Plasma functionalization for cyclic transition between neutral and charged excitons in monolayer MoS2
- Authors
- Kim, Y.; Jhon, Y. I.; Park, J.; Kim, C.; Lee, S.; Jhon, Y. M.
- Issue Date
- 2016-02-22
- Publisher
- NATURE RESEARCH
- Citation
- SCIENTIFIC REPORTS, v.6
- Abstract
- Monolayer MoS2 (1L-MoS2) has photoluminescence (PL) properties that can greatly vary via transition between neutral and charged exciton PLs depending on carrier density. Here, for the first time, we present a chemical doping method for reversible transition between neutral and charged excitons of 1L-MoS2 using chlorine-hydrogen-based plasma functionalization. The PL of 1L-MoS2 is drastically increased by p-type chlorine plasma doping in which its intensity is easily tuned by controlling the plasma treatment duration. We find that despite their strong adhesion, a post hydrogen plasma treatment can very effectively dedope chlorine adatoms in a controllable way while maintaining robust structural integrity, which enables well-defined reversible PL control of 1L-MoS2. After exhaustive chlorine dedoping, the hydrogen plasma process induces n-type doping of 1L-MoS2, degrading the PL further, which can also be recovered by subsequent chlorine plasma treatment, extending the range of tunable PL into a bidirectional regime. This cyclically-tunable carrier doping method can be usefully employed in fabricating highly-tunable n- and p-type domains in monolayer transition-metal dichalcogenides suitable for two-dimensional electro-optic modulators, on-chip lasers, and spin-and valley-polarized light-emitting diodes.
- Keywords
- MOLYBDENUM-DISULFIDE MOS2; SATURABLE ABSORBER; LIGHT-EMISSION; LAYER; PHOTOLUMINESCENCE; EVOLUTION; DYNAMICS; DIODES; BULK; WS2; MOLYBDENUM-DISULFIDE MOS2; SATURABLE ABSORBER; LIGHT-EMISSION; LAYER; PHOTOLUMINESCENCE; EVOLUTION; DYNAMICS; DIODES; BULK; WS2; plasma; functionalization; MoS2
- ISSN
- 2045-2322
- URI
- https://pubs.kist.re.kr/handle/201004/124375
- DOI
- 10.1038/srep21405
- Appears in Collections:
- KIST Article > 2016
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