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Growth, microstructure, structural and optical properties of PVP-capped CdS nanoflowers for efficient photocatalytic activity of Rhodamine B

Highlights: • Synthesis of un-capped and PVP-capped CdS microstructures by Hydrothermal. • Growth of both the flower and dendrite microstructures controlled by the growth time. • Phase transition of CdS from cubic zinc blend to hexagonal by the growth time. • CdS flowers enhanced the photocatalytic performance of RhB under visible light. • PVP-capped CdS showed the highest degradation of 95% of RhB within 120 min. - Abstract: Size and structure tunability of polyvinyl pyrolidone (PVP) capped cadmium sulfide (PVP-capped CdS) flowers were synthesized by controlling the reaction time. XRD pattern indicated a phase transition from the cubic zinc blend to the hexagonal phase of CdS powder as the reaction time increased. As per the microstructure analysis with respect to the reaction time, the spherical nanoparticles were transformed in to the flower like morphology consisting of sword like nanorods and confirmed by the bright field images of TEM, while, HR-TEM images showed the uniform lattice spacing. UV-spectra exhibited a red shift due to the excitations of CdS nanoparticles. The near band edge (NBE) peak of PVP-capped CdS was completely diminished which indicated to sulphur vacancies on the surface of flowers. The photocatalytic activity of PVP-capped CdS flowers was detected the fast degradation of Rhodamine B (RhB) dye (95% for 120 min) by irradiation of visible light.

36 MATERIALS SCIENCE↗

Raspberry—like monodispersity ZnO microspheres for photodegradation of rhodamine B

Highlights: • Rasberry-like ZnO microspheres were successfully prepared through a F108-assisted one-pot hydrothermal route. • The resulting ZnO microspheres are composed of many small nanoparticles, generating a unique rough surface. • The surface rough and the diameter of the microspheres can be easily tuned only by changing the composition of the precursor. • The Au decorated-ZnO composite demonstrates better photocatalytic activities for degradation of RhB than the pristine ZnO micropheres. - Abstract: In the article, we propose a simple and effective one-pot hydrothermal approach for synthesis of raspberry-like ZnO microspheres, where triblockpoly (ethylene oxide)-poly (propylene oxide)-poly (ethylene oxide), triethanolamine, ethylene glycol acts as the structure-directing agent (SDA), co-template, and solvent, respectively. They are together responsible for the growth of ZnO products with uniform morphology, high crystallinity, and good monodispersity. The resulting ZnO microspheres possess rough surface, which are composed of many small nanoparticles. Moreover, the surface roughness and the diameter of the microspheres can be easily tuned only by changing the composition of the precursor. Meanwhile, the photodegradation behavior of the products is also tested by selecting the rhodamine B (RhB) as the model pollutant. The photocatalytic results indicate that the raspberry-like ZnO products exhibit excellent photocatalytic activity. In particular, the Au decorated-ZnO composite demonstrates an enhanced photocatalytic activity towards degradation of RhB under UV irradiation compared with the pristine ZnO microspheres.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Fabrication of In2O3/TiO2 nanotube arrays hybrids with homogeneously developed nanostructure for photocatalytic degradation of Rhodamine B

Highlights: • A new class of plate-like In{sub 2}O{sub 3}/TNAs photocatalyst is successfully fabricated. • The obtained In{sub 2}O{sub 3}/TNAs hybrid presents a well-aligned nanotubular structure. • In{sub 2}O{sub 3} particles are dispersed homogeneously on TNAs without blocking the nozzles. • In{sub 2}O{sub 3}/TNAs hybrid shows a much enhanced Rhodamine B degradation efficiency. • In{sub 2}O{sub 3}/TNAs hybrid demonstrates an excellent recycling capability. - Abstract: To enhance the photocatalytic recycling capability of the TiO{sub 2}-based photocatalysts, a new kind of plate-like In{sub 2}O{sub 3}/TiO{sub 2} nanotube array (TNA) hybrids is fabricated herein by constructing TNAs via an anodization method followed by doping In{sub 2}O{sub 3} via a solvothermal method. The obtained In{sub 2}O{sub 3}/TNA hybrid demonstrates a well-aligned nanotubular structure with homogeneous dispersion of In{sub 2}O{sub 3} nanoparticles. It shows a much higher degradation rate of 77% after 2 h compared to TNA (37%). In addition, the plate-like feature endows the photocatalysts with an excellent recycling capability. These superior photocatalytic degradation performances can be ascribed to the following factors: (1) the enhanced light absorption ability and efficient separation of photoexcited electron-hole pairs derived from the formation of the heterostructure between the interface of TiO{sub 2} and In{sub 2}O{sub 3}; (2) the efficient transport of reactant molecules provided by the well-defined TNAs and the homogeneous distribution of the In{sub 2}O{sub 3} nanoparticles without blocking the nanotubes.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Three-dimensional MoO3 nanoflowers assembled with nanosheets for rhodamine B degradation under visible light

