EFFECT OF SILVER NANOPARTICLES ON THE FLUORESCENCE INTENSITY OF RHODAMINE 6G AND SULFORHODAMINE 101

2016 ◽  
Vol 75 (11) ◽  
pp. 1001-1008
Author(s):  
S.V. Nikolayev ◽  
V. V. Pozhar ◽  
M. I. Dzyubenko ◽  
K. S. Nikolayev
2016 ◽  
Vol 21 (2) ◽  
pp. 53-58 ◽  
Author(s):  
S. Nikolayev ◽  
◽  
V. Pozhar ◽  
M. Dzyubenko ◽  
K. Nikolayev

2015 ◽  
Vol 2015 ◽  
pp. 1-8 ◽  
Author(s):  
Md. Wahadoszamen ◽  
Arifur Rahaman ◽  
Nabil Md. Rakinul Hoque ◽  
Aminul I Talukder ◽  
Kazi Monowar Abedin ◽  
...  

A dispersive Raman spectrometer was used with three different excitation sources (Argon-ion, He-Ne, and Diode lasers operating at 514.5 nm, 633 nm, and 782 nm, resp.). The system was employed to a variety of Raman active compounds. Many of the compounds exhibit very strong fluorescence while being excited with a laser emitting at UV-VIS region, hereby imposing severe limitation to the detection efficiency of the particular Raman system. The Raman system with variable excitation laser sources provided us with a desired flexibility toward the suppression of unwanted fluorescence signal. With this Raman system, we could detect and specify the different vibrational modes of various hazardous organic compounds and some typical dyes (both fluorescent and nonfluorescent). We then compared those results with the ones reported in literature and found the deviation within the range of ±2 cm−1, which indicates reasonable accuracy and usability of the Raman system. Then, the surface enhancement technique of Raman spectrum was employed to the present system. To this end, we used chemically prepared colloidal suspension of silver nanoparticles as substrate and Rhodamine 6G as probe. We could observe significant enhancement of Raman signal from Rhodamine 6G using the colloidal solution of silver nanoparticles the average magnitude of which is estimated to be 103.


2021 ◽  
Vol 26 (3) ◽  
pp. 24-29
Author(s):  
S. Nikolaiev ◽  
◽  
V. Pozhar ◽  
M. Dzyubenko ◽  
K. Nikolaiev ◽  
...  

Subject and Purpose. The article is concerned with the spectral-luminescent and lasing characteristics of the radiation from solid-state active media based on polyurethane activated by a binary mixture of dyes. The purpose of these studies is to demonstrate a possibility of the spectral range expansion of the emission from solid-state dye lasers with polyurethane active elements. Methods and Methodology. Specially prepared samples of polyurethane active media having the same donor (Rhodamine 6G) concentration but various acceptor (Sulforhodamine 101) concentrations are experimentally studied for their spectral-luminescent and lasing characteristics. Results. The main spectroscopic characteristics of Rhodamine 6G and Sulforhodamine 101 in polyurethane have been measured, the nonradiative energy transfer parameters in this molecular pair estimated. It has been demonstrated that the matrix emission spectrum can be purposefully transformed by selection of relative concentrations of dyes in the mixture. In a broadband resonator, either a single- or two-band emission with different positions and various intensities of spectral bands is observed depending on the acceptor concentration. In a dispersive resonator under the same conditions, the tuning range of the lasing spectrum expands and extends to the longer wavelengths. Conclusion. The prospects of using donor-acceptor dye mixtures for improving spectral characteristics of polyurethane active elements in solid-state dye lasers have been confirmed. It has been shown that signatures of the emission characteristics of these media are governed by the mechanism of the excitation energy transfer between dye molecules. Lasing has been obtained on polyurethane matrices with the emission wavelength tuning throughout the “green-red” region of the spectrum.


2013 ◽  
Vol 631-632 ◽  
pp. 18-21 ◽  
Author(s):  
Zhi Liang Jiang ◽  
Mei Ling Tang ◽  
Qing Ye Liu ◽  
Ai Hui Liang

In the condition of 1.24 mmol/L EDTANa2, 16.7 mmol/L NaCl and 0.17 mmol/L Tris, the substrate chain of double-stranded DNA (dsDNA) could be cracked by Pb2+ to release single-stranded DNA (ssDNA) that adsorb onto AuPd nanoparticle (AuPdNP) and form stable AuPdNP-ssDNA, but the dsDNA can not protect AuPdNP that were aggregated to big AuPdNP aggregations (AuPdNPA) under the action of NaCl. The AuPdNP-ssDNA and AuPdNPA could be separated by centrifugation. With the concentration of Pb2+ increased, the released ssDNA increased, the AuPdNP-ssDNA in centrifugation solution increased and the catalytic effect enhanced on the fluorescence quenching reaction of Rhodamine 6G (Rh6G) and NaH2PO2, which led the fluorescence intensity at 552nm to decrease. The decreased fluorescence intensity (ΔF552nm) was linear to the concentration of Pb2+ in the range of 0.33-8.00 nmol/L, a detection limit of 0.21 nmol/L. The proposed method was applied to detect Pb2+ in water samples, with satisfactory results.


