Quantum Yields of Crude Oils

1996 ◽  
Vol 50 (12) ◽  
pp. 1563-1568 ◽  
Author(s):  
Corie Y. Ralston ◽  
Xu Wu ◽  
Oliver C. Mullins

Fluorescence quantum yield measurements are reported for visible and UV excitation for neat and dilute crude oil solutions, extending earlier work with excitation in the long wavelength visible and the NIR. Large and monotonically increasing quantum yields are found with shorter wavelength excitation (to 325 nm), and all crude oils are shown to have nearly the same relative dependence of quantum yield on excitation wavelength. These observations are explained by the energy dependence of internal conversion. Dilute solutions of light crude oils exhibit higher quantum yields than those of heavy crude oils because of their lack of large chromophores. The fraction of fluorescence emission resulting from electronic energy transfer (with subsequent fluorescence emission) for neat crude oils was previously shown to vary from ∼100% for ultraviolet excitation to ∼0% for near-infrared excitation; this large variation correlates well with and is explained by the very large variation in quantum yields with excitation wavelength. Comparison of quantum yields from neat and dilute solutions shows that quenching is the other major process which occurs with chromophore interactions. The quantum yields of a maltene and resin are large and similar, while the asphaltene exhibits much smaller quantum yields because of its lack of small chromophores.

1995 ◽  
Vol 49 (6) ◽  
pp. 754-764 ◽  
Author(s):  
Taggart D. Downare ◽  
Oliver C. Mullins

Fluorescence emission spectra and absolute quantum yields have been measured for ten diverse crude oils at various concentrations over a broad range of excitation and emission wavelengths in the visible and the near-infrared. Energy transfer produces large red shifts and large widths in the fluorescence emission spectra for shorter wavelength excitation particularly for heavier crude oils. However, the effects of energy transfer are nearly absent for near-infrared excitation; all crude oils exhibit nearly the same emission spectra for long wavelength excitation. In addition, the fraction of emission resulting from collisional energy transfer relative to nascent emission is almost independent of oil type; it is governed by quantum yield characteristics. Absolute fluorescence quantum yields of ten crude oils (and three rhodamine dyes for validation) were measured with respect to scattering of latex microspheres in distilled water. Fluorescence quantum yields vary systematically with crude oil type as well as excitation wavelength; quantum yields are lower for high fluorophore concentrations (heavy crude oils) and for longer wavelength excitation. Stern-Volmer analyses of the quantum yields indicate that simple models apply and show the relative quenching rates for different excitation wavelengths.


2021 ◽  
Author(s):  
WEN-SHUO KUO ◽  
Chia-Yuan Chang ◽  
Ping-Ching Wu ◽  
Jiu-Yao Wang

Abstract BackgroundNitrogen doping and amino-group functionalization, which result in strong electron donation, can be achieved through chemical modification. Large π-conjugated systems of graphene quantum dot (GQD)-based materials acting as electron donors can be chemically manipulated with low two-photon excitation energy in a short photoexcitation time for improving the charge transfer efficiency of sorted nitrogen-doped amino acid–functionalized GQDs (sorted amino-N-GQDs). ResultsIn this study, a self-developed femtosecond Ti-sapphire laser optical system (222.7 nJ pixel−1 with 100-170 scans, approximately 0.65-1.11 s of total effective exposure times; excitation wavelength: 960 nm in the near-infrared II region) was used for chemical modification. The sorted amino-N-GQDs exhibited enhanced two-photon absorption, post-two-photon excitation stability, two-photon excitation cross-section, and two-photon luminescence through the radiative pathway. The lifetime and quantum yield of the sorted amino-N-GQDs decreased and increased, respectively. Furthermore, the sorted amino-N-GQDs exhibited excitation-wavelength-independent photoluminescence in the near-infrared region and generated reactive oxygen species after two-photon excitation. An increase in the size of the sorted amino-N-GQDs boosted photochemical and electrochemical efficacy and resulted in high photoluminescence quantum yield and highly efficient two-photon photodynamic therapy. ConclusionThe sorted dots can be used in two-photon contrast probes for tracking and localizing analytes during two-photon imaging in a biological environment and for conducting two-photon photodynamic therapy for eliminating infectious microbes.


2017 ◽  
Vol 46 ◽  
pp. 234-240
Author(s):  
Wen Juan Dong ◽  
Ji Yan Han ◽  
Xin Wu ◽  
Li Fan ◽  
Wen Ting Liang

A novel near-infrared fluorescence quenching method has been developed for the determination of hydrogen peroxide based on N-acetyl-L-cysteine-capped gold nanoparticles (NAC-AuNPs) as a fluorescence probe. The prepared gold nanoparticles with the size of about 1.91 nm exhibited strong near-infrared fluorescence emission at 693 nm with excitation wavelength at 450 nm in aqueous solution. The fluorescence intensity of NAC-AuNPs was quenched dramatically by adding hydrogen peroxide. Therefore, it could be used to detect hydrogen peroxide based on the fluorescence quenching intensity was linear with the concentration of hydrogen peroxide. Under the optimal experimental conditions, the linear range and detection limit were 1.0×10-6 –3.0×10-2 mol/L and 1.0×10-7 mol/L, respectively. The possible quenching mechanism was investigated by time-resolved fluorescence spectroscopy. The proposed method was simple, sensitive and showed good repeatability and stability.


2019 ◽  
Author(s):  
Laura Abad Galán ◽  
Satoshi Wada ◽  
Lee Cameron ◽  
Alexandre N. Sobolev ◽  
Yasuchika Hasegawa ◽  
...  

