559 research outputs found
Back-action Induced Non-equilibrium Effect in Electron Charge Counting Statistics
We report our study of the real-time charge counting statistics measured by a
quantum point contact (QPC) coupled to a single quantum dot (QD) under
different back-action strength. By tuning the QD-QPC coupling or QPC bias, we
controlled the QPC back-action which drives the QD electrons out of thermal
equilibrium. The random telegraph signal (RTS) statistics showed strong and
tunable non-thermal-equilibrium saturation effect, which can be quantitatively
characterized as a back-action induced tunneling out rate. We found that the
QD-QPC coupling and QPC bias voltage played different roles on the back-action
strength and cut-off energy.Comment: 4 pages, 4 figures, 1 tabl
(2R)-2-Cinnamoylamino-N-[5-(4-methoxyphenyl)-1,3,4-thiadiazol-2-yl]propanamide
The asymmetric unit of the title compound, C21H20N4O3S, contains two independent molecules. The dihedral angles between the two benzene rings are 47.6 (1) and 30.2 (1)°, the corresponding values between the p-methoxybenzene and thiadiazol rings are 12.3 (1) and 24.7 (1)°, respectively, for the two molecules. The conformations of the N—H and C=O bonds are anti with respect to each other. The enone groups show a trans configuration. The crystal structure is stabilized by N—H⋯O and N—H⋯N interactions. The absolute structure could not be determined from the X-ray data but the absolute configuration has been assigned by reference to an unchanging chiral centre in the synthetic procedure
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