Efficient Conversion of CO2 to CO Using Tin and Other Inexpensive and Easily Prepared Post-Transition Metal Catalysts

• Published in: Journal of the American Chemical Society 2015-04, Vol.137 (15), p.5021-5027
• Main Authors: Medina-Ramos, Jonnathan, Pupillo, Rachel C, Keane, Thomas P, DiMeglio, John L, Rosenthal, Joel
• Format: Article
• Language: English
• Subjects: INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/ja5121088

The development of affordable electrocatalysts that can drive the reduction of CO2 to CO with high selectivity, efficiency, and large current densities is a critical step on the path to production of liquid carbon-based fuels. In this work, we show that inexpensive triflate salts of Sn2+, Pb2+, Bi3+, and Sb3+ can be used as precursors for the electrodeposition of CO2 reduction cathode materials from MeCN solutions, providing a general and facile electrodeposition strategy, which streamlines catalyst synthesis. The ability of these four platforms to drive the formation of CO from CO2 in the presence of [BMIM]­OTf was probed. The electrochemically prepared Sn and Bi catalysts proved to be highly active, selective, and robust platforms for CO evolution, with partial current densities of j CO = 5–8 mA/cm2 at applied overpotentials of η < 250 mV. By contrast, the electrodeposited Pb and Sb catalysts do not promote rapid CO generation with the same level of selectivity. The Pb material is only ∼10% as active as the Sn and Bi systems at an applied potential of E = −1.95 V and is rapidly passivated during catalysis. The Sb-comprised cathode material shows no activity for conversion of CO2 to CO under analogous conditions. When taken together, this work demonstrates that 1,3-dialkylimidazoliums can promote CO production, but only when used in combination with an appropriately chosen electrocatalyst material. More broadly, these results suggest that the interactions between CO2, the imidazolium promoter, and the cathode surface are all critical to the observed catalysis.