Organic materials are attractive for photovoltaics primarily because of the prospect of high throughput solution-processible manufacturing using roll-to-roll or spray deposition. In the formation of polymer based photovoltaic devices, the aspect that limits the power conversion efficiency is the bottleneck between short diffusion lengths of the excited states (excitons) in polymers, in the range of 10-20 nm. Optical absorption length, which is in the range of 50-200 nm and much larger than the exciton diffusion length, poses the limit on charge generation and collection. It is important to achieve complete optical absorption in active layers much thinner than optical absorption length to minimize losses due to recombination of charge carriers. Previously, light trapping techniques have been coupled with organic solar cell but without significant success. In this paper, three-dimensional sub micron grating structure is analyzed using finite element method (FEM) simulations for finding the optical absorption in different layers of solar cell to optimize the photonic concentrator effect of the grating structure. The energy dissipation of electromagnetic field in the active layer is studied as a function of active layer thickness, grating pitch and height. The superiority of grating structure in terms of light trapping feature as compared to planar geometry is clearly demonstrated by simulation results.

To investigate the feasibility of a 3D integrated all-solid-state micro-battery, the deposition of several battery materials was investigated. Deposition techniques where used that are in principle able to deposit step conformally in 3D structures: ALD was used to create a conductive Pt current collector, and LPCVD was applied for the deposition of poly-silicon anodes and LiCoO2 cathodes. The layers, initially deposited on planar substrates, showed the expected physical and electrochemical behavior and are in principle suitable for solid state micro-batteries.

This work presents recent results on outdoor characterisation of high efficiency luminescent solar concentrators. Outdoor measurements at 25�C and corrected to 1000 W/m2 have been compared with indoor characterization according to the international standards for conventional photovoltaic devices. Dependence of electrical parameters with temperature is also shown, together with results of various 1-day monitoring campaigns of luminescent concentrators performance under varying irradiance conditions. Results highlight the importance of those devices as potentially cheap, residential concentrating systems.

The US Navy continues to pursue electrochemical power sources with high energy density for low rate, long endurance undersea applications. The direct electro-oxidation and electro-reduction of sodium borohydride and hydrogen peroxide are being investigated to meet these goals. In an effort to minimize polarization losses and increase power density, a novel carbon microfiber array (CMA) electrode is being investigated.

The CMA is composed of 750 micron long, 10 micron diameter graphite fibers that protrude from a current collector like blades of grass. The CMA was developed for the direct reaction of peroxide in the Mg-H2O2 semi fuel cell. [1] There, the high surface area of the microfiber cathode reduces peroxide concentration polarization, resulting in increased power and energy density. For this work the CMA architecture was adapted into a novel membrane electrode assembly and evaluated in the direct BH4- / H2O2 fuel cell. The unique feature of this architecture vs. traditional membrane electrode assemblies (MEAs) is how all three components of the triple boundary interface are optimized: electrical connectivity, ionic connectivity and mass transport. The current iteration of this electrode architecture utilizes a carbon cloth that has been hot pressed into N115 membrane. This component is then placed over the CMFA electrode. The carbon microfibers of the CMFA protrude up into the carbon cloth matrix forming a 3-dimewnsional, interdigitated electrode architecture. The result of this modification is improved electrolyte flow through the CMFA and improved utilization of the surface area afforded by the carbon microfibers that was not observed in the non modified CMFA. Half cell polarization measurements were obtained simultaneously with the fuel cell polarization. Initial results using this modified CMFA electrode architecture show that the polarization losses observed for both the reduction of hydrogen peroxide and for the oxidation of borohydride were 5.2 times lower than for the non-modified CMAs electrode (0.014 ohms vs. 0.074 ohms). Comparing these results to those calculated from the literature [2, 3], where traditional membrane electrode assemblies were used for borohydride oxidation, 5 and 2.6 time improvements were obtained (0.07 ohms and 0.037 ohms were the effective resistive losses seen in the anode half cell polarizations).