Fig. 4: Electrochemical CO2R performance on Cu0.9Zn0.1 catalysts fabricated by co-sputtering and wet-chemical-etching at pH 1–13.5. | Nature Communications

Fig. 4: Electrochemical CO2R performance on Cu0.9Zn0.1 catalysts fabricated by co-sputtering and wet-chemical-etching at pH 1–13.5.

From: Accelerating electrochemical CO2 reduction to multi-carbon products via asymmetric intermediate binding at confined nanointerfaces

Fig. 4

a C2+ FEs at different current densities at pH 1, 4, 7, and 13.5, respectively. b Single-pass C2+ yield at different CO2 flow rates and current densities at pH 1, 4, 7, and 13.5 in a 13.5 cm2 cell. c CO2R stability curves with C2+ FEs at pH 4, 7, and 13.5 in a three-electrode flow cell. Current densities were optimized: 400 mA cm−2 at pH 4, 300 mA cm−2 at pH 7, and 150 mA cm−2 at pH 13.5, respectively (spheres: C2+ FEs, lines: cathodic potentials). d C2+/C1 ratios at different current densities at pH 1, 4, 7, and 13.5. e Comparison of C2+ FE, single-pass C2+ yield, and full-cell C2+ EE with previous reports (solid sphere: C2+ in electrocatalysis, hollow sphere: C2–4 in thermocatalysis, Supplementary Tables 20, 21). f C2+ energy efficiency (EE) at different current densities at pH 1, 4, 7, and 13.5 (sphere: cathodic C2+ EE, square: full-cell C2+ EE). g CO2R stability with C2+ and ethylene FEs at 150 mA cm−2 for Cu0.9Zn0.1 coated with graphite/carbon nanoparticles using a slim two-electrode flow-cell (The changed current density cycles consist of the work period at −150 mA cm−2 for 120 s (lower black line) and the regeneration period at −1 mA cm−2 for 30 s (upper black line)). Error bars in a, b, d, f represent the standard deviation based on three independent measurements.

Back to article page