High-efficiency Silicon Solar Cells: A Review

Over the past few decades, crystalline silicon solar cells have been extensively studied due to their high efficiency, high reliability, and low cost. In addition, these types of cells lead the industry and account for more than half of the market. For the foreseeable future, Si will still be a critical material for photovoltaic devices in the solar cell industry. In this paper, we discuss key issues, cell concepts, and the status of recent high-efficiency crystalline silicon solar cells.     

Exploiting ILP, TLP, and DLP with the polymorphous trips architecture

The Tera-op reliable intelligently adaptive processing system (TRIPS) architecture seeks to deliver system-level configurability to applications and runtime systems. It does so by employing the concept of polymorphism, which permits the runtime system to configure the hardware execution resources to match the mode of execution and demands of the compiler and application.     

Travelling-wave photodetectors with 172-GHz bandwidth and 76-GHzbandwidth-efficiency product

Results of the first fabrication and measurement of travelling-wave photodetectors are reported. The devices have bandwidths as high as 172 GHz, the highest reported for a p-i-n photodetector, and bandwidth-efficiency products as large as 76 GHz, the largest reported for any photodetector without gain. Comparisons with vertically illuminated and waveguide photodetectors fabricated on the same wafer establish the superior performance of travelling-wave photodetectors. Microwave loss on the travelling-wave photodetector structure is identified as a bandwidth limitation     

Study of Magnetic and Electrical Properties of Poly(o-phenylenediamine)/Manganese Substituted ZnFe2O4 Nanocomposites

Journal of Inorganic and Organometallic Polymers and Materials - Different concentrations of ZnFe2O4 and manganese substituted ZnFe2O4 nanoparticles (10%, 20% and 30%) dispersed...     

Observations on the role of oxide scales in high-temperature erosion-corrosion of alloys

The results are presented of exposure to a controlled high-temperature erosive gas stream of a series of alloys, which were selected to represent the range of microstructures and mechanical properties available in commercial high-temperature alloys. Analysis of the kinetic and morphological data suggested that the high-temperature oxidation behavior of a given alloy plays a very important role in determining its erosion-corrosion behavior under the conditions studied. In terms of relative behavior, alloys which are weak but ductile at temperature, and which form tenacious oxide scales, exhibited the highest resistance to high-temperature erosion-corrosion. Simple models were developed to describe the expected interaction between high-temperature oxidation and erosion.     

Corrosion of Fe-10Al-Cr alloys by coal char

Corrosion of iron-base alloys at 982°C (1800°F) by coal char is observed and the phase morphologies are discussed. No sulfidation was observed at 50 hr exposure. After 100 hr internal aluminum-rich sulfides were observed along with thick outer scales of iron oxide. The species causing the hightemperature-induced corrosion are probably sulfides and sulfates, present in most coal chars. Possible mechanisms for the corrosion are also discussed.Department of Materials Science and Mineral Engineering.     

Structure of polyurethane elastomers. X-ray diffraction and conformational analysis of MDI-propandiol and MDI-ethylene glycol hard segments

X-ray diffraction and conformational analysis have been used to investigate the structure of polyurethane hard segments prepared from diphenylmethane 4,4′-diisocyanate (MDI) with propandiol (PDO) and ethylene glycol (EDO) as chain extenders. The results are compared with those obtained previously for MDI-butandiol (BDO) hard segments. In the latter system, the poly(MDI-BDO) chains are fully extended with an all-trans conformation for the O(CH₂)₄O unit, and a monomer repeat of 18.95 Å. The unit cell is triclinic with a tilted base plane such that adjacent chains are staggered along the fibre axis. In contrast both poly(MDI-PDO) and poly(MDI-EDO) adopt unstaggered structures, i.e. the chains are in register and the unit cell base planes are perpendicular to the chain axis. The monomer repeats of 16.2 Å for poly(MDI-PDO) and 15.0 Å for poly(MDI-EDO) are shorter than the predicted repeats for fully-extended chains, indicating that these polymers have contracted conformations containing some gauche CH₂ groups. Conformational analysis shows that the 16.2 Å repeat for poly(MDI-PDO) can be achieved with the O(CH₂)₃O unit in the trans-gauche⁺-gauche⁺-trans or gauche⁺-trans-trans-gauche⁺ conformations. Similarly the 15.0 Å repeat for poly(MDI-EDO) is predicted for the gauche⁺-trans-gauche^? conformation for the O(CH₂)₂O unit. These conformations are of higher energy than the all-trans fully-extended chains. This may explain the higher crystalline perfection of the poly(MDI-BDO) hard segments, for which crystallization in the all-trans form will probably provide a greater driving force for phase separation.     

Conformational analysis of poly(MDI-butandiol) hard segment in polyurethane elastomers

As part of our study of the structure of the hard segments of polyurethane elastomers, we have used conformational analysis to predict the conformation of the polyurethane chain formed from diphenylmethane 4,4′-diisocyanate (MDI), with butandiol as the chain extender. X-ray diffraction indicates the chain conformation is highly extended in the solid state, with a monomer repeat of 18.95 Å. The chain conformation can be predicted from the interaction between the large contiguous groups. Semiempirical and CNDO/2 molecular orbital calculations have been used to investigate the phenyl-phenyl, phenyl-urethane, and urethane-butandiol interactions. Minimum energy for the diphenyl-methane section occurs for a CCH₂C bridge angle of θ = 110°. However, the more likely conformation in the polymer is probably that at the subsidiary minimum at θ = 118°, in which the phenyl rings are mutually perpendicular, which is comparable to the conformation seen for model compounds. For the phenyl-urethane interactions the energy minimum is at $\text{ч = ±90°}$, with the combination $\text{(ч}{}_1\text{, ч}{}_2\text{) = (?90°, +90°)}$ leading to the necessary extended conformation. Calculations for the butandiol segment favour an all-trans conformation which is coplanar with the urethane groups. The predicted conformation of the polymer chain has a fibre repeat which matches the observed value, and this cannot be attained if the butandiol unit contains any gauche bonds. Model compounds show large variations for the phenyl-urethane conformation from the predicted minimum at $\text{ч = ±90°}$, indicating the importance of intermolecular stacking forces in determining the polymer conformation. However, provided the adjacent butandiol and urethane groups are coplanar, the fibre repeat is relatively insensitive to variations of ч.     

A two‐station embossing process for rapid fabrication of surface microstructures on thermoplastic polymers

An embossing strategy involving a hot station and a cold station for sequentially heating and cooling the embossing tool was investigated to reduce cycle times in hot embossing polymer microstructures. Experimental studies showed that aluminum stamps with a thickness of 1.4 mm can be rapidly heated from room temperature to 200°C in 3 s using contact heating against a hot station at 250°C. Microchannels and microlenses were successfully embossed onto high‐density polyethylene and acrylonitrile–butadiene–styrene substrates using a heating time less than 3 s and a total cycle time around 10 s. The two‐station embossing process for the microlens was also numerically studied. The simulated filling behavior agreed with the experimental observation and the predicted thermal and deformation history of the polymer offered a good explanation on the experimentally observed process characteristics. POLYM. ENG. SCI., 47:530–539, 2007. © 2007 Society of Plastics Engineers.