Unraveling the Highly Complex Nature of Antimony on Pt(111)
Source abstract
Abstract
Abstract Understanding the growth behavior of group‐V elements on metal surfaces provides valuable information that can shed light on the feasibility of tailoring atomically thin monoelemental 2D polymorphs composed of pnictogens on these metallic substrates. Here, by combining scanning tunneling microscopy (STM), low energy electron diffraction and Auger electron spectroscopy measurements under ultra‐high vacuum conditions, a wide variety of Sb reconstructions on single‐crystal Pt(111) are identified and characterized. At Sb coverage of ≈0.2 ML, STM data are compatible with a scenario in which Sb atoms are randomly embedded into the topmost layer of Pt, in a substitutional configuration and without establishing a periodic structure. This disorder is robust against thermal annealing and quenching. Increasing the surface coverage and whether or not the sample is annealed, different well‐ordered Sb phases are formed. The Sb structures synthesized at room temperature without any heating process are best interpreted as surface alloys that involve only the first atomic layer. In contrast, experimental evidence points towards the development of multilayer alloy phases for the annealed samples.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Surface and Thin Film Phenomena · Graphene research and applications · Topological Materials and Phenomena
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Departamento de Física de la Materia Condensada Universidad Autónoma de Madrid Madrid E‐28049 Spain
Instituto Nicolás Cabrera Universidad Autónoma de Madrid Madrid E‐28049 Spain
Condensed Matter Physics Center (IFIMAC) Universidad Autónoma de Madrid Madrid E‐28049 Spain
References (58)
Show source-provided references
1. 10.1126/science.110289610.1126/science.1102896 ↗
2. 10.1038/nmat480210.1038/nmat4802 ↗
3. 10.1039/C8CS00823J10.1039/C8CS00823J ↗
4. 10.1002/adfm.20200288510.1002/adfm.202002885 ↗
5. 10.1103/RevModPhys.81.10910.1103/RevModPhys.81.109 ↗
6. 10.1021/nl301047g10.1021/nl301047g ↗
7. 10.1021/nl304347w10.1021/nl304347w ↗
8. 10.1088/1367-2630/16/9/09500210.1088/1367-2630/16/9/095002 ↗
9. 10.1021/acsnano.8b0700610.1021/acsnano.8b07006 ↗
10. 10.1021/acs.nanolett.8b0042910.1021/acs.nanolett.8b00429 ↗
11. 10.1021/acs.nanolett.9b0244410.1021/acs.nanolett.9b02444 ↗
12. 10.1103/PhysRevB.89.20141210.1103/PhysRevB.89.201412 ↗
13. 10.1039/C7CP02949G10.1039/C7CP02949G ↗
14. 10.1021/acsnano.8b0146710.1021/acsnano.8b01467 ↗
15. 10.1039/C8NR00648B10.1039/C8NR00648B ↗
16. 10.1103/PhysRevB.102.12541810.1103/PhysRevB.102.125418 ↗
17. 10.1063/1.486096410.1063/1.4860964 ↗
18. 10.1016/j.elspec.2016.09.00510.1016/j.elspec.2016.09.005 ↗
19. 10.1088/1361-6528/abd97410.1088/1361-6528/abd974 ↗
20. 10.1021/acsami.5b0244110.1021/acsami.5b02441 ↗
21. 10.1002/anie.20141124610.1002/anie.201411246 ↗
22. 10.1038/ncomms1258510.1038/ncomms12585 ↗
23. 10.1038/srep1610810.1038/srep16108 ↗
24. Gibaja C. · Angew. Chem., Int. Ed. · 2016 · 55 · 14343
25. 10.1002/adma.20160212810.1002/adma.201602128 ↗
26. 10.1021/acsnano.9b0437710.1021/acsnano.9b04377 ↗
27. 10.1002/adma.20180613010.1002/adma.201806130 ↗
28. 10.1021/acs.nanolett.7b0211110.1021/acs.nanolett.7b02111 ↗
29. 10.1116/1.57839910.1116/1.578399 ↗
30. 10.1016/0039-6028(94)90377-810.1016/0039-6028(94)90377-8 ↗
31. 10.1016/0039-6028(96)00609-710.1016/0039-6028(96)00609-7 ↗
32. 10.1142/S0218625X9700154110.1142/S0218625X97001541 ↗
33. 10.1016/S0039-6028(98)00509-310.1016/S0039-6028(98)00509-3 ↗
34. 10.1103/PhysRevB.57.412710.1103/PhysRevB.57.4127 ↗
35. 10.1016/S0039-6028(99)00344-110.1016/S0039-6028(99)00344-1 ↗
36. 10.1016/S0039-6028(99)01185-110.1016/S0039-6028(99)01185-1 ↗
37. 10.1103/PhysRevB.61.1398310.1103/PhysRevB.61.13983 ↗
38. 10.1016/S0039-6028(02)01488-710.1016/S0039-6028(02)01488-7 ↗
39. 10.1016/S0039-6028(02)01556-X10.1016/S0039-6028(02)01556-X ↗
40. 10.1016/j.susc.2004.05.02110.1016/j.susc.2004.05.021 ↗
41. 10.1016/j.susc.2004.09.00510.1016/j.susc.2004.09.005 ↗
42. 10.1016/j.susc.2005.03.03410.1016/j.susc.2005.03.034 ↗
43. 10.1116/1.290524910.1116/1.2905249 ↗
44. 10.1103/PhysRevLett.71.243710.1103/PhysRevLett.71.2437 ↗
45. 10.1088/0953-8984/12/35/30410.1088/0953-8984/12/35/304 ↗
46. 10.1016/j.chemphys.2006.01.02910.1016/j.chemphys.2006.01.029 ↗
47. 10.1103/PhysRevB.80.24541110.1103/PhysRevB.80.245411 ↗
48. 10.1103/PhysRevLett.107.11680310.1103/PhysRevLett.107.116803 ↗
49. 10.1103/PhysRevB.75.24541210.1103/PhysRevB.75.245412 ↗
50. 10.1016/j.susc.2008.03.00810.1016/j.susc.2008.03.008 ↗
51. 10.1088/1367-2630/11/6/06304610.1088/1367-2630/11/6/063046 ↗
52. Dong G. C. · Phys. Rev. Lett. · 2010 · 104 · 4
53. 10.1063/1.167910610.1063/1.1679106 ↗
54. 10.1016/0039-6028(81)90176-X10.1016/0039-6028(81)90176-X ↗
55. 10.1103/PhysRevB.44.392610.1103/PhysRevB.44.3926 ↗
56. K. E. Hermann (FHI) and M. A. Van Hove (HKBU) LEEDpat (version 4.2) 2014; see alsohttp://www.fhi-berlin.mpg.de/KHsoftware/LEEDpat/index.html.
57. 10.1103/PhysRevB.67.23541010.1103/PhysRevB.67.235410 ↗
58. 10.1063/1.243241010.1063/1.2432410 ↗