Synthesis of PtSn4 Intermetallic Nanodisks through a Galvanic Replacement Mechanism
Source abstract
Abstract
Intermetallic compounds with ordered crystal structures are attractive materials with extensive applications in many fields. PtSn4, the most Sn-rich Pt–Sn intermetallic compound discovered so far, has special physical and catalytical properties because of the “Sn–Pt–Sn” layered crystal structure. However, studies on the property of PtSn4 have been limited to the single crystal due to the lack of success in preparing PtSn4 nanomaterials. Here, starting from Sn nanoparticles, we demonstrated the preparation of monodisperse pure-phase PtSn4 intermetallic nanodisks (PtSn4 NDs) based on a galvanic replacement mechanism. The structure of the as-synthesized PtSn4 NDs was carefully characterized and analyzed. A systematic study on the PtSn4 formation mechanism and kinetics confirms that the galvanic replacement mechanism governs the formation of PtSn4 NDs. In electrocatalytic furfural reduction, PtSn4 NDs effectively suppress the major competitive hydrogen evolution reaction and show faradaic efficiency superior to Pt nanoparticles.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Semiconductor materials and interfaces · Electrocatalysts for Energy Conversion · Semiconductor materials and devices
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, Iowa State University, Ames, Iowa 50011, United States
Department of Chemistry, University of Virginia, Charlottesville, Virginia 22904, United States
The U.S. Department of Energy, Ames Laboratory, Ames, Iowa 50011, United States
Funding
Division of Chemistry · Division of Chemical, Bioengineering, Environmental, and Transport Systems · Iowa State University
References (34)
Show source-provided references
1. 10.1073/pnas.210402611810.1073/pnas.2104026118 ↗
2. 10.1002/anie.20210721010.1002/anie.202107210 ↗
3. 10.1038/s41929-017-0022-010.1038/s41929-017-0022-0 ↗
4. 10.1038/s41929-021-00730-x10.1038/s41929-021-00730-x ↗
5. 10.1126/science.abd444110.1126/science.abd4441 ↗
6. 10.1038/s41467-021-23517-x10.1038/s41467-021-23517-x ↗
7. 10.1038/s41929-019-0334-310.1038/s41929-019-0334-3 ↗
8. 10.1038/s41586-021-03870-z10.1038/s41586-021-03870-z ↗
9. 10.1126/science.abg789410.1126/science.abg7894 ↗
10. 10.1088/1742-6596/1199/1/01203710.1088/1742-6596/1199/1/012037 ↗
11. 10.34133/2020/464350710.34133/2020/4643507 ↗
12. 10.1038/nphys371210.1038/nphys3712 ↗
13. 10.1002/anie.20190610910.1002/anie.201906109 ↗
14. 10.1039/c9ta10097k10.1039/c9ta10097k ↗
15. 10.1016/j.apsusc.2020.14592510.1016/j.apsusc.2020.145925 ↗
16. 10.1126/science.abj998010.1126/science.abj9980 ↗
17. 10.1016/j.poly.2015.09.03310.1016/j.poly.2015.09.033 ↗
18. 10.1039/c9ce00356h10.1039/c9ce00356h ↗
19. 10.1021/cm500719710.1021/cm5007197 ↗
20. 10.1039/b712035d10.1039/b712035d ↗
21. 10.1021/acscatal.5b0228110.1021/acscatal.5b02281 ↗
22. 10.1021/ja062799610.1021/ja0627996 ↗
23. 10.1021/ja069032y10.1021/ja069032y ↗
24. 10.1021/ar800018v10.1021/ar800018v ↗
25. 10.1038/s41467-020-16830-410.1038/s41467-020-16830-4 ↗
26. 10.1126/science.107722910.1126/science.1077229 ↗
27. 10.1126/science.123475110.1126/science.1234751 ↗
28. 10.1021/jacs.0c0945810.1021/jacs.0c09458 ↗
29. 10.1126/sciadv.abg193410.1126/sciadv.abg1934 ↗
30. 10.1021/jacs.6b0655810.1021/jacs.6b06558 ↗
31. 10.1021/acsami.1c0930110.1021/acsami.1c09301 ↗
32. 10.1021/acsnano.6b0339610.1021/acsnano.6b03396 ↗
33. 10.1039/c7nr01047h10.1039/c7nr01047h ↗
34. 10.1039/c5ee02666k10.1039/c5ee02666k ↗