Journal
JOURNAL OF MATERIALS SCIENCE
Volume 56, Issue 2, Pages 1255-1271Publisher
SPRINGER
DOI: 10.1007/s10853-020-05278-y
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- Istituto Italiano di Tecnologia within the CRUI-CARE Agreement
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High levels of atmospheric carbon dioxide are considered a main cause of global warming. Electrochemical conversion of CO2 into valuable chemicals and fuels has promising potential for practical and sustainable devices. Efforts have been focused on designing inexpensive, active, and selective catalysts produced through green methods, with copper-based materials showing enhanced activity and selectivity for CO reduction.
High level of atmospheric carbon dioxide (CO2) concentration is considered one of the main causes of global warming. Electrochemical conversion of CO(2)into valuable chemicals and fuels has promising potential to be implemented into practical and sustainable devices. In order to efficiently realize this strategy, one of the biggest efforts has been focused on the design of catalysts which are inexpensive, active and selective and can be produced through green and up-scalable routes. In this work, copper-based materials are simply synthesized via microwave-assisted process and carefully characterized by physical/chemical/electrochemical techniques. Nanoparticle with a cupric oxide (CuO) surface as well as various cuprous oxide (Cu2O) cubes with different sizes is obtained and used for the CO(2)reduction reaction. It is observed that the Cu2O-derived electrodes show enhanced activity and carbon monoxide (CO) selectivity compared to the CuO-derived one. Among various Cu2O catalysts, the one with the smallest cubes leads to the best CO selectivity of the electrode, attributed to a higher electrochemically active surface area. Under applied potentials, all Cu2O cubes undergo structural and morphological modification, even though the cubic shape is retained. The nanoclusters formed during the material evolution offer abundant and active reaction sites, leading to the high performance of the Cu2O-derived electrodes. [GRAPHICS] .
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