4.6 Article

Photo-Responsive Molecular Junctions Activated by Perovskite/Graphene Heterostructure Electrode

期刊

ADVANCED OPTICAL MATERIALS
卷 10, 期 11, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adom.202200049

关键词

charge transport; Landauer formalism; molecular electronics; perovskites; self-assembled monolayers

资金

  1. National Research Foundation of Korea (NRF) [2021R1A2C3004783, 2021R1C1C1010266]
  2. NRF - Ministry of Science and ICT (MSIT) of Korea [2021M3H4A1A02049651]
  3. Samsung Electronics Co., Ltd [IO201211-08047-01]
  4. Ministry of Trade, Industry & Energy of Korea [20013621]
  5. NRF - MSIT of Korea [2019R1A6A1A10073437]
  6. National Research Foundation of Korea [2021R1C1C1010266, 2021R1A2C3004783] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

In this study, the authors enhanced the photoresponsivity of molecular junction devices by using organohalide perovskite/graphene heterojunction and investigated the role of self-assembled monolayer (SAM) in enhancing the photoresponsivity. They also elucidated the mechanism of light-induced coupling. These findings contribute to the design of high-performance molecular optoelectronic devices.
Photoresponsivity is a fundamental process that constitutes optoelectronic devices. In molecular junction devices, one of the most adopted strategies is to employ photoactive molecules that can undergo conformational change upon light illumination as the conduction channel. However, such devices suffer from their relatively low photoresponsivity, long switching time, and unidirectional switching. In this study, the authors employed organohalide perovskite (OHP)/graphene heterojunction as a photoactive electrode that acted a source of photo-generated carriers collected as photocurrent in self-assembled monolayer (SAM)-based molecular junctions. This hybrid device architecture of perovskite/graphene/SAM allows the molecular junctions to attain a high photoresponsivity with molecules that have intrinsically little photoresponse. The authors elucidate the role of the molecular SAM in enhancing the photoresponsivity by systematically examining the transport and charge transfer processes at the graphene/SAM interface via molecules with different intrinsic dipole moments. This, corroborated with a theoretical analysis, reveals the origin of the observed photoresponsivity as light-induced coupling between the SAM and the OHP/graphene electrode within the orbital-mediated resonant tunnelling transport regime. These findings advance the understanding of photo-induced charge transport in molecular junctions with heterointerfaces, providing a road-map for designing high-performance molecular optoelectronic devices based on hybrid device architecture.

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