Affiliation:
1. Department of Chemistry and Centre for Atomic Engineering of Advanced Materials Key Laboratory of Structure and Functional Regulation of Hybrid Materials of Ministry of Education Institutes of Physical Science and Information Technology and Anhui Province Key Laboratory of Chemistry for Inorganic/Organic Hybrid Functionalized Materials Anhui University 230601 Hefei China
Abstract
AbstractRecently, CO2 hydrogenation had a new breakthrough resulting from the design of catalysts to effectively activate linear CO2 with symmetry‐breaking sites. However, understanding the relationship between symmetry‐breaking sites and catalytic activity at the atomic level is still a great challenge. In this study, a set of gold‐copper alloy Au13Cux (x=0–4) nanoclusters were used as research objects to show the symmetry‐controlled breaking structure on the surface of nanoclusters with the help of manipulability of the Cu atoms. Among them, Au13Cu3 nanocluster displays the highest degree of symmetry‐breaking on its crystal structure compared with the other nanoclusters in the family. Where the three copper atoms occupying the surface of the icosahedral kernel unevenly with one copper atom is coordinately unsaturated (CuS2 motif relative to CuS3 motif). As expected, Au13Cu3 has an excellent hydrogenation activity of CO2, in which the current density is as high as 70 mA cm−2 (−0.97 V) and the maximum FECO reaches 99 % at −0.58 V. Through the combination of crystal structures and theoretical calculations, the excellent catalytic activity of Au13Cu3 is revealed to be indeed closely related to its asymmetric structure.
Funder
National Natural Science Foundation of China
Cited by
2 articles.
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