Highlights: • The orthorhombic three-dimensional MoO{sub 3} nanoflowers were synthesized by the modified hydrothermal method. • Using different amount of HCl to transfer from the h-MoO{sub 3} to the α-MoO{sub 3} was well discussed. • Better pore sizes and surface areas of the three-dimensional MoO{sub 3} nanoflowers accelerate the photodegradation process of RhB. • The three-dimensional MoO{sub 3} nanoflowers showed the photocatalytic activity (91.57%). • This methodology should be useful for preparing other nanostructured catalysts. - Abstract: Three-dimensional hierarchical nanoflowers self-assembled with the orthorhombic molybdenum oxide (α-MoO{sub 3}) nanoflowers were synthesized by the modified hydrothermal method. The structure characterizations of the three-dimensional α-MoO{sub 3} nanoflowers were carried out by scanning electron microscope (SEM), Energy Disperse Spectroscopy (EDS), X-ray diffraction (XRD) and nitrogen adsorption-desorption measurement. Moreover, the three-dimensional α-MoO{sub 3} nanoflowers as photocatalyst exhibited enhanced photocatalytic activity towards photodegradation of Rhodamine B (RhB) under xenon (Xe) lamp irradiation. The results of SEM, EDS, XRD and nitrogen adsorption-desorption measurement showed the three-dimensional α-MoO{sub 3} nanoflowers have a better morphology, pore size (7.99 nm) and surface areas (50.788 m{sup 2} g{sup −1}) than hexagonal MoO{sub 3} (h-MoO{sub 3}) nanosheets, photocatalytic activity studies confirmed that the three-dimensional α-MoO{sub 3} nanoflowers photocatalyst exhibits a high visible-light-driven activity for photodegradation of RhB solution of 91.57% within 160 min under Xe lamp irradiation. A mechanism was also proposed for the degradation of RhB by three-dimensional α-MoO{sub 3} nanoflowers.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

XPS study of Rhodamine B doped PVA nanocomposite films as a function of annealing

The bonding properties of PVA thin films are explored as a function of annealing in pure and Rhodamine B doped self-standing films. X-ray photoelectron spectroscopy measurements have shown high quality, impurity free films, where the bonding is found between C and O elements in agreement with the standard data of polymers. Upon annealing, the bonds break and signals come only from elemental carbon and oxygen at their respective binding energy positions. The experiments are able to show that upon annealing at 65° C, all the bonds break and hence electronic properties are completely modified.

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗

SERS Theory: The Chemical Effect of Rhodamine 6G Adsorption on Silver Surfaces on Its Raman Spectrum

