Engineering Papers⌕ Search

SEARCH · Engineering Papers

Results for “DYES”

Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 235 records · Page 13

Modulating upconversion luminescence through fluorescent dyes

In our work, we report an effective method to tune the upconversion emission of NaGdF{sub 4}:Yb{sup 3+},Er{sup 3+}@NaYF{sub 4} core/shell nanoparticles. The shell thickness-dependent upconversion luminescence of NaGdF{sub 4}:Yb{sup 3+},Er{sup 3+}@NaYF{sub 4} core/shell and the dye Rhodamine-B(RhB) composite were discussed in detail. It is found that the fluorescent dye RhB can remarkably improve the violet emission of the upconversion nanoparticles (UCNPs) and simultaneously generating the 605 nm yellow emission through energy transfer. Importantly, it is revealed that the effective energy transfer distance between upconversion nanoparticles and RhB is shorter than 18 nm in the media of NaYF{sub 4}. These results open a novel way for determining the energy transfer distance between the upconversion nanoparticles and the dyes and simultaneously tuning the emission brightness and the spectrum covering range of the upconversion nanoparticles for meeting the requirement in the application fields of light source, colorful display, biological imaging, and fluorescent probes. - Graphical abstract: TEM images of core/shell upconversion nanoparticles and the illustration of Energy transfer distance UCNPs and Rhodamine-B molecular. Display Omitted - Highlights: • The upconversion nanoparticles with controlled surface morphology and shell thickness were prepared by thermal decomposition method. The emission brightness and the spectrum covering range of the upconversion nanoparticles can be tuned. • The fluorescent dye RhB can remarkably improve the violet emission of the upconversion nanoparticles and simultaneously generating the 605 nm yellow emission through energy transfer. • It is the first reported that the effective energy transfer distance between upconversion nanoparticles and RhB is shorter than 18 nm in the media of NaYF{sub 4}.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Preparation and performance study of MgFe{sub 2}O{sub 4}/metal–organic framework composite for rapid removal of organic dyes from water

In present study, a stable and magnetic metal-organic framework (MOF) material was synthesized by simple solvothermal method as adsorbent to rapid removal of two organic dyes, the Rhodamine B (RB) and Rhodamine 6G (Rh6G), in water samples. The prepared material showed great characteristics of large surface area (519.86 m{sup 2} g{sup −1}), excellent magnetic responsivity (35.00 emu g{sup −1}) and rapid removal (within 5 min). Maximum adsorption capacities of the magnetic material toward RB and Rh6G were up to 219.78 and 306.75 mg g{sup −1}, respectively. Adsorption kinetics suggested the adsorption process met the pseudo-second-order kinetic model. The prepared material could be reused at least 10 times by washing with acetonitrile solution, the relative standard deviation (RSD) of these ten cycles removal efficiency was 4.8%. In conclusion, good chemical inertness, a mechanical/water stability and super-hydrophilicity feature made this MOF a promising adsorbent for targets removal from environmental water sample. - Graphical abstract: The magnetic MgFe{sub 2}O{sub 4}/metal–organic framework with ultra-high adsorption capacity towards rhodamine dyes showed rapid removal efficiency (within 5 min) and good reusability (at least 10 times). Display Omitted - Highlights: • A stable and magnetic MgFe{sub 2}O{sub 4}@MOF material was synthesized as adsorbent to rapid removal of organic dyes. • The material in this article could rapidly sequestered rhodamine dyes within 5 min. • The maximum adsorption capacities of the magnetic material were high.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

A recyclable and highly active Co{sub 3}O{sub 4} nanoparticles/titanate nanowire catalyst for organic dyes degradation with peroxymonosulfate

