Abstract
Electrochemical reduction of CO 2 to formate is a promising approach to utilize intermittent renewable energy for high-value chemical storage and to mitigate carbon pollution. Demanding applied targets for this process require that the reaction is sustained at a high current density with near-unity product efficiency. In this issue of Joule , Zheng and De Luna et al. show that incorporating sulfur into tin catalysts greatly increases the reaction rate while maintaining high selectivity and robust stability.
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