4,947 research outputs found
Quantitation of buried contamination by use of solvents
Experiments directed at determining the potential of reclaimed silicone polymers for reuse are described
On Internal Fracture of Solids
Initiation and propagation of internal fracture in solid
Quantitation of buried contamination by use of solvents
Spore recovery form cured silicone potting compounds using amine solvents to degrade the cured polymers was investigated. A complete list of solvents and a description of the effect of each on two different silicone polymers is provided
Efficient orthogonal control of tunnel couplings in a quantum dot array
Electrostatically-defined semiconductor quantum dot arrays offer a promising
platform for quantum computation and quantum simulation. However, crosstalk of
gate voltages to dot potentials and inter-dot tunnel couplings complicates the
tuning of the device parameters. To date, crosstalk to the dot potentials is
routinely and efficiently compensated using so-called virtual gates, which are
specific linear combinations of physical gate voltages. However, due to
exponential dependence of tunnel couplings on gate voltages, crosstalk to the
tunnel barriers is currently compensated through a slow iterative process. In
this work, we show that the crosstalk on tunnel barriers can be efficiently
characterized and compensated for, using the fact that the same exponential
dependence applies to all gates. We demonstrate efficient calibration of
crosstalk in a quadruple quantum dot array and define a set of virtual barrier
gates, with which we show orthogonal control of all inter-dot tunnel couplings.
Our method marks a key step forward in the scalability of the tuning process of
large-scale quantum dot arrays.Comment: 8 pages, 7 figure
Transition Mechanisms of Two Interacting DX Centers in N-Type AlGaAs using Reverse-Bias Deep Level Transient Spectroscopy and Temperature-Dependent Pulse-Width Reverse-Bias Deep Level Transient Spectroscopy Methods
The reverse-bias pulsed deep level transient spectroscopy (RDLTS) and a new temperature-dependent pulse-width RDLTS (TDP RDLTS) technique are reported to study the electric-field effect on carrier emission rates and the direct interaction between double DX centers recently detected in the Se:Al0.6Ga0.4As N confinement layer of the AlGaAs/GaAs single-quantum-well laser diodes. Traditional RDLTS measurements, with constant pulse width tp, prove that the two DX centers, Et1 and Et2, have strong direct emission interaction. Furthermore, the new TDP-RDLTS technique enables one to evaluate this direct transition time constant. Possible mechanisms for this interstate transition at different temperature ranges are provided and the new broadening effect due to this interstate transition is also reported here for the first time. Field-enhanced emission rates are calculated
Picoliter-volume inkjet printing into planar microdevice reservoirs for low-waste, high-capacity drug loading.
Oral delivery of therapeutics is the preferred route for systemic drug administration due to ease of access and improved patient compliance. However, many therapeutics suffer from low oral bioavailability due to low pH and enzymatic conditions, poor cellular permeability, and low residence time. Microfabrication techniques have been used to create planar, asymmetric microdevices for oral drug delivery to address these limitations. The geometry of these microdevices facilitates prolonged drug exposure with unidirectional release of drug toward gastrointestinal epithelium. While these devices have significantly enhanced drug permeability in vitro and in vivo, loading drug into the micron-scale reservoirs of the devices in a low-waste, high-capacity manner remains challenging. Here, we use picoliter-volume inkjet printing to load topotecan and insulin into planar microdevices efficiently. Following a simple surface functionalization step, drug solution can be spotted into the microdevice reservoir. We show that relatively high capacities of both topotecan and insulin can be loaded into microdevices in a rapid, automated process with little to no drug waste
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