This paper proposes an empirical relation, which represents
noise bias condition dependence for a silicon N-channel MOSFET. No matter whether the MOSFET is operated in linear or saturation region, bias condition dependence is found to be well described by a power function of voltage gain. By introducing a device's intrinsic
noise emf vnc(ƒ), which is independent from bias condition, and empirical parameter β, input-referred
noise voltage vni(ƒ) is clarified to be a function of vnc(ƒ), β, and voltage gain
, i.e.
. This relation implies that
noise voltage depends implicitly on bias condition through voltage gain, because transconductance gm and drain-source differential conductance gDS depend on bias condition. If β − 1 value is negligible, vni(ƒ) = vnc(ƒ) is almost independent from bias condition, whereas, if β − 1 value is not negligible, bias condition dependence for vni(ƒ) appears to be observed. The β deviation from unity, which characterizes bias condition dependence, measures the difference between signal amplification and
noise amplification. 相似文献
Semiclathrate hydrates are water-based host-guest compounds formed from aqueous solutions of ionic guest substances. These materials can greatly moderate formation pressures and temperatures from canonical gas hydrates. This is a significant advantage for industrial applications such as gas separation and storage. \(\hbox {N}_{2}\) gas is a major component contained in various flue gases and is usually mixed with \(\hbox {CO}_{2}\). Semiclathrate hydrates can separate these gases under moderate thermodynamic conditions. Tetra-n-butylammonium bromide (TBAB) is a widely used ionic guest substance. To develop the application technologies and their theoretical models, solubility data of \(\hbox {N}_{2}\) gas in TBAB aqueous solutions are required. In this study, we report \(\hbox {N}_{2}\) gas solubility measured by an absolute gravimetric method for the semiclathrate hydrate formation system of \(\hbox {TBAB} + \hbox {H}_{2}\hbox {O} + \hbox {N}_{2}\). The measurement pressures, temperatures and TBAB mass fractions were 3 MPa, 5 MPa and 7 MPa, 292.15 K, 302.15 K and 307.15 K, and 0 (pure water), 0.10, 0.20, 0.32 and 0.40, respectively. The uncertainties were 0.056 MPa, 0.44 K and 0.00012 in mole fraction. Although the technical difficulty lays on measurements of small \(\hbox {N}_{2}\) gas solubility by the absolute gravimetric method, our data implied the unique gas dissolution property of aqueous TBAB solution depending on the TBAB concentration. The aqueous TBAB solutions with mass fractions of 0.10 and 0.20 had similar \(\hbox {N}_{2}\) gas solubility as that in pure water. With higher mass fractions, 0.32 and 0.40, the \(\hbox {N}_{2}\) gas solubility slightly increased from that in pure water, which implies the salting-in effect of TBAB. 相似文献
The thermoelectric properties of TiN/MgO surface nanostructures have been determined using first-principles calculations based on the nonequilibrium Green’s function (NEGF) method. Through structural modification of the surfaces at the atomistic level, we find that the metallic TiN thin-film layer becomes semiconducting with a small bandgap, which enhances the Seebeck coefficient, while the electrical conductivity remains high at room temperature. Hence, a much larger thermoelectric figure of merit is obtained compared with bulk. These findings indicate the possibility of designing thermoelectric devices with surface nanostructures. 相似文献
Oxygen self-diffusion coefficients were determined for two Al2O3 single crystals by the isotope-exchange technique, using chemically polished and Ar -ion-milled samples. Results represented by D=562 exp[–665(kJ/mol)/RT] cm2/s are lower than those for diamond-paste-finished samples and near Reed and Wuensch's results. The oxygen diffusion coefficient determined using crushed particles and the microscopically measured ratio of surface area to volume agreed with these values 相似文献
A method of preparation of an urethane emulsion which provides thermosetting film is described here. By reacting a urethane prepolymer containing terminal isocyanate groups with diethylenetriamine in the presence of ketones, poly(urethane-urea-amine) was prepared. In other organic solvents, however, gelation occurred immediately and preparation of polyurethane-urea-amine was not successful. The function of ketone was ascribed to the tentative formation of a Schiff base between the primary amino group of diethylenetriamine and ketone in situ, and the reaction of primary amine with isocyanate was partly masked to prevent gelation. Then the free amino group is generated when the polymer is treated with epichlorohydrin and the reaction occurs between them. After the solution was neutralized with an aqueous acid, the solvent was removed in vacuo to give a stable self-emulsifiable thermosetting urethane emulsion. Typical mechanical properties of film from this urethane emulsion are also given here. 相似文献
For analyses of dynamic ultrastructures of erythrocyte intramembranous particles (IMPs) in situ, a quick-freezing method was used to stabilize the flow behavior of erythrocytes embedded in vitreous ice. Fresh human blood was jetted at various pressures through artificial tubes, in which the flowing erythrocytes were elongated from biconcave discoid shapes to elliptical ones, and quickly frozen in liquid isopentane-propane cryogen (-193 degrees C). They were freeze-fractured using a scalpel in liquid nitrogen, and routinely prepared for replica membranes. Many IMPs were observed on the protoplasmic freeze-fracture face (P-face) of the erythrocyte membranes. Some control erythrocytes under nonflowing or stationary conditions showed IMPs with their random distribution. However, other jetted erythrocytes under flowing conditions showed variously sized IMPs with much closer distribution. They were also arranged into parallel rows in some parts, and aggregated together. This quick-freezing method enabled for the first time the visualization of time-dependent topology and the molecular alteration of IMPs in dynamically flowing erythrocytes. 相似文献
Different multilayer Mg AZ31 and SS304L steel sheet combinations were prepared with different volume fractions of Mg. Isolated stress–strain curves of the Mg layers showed significant improvements in the strength and elongation of multilayer samples. Results indicated that in the most extreme situation with the lowest Mg volume fraction (Vf = 0.39), the ultimate strength was increased by 25 pct to 370 MPa and the elongation was improved by 70 pct to 0.34. Investigation of the fracture surface showed that failure occurs by the coalescence of cracks close to the interface region. The improved strength of the multilayer samples was due to the combined effect of surface crack prevention by the steel layer and the higher work-hardening rate caused by the possible increased activity of non-basal systems. It is suggested that the stronger work-hardening behavior and the enhanced activity of non-basal systems in the multilayer samples were due to the formation of new stress components in the transverse direction. The larger the volume fraction of steel in the multilayer, the longer the distance remaining unstrained before the UTS.