Abstract:
Measurement of capacitance and derivative capacitance (dC/dV) on a semiconductor structure under light-pumped condition is documented to measure carrier lifetime with a spatial resolution limited by physical law, depending on material properties (10 nm 100µm). An atomic force microscope or probe-station is used to position a nanometer scale tip over the surface of a semiconductor material to be probed, which is also illuminated with a controlled light source for carrier generation. The capacitance-voltage (C-V) curves or dC/dV versus voltage curves between the tip and the semiconductor are measured under these illuminating conditions with a sensitive capacitance sensor. The unique method for transient spectroscopy incorporates a unique control system and procedure in which capacitance or dC/dV signal are measured as a function of time synchronized to changing the illuminating condition. The capacitance transient can be measured at any dc voltage, but particularly useful information such as carrier density is obtained if the probe is biased at the semiconductor flatband voltage. A simple, one-dimensional model is used to determine, from the measurement of C-V or dC/dV curves, capacitance transients, and frequency-dependent capacitance variance, the carrier recombination rate, and carrier generation and recombination lifetimes in the semiconductor with a microscopic spatial resolution: The limitation of spatial resolution of this measurement is by physical law not by instrumentation. The invention encompasses several methods of acquiring the carrier lifetime on time scales of microseconds and longer with a highly localized probe which are unique with respect to previous practices. The method can easily be incorporated into various commercial instruments such as atomic force microscope, surface profiler, and probe station.
Abstract:
A composition formed from Group II fluorides in which the composition has little or no intrinsic birefringence at a selected wavelength. The composition is a mixed solid solution of CaF 2 with a second crystal of SrF 2 or BaF 2 . The resulting composition is in the form of Ca 1-x Sr x F 2 or Ca 1-x Ba x F 2 , or a combination of SrF 2 and BaF 2 , in the form of Ca 1-x-y Sr x Ba y F 2 . The specific form of the composition that effectively nulls out the intrinsic birefringence at a selected wavelength within the UV range is determined in one preferred method from the magnitudes of the intrinsic birefringences of the components, CaF 2 , SrF 2 , and BaF 2 .
Abstract:
The invention is related to a non-biotinylated bacteriophage that comprises a nucleic acid sequence encoding a biotinylation domain; a complex that comprises a biotinylated bacteriophage and a biotin-specif ic ligand- conjugated biocon jugate; and a method of detecting a bacterial cell in a sample comprising contacting the sample with a non-biotinylated bacteriophage that comprises a nucleic acid sequence encoding a biotinylation domain, wherein the bacteriophage is specific to the bacterial cell.
Abstract:
The various embodiments described herein include methods, devices, and systems for operating superconducting circuits. In one aspect, an electric circuit includes: (1) a superconductor component having a first terminal at a first end and a second terminal at a second end; (2) a gate component thermally-coupled to the superconductor component at a first location between the first terminal and the second terminal, where the gate component is thermally-coupled via a first section of the gate component; and where the gate component has a smallest width at the first section so as to focus resistive heating toward the superconductor component.
Abstract:
Described herein are methods for making genetically modified cells by introducing combinations of genetic variants (designed or random) or constructs (genes or otherwise arbitrary DNA) into a population of cells, and for tracking each variant combination by sequentially building an array of barcodes at a common locus (chromosomal or plasmid), termed the barcode locus. Also described are the cells made by such methods.