105 research outputs found
Direct thermal conductance measurements on suspended monocrystalline nanostructures
We describe and demonstrate a new class of devices that enable direct thermal conductance measurements on monocrystalline nanostructures. These are possible through our newly developed techniques for three-dimensional, successive surface nanomachining of GaAs-based heterostructures. Our methods allow the patterning of complex devices comprising electrically insulating, mesoscopic thermal conductors with separate, thermal transducers in situ. Intimate thermal contact between these elements is provided by their epitaxial registry. Low-temperature thermal conductance measurements indicate that phonon boundary scattering in these initial nanometer is scale structures is partially specular. These devices offer promise for ultrasensitive bolometry and calorimetry
Phonon scattering mechanisms in suspended nanostructures from 4 to 40 K
We have developed specially designed semiconductor devices for the measurement of thermal conductance in suspended nanostructures. By means of a novel subtractive comparison, we are able to deduce the phonon thermal conductance of individual nanoscale beams of different geometry and dopant profiles. The separate roles of important phonon scattering mechanisms are analyzed and a quantitative estimation of their respective scattering rates is obtained using the Callaway model. Diffuse surface scattering proves to be particularly important in the temperature range from 4 to 40 K. The rates of other scattering mechanisms, arising from phonon-phonon, phonon-electron, and phonon-point defect interactions, also appear to be significantly higher in nanostructures than in bulk samples
Tunability of the dielectric response of epitaxially strained SrTiO3 from first principles
The effect of in-plane strain on the nonlinear dielectric properties of
SrTiO3 epitaxial thin films is calculated using density-functional theory
within the local-density approximation. Motivated by recent experiments, the
structure, zone-center phonons, and dielectric properties with and without an
external electric field are evaluated for several misfit strains within +-3% of
the calculated cubic lattice parameter. In these calculations, the in-plane
lattice parameters are fixed, and all remaining structural parameters are
permitted to relax. The presence of an external bias is treated approximately
by applying a force to each ion proportional to the electric field. After
obtaining zero-field ground state structures for various strains, the
zone-center phonon frequencies and Born effective charges are computed,
yielding the zero-field dielectric response. The dielectric response at finite
electric field bias is obtained by computing the field dependence of the
structure and polarization using an approximate technique. The results are
compared with recent experiments and a previous phenomenological theory. The
tunability is found to be strongly dependent on the in-plane lattice parameter,
showing markedly different behavior for tensile and compressive strains. Our
results are expected to be of use for isolating the role of strain in the
tunability of real ultrathin epitaxial films.Comment: 11 pages, with postscript figures embedded. Uses REVTEX and epsf
macros. Also available at
http://www.physics.rutgers.edu/~dhv/preprints/ant_srti/index.htm
Analogies of structural instabilities in EuTiO3 and SrTiO3
Specific heat measurements and theoretical calculations reveal an intimate
analogy between EuTiO3 and SrTiO3. For EuTiO3 a hitherto unknown specific heat
anomaly is discovered at TA=282(1)K which is analogous to the well known
specific heat anomaly of SrTiO3 at TA=105K caused by an antiferrodistortive
transition. Since the zone center soft phonon mode observed in both systems can
be modeled with the same parameters we ascribe the new 282(1)K instability of
EuTiO3 to an antiferrodistortive phase transition. The higher transition
temperature of EuTiO3 as compared to SrTiO3 results from spin phonon coupling.Comment: PRB to be published, 12 pages, 3 Figure
Analytical characteristics and comparative evaluation of Aptima HCV quant Dx assay with the Abbott RealTime HCV assay and Roche COBAS AmpliPrep/COBAS TaqMan HCV quantitative test v2.0
Abstract Background The Aptima HCV Quant Dx assay (Aptima assay) is a fully automated quantitative assay on the Panther® system. This assay is intended for confirmation of diagnosis and monitoring of HCV RNA in plasma and serum specimens. The purpose of the testing described in this paper was to evaluate the performance of the Aptima assay. Methods The analytical sensitivity, analytical specificity, precision, and linearity of the Aptima assay were assessed. The performance of the Aptima assay was compared to two commercially available HCV assays; the Abbott RealTime HCV assay (Abbott assay, Abbott Labs Illinois, USA) and the Roche COBAS Ampliprep/COBAS Taqman HCV Quantitative Test v2.0 (Roche Assay, Roche Molecular Systems, Pleasanton CA, USA). The 95% Lower Limit of Detection (LoD) of the assay was determined from dilutions of the 2nd HCV WHO International Standard (NIBSC 96/798 genotype 1) and HCV positive clinical specimens in HCV negative human plasma and serum. Probit analysis was performed to generate the 95% predicted detection limits. The Lower Limit of Quantitation (LLoQ) was established for each genotype by diluting clinical specimens and the 2nd HCV WHO International Standard (NIBSC 96/798 genotype 1) in HCV negative human plasma and serum. Specificity was determined using 200 fresh and 536 frozen HCV RNA negative clinical specimens including 370 plasma specimens and 366 serum specimens. Linearity for genotypes 1 to 6 was established by diluting armored RNA or HCV positive clinical specimens in HCV negative serum or plasma from 8.08 log IU/mL to below 1 log IU/mL. Precision was tested using a 10 member panel made by diluting HCV positive clinical specimens or spiking armored RNA into HCV negative plasma and serum. A method comparison was conducted against the Abbott assay using 1058 clinical specimens and against the Roche assay using 608 clinical specimens from HCV infected patients. In addition, agreement between the Roche assay and the Aptima assay using specimens with low HCV concentrations (</= 25 IU/mL by Roche) was tested using 107 clinical specimens. Results The 95% LoD was 5.1 IU/mL or lower for serum and 4.8 IU/mL or lower for plasma depending on the HCV genotype. The LLoQ for the assay was 10 IU/mL. Specificity was 100% with 95% confidence intervals of 99.6 to 100% for serum and plasma data combined. The assay demonstrated good linearity across the range for all genotypes. The Precision as estimated by the standard deviation (sd) was 0.17 log or lower across the range of the assay for both serum and plasma. HCV viral load results were compared using the Aptima assay and the Abbott assay giving a slope of 1.06, an intercept of 0.08 and an R2 of 0.98. HCV viral load results were compared for the Aptima and Roche assays giving a slope of 1.05, an intercept of −0.12 and an R2 of 0.96. Positive and negative agreement for the Aptima assay vs the Roche assay was 89% for low level specimens. Conclusion The Aptima assay is a highly sensitive and specific assay. The assay gave comparable HCV viral load results when compared to the Abbott and Roche assays. The performance of the Aptima assay makes it an excellent candidate for the detection and monitoring of HCV
Magnetic field dependence of the exciton energy in a quantum disk
The groundstate energy and binding energy of an exciton, confined in a^M
quantum disk, are calculated as a function of an external magnetic field. The
confinement potential is a hard wall of finite height. The diamagnetic shift is
investigated for magnetic fields up to 40. Our results are applied to
self-assembled quantum dots and very good
agreement with experiments is obtained. Furthermore, we investigated the
influence of the dot size on the diamagnetic shift by changing the disk radius.
The exciton excited states are found as a function of the magnetic field. The
relative angular momentum is not a quantum number and changes with the magnetic
field strength.Comment: 10 pages, 17 figure
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