Sodium ions of TNWs were exchanged with hydrogen ions, and this protocol was very suitable for capturing high density of cobalt ions. Meanwhile, the fabricated Co{sub 3}O{sub 4}/TNWs nano-material presented a highly catalytic and stable activity for dye degradation. - Highlights: • Co{sub 3}O{sub 4} nanoparticles were deposited on the pretreated TNWs surface. • The TNWs treated by hydrogen ions captures higher density of cobalt ions. • The Co{sub 3}O{sub 4}/TNWs catalyst possesses highly efficiency for dyes degradation with oxone. - Abstract: In this paper, we reported a recyclable and highly active porous catalyst of titanate nanowires (TNWs) coated with well-distributed Co{sub 3}O{sub 4} nanoparticles (NPs) (Co{sub 3}O{sub 4}/TNWs). Sodium ions of TNWs were exchanged with hydrogen ions in the dilute nitric acid, and this protocol was very suitable for capturing cobalt ions. X-ray diffraction (XRD) demonstrated the existence of Co{sub 3}O{sub 4} phase with unique lattice planes, such as (2 2 0), (3 1 1) and (5 1 1). Electron microscopes (FE-SEM and TEM) indicated that the Co{sub 3}O{sub 4} NPs with an average diameter of 22 ± 3 nm were coated uniformly on TNWs surface (average diameter: 37 ± 5.5 nm), and the Co{sub 3}O{sub 4} NPs mainly exposed their (2 2 0) and (2 2 2) active planes. XPS analysis confirms the formation of Co{sub 3}O{sub 4} phase by the presence of Co 2p peaks at 780.1 eV (2p 3/2) and 795.5 eV (2p 1/2). Methylene blue (MB) and other organic dyes (rhodamine B (RhB) and methyl orange (MO)) were chosen as target compounds for catalytic degradation under indoor scattering light. Compared to the original Co{sub 3}O{sub 4}/TNWs catalyst, the catalytic efficiency of nanoscaled catalyst with oxone for MB was about 15 times higher, and the MB solution (10 mg L{sup −1}) was completely degraded within 8 min. The catalytic activity of recycled catalyst used in the sixth run still remained very active, and the degradation time for MB was only 16 min. The nanosized catalyst also had a high activity for dyes of RhB (10 mg L{sup −1}) and MO (10 mg L{sup −1}), as the degradation efficiencies of RhB and MO after 10 min of contact time were about 90.2% and 92.6%, respectively.

36 MATERIALS SCIENCE↗

Cost-effective fabrication of (g-C3N4 + Mo) added photostable ZnO thin films for enhanced visible light responsive photocatalytic dye degradation

Highlights: • First report on ZnO:Mo/GCN films prepared by simple cost-effective jet nebulizer spray method for dye degradation. • A remarkable enhancement in the photocatalytic dye degradation efficiency is achieved for ZnO. • The mechanism for the enhanced degradation is explained on the basis of the obtained point of zero charge values. • Optical, PL, SEM and XPS studies support the discussion on the photocatalytic property of ZnO:Mo/GCN. - Abstract: The photocatalytic activity of ZnO:Mo/GCN (ZnO:Molybdenum/g-C{sub 3}N{sub 4}) thin films deposited using a simple cost-effective jet nebulizer spray pyrolysis technique with different Mo doping concentrations (1,2 and 3 at.%) was studied. The photocatalytic degradation test was carried out against Methylene blue (MB) and Rhodamine B (RhB) dyes under visible light. It is found that thin film of ZnO:Mo/GCN with 1 at.% of Mo exhibits superior photocatalytic efficiency compared with the other samples. The degradation rate constant of this sample is 0.0727 and 0.0268 min{sup −1} for the tested MB and RhB dyes, respectively which are nearly two times and four times greater than the respective rate constant values of pristine ZnO. The mechanism involved in the enhanced photocatalytic activity is addressed with the help of obtained results. The properties of the deposited samples are correlated appropriately with the photocatalytic efficiency of the samples. The photostability of the prepared catalysts is tested experimentally.

36 MATERIALS SCIENCE↗

A Step Toward Efficient Panchromatic Multi-Chromophoric Sensitizers for Dye Sensitized Solar Cells

Panchromatic dyes with absorption profiles extending into the near infra-red are of interest to researchers in the field of dye sensitized solar cells (DSSCs), as they offer potential access to a wide energy range of photons necessary to enhance solar to electric power conversion efficiencies (PCEs). In this report, a porphyrin with a Soret band absorbing at high energy is combined with a squaraine absorbing at low energy $via$ an acetylene linker to form a bichromophoric sensitizer with molar extinctions on the order of 10 5 M -1 cm -1 and an incident photon-to-current efficiency (IPCE) onset of ~850 nm. Various bulky substituents were installed on both the porphyrin and squaraine moieties, and conjugation was increased with π-bridge spacers to achieve a PCE of 7.6%, which is up to 15% higher than a comparable squaraine-only dye. For the most part, charge injection dynamics indicate slower charge injection rates and lower injection quantum yields for these bichromophoric sensitizers compared to non-porphyrin squaraine-based DSSC sensitizers. Nevertheless, higher PCE was observed for most porphyrincontaining dyes due largely to increased panchromaticity.

