Browsing by Subject "Molecules"

Now showing 1 - 20 of 45

Open Access
A Twist in biphthalimide-based chromophores enables thermally activated delayed fluorescence
(American Chemical Society, 2024-04-18) Debnath, S.; Ramkissoon, P.; Vonder Haar, A.L.; Salzner, Ulrike; Smith, T.A.; Musser, A.J.; Patil, S.
Thermally activated delayed fluorescence (TADF) emitters, which convert nonemissive triplets into emissive singlets, have garnered tremendous impetus as next-generation organic electroluminescent materials. Employing donor−acceptor (D−A) designs to produce intramolecular charge transfer (ICT) states is considered an attractive strategy to effectively reduce the singlet− triplet ($ΔE_{ST}$) gap, thereby enhancing reverse intersystem crossing (rISC) in TADF emitters. Herein, we report two ICT chromophores (BP-1TPA and BP-2TPA) utilizing a rational design strategy based on a twisted biphthalimide acceptor core integrated with varying triphenylamine donors. We accomplish efficient TADF emission with a high photoluminescence quantum yield (PLQY) of ∼80% at ambient conditions from poly(methyl methacrylate)-doped films of these chromophores. Twisting the acceptor core ensures the separation of natural transition orbitals, leading to small $ΔE_{ST}$ and generates an intermediate triplet excited state to facilitate rISC. The present study, therefore, sheds light on how delayed fluorescence can be realized from a simple twisted phthalimide core by rational molecular engineering and enables new insights toward exploring the aromatic imide class of molecules as potential organic light-emitting materials.
Open Access
Absorption enhancement of molecules in the weak plasmon-exciton coupling regime
(Optical Society of American (OSA), 2014) Balci, S.; Karademir, E.; Kocabas, C.; Aydınlı, Atilla
We report on the experimental and theoretical investigations of enhancing the optical absorption of organic molecules in the weak plasmon-exciton coupling regime. A metal-organic hybrid structure consisting of dye molecules embedded in the polymer matrix is placed in close vicinity to thin metal films. We have observed a transition from a weak coupling regime to a strong coupling one as the thickness of the metal layer increases. The results indicate that absorption of the self-assembled J-aggregate nanostructures can be increased in the weak plasmon-exciton coupling regime and strongly quenched in the strong coupling regime. A theoretical model based on the transfer-matrix method qualitatively confirms the experimental results obtained from polarization-dependent spectroscopic reflection measurements.
Open Access
Antigenic GM3 lactone mimetic molecule integrated mannosylated glycopeptide nanofibers for the activation and maturation of dendritic cells
(American Chemical Society, 2017) Gunay, Gokhan; Ekiz, Melis Sardan; Ferhati, X.; Richichi, B.; Nativi, C.; Tekinay, Ayse B.; Güler, Mustafa O.
The ability of dendritic cells to coordinate innate and adaptive immune responses makes them essential targets for vaccination strategies. Presentation of specific antigens by dendritic cells is required for the activation of the immune system against many pathogens and tumors, and nanoscale materials can be functionalized for active targeting of dendritic cells. In this work, we integrated an immunogenic, carbohydrate melanoma-associated antigen-mimetic GM3-lactone molecule into mannosylated peptide amphiphile nanofibers to target dendritic cells through DC-SIGN receptor. Based on morphological and functional analyses, when dendritic cells were treated with peptide nanofiber carriers, they showed significant increase in antigen internalization and a corresponding increase in the surface expression of the activation and maturation markers CD86, CD83 and HLA-DR, in addition to exhibiting a general morphology consistent with dendritic cell maturation. These results indicate that mannosylated peptide amphiphile nanofiber carriers are promising candidates to target dendritic cells for antigen delivery. © 2017 American Chemical Society.
