Abstract
A cobalt bis(iminopyridine) complex is a highly active electrocatalyst for water reduction, with an estimated apparent second order rate constant k(app) ≤ 10(7) M(-1)s(-1) over a range of buffer/salt concentrations. Scan rate dependence data are consistent with freely diffusing electroactive species over pH 4-9 at room temperature for each of two catalytic reduction events, one of which is believed to be ligand based. Faradaic H(2) yields up to 87 ± 10% measured in constant potential electrolyses (-1.4 V vs SCE) confirm high reactivity and high fidelity in a catalyst supported by the noninnocent bis(iminopyridine) ligand. A mechanism involving initial reduction of Co(2+) and subsequent protonation is proposed.
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