Activating room temperature phosphorescence by organic materials using synergistic effects

2019 ◽  
Vol 7 (2) ◽  
pp. 230-236 ◽  
Author(s):  
Xianggui Kong ◽  
Xinrui Wang ◽  
Huimin Cheng ◽  
Yufei Zhao ◽  
Wenying Shi

We present a design principle to activate highly efficient organic room temperature phosphorescent (ORTP) of carbon dots (CDs), with layered double hydroxides (LDHs) as the host matrix, that utilizes three synergistic effects,i.e.structural confinement effect, heavy atom effect, and chemical bonding.

2021 ◽  
Author(s):  
Shangwei Feng ◽  
Qiuqin Huang ◽  
Shuming Yang ◽  
Zhenghuan Lin ◽  
Qidan Ling

Organic-inorganic hybrid metal halides have attracted intensive attention because of their unique electronic structure and solution processability. They have rigid micro/nano structure and heavy atom effect, which has obvious advantages...


2020 ◽  
Author(s):  
Heather Higginbotham ◽  
Masato Okazaki ◽  
Piotr de Silva ◽  
Satoshi Minakata ◽  
Youhei Takeda ◽  
...  

Room temperature phosphorescence materials offer great opportunities for applications in optoelectronics, due to their unique photophysical characteristics. However, purely organic emitters that can realize distinct electrophosphorescence are rarely exploited. Herein a new approach for designing heavy-atom-free organic room temperature phosphorescence emitters for organic light-emitting diodes is presented. The subtle tuning of the energy diagrams of singlet and triplet excited states by appropriate choice of host matrix allows tailored emission properties and switching of emission channels between thermally activated delayed fluorescence and room temperature phosphorescence. Moreover, an efficient and heavy-atom-free room temperature phosphorescence organic light-emitting diodes using the developed emitter is realized.


2021 ◽  
Author(s):  
Xiang Ma ◽  
Zi-Ang Yan ◽  
Xiaohan Lin ◽  
Siyu Sun ◽  
He Tian

Pure organic room-temperature phosphorescence (RTP) materials have attracted wide attention for their easy preparation, low toxicity and applications in professional fields such as bioimaging and anti-counterfeiting. Developing phosphorescent systems with more universality and less difficulty in synthesis has long been the pursuit of materials scientists. By employing polymeric quaternary ammonium salt with an ionic bonding matrix and heavy atoms, commercial fluorescent dyes are directly endowed with phosphorescence emission. In a single amorphous polymer, the external heavy-atom effect generates excited triplet states, which are further stabilized by the rigid polymer matrix. This study proposed a new general strategy to design and develop pure organic RTP materials starting from the vast library of organic dyes without complicated chemical synthesis.


2018 ◽  
Vol 122 (32) ◽  
pp. 6578-6584 ◽  
Author(s):  
Connor J. Easley ◽  
Magi Mettry ◽  
Emily M. Moses ◽  
Richard J. Hooley ◽  
Christopher J. Bardeen

2021 ◽  
Author(s):  
Shimpei Goto ◽  
Yuya Nitta ◽  
Nicolas Decarli ◽  
Leonardo Evaristo de Sousa ◽  
Patrycja Stachelek ◽  
...  

<div><div><div><p>A new twisted donor–acceptor–donor (D–A–D) multi-photofunctional organic molecule comprising of phenoselenazine as the electron-donors (Ds) and dibenzo[a,j]phenazine (DBPHZ) as the electron-acceptor (A) has been developed. The developed selenium-incorporated D–A–D compound is featured with multi-color polymorphism, distinct mechanochromic luminescence, chemically-stimulated luminochromism, thermally-activated delayed fluorescence, and room- temperature phosphorescence. The internal heavy atom effect on the photophysical properties of the D–A–D system has been investigated through the comparison with the physicochemical properties of a previously developed sulfur analogue and a tellurium analogue.</p></div></div></div>


2020 ◽  
Author(s):  
Heather Higginbotham ◽  
Masato Okazaki ◽  
Piotr de Silva ◽  
Satoshi Minakata ◽  
Youhei Takeda ◽  
...  

Room temperature phosphorescence materials offer great opportunities for applications in optoelectronics, due to their unique photophysical characteristics. However, purely organic emitters that can realize distinct electrophosphorescence are rarely exploited. Herein a new approach for designing heavy-atom-free organic room temperature phosphorescence emitters for organic light-emitting diodes is presented. The subtle tuning of the energy diagrams of singlet and triplet excited states by appropriate choice of host matrix allows tailored emission properties and switching of emission channels between thermally activated delayed fluorescence and room temperature phosphorescence. Moreover, an efficient and heavy-atom-free room temperature phosphorescence organic light-emitting diodes using the developed emitter is realized.


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