Please use this identifier to cite or link to this item:
Title: Limitations of the X-ray photoelectron spectroscopy technique in the study of electroactive polymers
Authors: Neoh, K.G. 
Kang, E.T. 
Tan, K.L. 
Issue Date: 30-Jan-1997
Citation: Neoh, K.G.,Kang, E.T.,Tan, K.L. (1997-01-30). Limitations of the X-ray photoelectron spectroscopy technique in the study of electroactive polymers. Journal of Physical Chemistry B 101 (5) : 726-731. ScholarBank@NUS Repository.
Abstract: Polyaniline (PAN) and polypyrrole (PPY) were analyzed by X-ray photoelectron spectroscopy (XPS) and bulk analytical techniques. A systematic comparison of the results was carried out to determine the effects of anion size, synthesis methods, and the nature of the polymer (powder or film) on the variation between the surface and bulk compositions. Good agreement between the XPS and bulk analytical results is generally obtained for chemically synthesized polyaniline (in powder form). However, these two methods may give substantial discrepancies in the analysis of anion concentration in as-cast polyaniline base films subjected to re-doping by acids. Such discrepancies are also found in the analysis of as-synthesized polypyrrole doped by large anions and polypyrrole base films and powders after re-doping by acids. In these cases the XPS technique tends to give anion concentrations that are significantly higher than the bulk values. In some of these cases the high surface anion concentration supports a high proportion of positively charged nitrogens (>50% for polyaniline, >30% for polypyrrole), which must involve the protonation of some amine units in addition to all of the imine units. However, in actuality, the re-doping process can only replenish the anions to less than half of the original bulk concentration in polypyrrole.
Source Title: Journal of Physical Chemistry B
ISSN: 10895647
Appears in Collections:Staff Publications

Show full item record
Files in This Item:
There are no files associated with this item.

Page view(s)

checked on Dec 29, 2019

Google ScholarTM


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.