Green syntheses of stable and efficient organic dyes for organic hybrid light-emitting diodes
Green syntheses of stable and efficient organic dyes for organic hybrid light-emitting diodes
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DOI:
10.1039/d1tc01567b
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发表时间:
2021-05-13
影响因子:
6.4
通讯作者:
Luscombe, Christine K.
中科院分区:
文献类型:
--
作者:
Huang, Yunping;Cohen, Theodore A.;Luscombe, Christine K.
Organic hybrid light-emitting diodes (hybrid-LEDs) employ organic dyes as light converters on top of commercial blue inorganic LEDs, replacing incumbent inorganic phosphor light converters synthesized from rare-earth and/or toxic metallic elements to optimize device environmental sustainability. Here, we present two naturally derived organic dyes for hybrid-LEDs, highlighting stability and efficiency enhancement based on a novel "acceptor-acceptor" molecular design. This "acceptor-acceptor" skeleton comprises theobromine and thiadiazole, two electron-withdrawing groups that lower energy levels and suppress photooxidation. This differentiates these dyes from the widely adopted "donor-acceptor" skeleton, where photooxidation is facilitated by the presence of electron-donating units. Simultaneously, sidechains on organic dyes used to enhance solution processability, crucial for film transparency, introduce an additional photooxidation pathway. With this "acceptor-acceptor" skeleton, the destabilization from sidechains was offset by the stability enhancement from the electronic effects in the backbone. When blended within an industrial polymer, poly(styrene-butadiene-styrene) (SBS), their enhanced solubility enables the formation of highly transparent films, crucial for reducing scattering loss in LEDs. Furthermore, resultant dye-SBS films achieved photoluminescence quantum yields (PLQYs) of around 90% under ambient conditions. Taking advantage of their transparency and solution processability, we fabricated a waveguide with this theobromine-dye-SBS composite, which was subsequentially assembled into an edge-lit LED device of no glare and enhanced aesthetics.