2016 ◽  
Author(s):  
Ilia G. Samusev ◽  
Nadezhda S. Tikhomirova ◽  
Vasiliy A. Slezhkin ◽  
Andrey Yu. Zyubin ◽  
Valery V. Bryukhanov ◽  
...  

2019 ◽  
Vol 85 (12) ◽  
pp. 84-95
Author(s):  
Olga Zaporozhets ◽  
Sergey Kulichenko ◽  
Sergey Lelyushok ◽  
Viktoriia Klovak

The influence of cationic, anionic, nonionic surfactants and their mixtures on the fluorescence characteristics of rhodamine 6G and Rho-damine C solutions has been investigated. The fluorescence intensity of aqueous solutions of rhodamine 6G and in the presence of cetylpyridinium chloride and sodium dodecyl sulfate has almost unchanged throughout the pH range. The fluorescence intensity of aqueous and water-micellar rhodamine C solutions has been increased in the pH 1-4 range; the signal has been remained unchanged at high pH values. The studies have been carried out at pH 4 for rhodamine 6G and at pH 10 for rhodamine C. The fluorescence characteristics of water-micellar dye - surfactant - non-ionic surfactant systems have been performed at a concentration of Triton X-100 of 3.4·10‑2 mol/l. The interaction with cationic surfactants has shown differences character between the I=f(n) dependences for aqueous solutions of highly hydrophobic rhodamine 6G and more hydrophilic rhodamine C. The study of the effect of the hydrocarbon radical length on the intensity of the fluorescence of rhodamine 6G and rhodamine C has been carried out at two concentrations of cationic surfactants: under the condition of the formation of stoichiometric associates dye with cationic surfactant and in the region of the micellar concentrations of cationic surfactants. The character of the influence of the length of the hydrocarbon radical cationic surfactants on the fluorescence intensity of the dyes can be explained by the increasing role of hydrophobic interactions and the enhancement of solubilization in systems involving long-chain surfactants. The difference in the nature of the associates of rhodamine 6G and rhodamine C with hydrophobic and moderately hydrophobic cationic surfactants has been counterbalanced in the presence of Triton X-100. Reduction of fluorescence intensity of rhodamine 6G in domicile solutions of anionic sodium dodecyl sulfate has been established. The method of fluorescence detection of sodium dodecyl sulfate in reaction with rhodamine 6G has been proposed. The method has been tested in determining of anionic surfactants in the waters after washing clothes.


Materials ◽  
2020 ◽  
Vol 13 (22) ◽  
pp. 5168
Author(s):  
Elżbieta Szczepańska ◽  
Anna Synak ◽  
Piotr Bojarski ◽  
Paweł Niedziałkowski ◽  
Anna Wcisło ◽  
...  

The present work describes synthesis, characterization, and use of a new dansyl-labelled Ag@SiO2 nanocomposite as an element of a new plasmonic platform to enhance the fluorescence intensity. Keeping in mind that typical surface plasmon resonance (SPR) characteristics of silver nanoparticles coincide well enough with the absorption of dansyl molecules, we used them to build the core of the nanocomposite. Moreover, we utilized 10 nm amino-functionalized silica shell as a separator between silver nanoparticles and the dansyl dye to prevent the dye-to-metal energy transfer. The dansyl group was incorporated into Ag@SiO2 core-shell nanostructures by the reaction of aminopropyltrimethoxysilane with dansyl chloride and we characterized the new dansyl-labelled Ag@SiO2 nanocomposite using transmission electron microscopy (TEM) and Fourier-transform infrared spectroscopy (FTIR). Additionally, water wettability measurements (WWM) were carried out to assess the hydrophobicity and hydrophilicity of the studied surface. We found that the nanocomposite deposited on a semitransparent silver mirror strongly increased the fluorescence intensity of dansyl dye (about 87-fold) compared with the control sample on the glass, proving that the system is a perfect candidate for a sensitive plasmonic platform.


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