Abstract
We report a highly active copper-based catalyst for electrochemical CO2 reduction. Electrochemical analysis revealed that the maximum turnover frequency for CO2 to CO conversion reached 1 460 000 s-1 at an overpotential (η) of 0.85 V. Surprisingly, this value is more than 1 000 000 times higher than those of other reported copper-based molecular catalysts.
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