Improved Operational Stability of Polymer Light-Emitting Diodes Based on Silver Nanowire Electrode Through Pre-Bias Conditioning Treatment

2014 ◽  
Vol 24 (41) ◽  
pp. 6465-6472 ◽  
Author(s):  
Yonghee Lee ◽  
Minwon Suh ◽  
Donghyuk Kim ◽  
Dongchan Lee ◽  
Hyein Chang ◽  
...  
2020 ◽  
Author(s):  
Hiroaki Jinno ◽  
Tomoyuki Yokota ◽  
Mari Koizumi ◽  
Wakako Yukita ◽  
Masahiko Saito ◽  
...  

Abstract Flexible organic optical devices have been used extensively in next-generation wearable electronics owing to advantages such as light-weight, thinness, and flexibility. Making such organic optical devices ultrathin enables long-term monitoring of health conditions owing to the increased conformability of ultrathin devices to human skin. Long-term biological signal monitoring also requires the integration of organic optical devices with an energy harvesting power sources which does not require recharging; to make devices self-powered. However, system-level integration of such thin organic optical sensors with power sources is challenging. An important obstacle to this type of integration is the insufficient operational stability of ultrathin organic light-emitting diodes under ambient air conditions. Here we develop an ultrathin self-powered organic optical system for photoplethysmogram (PPG) monitoring. This system consists of three types of ultrathin electronic devices: polymer light-emitting diodes (PLEDs), organic solar cells, and organic photodetectors. By adopting an inverted structure and a polyethylenimine ethoxylated layer doped with 8-hydroxyquinolinato-lithium as the electron-transport layer, PLEDs exhibit improved operational stability under ambient air conditions without external encapsulation. Ultraflexible PLEDs with no passivation retain 70% of the initial luminance lifetime of 11.3 h under ambient air. Integrated optical sensors exhibit a high linearity with the light intensity exponent of 0.98 by PLED light source. Such self-powered, ultraflexible PPG sensors can perform long-term stable monitoring of blood pulse signals on human hands.


2011 ◽  
Vol 23 (46) ◽  
pp. 5563-5567 ◽  
Author(s):  
Lu Li ◽  
Zhibin Yu ◽  
Weili Hu ◽  
Chia-hao Chang ◽  
Qi Chen ◽  
...  

2010 ◽  
Vol 23 (5) ◽  
pp. 664-668 ◽  
Author(s):  
Zhibin Yu ◽  
Qingwu Zhang ◽  
Lu Li ◽  
Qi Chen ◽  
Xiaofan Niu ◽  
...  

2012 ◽  
Vol 14 (41) ◽  
pp. 14249 ◽  
Author(s):  
Lu Li ◽  
Zhibin Yu ◽  
Chia-hao Chang ◽  
Weili Hu ◽  
Xiaofan Niu ◽  
...  

2000 ◽  
Vol 660 ◽  
Author(s):  
Thomas M. Brown ◽  
Ian S. Millard ◽  
David J. Lacey ◽  
Jeremy H. Burroughes ◽  
Richard H. Friend ◽  
...  

ABSTRACTThe semiconducting-polymer/injecting-electrode heterojunction plays a crucial part in the operation of organic solid state devices. In polymer light-emitting diodes (LEDs), a common fundamental structure employed is Indium-Tin-Oxide/Polymer/Al. However, in order to fabricate efficient devices, alterations to this basic structure have to be carried out. The insertion of thin layers, between the electrodes and the emitting polymer, has been shown to greatly enhance LED performance, although the physical mechanisms underlying this effect remain unclear. Here, we use electro-absorption measurements of the built-in potential to monitor shifts in the barrier height at the electrode/polymer interface. We demonstrate that the main advantage brought about by inter-layers, such as poly(ethylenedioxythiophene)/poly(styrene sulphonic acid) (PEDOT:PSS) at the anode and Ca, LiF and CsF at the cathode, is a marked reduction of the barrier to carrier injection. The electro- absorption results also correlate with the electroluminescent characteristics of the LEDs.


2021 ◽  
Vol 9 (36) ◽  
pp. 12068-12072
Author(s):  
Wentao Li ◽  
Jiaxiang Liu ◽  
Baowen Wang ◽  
Siyu Hou ◽  
Xingqiang Lü ◽  
...  

Based on geometrical isomerisation of [Ir(C^N1)(C^N2)((N^O))]-tris-heteroleptic Ir(iii)-complexes, the augmented transition dipole transition (TMD) with a preferential horizontal orientation, which is beneficial for their NIR-phosphorescence, is reported.


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