Manin-Olshansky triples for Lie superalgebras

Following V. Drinfeld and G. Olshansky, we construct Manin triples (\fg, \fa, \fa^*) such that \fg is different from Drinfeld's doubles of \fa for several series of Lie superalgebras \fa which have no even invariant bilinear form (periplectic, Poisson and contact) and for a remarkable exception. Straightforward superization of suitable Etingof--Kazhdan's results guarantee then the uniqueness of $q$-quantization of our Lie bialgebras. Our examples give solutions to the quantum Yang-Baxter equation in the cases when the classical YB equation has no solutions. To find explicit solutions is a separate (open) problem. It is also an open problem to list (\`a la Belavin-Drinfeld) all solutions of the {\it classical} YB equation for the Poisson superalgebras \fpo(0|2n) and the exceptional Lie superalgebra \fk(1|6) which has a Killing-like supersymmetric bilinear form but no Cartan matrix

Hot Spots on the Fermi Surface of Bi2212: Stripes versus Superstructure

In a recent paper Saini et al. have reported evidence for a pseudogap around (pi,0) at room temperature in the optimally doped superconductor Bi2212. This result is in contradiction with previous ARPES measurements. Furthermore they observed at certain points on the Fermi surface hot spots of high spectral intensity which they relate to the existence of stripes in the CuO planes. They also claim to have identified a new electronic band along Gamma-M1 whose one dimensional character provides further evidence for stripes. We demonstrate in this Comment that all the measured features can be simply understood by correctly considering the superstructure (umklapp) and shadow bands which occur in Bi2212.Comment: 1 page, revtex, 1 encapsulated postscript figure (color

Analytical Gradients for Projection-Based Wavefunction-in-DFT Embedding

Projection-based embedding provides a simple, robust, and accurate approach for describing a small part of a chemical system at the level of a correlated wavefunction method while the remainder of the system is described at the level of density functional theory. Here, we present the derivation, implementation, and numerical demonstration of analytical nuclear gradients for projection-based wavefunction-in-density functional theory (WF-in-DFT) embedding. The gradients are formulated in the Lagrangian framework to enforce orthogonality, localization, and Brillouin constraints on the molecular orbitals. An important aspect of the gradient theory is that WF contributions to the total WF-in-DFT gradient can be simply evaluated using existing WF gradient implementations without modification. Another simplifying aspect is that Kohn-Sham (KS) DFT contributions to the projection-based embedding gradient do not require knowledge of the WF calculation beyond the relaxed WF density. Projection-based WF-in-DFT embedding gradients are thus easily generalized to any combination of WF and KS-DFT methods. We provide numerical demonstration of the method for several applications, including calculation of a minimum energy pathway for a hydride transfer in a cobalt-based molecular catalyst using the nudged-elastic-band method at the CCSD-in-DFT level of theory, which reveals large differences from the transition state geometry predicted using DFT.Comment: 15 pages, 4 figure

Kosterlitz-Thouless transition of quantum XY model in two dimensions

The two-dimensional $S=1/2$ XY model is investigated with an extensive quantum Monte Carlo simulation. The helicity modulus is precisely estimated through a continuous-time loop algorithm for systems up to $128 \times 128$ near and below the critical temperature. The critical temperature is estimated as $T_{\rm KT} = 0.3427(2)J$. The obtained estimates for the helicity modulus are well fitted by a scaling form derived from the Kosterlitz renormalization group equation. The validity of the Kosterlitz-Thouless theory for this model is confirmed.Comment: 8 pages, 2 tables, 6 figure

Extraction of the Electron Self-Energy from Angle Resolved Photoemission Data: Application to Bi2212

The self-energy $\Sigma({\bf k},\omega)$, the fundamental function which describes the effects of many-body interactions on an electron in a solid, is usually difficult to obtain directly from experimental data. In this paper, we show that by making certain reasonable assumptions, the self-energy can be directly determined from angle resolved photoemission data. We demonstrate this method on data for the high temperature superconductor $Bi_2Sr_2CaCu_2O_{8+x}$ (Bi2212) in the normal, superconducting, and pseudogap phases.Comment: expanded version (6 pages), to be published, Phys Rev B (1 Sept 99

The Schwaigerian driver transfer technique and the Thevenin's and the Norton's theorem Final report

Graphical technique for analyzing series-parallel networks by rectangular diagrams in solving power distribution problem

Spectroscopy of 87Sr^{87}\text{Sr} triplet Rydberg states

A combined experimental and theoretical spectroscopic study of high-$n$, ${30 \lesssim n \lesssim 100}$, triplet $\text{S}$ and $\text{D}$ Rydberg states in $^{87}\text{Sr}$ is presented. $^{87}\text{Sr}$ has a large nuclear spin, ${I=9/2}$, and at high-$n$ the hyperfine interaction becomes comparable to, or even larger than, the fine structure and singlet-triplet splittings which poses a considerable challenge both for precision spectroscopy and for theory. For high-$n$ $\text{S}$ states, the hyperfine shifts are evaluated non-perturbatively taking advantage of earlier spectroscopic data for the ${I=0}$ isotope $^{88}\text{Sr}$, which results in good agreement with the present measurements. For the $\text{D}$ states, this procedure is reversed by first extracting from the present $^{87}\text{Sr}$ measurements the energies of the $^{3}\text{D}_{1,2,3}$ states to be expected for isotopes without hyperfine structure ($^{88}\text{Sr}$) which allows the determination of corrected quantum defects in the high-$n$ limit.Comment: 13 pages, 8 figure

Probing Nonlocal Spatial Correlations in Quantum Gases with Ultra-long-range Rydberg Molecules

We present photo-excitation of ultra-long-range Rydberg molecules as a probe of spatial correlations in quantum gases. Rydberg molecules can be created with well-defined internuclear spacing, set by the radius of the outer lobe of the Rydberg electron wavefunction $R_n$. By varying the principal quantum number $n$ of the target Rydberg state, the molecular excitation rate can be used to map the pair-correlation function of the trapped gas $g^{(2)}(R_n)$. We demonstrate this with ultracold Sr gases and probe pair-separation length scales ranging from $R_n = 1400 - 3200$ $a_0$, which are on the order of the thermal de Broglie wavelength for temperatures around 1 $\mu$K. We observe bunching for a single-component Bose gas of $^{84}$Sr and anti-bunching due to Pauli exclusion at short distances for a polarized Fermi gas of $^{87}$Sr, revealing the effects of quantum statistics.Comment: 6 pages, 5 figure

Creation of Rydberg Polarons in a Bose Gas

We report spectroscopic observation of Rydberg polarons in an atomic Bose gas. Polarons are created by excitation of Rydberg atoms as impurities in a strontium Bose-Einstein condensate. They are distinguished from previously studied polarons by macroscopic occupation of bound molecular states that arise from scattering of the weakly bound Rydberg electron from ground-state atoms. The absence of a $p$-wave resonance in the low-energy electron-atom scattering in Sr introduces a universal behavior in the Rydberg spectral lineshape and in scaling of the spectral width (narrowing) with the Rydberg principal quantum number, $n$. Spectral features are described with a functional determinant approach (FDA) that solves an extended Fr\"{o}hlich Hamiltonian for a mobile impurity in a Bose gas. Excited states of polyatomic Rydberg molecules (trimers, tetrameters, and pentamers) are experimentally resolved and accurately reproduced with FDA.Comment: 5 pages, 3 figure