10,937 research outputs found
Integrable dispersionless KdV hierarchy with sources
An integrable dispersionless KdV hierarchy with sources (dKdVHWS) is derived.
Lax pair equations and bi-Hamiltonian formulation for dKdVHWS are formulated.
Hodograph solution for the dispersionless KdV equation with sources (dKdVWS) is
obtained via hodograph transformation. Furthermore, the dispersionless
Gelfand-Dickey hierarchy with sources (dGDHWS) is presented.Comment: 15 pages, to be published in J. Phys. A: Math. Ge
Current rectification by asymmetric molecules: An ab initio study
We study current rectification effect in an asymmetric molecule
HOOC-CH-(CH) sandwiched between two Aluminum electrodes using
an {\sl ab initio} nonequilibrium Green function method. The conductance of the
system decreases exponentially with the increasing number of CH. The
phenomenon of current rectification is observed such that a very small current
appears at negative bias and a sharp negative differential resistance at a
critical positive bias when . The rectification effect arises from the
asymmetric structure of the molecule and the molecule-electrode couplings. A
significant rectification ratio of 38 can be achieved when .Comment: to appear in J. Chem. Phy
Generation of Narrow-Band Polarization-Entangled Photon Pairs for Atomic Quantum Memories
We report an experimental realization of a narrow-band polarization-entangled
photon source with a linewidth of 9.6 MHz through cavity-enhanced spontaneous
parametric down-conversion. This linewidth is comparable to the typical
linewidth of atomic ensemble based quantum memories. Single-mode output is
realized by setting a reasonable cavity length difference between different
polarizations, using of temperature controlled etalons and actively stabilizing
the cavity. The entangled property is characterized with quantum state
tomography, giving a fidelity of 94% between our state and a maximally
entangled state. The coherence length is directly measured to be 32 m through
two-photon interference.Comment: 4 pages, 4 figure
Adsorption of hydrogen molecules on the platinum-doped boron nitride nanotubes
Adsorption of hydrogen molecules on platinum-doped single-walled zigzag (8,0) boron nitride (BN) nanotube is investigated using the density-functional theory. The Pt atom tends to occupy the axial bridge site of the BN tube with the highest binding energy of −0.91 eV. Upon Pt doping, several occupied and unoccupied impurity states are induced, which reduces the band gap of the pristine BN nanotube. Upon hydrogen adsorption on Pt-doped BN nanotube, the first hydrogen molecule can be chemically adsorbed on the Pt-doped BN nanotube without crossing any energy barrier, whereas the second hydrogen molecule has to overcome a small energy barrier of 0.019 eV. At least up to two hydrogen molecules can be chemically adsorbed on a single Pt atom supported by the BN nanotube, with the average adsorption energy of −0.365 eV. Upon hydrogen adsorption on a Pt-dimer-doped BN nanotube, the formation of the Pt dimer not only weakens the interaction between the Pt cluster and the BN nanotube but also reduces the average adsorption energy of hydrogen molecules. These calculation results can be useful in the assessment of metal-doped BN nanotubes as potential hydrogen storage media
Adsorption of hydrogen molecules on the platinum-doped boron nitride nanotubes
Adsorption of hydrogen molecules on platinum-doped single-walled zigzag (8,0) boron nitride (BN) nanotube is investigated using the density-functional theory. The Pt atom tends to occupy the axial bridge site of the BN tube with the highest binding energy of −0.91 eV. Upon Pt doping, several occupied and unoccupied impurity states are induced, which reduces the band gap of the pristine BN nanotube. Upon hydrogen adsorption on Pt-doped BN nanotube, the first hydrogen molecule can be chemically adsorbed on the Pt-doped BN nanotube without crossing any energy barrier, whereas the second hydrogen molecule has to overcome a small energy barrier of 0.019 eV. At least up to two hydrogen molecules can be chemically adsorbed on a single Pt atom supported by the BN nanotube, with the average adsorption energy of −0.365 eV. Upon hydrogen adsorption on a Pt-dimer-doped BN nanotube, the formation of the Pt dimer not only weakens the interaction between the Pt cluster and the BN nanotube but also reduces the average adsorption energy of hydrogen molecules. These calculation results can be useful in the assessment of metal-doped BN nanotubes as potential hydrogen storage media
Effects of relative orientation of the molecules on electron transport in molecular devices
Effects of relative orientation of the molecules on electron transport in
molecular devices are studied by non-equilibrium Green's function method based
on density functional theory. In particular, two molecular devices, with the
planer Au and Ag clusters sandwiched between the Al(100) electrodes
are studied. In each device, two typical configurations with the clusters
parallel and vertical to the electrodes are considered. It is found that the
relative orientation affects the transport properties of these two devices
completely differently. In the Al(100)-Au-Al(100) device, the conductance
and the current of the parallel configuration are much larger than those in the
vertical configuration, while in the Al(100)-Ag-Al(100) device, an
opposite conclusion is obtained
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