Achieving efficient pure-red emission in perovskite-based high-definition display applications remains challenging due to persistent spectral, thermodynamic, and operational instability. Although significant progress has been made using red-emitting quasi-2D perovskites, quantum dots, and mixed-halide perovskites, their performance under operational conditions often remains limited. Here, we address these challenges by embedding mixed-halide perovskite nanocrystals (PeNCs) into a polymer matrix to create a donor-acceptor architecture. This hybrid system stabilizes the nanocrystals and enables efficient energy transfer Förster resonance energy transfer (FRET). We observe enhanced acceptor photoluminescence and reduced donor lifetimes, confirming the effective FRET-mediated energy transfer arising from optimal spectral overlap. With a FRET rate of 0.18 ps and a FRET efficiency of 88.9%, our approach provides spectrally stable, enhanced pure-red emission. Moreover, it demonstrates a pathway for designing customized energy cascades, paving the way for next-generation optoelectronic devices with improved stability and performance.
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http://dx.doi.org/10.1039/d4nr05253f | DOI Listing |
Nanoscale
March 2025
Centre for Nano Science and Engineering, Indian Institute of Science, Bengaluru 560012, Karnataka, India.
Achieving efficient pure-red emission in perovskite-based high-definition display applications remains challenging due to persistent spectral, thermodynamic, and operational instability. Although significant progress has been made using red-emitting quasi-2D perovskites, quantum dots, and mixed-halide perovskites, their performance under operational conditions often remains limited. Here, we address these challenges by embedding mixed-halide perovskite nanocrystals (PeNCs) into a polymer matrix to create a donor-acceptor architecture.
View Article and Find Full Text PDFLight Sci Appl
March 2025
Wuhan National Laboratory for Optoelectronics (WNLO) and School of Optical and Electronic Information, Huazhong University of Science and Technology (HUST), 1037 Luoyu Road, Wuhan, Hubei, 430074, China.
Vacuum-deposited perovskite light-emitting diodes (PeLEDs) have demonstrated significant potential for high-color-gamut active-matrix displays. Despite the rapid advance of green PeLEDs, red ones remain a considerable challenge because of the inferior photophysical properties of vacuum-deposited red-light-emitting materials. Here, a rationally designed fluorine-modified phosphine oxide additive was introduced to in-situ passivate vacuum-deposited perovskites.
View Article and Find Full Text PDFAdv Mater
March 2025
Department of Electrical and Electronic Engineering, the University of Hong Kong, Hong Kong, P. R. China.
Lead-halide perovskite nanocrystals (PNCs) exhibit significant potential for advancing foldable perovskite light-emitting diodes (F-PLEDs) due to their discrete crystalline morphology, bright emission across an extensive color gamut, and remarkable color purity; however, their progression remains in the early stages with the concerns of inadequate performance and mechanical instability. This study proposes a ligand strategy employing tribenzyl organic cation (tribenzylamine, TBA) carried multidentate X-type Lewis soft base (sodium acid pyrophosphate, SAPP) to address the challenges above simultaneously. Specifically, the use of multibranched aromatic ligands considerably improved the adhesion force between PNCs and adjacent layers, enhancing mechanical stability during folding, while the control sample shows deleterious cracks.
View Article and Find Full Text PDFNature
February 2025
State Key Laboratory of Advanced Chemical Power Sources, Frontiers Science Center for New Organic Matter, Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), College of Chemistry, Nankai University, Tianjin, People's Republic of China.
Ultrasmall CsPbI perovskite quantum dots (QDs) are the most promising candidates for realizing efficient and stable pure-red perovskite light-emitting diodes (PeLEDs). However, it is challenging for ultrasmall CsPbI QDs to retain their solution-phase properties when they assemble into conductive films, greatly hindering their device application. Here we report an approach for in situ deposit stabilized ultrasmall CsPbI QD conductive solids, by constructing CsPbI QD/quasi-two-dimensional (quasi-2D) perovskite heteroepitaxy.
View Article and Find Full Text PDFJ Colloid Interface Sci
February 2025
CAS Key Laboratory of Design and Assembly of Functional Nanostructures, and Fujian Key Laboratory of Nanomaterials Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou 350002 PR China; Fujian Science & Technology Innovation Laboratory for Optoelectronic Information of China, Fuzhou 350108 PR China; University of Chinese Academy of Sciences, Beijing 100049 PR China; Xiamen Key Laboratory of Rare Earth Photoelectric Functional Materials, Xiamen Research Center of Rare Earth Materials, Haixi Institute, Chinese Academy of Sciences, Xiamen 361021 PR China. Electronic address:
Iodide-bromide mixed perovskites have attracted significant attention for achieving pure-red emission. However, halide migration hinders the development of efficient and stable devices. We introduce an in situ crystallization regulation strategy using post-annealing to optimize pure-red CsPb(Br/I)/PVDF composite films.
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