Issue 46, 2018

Realization of high-power-efficiency white electroluminescence from a single polymer by energy-level engineering

Abstract

Single white light-emitting polymers (SWPs) represent a high-fidelity system for generating white light emission from polymers without phase separation compared to polymer blend systems. However, their device performance so far has been limited because of the unwanted hole scattering caused by an energy-level mismatch between emitters and hosts, and the large injection barrier at the polymer/anode interface. Here, we report novel poly(arylene phosphine oxide)-based all-phosphorescent SWPs by using the combination of a high-HOMO-level blue phosphor and high-HOMO-level poly(arylene phosphine oxide) host to achieve a low turn-on voltage of 2.8 V, high external quantum efficiency of 18.0% and remarkable power efficiency of 52.1 lm W−1, which makes them the most efficient SWPs so far. This record power efficiency is realized by using the high-HOMO-level blue phosphor to eliminate the hole scattering effect and by using the high-HOMO-level polymer host to reduce the hole injection barrier. This result represents an important progress in SWPs to achieve efficiency surpassing that of the polymer blends currently used for solution-processed white organic light-emitting diodes (WOLEDs) and even comparable with that of the small molecules used for vacuum-deposited WOLEDs.

Graphical abstract: Realization of high-power-efficiency white electroluminescence from a single polymer by energy-level engineering

Supplementary files

Article information

Article type
Edge Article
Submitted
22 8月 2018
Accepted
18 9月 2018
First published
19 9月 2018
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2018,9, 8656-8664

Realization of high-power-efficiency white electroluminescence from a single polymer by energy-level engineering

S. Shao, S. Wang, X. Xu, Y. Yang, J. Lv, J. Ding, L. Wang, X. Jing and F. Wang, Chem. Sci., 2018, 9, 8656 DOI: 10.1039/C8SC03753A

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