Enhancing device characteristics of InP quantum dot LED through structural modification with polyethylene glycol blend

IF 4 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY
Jaeseung Kim , Ji Ho Roh , Thi Na Le , Min Woo Hyeon , Bong Hoon Cha , Min Chul Suh , Hyunjung Kim
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引用次数: 0

Abstract

This study explored the integration of polyethylene glycol (PEG) into InP-based quantum dot (QD) light-emitting diodes (LEDs). By 5 wt% of PEG 400 blended into the QD emission layer (EML), we achieved an enhancement in both current efficiency (100 %) and external quantum efficiency (91 %). X-ray reflectivity revealed significant morphological changes in the QD EML upon PEG incorporation, primarily manifesting as increased thickness in the dense surface region without affecting the total thickness. This adjustment influenced electron density distribution, impacting hole and electron flow. Overall, the addition of PEG not only improved the electrical properties of QD LEDs but also reshaped the internal morphology of the QD EML. Notably, the efficiency improvements observed rival those achieved by integrating traditional hole transport materials into QD EMLs.

通过聚乙二醇混合物的结构改性提高 InP 量子点 LED 的器件特性
本研究探讨了将聚乙二醇(PEG)整合到基于 InP 的量子点(QD)发光二极管(LED)中的问题。通过在 QD 发射层 (EML) 中掺入 5 wt% 的 PEG 400,我们提高了电流效率(100%)和外部量子效率(91%)。X 射线反射率显示,掺入 PEG 后,QD EML 的形态发生了显著变化,主要表现为致密表面区域的厚度增加,但不影响总厚度。这种调整影响了电子密度分布,对空穴和电子流产生了影响。总之,添加 PEG 不仅改善了 QD LED 的电学特性,还重塑了 QD EML 的内部形态。值得注意的是,所观察到的效率提高与将传统空穴传输材料集成到 QD EML 中实现的效率提高不相上下。
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来源期刊
Synthetic Metals
Synthetic Metals 工程技术-材料科学:综合
CiteScore
8.30
自引率
4.50%
发文量
189
审稿时长
33 days
期刊介绍: This journal is an international medium for the rapid publication of original research papers, short communications and subject reviews dealing with research on and applications of electronic polymers and electronic molecular materials including novel carbon architectures. These functional materials have the properties of metals, semiconductors or magnets and are distinguishable from elemental and alloy/binary metals, semiconductors and magnets.
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