Silver nanoparticle size–dependent measurement of quantum efficiency of Rhodamine 6G

The plasmonic absorption band of silver nanoparticles in the visible range of electromagnetic spectrum has been successfully exploited to alter the emission characteristics of the Rhodamine 6G dye molecule. The influence of the nanoparticle size on the fluorescence quantum yield of Rhodamine 6G is interrogated via steady state fluorescence as well as dual beam thermal lens technique. The potential of the thermal lens technique that probe nonradiative path in contrast to radiative path exhibited in the fluorescence spectra as a complementary method to measure the quantum yield of a dye molecule is exploited. Analysis of the results clearly indicates that the particle size and the spectral overlap between the emission spectra of Rhodamine 6G, and absorption spectra of the silver nanoparticles determine the quantum yield value of dye–nanoparticle mixture.     

Study of concentration-dependent quantum yield of Rhodamine 6G by gold nanoparticles using thermal-lens technique

Tailoring optical properties of the dye molecules using metal nanoparticles is a burgeoning area of research. In this work, we report our results on the studies of how the absorption and emission behavior of Rhodamine 6G dye is tailored using gold nanoparticles. Furthermore, the influence of dye concentration on these properties for a given concentration of nanoparticles in the dye-nanoparticle mixture is investigated. In addition, the difference between the concentration-dependent fluorescence quantum yield of the dye molecules is measured in the absence and presence of nanoparticles using the dual-beam thermal-lens technique. Our absorption spectral studies show additional spectral features due to nanoparticle aggregation on interaction with cationic Rhodamine 6G dye. Dye concentration-dependent steady-state fluorescence studies in the presence of nanoparticles indicate a blue shift in peak fluorescence emission wavelength. The quantum yield value measured using thermal-lens technique exhibit a non-monotonic behavior with dye concentration with substantial quenching for lower dye concentrations. The results are interpreted in terms of dye–nanoparticle interaction and the formation of dye shell around the nanoparticle.     

Fluorescence quenching in dyes under an optically thin approximation

Kinetic analysis of the energy level scheme of a dye molecule yields expression for the fluorescence quantum yield. The quantum yield is dependent on molecular parameters and laser pulse characteristics. Calculations show quenching of fluorescence quantum yield due to excited state absorption. Earlier studies on quenching of fluorescence have been discussed quantitatively under an optically thin approximation.     

Synthesis and Properties of a New Photostable Soluble Perylene Dye: N,N'-Di-(1-Dehydroabietyl) Perylene-3,4,9,10-Bis(Dicarboximide)

N,N'-Di-(-1-Dehydroabietyl) perylene-3,4,9,10-bis(dicarboximide) is prepared in 95% yield by the condensation of perylene 3,4,9,10-tetracarboxylic dianhydride with dehydroabietyl amine. Thermal and photostable bright red-orange dye is measured to have a fluorescence quantum yield of unity, Q_f=1, in chloroform solutions. Solubility of the dye is 1.8 g/L in chloroform. The diimide is an ideal reference probe for fluorescence quantum yield measurements in 500—650 nm region and also very interesting dye for chemiluminescent light devices.     

Thermal lens technique to evaluate the fluorescence quantum yield of a schiff base

The fluorescence spectrum of the schiff base obtained from salicylaldehyde and 2-aminophenol is studied using an argon-ion laser as the excitation source and its fluorescence quantum yield (Q_f) is determined using a thermal lens method. This is a nondestructive technique that gives the absolute value of Q_f without the need for a fluorescence standard. The quantum-yield values are calculated for various concentrations of the solution in chloroform and also for various excitation wavelengths. The value of Q_f is relatively high, and is concentration dependent. The maximum value of Q_f obtained is nearly 0.78. The high value of the fluorescence quantum yield will render the schiff base useful as a fluorescent marker for biological applications. Photostability and gain studies will assess its suitability as a laser dye. PACS 42.55.Mv; 42.62.Cf; 42.62.Fi; 42.70.Hj     

Effect of concentration on optical properties of dyes incorporated into polyvinyl alcohol films

The quantum yield, lifetime and anisotropy of fluorescence emitted by molecules of neutral red dye incorporated into polyvinyl polymer films were studied as a function of dye concentration. From the data a mechanism of excitation quenching by dye monomers bound to the polymer matrix is suggested.     

