Measurements of Carrier Generation-Recombination Parameters in Silicon Solar Cell Material Using MOS Techniques

Modified and new measurement techniques were developed for determining the carrier generation-recombination (G-R) parameters in silicon solar cell material under carrier deficit and low-level carrier excess conditions using MOS-based test structures. The structures mainly consisted of ring-dot MOS Capacitors (MOS-C) and Schottky-Drained Gate-Controlled Diodes (SGCD). Sample G-R parameters were extracted from n-type high quality silicon solar cell material. Additional measurements were also performed on low-quality ntype silicon substrates for comparison purposes. The photoaccelerated MOS-C Capacitance-time (C-t) transient measurement technique, modified from the standard C-t method, allows one to drastically reduce the observation time in deducing the carrier generation lifetime (Tg) by simply illuminating the test structure during the transient. In applying the technique to MOS-C’s (which exhibited generation lifetime on the order of I msec) the observation time was reduced by approximately an order of magnitude. This is important in dealing with solar cell material because of typically long generation lifetimes. The SGCD structure, which consisted of an extended Schottky diode located next to an MOS-C, was developed and utilized for extracting the surface generation velocity (sg). The measurement is based on recording two C-t transients at Vd = 0 and at Vd = V t , respectively. The structure has a distinct advantage over the conventional PN junction GCD in that it is only slightly more complicated to fabricate and interrogate than a simple MOS-C. It was also demonstrated that steady-state deep-depletion C-V characteristics can be obtained using the SGCD structure. An MOS-C photo/forward-sweep measurement technique was primarily developed to extract the recombination lifetime (rp for n-type substrates) under low-level carrier excess conditions. The new technique is based on the change in inversion capacitance in response to a set of illumination and forward-sweep voltages applied to the MOS-C. The technique conveniently allows one to extract the recombination lifetime under room temperature conditions and was successfully applied to MOS-C’s fabricated on high quality silicon solar cell substrates

Diffusion in low-dimensional lipid membranes

The diffusion behavior of biological components in cellular membranes is vital to the function of cells. By collapsing the complexity of planar 2D membranes down to one dimension, fundamental investigations of bimolecular behavior become possible in one dimension. Here we develop lipid nanolithography methods to produce membranes, under fluid, with widths as low as 6 nm but extending to microns in length. We find reduced lipid mobility, as the width is reduced below 50 nm, suggesting different lipid packing in the vicinity of boundaries. The insertion of a membrane protein, M2, into these systems, allowed characterization of protein diffusion using high-speed AFM to demonstrate the first membrane protein 1D random walk. These quasi-1D lipid bilayers are ideal for testing and understanding fundamental concepts about the roles of dimensionality and size on physical properties of membranes from energy transfer to lipid packing

Programmed Bending Reveals Dynamic Mechanochemical Coupling in Supported Lipid Bilayers

In living cells, mechanochemical coupling represents a dynamic means by which membrane components are spatially organized. An extra-ordinary example of such coupling involves curvature-dependent polar localization of chemically-distinct lipid domains at bacterial poles, which also undergo dramatic reequilibration upon subtle changes in their interfacial environment such as during sporulation. Here, we demonstrate that such interfacially-triggered mechanochemical coupling can be recapitulated in vitro by simultaneous, real-time introduction of mechanically-generated periodic curvatures and attendant strain-induced lateral forces in lipid bilayers supported on elastomeric substrates. In particular, we show that real-time wrinkling of the elastomeric substrate prompts a dynamic domain reorganization within the adhering bilayer, producing large, oriented liquid-ordered domains in regions of low curvature. Our results suggest a mechanism in which interfacial forces generated during surface wrinkling and the topographical deformation of the bilayer combine to facilitate dynamic reequilibration prompting the observed domain reorganization. We anticipate this curvature-generating model system will prove to be a simple and versatile tool for a broad range of studies of curvature-dependent dynamic reorganizations in membranes that are constrained by the interfacial elastic and dynamic frameworks such as the cell wall, glycocalyx, and cytoskeleton