14 SOLAR ENERGY↗

Ruthenium Dye Excitations and Relaxations in Natural Sunlight

Solar harvesting devices using dyes convert the sun's energy to usable forms. The photophysics involved are generally investigated using time-resolved spectroscopic experiments with femtosecond to nanosecond resolution. We show that a kinetic framework constructed from transient and linear absorption measurements of metal-ligand charge transfer states for a set of ruthenium complexes in solution can be used to simulate the steady-state dynamics of dyes adsorbed on a substrate under diffuse solar radiation. Even though the intensity of sunlight is relatively low, double excitations to higher excited states can occur. The steady-state populations show that the dyes' triplet state is the main species present besides the ground state. While small, these persistent excited populations can influence reactivity over the extended periods of time that the systems operate. The results show that non-radiative and optical events (dye -1 s -1 ) within the singlet manifold and from the triplet state exhibit a dependence on ligand substituents.

14 SOLAR ENERGY↗

Emission lifetimes of a fluorescent dye under shock compression

The emission lifetimes of rhodamine 6G (R6G), were measured under shock compression to 9.1 GPa, with the dual intent of better understanding molecular photophysics in extreme environments and assessing the usefulness of fluorescence lifetime microscopy to measure spatially-dependent pressure distributions in shocked microstructured media. R6G was studied as free dye dissolved in poly-methyl methacrylate (PMMA), or dye encapsulated in silica microparticles suspended in PMMA. Thin layers of these materials in impedance-matched geometries were subjected to planar single-stage shocks created by laser-driven flyer plates. A synchronized femtosecond laser excited the dye at selected times relative to flyer plate arrival and the emission lifetimes were measured with a streak camera. Lifetimes decreased when shocks arrived. The lifetime decrease was attributed to a shock-induced enhancement of R6G nonradiative relaxation. At least part of the relaxation involved shock-enhanced intersystem crossing. For free dye in PMMA, the lifetime decrease during the shock was shown to be a linear function of shock pressure from 0-9 GPa, with a slope of -0.22 ns·GPa -1 . Furthermore, the linear relationship makes it simple to convert lifetimes into pressures. Lifetime measurements in shocked microenvironments may be better than emission intensity measurements, since lifetimes are sensitive to the surrounding environment, but insensitive to intensity variations associated with the motion and optical properties of a dynamically changing structure.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Excited Carrier Dynamics in a Dye-Sensitized Niobate Nanosheet Photocatalyst for Visible-Light Hydrogen Evolution

