU - Wang, Fei
AU - Bu, Xiuming
AU - Lai, Zhengxun
AU - Kang, Xiaolin
AU - Xie, Pengshan
AU - Quan, Quan
AU - Liu, Chuntai
AU - Ho, Johnny C.
N1 - Funding Information:
W.W. and S.P.Y. contributed equally to this work. This research was financially supported by the Research Fellow Scheme (No. RFS2021‐1S04) and the Theme‐based Research (No. T42‐103/16‐N) of the Research Grants Council of Hong Kong SAR, China, and Foshan Innovative and Entrepreneurial Research Team Program (No. 2018IT100031).
Publisher Copyright:
© 2021 Wiley-VCH GmbH.
PY - 2021/11/18
Y1 - 2021/11/18
N2 - Due to their excellent properties, ternary GaAsxSb1−x nanowires have been extensively investigated to enable various nanodevice structures. However, the surfactant effect of antimony has a notorious impact on the surface morphology and electrical properties of prepared Sb-rich nanowires, restricting their practical utilization. Herein, through the in situ passivation effect of thiourea, highly-crystalline, uniform, and thin GaAsxSb1−x nanowires (x ≤ 0.34) are successfully achieved. In contrast to low-melting-point sulfur powders typically used in surfactant-assisted chemical vapor deposition, thiourea has a relatively higher melting point, facilitating the more controllable formation of SbxSy layer on the nanowire surface to minimize the radial growth and to stabilize the sidewalls for high-quality Sb-rich nanowires. When configured into field-effect transistors, the obtained GaSb nanowires exhibit excellent device performance with a hole mobility of over 200 cm2 V−1 s−1. The optimal GaAs0.18Sb0.82 device yields an impressive responsivity of 5.4 × 104 A W−1 and an external quantum efficiency of 4.4 × 106% under near-infrared light illumination. Importantly, the rise and decay times are as efficient as 80 and 104 µs, respectively, which are better than any values reported for GaAsSb nanowire photoconductors to date. All these results demonstrate the promising potential of GaAsxSb1−x nanowires for high-mobility electronics and ultrafast near-infrared optoelectronics.
AB - Due to their excellent properties, ternary GaAsxSb1−x nanowires have been extensively investigated to enable various nanodevice structures. However, the surfactant effect of antimony has a notorious impact on the surface morphology and electrical properties of prepared Sb-rich nanowires, restricting their practical utilization. Herein, through the in situ passivation effect of thiourea, highly-crystalline, uniform, and thin GaAsxSb1−x nanowires (x ≤ 0.34) are successfully achieved. In contrast to low-melting-point sulfur powders typically used in surfactant-assisted chemical vapor deposition, thiourea has a relatively higher melting point, facilitating the more controllable formation of SbxSy layer on the nanowire surface to minimize the radial growth and to stabilize the sidewalls for high-quality Sb-rich nanowires. When configured into field-effect transistors, the obtained GaSb nanowires exhibit excellent device performance with a hole mobility of over 200 cm2 V−1 s−1. The optimal GaAs0.18Sb0.82 device yields an impressive responsivity of 5.4 × 104 A W−1 and an external quantum efficiency of 4.4 × 106% under near-infrared light illumination. Importantly, the rise and decay times are as efficient as 80 and 104 µs, respectively, which are better than any values reported for GaAsSb nanowire photoconductors to date. All these results demonstrate the promising potential of GaAsxSb1−x nanowires for high-mobility electronics and ultrafast near-infrared optoelectronics.
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U2 - 10.1002/adom.202101289
DO - 10.1002/adom.202101289
M3 - Article
AN - SCOPUS:85115319796
SN - 2195-1071
VL - 9
JO - Advanced Optical Materials
JF - Advanced Optical Materials
IS - 22
M1 - 2101289
ER -