Aqueous electromigration of single-walled carbon nanotubes and co-electromigration with copper ions
Author(s) -
Pavan M. V. Raja,
Gibran L. Esquenazi,
Kourtney Wright,
Cathren E. Gowenlock,
Bruce E. Brinson,
Shirin Alexander,
Daniel R. Jones,
Varun Shenoy Gangoli,
Andrew R. Barron
Publication year - 2018
Publication title -
nanoscale
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.038
H-Index - 224
eISSN - 2040-3372
pISSN - 2040-3364
DOI - 10.1039/c8nr06485g
Subject(s) - electromigration , copper , materials science , adsorption , carbon nanotube , aqueous solution , ion , pulmonary surfactant , metal , inorganic chemistry , chemical engineering , carbon fibers , nanotechnology , chemistry , metallurgy , composite material , organic chemistry , composite number , engineering
The electromigration behaviour of raw and acid purified single walled carbon nanotubes (SWCNTs) in dilute aqueous systems (0.0034 mg mL -1 ), in the absence of surfactant, with the addition of either 0.85 M acetic acid or 0.1 M CuSO 4 , was evaluated using a 2-inch copper cathode and either a 2-inch copper or 0.5-inch platinum anode. The results showed that the electromigration of raw SWCNTs (with a high catalyst residue) in the presence of CuSO 4 resulted in the formation of a Cu-SWCNT composite material at the cathode. In contrast, acid purified SWCNTs were observed to diffuse to a copper anode, creating fibrillated agglomerates with "rice-grain"-like morphologies. Upon acidification with acetic acid (or addition of CuSO 4 ) the direction of electromigration reversed towards the cathode as a result of coordination of Cu 2+ o the functional groups on the SWCNT overcoming the inherent negative charge of the acid purified SWCNTs. The result was the co-deposition of SWCNTs and Cu metal on the cathode. Addition of 0.005 M EDTA sequesters some of the Cu 2+ and resulted in the separation of metal decorated SWCNTs to the cathode and un-decorated SWCNTs to the anode. The resulting SWCNT and Cu/SWCNT deposits were characterized by Raman spectroscopy, XPS, SEM, EDS, and TEM.
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