Critical oxide thickness for efficient single-walled carbon nanotube growth on silicon using thin SiO2 diffusion barriers

被引:40
作者
Simmons, Jason M.
Nichols, Beth M.
Marcus, Matthew S.
Castellini, Olivia M.
Hamers, Robert J.
Eriksson, Mark A.
机构
[1] Univ Wisconsin, Dept Phys, Madison, WI 53706 USA
[2] Univ Wisconsin, Dept Chem, Madison, WI 53706 USA
关键词
carbon nanotubes; catalysis; chemical vapor deposition; photoelectron spectroscopy;
D O I
10.1002/smll.200600095
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The ability to integrate carbon nanotubes, especially single-walled carbon nanotubes, seamlessly onto silicon would expand their range of applications considerably. Though direct integration using chemical vapor deposition is the simplest method, the growth of single-walled carbon nanotubes on bare silicon and on ultrathin oxides is greatly inhibited due to the formation of a noncatalytic silicide. Using X-ray photoelectron spectroscopy, we show that silicide formation occurs on ultrathin oxides due to thermally activated metal diffusion through the oxide. Silicides affect the growth of single-walled nanotubes more than multi-walled nanotubes due to the increased kinetics at the higher single-walled nanotube growth temperature. We demonstrate that nickel and iron catalysts, when deposited on clean silicon or ultrathin silicon dioxide layers, begin to form silicides at relatively low temperatures, and that by 900 degrees C, all of the catalyst has been incorporated into the silicide, rendering it inactive for subsequent single-walled nanotube growth. We further show that a 4-nm silicon dioxide layer is the minimum diffusion barrier thickness that allows for efficient single-walled nanotube growth.
引用
收藏
页码:902 / 909
页数:8
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