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ToF‐SIMS study of stages in the electrochemical growth of insulating poly(o‐aminophenol) films
Author(s) -
Carbone M. E.,
Ciriello R.,
Salvi A. M.,
Castle J. E.
Publication year - 2016
Publication title -
surface and interface analysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.52
H-Index - 90
eISSN - 1096-9918
pISSN - 0142-2421
DOI - 10.1002/sia.5968
Subject(s) - monomer , cyclic voltammetry , polymer , platinum , x ray photoelectron spectroscopy , electrochemistry , electrode , substrate (aquarium) , chemistry , thin film , conductive polymer , polymer chemistry , materials science , analytical chemistry (journal) , chemical engineering , nanotechnology , organic chemistry , catalysis , oceanography , engineering , geology
Previous XPS investigations of insulating poly(o‐aminophenol) (PoAP), electrosynthesized by cyclic voltammetry on Pt substrates, revealed the formation of a thin film of about 7 nm of thickness, firmly adherent onto the electrode surface and stable even under Ultra High Vacuum (UHV) conditions. A constant repeat formula made of alternating quinoneimine and monomer units was derived with polymer chains terminating as carbonyl‐type groups. Based on these findings, we have continued our investigation on insulating PoAP by employing time‐of‐flight SIMS whose superior surface sensitivity is well‐known. The aim was to corroborate the polymer structure with particular reference to the top surface layers in view of possible bio‐applications and to understand the possible way of interaction with the underlying platinum electrode surface. In order to do this, we analyzed PoAP films grown at different levels of the electrochemical synthesis (1, 5, and 20 scan cycles) and the platinum substrate itself. The individuation of the main characteristic fragments and the behavior of their intensity by varying the stage of the electropolymerization allowed to confirm the polymer structure and the presence of terminating carbonyl groups. Remarkably, from the analysis of the PoAP/Pt interface at the early stage of the polymer formation, it was possible to discern that polymer chains tend to interact with the electrode surface preferentially by the nitrogen atom of the oxidized monomers. Copyright © 2016 John Wiley & Sons, Ltd.