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. Additionally, TBA-SAPP ligands effectively eliminate the defects in PNC film, yielding exceptional photoluminescence properties with a near-unity quantum yield. Consequently, the multifunctional ligands improved F-PLEDs to achieve a record-high external quantum efficiency (EQE) of 16.2% compared to the previously reported pure-red flexible PLEDs and display substantially improved spectral and operational stability. Equally important, these devices demonstrate robust mechanical properties, enduring a small folding radius of 1 mm for 5000 cycles. This ligand strategy is anticipated to inspire relevant research in PNCs and promote the realization of highly efficient and mechanically stable F-PLEDs.
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http://dx.doi.org/10.1002/adma.202415211 | DOI Listing |
Adv 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 PDFAmino Acids
January 2020
Institutul National de Cercetare Dezvoltare pentru Electrochimie si Materie Condensata, Str. Dr. A. Paunescu Podeanu, Nr. 144, 300569, Timisoara, Romania.
The task of this work was to investigate the extraction capacity of various calixarenes for free and esterified amino acids from aqueous acid phases. Furthermore, this method was applied to aqueous extracts of Helleborus purpurascens. Generally, it is known that calixarenes can be used as extractants for ammonium compounds due to π-cation and lone pair cation interactions.
View Article and Find Full Text PDFOrg Biomol Chem
March 2018
Organic Chemistry Laboratory, Department of Chemistry, National and Kapodistrian University of Athens, 10571, Athens, Greece.
A number of environmental pollutants and endogenous oxidation agents form 1-(2-deoxy-β-d-ribofuranosyl)-5-hydroxy-5-methylhydantoin (HydT), an important DNA lesion resulting from thymidine oxidation. In this paper, two intermediates, postulated in the formation of HydT, have been characterised for the first time. The first, N1-formyl-N3-pyruvoylurea intermediate, was produced by the ozonolysis reaction of 2',3',5'-tri-O-acetylribo-, 3',5'-di-O-TBS- and N3,O3',O5-tribenzyl-protected thymidines and was shown to produce, upon decomposition and depending on the protecting group and the conditions, HydT alone, or together with protected-β-d-ribofuranosyl-N1-formylurea and formamide products.
View Article and Find Full Text PDFActa Crystallogr Sect E Struct Rep Online
January 2010
Department of Chemistry, Shahid Beheshti University, G. C., Evin, Tehran 1983963113, Iran.
In the title compound, (C(21)H(22)N)(2)[AuCl(4)]Cl, the Au(III) atom adopts a square-planar coordination geometry defined by four chloride ions. In the crystal structure, inter-molecular N-H⋯Cl hydrogen bonds link the organic cations and the uncoordinated chloride ion.
View Article and Find Full Text PDFBioorg Med Chem
June 2004
Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, Flemingovo nám. 2, 166 10 Prague 6, Czech Republic.
Treatment of 6-bromomethyl- or 6-dibromomethyl-5-nitropyrimidine-2,4-diamine with KCN gave the same product--(2,6-diamino-5-nitropyrimidinyl)acetonitrile. Benzylation of the nitrile took place on the alpha-carbon to the cyano group preferentially affording the corresponding mono- and dibenzyl derivative, whose reductive cyclization resulted in 7-benzyl-5H-pyrrolo[3,2-d]pyrimidine-2,4-diamine and 7,7-dibenzyl-7H-pyrrolo[3,2-d]pyrimidine-2,4,6-triamine, respectively. Suitability of the protection of N(2) and N(4) atoms with benzyl, acetyl, or benzoyl groups was also investigated.
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