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Flux-Dependent Growth Kinetics and Diameter Selectivity in Single-Wall Carbon Nanotube Arrays
被引:32
作者:
Geohegan, David B.
[1
]
Puretzky, Alex A.
[1
]
Jackson, Jeremy J.
[1
]
Rouleau, Christopher M.
[1
]
Eres, Gyula
[2
]
More, Karren L.
[2
]
机构:
[1] Oak Ridge Natl Lab, Ctr Nanophase Mat Sci, Oak Ridge, TN 37831 USA
[2] Oak Ridge Natl Lab, Div Mat Sci & Technol, Oak Ridge, TN 37831 USA
来源:
关键词:
single wall carbon nanotubes;
chemical vapor deposition;
induction time;
nucleation;
growth rate;
kinetics;
in situ;
real-time;
diagnostics;
pulsed growth;
diameter distribution;
flux;
aligned;
partial pressure;
CHEMICAL-VAPOR-DEPOSITION;
FILAMENT GROWTH;
MODEL;
WATER;
NUCLEATION;
CATALYST;
NICKEL;
TIME;
D O I:
10.1021/nn2030397
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
The nucleation and growth kinetics of single-wall carbon nanotubes in aligned arrays have been measured using fast pulses of acetylene and in situ optical diagnostics in conjunction with low pressure chemical vapor deposition (CVD). Increasing the acetylene partial pressure is shown to decrease nucleation times by,three orders of magnitude, permitting aligned nanotube arrays to nucleate and grow to micrometers lengths within single gas pulses at high (up to 7 mu m/s) peak growth rates and short similar to 0.5 s times. Low-frequency Raman scattering (>10 cm(-1)) and transmission electron microscopy measurements show that increasing the feedstock flux In both continuous- and pulsed-CVD shifts the product distribution to large single-wall carbon nanotube diameters >2.5 nm. Sufficiently high acetylene partial pressures In pulsed-CVD appear to temporarily terminate the growth of the fastest-growing, small-diameter nanotubes by overcoating the more catalytically active, smaller catalyst nanoparticles within the ensemble with non-nanotube carbon in agreement with a growth model. The results indicate that subsets of catalyst nanoparticle ensembles nucleate, grow, and terminate growth within different flux ranges according to their catalytic activity.
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页码:8311 / 8321
页数:11
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