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Metal-Organic Framework Supported Low-Nuclearity Cluster Catalysts for Highly Selective Carbon Dioxide Electroreduction to Ethanol.

Authors :
Shao B
Huang D
Huang RK
He XL
Luo Y
Xiang YL
Jiang LB
Dong M
Li S
Zhang Z
Huang J
Source :
Angewandte Chemie (International ed. in English) [Angew Chem Int Ed Engl] 2024 Nov 04; Vol. 63 (45), pp. e202409270. Date of Electronic Publication: 2024 Jul 31.
Publication Year :
2024

Abstract

It is still a great challenge to achieve high selectivity of ethanol in CO <subscript>2</subscript> electroreduction reactions (CO <subscript>2</subscript> RR) because of the similar reduction potentials and lower energy barrier of possible other C <subscript>2+</subscript> products. Here, we report a MOF-based supported low-nuclearity cluster catalysts (LNCCs), synthesized by electrochemical reduction of three-dimensional (3D) microporous Cu-based MOF, that achieves a single-product Faradaic efficiency (FE) of 82.5 % at -1.0 V (versus the reversible hydrogen electrode) corresponding to the effective current density is 8.66 mA cm <superscript>-2</superscript> . By investigating the relationship between the species of reduction products and the types of catalytic sites, it is confirmed that the multi-site synergism of Cu LNCCs can increase the C-C coupling effect, and thus achieve high FE of CO <subscript>2</subscript> -to-ethanol. In addition, density functional theory (DFT) calculation and operando attenuated total reflectance surface-enhanced infrared absorption spectroscopy further confirmed the reaction path and mechanism of CO <subscript>2</subscript> -to-EtOH.<br /> (© 2024 Wiley-VCH GmbH.)

Details

Language :
English
ISSN :
1521-3773
Volume :
63
Issue :
45
Database :
MEDLINE
Journal :
Angewandte Chemie (International ed. in English)
Publication Type :
Academic Journal
Accession number :
38880988
Full Text :
https://doi.org/10.1002/anie.202409270