PTAA/TPBi Host–Guest Engineering Enables High‐Brightness Yellow Carbon Dot Based Light‐Emitting Diodes through Electron Confinement

Abstract Carbon dots have been extensively studied as a ‐stable, tunable, and environmentally friendly light‐emitting material in light‐emitting diodes. However, it has been found that no matter how the properties of carbon dots (CDs) are optimized, the device performance is still unsatisfactory, and even solid‐state CDs with high quantum yields do not necessarily imply better device performance. In this study, CDs are doped into host materials— to form an emissive layer. When excited by an applied electric field, the CDs act as luminescent guest molecules, while the host material provides the desired charge transport properties and stability. This method‐ improves the morphology of the emissive layer and balances the charge transport and distribution, thus increasing the charge compounding efficiency and improving the device performance, with poly[bis(4‐phenyl)(2,4,6‐trimethylphenyl)amine] as the hole transport layer and 1,3,5‐tris(1‐phenyl‐1H‐benzimidazol‐2‐yl)benzene as the host material doped with CDs, the luminance is as high as 9754 cd m −2 and the efficiency is 8.53 cd A −1 . The results of the study show that in addition to the synthesis of highly efficient solid‐state fluorescent CDs, the design of the device structure and the development of more efficient hole‐transporting materials are also key factors to improve the performance of CDs‐based light‐emitting diodes.

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Publication Details

Journal
Advanced Materials Interfaces
Published
2025-10-22
DOI
https://doi.org/10.1002/admi.202500731
Primary Topic
Carbon and Quantum Dots Applications
Type
article
Field-Weighted Citation Impact
0.00

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article

PTAA/TPBi Host–Guest Engineering Enables High‐Brightness Yellow Carbon Dot Based Light‐Emitting Diodes through Electron Confinement

Xingming Bian, Tan Zhanao, Lin Liu, Shaoqi Zhang et al.
Advanced Materials Interfaces
Carbon and Quantum Dots Applications
article

PTAA/TPBi Host–Guest Engineering Enables High‐Brightness Yellow Carbon Dot Based Light‐Emitting Diodes through Electron Confinement

Xingming Bian, Tan Zhanao, Lin Liu, Shaoqi Zhang, Yiming Bai, Yu Li, Yang Wang, Wang Fuzhi, Liu Yina, Yue Shuaifei
article en

Abstract

Abstract Carbon dots have been extensively studied as a ‐stable, tunable, and environmentally friendly light‐emitting material in light‐emitting diodes. However, it has been found that no matter how the properties of carbon dots (CDs) are optimized, the device performance is still unsatisfactory, and even solid‐state CDs with high quantum yields do not necessarily imply better device performance. In this study, CDs are doped into host materials— to form an emissive layer. When excited by an applied electric field, the CDs act as luminescent guest molecules, while the host material provides the desired charge transport properties and stability. This method‐ improves the morphology of the emissive layer and balances the charge transport and distribution, thus increasing the charge compounding efficiency and improving the device performance, with poly[bis(4‐phenyl)(2,4,6‐trimethylphenyl)amine] as the hole transport layer and 1,3,5‐tris(1‐phenyl‐1H‐benzimidazol‐2‐yl)benzene as the host material doped with CDs, the luminance is as high as 9754 cd m −2 and the efficiency is 8.53 cd A −1 . The results of the study show that in addition to the synthesis of highly efficient solid‐state fluorescent CDs, the design of the device structure and the development of more efficient hole‐transporting materials are also key factors to improve the performance of CDs‐based light‐emitting diodes.

Advanced Materials InterfacesVol. 12(23)
North China Electric Power University (CN), Hebei University of Technology (CN), Beijing University of Chemical Technology (CN)
National Natural Science Foundation of China, Hebei University, Hebei University of Technology, State Key Laboratory of Reliability and Intelligence of Electrical Equipment
Openalex Percentile: Top 76%
Carbon and Quantum Dots Applications
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