The SERS spectra of small organic molecules can be very sensitive to the physisorption or chemisorption of the molecules onto metallic surfaces. However it is challenging to model the results, as typical SERS substrates have a broad distribution of possible surface sites, and the populations of these sites and the SERS enhancement factors associated with them are very difficult to determine, especially when electromagnetic hot spots dominate the observed spectra. However it is important to account for these effects if one is to make a quantitative interpretation of measured SERS spectra. Indeed, the influence of different sites is important to both the electromagnetic and chemical mechanisms in SERS, where the former mechanism is concerned with local field enhancement effects arising from plasmon excitation, while the latter arises from the effect of chemisorption induced charged transfer on the Raman intensities, as can be modeled using static limit Raman intensity calculations[1]. Extensive studies have been performed on simple organics like pyridine bound to gold and silver clusters, and it was found that both the chemical and electrodynamic enhancement factors associated with binding pyridine in various orientations result in noticeable changes in the SERS spectra compared to the gas phase spectrum of pyridine.[2] One of the most important benchmark molecules for SERS and TERS studies is Rhodamine 6G (R6G). This is a strongly fluorescent dye molecule in solution, but when adsorbed onto SERS substrates, its fluorescence is quenched, and the resulting SERS intensities are among the largest observed for any molecule. As a result R6G has played a crucial role in the development of single molecule SERS, and in the development of SERS substrates. [3, 4] Previously, the SERS spectrum of R6G has been modeled as if it were a gas phase molecule. Jensen and Schatz[5] incorporated resonant effects as well as vibronic effects and found that resonance excitation to the S1 excited state of R6G resulted in good agreement with spectra obtained from SERS experiments. In another study, intermolecular charge transfer was studied with R6G bound to a Ag2 cluster.[6] It is unclear if a cluster model as small as two silver atoms can accurately capture the surface effects of a nanoparticle with thousands of atoms. Recent single molecule, ultra high vacuum, tip enhanced Raman spectroscopy (SM-UHV-TERS) measurements for R6G[3] were moderately reproduced by gas phase resonance Raman calculations. Of particular importance in this work was the comparison of TERS spectra at room temperature with those at a low temperature of 10K. It was found that lowering the temperature led to both sharpening of the vibrational spectra, and shifts in the spectra (up to 20 cm-1 with some lines shifting red, some blue and some not at all), suggesting that the molecule transitions from a largely gas phase molecule at room temperature to being strongly chemisorbed at 10K. A potential energy distribution analysis performed by Chulhai and Jensen[3] showed that the modes that were shifted from the gas phase had vibrational activity associated with the ethylamine component of R6G, which is the likely moiety associated with Raman calculations. What remains unresolved concerning the SM-UHV-TERS studies of R6G is direct evidence that the chemical binding of R6G to a silver nanoparticle surfaces causes frequency shifts and/or intensity changes in the Raman scattering intensities of specific modes, especially those involving vibrations of the ethylamine moiety. The theoretical work described in this chapter directly addresses this issue by calculating Raman spectra for R6G interacting with a 20-atom silver cluster, and with a flat Ag(111) surface. Tetrahedral Ag20 is chosen for part of these studies as it provides a model nanoparticle structure that has a well-defined fragment of a (111) surface, as well as having edges and vertices that can be used to model coordinately unsaturated sites on a particle. In addition, Ag20 has been found to provide a reasonable reference structure for determining the chemical contribution to SERS enhancements.[1] Two different geometries of the Ag20/R6G system are considered in the present study, corresponding to two different binding configurations of R6G to a pristine Ag(111) surface. In addition, we study adsorption of R6G on a flat Ag(111) surface of using plane wave DFT calculations to determine optimized geometries and normal mode properties.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Electronic π-to-π* Excitations of Rhodamine Dyes Exhibit a Time-Dependent Kohn-Sham Theory “Cyanine Problem”

The longest-wavelength π-to-π* electronic excitations of rhodamine-like dyes (RDs) with different group16 heteroatoms (O, S, Se, Te) have been investigated. Time-dependent Kohn–Sham theory (TDKST) calculations were compared with coupled-cluster (CC) and equations-of-motion (EOM) CC results for π-to-π* singlet and triplet excitations. The RDs exhibit characteristics in the TDKST calculations that are very similar to previously investigated cyanine dyes, in the sense that the singlet energies obtained with nonhybrid functionals are too high compared with the CC results at the SD(T) level. The errors became increasingly larger for functionals with increasing amounts of exact exchange. TDKST with all tested functionals led to severe underestimations of the corresponding triplet excitations and overestimations of the singlet--triplet gaps. Long-range-corrected range-separated exchange and "optimal tuning" of the range separation parameter did not significantly improve the TDKST results. A detailed analysis suggests that the problem is differential electron correlation between the ground and excited states, which is not treated sufficiently by the relatively small integrals over the exchange-correlation response kernel that enters the excitation energy expression. As a result, numerical criteria are suggested that may help identify "cyanine-like" problems in TDKST calculations of excitation spectra.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Evaluation of Rhodamine B as a biomarker for assessing bait acceptance in wild pigs

