Enhancing carbon dioxide gas-diffusion electrolysis by creating a hydrophobic catalyst microenvironment
Nature Communications, ISSN: 2041-1723, Vol: 12, Issue: 1, Page: 136
2021
- 398Citations
- 379Captures
- 1Mentions
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations398
- Citation Indexes398
- 398
- CrossRef123
- Captures379
- Readers379
- 379
- Mentions1
- News Mentions1
- News1
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Durable CO2 conversion in the proton-exchange membrane system
Nature, Published online: 31 January 2024; doi:10.1038/s41586-023-06917-5 We develop a proton-exchange membrane system that reduces CO2 to formic acid at a catalyst that is derived from waste lead–acid batteries and in which a lattice carbon activation mechanism contributes.
Article Description
Electroreduction of carbon dioxide (CO) over copper-based catalysts provides an attractive approach for sustainable fuel production. While efforts are focused on developing catalytic materials, it is also critical to understand and control the microenvironment around catalytic sites, which can mediate the transport of reaction species and influence reaction pathways. Here, we show that a hydrophobic microenvironment can significantly enhance CO gas-diffusion electrolysis. For proof-of-concept, we use commercial copper nanoparticles and disperse hydrophobic polytetrafluoroethylene (PTFE) nanoparticles inside the catalyst layer. Consequently, the PTFE-added electrode achieves a greatly improved activity and Faradaic efficiency for CO reduction, with a partial current density >250 mA cm and a single-pass conversion of 14% at moderate potentials, which are around twice that of a regular electrode without added PTFE. The improvement is attributed to a balanced gas/liquid microenvironment that reduces the diffusion layer thickness, accelerates CO mass transport, and increases CO local concentration for the electrolysis.
Bibliographic Details
Springer Science and Business Media LLC
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