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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） ▾

  • Broad-Spectrum Tunable Photoluminescent Material Based on Cascade Fluorescence Resonance Energy Transfer between Three Fluorophores Encapsulated within the Self-Assembled Surfactant Systems

    摘要： A broad spectrum tunable photoluminescent material with dual encryption based on a two-step Fluorescence Resonance Energy Transfer (FRET) between Pyrene (Py), Coumarin480 (Cou480) and Rhodamine6G (R6G) in micelles of SDS and bmimDS is presented. The phenomenon is achievable due to the encapsulation of the fluorophores within these micelles. The transfer of energy as FRET between the pair Py and Cou480 showed ON at 336 nm and OFF at 402 nm in contrast to the FRET observed between the pair Cou480 and R6G that showed ON at 402nm and OFF at 336 nm. However, the transfer of energy as FRET occurs from Py to R6G in the presence of Cou480 when excited at 336 nm, thereby making it a chain of three fluorophores with Cou480 acting as a relay fluorophore receiving energy from Py and transferring it to R6G. The different FRET scenarios between the three fluorophores in micelles provide a window for the generation of a matrix of colors, which occupies a significant 2D area in the chromaticity diagram, having potential applications in security printing. The different fluorophoric ratios generate different colors based on their individual photonic emissions and the FRET processes taking place between them. Writing tests were carried out using varied ratios of the fluorophores in the micellar systems producing different colored outputs under the UV light with insignificant visibility under the white light. We envision that this as-discovered three fluorophoric FRET system could form the basis for the future development of multi-FRET light-harvesting devices and anti-counterfeiting security inks based on much simpler non-covalent interaction aided encapsulation of the fluorophores within the self-assembled soft systems.

    关键词： micelles,security printing,Rhodamine6G (R6G),SDS,Pyrene (Py),Coumarin480 (Cou480),bmimDS,Fluorescence Resonance Energy Transfer (FRET),photoluminescent material

    更新于2025-11-19 16:46:39

  • Water-sensitive ratiometric fluorescent probes and application to test strip for rapid and reversible detection of water

    摘要： Naphthalimide-decorated fluorinated acetamides 1 and 2 were developed as solvent-sensitive dual emissive fluorescence probes. Particularly, 1 exhibited dual emission with a large Stokes shift for water, DMF, and DMSO solvents over other various organic solvents. The dual emission might be due to the increase of intramolecular charge transfer (ICT) of the naphthalimide moiety through the association of the difluorinated acetamide group with the solvent molecules. The 1 can give rise to a ratiometric change in the dual emission and a visual fluorescent color change depending on the water contents in organic solvents, including ethanol, methanol, acetonitrile and DMF solvents. Moreover, the 1-impregnated paper strips showed a rapid and easy-to-visualize fluorescent color change enabling water detection in organic solvents. These simple-to-use paper strips were also found to be reusable over 20 times.

    关键词： Naphthalimide,Ratiometric fluorescence probe,Reusable test strip,Intramolecular charge transfer (ICT),Water detection

    更新于2025-11-19 16:46:39

  • Tunable Photophysical Properties of Thiophene Based Chromophores: Conjoined Experimental and Theoretical Investigation

    摘要： In this paper we report synthesis and photophysical properties of six novel thiophene derivatives (ThD) with D-π-A structure. The subject of this work are three nitrophenyls (1) BT-Th-NO2 and three benzonitriles (2) BT-Th-CN, substituted at different positions of aromatic ring ((a) ortho-, (b) meta- or (c) para-). Dyes were obtained using simple three-step synthesis and their chemical structures were confirmed by 1H and 13C NMR, IR as well as high resolution mass spectrometry. The influence of positional isomerism on optical properties has been explored experimentally and theoretically. The photophysical properties were investigated using steady-state as well as time-resolved spectroscopy and the obtained results were supported by quantum-chemical calculations. TD-DFT calculations indicated that charge-transfer strength can be correlated with the observed optical properties. In addition, the influence of the acceptor position on photoluminescence spectra, fluorescence quantum yields and emission lifetimes was specified. We show that ThD optical properties can be tuned in wide spectral range by the change made in only single step of synthesis reaction.

