From N-type doping to phase transition in large-area MoS 2 via controlled sulfur vacancy formation
Source abstract
Abstract
Precise and damage-free doping of two-dimensional semiconductors is essential for advancing their use in nano-electronic and optoelectronic devices. Here, we present a controllable strategy for n-type doping and phase engineering of monolayer MoS2 by tuning sulfur vacancy formation using energy-controlled Ar+ ion treatment. This method enables selective top-layer sulfur removal without disrupting the underlying lattice, leading to enhanced n-type conductivity. Extended plasma exposure induces a phase transition from the semiconducting 2H phase to the metallic 1T phase, as confirmed by Raman, photoluminescence, and X-ray photoelectron spectroscopy. Doped devices exhibit improved electrical and optoelectronic performance, including higher on-current, carrier mobility, and photoresponsivity. Additionally, selective formation of 1T contacts at the source/drain regions further reduces contact resistance and boosts injection efficiency. Al2O3 encapsulation is shown to suppress surface oxidation during O2 plasma exposure, maintaining device stability. This work demonstrates that plasma-assisted defect and phase control offers a practical and scalable pathway to tailor the electronic properties of 2D semiconductors.
Source: europepmc · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: 2D Materials and Applications · MXene and MAX Phase Materials · Chalcogenide Semiconductor Thin Films
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Semiconductor Convergence Engineering, Sungkyunkwan University, Gyeonggi-do 16419, Republic of Korea
Department of Advanced Materials Science & Engineering, Sungkyunkwan University, Gyeonggi-do 16419, Republic of Korea
Department of Display Engineering, Sungkyunkwan University, Gyeonggi-do 16419, Republic of Korea
College of Information and Communication Engineering, Sungkyunkwan University, Gyeonggi-do 16419, Republic of Korea
Funding
Ministry of Trade, Industry and Energy · National Research Foundation of Korea
References (44)
Show source-provided references
1. Radisavljevic · Nat. Nanotechnol. · 2011 · 6 · 14710.1038/nnano.2010.279 ↗
2. Lopez-Sanchez · Nat. Nanotechnol. · 2013 · 8 · 49710.1038/nnano.2013.100 ↗
3. Splendiani · Nano Lett. · 2010 · 10 · 127110.1021/nl903868w ↗
4. Mak · Phys. Rev. Lett. · 2010 · 105 · 13680510.1103/PhysRevLett.105.136805 ↗
5. Dumcenco · ACS Nano · 2015 · 9 · 461110.1021/acsnano.5b01281 ↗
6. Y.-H.Lee , X.-Q.Zhang , W.Zhang , M.-T.Chang , C.-T.Lin , K.-D.Chang , Y.-C.Yu , J. T.-W.Wang , C.-S.Chang , L.-J.Li , et al. , arXiv , 2012, preprint, arXiv:1202.5458, 10.48550/arXiv.1202.545810.48550/arXiv.1202.5458 ↗
7. Yang · Sci. Rep. · 2023 · 13 · 837810.1038/s41598-023-35596-5 ↗
8. Azcatl · Nano Lett. · 2016 · 16 · 543710.1021/acs.nanolett.6b01853 ↗
9. Tan · Nanoscale · 2021 · 13 · 1527810.1039/D1NR03917B ↗
10. Kim · J. Mater. Chem. C · 2020 · 8 · 184610.1039/C9TC05548G ↗
11. Telkhozhayeva · Adv. Funct. Mater. · 2024 · 34 · 240461510.1002/adfm.202404615 ↗
12. Qiu · Nat. Commun. · 2013 · 4 · 264210.1038/ncomms3642 ↗
13. Hong · Nat. Commun. · 2015 · 6 · 629310.1038/ncomms7293 ↗
14. Rajput · Commun. Mater. · 2024 · 5 · 19010.1038/s43246-024-00632-y ↗
15. Zhao · Nat. Commun. · 2023 · 14 · 4410.1038/s41467-022-35651-1 ↗
16. Hong · Nat. Commun. · 2015 · 6 · 629310.1038/ncomms7293 ↗
17. Kang · ACS Appl. Mater. Interfaces · 2024 · 16 · 4384910.1021/acsami.4c08549 ↗
18. Liu · Small · 2017 · 13 · 160296710.1002/smll.201602967 ↗
19. Chee · Nanoscale · 2017 · 9 · 933310.1039/C7NR01883E ↗
20. Kim · ACS Appl. Electron. Mater. · 2022 · 4 · 379410.1021/acsaelm.2c00379 ↗
21. Chakraborty · Phys. Rev. B:Condens. Matter Mater. Phys. · 2012 · 85 · 16140
22. Yao · Nanomaterials · 2019 · 9 · 84410.3390/nano9060844 ↗
23. Jung · 2D Mater. · 2019 · 6 · 02502410.1088/2053-1583/ab070c ↗
24. Chakraborty · Phys. Rev. B:Condens. Matter Mater. Phys. · 2012 · 85 · 16140310.1103/PhysRevB.85.161403 ↗
25. Hossen · Nano Sel. · 2024 · 6 · e20240010310.1002/nano.202400103 ↗
26. Mouri · Nano Lett. · 2013 · 13 · 594410.1021/nl403036h ↗
27. Yang · Nano Lett. · 2014 · 14 · 627510.1021/nl502603d ↗
28. Kim · ACS Appl. Mater. Interfaces · 2017 · 9 · 1196710.1021/acsami.6b15886 ↗
29. Eda · Nano Lett. · 2011 · 11 · 511110.1021/nl201874w ↗
30. Kim · ACS Appl. Mater. Interfaces · 2017 · 9 · 1196710.1021/acsami.6b15886 ↗
31. Tang · J. Mater. Chem. C · 2018 · 6 · 956110.1039/C8TC03430C ↗
32. Park · Adv. Sci. · 2021 · 8 · 200276810.1002/advs.202002768 ↗
33. Luo · Appl. Catal., B · 2021 · 299 · 12066410.1016/j.apcatb.2021.120664 ↗
34. Abidi · Nanoscale · 2024 · 16 · 1983410.1039/D4NR02518K ↗
35. Qiu · Nat. Commun. · 2013 · 4 · 264210.1038/ncomms3642 ↗
36. Cheng · Nano Res. · 2024 · 17 · 325310.1007/s12274-023-6235-8 ↗
37. Cheng · J. Mater. Chem. C · 2024 · 12 · 279410.1039/D3TC04605B ↗
38. He · J. Mater. Chem. C · 2025 · 13 · 574610.1039/D4TC05001K ↗
39. Ho · Phys. Status Solidi RRL · 2015 · 9 · 18710.1002/pssr.201409561 ↗
40. Leonhardt · ACS Appl. Mater. Interfaces · 2019 · 11 · 4269710.1021/acsami.9b11550 ↗
41. Valsaraj · 2D Mater. · 2015 · 2 · 04500910.1088/2053-1583/2/4/045009 ↗
42. Na · Nanoscale · 2014 · 6 · 43310.1039/C3NR04218A ↗
43. Kim · Appl. Surf. Sci. · 2024 · 670 · 16057010.1016/j.apsusc.2024.160570 ↗
44. Lin · Appl. Surf. Sci. · 2018 · 443 · 42110.1016/j.apsusc.2018.02.225 ↗