Browsing by Subject "Anodes"

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Open Access
Characterization of thermally poled germanosilicate thin films
(Optical Society of American (OSA), 2004) Ozean, A.; Digonnet, M.J.F.; Kino G.S.; Ay F.; Aydınlı, Atilla
We report measurements of the nonlinearity profile of thermally poled low-loss germanosilicate films deposited on fused-silica substrates by PECVD, of interest as potential electro-optic devices. The profiles of films grown and poled under various conditions all exhibit a sharp peak ∼0.5 μm beneath the anode surface, followed by a weaker pedestal of approximately constant amplitude down to a depth of 13-16 μm, without the sign reversal typical of poled undoped fused silica. These features suggest that during poling, the films significantly slow down the injection of positive ions into the structure. After local optimization, we demonstrate a record peak nonlinear coefficient of ∼1.6 pm/V, approximately twice as strong as the highest reliable value reported in thermally poled fused silica glass, a significant improvement that was qualitatively expected from the presence of Ge. ©2004 Optical Society of America.
Open Access
Lithium salt-nonionic surfactant lyotropic liquid crystalline gel-electrolytes with redox couple for dye sensitized solar cells
(Royal Society of Chemistry, 2016) Yılmaz, E.; Olutaş, E. B.; Barım, G.; Bandara, J.; Dag, Ö.
Lithium salt (LiCl, LiBr, LiI, or LiNO3) and a non-ionic surfactant (such as 10-lauryl ether, C12E10) form lyotropic liquid crystalline (LLC) mesophases in the presence of a small amount of water. The mesophases can be prepared as gels by mixing all the ingredients in one pot or in the solution phase that they can be prepared by coating over any substrate where the LLC phase is formed by evaporating excess solvent. The second method is easier and produces the same mesophase as the first method. A typical composition of the LLC phases consists of 2-3 water per salt species depending on the counter anion. The LiI-C12E10 mesophases can also be prepared by adding I2 to the media to introduce an I-/I3 - redox couple that may be used as a gel-electrolyte in a dye-sensitized solar cell. Even though the mesophases contain a large amount of water in the media, this does not affect the cell performance. The water molecules in the mesophase are in the hydration sphere of the ions and do not act like bulk water, which is harmful to the anode of the dye-sensitized solar cells (DSSC). There are two major drawbacks of the salt-surfactant LLC mesophases in the DSSCs; one is the diffusion of the gels into the pores of the anode electrode and the other is the low ionic conductivity. The first issue was partially overcome by introducing the gel content as a solution and the gelation was carried in/over the pores of the dye modified titania films. To increase the ionic conductivity of the gels, other salts (such as LiCl, LiBr, and LiNO3) with better ionic conductivity were added to the media, however, those gels behave less effectively than pure LiI/I2 systems. Overall, the DSSCs constructed using the LLC electrolyte display high short circuit current (Isc of around 10 mA), high open circuit voltage (Voc of 0.81 V) and good fill factor (0.69) and good efficiency (3.3%). There is still room for improvement in addressing the above issues in order to enhance the cell efficiency by developing new methods of introducing the gel-electrolytes into the mesopores of the anode electrode.
Open Access
Mo2C as a high capacity anode material: a first-principles study
(Royal Society of Chemistry, 2016) Çakir, D.; Sevik, C.; Gülseren, O.; Peeters, F. M.
The adsorption and diffusion of Li, Na, K and Ca atoms on a Mo2C monolayer are systematically investigated by using first principles methods. We found that the considered metal atoms are strongly bound to the Mo2C monolayer. However, the adsorption energies of these alkali and earth alkali elements decrease as the coverage increases due to the enhanced repulsion between the metal ions. We predict a significant charge transfer from the ad-atoms to the Mo2C monolayer, which indicates clearly the cationic state of the metal atoms. The metallic character of both pristine and doped Mo2C ensures a good electronic conduction that is essential for an optimal anode material. Low migration energy barriers are predicted as small as 43 meV for Li, 19 meV for Na and 15 meV for K, which result in the very fast diffusion of these atoms on Mo2C. For Mo2C, we found a storage capacity larger than 400 mA h g-1 by the inclusion of multilayer adsorption. Mo2C expands slightly upon deposition of Li and Na even at high concentrations, which ensures the good cyclic stability of the atomic layer. The calculated average voltage of 0.68 V for Li and 0.30 V for Na ions makes Mo2C attractive for low charging voltage applications.
Open Access
Synthesis of mesoporous lithium titanate thin films and monoliths as an anode material for high-rate lithium-ion batteries
(Wiley-VCH Verlag, 2016) Balcı, F. M.; Kudu, Ö. U.; Yılmaz, E.; Dag, Ö.
Mesoporous Li4Ti5O12 (LTO) thin film is an important anode material for lithium-ion batteries (LIBs). Mesoporous films could be prepared by self-assembly processes. A molten-salt-assisted self-assembly (MASA) process is used to prepare mesoporous thin films of LTOs. Clear solutions of CTAB, P123, LiNO3, HNO3, and Ti(OC4H9)4 in ethanol form gel-like meso-ordered films upon either spin or spray coating. In the assembly process, the CTAB/P123 molar ratio of 14 is required to accommodate enough salt species in the mesophase, in which the LiI/P123 ratio can be varied between molar ratios of 28 and 72. Calcination of the meso-ordered films produces transparent mesoporous spinel LTO films that are abbreviated as Cxx-yyy-zzz or CAxx-yyy-zzz (C=calcined, CA=calcined–annealed, xx=LiI/P123 molar ratio, and yyy=calcination and zzz=annealing temperatures in Celsius) herein. All samples were characterized by using XRD, TEM, N2-sorption, and Raman techniques and it was found that, at all compositions, the LTO spinel phase formed with or without an anatase phase as an impurity. Electrochemical characterization of the films shows excellent performance at different current rates. The CA40-350-450 sample performs best among all samples tested, yielding an average discharge capacity of (176±1) mA h g−1 at C/2 and (139±4) mA h g−1 at 50 C and keeping 92 % of its initial discharge capacity upon 50 cycles at C/2.