ABSTRACT Worldwide, there is growing interest in the use of pharmaceutical baits to control populations of wild pigs ( Sus scrofa ). In this study we evaluated the utility of Rhodamine B (RB), a chemical marker commonly used in wildlife research and management, as a potential biomarker for quantifying bait uptake in wild pigs. Thirty wild pigs were live‐trapped, transported to a captive facility on the Department of Energy's Savannah River Site located in South Carolina, USA, during autumn 2013, and administered RB orally at a dosage of 30 mg/kg. Eight vibrissae and guard hairs were collected pre‐ and post‐RB exposure (7 or 14 days) and evaluated for the presence of RB using fluorescence microscopy. No evidence of RB marking was observed in any samples collected pre‐RB administration. In contrast, we observed fluorescent marking post‐RB exposure that was indicative of the presence of RB for all individuals, with 98% of vibrissae and 100% of guard hairs exhibiting RB marks. The uniform detection of RB among individuals and consistent manifestation of marks in both guard hair and vibrissae, samples that easily can be collected and stored by untrained field personnel from live or deceased pigs, suggests that RB is an effective biomarker for use in large‐scale management programs to control wild pigs. In particular, our results, combined with previous studies evaluating uptake of RB in other species, suggest that RB can be used to develop baiting programs to deliver pharmaceuticals to free‐ranging wild pigs, as well as evaluate the potential impacts of pig baits on non‐target species. © 2014 The Wildlife Society.

Beasley, James↗

Synthesis, Characterization and Experimental Studies of Nano Zn–Al–Fe{sub 3}O{sub 4} Blended Alginate/Ca Beads for the Adsorption of Rhodamin B

In the present study, adsorptive removal of rhodamin-B (RMN-B) from aqueous solution was investigated by using nano Zn–Al–Fe{sub 3}O{sub 4} incorporated sodium alginate (SA) beads. SA is a natural polysaccharide, non toxic and biodegradable material. The incorporation of Zn–Al–Fe{sub 3}O{sub 4} into SA was done by ionic polymerization method using CaCl{sub 2}. A batch mode study was used for the adsorption of RMN-B onto Zn–Al–Fe{sub 3}O{sub 4}/ alginate beads. The adsorption efficiency of RMN-B was investigated by the following modeling equations like Freundlich, Langmuir, Pseudo-first order, Pseudo-second order, Intraparticle diffusion, Gibbs free energy, Enthalpy and Entropy. The predicted experimental results of various modeling equations were implied that the process follow Langmuir and pseudo-second order equations. The intraparticle diffusion parameters indicate that the diffusion between RMN-B and nano beads were predominant in throughout of process. The surface morphology of nano beads of before and after adsorption were show that RMN-B is strongly adhered on whole surface of the nano material. The FTIR spectrum indicates that the RMN-B strongly adsorbed on the surface and TGA study reveals that the alginate/Zn–Al–Fe{sub 3}O{sub 4}/Ca material has an excellent temperature withstand capacity.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Solution synthesis of two-dimensional zinc oxide (ZnO)/molybdenum disulfide (MoS 2 ) heterostructure through reactive templating for enhanced visible-light degradation of rhodamine B

Numerous inorganic materials have been identified as potential candidates for high-performance photocatalysts. However, their solar-to-energy conversion efficiencies still fail to meet commercial requirements. Here, the main hurdle is the rapid recombination of photoexcited electrons and holes in single-phase materials. A viable predicted approach to suppress charge recombination is coupling two materials to form a two-dimensional (2D) heterostructure that physically separates photoinduced electrons and holes in different layers. In this work, the heterostructure-based paradigm was tested and a scalable solution synthesis of epitaxial ZnO-MoS 2 heterostructure was developed. A 2D ZnO-MoS 2 heterostructure was synthesized under hydrothermal conditions by stabilizing intermediate Zn-hydroxide states on a functionalized MoS 2 surface. Detailed characterization showed the formation of multilayer heterostructure with MoS 2 flakes intercalated between large size ZnO plates. The performance of this heterostructure was evaluated using photocatalytic degradation of rhodamine B. A degradation efficiency of 70% was measured within 90 minutes of visible-light irradiation, almost doubling the efficiency of the corresponding single-phase materials or their physical mixtures.

