TY - JOUR
T1 - Progress and Perspectives of Electrochemical CO2 Reduction on Copper in Aqueous Electrolyte
AU - Nitopi, Stephanie A.
AU - Bertheussen, Erlend
AU - Scott, Søren Bertelsen
AU - Liu, Xinyan
AU - Engstfeld, Albert Kilian
AU - Horch, Sebastian
AU - Seger, Brian
AU - Stephens, Ifan
AU - Chan, Karen
AU - Hahn, Christopher
AU - Nørskov, Jens Kehlet
AU - Jaramillo, Thomas
AU - Chorkendorff, Ib
PY - 2019
Y1 - 2019
N2 - To date, copper is the only heterogeneous catalyst that has shown a propensity to produce valuable hydrocarbons and alcohols, such as ethylene and ethanol, from electrochemical CO2 reduction (CO2R). There are variety of factors that impact CO2R activity and selectivity, including the catalyst surface structure, morphology, composition, the choice of electrolyte ions and pH, and the electrochemical cell design. Many of these factors are often intertwined, which can complicate catalyst discovery and design efforts. Here we take a broad and historical view of these different aspects and their complex interplay in CO2R catalysis on Cu, with the purpose of providing new insights, critical evaluations, and guidance to the field with regard to research directions and best practices. First, we describe the various experimental probes and complementary theoretical methods that have been used to discern the mechanisms by which products are formed, and next we present our current understanding of the complex reaction networks for CO2R on Cu. We then analyze two key methods that have been used in attempts to alter the activity and selectivity of Cu: nanostructuring and the formation of bimetallic electrodes. Finally, we offer some perspectives on the future outlook for electrochemical CO2R.
AB - To date, copper is the only heterogeneous catalyst that has shown a propensity to produce valuable hydrocarbons and alcohols, such as ethylene and ethanol, from electrochemical CO2 reduction (CO2R). There are variety of factors that impact CO2R activity and selectivity, including the catalyst surface structure, morphology, composition, the choice of electrolyte ions and pH, and the electrochemical cell design. Many of these factors are often intertwined, which can complicate catalyst discovery and design efforts. Here we take a broad and historical view of these different aspects and their complex interplay in CO2R catalysis on Cu, with the purpose of providing new insights, critical evaluations, and guidance to the field with regard to research directions and best practices. First, we describe the various experimental probes and complementary theoretical methods that have been used to discern the mechanisms by which products are formed, and next we present our current understanding of the complex reaction networks for CO2R on Cu. We then analyze two key methods that have been used in attempts to alter the activity and selectivity of Cu: nanostructuring and the formation of bimetallic electrodes. Finally, we offer some perspectives on the future outlook for electrochemical CO2R.
U2 - 10.1021/acs.chemrev.8b00705
DO - 10.1021/acs.chemrev.8b00705
M3 - Journal article
C2 - 31117420
SN - 0009-2665
VL - 119
SP - 7610
EP - 7672
JO - Chemical Reviews
JF - Chemical Reviews
IS - 12
ER -