journal article·2025-05-07

Greatly Enhanced Radiative Recombination at High Exciton Density in Acid-Treated 2D Alloy

Matej Sebek, Gang Wu, Zeng Wang, Michael Sullivan, Debbie Hwee Leng Seng, Xiao Di Su, Nguyen Thi Kim Thanh, Jinghua Teng

ACS Applied Materials & Interfaces· Volume 17· Issue 18
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Abstract

Enhanced photoluminescence (PL) in transition metal dichalcogenides (TMDs) is critical for their application in optoelectronics. In this study, we report a 99 × PL enhancement in a superacid bis(trifluoromethane) sulfonimide (TFSI)-treated MoS 2(1– x ) Se 2 x alloy. The alloy’s optical bandgap is tunable by changing its stoichiometry, allowing for PL enhancement at tailored positions. The PL enhancement is robust even at high excitation power, overcoming the limitation of exciton–exciton annihilation observed in MoS 2 . Through molecular dynamics simulations and spectroscopic analysis, we demonstrate that the MoS 2(1– x ) Se 2 x monolayer inherently exhibits moderate strain, which shifts the van Hove singularity in the S-rich domain. Furthermore, density functional theory calculations reveal the absence of a pronounced van Hove feature in the alloy configuration. Our findings extend the range of materials amenable to superacid treatment and open new avenues for optoelectronic applications, particularly those requiring high excitation powers.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Perovskite Materials and Applications · 2D Materials and Applications · Quantum Dots Synthesis And Properties

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

Affiliations

Institute of Materials Research and Engineering, Agency for Science, Technology and Research, Fusionopolis Way 2, Singapore 138634, Singapore

Biophysics Group, Department of Physics & Astronomy, University College London, Gower Street, London WC1E 6BT, U.K.

Institute of High Performance Computing, Agency for Science, Technology and Research, 1 Kent Ridge Road, Singapore 119210, Singapore

UCL Healthcare Biomagnetics and Nanomaterials Laboratories, 21 Albemarle Street, London W1S 4BS, U.K.

Funding

Agency for Science, Technology and Research · National Research Foundation Singapore

References (56)

Show source-provided references
1. 10.1038/srep0921810.1038/srep09218 ↗
2. 10.1038/nphoton.2014.30410.1038/nphoton.2014.304 ↗
3. 10.1002/pssr.20151022410.1002/pssr.201510224 ↗
4. 10.1021/acs.nanolett.7b0076810.1021/acs.nanolett.7b00768 ↗
5. 10.1002/adma.20230224810.1002/adma.202302248 ↗
6. 10.1103/PhysRevB.90.20542210.1103/PhysRevB.90.205422 ↗
7. 10.1103/PhysRevLett.105.13680510.1103/PhysRevLett.105.136805 ↗
8. 10.1021/nn500532f10.1021/nn500532f ↗
9. 10.1002/smll.20190179110.1002/smll.201901791 ↗
10. 10.1021/acsnano.5b0440010.1021/acsnano.5b04400 ↗
11. 10.1021/acsami.7b0126210.1021/acsami.7b01262 ↗
12. 10.1021/acs.nanolett.9b0243110.1021/acs.nanolett.9b02431 ↗
13. 10.1039/C8NR00530C10.1039/C8NR00530C ↗
14. 10.1021/acs.nanolett.6b0053610.1021/acs.nanolett.6b00536 ↗
15. Li, Z., Bretscher, H., Zhang, Y., Delport, G., Xiao, J., Lee, A., Stranks, S. D., Rao, A.: Mechanistic insight to the chemical treatments of monolayer transition metal disulfides for photoluminescence enhancement. arXiv preprint arXiv:2009.11123, 2020.10.1038/s41467-021-26340-6 ↗
16. 10.1088/2515-7639/ad4c0510.1088/2515-7639/ad4c05 ↗
17. 10.1021/acsnano.7b0252110.1021/acsnano.7b02521 ↗
18. 10.1038/s41699-024-00443-210.1038/s41699-024-00443-2 ↗
19. 10.3390/app1108353010.3390/app11083530 ↗
20. 10.1126/science.aaw805310.1126/science.aaw8053 ↗
21. 10.1126/science.aad211410.1126/science.aad2114 ↗
22. 10.1126/science.abi919310.1126/science.abi9193 ↗
23. 10.1038/ncomms366110.1038/ncomms3661 ↗
24. 10.1038/s41467-018-03049-710.1038/s41467-018-03049-7 ↗
25. 10.1103/PhysRevB.93.20111110.1103/PhysRevB.93.201111 ↗
26. 10.1002/adma.20130438910.1002/adma.201304389 ↗
27. 10.1039/C5NR02652K10.1039/C5NR02652K ↗
28. 10.1039/D0RA07776C10.1039/D0RA07776C ↗
29. 10.1039/C5CP04653J10.1039/C5CP04653J ↗
30. 10.1063/5.002136110.1063/5.0021361 ↗
31. 10.1039/C4NR03716B10.1039/C4NR03716B ↗
32. 10.1016/j.electacta.2015.10.15310.1016/j.electacta.2015.10.153 ↗
33. 10.1038/s41467-017-01487-310.1038/s41467-017-01487-3 ↗
34. 10.1103/PhysRevB.88.12130110.1103/PhysRevB.88.121301 ↗
35. 10.1088/1674-1056/27/3/03780210.1088/1674-1056/27/3/037802 ↗
36. 10.1038/s41467-020-15023-310.1038/s41467-020-15023-3 ↗
37. 10.1063/1.497407210.1063/1.4974072 ↗
38. 10.1021/acs.nanolett.8b0171410.1021/acs.nanolett.8b01714 ↗
39. 10.1063/5.002465210.1063/5.0024652 ↗
40. 10.1038/s41467-018-05643-110.1038/s41467-018-05643-1 ↗
41. 10.1063/1.505369910.1063/1.5053699 ↗
42. 10.1021/acs.jpcc.2c0005110.1021/acs.jpcc.2c00051 ↗
43. 10.1021/acsami.1c0681210.1021/acsami.1c06812 ↗
44. 10.1063/1.143316410.1063/1.1433164 ↗
45. 10.1038/s41467-017-02684-w10.1038/s41467-017-02684-w ↗
46. 10.1103/PhysRevB.54.1064410.1103/PhysRevB.54.10644 ↗
47. 10.1007/s10853-018-2617-510.1007/s10853-018-2617-5 ↗
48. 10.1038/nature2515510.1038/nature25155 ↗
49. 10.1021/acsnano.9b0495710.1021/acsnano.9b04957 ↗
50. 10.1016/j.isci.2022.10394210.1016/j.isci.2022.103942 ↗
51. 10.1021/acsnano.0c0674510.1021/acsnano.0c06745 ↗
52. 10.1002/smll.20210660010.1002/smll.202106600 ↗
53. 10.1038/s41565-017-0022-x10.1038/s41565-017-0022-x ↗
54. 10.1088/0957-4484/26/17/17570210.1088/0957-4484/26/17/175702 ↗
55. 10.1038/nnano.2008.39910.1038/nnano.2008.399 ↗
56. 10.1364/OME.9.00162010.1364/OME.9.001620 ↗