Highly efficient white organic Light-Emitting diodes utilizing intermolecular interaction based on molecular geometry between host and deep blue Pt(Ⅱ) complex
- Authors
- Nam, Hyewon; Kim, Ki Ju; Ko, Soo-Byung; Kang, Sunwoo; Shin, Dong Jin; Kim, Jae-Min; Lee, Jun Yeob; Kim, Taekyung
- Issue Date
- 1-May-2024
- Publisher
- Elsevier B.V.
- Keywords
- Tandem; White organic light-emitting diodes; π-π interaction
- Citation
- Chemical Engineering Journal, v.487
- Journal Title
- Chemical Engineering Journal
- Volume
- 487
- URI
- https://scholarworks.bwise.kr/hongik/handle/2020.sw.hongik/33065
- DOI
- 10.1016/j.cej.2024.150294
- ISSN
- 1385-8947
1873-3212
- Abstract
- Previous studies on white organic light-emitting diodes (WOLEDs) using a single Pt dopant relied on square-planar Pt complexes, exhibiting various emission characteristics due to ligand-centered π-π interactions. However, this approach limits the range of the materials selections to those with excimer or aggregation-induced emission (AIE) properties. In this study, a new method for creating WOLEDs with a single Pt dopant is proposed. We observed the emergence of an intermolecular interaction, specifically the formation of an exciplex due to π-π interaction between the n-host (ET) and the Pt complex, leading to a low-energy yellow emission. By varying the mixing ratio of ET and Pt complex, a spectrum of emissions ranging from pure blue to yellow was achievable. Consequently, we constructed 3-stack tandem devices, leveraging color variations based on the ET:Pt ratio. As a result, we successfully achieved a cool white emission with a Color Rendering Index (CRI) of 66.7, International Commission on Illumination (CIE) coordinates of (0.294, 0.380). Additionally, through optimization of the device structure, external quantum efficiency (EQE) was enhanced from 18.3% to 21.9%. This novel and simple device architecture adjusting intermolecular interaction based on molecular geometry between ET and Pt(II) complex provides a solution to materials limitations in WOLEDs. © 2024 Elsevier B.V.
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