Bounds on three- and higher-distance sets

A finite set X in a metric space M is called an s-distance set if the set of distances between any two distinct points of X has size s. The main problem for s-distance sets is to determine the maximum cardinality of s-distance sets for fixed s and M. In this paper, we improve the known upper bound for s-distance sets in n-sphere for s=3,4. In particular, we determine the maximum cardinalities of three-distance sets for n=7 and 21. We also give the maximum cardinalities of s-distance sets in the Hamming space and the Johnson space for several s and dimensions.Comment: 12 page

Quantum Quench and Scaling of Entanglement Entropy

Global quantum quench with a finite quench rate which crosses critical points is known to lead to universal scaling of correlation functions as functions of the quench rate. In this work, we explore scaling properties of the entanglement entropy of a subsystem in a harmonic chain during a mass quench which asymptotes to finite constant values at early and late times and for which the dynamics is exactly solvable. When the initial state is the ground state, we find that for large enough subsystem sizes the entanglement entropy becomes independent of size. This is consistent with Kibble-Zurek scaling for slow quenches, and with recently discussed "fast quench scaling" for quenches fast compared to physical scales, but slow compared to UV cutoff scales.Comment: 6 pages, 5 figures; Major revision which affects the main result

Direct observation of a hydrophobic bond in loop-closure of a capped (-OCH2CH2-)n oligomer in water

The small r variation of the probability density P(r) for end-to-end separations of a -CH2CH3 capped (-OCH2CH2-)n oligomer in water is computed to be closely similar to the CH4 ... CH4 potential of mean force under the same circumstances. Since the aqueous solution CH4 ... CH4 potential of mean force is the natural physical definition of a primitive hydrophobic bond, the present result identifies an experimentally accessible circumstance for direct observation of a hydrophobic bond which has not been observed previously because of the low solubility of CH4 in water. The physical picture is that the soluble chain molecule carries the capping groups into aqueous solution, and permits them to find one another with reasonable frequency. Comparison with the corresponding results without the solvent shows that hydration of the solute oxygen atoms swells the chain molecule globule. This supports the view that the chain molecule globule might have a secondary effect on the hydrophobic interaction which is of first interest here. The volume of the chain molecule globule is important for comparing the probabilities with and without solvent because it characterizes the local concentration of capping groups. Study of other capping groups to enable X-ray and neutron diffraction measurements of P(r) is discussed.Comment: 4 pages, 3 figure

Control of quantum interference in molecular junctions: Understanding the origin of Fano and anti- resonances

We investigate within a coarse-grained model the conditions leading to the appearance of Fano resonances or anti-resonances in the conductance spectrum of a generic molecular junction with a side group (T-junction). By introducing a simple graphical representation (parabolic diagram), we can easily visualize the relation between the different electronic parameters determining the regimes where Fano resonances or anti-resonances in the low-energy conductance spectrum can be expected. The results obtained within the coarse-grained model are validated using density-functional based quantum transport calculations in realistic T-shaped molecular junctions.Comment: 5 pages, 5 figure

Crossover behavior and multi-step relaxation in a schematic model of the cut-off glass transition

We study a schematic mode-coupling model in which the ideal glass transition is cut off by a decay of the quadratic coupling constant in the memory function. (Such a decay, on a time scale tau_I, has been suggested as the likely consequence of activated processes.) If this decay is complete, so that only a linear coupling remains at late times, then the alpha relaxation shows a temporal crossover from a relaxation typical of the unmodified schematic model to a final strongly slower-than-exponential relaxation. This crossover, which differs somewhat in form from previous schematic models of the cut-off glass transition, resembles light-scattering experiments on colloidal systems, and can exhibit a `slower-than-alpha' relaxation feature hinted at there. We also consider what happens when a similar but incomplete decay occurs, so that a significant level of quadratic coupling remains for t>>tau_I. In this case the correlator acquires a third, weaker relaxation mode at intermediate times. This empirically resembles the beta process seen in many molecular glass formers. It disappears when the initial as well as the final quadratic coupling lies on the liquid side of the glass transition, but remains present even when the final coupling is only just inside the liquid (so that the alpha relaxation time is finite, but too long to measure). Our results are suggestive of how, in a cut-off glass, the underlying `ideal' glass transition predicted by mode-coupling theory can remain detectable through qualitative features in dynamics.Comment: 14 pages revtex inc 10 figs; submitted to pr

Derivation of Amplitude Equations by Renormalization Group Method

A proper formulation in the perturbative renormalization group method is presented to deduce amplitude equations. The formulation makes it possible not only avoiding a serious difficulty in the previous reduction to amplitude equations by eliminating all of the secular terms but also consistent derivation of higher-order correction to amplitude equations.Comment: 6 page, revte