113 research outputs found
Deceleration of a supersonic beam of SrF molecules to 120 m/s
We report on the deceleration of a beam of SrF molecules from 290 to 120~m/s.
Following supersonic expansion, the molecules in the (, )
low-field seeking states are trapped by the moving potential wells of a
traveling-wave Stark decelerator. With a deceleration strength of 9.6 km/s
we have demonstrated the removal of 85 % of the initial kinetic energy in a 4
meter long modular decelerator. The absolute amount of kinetic energy removed
is a factor 1.5 higher compared to previous Stark deceleration experiments. The
demonstrated decelerator provides a novel tool for the creation of highly
collimated and slow beams of heavy diatomic molecules, which serve as a good
starting point for high-precision tests of fundamental physics
Deceleration and trapping of heavy diatomic molecules using a ring-decelerator
We present an analysis of the deceleration and trapping of heavy diatomic
molecules in low-field seeking states by a moving electric potential. This
moving potential is created by a 'ring-decelerator', which consists of a series
of ring-shaped electrodes to which oscillating high voltages are applied.
Particle trajectory simulations have been used to analyze the deceleration and
trapping efficiency for a group of molecules that is of special interest for
precision measurements of fundamental discrete symmetries. For the typical case
of the SrF molecule in the (N,M) = (2, 0) state, the ring-decelerator is shown
to outperform traditional and alternate-gradient Stark decelerators by at least
an order of magnitude. If further cooled by a stage of laser cooling, the
decelerated molecules allow for a sensitivity gain in a parity violation
measurement, compared to a cryogenic molecular beam experiment, of almost two
orders of magnitude
Microcantilever equipped with nanowire template electrodes for multiprobe measurement on fragile nanostructures
Ebstein’s anomaly may be caused by mutations in the sarcomere protein gene MYH7
Ebstein's anomaly is a rare congenital heart malformation characterised by adherence of the septal and posterior leaflets of the tricuspid valve to the underlying myocardium. Associated abnormalities of left ventricular morphology and function including left ventricular noncompaction (LVNC) have been observed. An association between Ebstein's anomaly with LVNC and mutations in the sarcomeric protein gene MYH7, encoding β-myosin heavy chain, has been shown by recent studies. This might represent a specific subtype of Ebstein's anomaly with a Mendelian inheritance pattern. In this review we discuss the association of MYH7 mutations with Ebstein's anomaly and LVNC and its implications for the clinical care for patients and their family members.Congenital Heart Diseas
Investigation of the potential distribution in porous nanocrystalline TiO2 electrodes by electrolyte electroreflection
Ebstein's anomaly may be caused by mutations in the sarcomere protein gene MYH7
Ebstein's anomaly is a rare congenital heart malformation characterised by adherence of the septal and posterior leaflets of the tricuspid valve to the underlying myocardium. Associated abnormalities of left ventricular morphology and function including left ventricular noncompaction (LVNC) have been observed. An association between Ebstein's anomaly with LVNC and mutations in the sarcomeric protein gene MYH7, encoding β -myosin heavy chain, has been shown by recent studies. This might represent a specific subtype of Ebstein's anomaly with a Mendelian inheritance pattern. In this review we discuss the association of MYH7 mutations with Ebstein's anomaly and LVNC and its implications for the clinical care for patients and their family members
ChemInform Abstract: The Reduction of Hydrogen Peroxide at Silicon in Weak Alkaline Solutions
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