Efficient wettability-controlled electroreduction of CO<sub>2</sub> to CO at Au/C interfaces.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 32541875.
- Also identified by DOI 10.1038/s41467-020-16847-9 and PMC identifier 7295780.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
The electrochemical CO<sub>2</sub> reduction reaction (CO<sub>2</sub>RR) represents a very promising future strategy for synthesizing carbon-containing chemicals in a more sustainable way. In spite of great progress in electrocatalyst design over the last decade, the critical role of wettability-controlled interfacial structures for CO<sub>2</sub>RR remains largely unexplored. Here, we systematically modify the structure of gas-liquid-solid interfaces over a typical Au/C gas diffusion electrode through wettability modification to reveal its contribution to interfacial CO<sub>2</sub> transportation and electroreduction. Based on confocal laser scanning microscopy measurements, the Cassie-Wenzel coexistence state is demonstrated to be the ideal three phase structure for continuous CO<sub>2</sub> supply from gas phase to Au active sites at high current densities. The pivotal role of interfacial structure for the stabilization of the interfacial CO<sub>2</sub> concentration during CO<sub>2</sub>RR is quantitatively analysed through a newly-developed in-situ fluorescence electrochemical spectroscopic method, pinpointing the necessary CO<sub>2</sub> mass transfer conditions for CO<sub>2</sub>RR operation at high current densities.