Publication:
Electrochromism of Electropolymerized Metallophthalocyanines

dc.contributor.authorKOCA, ATIF
dc.contributor.authorsDemir, Faruk; Biyiklioglu, Zekeriya; Koca, Atif
dc.date.accessioned2022-03-13T12:45:35Z
dc.date.accessioned2026-01-10T18:14:13Z
dc.date.available2022-03-13T12:45:35Z
dc.date.issued2014
dc.description.abstractIn this paper, metallophthalocyanines (MPcs; M = 2H(+) (H2Pc); Ni2+ (NiPc) and Cu2+ (CuPc)) bearing electropolymerizable amino substituents were easily and controllably electropolymerized on the working electrodes as thin solid films and electrochromic properties of these films were studied in detail with the various electrochemical, in-situ spectroelectrochemical and in-situ electrocolorimetric analysis methods. Although H2Pc and CuPc showed reasonable electrochromic features, NiPc illustrated excellent electrochromic responses with the fast response times, high optic contrast and better optical and coulombic stabilities. Although, monomeric H2Pc, NiPc, and CuPc did not behave as electrochromic materials, surprisingly the electropolymerized films of these complexes illustrated electrochemically triggered color changes between cyan and yellow or red colors. H2Pc is the first example of the metal free phthalocyanine, whose electropolymerized film behaved as an anodic coloring material. (C) 2013 The Electrochemical Society. All rights reserved.
dc.identifier.doi10.1149/2.002403jes
dc.identifier.eissn1945-7111
dc.identifier.issn0013-4651
dc.identifier.urihttps://hdl.handle.net/11424/237807
dc.identifier.wosWOS:000332137100088
dc.language.isoeng
dc.publisherELECTROCHEMICAL SOC INC
dc.relation.ispartofJOURNAL OF THE ELECTROCHEMICAL SOCIETY
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectLUTETIUM(III) PHTHALOCYANINE
dc.subjectFILMS
dc.subjectGREEN
dc.subjectAL
dc.titleElectrochromism of Electropolymerized Metallophthalocyanines
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPageG6
oaire.citation.issue3
oaire.citation.startPageG1
oaire.citation.titleJOURNAL OF THE ELECTROCHEMICAL SOCIETY
oaire.citation.volume161

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