Please use this identifier to cite or link to this item:
http://hdl.handle.net/10397/111421
| DC Field | Value | Language |
|---|---|---|
| dc.contributor | Department of Applied Physics | en_US |
| dc.contributor | Research Centre for Data Science and Artificial Intelligence | en_US |
| dc.contributor | Research Centre for Nanoscience and Nanotechnology | en_US |
| dc.creator | Zhu, T | en_US |
| dc.creator | Zheng, C | en_US |
| dc.creator | Xu, L | en_US |
| dc.creator | Yang, M | en_US |
| dc.date.accessioned | 2025-02-27T04:12:13Z | - |
| dc.date.available | 2025-02-27T04:12:13Z | - |
| dc.identifier.uri | http://hdl.handle.net/10397/111421 | - |
| dc.language.iso | en | en_US |
| dc.publisher | American Physical Society | en_US |
| dc.rights | ©2024 American Physical Society | en_US |
| dc.rights | The following publication Zhu, T., Zheng, C., Xu, L., & Yang, M. (2024). Exciton dissociation in two-dimensional transition metal dichalcogenides: Excited states and substrate effects. Physical Review B, 110(15), 155416 is available at https://doi.org/10.1103/PhysRevB.110.155416. | en_US |
| dc.title | Exciton dissociation in two-dimensional transition metal dichalcogenides : excited states and substrate effects | en_US |
| dc.type | Journal/Magazine Article | en_US |
| dc.identifier.volume | 110 | en_US |
| dc.identifier.issue | 15 | en_US |
| dc.identifier.doi | 10.1103/PhysRevB.110.155416 | en_US |
| dcterms.abstract | Exciton dissociation plays a crucial role in the performance of optoelectronic devices based on two-dimensional (2D) transition metal dichalcogenides (TMDs). In this work, we investigate the effect of an in-plane electric field on the exciton resonance states in MX2 (M = Mo, W; X = S, Se) monolayers and few layers using the complex coordinate rotation method and the Lagrange-Laguerre polynomial expansion of the wave function. This technique enables accurate computation of both ground and excited excitonic states across a wide range of electric field strengths, overcoming limitations of previous perturbative approaches. Our calculations reveal that an electric field effectively dissociates excitons, with excited states being more easily dissociated than the ground state. The critical field for exciton dissociation is found to be smaller in WX2 monolayers compared to MoX2 monolayers due to the smaller exciton reduced mass. Furthermore, the presence of a dielectric substrate and an increase in the number of MX2 layers enhance the exciton susceptibility to the electric field, lowering the critical field for dissociation. The dependence of exciton properties on the number of MX2 layers can be well described by power functions. These findings provide valuable insights for the design and optimization of high-performance optoelectronic devices based on 2D TMDs. | en_US |
| dcterms.accessRights | open access | en_US |
| dcterms.bibliographicCitation | Physical review B : covering condensed matter and materials physics, 15 Oct. 2024, v. 110, no. 15, 155416 | en_US |
| dcterms.isPartOf | Physical review B : covering condensed matter and materials physics | en_US |
| dcterms.issued | 2024-10-15 | - |
| dc.identifier.scopus | 2-s2.0-85206491622 | - |
| dc.identifier.eissn | 2469-9950 | en_US |
| dc.identifier.artn | 155416 | en_US |
| dc.description.validate | 202502 bcch | en_US |
| dc.description.oa | Version of Record | en_US |
| dc.identifier.FolderNumber | OA_Others; a3484c, a3719 | - |
| dc.identifier.SubFormID | 50231, 50851 | - |
| dc.description.fundingSource | RGC | en_US |
| dc.description.fundingSource | Others | en_US |
| dc.description.fundingText | National Natural Science Foundation of China; National Key R&D Program of the Ministry of Science and Technology of China; Hong Kong Polytechnic University | en_US |
| dc.description.pubStatus | Published | en_US |
| dc.description.oaCategory | VoR allowed | en_US |
| Appears in Collections: | Journal/Magazine Article | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| PhysRevB.110.155416.pdf | 2.65 MB | Adobe PDF | View/Open |
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