2D heterostructure↗

Novel Y doped Bi{sub 2}WO{sub 6} photocatalyst: Hydrothermal fabrication, characterization and enhanced visible-light-driven photocatalytic activity for Rhodamine B degradation and photocurrent generation

Visible-light-driven (VLD) Yttrium (Y) ion doped Bi{sub 2}WO{sub 6} photocatalyst has been synthesized via a facile hydrothermal route. Incorporation of Y{sup 3} {sup +} into Bi{sub 2}WO{sub 6} lattice was successfully confirmed by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and ICP analysis. The microstructure and optical property of the as-prepared samples have been characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), nitrogen adsorption–desorption isotherm and UV–vis diffuse reflectance spectra (DRS). The photocatalytic experiments indicated that the Y-Bi{sub 2}WO{sub 6} showed a much higher photocatalytic activity than the pristine Bi{sub 2}WO{sub 6} for the degradation of Rhodamine B (RhB) and photocurrent (PC) generation. This enhancement should be ascribed to the slightly increased band gap and the generated defects by Y{sup 3} {sup +} doping, thus resulting in a much lower recombination rate of the photoinduced electrons and holes. Such a process was verified by the photoluminescence (PL) spectroscopy. In addition, the active species trapping experiments indicated that holes (h{sup +}) and superoxide radicals (·O{sub 2}{sup −}) play important roles in the photocatalytic reaction. - Highlights: • Novel Y-Bi{sub 2}WO{sub 6} photocatalyst has been synthesized by a facile hydrothermal route. • Y-Bi{sub 2}WO{sub 6} exhibits a much higher photocatalytic activity than pristine Bi{sub 2}WO{sub 6}. • Holes (h{sup +}) and superoxide radicals (·O{sub 2}{sup −}) are the two main active species. • Y{sup 3} {sup +} ion can result in a low recombination of photogenerated electron and hole.

36 MATERIALS SCIENCE↗

Graphene oxide based CdSe photocatalysts: Synthesis, characterization and comparative photocatalytic efficiency of rhodamine B and industrial dye

Highlights: ► CdSe–graphene is synthesized by hydrothermal method. ► Three molar solutions of CdSe were used making three different composites. ► RhB and Texbrite MST-L were used as sample dye solutions. ► Texbrite MST-L is photo degraded in visible light. ► UV-spectroscopic analysis was done to measure degradation. - Abstract: CdSe–graphene composites were prepared using simple “hydrothermal method” where the graphene surface was modified using different molar solutions of cadmium selenide (CdSe) in aqueous media. The characterization of CdSe–graphene composites were studied by X-ray diffraction (XRD), energy dispersive X-ray (EDX), scanning electron microscope (SEM), and with transmission electron microscope (TEM). The catalytic activities of CdSe-composites were evaluated by degradation of rhodamine B (RhB) and commercial industrial dye “Texbrite MST-L (TXT-MST)” with fixed concentration. The degradation was observed by the decrease in the absorbance peak studied by UV spectrophotometer. The decrease in the dye concentration indicated catalytic degradation effect by CdSe–graphene composites.

36 MATERIALS SCIENCE↗

Enhanced photosensitized degradation of rhodamine B on CdS/TiO{sub 2} nanocomposites under visible light irradiation