Dye-sensitized photocatalysts that consist of a light-absorbing dye and a wide gap oxide semiconductor have been studied extensively as components of solar energy conversion systems. Although surface modification by a metal and/or metal oxide has a significant impact on the photocatalytic efficiency, the mechanism by which these modifications increase the activity has not been fully understood. Here a dye-sensitized H 2 evolution system was constructed by using Pt-intercalated HCa 2 Nb 3 O 10 nanosheets, Ru(II) complex photosensitizers ([Ru(4,4’-(CH 3 ) 2- bpy) 2 (4,4’-(PO 3 H 2 ) 2- bpy)] 2+ and [Ru(4,4’-(CH 3 ) 2- bpy) 2 (4,4’-(CH 2 PO 3 H 2 ) 2- bpy)] 2+ , abbreviated as RuP 2+ and RuCP 2+ ; bpy = 2,2'-bipyridine), and amorphous Al 2 O 3 as building blocks. In the presence of iodide as the electron donor, the H 2 evolution rate from Pt/HCa 2 Nb 3 O 10 nanosheets sensitized by RuP 2+ was increased by modification of the nanosheets with Al 2 O 3 . On the other hand, Al 2 O 3 had a negative impact on the H 2 evolution rate when RuCP 2+ was employed. These hybrid materials were studied by transient diffuse reflectance spectroscopy and steady-state emission spectroscopy. A detailed analysis of the transient absorption profiles of the adsorbed Ru(II) complexes revealed that there are at least three states of the complexes on the nanosheet surface. The transient bleaching of the ground state absorbance had different lifetime components ranging from a few μs to several hundred μs, which mainly reflect back electron transfer rates from HCa 2 Nb 3 O 10 to the oxidized Ru(II) complexes. Here, the Al 2 O 3 modifier could inhibit not only the back electron transfer events but also electron injection from the excited state photosensitizer. Interestingly, the negative effect of Al 2 O 3 on the electron injection rate was negligible in the case of RuP 2+ , which also had a higher H 2 evolution rate. This work highlights that suppressing fast back electron transfer from Pt/HCa 2 Nb 3 O 10 to the oxidized Ru(II) complex, which occurs on a time scale of a few μs, and maximizing the electron injection efficiency are both necessary for improving dye-sensitized H 2 evolution.

14 SOLAR ENERGY↗

TiO 2 -Assisted Photoisomerization of Azo Dyes Using Self-Assembled Monolayers: Case Study on para -Methyl Red Towards Solar-Cell Applications

The optical and electronic properties of a TiO2 nanoparticle-assisted photo-isomerizable surface, prepared by an azo dye/TiO2 nanocomposite film, are examined experimentally and computationally. The azo dye, para-methyl red, undergoes photoisomerization at room temperature, catalyzed by the TiO2 nanoparticle supports, while it exhibits negligible photoisomerization in solvents under otherwise identical conditions. Density functional theory and time-dependent density functional theory are employed to explain the origin of this photoisomerization in these dye…TiO2 nanoparticle self-assembled monolayers (SAMs). The device performance of these SAMs when embedded into dye-sensitized solar cells is used to further elucidate the nature of this azo dye photoisomerization and relate it to the ensuing optoelectronic properties.

Zhang, Lei↗

Complications in complexation kinetics for lanthanides with DTPA using dye probe molecules in aqueous solution

The complexation kinetics for the polyaminopolycarboxylic ligand DTPA to lanthanides in acidic aqueous solution were investigated using the dye ligand displacement technique and stopped-flow spectroscopy. Significant rate differences were obtained for different dye probes used, indicating that the kinetics of the dissociation of the dye molecule significantly impacts the overall measured kinetics when using this common methodology. The conditions of the solution also influenced the dye-lanthanide-DTPA interactions, which reconciled previously disparate data in the literature.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Maximizing sunlight absorption in narrow bandgap semiconducting copper(I) iodides for enhanced photocatalytic dye degradation

Photocatalytic dye degradation leverages sunlight to break down dyes and pigments into safer, simpler molecules. Using a material that can absorb a broad range of the solar spectrum optimizes the speed and efficiency of this process. In this study, we explore a series of new, narrow bandgap copper iodide semiconductors (1.5–1.7 eV) with various dimensionalities (0D to 3D) to evaluate their photocatalytic efficiency in dye degradation. The most effective material achieved 95% degradation within just 27 minutes. Mass spectrometry provided a detailed insight and in-depth understanding into the degradation mechanism. All materials demonstrated excellent stability under ambient conditions, highlighting their promise as eco-friendly candidates for dye degradation in water purification.

Carignan, Gia M. [Rutgers Univ., Piscataway, NJ (U↗

Effect of methyl red dye on dielectric and conductivity properties of PEO/CdCl{sub 2} electrolytes

In this report the conductivity and dielectric properties of polyethylene oxide-cadmium chloride (PEO/CdCl{sub 2}) polymer electrolyte films doped with an azo dye methyl red (MR) are discussed. The films were prepared by solution casting technique at different concentrations of the dye in PEO/CdCl{sub 2} electrolyte. The thermal behavior, chemical interaction of the dye with the electrolyte and surface morphology were studied by differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM) respectively. The conductivity and dielectric properties were measured as a function of composition and temperature using complex impedance spectroscopy. The temperature dependent electrical conductivity of the films exhibited Arrhenius type behavior. Conductivity and dielectric results also signify the enhancement in the amorphous phase of the polymer electrolyte dye systems. The value of highest conductivity observed is 1.21x10{sup −4} at 343K and the conductivity of the film was enhanced by a three orders of magnitude.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