A conjugated <i>β</i>-triketone, tris(2-naphthoyl)methane (<b>tnm</b>H), has been synthesized and successfully utilized as an antenna moiety for sensitization of the trivalent lanthanoids Eu<sup>3+</sup><sub>,</sub>Sm<sup>3+</sup><sub>,</sub>Yb<sup>3+</sup>and Nd<sup>3+</sup>, in an isomorphous series of mononuclear complexes formulated as [Ln(<b>tnm</b>)<sub>3</sub>(DMSO)<sub>2</sub>] (Ln<sup>3+ </sup>= Nd<sup>3+</sup>, Sm<sup>3+</sup>, Eu<sup>3+</sup>, Gd<sup>3+</sup>and Yb<sup>3+</sup>). The photophysical properties of the materials were characterized as comprehensively as possible, with overall quantum yields, intrinsic quantum yields based on calculated radiative decays, and sensitization efficiencies reported. This investigation improves understanding of the sensitization processes occurring in the near-infrared (NIR) region systems in particular, where quantitative data is currently scarce. In fact, the [Yb(<b>tnm</b>)<sub>3</sub>(DMSO)<sub>2</sub>] and its deuterated analogue, [Yb(<b>tnm</b>)<sub>3</sub>(<i>d<sub>6</sub>-</i>DMSO)<sub>2</sub>], present high values of overall quantum yield of 4% and 6%, respectively, which makes them useful and readily accessible references for future investigation of NIR-emitting systems.


2017 ◽  
Vol 21 (12) ◽  
pp. 844-849
Author(s):  
Sergei G. Makarov ◽  
Günter Schnurpfeil ◽  
Elena A. Rychagova ◽  
Sergey Yu. Ketkov ◽  
Olga N. Suvorova ◽  
...  

The singlet oxygen ([Formula: see text]O[Formula: see text] quantum yield of the near-infrared absorbing ([Formula: see text] [Formula: see text] 839 nm) planar [Formula: see text]-conjugated binuclear zinc phthalocyanine (ZnPc) was measured and compared to the [Formula: see text]O[Formula: see text] quantum yields of the mononuclear and the planar binuclear phthalocyanine without [Formula: see text]-conjugation between Pc rings. In addition, the photooxidative stability of the [Formula: see text]-conjugated binuclear Pc was determined and compared to the stabilities of the mononuclear ZnPc and the known near-infrared photosensitizer, zinc tetra-tert-butylnaphthalocyanine ([Formula: see text] 761 nm). The results are explained by DFT calculations and cyclic voltammetry.


Synlett ◽  
2020 ◽  
Vol 31 (12) ◽  
pp. 1129-1134 ◽  
Author(s):  
Weiping Wang ◽  
Wen Lv

Photolysis reactions are widely utilized to release desired molecules under the control of light irradiation in the fields of photochemistry, biology, and drug delivery. In biological and medical applications, it is highly desired to increase the excitation wavelength for activating photolysis reactions, since the long-wavelength light (red or near-infrared light) has deep tissue penetration depth and low photocytotoxicity. Here, we briefly summarize current strategies of achieving long-wavelength light-excitable photolysis. We highlight our recently developed strategy of one-photon upconversion-like photolysis. Compared with the multiphoton upconversion-based photolysis, the one-photon strategy has a simpler energy transfer process and a higher ­energy utilization efficiency, providing a new path of activating photolysis reactions with increased excitation wavelength and photolysis quantum yield.


Author(s):  
V. Fidler ◽  
P. Kapusta ◽  
M. Nepras ◽  
J. Schroeder ◽  
I.V. Rubtsov ◽  
...  

Ultrafast time resolved fluorescence anisotropy decay measurements were performed to gain insight into the energy gap dependence of donor-acceptor inter-chromophoric coupling within one supra-molecule. Three new compounds, each consisting of two semi-rigidly linked and strongly coupled chromophores, were designed and synthesized for this study. Their general structure is donor-spacer-acceptor, where "donor" is phenylamino, pyrenylamino, or benzanthronylamino moiety, and acceptor is aminobenzanthrone. While being similar structurally, the compounds differ significantly in the excitation energy difference of the two chromophores in a supra-molecule. Experimental data show an ultrafast initial fluorescence emission anisotropy decrease (within less then 1 ps) when the excited state energies of the interacting chromophores are close to each other or equal. No such fast fluorescence anisotropy dynamics is observed for a compound with a large energy gap.


2011 ◽  
Vol 83 (12) ◽  
pp. 2213-2228 ◽  
Author(s):  
Albert M. Brouwer

The use of standards for the measurement of photoluminescence quantum yields (QYs) in dilute solutions is reviewed. Only three standards can be considered well established. Another group of six standards has been investigated by several independent researchers. A large group of standards is frequently used in recent literature, but the validity of these is less certain. The needs for future development comprise: (i) confirmation of the validity of the QY values of many commonly used standard materials, preferably in the form of SI traceable standards; (ii) extension of the set of standard materials to the UV and near-IR spectral ranges; and (iii) good standards or robust protocols for the measurements of low QYs.


2001 ◽  
Vol 05 (05) ◽  
pp. 460-464 ◽  
Author(s):  
JOHN W. OWENS ◽  
MARSHA ROBINS

This study correlates the photophysical properties of aluminum phthalocyanine tetrasulfonate (AlPcTs), zinc phthalocyanine tetrasulfonate (ZnPcTs), and phthalocyanine tetrasulfonate (PcTs) with their ability to kill human embryonic lung (HEL) cells. Photofrin, a proven anti-cancer drug, was used for comparison. The photophysical properties include fluorescence emission spectra, fluorescence quantum yields, singlet state and radiative lifetimes, quantum yield for triplet formation, and fluorescence rate constants. Results indicate that photodynamic efficacy correlates inversely with fluorescence quantum yield and fluorescence lifetime and directly with quantum yield for triplet formation.


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