journal article·2024-12

Liquid Metal Alloys Enable Efficient Formate Electrosynthesis

Haoling Huang, Xue Ding, Xinnan Mao, Yuchen Yan, Fang Lv, Binbin Pan, Wei Huang, Lu Wang, Na Han, Yanguang Li

Advanced Functional Materials· Volume 34· Issue 49
Publisher page

Abstract

Abstract Liquid metals are an interesting class of materials with the unique combination of metallic nature and liquid fluidity, and have recently been explored in many emerging fields. Their potential applications in catalysis, unfortunately, remain largely untapped. Herein, Ga‐mediated liquid metal alloying as an effective strategy is demonstrated to prepare functional alloys for catalysis. The alloying is carried out by dissolving indium or tin pellets in liquid gallium at room temperature or assisted by gentle heating, giving rise to binary Ga1−xInx and Ga1−xSnx liquid metal alloys with tunable chemical compositions. When further subjected to ultrasonication in water, they are ruptured into nanosized particles with liquid metal cores and thin surface oxide shells. Electrochemical measurements reveal that the liquid metal alloying significantly promotes electrocatalytic CO2 reduction to formate. Taking Ga0.75In0.25 as an example, its formate Faradaic efficiency is enhanced by 10%–20% compared to those of Ga and In, and its formate partial current density is 4–6 times larger than those of Ga and In. This enhancement is rationalized via computational simulations showing that the surrounding of In active sites with Ga atoms deactivates the undesirable reaction pathways to CO or H2, and facilitates selective formate electrosynthesis.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: CO2 Reduction Techniques and Catalysts · Advanced battery technologies research · Electrocatalysts for Energy Conversion

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

Affiliations

Institute of Functional Nano & Soft Materials (FUNSOM) Soochow University Suzhou 215123 China

Jiangsu Key Laboratory for Advanced Negative Carbon Technologies Soochow University Suzhou 215123 China

Macao Institute of Materials Science and Engineering (MIMSE) MUST‐SUDA Joint Research Center for Advanced Functional Materials Macau University of Science and Technology Taipa Macau SAR 999078 China

Funding

National Natural Science Foundation of China · Natural Science Foundation of Jiangsu Province · Collaborative Innovation Center of Suzhou Nano Science and Technology

References (52)

Show source-provided references
1. 10.1016/j.joule.2020.10.01210.1016/j.joule.2020.10.012 ↗
2. 10.1038/s41929-023-01083-310.1038/s41929-023-01083-3 ↗
3. 10.1039/C7CS00043J10.1039/C7CS00043J ↗
4. 10.1021/accountsmr.1c0014310.1021/accountsmr.1c00143 ↗
5. 10.1002/admt.20180042010.1002/admt.201800420 ↗
6. 10.1002/smll.20190339110.1002/smll.201903391 ↗
7. 10.1002/cctc.20230081410.1002/cctc.202300814 ↗
8. 10.1038/s41586-023-06082-910.1038/s41586-023-06082-9 ↗
9. 10.1126/science.aao424910.1126/science.aao4249 ↗
10. 10.1038/ncomms1006610.1038/ncomms10066 ↗
11. 10.1038/ncomms1543210.1038/ncomms15432 ↗
12. 10.1038/s41563-018-0084-710.1038/s41563-018-0084-7 ↗
13. 10.1038/s41467-019-08824-810.1038/s41467-019-08824-8 ↗
14. 10.1016/j.scib.2022.08.01110.1016/j.scib.2022.08.011 ↗
15. 10.1038/s41560-019-0450-y10.1038/s41560-019-0450-y ↗
16. 10.1039/D2EE00472K10.1039/D2EE00472K ↗
17. 10.1039/D0EE02981E10.1039/D0EE02981E ↗
18. 10.1126/science.aav350610.1126/science.aav3506 ↗
19. 10.1016/j.chempr.2018.08.01910.1016/j.chempr.2018.08.019 ↗
20. 10.1002/cssc.20160039410.1002/cssc.201600394 ↗
21. 10.1021/acs.iecr.7b0351410.1021/acs.iecr.7b03514 ↗
22. 10.1016/j.joule.2017.09.00310.1016/j.joule.2017.09.003 ↗
23. 10.1002/aenm.20190233810.1002/aenm.201902338 ↗
24. 10.1016/j.jechem.2018.12.00410.1016/j.jechem.2018.12.004 ↗
25. 10.1002/smsc.20210002910.1002/smsc.202100029 ↗
26. 10.1039/C8TA10959A10.1039/C8TA10959A ↗
27. 10.1002/anie.20210525610.1002/anie.202105256 ↗
28. 10.1038/nmat122310.1038/nmat1223 ↗
29. 10.1002/smtd.20230048210.1002/smtd.202300482 ↗
30. 10.1002/adma.20180561710.1002/adma.201805617 ↗
31. 10.1016/j.apcatb.2022.12137710.1016/j.apcatb.2022.121377 ↗
32. 10.1002/anie.20191483110.1002/anie.201914831 ↗
33. 10.1002/adfm.20210360110.1002/adfm.202103601 ↗
34. 10.1002/eem2.1250810.1002/eem2.12508 ↗
35. 10.1039/C9CY01396B10.1039/C9CY01396B ↗
36. 10.1007/BF0266367710.1007/BF02663677 ↗
37. 10.1007/BF0266748510.1007/BF02667485 ↗
38. 10.1021/jacs.2c0369810.1021/jacs.2c03698 ↗
39. 10.1002/adma.20220339110.1002/adma.202203391 ↗
40. 10.1021/acs.chemmater.0c0204710.1021/acs.chemmater.0c02047 ↗
41. 10.1002/sia.181710.1002/sia.1817 ↗
42. 10.1039/D2EE02147A10.1039/D2EE02147A ↗
43. 10.1002/anie.20221513610.1002/anie.202215136 ↗
44. 10.1039/C8TA08613C10.1039/C8TA08613C ↗
45. 10.1002/inf2.1225310.1002/inf2.12253 ↗
46. 10.1039/D0EE03756G10.1039/D0EE03756G ↗
47. 10.1038/s41578-021-00356-210.1038/s41578-021-00356-2 ↗
48. 10.1021/ja411388510.1021/ja4113885 ↗
49. 10.1039/C7TA07495F10.1039/C7TA07495F ↗
50. 10.1038/s41467-018-07419-z10.1038/s41467-018-07419-z ↗
51. 10.1002/anie.20210283210.1002/anie.202102832 ↗
52. 10.1016/j.apcatb.2021.11997910.1016/j.apcatb.2021.119979 ↗