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oe1(光电查) - 科学论文

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出版时间
  • 2018
研究主题
  • ac-dc difference
  • Thermal transfer standard
  • inductive voltage
  • uncertainty budget
  • pulse-driven ac Josephson voltage standard
应用领域
  • Measurement and Control Technology and Instruments
机构单位
  • National Institute of Metrology
1183 条数据
?? 中文（中国） ▾

  • Utilization of Ternary Europium Complex for Organic Electroluminescent Devices and as a Sensitizer to Improve Electroluminescence of Red-Emitting Iridium Complex

    摘要： Two new lanthanide complexes [Ln(hfaa)3(Py-Im)] [hfaa = hexafluoroacetylacetone, Py-Im = 2-(2-pyridyl)benzimidazole and Ln = Eu(III) (1) and Tb(III) (2)] were synthesized and characterized. An X-ray crystal structure determination confirms that complex 1 is eight-coordinate with a distorted trigonal dodecahedral geometry. It shows typical vivid red Eu(III) emission in the solid state, in solution, and in a polymer matrix. The observed lifetime (τobs) of complex 1 in the solid state, in dichloromethane (DCM) solution, and in thin films is 833.01, 837.95, and 626.16?715.69 μs, respectively, with a photoluminescence quantum yield QEuL ≈ 33% in DCM solution. Complex 2 displays a yellowish-green emission in the solid state (τobs ≈ 36.99 μs), while a near white-light emission in solution (x; 0.2574: y; 0.3371) and in thin films. Therefore, it is a potential candidate for generating single-component white light-emitting materials for solid-state lighting applications. The kinetic scheme for modeling energy-transfer processes shows that the main donor state for 1 is the ligand triplet state (T1) and that energy transfer occurs to both the 5D1 (56.55%) and 5D0 (40.58%) levels. We fabricated a series of single- and double-layer organic light-emitting devices using complex 1. The luminance of the optimized double-layer electroluminescence (EL) device was 373 cd/m2 with very low turn-on voltage of ～4.2 V. Complex 1 was further utilized as a sensitizer to improve the EL of a red-emitting iridium complex PQ2Ir(dpm) (PQ = phenylquinoly-N,C2′, dpm = dipivaloylmethane). The codoped device achieved a maximum brightness and maximum current efficiency (ηc) of 93 224 cd/m2 and 36.38 cd/A, respectively.

    关键词： electroluminescence,organic light-emitting devices,photoluminescence,energy transfer,lanthanide complexes

    更新于2025-11-20 15:33:11

  • Energy transfer behaviors and tunable luminescence in Tb3+/Eu3+ codoped oxyfluoride glass ceramics containing cubic/hexagonal NaYF4 nanocrystals

    摘要： For glass ceramics, glass crystallization and doping activators into nanocrystalline phases are the key factors determining optical performance, including energy transfer (ET) process. Herein, we propose a strategy to verify ET behaviors based on glass crystallization, elaborately selecting phase-transformed NaYF4: Tb3+, Eu3+ nanocrystals embedded transparent glass ceramics as a typical example. The ET behaviors from Tb3+ to Eu3+ are clarified via photoluminescence spectra, time-resolved spectra and decay curves. Impressively, the corresponding ET process in cubic NaYF4 turns out to be more efficient than that in hexagonal, in spite of a disorder-to-order transformation from cubic to hexagonal. The reason for this abnormal ET efficiency is that dopants prefer to be partitioned into the cubic NaYF4 rather than the hexagonal one during glass crystallization. This work provides keen insights into the relationship between glass crystallization and ET behaviors, which can also feed back to helpfully guide the design and fabrication of glass ceramics with superior optical performance.

    关键词： glass crystallization,cubic/hexagonal NaYF4,energy transfer

    更新于2025-11-20 15:33:11

  • Single-Composition White Light Emission from Dy3+ Doped Sr2CaWO6

    摘要： A series of Dy3+ ion doped Sr2CaWO6 phosphors with double perovskite structure were synthesized by traditional high temperature solid-state method. It was found that there is significant energy transfer between Dy3+ and the host lattice, and the intensities of emission peaks at 449 nm (blue), 499 nm (cyan), 599 nm (orange), 670 nm (red), and 766 nm (infra-red) can be changed by adjusting the concentration of dopant amount of Dy3+ ion in Sr2CaWO6. The correlated color temperature of Dy3+ ion doped Sr2CaWO6 phosphors can be tuned by adjusting the concentration of Dy3+ ion. Upon optimal doping at 1.00 mol% Dy3+, white light with chromaticity coordinate (0.34, 0.33) was emitted under excitation at 310 nm. Thus, single composition white emission is realized in Dy3+ doped Sr2CaWO6.

