98%
921
2 minutes
20
Lead-halide perovskite light-emitting diodes (PeLEDs) are intrinsically capable of delivering high efficiency at high current densities compared to conventional solution-processed light-emitting diodes. While such performance and relevant high radiance have been well demonstrated in green and near-infrared ones, blue PeLEDs have lagged far behind due to extremely severe luminance-efficiency roll-off, especially in the pure-blue region (<480 nm, a CIEy coordinate below 0.15). Here, by tackling the critical limitations of phosphonic acid functional carbazoles (PACs) as hole injection layers and simultaneously leveraging their advantages on hole injection, we achieved ultrabright pure blue PeLEDs with minimized efficiency roll-off at high brightness with a CIEy coordinate below 0.15. We show that devices based on prevailing small-molecule PACs generally exhibit significant leakage currents. This is due to a synergistic effect of uneven surface coverage from reverse micelle formation and the nanoisland structure of thin-film lead-halide perovskite emitters. By using polymeric PACs instead, we demonstrate bright blue PeLEDs showing a peak luminance of ∼29 800 cd m (478 nm, at a CIEy coordinate below 0.15). We also achieve a high brightness reaching ∼140 000 cd m under pulsed driven. Our study not only provides a useful guidance for developing bright blue PeLEDs but also resolves a long-standing puzzle regarding the interfacial properties of PACs and their impact on hole transport, and it helps with the further design of these materials for lead-halide perovskite applications.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acsnano.5c01879 | DOI Listing |
J Phys Chem Lett
September 2025
School of Materials Science and Engineering, Changchun University of Science and Technology, Changchun 130022, People's Republic of China.
Inverted quantum dot light-emitting diodes (QLEDs) show great promise for next-generation displays due to their compatibility with integrated circuit architectures. However, their development has been hindered by inefficient exciton utilization and charge transport imbalance. Here, we present a strategy for regulating charge-exciton dynamics through the rational design of a multifunctional hole transport layer (HTL), incorporating polyethylenimine ethoxylated (PEIE) as a protective interlayer in fully-solution-processed inverted red QLEDs.
View Article and Find Full Text PDFAdv Mater
September 2025
State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun, 130012, P. R. China.
Helicene-based circularly polarized luminescence (CPL) materials suffer from severely low color purity in circularly polarized organic light-emitting diodes (CP-OLEDs). Here, a novel molecular engineering strategy is introduced by replacing helicene containing continuous fused benzene rings with a multiple resonance (MR) framework comprising discontinuous fused benzene rings. This approach effectively suppresses high-frequency C─C bond stretching vibrations and enhances short-range charge transfer, enabling high color purity, CPL activity, and efficient thermally activated delayed fluorescence (TADF).
View Article and Find Full Text PDFInt J Dermatol
July 2025
Brigham and Women's Hospital, Boston, Massachusetts, USA.
ACS Appl Mater Interfaces
September 2025
Organic Electronic Materials Laboratory, Department of Information Display, College of Sciences, Kyung Hee University, Seoul 02447, Republic of Korea.
Solution-processed phosphorescent inverted organic light-emitting diodes (s-IOLEDs) have garnered significant attention due to their excellent stability and high performance. However, frequently used inorganic electron transport layers usually cause exciton dissociation at the emitting layer interface, leading to low device efficiency and severe efficiency roll-off. In this work, we designed a cross-linkable triazine-grafted electron transport copolymer (PPDPT--PBCB) with a high triplet energy (3.
View Article and Find Full Text PDFBeilstein J Nanotechnol
August 2025
Nanotechnology Lab, Research Laboratories of Saigon Hi-Tech Park, Lot I3, N2 Street, Tang Nhon Phu Ward, Ho Chi Minh City 70000, Vietnam.
Silver nanoprisms (AgNPrs) are promising candidates for surface-enhanced Raman scattering (SERS) due to their strong localized surface plasmon resonance and sharp tip geometry. In this study, AgNPrs were synthesized through a photochemical method by irradiating spherical silver nanoparticle seeds with 10 W green light-emitting diodes (LEDs; 520 ± 20 nm) for various periods of time up to 72 h. The growth mechanism was investigated through ultraviolet-visible spectroscopy, field-emission scanning electron microscopy, X-ray diffraction, and transmission electron microscopy analyses, confirming the gradual transformation of spherical seeds into AgNPrs.
View Article and Find Full Text PDF