4.8 Article

Trion-Mediated Forster Resonance Energy Transfer and Optical Gating Effect in WS2/hBN/MoSe2 Heterojunction

期刊

ACS NANO
卷 14, 期 10, 页码 13470-13477

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.0c05447

关键词

2D materials; transition metal dichalcogenides; trion; van der Waals heterostructure; Forster resonance energy transfer; photogating; optical spectroscopy

资金

  1. Singapore Ministry of Education Tier3 Programme Geometrical Quantum Materials [MOE2018-T3-1-002]
  2. AcRF Tier2 grant [MOE2017-T21-040]
  3. AcRF Tier1 grant [RG 194/17]
  4. Singapore National Research Foundation Competitive Research Programme Integrated On-chip Planar Coherent Light Sources [NRF-CRP-21-2018-0007]
  5. National Research Foundation-Agence Nationale de la Recherche (NRF-ANR) Grant [NRF2017-NRF-ANR005 2DCHIRAL]
  6. Elemental Strategy Initiative [JPMXP0112101001]
  7. JSPS KAKENHI [JP20H00354]
  8. CREST, JST [JPMJCR15F3]

向作者/读者索取更多资源

van der Waals two-dimensional layered heterostr uctures have recently emerged as a platform, where the interlayer couplings give rise to interesting physics and innitifunctionalities in optoelectronics. Such couplings can be rationally controlled by dielectric, separation, and stacking angles, which affect the overall charge or energy-transfer processes, and emergent.. potential landscape for twistronics. Herein, we report the efficient Forster resonance energy transfer (FRET) in WS2/hBN/MoSe2 heterostructure, probed by both steady-state and time resolved optical spectroscopy. We clarified the evolution behavior of the Mo electron hole pairs and free electrons from the trions, that is, 59.9% of the electron hole pairs could transfer into MoSe2 by FRET channels (similar to 38 ps) while the free electrons accumulate at the WS2/hBN interface to photogate MoSe2. This study presents a clear picture of the FRET process in two-dimensional transition-metal dichalcogenides' heterojunctions, which establishes the scientific foundation for developing the related heterojunction optoelectronic devices.

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