journal article·2016-09-07

Bifunctional Interface of Au and Cu for Improved CO2 Electroreduction

Seoin Back, Jun-Hyuk Kim, Yong-Tae Kim, Yousung Jung

Publisher page

Abstract

Gold is known currently as the most active single-element electrocatalyst for CO2 electroreduction reaction to CO. In this work, we combine Au with a second metal element, Cu, to reduce the amount of precious metal content by increasing the surface-to-mass ratio and to achieve comparable activity to Au-based catalysts. In particular, we demonstrate that the introduction of a Au-Cu bifunctional "interface" is more beneficial than a simple and conventional homogeneous alloying of Au and Cu in stabilizing the key intermediate species, *COOH. The main advantages of the proposed metal-metal bifunctional interfacial catalyst over the bimetallic alloys include that (1) utilization of active materials is improved, and (2) intrinsic properties of metals are less affected in bifunctional catalysts than in alloys, which can then facilitate a rational bifunctional design. These results demonstrate for the first time the importance of metal-metal interfaces and morphology, rather than the simple mixing of the two metals homogeneously, for enhanced catalytic synergies.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: CO2 Reduction Techniques and Catalysts · Electrocatalysts for Energy Conversion · Electrochemical Analysis and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Graduate School of EEWS, Korea Advanced Institute of Science and Technology (KAIST), 291 Daehakro, Daejeon 34141, Korea

Department of Energy System, School of Mechanical Engineering, Pusan National University, Busan 609-735, Korea

Hybrid Materials Solution National Core Research Center (NCRC), Pusan National University, Busan 609-735, Korea

Funding

National Research Foundation of Korea · Agency for Defense Development · Korea Institute of Energy Technology Evaluation and Planning

References (37)

Show source-provided references
1. 10.1021/jz101262710.1021/jz1012627 ↗
2. 10.1039/c0ee00071j10.1039/c0ee00071j ↗
3. 10.1021/cs501229810.1021/cs5012298 ↗
4. 10.1021/cs501600x10.1021/cs501600x ↗
5. 10.1021/jz201461p10.1021/jz201461p ↗
6. 10.1021/ja505791r10.1021/ja505791r ↗
7. 10.1021/jp509967m10.1021/jp509967m ↗
8. 10.1021/ja309317u10.1021/ja309317u ↗
9. 10.1021/ja509509910.1021/ja5095099 ↗
10. 10.1021/ja409445p10.1021/ja409445p ↗
11. 10.1038/nchem.36710.1038/nchem.367 ↗
12. 10.1038/nmat379510.1038/nmat3795 ↗
13. 10.1039/C5CP07717F10.1039/C5CP07717F ↗
14. 10.1038/ncomms594810.1038/ncomms5948 ↗
15. 10.1021/ja010963d10.1021/ja010963d ↗
16. 10.1038/nmat122310.1038/nmat1223 ↗
17. 10.1103/PhysRevLett.77.386510.1103/PhysRevLett.77.3865 ↗
18. 10.1103/PhysRevB.59.741310.1103/PhysRevB.59.7413 ↗
19. 10.1103/PhysRevB.50.1795310.1103/PhysRevB.50.17953 ↗
20. 10.1103/PhysRevB.59.175810.1103/PhysRevB.59.1758 ↗
21. 10.1016/0927-0256(96)00008-010.1016/0927-0256(96)00008-0 ↗
22. 10.1103/PhysRevB.13.518810.1103/PhysRevB.13.5188 ↗
23. 10.1021/jp047349j10.1021/jp047349j ↗
24. 10.1021/acscatal.5b0046210.1021/acscatal.5b00462 ↗
25. 10.1021/jz302115510.1021/jz3021155 ↗
26. 10.1016/j.susc.2011.04.02810.1016/j.susc.2011.04.028 ↗
27. 10.1038/nmat175210.1038/nmat1752 ↗
28. 10.1126/science.113594110.1126/science.1135941 ↗
29. 10.1038/nmat184010.1038/nmat1840 ↗
30. 10.1021/nl500037x10.1021/nl500037x ↗
31. 10.1021/cs300227s10.1021/cs300227s ↗
32. 10.1039/B615547B10.1039/B615547B ↗
33. 10.1038/nchem.12110.1038/nchem.121 ↗
34. 10.1063/1.481232310.1063/1.4812323 ↗
35. 10.1103/PhysRevB.45.1031410.1103/PhysRevB.45.10314 ↗
36. 10.1021/jp047576l10.1021/jp047576l ↗
37. 10.1023/A:101902061433610.1023/A:1019020614336 ↗