Abstract

Electrocatalytic carbon dioxide (CO<sub>2</sub>) reduction is considered as an economical and environmentally friendly approach to neutralizing and recycling greenhouse gas CO<sub>2</sub>. However, the design of preeminent and robust electrocatalysts for CO<sub>2</sub> electroreduction is still challenging. Herein, we report the <i>in-situ</i> growth of dense CuO<i><sub>x</sub></i> nanowire forest on 3D porous Cu foam (CuO<i><sub>x</sub></i>-NWF@Cu-F), which can be directly applied as a freestanding and binder-free working electrode for highly effective electrocatalytic CO<sub>2</sub> reduction. By adjusting the surface morphology and chemical composition of CuO<i><sub>x</sub></i> nanowires via surface reconstruction, large electrochemically active surface area and abundant Cu(+1) sites were generated, leading to remarkable activity for CO<sub>2</sub> electroreduction. The as-prepared hierarchical conductive electrode exhibited an enhanced Faradaic efficiency of 15.0% for ethanol formation (FE<sub>C<sub>2</sub></sub><sub>H<sub>5</sub></sub><sub>OH</sub>) and a total Faradaic efficiency of 69.4% for all carbonaceous compounds (FE<sub>C-total</sub>) at a mild applied potential of –0.45 V vs. RHE in 0.1 M KHCO<sub>3</sub> electrolyte. It achieved a 4-fold increase in FE<sub>C-total</sub> than that of Cu nanowire forest supported on 3D porous Cu foam (Cu-NWF@Cu-F) obtained by <i>in-situ</i> reduction of the CuO<i><sub>x</sub></i>-NWF@Cu-F via annealing at H<sub>2</sub> atmosphere, and thereby effectively suppressed the hydrogen evolution side-reaction.

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