Organic luminescent materials that exhibit thermally activated delayed fluorescence (TADF) can convert non-emissive triplet excitons into emissive singlet states through a reverse intersystem crossing (RISC) process. Therefore, they have tremendous potential for applications in organic light-emitting diodes (OLEDs). However, with the development of ultra-high definition 4K/8K display technologies, designing efficient deep-blue TADF materials to achieve the Commission Internationale de l'& Eacute;clairage (CIE) coordinates fulfilling BT.2020 remains a significant challenge. Here, an effective approach is proposed to design deep-blue TADF molecules based on hybrid long- and short-range charge-transfer by incorporation of multiple donor moieties into organoboron multiple resonance acceptors. The resulting TADF molecule exhibits deep-blue emission at 414 nm with a full width at half maximum (FWHM) of 29 nm, together with a thousand-fold increase in RISC rate. OLEDs based on the champion material achieve a record maximum external quantum efficiency (EQE) of 22.8% with CIE coordinates of (0.163, 0.046), approaching the coordinates of the BT.2020 blue standard. Moreover, TADF-assisted fluorescence devices employing the designed material as a sensitizer exhibit an exceptional EQE of 33.1%. This work thus provides a blueprint for future development of efficient deep-blue TADF emitters, representing an important milestone towards meeting the blue color gamut standard of BT.2020.Here, an effective approach is proposed to design deep-blue thermally activated delayed fluorescence molecules based on hybrid long- and short-range charge-transfer by incorporating multiple donor moieties into organoboron multiple resonance acceptors. The resulting molecule exhibits deep-blue emission, narrow spectra, and high reverse intersystem crossing rate. The organic light-emitting diode fabricated with the designed molecule records maximum external quantum efficiency of 22.8% with the Commission Internationale de l'& Eacute;clairage coordinates of (0.163, 0.046). image
Excited-State Engineering Enables Efficient Deep-Blue Light-Emitting Diodes Exhibiting BT.2020 Color Gamut / An R.-Z.; Sun Y.; Chen H.-Y.; Liu Y.; Privitera A.; Myers W.K.; Ronson T.K.; Gillett A.J.; Greenham N.C.; Cui L.-S.. - In: ADVANCED MATERIALS. - ISSN 1521-4095. - ELETTRONICO. - 36:(2024), pp. 2313602.1-2313602.8. [10.1002/adma.202313602]
Excited-State Engineering Enables Efficient Deep-Blue Light-Emitting Diodes Exhibiting BT.2020 Color Gamut
Privitera A.;
2024
Abstract
Organic luminescent materials that exhibit thermally activated delayed fluorescence (TADF) can convert non-emissive triplet excitons into emissive singlet states through a reverse intersystem crossing (RISC) process. Therefore, they have tremendous potential for applications in organic light-emitting diodes (OLEDs). However, with the development of ultra-high definition 4K/8K display technologies, designing efficient deep-blue TADF materials to achieve the Commission Internationale de l'& Eacute;clairage (CIE) coordinates fulfilling BT.2020 remains a significant challenge. Here, an effective approach is proposed to design deep-blue TADF molecules based on hybrid long- and short-range charge-transfer by incorporation of multiple donor moieties into organoboron multiple resonance acceptors. The resulting TADF molecule exhibits deep-blue emission at 414 nm with a full width at half maximum (FWHM) of 29 nm, together with a thousand-fold increase in RISC rate. OLEDs based on the champion material achieve a record maximum external quantum efficiency (EQE) of 22.8% with CIE coordinates of (0.163, 0.046), approaching the coordinates of the BT.2020 blue standard. Moreover, TADF-assisted fluorescence devices employing the designed material as a sensitizer exhibit an exceptional EQE of 33.1%. This work thus provides a blueprint for future development of efficient deep-blue TADF emitters, representing an important milestone towards meeting the blue color gamut standard of BT.2020.Here, an effective approach is proposed to design deep-blue thermally activated delayed fluorescence molecules based on hybrid long- and short-range charge-transfer by incorporating multiple donor moieties into organoboron multiple resonance acceptors. The resulting molecule exhibits deep-blue emission, narrow spectra, and high reverse intersystem crossing rate. The organic light-emitting diode fabricated with the designed molecule records maximum external quantum efficiency of 22.8% with the Commission Internationale de l'& Eacute;clairage coordinates of (0.163, 0.046). imageI documenti in FLORE sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.