Graphical abstract: The photosensitized degradation of RhB was largely enhanced by the synergistic effect of the RhB and CdS/TiO{sub 2} nanocomposite. The composite of the two inorganic semiconductors with appropriate oxidation reduction energy levels enhanced the charge separation and extended the absorption response to visible region. - Highlights: • CdS/TiO{sub 2} nanocomposites were synthesized by a simple hydrothermal method. • Samples prepared at 200 °C, 12 h, CdS/TiO{sub 2} = 12% possessed the best activity. • The photosensitized degradation of RhB was largely enhanced by the composite. • The better activity was due to the synergistic effect of the RhB and CdS/TiO{sub 2}. - Abstract: Visible-light-driven photocatalysts, CdS/TiO{sub 2} nanocomposites were synthesized by a simple hydrothermal method. Their formation and structures were characterized by X-ray diffractometer, transmission electron microscopy, diffuse reflectance spectroscopy, and X-ray photoelectron spectroscopy. Taking rhodamine B (RhB) as a model, their photocatalytic activities in aqueous phase under visible light irradiation (420 < λ < 800 nm) were tested. The results showed that the composite of CdS and TiO{sub 2} with appropriate oxidation reduction energy levels enhanced the charge separation and extended the absorption response into visible light region. Thus, the photosensitized degradation of RhB was largely enhanced. The degradation mechanism was explored concretely.

36 MATERIALS SCIENCE↗

Efficient removal rhodamine B over hydrothermally synthesized fishbone like BiVO{sub 4}

Graphical abstract: - Highlights: • Fishbone like BiVO{sub 4} product was synthesized through hydrothermal method. • BiVO{sub 4} sample was characterized by various characterization technologies. • Fishbone like BiVO{sub 4} presented outstanding photocatalytic performance. - Abstract: Fishbone like BiVO{sub 4} product has been successfully synthesized by a hydrothermal method without using any surfactant or template. The pH value was found to play an important role in the formation of this morphology. The band gap of the as-prepared fishbone like BiVO{sub 4} sample was estimated to be about 2.36 eV from the onset of UV–vis diffuse reflectance spectrum (UV–vis DRS) of the photocatalyst. The as-prepared fishbone like BiVO{sub 4} sample exhibited excellent visible-light-driven photocatalytic efficiency. Over this catalyst, the 100% degradation of rhodamine B (Rh B) (0.005 mmol L{sup −1}) was obtained after visible light irradiation (λ > 420 nm) for 180 min. This is much higher than that of bulk BiVO{sub 4} sample prepared by solid-state reaction. The reason for the differences in the photocatalytic activities of fishbone like BiVO{sub 4} sample and bulk BiVO{sub 4} sample was further investigated.

36 MATERIALS SCIENCE↗

Demonstration of Capture, Cooling, Tagging, and Spectroscopic Characterization of UV Photoproduct Ions in a Cryogenic Ion Trap: Application to 266 nm Photofragment Ions from Rhodamine 6G

We demonstrate a method to determine the structures of the primary photodissociation products from a cryogenically cooled parent ion. In this approach, a target ion is cooled by a pulse of buffer gas and tagged in a 20 K Paul trap. The cold ion is then photodissociated by pulsed (~5 ns) UV laser excitation, and the ionic products are trapped, cooled, and tagged by introduction of a second buffer gas pulse in the same trap. The tagged fragments are then ejected into a triple focusing, UV/vis/IR time-of-flight photofragmentation mass spectrometer which yields vibrational and electronic spectra of the mass-selected photofragments. Furthermore, these methods are demonstrated by application to the 266 nm photodissociation of the Rhodamine 6G cation to yield the R575 fragment ion based on loss of ethene as well as to a weaker secondary fragment arising from loss of m/z 43.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Adsorption and Solvation Modulate Rhodamine B Diffusion in Ethanol/Water-Filled Anodic Alumina Nanopores