Influence of interaction of chromophores, linked by the unconjugated chain, on the luminescence properties of biscyanine dyes

Deactivation of electronically excited state of chemically bound dimers – biscyanines with two chromophores linked by unconjugated chains and corresponding monomer dye was investigated. It was found that the quantum yield of dimer fluorescence is lower than that of a monomer dye. The amount of quantum yield of fluorescence decreases with the increase of chromophores interaction degree (the decrease of the isolating polymethylene bridge length). It is shown on the basis of the external heavy-atom effect studies that the decrease of biscyanines fluorescence ability is connected with the enhancment of singlet–triplet intersystem crossing (S₁T₁). It has been established that the probability of the triplet states population in biscyanines with chromophores in parallel arrangement is considerably higher than that in similar compounds with an angular arrangement of chromophores. The delayed fluorescence was observed in the case of dyes with parallel arrangment of chromophores.     

Photoluminescence properties of poly(thiophene-3yl-acetic acid 8-quinolinyl ester) in solution and in acid medium

The photoluminescence characteristics and quantum yields of poly(thiophene-3-yl-acetic acid 8-quinolinyl ester) have been studied. Fluorescence measurements indicate that fluorescence quantum efficiency increases with decreasing the concentration of polymer solution. The quantum yield of the polymer in the solution is higher than that of the Rhodamine B dye at lower concentration. The behaviour of photoluminescence property is studied under different acidic conditions. The fluorescence quenching is observed in the acid medium without any shift in the wavelength.     

Synthesis of a New Thermal and Photostable Reference Probe for Qf Measurement in Aqua: Water Soluble N,N′-bis-(2-Hydroxy-4-benzoic Acid)-3,4,9,10-perylenebis(dicarboximide)

N,N′-bis(2-hydroxy-4-benzoic acid)-3,4,9,10-perylenebis(dicarboximide) is synthesized from perylene 3,4,9,10-tetracarboxylic dianhydride and 4-amino-3-hydroxy benzoic acid in 90% yield. Together with the photostability the dye is also very stable thermally. The fluorescence quantum yield is measured as one, Q_f=1.The diimide dissolves in water at PH = 8 completely. The diimide is an ideal reference probe for fluorescence quantum yield measurements in 500–650 nm region and an attractive photosensitizer for the photoreactions occur in water.     

Enhancement of the fluorescence of triphenylmethane dyes caused by their interaction with nanoparticles from β-diketonate complexes

We have studied the absorption and fluorescence spectra of Malachite Green and Crystal Violet in aqueous and alcoholic-aqueous solutions in which nanoparticles from Ln(III) and Sc(III) diketonates are formed at concentrations of complexes in a solution of 5–30 μM. We have shown that, if the concentrations of the dyes in the solution are lower than 0.5 μM, dye molecules are incorporated completely into nanoparticles or are precipitated onto their surface. The fluorescence intensity of these incorporated and adsorbed Malachite Green and Crystal Violet molecules increases by several orders of magnitude compared to the solution, which takes place because of a sharp increase in the fluorescence quantum yields of these dyes and at the expense of the sensitization of their fluorescence upon energy transfer from β-diketonate complexes entering into the composition of nanoparticles. We have shown that, if there is no concentration quenching, the values of the fluorescence quantum yield of the Crystal Violet dye incorporated into nanoparticles and adsorbed on their surface vary from 0.06 to 0.13, i.e., are close to the fluorescence quantum yield of this dye in solid solutions of sucrose acetate at room temperature. The independence of the fluorescence quantum yield of Crystal Violet on the morphology of nanoparticles testifies to a high binding constant of complexes and the dye. The considerable fluorescence quantum yields of triphenylmethane dyes in nanoparticles and sensitization of their fluorescence by nanoparticle-forming complexes make it possible to determine the concentration of these dyes in aqueous solutions by the luminescent method in the range of up to 1 nM.     

