[1]
J. K. Campbell, L. Sun, R. M. Crooks, J. Am. Chem. Soc. Vol. 121 (1999), pp.3779-3780.
Google Scholar
[2]
C. G. Hu, W. L. Wang, S. X. Wang, et al., Vol. 12 (2003), pp.1295-1299.
Google Scholar
[3]
B. C. Yang, W. S. Wang, Physics and technology of thin film, 1997, University of Electronic Science and Technology of China, Chengduo, China, p.207 (in Chinese).
Google Scholar
[4]
M. S. P. Shaffer, X. Fan and A. H. Windle, dispersion and packing of carbon nanotubes, 36(11) (1998) 1603-1612.
DOI: 10.1016/s0008-6223(98)00130-4
Google Scholar
[5]
L. J. Bellamy, The infra-red spectra of complex molecules, Chapman and Hall, London, pp.183-194.
Google Scholar
[6]
J. Xu, M. C. Granger, Q. Chen, et al., Anal. Chem. Vol. 69 (1997), 591A-597A.
Google Scholar
[7]
S. Ferro, A. D. Battisti, Electrochimica Acta, Vol. 47 (2002), pp.1641-0. 4 -0. 2 0. 0 0. 2 0. 4 0. 6 0. 8 1. 0 1. 2 1. 4 -4 -2.
Google Scholar
[2] [4] Scan rate 100 mV s-1 10min n-CNT 20min n-CNT 10min m-CNT j (mA cm -2 ) Potential (V vs SCE) 0. 00 0. 05 0. 10 0. 15 0. 20 0. 25 0. 30.
Google Scholar
[1] [2] [3] [4] [5] [6] [7] [8] [10] min m-CNT.
Google Scholar
[20]
min n-CNT jpa ( mA cm -2 ) Scan rate / V s -1 Fig. 2. Cyclic voltammograms on the treated CNTs electrodes for 5 m mol L -1 FeSO4 in 1 mol L -1 Fig. 3. jpa changes with the scan rate on the treated CNTs electrodes for 5 m mol L -1 FeSO4 in 1 mol L -1.
Google Scholar