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机构地区:[1]中国科学院化学研究所,南京大学配位化学研究所
出 处:《分子催化》1996年第1期19-24,共6页Journal of Molecular Catalysis(China)
摘 要:合成了(2,9,16,23-四羧基)酞菁(H2TcPc)及其Co(Ⅱ)、Ru(Ⅲ)、Fe(Ⅲ)、Cu(Ⅱ)的配合物(CoTcPc、RuTcPc、FeTcPc、CuTcPc),用不可逆吸附法制备了这些化合物的玻碳修饰电极。研究这些修饰电极在酸性和碱性水溶液中对分子氧(O2)电还原的催化作用,发现酸性水溶液中,CoTcPc和RuTcPc修饰电极对电还原氧有催化活性,还原产物为过氧化氢;碱性水溶液中,四个配合物修饰电极对电还原氧都有催化活性,其中,FeTcPc还原氧的活性较好,它将分子氧(O2)一步直接还原为水。tetracarboxylphthocyanine(H2TcPc) and its Co(Ⅱ)、Fe(Ⅲ)、Cu(Ⅱ)、Ru(Ⅲ)coordination compounds(CoTcPc,FeTcPc,CuTcPc,RuTcPc) were synthesized and their chemical modified electrodes(CMEs) prepared.Activity of these CMEs towards the electroreduction of dioxygen in aqueous solution was investigated with cyclic voltammogram.The experiments showed that RuTcpc and CoTcPc were active in the acidic solution,with oxygen being reduced to peroxide;And CoTcPc,FeTcPc,CuTcPc,RuTcPc were active in the alkaline solution,with oxygen being reduced to peroxide on all the complexes with the exception of FeTcPc for which the reduction of dioxygen to water was observed.
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