9,9二炔丙基芴的合成和发光性能(英文)

芴与炔丙基溴在NaOH/PhCH2N+Me3C l催化作用下反应生成85%的二炔丙基芴(DPF).在10-4Pa真空中的ITO玻璃基板上沉积DPF制成EL器件.测得DPF特有的紫外可见吸收波段为337nm和354nm,其在432nm的蓝色光致发光(PL)光谱对应的光子能量是2.87eV.二炔丙基芴电致发光(EL)器件具有典型的矫正二极管性能,蓝色的电致发光光波以及12V的开启电压.由光谱扫描色度计PR-705测得色度值为(0.16,0.17),意味着器件发深蓝光.通过微分扫描热量计和热解重量分析仪研究DPF的热反应性能,其熔点和反应温度分别为117℃和247℃.

Phase transition and photoluminescence properties of Eu^3＋-doped ZnMoO4 red phosphors

Eu3＋-doped ZnMoO4 with different doping concentrations were synthesized by a hydrothermal method. The effects of Eu3＋ doping on the phase structure and photoluminescence （PL） properties of ZnMoO4 were investigated. The result showed that the introduction of Eu3~ could lead to phase transition of ZnMoO4. With the increase of Eu3-- doping amount, [3-ZnMoO4 was transformed to ct phase gradually, which led to different photoluminescence performances. The optimized doping concentration of Eu3＋ was 6 mol% for the highest emission intensity at 615 nm. Its CIE chromaticity coordinates were （0.667, 0.331）, which were very close to the values of standard chromaticity （0.67, 0.33） for National Television Standards Committee （NTSC） system. Therefore, Eu3＋-doped ZnMoO4 is considered to be a promising red-emitting phosphor for white LED applications.

Photoluminescence mechanisms of red-emissive carbon dots derived from non-conjugated molecules

Red-emissive carbon dots(R-CDs)have been widely studied because of their potential application in tissue imaging and optoelectronic devices.At present,most R-CDs are synthesized by using aromatic precursors,but the synthesis of R-CDs from non-aromatic precursors is challenging,and the emission mechanism remains unclear.Herein,different R-CDs were rationally synthesized using citric acid(CA),a prototype non-aromatic precursor,with the assistance of ammonia.Their structural evolution and optical mechanism were investigated.The addition of NH_(3)·H_(2)O played a key role in the synthesis of CA-based R-CDs,which shifted the emission wavelength of CA-based CDs from 423 to 667 nm.Mass spectrometry(MS)analysis indicated that the amino groups served as N dopants and promoted the formation of localized conjugated domains through an intermolecular amide ring,thereby inducing a significant emission redshift.The red-emissive mechanism of CDs was further confirmed by control experiments using other CA-like molecules(e.g.,aconitic acid,tartaric acid,aspartic acid,malic acid,and maleic acid)as precursors.MS,nuclear magnetic resonance characterization,and computational modeling revealed that the main carbon chain length of CA-like precursors tailored the cyclization mode,leading to hexatomic,pentatomic,unstable three/four-membered ring systems or cyclization failure.Among these systems,the hexatomic ring led to the largest emission redshift(244 nm,known for CA-based CDs).This work determined the origin of red emission in CA-based CDs,which would guide research on the controlled synthesis of R-CDs from other non-aromatic precursors.

A selective sensor for cyanide ion(CN^-) based on the inner filter effect of metal nanoparticles with photoluminescent carbon dots as the fluorophore

Herein, we report a plasmonic metal nanoparti- cle-involved sensor for cyanide ion based on the inner filter effect by using photoluminescent carbon dots as the signal reporter. With commercial bee pollen as the carbon resource, we synthesized photoluminescent nitrogen-doped carbon dots by a one-pot hydrothermal process, and their fluores- cence quantum yield reached as high as 10.2 % ± 0.5 %. Fluorescence measurements indicated that the fluorescence of the carbon dots was insusceptible to the presence of many environmentally ordinary ions. Thanks to this “inert” property, we then developed a turn-on fluorescent sensor for cyanide ion in an inner filter effect manner by using carbon dots as the fluorophore and gold or silver nanoparticle as the light absorber. This detection technique is expected to be used for other metal nanoparticles-carbon dots ensemble fluorescent assays.

Exceptionally efficient deep blue anthracene-based luminogens:design,synthesis,photophysical,and electroluminescent mechanisms

Achieving high-efficiency deep blue emitter with CIE_(y)<0.06(CIE,Commission Internationale de L’Eclairage)and external quantum efficiency(EQE)>10%has been a long-standing challenge for traditional fluorescent materials in organic light-emitting diodes(OLEDs).Here,we report the rational design and synthesis of two new deep blue luminogens:4-(10-(4’-(9 H-carbazol-9-yl)-2,5-dimethyl-[1,1’-biphe nyl]-4-yl)anthracen-9-yl)benzonitrile(2 M-ph-pCzAnBzt)and 4-(10-(4-(9 H-carbazol-9-yl)-2,5-dimethyl phenyl)anthracen-9-yl)benzonitrile(2 M-pCzAnBzt).In particular,2 M-ph-pCzAnBzt produces saturated deep blue emissions in a non-doped electroluminescent device with an exceptionally high EQE of 10.44% and CIE_(x,y)(0.151,0.057).The unprecedented electroluminescent efficiency is attributed to the combined effects of higher-order reversed intersystem crossing and triplet-triplet up-conversion,which are supported by analysis of theoretical calculation,triplet sensitization experiments,as well as nanosecond transient absorption spectroscopy.This research offers a new approach to resolve the shortage of high efficiency deep blue fluorescent emitters.