Fluorescence Quantum Yield Determination of Propylparaben Using Flow Injection Spectroscopy

The determination of the fluorescence quantum yield of Propylparaben is introduced and applied to L-tyrosine as a standard by a new approach that can be applied to the pharmaceutical compound utilised in this study. The quantum yield is a critical figure of quality for the optical nature of a fluorophore. Numerous investigations have considered the glitter in both pharmaceutical and nature compounds for its medical and industrial significance. A straightforward method is detailed here to decide the quantum yield of Propylparaben in solution as an element of the fluorescence concentration. For this reason, L-Tyrosine is chosen as a fluorescence standard perspective to gauge the Propylparaben fluorescence quantum yield. The impacts of pH, solvents and flow rate on the assessment of quantum yield and quantum efficiency, for the reference and the solutions of Propylparaben, have been investigated. The results indicated that these parameters significantly influence the accuracy of the method. Diverse methods are concentrated on to represent distinctive quantum yield advancements with the quantum efficiency. The impact of these parameters was likewise considered. In this study, the application of the single method may be taken into consideration to compute quantum yield of Propylparaben, which was 0.36, and this is an exceptionally basic and general technique to solve the imperative issue of luminescence quantum yield assurance of other fluorescence compounds.     

The Fluorescence Properties of Three Rhodamine Dye Analogues: Acridine Red,Pyronin Y and Pyronin B

The fluorescence spectra, fluorescence quantum yield, and fluorescence lifetime of Acridine Red (AR), Pyronin Y (PYY), and Pyronin B (PYB) in aqueous and organic solvents were measured by steady state fluorescence, time-correlated single photon counting, and electronic absorption methods. The rate constants of radiation and non radiation process (k_f and k_ic) were calculated to elucidate the structural effect on the fluorescence mechanism. The data for each compound are compared with that of the corresponding rhodamine dye. AR showed significant longer lifetime and higher quantum yield than PYY and PYB, because the alkyls on N atom enhance the internal conversion (IC), the longer the alkyl the faster the IC. However, the structural variation does not alter the rate constant of radiation process (k_f) but does change k_ic significantly. The phenyl in Rhodamine B or Rhodamine 6G shows only a slight effect on the fluorescence properties. Ethanol is the solvent in which all five compounds exhibit longest lifetime and highest fluorescence quantum yield.     

Effect of cooperative interactions in optical ensembles on the threshold characteristics of lasing in the case of coherent optical pumping

The dependence of the threshold pump energy of dye lasers on the quantum yield of fluorescence of active solutions in the case of laser excitation was studied. The rate of increase in the threshold pump energy was found to be considerably lower than the rate of decrease in quantum yield. The results were interpreted in terms of the development of the cooperative interaction between active centers in the high-intensity coherent pump field.

     

A Thermal and Photostable Reference Probe for Qf Measurements: Chloroform Soluble Perylene 3,4,9,10-Tetracarboxylic Acid-bis-N,N-Dodecyl Diimide

The synthesis of a chloroform soluble perylene 3, 4, 9, 10-tetracarboxylic acid-bis-N, N′-dodecyl diimide via condensation of perylene 3, 4, 9, 10-tetracarboxylic dianhydnde and 1, 12-diamino dodecane is described. The thermal analysis is shown thermal stabilities above 400°C. Thermal and photostable dye is measured to have a fluorescence quantum yield of unity, Q_f = 1.00, in chloroform solutions. Perylene bis-dodecyl diimide is an ideal reference probe for fluorescence quantum yield measurements in 500–650 nm region and a reliable soluble photosensitizer for solar photochemical applications.     

