Related Experiment Video
Updated: Jun 2, 2025

Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
Published on: April 10, 2018
Isolated Tin Enhanced CO Coverage-Regulation on Sn1Cu Alloy for Selective CO2 Electroreduction to C2+ Products
Yijiang Liu1, Zongye Yue1, Chenghao Jin1
1International Collaborative Center on Photoelectric Technology and Nano Functional Materials, Institute of Photonics & Photon-Technology, Northwest University, Xi'an, 710069, P. R. China.
Abstract:
Electricity-powered C─C coupling of CO2 represents an attractive strategy for producing valuable commodity chemicals with renewable energy, but it is still challenging to gain high C2+ selectivity at high current density. Here, a Sn1Cu single-atom alloy (SAA) is reported with isolated Sn atom embedded into the Cu lattice, as efficient ectrocatalyst for CO2 reduction. The as prepared Sn1Cu-SAA catalyst shows a maximal C2+ Faradaic efficiency of 79.3% at 800 mA cm-2, which can be kept stable for at least 16 h. The combination of in situ spectroscopy and DFT calculation reveal that the introduced Sn atom promote the activation of CO2 to *CO, and enhance the CO coverage on Sn1Cu-SAA. As results, the reaction barrier of C─C coupling pathway is significantly reduced, boosting the generation of C2+ products. These findings offer a novel sight for fabricating multicarbon products from CO2 via regulation the concentration of intermediates on catalytic interface.
More Related Videos
Related Concept Videos
Precipitation and Co-precipitation
Electrodeposition
Electrodeposition can...
Extraction: Advanced Methods
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation...
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Radical Reactivity: Concentration Effects

