The design and synthesis of highly efficient deep red (DR) and near-infrared (NIR) organic emitting materials with characteristic of thermally activated delayed fluorescence (TADF) still remains a great challenge. A strategy was developed to construct TADF organic solid films with strong DR or NIR emission feature. The triphenylamine (TPA) and quinoxaline-6,7-dicarbonitrile (QCN) were employed as electron donor (D) and acceptor (A), respectively, to synthesize a TADF compound, TPA-QCN. The TPA-QCN molecule with orange-red emission in solution was employed as a dopant to prepare DR and NIR luminescent solid thin films. The high doped concentration and neat films exhibited efficient DR and NIR emissions, respectively. The highly efficient DR and NIR organic light-emitting devices (OLEDs) were fabricated by regulating TPA-QCN dopant concentration in the emitting layers.

The design and preparation of metal-free organic materials that exhibit room-temperature phosphorescence (RTP) is a very attractive topic owing to potential applications in organic optoelectronic devices. Herein, we present a facile approach to efficient and long-lived organic RTP involving the doping of N-phenylnaphthalen-2-amine (PNA) or its derivatives into a crystalline 4,4'-dibromobiphenyl (DBBP) matrix. The resulting materials showed strong and persistent RTP emission with a quantum efficiency of approximately 20 % and a lifetime of a few to more than 100 milliseconds. Bright white dual emission containing blue fluorescence and yellowish-green RTP from the PNA-doped DBBP crystals was also confirmed by Commission Internationale de l'Eclairage (CIE) coordinates of (x=0.29-0.31, y=0.38-0.41).

Thermally activated delayed fluorescence (TADF) materials that are able to realize electroluminescence showing simultaneously narrow emission band, high color purity, and high efficiency are highly demanded for display applications. Up to now, a few blue emissive TADF materials with such characteristics have been reported, while green TADF materials with such features are extremely scarce. Herein, two TADF compounds with highly efficient narrowband bluish green/green emission (full‐width at half‐maximum (FWHM): 22 and 21 nm in toluene) induced by multiple resonance effect are reported. An optimized organic light‐emitting diode based on the green emissive compound shows a fairly narrow electroluminescent spectrum (FWHM: 33 nm), as well as an excellent color purity with the Commission Internationale de L'Eclairage (CIE) coordinates of (0.20, 0.65), which is a close resemblance to the standard green‐light CIE coordinates of (0.21, 0.71) defined by the National Television System Committee. Meanwhile, the maximum external quantum efficiency (EQE) up to 25.5% is achieved and a high EQE of 20.1% is maintained at a practical high luminance of 1000 cd m−2. The outstanding device performance of the compound makes it attractive for potential practical applications.

Herein, a ternary boron-oxygen-nitrogen embedded polycyclic aromatic hydrocarbon with multiple resonance thermally activated delayed fluorescence (MR-TADF), namely DBNO, is developed by adopting the para boron-πboron and para oxygen-π-oxygen strategy. The designed molecule presents a vivid green emission with a high photoluminescence quantum yield (96 %) and an extremely narrow full width at half maximum (FWHM) of 19 nm/ 0.09 eV, which surpasses all previously reported green TADF emitters to date. In addition, the long molecular structure along the transition dipole moment direction endows it with a high horizontal emitting dipole ratio of 96 %. The organic light-emitting diode (OLED) based on DBNO reveals a narrowband green emission with a peak at 504 nm and a FWHM of 24 nm/0.12 eV. Particularly, a significantly improved device performance is achieved by the TADFsensitization (hyperfluorescence) mechanism, presenting a FWHM of 27 nm and a maximum external quantum efficiency (EQE) of 37.1 %.

A pure organic molecule 2,6-di­(phenothiazinyl)­naphthalene (DPTZN) with room-temperature phosphorescence (RTP) features was developed. Remarkably, a triazine-benzimidazole-based molecule TRZ-BIM can significantly improve the RTP efficiency of DPTZN in DPTZN:TRZ-BIM blend films. The photoluminescence quantum yield (PLQY) of 10 wt % DPTZN:TRZ-BIM blend film is 38%. The RTP property of DPTZN:TRZ-BIM blend films was characterized by steady, time-resolved, and temperature-dependent emission spectra. An organic light-emitting diode (OLED) with 10 wt % DPTZN:TRZ-BIM blend film as the emitting layer showed a high maximum external quantum efficiency of 11.5%, current efficiency of 33.8 cd A–1, and power efficiency of 32.6 lm W–1. Herein, we have developed an efficient approach to achieve precious-metal-free organic films that can be employed to fabricate high-performance phosphorescence OLEDs.