Selection of metal–tellurium (M–Te) alloy as Recyclable Controlled Te Precursors for Wafer‐Scale Synthesis of M x Te y Thin Films
Source abstract
Abstract
ABSTRACT Wafer‐scale synthesis of metal telluride films has been hindered by the high volatility and limited reactivity of tellurium. To overcome this, we introduce a confined tellurization strategy utilizing in situ formed metal–tellurium (M–Te) alloys as controllable Te sources. Systematic investigation on appropriate metal species through cohesive energy calculations and experiments demonstrates that the cohesive energy of the source metal and metal‐to‐Te atomic ratio in the source bilayer are the key parameters dictating Te flux. Among many metals, Au–Te and Ag–Te alloys provide steady Te flux while preventing the delamination of M/Te bilayer (observed with Pt, Mo, Cu) after metal deposition on Te layer and the undesired co‐evaporation of metal (observed with In, Zn) during Te supply for M x Te y synthesis. With the Au–Te alloy, atomically‐smooth, single‐crystalline 4‐inch Si 2 Te 3 thin films are produced, which are the largest reported to date. The film thickness can be modulated by adjusting the Au/Te ratio, verified by structural and spectroscopic characterization. The generality of this concept is verified by synthesizing other tellurides, including MoTe 2 and Cr 2 Te 3 . The M–Te alloy source is recyclable by replenishing Te on the alloy, establishing this methodology as a robust and versatile platform for producing a wide range of high‐quality metal telluride films.
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Research context
OpenAlex topics: 2D Materials and Applications · Chalcogenide Semiconductor Thin Films · Advanced Thermoelectric Materials and Devices
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Material Science and Engineering Pohang University of Science and Technology (POSTECH) Pohang Republic of Korea
Department of Mechanical Engineering Dong‐A University (DAU) Busan Republic of Korea
Funding
National Research Foundation of Korea
References (66)
Show source-provided references
1. 10.1038/s41565-023-01413-310.1038/s41565-023-01413-3 ↗
2. 10.1038/s41565-020-00789-w10.1038/s41565-020-00789-w ↗
3. 10.1021/acsnano.0c0018010.1021/acsnano.0c00180 ↗
4. 10.1002/adma.20241571710.1002/adma.202415717 ↗
5. 10.1002/lpor.20250111910.1002/lpor.202501119 ↗
6. 10.1021/acs.nanolett.3c0239610.1021/acs.nanolett.3c02396 ↗
7. 10.1038/s41377-022-01047-510.1038/s41377-022-01047-5 ↗
8. 10.1063/5.020424810.1063/5.0204248 ↗
9. 10.1126/science.abq088310.1126/science.abq0883 ↗
10. 10.1021/acs.nanolett.8b0517410.1021/acs.nanolett.8b05174 ↗
11. Low Power Flexible Monolayer MoS2 Integrated Circuits
12. 10.1038/s41467‐021‐27195‐710.1038/s41467‐021‐27195‐7 ↗
13. 10.1038/s41565-021-01004-010.1038/s41565-021-01004-0 ↗
