Novel Ambiguities in the Seiberg-Witten Map and the Emergent Gravity

A homogeneous part of the Seiberg-Witten gauge equivalence relation for gauge fields can lead to solutions that involve matter fields in such a way that the gauge equivalence and the dimensional and index structures are preserved. In particular, we consider scalar fields coupled to U(1) gauge fields. The matter fields appear non-linearly in the map. As an application, we analyze the implication of this ambiguity to emergent gravity at the first order in noncommutative parameter and show that the new ambiguity restores the possibility of conformal coupling of real scalar density field that is coupled non-minimally to the emergent gravity induced by gauge fields -- a possibility that is strictly not allowed if we consider only the already known ambiguity in the Seiberg-Witten map.Comment: JHEP style, 10 pages, minor corrections, a version published in JHE

U(1) gauge invariant noncommutative Schr\"odinger theory and gravity

We consider the complex, massive Klein-Gordon field living in the noncommutative space, and coupled to noncommutative electromagnetic fields. After employing the Seiberg-Witten map to first order, we analyze the noncommutative Klein-Gordon theory as $c$, the velocity of light, goes to infinity. We show that the theory exhibits a regular "magnetic" limit only for certain forms of magnetic fields. The resulting theory is nothing but the Schr\"odinger theory in a gravitational background generated by the gauge fields.Comment: 15 pages, LaTe

Continuum Theory of Polymer Crystallization

We present a kinetic model of crystal growth of polymers of finite molecular weight. Experiments help to classify polymer crystallization broadly into two kinetic regimes. One is observed in melts or in high molar mass polymer solutions and is dominated by nucleation control with $G \sim \exp(1/T \Delta T)$, where $G$ is the growth rate and $\Delta T$ is the super-cooling. The other is observed in low molar mass solutions (as well as for small molecules) and is diffusion controlled with $G \sim \Delta T$, for small $\Delta T$. Our model unifies these two regimes in a single formalism. The model accounts for the accumulation of polymer chains near the growth front and invokes an entropic barrier theory to recover both limits of nucleation and diffusion control. The basic theory applies to both melts and solutions, and we numerically calculate the growth details of a single crystal in a dilute solution. The effects of molecular weight and concentration are also determined considering conventional polymer dynamics. Our theory shows that entropic considerations, in addition to the traditional energetic arguments, can capture general trends of a vast range of phenomenology. Unifying ideas on crystallization from small molecules and from flexible polymer chains emerge from our theory.Comment: 37 double-spaced pages including 8 figures, submitted to the Journal of Chemical Physic

Dynamics of Diblock Copolymers in Dilute Solutions

We consider the dynamics of freely translating and rotating diblock (A-B), Gaussian copolymers, in dilute solutions. Using the multiple scattering technique, we have computed the diffusion and the friction coefficients D_AB and Zeta_AB, and the change Eta_AB in the viscosity of the solution as functions of x = N_A/N and t = l_B/l_A, where N_A, N are the number of segments of the A block and of the whole copolymer, respectively, and l_A, l_B are the Kuhn lengths of the A and B blocks. Specific regimes that maximize the efficiency of separation of copolymers with distinct "t" values, have been identified.Comment: 20 pages Revtex, 7 eps figures, needs epsf.tex and amssymb.sty, submitted to Macromolecule

Determining the underlying Fermi surface of strongly correlated superconductors

The notion of a Fermi surface (FS) is one of the most ingenious concepts developed by solid state physicists during the past century. It plays a central role in our understanding of interacting electron systems. Extraordinary efforts have been undertaken, both by experiment and by theory, to reveal the FS of the high temperature superconductors (HTSC), the most prominent strongly correlated superconductors. Here, we discuss some of the prevalent methods used to determine the FS and show that they lead generally to erroneous results close to half filling and at low temperatures, due to the large superconducting gap (pseudogap) below (above) the superconducting transition temperature. Our findings provide a perspective on the interplay between strong correlations and superconductivity and highlight the importance of strong coupling theories for the characterization as well as the determination of the underlying FS in ARPES experiments

Bosonic resonating valence bond wave function for doped Mott insulators

We propose a new class of ground states for doped Mott insulators in the electron second-quantization representation. They are obtained from a bosonic resonating valence bond (RVB) theory of the t-J model. At half filling, the ground state describes spin correlations of the S=1/2 Heisenberg model very accurately. Its spin degrees of freedom are characterized by RVB pairing of spins, the size of which decreases continuously as holes are doped into the system. Charge degrees of freedom emerge upon doping and are described by twisted holes in the RVB background. We show that the twisted holes exhibit an off diagonal long range order (ODLRO) in the pseudogap ground state, which has a finite pairing amplitude, but is short of phase coherence. Unpaired spins in such a pseudogap ground state behave as free vortices, preventing superconducting phase coherence. The existence of nodal quasiparticles is also ensured by such a hidden ODLRO in the ground state, which is non-Fermi-liquid-like in the absence of superconducting phase coherence. Two distinct types of spin excitations can also be constructed. The superconducting instability of the pseudogap ground state is discussed and a d-wave superconducting ground state is obtained. This class of pseudogap and superconducting ground states unifies antiferromagnetism, pseudogap, superconductivity, and Mott physics into a new state of matter.Comment: 28 pages, 5 figures, final version to appear in Phys. Rev.

Berry's phase in noncommutative spaces

We introduce the perturbative aspects of noncommutative quantum mechanics. Then we study the Berry's phase in the framework of noncommutative quantum mechanics. The results show deviations from the usual quantum mechanics which depend on the parameter of space/space noncommtativity.Comment: 7 pages, no figur

Anomalous Dynamics of Forced Translocation

We consider the passage of long polymers of length N through a hole in a membrane. If the process is slow, it is in principle possible to focus on the dynamics of the number of monomers s on one side of the membrane, assuming that the two segments are in equilibrium. The dynamics of s(t) in such a limit would be diffusive, with a mean translocation time scaling as N^2 in the absence of a force, and proportional to N when a force is applied. We demonstrate that the assumption of equilibrium must break down for sufficiently long polymers (more easily when forced), and provide lower bounds for the translocation time by comparison to unimpeded motion of the polymer. These lower bounds exceed the time scales calculated on the basis of equilibrium, and point to anomalous (sub-diffusive) character of translocation dynamics. This is explicitly verified by numerical simulations of the unforced translocation of a self-avoiding polymer. Forced translocation times are shown to strongly depend on the method by which the force is applied. In particular, pulling the polymer by the end leads to much longer times than when a chemical potential difference is applied across the membrane. The bounds in these cases grow as N^2 and N^{1+\nu}, respectively, where \nu is the exponent that relates the scaling of the radius of gyration to N. Our simulations demonstrate that the actual translocation times scale in the same manner as the bounds, although influenced by strong finite size effects which persist even for the longest polymers that we considered (N=512).Comment: 13 pages, RevTeX4, 16 eps figure

Theory of Non-Reciprocal Optical Effects in Antiferromagnets: The Case Cr_2O_3

A microscopic model of non-reciprocal optical effects in antiferromagnets is developed by considering the case of Cr_2O_3 where such effects have been observed. These effects are due to a direct coupling between light and the antiferromagnetic order parameter. This coupling is mediated by the spin-orbit interaction and involves an interplay between the breaking of inversion symmetry due to the antiferromagnetic order parameter and the trigonal field contribution to the ligand field at the magnetic ion. We evaluate the matrix elements relevant for the non-reciprocal second harmonic generation and gyrotropic birefringence.Comment: accepted for publication in Phys. Rev.