Open Access
Colloidal quantum dot light-emitting diodes employing phosphorescent small organic molecules as efficient exciton harvesters
(American Chemical Society, 2014) Mutlugun, E.; Guzelturk, B.; Abiyasa, A. P.; Gao, Y.; Sun X. W.; Demir, Hilmi Volkan
Nonradiative energy transfer (NRET) is an alternative excitation mechanism in colloidal quantum dot (QD) based electroluminescent devices (QLEDs). Here, we develop hybrid highly spectrally pure QLEDs that facilitate energy transfer pumping via NRET from a phosphorescent small organic molecule-codoped charge transport layer to the adjacent QDs. A partially codoped exciton funnelling electron transport layer is proposed and optimized for enhanced QLED performance while exhibiting very high color purity of 99%. These energy transfer pumped hybrid QLEDs demonstrate a 6-fold enhancement factor in the external quantum efficiency over the conventional QLED structure, in which energy transfer pumping is intrinsically weak.
Open Access
Controlled enzymatic stability and release characteristics of supramolecular chiral peptide amphiphile nanofiber gels
(Elsevier B.V., 2017) Zengin, A.; Cinar, G.; Güler, Mustafa O.
Supramolecular bioarchitectures formed by assembly of achiral or chiral building blocks play important roles in various biochemical processes. Stereochemistry of amino acids is important for structural organization of peptide and protein assemblies and structure-microenvironment interactions. In this study, oppositely charged peptide amphiphile (PA) molecules with L-, D- and mixture of L- and D-amino acid conformations are coassembled into supramolecular nanofibers and formed self-supporting gels at pH 7.4 in water. The enzymatic stability of the PA nanofiber gels was studied in the presence of proteinase K enzyme, which digest a broad spectrum of proteins and peptides. The structural changes on the chiral PA nanofibers were also analyzed at different time periods in the presence of enzymatic activity. Controlled release of a model cargo molecule through the chiral PA nanofiber gels was monitored. The diffusivity parameters were measured for all gel systems. Release characteristics and the enzymatic stability of the peptide nanofiber gels were modulated depending on organization of the chiral PA molecules within the supramolecular assemblies.
Open Access
Cyclodextrin-functionalized mesostructured silica nanoparticles for removal of polycyclic aromatic hydrocarbons
(Academic Press Inc., 2017) Topuz, F.; Uyar, T.
Polycyclic aromatic hydrocarbons (PAHs) are the byproducts of the incomplete combustion of carbon-based fuels, and have high affinity towards DNA strands, ultimately exerting their carcinogenic effects. They are ubiquitous environmental contaminants, and can accumulate on tissues due to their lipophilic nature. In this article, we describe a novel concept for PAH removal from aqueous solutions using cyclodextrin-functionalized mesostructured silica nanoparticles (CDMSNs) and pristine mesostructured silica nanoparticles (MSNs). The adsorption applications of MSNs are greatly restricted due to the absence of surface functional groups on such particles. In this regard, cyclodextrins can serve as ideal functional molecules with their toroidal, cone-type structure, capable of inclusion-complex formation with many hydrophobic molecules, including genotoxic PAHs. The CDMSNs were synthesized by the surfactant-templated, NaOH-catalyzed condensation reactions of tetraethyl orthosilicate (TEOS) in the presence of two different types of cyclodextrin (i.e. hydroxypropyl-β-cyclodextrin (HP-β-CD) and native β-cyclodextrin (β-CD)). The physical incorporation of CD moieties was supported by XPS, FT-IR, NMR, TGA and solid-state 13C NMR. The CDMSNs were treated with aqueous solutions of five different PAHs (e.g. pyrene, anthracene, phenanthrene, fluorene and fluoranthene). The functionalization of MSNs with cyclodextrin moieties significantly boosted the sorption capacity (q) of the MSNs up to ∼2-fold, and the q ranged between 0.3 and 1.65 mg per gram CDMSNs, of which the performance was comparable to that of the activated carbon.
