Browsing by Subject "Lyotropic Liquid Crystal"

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    Effect of hygroscopicity of the metal salts on the formation and air stability of lyotropic liquid crystalline mesophases in hydrated salt-surfactant systems
    (Elsevier, 2014-11-01) Albayrak, C.; Barım, G.; Dag, Ö.
    It is known that alkali, transition metal and lanthanide salts can form lyotropic liquid crystalline (LLC) mesophases with non-ionic surfactants (such as CiH2i+1(OCH2CH2)jOH, denoted as CiEj). Here we combine several salt systems and show that the percent deliquescence relative humidity (%DRH) value of a salt is the determining parameter in the formation and stability of the mesophases and that the other parameters are secondary and less significant. Accordingly, salts can be divided into 3 categories: Type I salts (such as LiCl, LiBr, LiI, LiNO3, LiClO4, CaCl2, Ca(NO3)2, MgCl2, and some transition metal nitrates) have low %DRH and form stable salt–surfactant LLC mesophases in the presence of a small amount of water, type II salts (such as some sodium and potassium salts) that are moderately hygroscopic form disordered stable mesophases, and type III salts that have high %DRH values, do not form stable LLC mesophases and leach out salt crystals. To illustrate this effect, a large group of salts from alkali and alkaline earth metals were investigated using XRD, POM, FTIR, and Raman techniques. Among the different salts investigated in this study, the LiX (where X is Cl, Br, I, NO3 , and ClO4 ) and CaX2 (X is Cl, and NO3 ) salts were more prone to establish LLC mesophases because of their lower %DRH values. The phase behavior with respect to concentration, stability, and thermal behavior of Li(I) systems were investigated further. It is seen that the phase transitions among different anions in the Li(I) systems follow the Hofmeister series.
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    Investigation of lithium salt-nonionic surfactant mesophases and their applications in solar cells as gel electrolyte
    (2013) Barım, Gözde
    Some salts and some nonionic surfactants self-assemble together into lyotropic liquid crystalline (LLC) mesophases. The salt can be either in aqueous solution phase or in its molten phase in the self-assembly process. Concentrated aqueous solutions of lithium salts (LiCl, LiBr, or LiI) and pluronics (triblock copolymers, such as P65, P85, P103, or P123) or 10-lauryl ether (C12H25(CH2CH2O)10OH, denoted as C12EO10) type nonionic surfactant mesophases were investigated in this thesis work. The LLC mesophases are well ordered between 5.0 and 25.0 salt/pluronics and 2.0 and 10.0 salt/C12EO10 mole ratios, and remain stable for months under the ambient conditions. The water molecules remain as the hydrates under open atmosphere in the LLC mesophases of lithium salts-nonionic surfactants. The lithium salt-pluronic LLC mesophases are birefringent and have a hexagonal mesophase in a broad range of salt concentrations. The unit cell of the mesophases increases and a transition from the hexagonal to a cubic mesophases occurs upon increasing the salt content of the media. Moreover the LLC mesophases are ordered and stable up to 25.0 salt to pluronic mole ratio. At higher salt content, one can observe either a disordered phase or co-existence of salt crystals and mesophase. There is a big demand on the gel electrolytes for dye sensitized solar cells (DSSC) in order to overcome solvent problems caused by liquid electrolytes. The LLC mesophases of LiI, LiCl and LiBr salts with 10-lauryl ether (C12EO10) has been considered as gel-electrolyte for the DSSC. We demonstrate that the LiI/I2 couple can be incorporated into above LLC mesophases of various lithium salt-nonionic surfactant systems. Those LLC phases, with LiI/I2 couple have been characterized by means of diffraction, microscopy, spectroscopy and conductivity measurements. The LLC mesophases diffract at small angles and do not show any phase segregation upon incorporating the LiI/I2 redox couple. The LLC mesophases of these systems are 2D hexagonal, and they remain stable under ambient conditions for months. In the LLC media, the iodide ion and iodine molecule react to produce triodide ion in the media. The iodide/triodide (I- /I3 - ) redox couples containing gel electrolytes were formed and their solar performance was investigated by using a solar simulator and a cell consisting of a dye sensitized anode (FTO-dye modified TiO2), gel-electrolyte, and a cathode (FTO-Pt nanoparticles). The LLC mesophases of various lithium saltnonionic surfactant systems with the I- /I3 - redox couple were characterized using POM (Polarized Optical Microscope), XRD (X-ray Diffraction), FT-IR (Fourier Transform Infrared Spectroscopy) and Raman techniques. These new LLC mesophases can be used as gel electrolytes in solar cells after incorporation of redox couple into the media and display responses as good as commonly used liquid electrolytes.