» Articles » PMID: 33380454

Direct and Continuous Generation of Pure Acetic Acid Solutions Via Electrocatalytic Carbon Monoxide Reduction

Overview
Specialty Science
Date 2020 Dec 31
PMID 33380454
Citations 11
Authors
Affiliations
Soon will be listed here.
Abstract

Electrochemical CO or CO reduction to high-value C liquid fuels is desirable, but its practical application is challenged by impurities from cogenerated liquid products and solutes in liquid electrolytes, which necessitates cost- and energy-intensive downstream separation processes. By coupling rational designs in a Cu catalyst and porous solid electrolyte (PSE) reactor, here we demonstrate a direct and continuous generation of pure acetic acid solutions via electrochemical CO reduction. With optimized edge-to-surface ratio, the Cu nanocube catalyst presents an unprecedented acetate performance in neutral pH with other liquid products greatly suppressed, delivering a maximal acetate Faradaic efficiency of 43%, partial current of 200 mA⋅cm, ultrahigh relative purity of up to 98 wt%, and excellent stability of over 150 h continuous operation. Density functional theory simulations reveal the role of stepped sites along the cube edge in promoting the acetate pathway. Additionally, a PSE layer, other than a conventional liquid electrolyte, was designed to separate cathode and anode for efficient ion conductions, while not introducing any impurity ions into generated liquid fuels. Pure acetic acid solutions, with concentrations up to 2 wt% (0.33 M), can be continuously produced by employing the acetate-selective Cu catalyst in our PSE reactor.

Citing Articles

Observation of metal-organic interphase in Cu-based electrochemical CO-to-ethanol conversion.

Shen Y, Fang N, Liu X, Ling Y, Su Y, Tan T Nat Commun. 2025; 16(1):2073.

PMID: 40021652 PMC: 11871064. DOI: 10.1038/s41467-025-57221-x.


Solid-State-Electrolyte Reactor: New Opportunity for Electrifying Manufacture.

Liu C, Ji Y, Zheng T, Xia C JACS Au. 2025; 5(2):521-535.

PMID: 40017735 PMC: 11862930. DOI: 10.1021/jacsau.4c01183.


Switching CO-to-Acetate Electroreduction on Cu Atomic Ensembles.

Zhang L, Feng J, Wang R, Wu L, Song X, Jin X J Am Chem Soc. 2024; 147(1):713-724.

PMID: 39688936 PMC: 11726573. DOI: 10.1021/jacs.4c13197.


Investigation and Mitigation of Carbon Deposition over Copper Catalyst during Electrochemical CO Reduction.

DuanMu J, Wu Z, Gao F, Yang P, Niu Z, Zhang Y Precis Chem. 2024; 2(4):151-160.

PMID: 39473528 PMC: 11503900. DOI: 10.1021/prechem.4c00002.


Blended nexus molecules promote CO to l-tyrosine conversion.

Fan L, Zhu Z, Zhao S, Panda S, Zhao Y, Chen J Sci Adv. 2024; 10(36):eado1352.

PMID: 39241062 PMC: 11378904. DOI: 10.1126/sciadv.ado1352.


References
1.
Perez-Gallent E, Figueiredo M, Calle-Vallejo F, Koper M . Spectroscopic Observation of a Hydrogenated CO Dimer Intermediate During CO Reduction on Cu(100) Electrodes. Angew Chem Int Ed Engl. 2017; 56(13):3621-3624. DOI: 10.1002/anie.201700580. View

2.
Chu S, Cui Y, Liu N . The path towards sustainable energy. Nat Mater. 2016; 16(1):16-22. DOI: 10.1038/nmat4834. View

3.
Weng Z, Zhang X, Wu Y, Huo S, Jiang J, Liu W . Self-Cleaning Catalyst Electrodes for Stabilized CO Reduction to Hydrocarbons. Angew Chem Int Ed Engl. 2017; 56(42):13135-13139. DOI: 10.1002/anie.201707478. View

4.
Appel A, Bercaw J, Bocarsly A, Dobbek H, DuBois D, Dupuis M . Frontiers, opportunities, and challenges in biochemical and chemical catalysis of CO2 fixation. Chem Rev. 2013; 113(8):6621-58. PMC: 3895110. DOI: 10.1021/cr300463y. View

5.
Zhou G, Yang J . Formation of quasi-one-dimensional Cu2O structures by in situ oxidation of Cu(100). Phys Rev Lett. 2002; 89(10):106101. DOI: 10.1103/PhysRevLett.89.106101. View