    关键词： push-pull chromophores,Thiophene derivatives,TD-DFT,quantum yield,charge transfer

    更新于2025-11-19 16:46:39

  • High lying energy of charge-transfer states and small energetic offsets enabled by fluorinated quinoxaline-based alternating polymer and alkyl-thienyl side-chain modified non-fullerene acceptor

    摘要： Significant driving forces are the prerequisite to achieve fast and efficient charge separation in fullerene derivatives-based polymer solar cells to achieve high power conversion efficiency (PCE). However, the large driving forces both in photo-induced hole transfer (PHT) and in photo-induced electron transfer (PET) processes lead to significant energy losses, resulting in low open-circuit voltage in the devices. Recent studies indicate the driving forces in non-fullerene acceptors-based devices can be reduced to very low values but still with high PCE and low energy losses. Herein, we report a new donor:acceptor system with high lying energy of charge-transfer excitons (ECT) of 1.50 eV and very small driving forces (PHT of 0.28 eV and PET of 0.11 eV), in which a fluorinated quinoxaline-based alternating polymer (FTQ) and an alkyl-thienyl side-chain modified small molecule (ITIC-Th) are taken as the donor material and non-fullerene acceptor material, respectively. A high power conversion efficiency (PCE) of 8.19% with maximal external quantum efficiency of 71% are achieved successfully in FTQ:ITIC-Th-based device after appropriate thermal annealing treatment, indicating FTQ can be further applied as donor materials with other highly efficient NF-acceptors to achieve enhanced performances and low energy losses.

    关键词： Power conversion efficiency,Driving forces,Energy of charge-transfer states,Polymer solar cells

    更新于2025-11-14 17:28:48

  • Electrical and optical properties of organic light-emitting diodes with rhenium(I) complexes using DC and AC methods

    摘要： Four rhenium(I) tricarbonyl complexes with 1,10-phenanthroline and derivative bearing electron-donating CH3 and OCH3 substituents were doped into host material poly (9-vinylcarbazole) (PVK) with a mass ratio of 8% as the emissive layer in organic light-emitting diodes (OLEDs). All complexes showed photoluminescence in the solution and embedded into a PVK matrix (λmax～520–550 nm). The comparison with the bare PVK emission and the compound/PVK ?lm shows that the emission of the polymer was quenched through an energy transfer process from PVK to the dopant. The electrical properties of the devices with FTO/PEDOT:PSS/Complex:PVK/Al architecture were investigated using the DC method by curves of current density-voltage and the AC method as admittance spectroscopy, which showed that the behavior of the devices is controlled by charge carrier injection rather than bulk transport.

    关键词： Energy transfer,Re(I) complexes,Charge injection,Admittance spectroscopy,Emission,OLEDs

    更新于2025-11-14 17:28:48

  • Dopamine-functionalized upconversion nanoparticles as fluorescent sensors for organophosphorus pesticide analysis

    摘要： Organophosphorus pesticide (OP) residues in agricultural products, herbal medicines and environment have attracted increasing concerns because they cause high healthy risk. Herein, a tyrosinase-mediated photoinduced electron transfer system was constructed for OPs analysis by using dopamine-functionalized upconversion nanoparticles (UCNPs) as fluorescent (FL) sensors. Dopamine quinone was produced by tyrosinase-mediated oxidation of dopamine on the surface of UCNPs, which acted as electron accepter to quench the FL emission of UCNPs. The FL quenching was inhibited by OP since it inhibited the activity of tyrosinase. Chlorpyrifos was used as a model analyte to investigate the feasibility of the FL sensor for the analysis of OPs. Under the optimal conditions, chlorpyrifos can be analysed in a wide range of 1.0 ? 1000 ng mL?1, with a detection limit of 0.38 ng mL?1 (3σ). Some other groups pesticides, including organonitrogen pesticide, organochlorine pesticide and chloronicotinyl insecticide all showed negligible interference. The proposed sensor was successfully used to analyse chlorpyrifos spiked in Balloonflower and Angelica with acceptable recovery values of 95.4–120.0%, demonstrating its application potential for real samples. It exhibits some advantages like low cost, high sensitivity and free of autofluorescent interference and photobleaching.

    关键词： Tyrosinase,Photoinduced electron transfer,Fluorescent sensor,Organophosphorus pesticide,Upconversion nanoparticles,Chlorpyrifos

    更新于2025-11-14 17:15:25

  • Phosphorimetric determination of 4-nitrophenol using mesoporous molecular imprinting polymers containing manganese(II)-doped ZnS quantum dots

    摘要： Mesoporous molecularly imprinted polymers (MIPs) containing mangnanese-doped ZnS quantum dots (Mn-ZnS QDs) were prepared for specific recognition and detection of 4-nitrophenol (4-NP). The Mn-ZnS QDs display orange room-temperature phosphorescence with excitation/emission peaks at 295/590 nm and a decay time of 2.0 ms. In the presence of 4-NP, the orange phosphorescence is strongly reduced. Phosphorescence drops linearly in the 0.1–100 μM 4-NP concentration range, and the detection limit is 60 nM. The detection limit is far lower than the maximally allowed 4-NP concentrations in surface water and drinking water as specified by the U.S. Environmental Protection Agency. The intraday (n = 5) and interday (n = 6) spiked recovery rates were 96.0–104.5% and 97.9–107.9%, respectively, with relative standard deviations of 0.7–4.8% and 1.8–7.5% respectively. These MIPs integrated the characteristic features of phosphorimetry and molecular imprinting. Potential interference by competitive substances, background fluorescence or scattered light are widely reduced.

