Heterometallic cluster improves catalytic performance for proton reduction, suggesting new electrocatalyst designs.
A heterometallic thiomolybdate cluster, Cp*3CoMo2S4 (Cp* = 1,2,3,4,5-pentamethylcyclopentadienide) has been synthesized and identified as a molecular electrocatalyst for proton reduction in dimethylformamide. Compared with its homometallic congener (Cp*3Mo3S4), cobalt incorporation improves activity by lowering the overpotential for proton reduction, consistent with the contrasting catalytic performance of MoS2 and its Co-doped derivative. Isolation of the reduced form of Cp*3CoMo2S4 and subsequent reactivity studies provide insight into the reaction pathway. These findings establish Cp*3CoMo2S4 as a molecular model for extended sulfide materials.
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Patra et al. (2025) studied this question.
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