Abstract
Energetically efficient electrochemical reduction of CO2 would offer the possibility of storing electricity from renewables in the form of fuels and other valuable chemicals. It may also help mitigate the increase of atmospheric CO2 associated with global warming. However, the process suffers from a low energy efficiency because of the large overpotentials required. In aqueous electrolytes, the competing hydrogen evolution reaction also decreases the faradaic efficiency (which contributes to the low energy efficiency of the process). Recent claims of high faradaic efficiency and low overpotentials for the reduction of CO2 in room-temperature ionic liquids (RTILs) and RTIL–water mixtures have spurred considerable research. Here, we offer a critical review of those claims and of recent work aimed at understanding the details of this important reaction in these nonconventional electrolytes.
| Original language | English |
|---|---|
| Pages (from-to) | 80-88 |
| Number of pages | 9 |
| Journal | Current Opinion in Electrochemistry |
| Volume | 23 |
| DOIs | |
| Publication status | Published - Oct 2020 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
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SDG 13 Climate Action
Keywords
- CO reduction reaction
- Computational methods
- In situ spectroscopy
- Room-temperature ionic liquids
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