Unknown

Dataset Information

0

Overpotential for CO2 electroreduction lowered on strained penta-twinned Cu nanowires.


ABSTRACT: Based on first-principles calculations, we predict that penta-twinned Cu nanowires (NWs) are superior to conventional Cu catalysts for CO2 electroreduction. The penta-twinned NWs possess a combination of ultrahigh mechanical strength, large surface-to-volume ratios and an abundance of undercoordinated adsorption sites, all desirable for CO2 electroreduction. In particular, we show that the penta-twinned Cu NWs can withstand elastic strains orders of magnitude higher than their conventional counterpart, and as a result their CO2 electroreduction activities can be significantly enhanced by elastic tensile strains. With a moderate tensile strain, the bias potential for methane production at a decent current density (2 mA cm-2) can be reduced by 50%. On the other hand, the competing hydrogen evolution reaction can be suppressed by the tensile strains. The presence of H at the NW surface is found to have a minor effect on CO2 electroreduction. Finally, we propose to use graphene as a substrate to stretch deposited Cu NWs.

SUBMITTER: Chen Z 

PROVIDER: S-EPMC5508656 | biostudies-literature | 2015 Dec

REPOSITORIES: biostudies-literature

altmetric image

Publications

Overpotential for CO<sub>2</sub> electroreduction lowered on strained penta-twinned Cu nanowires.

Chen Zhengzheng Z   Zhang Xu X   Lu Gang G  

Chemical science 20150819 12


Based on first-principles calculations, we predict that penta-twinned Cu nanowires (NWs) are superior to conventional Cu catalysts for CO<sub>2</sub> electroreduction. The penta-twinned NWs possess a combination of ultrahigh mechanical strength, large surface-to-volume ratios and an abundance of undercoordinated adsorption sites, all desirable for CO<sub>2</sub> electroreduction. In particular, we show that the penta-twinned Cu NWs can withstand elastic strains orders of magnitude higher than th  ...[more]

Similar Datasets

| S-EPMC6559126 | biostudies-literature
| S-EPMC9255670 | biostudies-literature
| S-EPMC4308715 | biostudies-literature
| S-EPMC8154520 | biostudies-literature