Optimizing Cu+-Cu0 synergy by operando tracking of Cu2O nanocatalysts during the electrochemical CO2 reduction reaction

Abstract

Tracking the evolution of electrocatalysts over oxide-derived Cu materials during the electrochemical CO2 reduction reaction (eCO2RR) is pivotal for optimizing the product selectivity toward desired multi-carbon (C2+) products. However, the identification of the true intermediate active catalyst is still unclear. Here, we adopted a multi-modal characterization approach, primarily based on operando powder X-ray diffraction and operando micro-Raman spectroscopy, to study three Cu2O precursors with different morphologies, namely, octahedral (O-), cubic (C-), and nanowire (N-Cu2O). This multi-modal approach allows us to investigate the Cu2O nano-crystallites from the interface to the bulk structure. The results suggested notably different electrochemical reduction kinetics. 26.1% O-Cu2O and 90.6% C-Cu2O were reduced to much smaller Cu(0) domains after two hours of time-on-stream; N-Cu2O, with notably higher surface-to-volume ratio, was completely reduced within 45 min of time-on-stream. We accordingly observed a structure-reactivity correlation where a more intricate Cu2O/Cu grain network (and hence Cu+-Cu0 junctions) as observed in O-Cu2O, can lead to stable and quantitative production of ethylene at the Faradic efficiency of around 40% (in stark contrast to those of C- and N-Cu2O). The synergy between the Cu2O and Cu phases was also verified by density functional theory calculations. The upshifted d-band center of Cu2O/Cu in O-Cu2O is the most conducive toward the production of ethylene, whereas the downshifted d-band center of Cu2O/Cu in C-Cu2O leads to a decreased production of ethylene in the expense of unwanted production of hydrogen. We envisage that system optimization and design of new catalysts will become more facile and efficient using a related multi-modal operando characterization philosophy.