AVS2008 Session EN+AS+TF+VT+NC-WeA: Energy: Tools and Approaches

Wednesday, October 22, 2008 1:40 PM in Room 203

Wednesday Afternoon

Time Period WeA Sessions | Abstract Timeline | Topic EN Sessions | Time Periods | Topics | AVS2008 Schedule

Start Invited? Item
1:40 PM EN+AS+TF+VT+NC-WeA-1 Continuous, In-Line Processing of CdS/CdTe Devices
W.S. Sampath (Colorado State University); R.A. Enzenroth, K.L. Barth (AVA Solar Inc.); V. Manivannan (Colorado State University); K. Barricklow, P. Noronha (AVA Solar Inc.)
A continuous, in-line process suitable for high throughput manufacturing of CdS/CdTe photovoltaic devices has been demonstrated. Utilizing this process, devices with efficiencies of 13% has been fabricated with a low iron soda lime glass (3”x3”) with ant-reflection coatings. The process has been extended to large area devices (16” x16” substrate size). After CdCl2 treatment, devices showed Voc > 700 mV and Jsc > 20 mA/cm2. This performance is similar to the performance of small area devices which showed good stability. Also we have employed many methods including Spectroscopic Ellipsometry (SE) as a non-destructive tool to characterize CdS/CdTe heterojunction specifically studying the effects of processing on the optical properties of the thin-film layers.
2:20 PM EN+AS+TF+VT+NC-WeA-3 Molecular Dynamics and Experimental Investigations of Reversible Absorption of H2, CH4, and CO2 in Calixarenes
J.L. Daschbach, P.K. Thallapally, B.P. McGrail, L.X. Dang (Pacific Northwest National Laboratory)
Molecular solids based on calix[4]arenes have been shown to exhibit reversible absorption of small gas molecules, and remain stable, at temperatures above 400 K. As such, they are interesting as prototypical molecular systems for storing guests like hydrogen and methane, and potentially selectively trapping carbon dioxide in hydrocarbon based systems. We have conducted high-pressure and temperature gas absorption experiments with low density p-tert-butylcalix[4]arene (TBC4) in which calixarenes are slightly offset to form a skewed capsule with an estimated free volume of 235 Å3. Hydrogen and methane absorption near 300 K were 1.0 and 2.2 wt% respectively. Carbon dioxide is absorbed at a 1:1 loading per TBC4 molecule at 3 atm. In recent work we have shown that the high density form of TBC4 will absorb CO2 at 3 atm, undergoing a phase transformation in the process, and it can be reversibly cycled between these states using moderate combinations of temperature and pressure. Somewhat surprisingly, we have found that TBC4 can be loaded with up to two CO2 per TBC4 molecule. We have used empirical molecular simulation techniques to study the dynamics of CO2 and CH4 in TBC4. The rattling motion of the absorbed small molecules have been characterized using velocity autocorrelation. The coupling to the host lattice is probed by temperature dependent calculations. The effects of increased loading are studied up to the 2:1 loading of CO2, and clearly show differences in the host-guest coupling for molecules outside the cavities relative to the cage entrapped molecules. The free energy of absorption of CH4 and CO2 is studied under range of conditions by thermodynamic integration. These data support the experimental observations that these molecules can be reversibly absorbed at moderate pressures and temperatures.
2:40 PM EN+AS+TF+VT+NC-WeA-4 Sustainable Energy and the Role of Advanced Electron Microscopy
D.J. Stokes, B. Freitag, D.H.W. Hubert (FEI Company, The Netherlands)
Advanced electron microscopy, using the latest aberration-corrected and monochromated (scanning) transmission electron microscopes (S/TEM) is helping to bring new scientific and technological insights that are advancing progress in areas such as health, energy and the environment. Specifically, with global energy resources under increasing pressure, great efforts are being made to develop new nanomaterials that will lead to renewable energy sources and increased efficiency, to sustain energy supplies into the long term future whilst helping to preserve and protect the Earth’s environment. To get there, we are being taken to atomic realms such that, to tailor new nanomaterials for specific functions, it is essential to precisely understand, accurately control and truly visualize structure-property relations at an unprecedented level. The atomic structure of nanomaterials and the energy needed for their function can be optimized by the fundamental understanding of catalytic behavior of nanoparticles and by a better understanding of the physical properties on the atomic level of systems such as solar cells, fuel cells and light sources (LEDs). This requires advanced tools that allow us to see down to the individual atoms and sense their chemical environment. It means having the ability to perform experiments in situ, to follow specific chemical reactions and physical processes, and there is a need to be able to do this in multi-dimensions, both spatial and temporal. We discuss and demonstrate the role of advanced electron microscopy in answering some of the most challenging and fundamental scientific questions in the field of catalysis, ranging from electron tomographic 3D reconstruction of the crystal facets of catalyst nanoparticles and aberration-corrected imaging correlated with density functional theory for elucidating precise atomic positions, to in situ studies of catalytic reactions for visualization of otherwise unseen intermediate nanostructures. These examples relate the nanostructures investigated to the property manifested by that particular structure, enabling us to gain new information about catalytic function.
3:00 PM EN+AS+TF+VT+NC-WeA-5 Investigation of Low Temperature-Annealed TiO2 Electrodes Prepared by Sol-Gel Technique for the Fabrication of Dye-Sensitized Solar Cells
M.F. Hossain, S. Biswas, M. Shahjahan, A. Majumder, T. Takahashi (University of Toyama, Japan)
Dye sensitized solar cells (DSCs) are considered as a low cost alternative to conventional p-n junction solar cell devices. The high light-to-energy conversion efficiencies achieved with dye sensitized solar cells (DSCs) may be attributed to the nanoporous TiO2 electrode. Among the various techniques for the preparation of TiO2 photo-electrode, the relatively simple sol gel method is the most widely used because of its ability to obtain films with tailored properties on large, curved substrates, and also it is a low temperature process. Crystallinity is one of the key factors behind the photovoltaic performances of TiO2; therefore achievement of better crystallinity at relatively low temperature is an important issue. In our present study, the titanium dioxide porous films were deposited on SnO2:F coated glass by sol–gel technique; where, an alcoholic solution of tetra-buthylorthotitane was hydrolysed in a water/alcohol/acetic acid mixture. These films were transparent and crack free. For this investigation; annealing temperature and number of coating layers were varied. All the films were annealed at different annealing temperatures, ranging from 350 to 500°C. Sufficiently good crystalline samples were obtained by annealing at 350°C. The X-ray diffraction patterns of all TiO2 films confirmed the anatase structure. The surface morphology of the films has been observed by atomic force microscope and field emission scanning electron microscope. The morphology of TiO2 thin films strongly depends on annealing temperatures and number of coatings. Incident photon-to-current conversion efficiency is calculated for all the solar cells with different TiO2 thin films to evaluate the economic viability of this technique. It has been observed that the photoelectric conversion efficiency of DSCs increases with the optimization of annealing temperature as well as with the increase of the numbers of layers.
Time Period WeA Sessions | Abstract Timeline | Topic EN Sessions | Time Periods | Topics | AVS2008 Schedule