Open Access
Cytotoxicity of multifunctional surfactant containing capped mesoporous silica nanoparticles
(Royal Society of Chemistry, 2016) Yildirim, A.; Turkaydin, M.; Garipcan, B.; Bayındır, Mehmet
This paper reports the synthesis of silica capped surfactant (cetyltrimethylammonium bromide; CTAB) and dye (Rose Bengal; RB) containing mesoporous silica nanoparticles (MSNs). Capping the pores of the surfactant containing MSNs with a thin silica layer decreased the immediate surfactant originated cytotoxicity of these particles without affecting their long term (3 days) cytotoxicity. Also, the silica capping process almost completely prevented the hemolytic activity of the surfactant containing MSNs. In addition, improved uptake of silica capped MSNs compared to the uncapped particles by cancer cells was demonstrated. The delayed cytotoxicity, low hemolytic activity, and better cellular uptake of the silica capped MSNs make them promising for the development of safe (i.e. with fewer side effects) yet efficient theranostic agents. These nanocarriers may release the loaded cytotoxic molecules (CTAB) mostly after being accumulated in the tumor site and cause so minimal damage to the normal tissues and blood components. In addition, the nanoscale confinement of RB molecules inside the pores of MSNs makes the particles brightly fluorescent. Furthermore, it was demonstrated that due to the singlet oxygen generation capability of the RB dye the silica capped MSNs can be also used for photodynamic therapy of cancer. © 2016 The Royal Society of Chemistry.
Open Access
Effects of temperature, pH and counterions on the stability of peptide amphiphile nanofiber structures
(Royal Society of Chemistry, 2016) Ozkan A.D.; Tekinay, A. B.; Güler, Mustafa O.; Tekin, E. D.
Peptide amphiphiles are a class of self-assembling molecules that are widely used to form bioactive nanostructures for various applications in bionanomedicine. However, peptide molecules can exhibit distinct behaviors under different conditions, suggesting that environmental variables such as temperature, pH, electrolytes and the presence of biological factors may greatly affect the self-assembly process. In this work, we used united-atom molecular dynamics simulations to understand the effects of three counterions (Na+, Ca2+ at pH 7 and Cl- at pH 2) and temperature change on the stability of the lauryl-VVAGERGD peptide amphiphile self-assembly. This molecule contains a bioactive RGD peptide sequence and has been shown to support cellular adhesion and proliferation in vitro. A 19-layered peptide nanostructure, containing 12 peptide amphiphile molecules per layer, was previously shown to exhibit optimal stability and it was used as the model nanofiber system. Peptide backbone stability was studied under increasing temperatures (300-358 K) using the number of hydrogen bonds and root-mean-square deviations of nanofiber size. At higher temperatures, fiber disintegration was observed to be dependent on the type of counter-ion used for nanofiber formation. Interestingly, rapid heating to higher temperatures could sometimes reestablish the integrity of the nanofiber backbone, possibly by allowing the system to bypass an energy barrier and assuming a more thermodynamically stable configuration. As counterion identity was observed to exhibit remarkable effects on the thermal stability of peptide nanofibers, we suggest that these behaviors should be considered while developing new materials for potential applications.
Open Access
Efficient removal of polycyclic aromatic hydrocarbons and heavy metals from water by electrospun nanofibrous polycyclodextrin membranes
(American Chemical Society, 2019) Çelebioğlu, Aslı; Topuz, Fuat; Yıldız, Zehra İrem; Uyar, Tamer
Here, a highly efficient membrane based on electrospun polycyclodextrin (poly-CD) nanofibers was prepared and exploited for the scavenging of various polycyclic aromatic hydrocarbons (PAHs) and heavy metals from water. The poly-CD nanofibers were produced by the electrospinning of CD molecules in the presence of a cross-linker (i.e., 1,2,3,4-butanetetracarboxylic acid), followed by heat treatment to obtain an insoluble poly-CD nanofibrous membrane. The membrane was used for the removal of several PAH compounds (i.e., acenaphthene, fluorene, fluoranthene, phenanthrene, and pyrene) and heavy metals (i.e., Pb2+, Ni2+, Mn2+, Cd2+, Zn2+, and Cu2+) from water over time. Experiments were made on the batch sorption of PAHs and heavy metals from contaminated water to explore the binding affinity of PAHs and heavy metals to the poly-CD membrane. The equilibrium sorption capacity (qe) of the poly-CD nanofibrous membrane was found to be 0.43 ± 0.045 mg/g for PAHs and 4.54 ± 0.063 mg/g for heavy metals, and the sorption kinetics fitted well with the pseudo-second-order model for both types of pollutants. The membrane could be recycled after treatment with acetonitrile or a 2% nitric acid solution and reused up to four times with similar performance. Further, dead-end filtration experiments showed that the PAH removal efficiencies were as high as 92.6 ± 1.6 and 89.9 ± 4.8% in 40 s for the solutions of 400 and 600 μg/L PAHs, respectively. On the other hand, the removal efficiencies for heavy metals during the filtration were 94.3 ± 5.3 and 72.4 ± 23.4% for 10 and 50 mg/L solutions, respectively, suggesting rapid and efficient filtration of heavy metals and PAHs by the nanofibrous poly-CD membrane.