High-resolution 3D-printed plastic scintillators with tertiary dye

Additive manufacturing offers efficient production of plastic scintillators with nontrivial geometries using vat polymerization, allowing fabrication of geometries which would be difficult or even impossible to produce using conventional subtractive manufacturing. This work presents a novel photocurable scintillator formula that includes coumarin 450 as a tertiary dye to enable high-resolution 3D printing via the manipulation of the 405 nm cure light. Bulk photocured and 3D printed (with and without tertiary dye) samples were compared through observational assessment and spectral response. All samples showed pulse shape discrimination between neutron and gamma events. Inclusion of the tertiary dye has minimal impact on emission spectrum and light output, but significant impact on print resolution as shown by comparison of printed high-complexity geometries and feature resolution test objects. With the use of a cure-limiting dye, unsupported features — such as freestanding pillars — were resolvable down to 0.7 mm. Even finer resolution at or below 0.1 mm was achieved in fully supported, integrated structures printed with off-the-shelf 405 nm desktop 3D printer. Scintillators demonstrated a light output up to 50% of EJ-200 with a PSD figure of merit up to 1.35 at 0.9–1.1 MeVee.

36 MATERIALS SCIENCE↗

Luminescence and Nonlinear Optical Properties of Hybrid Associates of Ag{sub 2}S Quantum Dots with Molecules of Thiazine Dyes

Spectral, kinetic, and nonlinear optical regularities that demonstrate the exchange of electronic excitations between the components of hybrid associates of Ag{sub 2}S colloid quantum dots (1.7–1.8 nm) in gelatin with molecules of thiazine dyes (Ds) are found. When the IR luminescence of Ag{sub 2}S quantum dots (QDs) is excited by radiation from the thionine absorption region, its enhancement due to nonradiative resonant energy transfer is observed. The association with methylene-blue molecules blocked the IR luminescence of Ag{sub 2}S QDs upon its excitation by radiation from the absorption region of the dye due to the transfer of charge carriers. It is demonstrated that the hybrid association of thionine molecules and Ag{sub 2}S QDs adversely affects the nonlinear optical properties of the latter, which manifests itself in inverse saturated absorption by the action of 10-ns second-harmonic pulses (532 nm) of a Nd{sup 3+}:YAG laser. For the associates of Ag{sub 2}S QDs with methylene-blue molecules, the radiation focusing caused by the transfer of charge carriers from the dye and the change in the population of small traps in nanocrystals is found. It is concluded that the direction of the transfer of electronic excitations and the photophysical processes in these objects are determined by the mutual arrangement of the HOMO–LUMO levels of the dye with respect to the levels of dimensional quantization of the Ag{sub 2}S QDs.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Chemically Cross-Linked Cellulose Nanocrystal Aerogels for Effective Removal of Cation Dye

In this study, porous aerogels were prepared by directional freeze-drying via cross-linking cellulose nanocrystals (CNCs) with poly(methyl vinyl ether-co-maleic acid) (PMVEMA) and poly(ethylene glycol) (PEG). The thermal properties and physical adsorption performance toward cation methylene blue dye of the obtained CNC aerogels were investigated. The maximum degradation temperature was increased from 324°C of CNCs to 355°C of cross-linked CNC aerogels. The dye adsorption isotherm results showed that the maximum methylene blue adsorption capacity of CNC aerogels was 116.2 mg g −1 , according to the Langmuir model, which was mainly due to the electrostatic attractions between negatively charged carboxyl groups or sulfonate groups on the CNC aerogles and cation MB molecules. The reusability test showed that the CNC aerogels contained the same dye adsorption performance in five adsorption/desorption cycles. Overall, this study described an ideal alternative for water purification with high dye adsorption capacity and enhanced physical performance.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Effect of Random Nanostructured Metallic Environments on Spontaneous Emission of HITC Dye