14. 10.1002/adma.20200660110.1002/adma.202006601 ↗
15. 10.1002/admi.20210236010.1002/admi.202102360 ↗
16. 10.1038/s41467-021-23711-x10.1038/s41467-021-23711-x ↗
17. 10.1038/s41699-021-00264-710.1038/s41699-021-00264-7 ↗
18. 10.1021/acs.chemmater.7b0160510.1021/acs.chemmater.7b01605 ↗
19. 10.1002/adma.20220337310.1002/adma.202203373 ↗
20. 10.1021/acs.chemrev.0c0119110.1021/acs.chemrev.0c01191 ↗
21. 10.1021/acs.chemrev.3c0085110.1021/acs.chemrev.3c00851 ↗
22. 10.1021/acsnano.5c1542210.1021/acsnano.5c15422 ↗
23. 10.1021/acsnano.4c0286310.1021/acsnano.4c02863 ↗
24. 10.1038/s41467-017-02238-010.1038/s41467-017-02238-0 ↗
25. 10.1002/adma.20160347110.1002/adma.201603471 ↗
26. 10.1021/acsnano.0c0943010.1021/acsnano.0c09430 ↗
27. 10.1039/D0NR01730B10.1039/D0NR01730B ↗
28. 10.1002/adma.20170726010.1002/adma.201707260 ↗
29. 10.1021/acsanm.9b0177410.1021/acsanm.9b01774 ↗
30. 10.1002/adma.20170527010.1002/adma.201705270 ↗
31. 10.1002/adma.20210225210.1002/adma.202102252 ↗
32. 10.1038/s41928-020-0396-x10.1038/s41928-020-0396-x ↗
33. 10.1038/s41467‐023‐40448‐x10.1038/s41467‐023‐40448‐x ↗
34. 10.3390/nano1223413310.3390/nano12234133 ↗
35. 10.1063/5.026261910.1063/5.0262619 ↗
36. 10.1021/nl504330g10.1021/nl504330g ↗
37. 10.1063/1.170928710.1063/1.1709287 ↗
38. 10.1063/1.494856510.1063/1.4948565 ↗
39. 10.1021/acs.nanolett.5c0508510.1021/acs.nanolett.5c05085 ↗
40. 10.1002/adfm.20210108610.1002/adfm.202101086 ↗
41. 10.1038/s41699-025-00553-510.1038/s41699-025-00553-5 ↗
42. 10.1016/0022‐0248(93)90501‐M10.1016/0022‐0248(93)90501‐M ↗
43. 10.1016/0022-0248(92)90572-Z10.1016/0022-0248(92)90572-Z ↗
44. 10.1016/j.calphad.2008.09.00910.1016/j.calphad.2008.09.009 ↗
45. 10.1021/nn202996r10.1021/nn202996r ↗
46. 10.1021/jacs.6b1107610.1021/jacs.6b11076 ↗
47. 10.1038/s41928‐024‐01158‐410.1038/s41928‐024‐01158‐4 ↗
48. 10.1002/smsc.20230014410.1002/smsc.202300144 ↗
49. 10.1021/acsnano.0c0593610.1021/acsnano.0c05936 ↗
50. 10.1002/smll.20210214610.1002/smll.202102146 ↗
51. 10.1002/admi.20180173310.1002/admi.201801733 ↗
52. 10.1021/acsmaterialslett.3c0039510.1021/acsmaterialslett.3c00395 ↗
53. 10.1021/acs.jpcc.2c0190510.1021/acs.jpcc.2c01905 ↗
54. 10.1039/D4NR00687A10.1039/D4NR00687A ↗
55. 10.1103/PhysRevB.54.1116910.1103/PhysRevB.54.11169 ↗
56. 10.1016/0927‐0256(96)00008‐010.1016/0927‐0256(96)00008‐0 ↗
57. 10.1103/PhysRevLett.77.386510.1103/PhysRevLett.77.3865 ↗
58. 10.1103/PhysRevB.13.518810.1103/PhysRevB.13.5188 ↗
59. 10.1063/1.338234410.1063/1.3382344 ↗
60. 10.1021/acsami.3c0126710.1021/acsami.3c01267 ↗
61. 10.1021/acs.inorgchem.5c0408410.1021/acs.inorgchem.5c04084 ↗
62. 10.1002/sstr.20250004810.1002/sstr.202500048 ↗
63. 10.1038/s41467‐020‐15933‐210.1038/s41467‐020‐15933‐2 ↗
64. 10.1016/j.commatsci.2020.11022810.1016/j.commatsci.2020.110228 ↗
65. 10.1039/C4RA10726H10.1039/C4RA10726H ↗
66. 10.1063/1.503750010.1063/1.5037500 ↗