Interaction-induced corrections to conductance and thermopower in quantum wires
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The electrochemical reactions of solid oxide fuel cells occur in the region where gas-phase species, electrode, and electrolyte coincide. When the electrode is an ionic insulator and the electrolyte is an electronic insulator, this triple phase boundary is assumed to have atomic dimensions. For this study, we use photoemission electron microscopy to show that the reduced surface of the electrolyte yttria-stabilized zirconia (YSZ) has a sharp electronic metal-insulator boundary near Pt negative electrodes. The electronic conductivity of the reduced YSZ allows for oxygen reduction, allowing the reduced YSZ to behave as an extended triple phase boundary. This extended triple phase boundary can be many microns in size, depending on oxygen pressure, temperature, applied voltage, and time.
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The electrical properties of composite films based on conductive polymer PEDOT: PSS, graphene oxide (GO), and titanium dioxide nanoparticles (TiO{sub 2}) (PEDOT: PSS– TiO{sub 2} and GO–TiO{sub 2}) used as contact layers of organic and perovskite photovoltaic structures have been studied. As a result of the study of morphology by atomic force microscopy, it was found that the PEDOT: PSS–TiO{sub 2} and GO–TiO{sub 2} films have a globular structure with a grain size of ~200–300 nm. The current–voltage characteristics of the PEDOT: PSS–TiO{sub 2} and GO–TiO{sub 2} films are measured in the temperature range of 80–300 K, the dependences of the resistivity versus temperature, ρ(T), which have an activation character, are obtained. It is established that as the temperature decreases, the ρ(T) dependences show a transition from large values of the activation energy (570 meV and 329 meV) to lower values (25 meV and 2.2 meV) for the PEDOT: PSS–TiO{sub 2} and GO–TiO{sub 2} films, respectively. The mechanisms of transport of charge carriers in the materials studied are discussed.
The "data collection" basically involves setting up the thermal wave frequency, laser scan distance, and other parameters related to the experimental setup. The modification of this code is minor and the details of this code can be found in the earlier patent ("thermal conductivity microscope"). The "data analysis" instead, replaces the simplified analytical model by a more complete analytical model, and used a "thermoquadruple" method to solve the analytical model. The efficiency is orders of magnitude improved and the accuracy is also better. Meanwhile, the previous model can only handle a two-layer sample structure. The new, complete model can handle materials with multiple layers (any given number), which is necessary to handle post ion irradiated materials.
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The lithium-air (Li-air) technology developed by EDF uses an air electrode which works with an aqueous electrolyte, which prevent the use of unprotected lithium metal electrode. A Li+ ionic conductor glass ceramic is used to separate the aqueous electrolyte compartment from the negative lithium electrode. However, this glass-ceramic is not stable in contact with lithium, it is thus necessary to add a protective buffer layer. In another hand, this protection should ideally resist to lithium dendritic growth. It is in this context that this research project which has as goal the development of a protective buffer layer based on block copolymer electrolytes (BCE) between the lithium metal and the lithium ionic conductor ceramic, for lithium-air battery. In a first part, the BCE is studied in lithium-lithium symmetric cells, in order to determine their electrochemical properties such as ionic conductivity, steady state transference number, and finally their resistance to dendritic growth during cycling. Several characterization techniques were employed and especially hard X-ray micro-tomography to analyze the lithium morphology before and after cycling. For single-ion BCE, we expect to suppress dendritic growth, however, we report here for the first time, the visualization of a homogeneous growth of lithium but the formation of dense lithium objects. In another part, the composite BCE-ceramic is studied by electrochemical impedance spectroscopy (EIS). The cycling of lithium-composite-lithium symmetric cells and the analysis of the EIS measurement after each cycle permit to determine if the dendrites have cross the protective layer and are in contact with the ceramic. Besides, the quantification of the polarization loss at the interface polymer-ceramic is evaluated by polarization experiments. This contribution is found to be small.
Doping limits, band gaps, work functions and energy band alignments of undoped and donor-doped transparent conducting oxides ZnO, In{sub 2}O{sub 3}, and SnO{sub 2} as accessed by X-ray and ultraviolet photoelectron spectroscopy (XPS/UPS) are summarized and compared. The presented collection provides an extensive data set of technologically relevant electronic properties of photovoltaic transparent electrode materials and illustrates how these relate to the underlying defect chemistry, the dependence of surface dipoles on crystallographic orientation and/or surface termination, and Fermi level pinning.
Cylindrical calorimeter designed to measure temperature dependent thermal conductivity for high performance insulation
Thermal analysis of electrical cylindrical calorimeter used for multilayer insulation thermal conductivity tests - Vol. 1
The core sample is heated from the outside at a known rate and the rise in temperature at the surface of the core tube is measured. Because the temperature at the surface, increasing with time, is a function of the thermal properties of both the core tube and the sample, the thermal properties of the sample can be estimated by comparing the measured temperature with the theory, provided that the thermal properties of the core tube are known. Thus it is not necessary to extract the sample from the core tube to make the measurements. Neither is it necessary to insert a heater, or temperature sensor, into the sample within the core tube, as would be required if another method were applied. The sample remains intact after the measurements. The temperature change in the sample can be kept to a minimum as long as the thermal conductivity determination is possible with a reasonable precision. If the radiative method of heat transfer is chosen, the core tube will only be in mechanical contact with the sample holder and a sensor attached to the core tube to measure the surface temperature, thereby greatly reducing the possibility of disturbing the sample.
A physically transparent approximate theory of phonon decay rates is presented starting from a pair potential model of the interatomic forces in an insulator or semiconductor. The theory applies in the classical regime and relates the 3-phonon decay rate to the third derivative of the pair potential. Phonon dispersion relations do not need to be calculated, as sum rules relate all the needed quantities directly to the pair potential. The Brillouin zone averaged phonon lifetime turns out to involve a dimensionless measure of the anharmonicity multiplied by an effective density of states for 3-phonon decay. Results are given for rare gas and alkali halide crystals. For rare gases, the results are in good agreement with more elaborate perturbation calculations. Comparison to experimental data on phonon linewidths and thermal conductivity are made.
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