Hostname: page-component-848d4c4894-pjpqr Total loading time: 0 Render date: 2024-07-02T21:21:03.534Z Has data issue: false hasContentIssue false
  • English
  • Français

A Novel Conducting Polymer with O-S-S-O Bonds for Positive Material:Poly(2,2′-Diaminobenzyloxydisulfide)

Published online by Cambridge University Press:  10 February 2011

Y. Z. Su ,
W. S. Ma  and
K. C. Gong
Y. Z. Su
Affiliation:
Polymer Structure & Modification Res. Lab., South China University of Technology, Guangzhou, China 510641, [email protected]
W. S. Ma
Affiliation:
Polymer Structure & Modification Res. Lab., South China University of Technology, Guangzhou, China 510641, [email protected]
K. C. Gong
Affiliation:
Polymer Structure & Modification Res. Lab., South China University of Technology, Guangzhou, China 510641, [email protected]
Get access

Abstract

Organic disulfide compounds has been proposed as a new class of high-energy storage material. Poly(2,2'-diaminobenzyloxydisulfide), a novel conducting polymer having O-S-S-O bond joined two moieties of anilines, is synthesized both chemically and electrochemically as a new positive storage material. It exhibits conductivity in the region of 10-3 S cm-1 by the fourprobe method and the O-S-S-0 bonds in it are confirmed by Fourie Transform Raman Spectroscopy(FT-RS) and Fourie Transform Infrared Spectroscopy(FT-IR). The poly(2,2'- diaminobenzyloxydisulfide) films are formed by electropolymerization from a AN/THF solution containing 0. IM LiClO4, 0. IM HCl and 0.05 M 2,2'-diaminobenzyloxydisulfide monomer on Pt electrode under continuous cycling between -0.30V and 1.20V vs Ag/AgCl(sat. KCI) at scanning rate 50mv s-1. The cyclic voltammetry shows its electrochemical behaviour is similar to polyaniline. The redox peak current of the cyclic voltammograms increase with increasing of the cyclic numbers.

Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 575: Symposium CC – New Materials for Batteries & Fuel Cells , 1999 , 403
Copyright
Copyright © Materials Research Society 2000

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

1. Visco, S. J., Maihe, C. C., L. C. De Jonghe and Amand, M. B., J. Electrochem. Soc., 136, p. 661(1991).Google Scholar
2. Naoi, K., Menda, M., Ooike, H. and Oyama, N., Proc. 31st Bat. Symp. Jpn., p. 31(1990).Google Scholar
3. Oyama, N., Pope, J. M. and Sotomura, T., J. Electrochem. Soc., 144, p. L47(1997).Google Scholar
4. Gong, K. C. and Ma, W. S., Mat. Res. Soc. Symp., 461, p. 87(1997).Google Scholar
5. Yu, L., Wang, X. H., and Li, J., J. Power Souce, 73, p. 261(1998).Google Scholar
6. Naoi, K., Kawase, K., and Inoue, Y., J. Electrochem. Soc., 144, p. L170(1997).Google Scholar
7. Picar, S., Genies, E., J. Electroanal. Chem., 408 p. 53(1996).Google Scholar
8. Naoi, K., Kawase, K., Mori, M. and Komiyama, M., Mat. Res. Soc. Symp., 496, p. 309(1998).Google Scholar
9. Liu, M., Visco, S. J. and L. C. De Jonghe and Amand, M. B., J. Electrochem. Soc., 138, p. 1891(1991).Google Scholar
10. Osaka, T., Nakajima, T., Naoi, K. and Owens, B. B., J. Electrochem. Soc., 137, p.2139(1990).Google Scholar
11. Tardif, D. L., Williams, C. R., Harpp, D. N., J. Am. Chem. Soc., 117, p. 9067(1995).Google Scholar
12. Zotti, G., Cattarub, S. and Comisso, N., J. Electroanal. Chem., 239, p. 387(1988).Google Scholar