98%
921
2 minutes
20
Acidic CO electroreduction using diluted CO (as in flue gas) as the feedstock can simultaneously circumvent the CO purification step and lower the carbon loss in conventional alkaline or neutral electrolyte, and thus is highly desired but has rarely been achieved thus far. Herein, we report a simple and general strategy using an imidazolium-based anion-exchange ionomer as the coating layer, which could enrich the diluted CO to generate a high local CO concentration, and simultaneously block the proton transport to the cathode surface to suppress the competing hydrogen evolution reaction. As a result, the ionomer-modified Cu catalyst can achieve an efficient electroreduction of diluted CO (15 vol% CO) to multicarbon (C) products in strong acid (pH 0.8), with a high C Faradaic efficiency of 70.5% and a high single-pass carbon efficiency of 73.6% at a current density of 800 mA cm, competitive with that obtained with pure CO. These findings provide opportunity for the direct electrochemical conversion of flue gas into valuable products with high efficiency.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12075586 | PMC |
http://dx.doi.org/10.1038/s41467-025-59783-2 | DOI Listing |
Adv Mater
August 2025
Department of Chemistry, Northwestern University, Evanston, IL, 60208, USA.
Copper catalyst morphology, faceting, and oxidation state are each known to impact selectivity in the electroreduction of CO. Copper oxide precatalysts are synthesized using flash Joule heating and rapid cooling, and it is observed that temperature ramp rates can be used to control morphology, enabling us to implement ≈10 nm-sized intragrain features within ≈35 nm grains. It is found that the structural features of the precatalysts are substantially transferred to Cu catalysts that are formed when they are employed in CO electroreduction in a membrane electrode assembly electrolyzer.
View Article and Find Full Text PDFNat Commun
August 2025
Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), Renewable Energy Conversion and Storage Center (RECAST), Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), College of Chemistry, Nankai University, Tianjin, 300071, China. huan.wang0520@nankai
The electrocatalysis of flue gas into CO in membrane electrode assembly (MEA) provides a sustainable route for realizing practical CO electrolysis technology but suffers from restricted CO mass transport due to thick gas boundary layer (GBL) and weak concentration gradient. Inspired by nutrient diffusion mechanism in plant, we introduce the concept of self-reinforced CO concentration gradient, which is realized via porous carbon nanosheets (PC) as soil for enriching CO and single-atomic Ni-doped carbon nanotubes (Ni-CNTs) as rhizome for electro-catalyzing CO. A combined experimental and simulation study reveals optimal length of Ni-CNTs on PC reduces the GBL thickness and spontaneously enhances CO concentration gradient, synergistically breaking the limitation of CO transport.
View Article and Find Full Text PDFJ Am Chem Soc
June 2025
Key Laboratory of Synthetic and Biological Colloids, Ministry of Education, School of Chemical and Material Engineering, Jiangnan University, Wuxi 214122, China.
The electrochemical CO reduction reaction (CORR) to ethanol represents a sustainable avenue to close the carbon cycle and produce renewable fuels, yet challenges persist in achieving high selectivity and activity under industrially relevant dilute CO streams. Herein, we realize an efficient ethanol electrosynthesis by coating Cu catalysts with β-hydroxy ketone-based covalent organic polymers (COP), which not only activate CO but also balance the *CHO/*CO flux at the catalyst-electrolyte interface. The COP coated Cu NPs (Cu+COP) exhibits unprecedented FE of 54.
View Article and Find Full Text PDFNat Commun
May 2025
Department of Mechanical and Industrial Engineering, University of Toronto, Toronto, ON, Canada.
Electrocatalysis offers a promising route to convert CO into alcohols, which is most efficient in a two-step cascade reaction with CO-to-CO followed by CO-to-alcohol. However, current alcohol-producing CO/CO electrolyzers suffer from low selectivity or alcohol crossover, resulting in alcohol concentrations of less than 1%, which are further diluted in downstream cold-traps. As a result, electrocatalytic alcohol production has yet to be scaled beyond the lab (1-10 cm).
View Article and Find Full Text PDFAngew Chem Int Ed Engl
July 2025
Key Laboratory for Soft Chemistry and Functional Materials, School of Chemistry and Chemical Engineering, School of Energy and Power Engineering, Nanjing University of Science and Technology, Ministry of Education, Nanjing, 210094, P.R. China.
Using high-purity oxygen (O) for electrofixation would increase the production cost of hydrogen peroxide (HO) because of requiring complex pre-treatment procedures. Atmospheric air is an abundant source, but the direct air electrofixation has proved to be very challenging, that in common conception against nitrogen (N) in the system. According to the Le Chatelier's principle, O concentration is diluted by N (78%) in atmospheric air, which reduces overall reaction rates/equilibrium.
View Article and Find Full Text PDF