Highly efficient electro-reduction of CO2 to formic acid by nano-copperElectronic supplementary information (ESI) available: Details for confined jet mixer, morphology of CuO catalyst layers, analytical characterisation of electrolysis products and impedance spectroscopy model included. See DOI: 10.1039/c6ta04874a
Ultra-fine copper( ii ) oxide nanoparticles were used for the electrocatalytic reduction of CO 2 to formic acid at high Faradaic efficiencies. The nanoparticles were directly synthesised via continuous hydrothermal flow synthesis (CHFS) process, which used water as a solvent and reagent. The as-prep...
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Main Authors | , , |
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Format | Journal Article |
Published |
13.09.2016
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Online Access | Get full text |
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Summary: | Ultra-fine copper(
ii
) oxide nanoparticles were used for the electrocatalytic reduction of CO
2
to formic acid at high Faradaic efficiencies. The nanoparticles were directly synthesised
via
continuous hydrothermal flow synthesis (CHFS) process, which used water as a solvent and reagent. The as-prepared nanoparticles were subsequently formulated into Nafion based inks. For the electroreduction of CO
2
, the influence of Nafion fraction on the Faradaic efficiencies and overpotential (for formic acid production), was explored over a wide potential range. The highest Faradaic efficiency for formic acid production (61%) was observed with a 25 wt% Nafion fraction, at a potential of −1.4 V
vs.
Ag/AgCl. Some insights into the significant increase in Faradaic efficiency for the production of formic acid with the optimum Nafion content, was elucidated with electrochemical impedance spectroscopy.
Ultra-fine copper(
ii
) oxide nanoparticles were used for the electrocatalytic reduction of CO
2
to formic acid at high Faradaic efficiencies. |
---|---|
Bibliography: | Electronic supplementary information (ESI) available: Details for confined jet mixer, morphology of CuO catalyst layers, analytical characterisation of electrolysis products and impedance spectroscopy model included. See DOI 10.1039/c6ta04874a |
ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/c6ta04874a |