In this paper, we discuss a general procedure by which nonlinear power spectral densities (PSDs) of the harmonic oscillator can be calculated in both the quantum and classical regimes. We begin with an introduction of the damped and undamped classica
l harmonic oscillator, followed by an overview of the quantum mechanical description of this system. A brief review of both the classical and quantum autocorrelation functions (ACFs) and PSDs follow. We then introduce a general method by which the kth-order PSD for the harmonic oscillator can be calculated, where $k$ is any positive integer. This formulation is verified by first reproducing the known results for the $k = 1$ case of the linear PSD. It is then extended to calculate the second-order PSD, useful in the field of quantum measurement, corresponding to the $k = 2$ case of the generalized method. In this process, damping is included into each of the quantum linear and quadratic PSDs, producing realistic models for the PSDs found in experiment. These quantum PSDs are shown to obey the correspondence principle by matching with what was calculated for their classical counterparts in the high temperature, high-Q limit. Finally, we demonstrate that our results can be reproduced using the fluctuation-dissipation theorem, providing an independent check of our resultant PSDs.
The topological physics of quantum Hall states is efficiently encoded in purely topological quantum field theories of the Chern-Simons type. The reliable inclusion of low-energy dynamical properties in a continuum description however typically requir
es proximity to a quantum critical point. We construct a field theory that describes the quantum transition from an isotropic to a nematic Laughlin liquid. The soft mode associated with this transition approached from the isotropic side is identified as the familiar intra-Landau level Girvin-MacDonald-Platzman mode. We obtain z=2 dynamic scaling at the critical point and a description of Goldstone and defect physics on the nematic side. Despite the very different physical motivation, our field theory is essentially identical to a recent geometric field theory for a Laughlin liquid proposed by Haldane.
A growing list of experiments show orthorhombic electronic anisotropy in the iron pnictides, in some cases at temperatures well above the spin density wave transition. These experiments include neutron scattering, resistivity and magnetoresistance me
asurements, and a variety of spectroscopies. We explore the idea that these anisotropies stem from a common underlying cause: orbital order manifest in an unequal occupation of $d_{xz}$ and $d_{yz}$ orbitals, arising from the coupled spin-orbital degrees of freedom. We emphasize the distinction between the total orbital occupation (the integrated density of states), where the order parameter may be small, and the orbital polarization near the Fermi level which can be more pronounced. We also discuss light-polarization studies of angle-resolved photoemission, and demonstrate how x-ray absorption linear dichroism may be used as a method to detect an orbital order parameter.