Fluorescence quantum yield of rhodamine 6G using pulsed photoacoustic technique

Experimental method for measuring photoacoustic(PA) signals generated by a pulsed laser beam in liquids is described. The pulsed PA technique is found to be a convenient and accurate method for determination of quantum yield in fluorescent dye solutions. Concentration dependence of quantum yield of rhodamine 6G in water is studied using the above method. The results indicate that the quantum yield decreases with increase in concentration in the quenching region in agreement with the existing reports based on radiometric measurements.     

高浓度若丹明6G溶液荧光寿命的测量

本文提出一种测量高浓度溶液荧光寿命的方法.利用这种方法测量了浓度范围从1×10-6至1×10-2mol·L-1的Rh6G乙醇溶液的荧光寿命.并证明了在这个浓度范围内,Stern-Volmer公式仍然成立.     

Mechanisms of Fluorescence Quenching in Donor—Acceptor Labeled Antibody—Antigen Conjugates

The cyanine dyes Cy5 and Cy5.5 are presented as a new long wavelength-excitable donor-acceptor dye pair for homogeneous fluoroimmunoassays. The deactivation pathways responsible for the quenching of the fluorescence of the antibody-bound donor are elucidated. Upon binding of the donor dye to the antibodies at low dye/protein ratios, its fluorescence quantum yield rises to unity. Higher dye/protein ratios lead to progressive aggregation of the dyes, which results in quenching of monomer fluorescence due to resonance energy transfer (RET) from the monomers to the nonfluorescent dimers. The dependence of the quenching efficiency on the labeling ratio is described quantitatively by assuming a Poisson distribution of the dyes over the antibodies. The maximum fluorescence intensity per antibody is obtained at a labeling ratio of 4. Upon formation of the antibody-antigen complex, electron transfer and RET to the antigen-bound acceptor dye occur. Steady-state and time-resolved fluorescence measurements reveal that approximately 50% of the donor quenching is due to RET, while the residual quenching effect is caused by the static quenching process.     

Enhanced Emission Induced by FRET from a Long-Lifetime, Low Quantum Yield Donor to a Long-Wavelength, High Quantum Yield Acceptor

We report observation of high quantum yield, long-lifetime fluorescence from a red dye BO-PRO-3 excited by resonance energy transfer (RET). The acceptor fluorescence was highly enhanced upon binding to the donor-labeled DNA. A ruthenium complex (Ru) was chosen as a donor in this system because of its long fluorescence lifetime. Both donor and acceptor were non-covalently bound to DNA. Emission from the donor-acceptor system (DA) at wavelengths exceeding 600 nm still preserves the long-lifetime component of the Ru donor, retaining average fluorescence lifetimes in the range of 30–50 ns. Despite the low quantum yield of the Ru donor in the absence of acceptor, its overall quantum yield of the DA pair was increased by energy transfer to the higher quantum yield acceptor BO-PRO-3. The wavelength-integrated intensity of donor and acceptor bound to DNA was many-fold greater than the intensity of the donor and acceptor separately bound to DNA. The origin of this effect is due to an efficient energy transfer from the donor, competing with non-radiative depopulation of the donor excited state. The distinctive features of DA complexes can be used in the development of a new class of engineered luminophores that display both long lifetime and long-wavelength emission. Similar DA complexes can be applied as proximity indicators, exhibiting strong fluorescence of adjacently located donors and acceptors over the relatively weak fluorescence of separated donors and acceptors.     

Photo-physical properties and quantum yield of some laser dyes in new polymer host

The field of laser dyes-active solid polymer materials is a promising field and quite competitive with liquid dye lasers. This paper investigates some photo-physical parameters of pyromethene (PM-567, PM-597) and Rhodamine B dyes incorporated into glycidyl methacrylate (GMA) promising polymeric host matrix. These parameters are: absorption and emission cross-sections, fluorescence lifetime and quantum yield, in addition to FT-Raman spectra as an indication for binding the dye molecules with the backbones of GMA polymeric chain.