    关键词： double perovskite,energy transfer,white light-emitting,photoluminescence

    更新于2025-11-20 15:33:11

  • Energy transfer in and fluorescence studies of the Eu-Tb doped BPA-phen system

    摘要： To enhance the red emission efficiency of Eu3+ complexes, [Eu/Tbx(BPA)3phen] (BPA = bisphenol A, phen = 1,10-phenanthroline) is designed and synthesized. The complexes are characterized fully and their luminescence properties are evaluated. Co-fluorescence is detected in the Eu/Tbx(BPA)3phen complexes, and the existence of Tb3+ enhances the luminescence intensity of the central Eu3+ because of the intramolecular energy transfer from the 5D4 level of Tb3+ to the 5D0 level of Eu3+. The luminescence intensity of europium ions at 615 nm is the highest for Eu/Tb1(BPA)3phen. To improve the thermal stabilities and mechanical properties of pure complexes, Eu/Tb1(BPA)3phen/PAN (PAN = polyacrylonitrile) is used to fabricate fibres by electrospinning. Compared with Eu/Tb1(BPA)3phen (τ = 1.1087 ms), the fibres have a longer fluorescence lifetime of 1.533 ms. The fibres also retain a high quantum yield of 47.16%. Thus, the flexible luminescent fibres have potential applications in many fields.

    关键词： electrospinning,Bisphenol A,energy transfer,luminescence

    更新于2025-11-20 15:33:11

  • Tuning the luminescence of nitrogen-doped graphene quantum dots synthesized by pulsed laser ablation in liquid and their use as a selective photoluminescence on–off–on probe for ascorbic acid detection

    摘要： In this work, nitrogen-doped graphene quantum dots (N-GQDs) were synthesized by pulsed laser ablation in liquid using Nd:YAG laser (532 nm). Graphite target was ablated in dimethylformamide, as solvent and nitrogen source, and the microstructure as well as optical properties of N-GQDs were studied. The N-GQDs structure consists of a graphitic core with oxygen and nitrogen functionalities and particle size about 3 nm, as demonstrated by X-ray photoelectron spectroscopy, Raman spectroscopy and transmission electron microscopy. The as-prepared N-GQDs structure was modified by solvothermal treatment at 65, 90 and 120 °C reducing the oxygen functional groups, adding nitrogen and restoring the π-conjugated structure of N-GQD. The N-GQDs exhibit UV-Vis absorption spectrum with the characteristic π-π* and n – π* electronic transitions of the GQDs with a large amount of oxygen and nitrogen functionalities. These N-GQDs exhibited a visible light photoluminescence centered at 486 nm upon an excitation of 410 nm and the photoluminescence intensity enhanced up to 4.05% of quantum yield after solvothermal treatment. The N-GQDs dispersion was used for selective detection of ascorbic acid, through a signal-off and signal-on system. The results show the use of N-GQDs as a competent photoluminescence sensor for metal ions and ascorbic acid.

    关键词： Fluorescence quenching,electron transfer,carbon nanoparticles

    更新于2025-11-19 16:56:42

  • Sensitized photochemical CO2 reduction by hetero-Pacman compounds linking a Re(I) tricarbonyl with a porphyrin unit

    摘要： The hetero-Pacman architecture places two different metal coordination sites in close proximity, which can support efficient energy and/or electron transfer and allow for cooperative activation of small molecules. Herein, we present the synthesis of dyads consisting of a porphyrin unit as photosensitizer and a rhenium unit as catalytically active site, which are held together by the rigid xanthene backbone. Mononuclear [(NN)Re(CO)3(Cl)] complexes for CO2 reduction where NN represents a bidentate diimine ligand (e.g. bipyridine or phenanthroline) lack light absorption in the visible region, resulting in poor photocatalysis upon illumination with visible light. In order to improve their visible light absorption, we have focused on the incorporation of a strongly absorbing free base or zinc porphyrin unit. Resulting photocatalytic experiments showed a strong dependence of catalytic performance on both the type of photosensitizer and also the excitation wavelengths. Most notably, the intramolecular hetero-Pacman system containing a zinc porphyrin unit showed much better catalytic activity in the visible region (excitation wavelengths >450 nm) than the free base version, the corresponding mononuclear rhenium compound or an intermolecular system comprised of a 1:1 mixture of the mononuclear analogues.

