1,116 research outputs found
Time-dependent Aharonov-Bohm effect on the noncommutative space
We study the time-dependent Aharonov-Bohm effect on the noncommutative space.
Because there is no net Aharonov-Bohm phase shift in the time-dependent case on
the commutative space, therefore, a tiny deviation from zero indicates new
physics. Based on the Seiberg-Witten map we obtain the gauge invariant and
Lorentz covariant Aharonov-Bohm phase shift in general case on noncommutative
space. We find there are two kinds of contribution: momentum-dependent and
momentum-independent corrections. For the momentum-dependent correction, there
is a cancellation between the magnetic and electric phase shifts, just like the
case on the commutative space. However, there is a non-trivial contribution in
the momentum-independent correction. This is true for both the time-independent
and time-dependent Aharonov-Bohm effects on the noncommutative space. However,
for the time-dependent Aharonov-Bohm effect, there is no overwhelming
background which exists in the time-independent Aharonov-Bohm effect on both
commutative and noncommutative space. Therefore, the time-dependent
Aharonov-Bohm can be sensitive to the spatial noncommutativity. \draftnote{The
net correction is proportional to the product of the magnetic fluxes through
the fundamental area represented by the noncommutative parameter , and
through the surface enclosed by the trajectory of charged particle.} More
interestingly, there is an anti-collinear relation between the logarithms of
the magnetic field and the averaged flux (N is the number of
fringes shifted). This nontrivial relation can also provide a way to test the
spatial noncommutativity. For , our estimation on the
experimental sensitivity shows that it can reach the scale. This
sensitivity can be enhanced by using stronger magnetic field strength, larger
magnetic flux, as well as higher experimental precision on the phase shift.Comment: 12 pages, 1 figure; v2, accepted version by PL
The one-dimensional polymer poly[[aquaÂ(2,2′-bipyridine)cadmium(II)]-μ-trans-stilbene-4,4′-dicarboxylÂato]
In the title polymer, [Cd(C16H10O4)(C10H8N2)(H2O)]n, the CdII ion is in a strongly distorted octaÂhedral geometry, being coordinated by two N atoms from a 2,2′-bipyridine ligand, three carboxylate O atoms from two symmetry-related trans-stilbene-4,4′-dicarboxylÂate dianions and one water molÂecule. The stilbene ligand lies on an inversion centre at the midpoint of the central C=C bond. This feature generates the polymeric structure: adjacent CdII ions are bridged by trans-stilbene-4,4′-dicarboxylÂate dianions, giving rise to a one-dimensional structure. The coordinated water molÂecule is involved in interchain O—H⋯O hydrogen bonds
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