Confinement of solvents and solutes within nanoporous materials frequently leads to the emergence of unique mass transport behaviors that, once fully understood, may lead to improved chemical separations. Here, the diffusion of Rhodamine B (RhB) dye within 10 and 20 nm diameter anodic aluminum oxide (AAO) nanopores filled with binary ethanol/water mixtures is investigated. Mixture compositions spanning from pure ethanol to pure water are employed. The results of confocal fluorescence correlation spectroscopy studies reveal that RhB diffusion occurs by a two-component mechanism comprising composition-dependent fast and slow motions, characterized by diffusion coefficients D f and D s . The results are consistent with those of previous studies performed under more limited conditions [J. Phys. Chem. C, 2023, 127, 411-420]. The fast component scales with mixture viscosity and is assigned to hindered bulk-like diffusion in central pore regions. Slow diffusion likely involves adsorption of RhB to the pore surface and may be described by a desorption mediated mechanism. The occurrence of RhB adsorption to the AAO surface is verified at the single-molecule level by wide-field fluorescence imaging of membrane cross-sectional surfaces. Unique composition dependent trends in the autocorrelation amplitude and in D s that mimic bulk RhB solubility are revealed. D s is found to be smallest in pure ethanol and pure water and largest in intermediate mixtures. These results suggest that RhB surface adsorption is strongest in the pure liquids and weakest in mixtures of intermediate composition, where the dye is least soluble, and most soluble, respectively. As a result, molecular dynamics simulations reveal that a water layer appears on the pore surface under most conditions, while RhB is solvated primarily by ethanol. The composition dependence of RhB diffusion is concluded to reflect its solvation dependent interactions with the pore walls.

36 MATERIALS SCIENCE↗

Pressure-Induced Stacking of Rhodamine 6G Molecules

Extended conjugation of molecular π systems are of great significance for solar cells and organic light-emitting diodes as these can serve as new light absorbing and emitting chromophores. This research demonstrates the potential of using pressure and solvent environment to create larger assemblies of molecular π-conjugated systems. Here, we selected rhodamine 6G (Rh6G) to study the pressure-induced stacking of molecules in three different solvents: methanol (MeOH), isopropanol (IPA), and 16:3:1 mixture of methanol: ethanol: water (MEW). Absorption, emission, and fluorescence lifetime were studied at pressures up to 11.38 GPa. We found that pressure-induced stacking mechanisms can present solvent dependence: high pressures tend to create emissive Haggregates in MeOH and MEW, but excimers in IPA. This work guides and demonstrates routes to stacking of organic molecules using high pressures and provides fundamental insights into the formation of extended conjugation π systems.

Johnson, Kade [Univ. of Texas at San Antonio, TX (↗

Super-Resolved Single-Molecule Tracking Studies of Rhodamine B Accumulation on Fresh and Aged Polyethylene Terephthalate

It is well-known that toxic organic micropollutants (OMs) accumulate on the surfaces of microplastics. However, much remains to be learned about the exact molecular level mechanisms of OM accumulation and how these evolve as the plastics age. In this work, super-resolved single-molecule tracking (SMT) is used for the first time to investigate the accumulation of Rhodamine B (RhB) dye on fresh and artificially aged polyethylene terephthalate (PET) surfaces. PET thin films serve as models for microplastics, while RhB serves as a proxy for the OMs they accumulate. Artificial aging of the films is accomplished by exposing them in a UV-ozone chamber. Water contact angle, spectroscopic ellipsometry, and carbonyl index measurements reveal a gradual decrease in film hydrophobicity, thickness, and carbonyl content with age. Atomic force microscopy (AFM) data reveal an increase in surface roughness and confirm that the films remain largely intact and continuous across the aging times explored. In SMT experiments, wide-field fluorescence videos acquired from the water/PET interface under 7.5 pM RhB reveal both mobile and immobile dye molecules. Measurements of the frame-to-frame displacements of the dye show that diffusion occurs by a desorption-mediated mechanism and that the diffusion rate varies with PET film age. The surface density of mobile dye molecules decreases with increasing PET age, while the population of immobile molecules becomes relatively larger, suggesting an age-dependent transformation of the mechanism(s) by which the dye is accumulated. SMT data reveal that both mobile and immobile molecules repeatedly adsorb over the same surface sites, consistent with the emergence of nanoscale PET surface heterogeneity also revealed by AFM. Estimates of the adsorption coefficients are obtained using a nearest-neighbor analysis, giving values from 9.9 × 10 5 to 2.1 × 10 6 M –1 for immobile molecules and from 1.8 × 10 5 to 2.5 × 10 5 M –1 for mobile molecules on fresh and 5 min aged PET, respectively. Here, anomalous age-dependent variations in the velocity of molecular motion on the PET surface and in the population of immobile molecules are shown to correlate with changes in the strength of RhB adsorption.

Adsorption↗