On the dendritic growth and field emission of amorphous AlQ3 nanowires

被引:21
作者
Cho, Chun-Pei [2 ]
Perng, Tsong-Pyng [1 ,3 ]
机构
[1] Natl Tsing Hua Univ, Dept Mat Sci & Engn, Hsinchu 30013, Taiwan
[2] Natl Chi Nan Univ, Dept Appl Mat & Optoelect Engn, Nantou 54561, Taiwan
[3] Yuan Ze Univ, Dept Chem Engn & Mat Sci, Chungli 32003, Taiwan
关键词
AlQ(3) nanowires; Dendritic growth; Photoluminescence; Field emission; SILICON-CARBIDE NANOWIRES; DIP-PEN NANOLITHOGRAPHY; DIMENSIONAL NANOMATERIALS; THIN-FILMS; NANOPARTICLES; ARRAYS; FABRICATION; POLYMERS; NANORODS; ELECTROLUMINESCENCE;
D O I
10.1016/j.orgel.2009.10.007
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Amorphous AlQ(3) nanowires were fabricated by vapor condensation under a cold trap. Their diameter distributed in a small range of 35-60 nm, but their length was dramatically changed by working pressure. Longer and thinner nanowires could be obtained at a lower working pressure. The most appropriate condition to fabricate long and fine nanowires was to set boat temperature at 410 degrees C and to control the working pressure of Ar at 1.33 x 10(-3)-3.99 x 10(3) Pa. A higher density of nanowires was observed at a lower working pressure. The dendritic growth mechanism caused by a temperature gradient was proposed to explain the formation of branched nanowires. Due to the absence of quantum confinement effect, the nanowires did not exhibit a PL blue shift as their sizes shrank. When higher density of nanowires were formed at a lower working pressure, stronger PL intensity could be revealed on the emission spectra. The amorphous nanowires also exhibited field-emission behavior. Their Eturn-on ranged from 3 to 20 V/mu m and frequently approximated to 10 V/mu m, comparable to those of most inorganic 1D nanostructures but somewhat larger than that of CNTs. Larger thickness caused by a higher deposition rate at a higher boat temperature could lead to a smaller Eturn-on. Crown Copyright (C) 2009 Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:115 / 122
页数:8
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