Open Access
Electrospinning of polymer-free nanofibers from cyclodextrin inclusion complexes
(American Chemical Society, 2011) Çelebioğlu, Aslı; Uyar, Tamer
The electrospinning of polymer-free nanofibers from highly concentrated (160%, w/v) aqueous solutions of hydroxypropyl-β-cyclodextrin (HPβCD) and its inclusion complexes with triclosan (HPβCD/triclosan-IC) was achieved successfully. The dynamic light scattering (DLS) and rheology measurements indicated that the presence of considerable HPβCD aggregates and the high solution viscosity were the key factors in obtaining electrospun HPβCD and HPβCD/ triclosan-IC nanofibers without the use of any polymeric carrier. The HPβCD and HPβCD/triclosan-IC solutions containing 20% (w/w) urea yielded no fibers but only beads and splashes because of the depression of the self-aggregation of the HPβCD. The inclusion complexation of triclosan with HPβCD was studied by isothermal titration calorimetry (ITC) and turbidity measurements. The characteristics of the HPβCD and HPβCD/triclosan-IC nanofibers were investigated by Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), X-ray diffraction (XRD), and differential scanning calorimetry (DSC). It was found that the electrospinning of HPβCD/triclosan-IC solution having a 1:1 molar ratio was optimal for obtaining nanofibers without any uncomplexed guest molecules.
Open Access
Electrostatics of Polymer Translocation Events in Electrolyte Solutions
(American Institute of Physics Inc., 2016) Buyukdagli, S.; Ala-Nissila, T.
We develop an analytical theory that accounts for the image and surface charge interactions between a charged dielectric membrane and a DNA molecule translocating through the membrane. Translocation events through neutral carbon-based membranes are driven by a competition between the repulsive DNA-image-charge interactions and the attractive coupling between the DNA segments on the trans and the cis sides of the membrane. The latter effect is induced by the reduction of the coupling by the dielectric membrane. In strong salt solutions where the repulsive image-charge effects dominate the attractive trans-cis coupling, the DNA molecule encounters a translocation barrier of ∼10 kBT. In dilute electrolytes, the trans-cis coupling takes over image-charge forces and the membrane becomes a metastable attraction point that can trap translocating polymers over long time intervals. This mechanism can be used in translocation experiments in order to control DNA motion by tuning the salt concentration of the solution.
Open Access
Elucidating the barriers on direct water splitting: key role of oxygen vacancy density and coordination over PbTiO3 and TiO2
(American Chemical Society, 2021-01-28) Ersen, M.; Ellialtıoğlu, Ş.; Gülseren, Oğuz; Uner, D.