    关键词： Room-temperature phosphorescence,Mesoporous molecularly imprinted polymers,Photoinduced electron-transfer,4-Nitrophenol,Decay time

    更新于2025-11-14 17:04:02

  • Electrochemiluminescence sensing platform for ultrasensitive DNA analysis based on resonance energy transfer between graphitic carbon nitride quantum dots and gold nanoparticles

    摘要： Electrogenerated chemiluminescence (ECL) of semiconductor quantum dots (QDs) is considered as a powerful technique in the fabrication of biosensor, however, the inherent toxicity of the heavy metal ion containing in QDs limits their further applications. Thus, searching for environment-friendly luminescent nanomaterials with high electrochemiluminescence (ECL) e?ciency is an urgent goal. In this work, a solid-state method under low temperature was adopted to prepare graphitic carbon nitride quantum dots (g-CNQDs). By using coreactant K2S2O8, a strong cathodic ECL signal of g-CNQDs could be observed in phosphate bu?er. A novel ECL resonance energy transfer procedure was constructed between g-CNQDs (emitter) and gold nanoparticles (acceptor). A signal probe was formed by connecting gold nanoparticles at the hairpin DNA (Hai-DNA) terminal. When the signal probe was anchored on g-CNQDs, ECL resonance energy transfer occurred due to the ECL quenching of gold nanoparticles to g-CNQDs. This phenomenon decreased the ECL signal. In the presence of target DNA (T-DNA), the looped structure of Hai-DNA could be destroyed by T-DNA, and gold nanoparticles were separated from g-CNQDs. Accordingly, the ECL resonance energy transfer procedure was hindered, and the ECL signal was recovered again. The ECL intensities exhibited linear correlation with the logarithm of T-DNA concentration from 0.02 fM to 0.1 pM, and the limit of detection was 0.01 fM (3σ). With the developed ECL resonance energy transfer system, good selectivity and high sensitivity were achieved in T-DNA detection.

    关键词： Graphitic carbon nitride quantum dots,Electrochemiluminescence,DNA,Resonance energy transfer,Biosensor

    更新于2025-11-14 17:04:02

  • Aggregation-induced phosphorescence quenching method for the detection of picric acid based on melamine-passivated Mn-doped ZnS quantum dots

    摘要： Melamine (MA)-passivated Mn-doped ZnS quantum dots (QDs) were synthesized by a hydrothermal method. The MA-passivated QDs can form a charge-transfer complex with picric acid (PA) at 80 °C, thereby quenching the phosphorescence of the QDs. A sensitive method for detecting PA was established based on this principle of phosphorescence quenching. When the PA concentration ranged from 2.0–180 ng mL–1, the concentration was linearly related to the quenching intensity of the QDs, with a detection limit of 1.4 ng mL–1. When applied to detect PA in environmental water samples, the proposed method showed superior analytical performance compared with other PA analysis methods. Furthermore, we verified the static quenching mechanism by density functional theory. MA on the surface of QDs and PA formed a stable structure with a binding energy of 12.43 eV.

    关键词： Melamine,Picric Acid,Mn-doped quantum dots,Charge-transfer Complex,Phosphorescence

    更新于2025-11-14 17:04:02

  • A novel photoelectrochemical biosensor for the sensitive detection of dual microRNAs using molybdenum carbide nanotubes as nanocarriers and energy transfer between CQDs and AuNPs

    摘要： Herein, a novel photoelectrochemical (PEC) biosensor was developed for the ultrasensitive detection of dual microRNAs (miRNAs), with the detection being based on energy transfer (ET) between carbon quantum dots (CQDs) and gold nanoparticles (AuNPs). The PEC platform consisted of a CQDs@Mo2C nanotube modified ITO electrode. Two hairpin probes (H1 and H2) carrying the Au NPs were used “switch off” and “switch on” the PEC signal of the CQDs, with a close approach of the tagged AuNPs to the CQDs quenching the PEC signal. The introduction of different miRNAs (miRNA-159b and miRNA-166a) altered the interparticle distance between the AuNPs and CQDs, thereby affecting the intensity of the PEC response. This approach allowed the highly sensitive detection of both miRNA-159b and miRNA-166a. The linear range of the biosensor for miRNA-159b and miRNA-166a detection were 0.5–5000 fM, with low detection limits of 0.15 fM and 0.21 fM, respectively. To our knowledge, this is the first reported CQDs-based ET biosensor for the PEC detection of dual miRNAs. Results suggest that this approach offers a promising platform for the ultrasensitive detection of multiple miRNAs.

    关键词： MicroRNA detection,AuNPs,Photoelectrochemistry,Energy transfer,CQDs@Mo2C

    更新于2025-11-14 17:03:37