Açık Akademik Arşiv Sistemi

Electrocatalytic activity of phthalocyanines bearing thiophenes for hydrogen production from water

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dc.contributor.authors Osmanbas, OA; Koca, A; Kandaz, M; Karaca, F;
dc.date.accessioned 2020-02-24T14:14:12Z
dc.date.available 2020-02-24T14:14:12Z
dc.date.issued 2008
dc.identifier.citation Osmanbas, OA; Koca, A; Kandaz, M; Karaca, F; (2008). Electrocatalytic activity of phthalocyanines bearing thiophenes for hydrogen production from water. INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 33, 3288-3281
dc.identifier.issn 0360-3199
dc.identifier.uri https://doi.org/10.1016/j.ijhydene.2008.04.018
dc.identifier.uri https://hdl.handle.net/20.500.12619/44695
dc.description.abstract in this work, voltammetric and spectroelectrochemical properties and electrocatalytic activities of thiophene-derivatized metallophthalocyanines for hydrogen production were investigated. Observation of reversible multi-electron reduction processes in the voltammetric analysis of the complexes is an indicator of the possible usage of the complexes as an electrocatalyst for the reduction of proton in aqueous solution. Electrocatalytic studies indicate that cobalt phthalocyanine modified electrodes catalyze the proton reduction by the electro-reduced [(CoPc-2)-Pc-1](-1) and/or [(CoPc-3)-Pc-1](-2) species depending on the pH of the solution. Zinc and copper phthalocyanine complexes do not catalyze the proton reduction reaction substantially. Electrode modification techniques affect the catalytic proton reduction activity of the complexes considerably. The most successful activity is recorded at pH 1.5 with the electrode modified by electropolymerization and dip coating of the CoPc on the GCE electrode.(C) 2008 International Association for Hydrogen Energy. Published by Elsevier Ltd. All rights reserved.
dc.language English
dc.publisher PERGAMON-ELSEVIER SCIENCE LTD
dc.subject Energy & Fuels
dc.title Electrocatalytic activity of phthalocyanines bearing thiophenes for hydrogen production from water
dc.type Article
dc.identifier.volume 33
dc.identifier.startpage 3281
dc.identifier.endpage 3288
dc.contributor.department Sakarya Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü
dc.contributor.saüauthor Kandaz, Mehmet
dc.relation.journal INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
dc.identifier.wos WOS:000258518000004
dc.identifier.doi 10.1016/j.ijhydene.2008.04.018
dc.contributor.author Kandaz, Mehmet


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