In this work, using the state-of-the-art first-principles calculations based on density functional theory, we found that the concentration and coordination of surface oxygen vacancies with respect to each other were critical for the direct water-splitting reaction on the (001) surfaces of PbTiO3 and TiO2. For the water-splitting reaction to happen on TiO2-terminated surfaces, it is necessary to have two neighboring O vacancies acting as active sites that host two adsorbing water molecules. However, eventual dissociation of O–H bonds is possible only in the presence of an additional nearest-neighbor O vacancy. Unfortunately, this necessary third vacancy inhibits the formation of molecular hydrogen by trapping the dissociated H atoms on TiO2-terminated surfaces. Formation of up to three O vacancies is energetically less costly on both terminations of PbTiO3(001) surfaces compared with those on TiO2; the presence of Pb leads to weaker O bonds over these surfaces. Molecular hydrogen formation is more favorable on the PbO-terminated surface of PbTiO3, requiring only two neighboring oxygen vacancies. However, the hydrogen molecule is retained near the surface by weak van der Waals forces. Our study indicates two barriers leading to low productivity of direct water-splitting processes. First and foremost, there is an entropic barrier imposed by the requirement of at least two nearest-neighbor O vacancies, sterically hindering the process. Furthermore, there are also enthalpic barriers of formation on TiO2-terminated surfaces or removal of H2 molecules from the PbO-terminated surface. The requirement dictating three nearest-neighbor oxygen vacancies for hydrogen evolution is also consistent with the chemical intuition: The nearest neighbor of the formed hydrogen should be reduced enough to inhibit spontaneous oxidation under ambient conditions.
Open Access
Enhanced interactions of amino acids and nucleic acid bases with bare black phosphorene monolayer mediated by coadsorbed species
(American Chemical Society, 2019) Kadıoğlu, Y.; Görkan, T.; Üzengi-Aktürk, O.; Aktürk, E.; Çıracı, Salim
In this paper, we characterize amino acids and nucleic acid bases (nucleobases), such as glutamine, histidine, tyrosine, adenine, guanine, cytosine, and thymine, and examine their interaction with bare, as well as with gold cluster and Ti adatom covered, black phosphorene (α-P) monolayers using density functional theory. The binding of these amino acids and nucleobases to the bare α-P monolayer is realized generally through weak van der Waals interaction and comprises only a small amount of charge exchange. Accordingly, the electronic energy structures of adsorbates and underlying substrate are not affected significantly. However, the electronic structure of bare α-P is significantly affected upon adsorption of a gold cluster and a single Ti adatom; depending on the size of the adsorbate and the symmetry of their coverage, the energy band gap can be tuned and permanent magnetic moments can be attained. Additionally, the adsorption of amino acids or nucleobases to these adsorbates on an α-P monolayer results in enhanced binding and hence makes their sustainable fixation on α-P monolayer possible. In particular, a semiconducting Au decorated α-P monolayer undergoes a metal–insulator transition upon the adsorption of tyrosine. This and similar effects favor the α-P monolayer in biosensor applications. In contrast to the situation with adsorbates, the binding of amino acid is not enhanced when it adsorb to patterned vacancy or divacancy sites of the α-P monolayer. Our study shows that the absorbance of the bare α-P monolayer can be enhanced by coating with amino acid and nucleobases. The absorbance spectrum can be further modified by the adsorption of these molecules to gold atoms on the α-P monolayer.
Open Access
The formation and characterization of cyclodextrin functionalized polystyrene nanofibers produced by electrospinning
(2009) Uyar, Tamer; Havelund, R.; Hacaloglu J.; Zhou X.; Besenbacher F.; Kingshott P.
Polystyrene (PS) nanofibers containing the inclusion complex forming beta-cyclodextrin (β-CD) were successfully produced by electrospinning aimed at developing functional fibrous nanowebs. By optimization of the electrospinning parameters, which included varying the relative concentration of PS and β-CD in the solutions, bead-free fibers were produced. Homogeneous solutions of β-CD and PS in dimethylformamide (DMF) were used with concentrations of PS varying from 10% to 25% (w/v, with respect to DMF), and β-CD concentrations of 1% to 50% (w/w, with respect to PS). The presence of β-CD facilitated the production of bead-free PS fibers even from lower polymer concentrations as a result of the higher conductivity of the PS/CD solutions. The morphology and the production of bead-free PS/CD fibers were highly dependent on the β-CD contents. Transmission electron microscope (TEM) and atomic force microscope (AFM) images showed that incorporation of β-CD yielded PS fibers with rougher surfaces. Thermogravimetric analysis (TGA) and direct insertion probe pyrolysis mass spectroscopy (DP-MS) results confirmed the presence of β-CD in the PS fibers. X-ray diffraction (XRD) spectra of the fibers indicated that the β-CD molecules are distributed within the PS matrix without any phase separated crystalline aggregates up to 40% (w/w) β-CD loading. Furthermore, chemical analyses by Fourier transform infrared (FTIR) spectroscopy studies confirm that β-CD molecules are located within the PS fiber matrix. Finally, preliminary investigations using x-ray photoelectron spectroscopy (XPS) and time-of-flight static secondary ion mass spectrometry (ToF-static-SIMS) show the presence of the cyclodextrin molecules in the outer molecular layers of the fiber surfaces. The XPS and ToF-SIMS findings indicate that cyclodextrin functionalized PS webs would have the potential to be used as molecular filters and/or nanofilters for the purposes of filtration/purification/separation owing to surface associated β-CD molecules which have inclusion complexation capability. © 2009 IOP Publishing Ltd.
