Single Pass CO<sub>2</sub> Conversion Exceeding 85% in the Electrosynthesis of Multicarbon Products via Local CO<sub>2</sub> Regeneration
Colin P. O’Brien, Rui Kai Miao, Shijie Liu, Yi Xu, Geonhui Lee, Anthony Robb, Jianan Erick Huang, Ke Xie, Koen Bertens, Christine M. Gabardo, Jonathan P. Edwards, Cao‐Thang Dinh, Edward H. Sargent, David Sinton
Abstract
The carbon dioxide reduction reaction (CO2RR) presents the opportunity to consume CO2 and produce desirable products. However, the alkaline conditions required for productive CO2RR result in the bulk of input CO2 being lost to bicarbonate and carbonate. This loss imposes a 25% limit on the conversion of CO2 to multicarbon (C2+) products for systems that use anions as the charge carrier—and overcoming this limit is a challenge of singular importance to the field. Here, we find that cation exchange membranes (CEMs) do not provide the required locally alkaline conditions, and bipolar membranes (BPMs) are unstable, delaminating at the membrane–membrane interface. We develop a permeable CO2 regeneration layer (PCRL) that provides an alkaline environment at the CO2RR catalyst surface and enables local CO2 regeneration. With the PCRL strategy, CO2 crossover is limited to 15% of the amount of CO2 converted into products, in all cases. Low crossover and low flow rate combine to enable a single pass CO2 conversion of 85% (at 100 mA/cm2), with a C2+ faradaic efficiency and full cell voltage comparable to the anion-conducting membrane electrode assembly.