Applications of DFT to the theory of twentieth-century harmony

Music theorists have only recently, following groundbreaking work by Quinn, recognized the potential for the DFT on pcsets, initially proposed by Lewin, to serve as the foundation of a theory of harmony for the twentieth century. This paper investigates pcset “arithmetic” – subset structure, transpositional combination, and interval content – through the lens of the DFT. It discusses relationships between interval classes and DFT magnitudes, considers special properties of dyads, pcset products, and generated collections, and suggest methods of using the DFT in analysis, including interpreting DFT magnitudes, using phase spaces to understand subset structure, and interpreting the DFT of Lewin’s interval function. Webern’s op. 5/4 and Bartok’s String Quartet 4, iv, are discussed.Accepted manuscrip

Quantum Cluster Variables via Serre Polynomials

For skew-symmetric acyclic quantum cluster algebras, we express the quantum $F$-polynomials and the quantum cluster monomials in terms of Serre polynomials of quiver Grassmannians of rigid modules. As byproducts, we obtain the existence of counting polynomials for these varieties and the positivity conjecture with respect to acyclic seeds. These results complete previous work by Caldero and Reineke and confirm a recent conjecture by Rupel.Comment: minor corrections, reference added, example 4.3 added, 38 page

Decontextualizing contextual inversion

Contextual inversion, introduced as an analytical tool by David Lewin, is a concept of wide reach and value in music theory and analysis, at the root of neo-Riemannian theory as well as serial theory, and useful for a range of analytical applications. A shortcoming of contextual inversion as it is currently understood, however, is, as implied by the name, that the transformation has to be defined anew for each application. This is potentially a virtue, requiring the analyst to invest the transformational system with meaning in order to construct it in the first place. However, there are certainly instances where new transformational systems are continually redefined for essentially the same purposes. This paper explores some of the most common theoretical bases for contextual inversion groups and considers possible definitions of inversion operators that can apply across set class types, effectively decontextualizing contextual inversions.Accepted manuscrip

Spectroscopy of the a^3\Sigma_u^+ state and the coupling to the X^1\Sigma_g^+ state of K_2

We report on high resolution Fourier-transform spectroscopy of fluorescence to the a^3\Sigma_u^+ state excited by two-photon or two-step excitation from the X^1\Sigma_g^+ state to the 2^3\Pi_g state in the molecule K_2. These spectroscopic data are combined with recent results of Feshbach resonances and two-color photoassociation spectra for deriving the potential curves of X^1\Sigma_g^+ and a^3\Sigma_u^+ up to the asymptote. The precise relative position of the triplet levels with respect of the singlet levels was achieved by including the excitation energies from the X^1\Sigma_g^+ state to the 2^3\Pi_g state and down to the a^3\Sigma_u^+ state in the simultaneous fit of both potentials. The derived precise potential curves allow for reliable modeling of cold collisions of pairs of potassium atoms in their ^2S ground state

Ab initio calculation of the KRb dipole moments

The relativistic configuration interaction valence bond method has been used to calculate permanent and transition electric dipole moments of the KRb heteronuclear molecule as a function of internuclear separation. The permanent dipole moment of the ground state $X^1\Sigma^+$ potential is found to be 0.30(2) $ea_0$ at the equilibrium internuclear separation with excess negative charge on the potassium atom. For the $a^3\Sigma^+$ potential the dipole moment is an order of magnitude smaller (1 $ea_0=8.47835 10^{-30}$ Cm) In addition, we calculate transition dipole moments between the two ground-state and excited-state potentials that dissociate to the K(4s)+Rb(5p) limits. Using this data we propose a way to produce singlet $X^1\Sigma^+$ KRb molecules by a two-photon Raman process starting from an ultracold mixture of doubly spin-polarized ground state K and Rb atoms. This Raman process is only allowed due to relativistic spin-orbit couplings and the absence of gerade/ungerade selection rules in heteronuclear dimers.Comment: 16 pages, 7 figure

Global analysis of data on the spin-orbit coupled A1Σu+A^{1}\Sigma_{u}^{+} and b3Πub^{3}\Pi_{u} states of Cs2

We present experimentally derived potential curves and spin-orbit interaction functions for the strongly perturbed $A^{1}\Sigma_{u}^{+}$ and $b^{3}\Pi_{u}$ states of the cesium dimer. The results are based on data from several sources. Laser-induced fluorescence Fourier transform spectroscopy (LIF FTS) was used some time ago in the Laboratoire Aim\'{e} Cotton primarily to study the $X ^{1}\Sigma_{g}^{+}$ state. More recent work at Tsinghua University provides information from moderate resolution spectroscopy on the lowest levels of the $b^{3}\Pi_{0u}^{\pm}$ states as well as additional high resolution data. From Innsbruck University, we have precision data obtained with cold Cs$_{2}$ molecules. Recent data from Temple University was obtained using the optical-optical double resonance polarization spectroscopy technique, and finally, a group at the University of Latvia has added additional LIF FTS data. In the Hamiltonian matrix, we have used analytic potentials (the Expanded Morse Oscillator form) with both finite-difference (FD) coupled-channels and discrete variable representation (DVR) calculations of the term values. Fitted diagonal and off-diagonal spin-orbit functions are obtained and compared with {\it ab initio} results from Temple and Moscow State universities

High-precision calculations of van der Waals coefficients for heteronuclear alkali-metal dimers

Van der Waals coefficients for the heteronuclear alkali-metal dimers of Li, Na, K, Rb, Cs, and Fr are calculated using relativistic ab initio methods augmented by high-precision experimental data. We argue that the uncertainties in the coefficients are unlikely to exceed about 1%.Comment: 11 pages, 2 figs, graphicx.st

Theoretical model for ultracold molecule formation via adaptive feedback control

We investigate pump-dump photoassociation of ultracold molecules with amplitude- and phase-modulated femtosecond laser pulses. For this purpose a perturbative model for the light-matter interaction is developed and combined with a genetic algorithm for adaptive feedback control of the laser pulse shapes. The model is applied to the formation of 85Rb2 molecules in a magneto-optical trap. We find for optimized pulse shapes an improvement for the formation of ground state molecules by more than a factor of 10 compared to unshaped pulses at the same pump-dump delay time, and by 40% compared to unshaped pulses at the respective optimal pump-dump delay time. Since our model yields directly the spectral amplitudes and phases of the optimized pulses, the results are directly applicable in pulse shaping experiments

Theoretical overview of atomic parity violation. Recent developments and challenges

Recent advances in interpreting the most accurate to-date measurement of atomic parity violation in Cs are reviewed. The inferred nuclear weak charge, Q_W = - 72.65(28)_expt (36)_theor, agrees with the prediction of the standard model at 1 sigma level. Further improved interpretation is limited by an accuracy of solving basic correlation problem of atomic structure. We report on our progress in solving this problem within the relativistic coupled-cluster formalism. We include single-, double- and triple- electronic excitations in the coupled-cluster expansion. Numerical results for energies, electric-dipole matrix elements, and hyperfine-structure constants of Cs are presented.Comment: PAVI'06 proceedings + EJPA; refs + SM Qw fixe