Open Access
Förster-type nonradiative energy transfer for assemblies of arrayed nanostructures: confinement dimension vs stacking dimension
(American Chemical Society, 2014-02-11) Hernandez-Martinez, P. L.; Govorov, A. O.; Demir, Hilmi Volkan
Forster-type nonradiative energy transfer (NRET) provides us with the ability to transfer excitation energy between proximal nanostructures with high efficiency under certain conditions. Nevertheless, the well-known Forster theory was developed for the case of a single donor (e.g., a molecule, a dye) together with single acceptor. There is no complete understanding for the cases when the donors and the acceptors are assembled in nanostructure arrays, though there are special cases previously studied. Thus, a comprehensive theory that models Forster-type NRET for assembled nanostructure arrays is required. Here, we report a theoretical framework of generalized theory for the Forster-type NRET with mixed dimensionality in arrays. These include combinations of arrayed nanostructures made of nanoparticles (NPs) and nanowires (NWs) assemblies in one-dimension (1D), two-dimension (2D), and three-dimension (3D) completing the framework for the transfer rates in all possible combinations of different confinement geometries and assembly architectures, we obtain a unified picture of NRET in assembled nanostructures arrays. We find that the generic NRET distance dependence is modified by arraying the nanostructures. For an acceptor NP the rate distance dependence changes from gamma alpha d(-6) to gamma alpha d(-5) when they are arranged in a ID stack, and to gamma alpha d(-4) when in a 2D array, and to gamma alpha d(-3) when in a 3D array. Likewise, an acceptor NW changes its distance dependence from gamma alpha d(-5) to gamma alpha d(-4) when they are arranged in a 1D array and to gamma alpha d(-3) when in a 2D array. These finding shows that the numbers of dimensions across which nanostructures are stacked is equally critical as the confinement dimension of the nanostructure in determining the NRET kinetics.
Open Access
Functional electrospun polystyrene nanofibers incorporating α-, β-, and γ-cyclodextrins: Comparison of molecular filter performance
(2010) Uyar, Tamer; Havelund, R.; Hacaloglu, J.; Besenbacher, F.; Kingshott, P.
Electrospinning has been used to successfully create polystyrene (PS) nanofibers containing either of three different types of cyclodextrin (CD); α-CD, β-CD, and γ-CD. These three CDs are chosen because they have different sized cavities that potentially allow for selective inclusion complex (IC) formation with molecules of different size or differences in affinity of IC formation with one type of molecule. The CD containing electrospun PS nanofibers (PS/CD) were initially characterized by scanning electron microscopy (SEM) to determine the uniformity of the fibers and their fiber diameter distributions. X-ray photoelectron spectroscopy (XPS) was used to quantitatively determine the concentration of each CD on the different fiber surfaces. Static time-of-flight secondary ion mass spectrometry (static-ToF-SIMS) showed the presence of each type of CD on the PS nanofibers by the detection of both the CD sodium adduct molecular ions (M + Na+) and lower molecular weight oxygen containing fragment ions. The comparative efficiency of the PS/CD nanofibers/nanoweb for removing phenolphthalein, a model organic compound, from solution was determined by UV-vis spectrometry, and the kinetics of phenolphthalein capture was shown to follow the trend PS/α-CD > PS/β-CD > PS/γ-CD. Direct pyrolysis mass spectrometry (DP-MS) was also performed to ascertain the relative binding strengths of the phenolphthalein for the CD cavities, and the results showed the trend in the interaction strength was β-CD > γ-CD > α-CD. Our results demonstrate that nanofibers produced by electrospinning that incorporate cyclodextrins with different sized cavities can indeed filter organic molecules and can potentially be used for filtration, purification, and/or separation processes. © 2010 American Chemical Society.
