Fig. 3: Monitoring CO2 reduction/CO oxidation interconversion via electrochemistry. | Nature Communications

Fig. 3: Monitoring CO2 reduction/CO oxidation interconversion via electrochemistry.

From: Energy-efficient CO2/CO interconversion by homogeneous copper-based molecular catalysts

Fig. 3

A The comparative cyclic voltammograms of 1 mM C1 recorded under 1 atmospheric (atm) CO2 in DMF (purple trace) and 0.2 M water containing DMF (green trace). B The analogous data measured for 1 mM C2 recorded in DMF (green trace) and 0.45 M water containing DMF (blue trace). The scan rate for these experiments were 0.1 V/s and nBu4N+BF4- was used as electrolyte. The comparative cyclic voltammograms of C 0.5 mM C1 under 1 atm Ar (red dotted trace) and 1 atm CO2 (solid blue trace), and D 0.5 mM C2 under 1 atm Ar (green dotted trace) and 1 atm CO2 (solid purple trace) in an aqueous solution of pH 6.5. The scan rate for these experiments were 1.0 V/s and Na2SO4 was used as electrolyte. The cyclic voltammograms of E 0.5 mM C1 (solid blue trace) and F 0.5 mM C2 (solid purple trace) under 1 atm of 1:1 CO2/CO mixture. The blank data under analogous conditions are shown in black dotted trace. The scan rate for these experiments were 0.1 V/s and Na2SO4 was used as electrolyte. The horizontal arrows in (A–F) signify the initial scan direction. The electrocatalytic CO2 reduction and CO oxidation responses are represented by the blue and red boxes, respectively.

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