Abstract
Upgrading carbon dioxide/monoxide to multi-carbon C2+ products using renewable electricity offers one route to more sustainable fuel and chemical production. One of the most appealing products is acetate, the profitable electrosynthesis of which demands a catalyst with higher efficiency. Here, a coordination polymer (CP) catalyst is reported that consists of Cu(I) and benzimidazole units linked via Cu(I)-imidazole coordination bonds, which enables selective reduction of CO to acetate with a 61% Faradaic efficiency at −0.59 volts versus the reversible hydrogen electrode at a current density of 400 mA cm−2 in flow cells. The catalyst is integrated in a cation exchange membrane-based membrane electrode assembly that enables stable acetate electrosynthesis for 190 h, while achieving direct collection of concentrated acetate (3.3 molar) from the cathodic liquid stream, an average single-pass utilization of 50% toward CO-to-acetate conversion, and an average acetate full-cell energy efficiency of 15% at a current density of 250 mA cm−2. © 2023 Wiley-VCH GmbH.
| Original language | English |
|---|---|
| Article number | 2209567 |
| Journal | Advanced Materials |
| Volume | 35 |
| Issue number | 10 |
| Online published | 30 Dec 2022 |
| DOIs | |
| Publication status | Published - 9 Mar 2023 |
| Externally published | Yes |
Research Keywords
- acetate
- CO/CO2 reduction
- coordination polymers
- electrosynthesis
- MEA