Open Access
Generalized theory of förster-type nonradiative energy transfer in nanostructures with mixed dimensionality
(American Chemical Society, 2013-04-16) Hernandez-Martinez, P. L.; Govorov, A. O.; Demir, Hilmi Volkan
Forster-type nonradiative energy transfer (NRET) is widely used, especially utilizing nanostructures in different combinations and configurations. However, the existing well-accepted Forster theory is only for the case of a single particle serving as a donor together with another particle serving as an acceptor. There are also other special cases previously studied; however, there is no complete picture and unified understanding. Therefore, there is a strong need for a complete theory that models Forster-type NRET for the cases of mixed dimensionality including all combinations and configurations. We report a generalized theory for the Forster-type, NRET, which includes the derivation of the effective dielectric function due to the donor in different confinement geometries and the derivation of transfer rates distance dependencies due to the acceptor in different confinement geometries, resulting in a complete picture and understanding of the mixed dimensionality.
Open Access
Generation of soliton molecules with independently evolving phase in a mode-locked fiber laser
(Optical Society of America, 2010) Ortaç, Bülend; Zaviyalov, A.; Nielsen, C.K.; Egorov, O.; Iliew, R.; Limpert, J.; Lederer, F.; Tünnermann, A.
We report the experimental generation of two-soliton molecules in an ytterbium-doped fiber laser. These molecules exhibit an independently evolving phase and are characterized by a regular spectral modulation pattern with a modulation depth of 80%. © 2010 Optical Society of America.
Open Access
Heat transfer through dipolar coupling: Sympathetic cooling without contact
(American Physical Society, 2016) Renklioglu, B.; Tanatar, Bilal; Oktel, M. Ö.
We consider two parallel layers of dipolar ultracold Fermi gases at different temperatures and calculate the heat transfer between them. The effective interactions describing screening and correlation effects between the dipoles in a single layer are modeled within the Euler-Lagrange Fermi-hypernetted-chain approximation. The random-phase approximation is used for the interactions across the layers. We investigate the amount of transferred power between the layers as a function of the temperature difference. Energy transfer arises due to the long-range dipole-dipole interactions. A simple thermal model is established to investigate the feasibility of using the contactless sympathetic cooling of the ultracold polar atoms and molecules. Our calculations indicate that dipolar heat transfer is effective for typical polar molecule experiments and may be utilized as a cooling process.
Open Access
Influence of gold-silica nanoparticles on the performance of small-molecule bulk heterojunction solar cells
(Elsevier BV * North-Holland, 2015) Xu, X.; Kyaw, A. K. K.; Peng, B.; Xiong, Q.; Demir, Hilmi Volkan; Wang Y.; Wong, T. K. S.; Sun, X. W.
Light trapping by gold (Au)-silica nanospheres and nanorods embedded in the active layer of small-molecule (SM) organic solar cell has been systematically compared. Nanorod significantly outperforms nanosphere because of more light scattering and higher quality factor for localized surface plasmon resonance (LSPR) triggered by nanorods. The optimum concentration of nanorod was characterized by charge carrier transport and morphology of the active layers. At optimum nanorod concentration, almost no change in the morphology of the active layer reveals that LSPR and scattering effects rather than the morphology are mainly responsible for the enhanced power conversion efficiency. In addition, the preliminary lifetime studies of the SM solar cells with and without Au-silica nanorods were conducted by measuring the current density-voltage characteristics over 20 days. The results show that plasmonic device with nanorods has no adverse impact on the device stability