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Investigation of the electrocatalytic activity of metalophthalocyanine complexes for hydrogen production from water

机译:金属酞菁配合物对水制氢的电催化活性研究

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The electrocatalytic proton reduction activity of metallophthalocyanines was investigated by using Nafion (Nf) membrane on ITO electrode embedding different metallophthalocyanine derivatives such as cobalt phthalocyanine (CoPc) and palladium phthalocyanine (PdPc) carrying tetra tricarbetoxyethyl groups. Electrocatalytic studies of CoPc indicated that the proton reduction was catalyzed by the CoPc via the electroreduced Co~ⅠPc(-2) or Co~ⅠPc(-1). PdPc modified ITO electrode exhibited only one cathodic wave which can be easily attributed to the proton reduction. Comparison of this wave with the bare electrode indicates that the complex does not work as a catalyst for proton reduction. Analysis of the CVs of CoPc at different pHs indicates that activity of CoPc varies arbitrarily with increasing pH. The most successful activity is at pH 2.2.
机译:利用Nafion(Nf)膜在ITO电极上嵌入了带有四三碳氧羰基乙基的钴酞菁(CoPc)和酞菁钯(PdPc)等不同的金属酞菁衍生物,研究了金属酞菁的电催化质子还原活性。 CoPc的电催化研究表明,质子还原是通过电还原的Co〜ⅠPc(-2)或Co〜ⅠPc(-1)催化的。 PdPc修饰的ITO电极仅表现出一个阴极波,可以很容易地归因于质子的还原。该波与裸电极的比较表明该络合物不能用作质子还原的催化剂。 CoPc在不同pH值下的CV分析表明,CoPc的活性随pH值的增加而任意变化。最成功的活性是在pH 2.2下。

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