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Issue 48, 2016
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One dimensional metal dithiolene (M = Ni, Fe, Zn) coordination polymers for the hydrogen evolution reaction

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Abstract

Immobilization of metal complexes to electrode surfaces has emerged as an attractive strategy to combine homogeneous and heterogeneous catalysis. We recently reported the immobilization of cobalt dithiolene catalytic units via incorporation into extended one and two dimensional (1D and 2D) frameworks. We extend here this methodology to the formation of 1D nickel, iron, and zinc dithiolene coordination polymers based on benzene-1,2,4,5-tetrathiolate (BTT) frameworks and investigate their catalytic H2-evolving activities under fully aqueous conditions. The nickel dithiolene coordination polymer is an active electrocatalyst for the hydrogen evolution reaction (HER). An overpotential of 470 mV was required to reach a current density of 10 mA cm−2 at pH 1.3, making this system one of the best performing heterogenized molecular catalysts for HER. This overpotential is 90 mV lower than that of the cobalt analogue, suggesting that the nickel coordination polymer is a more efficient H2-evolving catalyst. Additionally, no decrease in activity is observed for the nickel polymer during the first hour of electrolysis, indicating that it is stable under prolonged electrolysis.

Graphical abstract: One dimensional metal dithiolene (M = Ni, Fe, Zn) coordination polymers for the hydrogen evolution reaction

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Publication details

The article was received on 17 Aug 2016, accepted on 11 Nov 2016 and first published on 14 Nov 2016


Article type: Paper
DOI: 10.1039/C6DT03257E
Dalton Trans., 2016,45, 19311-19321

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    One dimensional metal dithiolene (M = Ni, Fe, Zn) coordination polymers for the hydrogen evolution reaction

    C. A. Downes and S. C. Marinescu, Dalton Trans., 2016, 45, 19311
    DOI: 10.1039/C6DT03257E

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