    关键词： photocatalysis,CO2 reduction,electron transfer,porphyrin,rhenium

    更新于2025-11-19 16:56:35

  • Manipulating the Phase Distributions and Carrier Transfers in Hybrid Quasi-Two-Dimensional Perovskite Films

    摘要： Quasi two-dimensional perovskites are promising alternatives to conventional three-dimensional perovskites because of their high stability and easy tunability. However, controlling the phase distribution according to device architecture remains a major challenge. Here, the manipulation of phase purity and vertical distribution proven by ultrafast transient absorption spectroscopy, and their effect on device characteristics are reported. By adding ethyl acetate as antisolvent, the growth direction of the perovskite film is flipped. CH3NH3Cl and dimethyl sulfoxide are used to slow the growth rate of the crystal, which gives better phase purity. The direction of carrier transfer is tuned accordingly. It is found that solar cell performance is more sensitive to phase purity relative to vertical distribution. These findings are of importance for the applications of quasi-2D perovskites in different types of devices that require to change phase purity and vertical distribution.

    关键词： solar cells,carrier transfer,vertical distribution,phase purity,quasi-2D perovskite

    更新于2025-11-19 16:56:35

  • Excited state intramolecular single proton transfer mechanism of pigment yellow 101 in solid state: Experiment and DFT calculation

    摘要： To investigate fluorescence mechanism of Pigment Yellow 101 (P. Y. 101) in solid state, three aromatic aldehyde azines (1-3) including P. Y. 101 have been synthesized and compared with each other. Results indicated that P. Y. 101 prepared by solvothermal method is actually the mixture of two polymorphs, whose molecular packing mode can be transformed into each other by recrystallizing or external stimuli such as pressure and grinding. The ESIPT properties of 1-3 were investigated by DFT/TD-DFT calculations and time-correlated single photon counting (TCSPC) technique. Both experimental and theoretical results revealed that the dual fluorescence properties of P. Y. 101 in solid state are ascribed to the excited-state intramolecular single proton transfer fluorescence emissions of two structurally different polymorphs rather than the results of the sequential or concerted excited-state intramolecular double proton transfers, which provide a potential valuable tool for developing multistimuli-responsive luminescent materials.

    关键词： Aromatic aldehyde azines,DFT calculation,P. Y. 101,Excited-state intramolecular proton transfer,Polymorphs

    更新于2025-11-19 16:56:35

  • Tuning the Functional Groups on Carbon Nanodots and Antioxidant Studies

    摘要： Carbon nanodots (CNDs) have shown good antioxidant capabilities by scavenging oxidant free radicals such as diphenyl-1-picrylhydrazyl radical (DPPH?) and reactive oxygen species. While some studies suggest that the antioxidation activities associate to the proton donor role of surface active groups like carboxyl groups (–COOH), it is unclear how exactly the extent of oxidant scavenging potential and its related mechanisms are influenced by functional groups on CNDs’ surfaces. In this work, carboxyl and the amino functional groups on CNDs’ surfaces are modified to investigate the individual influence of intermolecular interactions with DPPH? free radical by UV-Vis spectroscopy and electrochemistry. The results suggest that both the carboxyl and the amino groups contribute to the antioxidation activity of CNDs through either a direct or indirect hydrogen atom transfer reaction with DPPH?.

    关键词： carbon nanodots,radical scavenging,electro-chemistry,functional groups,antioxidation,charge transfer

    更新于2025-11-19 16:56:35

  • Reconstructing Dual‐Induced {0 0 1} Facets Bismuth Oxychloride Nanosheets Heterostructures: An Effective Strategy to Promote Photocatalytic Oxygen Evolution

    摘要： Sunlight-driven photocatalytic water splitting to generate oxygen (O2) is a promising approach for utilizing solar energy. Herein, direct Z-scheme heterostructure photocatalysts composed of ultrathin Bi3O4Cl and BiOCl nanosheets are rationally fabricated via alkaline chemical etching and solvent exfoliation for O2 evolution under visible light. With AgNO3 and FeCl3 as the electron scavenger, the optimized ultrathin Bi3O4Cl/BiOCl exhibits prominent photocatalytic activity for O2 production under visible-light illumination and the production rate (58.6 μmol g?1 h?1) is much higher than the nanocrystal heterostructure (28.5 μmol g?1 h?1). This ultrathin heterostructure system can efficiently transfer the electrons, which leads to a considerable improvement in the photocatalytic performance. Due to the suitable band edge potentials and the intense electronic interaction between two-dimensional (2D) Bi3O4Cl and 2D BiOCl, as confirmed by theoretical computations, photoluminescence, and photoelectricity tests, the ultrathin heterojunction with an internal electric field has a highly remarkable charge transfer. The intimate interface contact and {0 0 1} facets effect promote the high photocatalytic performance of the ultrathin Bi3O4Cl/BiOCl heterostructure.

    关键词： remarkable charge transfer,ultrathin Bi3O4Cl/BiOCl heterostructure,facets effect,photocatalysis

    更新于2025-11-19 16:51:07