STRUCTURAL AND ELECTROCHROMIC PROPERTIES OF SOL-GEL DERIVED NI(SI)-OXIDE FILMS

Citation
A. Surca et al., STRUCTURAL AND ELECTROCHROMIC PROPERTIES OF SOL-GEL DERIVED NI(SI)-OXIDE FILMS, Journal of electroanalytical chemistry [1992], 433(1-2), 1997, pp. 57-72
Citations number
49
Journal title
Journal of electroanalytical chemistry [1992]
ISSN journal
15726657 → ACNP
Volume
433
Issue
1-2
Year of publication
1997
Pages
57 - 72
Database
ISI
SICI code
Abstract
In our recent publication we reported the FT-IR spectroscopic analysis of Ni-oxide films [A. Surca, B. Orel, B. Pihlar, P. Bukovec, J. Elect roanal. Chem. 408 (1996) 83] prepared from aqueous sols containing a n ickel sulphate precursor and polyvinylalcohol as an additive to improv e the optical quality of the films. Films with improved adherence on I TO coated glass were deposited via the sol-gel route using a dip-coati ng technique from sols containing in addition a nickel sulphate precur sor 3-aminopropyltrimethoxysilane (3-APMS), Heat treatment at 300 degr ees C produced Ni(Si)-oxide films whose IR spectra resemble the alpha( II)-Ni(OH)(2) phase with NiO (bunsenite) nanocrystalline inclusions as was shown by X-ray diffraction analysis. The electrochromic effect wi th colouring/bleaching changes up to 55% was noted in 0.1 M LiOH. The colouration efficiency (eta) which is defined as the change in optical density per unit of inserted charge (Delta OD/Q) was up to 26 cm(2)C( -1). Evolution of newly formed phases appearing during extensive (up t o 200 cycles) potential cycling revealed the transformation of the as- deposited alpha(II)-Ni(OH)(2) phase to beta(III)-NiOOH and beta(II)-Ni OOH2 phases. In films cycled potentially more than 150 times in 0.1 M LiOH an irreversible transformation of the beta(III)-NiOOH phase into the gamma(III)-NiOOH phase was observed. From these results it was con cluded that Ni(Si)-oxide films follow the Bode scheme [H. Bode, K. Deh melt, J. Witte, Electrochim, Acta 11 (1966) 1079] when cycled potentia lly in protic electrolyte. (C) 1997 Elsevier Science S.A.