We have studied emission kinetics of HITC laser dye on top of glass, smooth Au films, and randomly structured porous Au nanofoams. The observed concentration quenching of luminescence of highly concentrated dye on top of glass (energy transfer to acceptors) and the inhibition of the concentration quenching in vicinity of smooth Au films were in accord with our recent findings. Intriguingly, the emission kinetics recorded in different local spots of the Au nanofoam samples had a spread of the decay rates, which was large at low dye concentrations and became narrower with increase of the dye concentration. We infer that in different subvolumes of Au nanofoams, HITC molecules are coupled to the nanofoams weaker or stronger. The inhibition of the concentration quenching in Au nanofoams was stronger than on top of smooth Au films. This was true for all weakly and strongly coupled subvolumes contributing to the spread of the emission kinetics. The experimental observations were explained using theoretical model accounting for change in the Förster radius caused by the strong energy transfer to metal.

36 MATERIALS SCIENCE↗

Using Vertically Aligned Carbon Nanofiber Arrays on Rigid or Flexible Substrates for Delivery of Biomolecules and Dyes to Plants

The delivery of biomolecules and impermeable dyes to intact plants is a major challenge. Nanomaterials are up-and-coming tools for the delivery of DNA to plants. As exciting as these new tools are, they have yet to be widely applied. Nanomaterials fabricated on rigid substrate (backing) are particularly difficult to successfully apply to curved plant structures. This study describes the process for microfabricating vertically aligned carbon nanofiber arrays and transferring them from a rigid to a flexible substrate. We detail and demonstrate how these fibers (on either rigid or flexible substrates) can be used for transient transformation or dye (e.g., fluorescein) delivery to plants. We show how VACNFs can be transferred from rigid silicon substrate to a flexible SU-8 epoxy substrate to form flexible VACNF arrays. Further, to overcome the hydrophobic nature of SU-8, fibers in the flexible film were coated with a thin silicon oxide layer (2-3 nm). To use these fibers for delivery to curved plant organs, we deposit a 1 µL droplet of dye or DNA solution on the fiber side of VACNF films, wait 10 min, place the films on the plant organ and employ a swab with a rolling motion to drive fibers into plant cells. With this method, we have achieved dye and DNA delivery in plant organs with curved surfaces.

59 BASIC BIOLOGICAL SCIENCES↗

Lewis Acid-Assisted Isotopic 18 F- 19 F Exchange in BODIPY Dyes: Facile Generation of Positron Emission Tomography/Fluorescence Dual Modality Agents for Tumor Imaging

Positron emission tomography (PET) is a powerful technique for imaging biological pathways in vivo, particularly those that are key targets in disease processes. In contrast, fluorescence imaging has demonstrated to be a superior method for image-guided surgery, such as tumor removal. Although the integration of PET and optical imaging could provide an attractive strategy for patient management, there is a significant shortage of established platforms/methods for PET/optical probe construction. In this study, various reaction conditions were explored to develop a simple and fast method allowing for the introduction of [ 18 F]-fluoride into BODIPY dyes. Through a systematic optimization of the reaction conditions, we found that BODIPY dyes, including commercial amine-reactive BODIPY succinimidyl esters, may be converted into their radioactive analogues in the matter of minutes via a 18 F- 19 F isotopic exchange reaction promoted by a Lewis acid such as SnCl 4 . An integrin-targeting RGD peptide was also conjugated with [ 18 F]BODIPY® R6G , derived from the commercially available BODIPY® R6G fluorescent tag, to provide a [ 18 F]-RGD conjugate in 82% yield. In vivo evaluation of this imaging probe showed a discernible tumor uptake in the U87MG xenograft model. The dual modality imaging properties of the probe was confirmed by ex vivo fluorescence and microPET imaging experiments. In summary, in the matter of minutes, BODIPY dyes were converted into their “hot” radioactive analogues via a 18 F- 19 F isotopic exchange reaction promoted by a Lewis acid. This approach, which can be applied to commercial BODIPY dyes, provides easy access to positron emission tomography/fluorescence dual modality imaging agents.

18F-19F exchange↗