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Register a new userSupersymmetry and eigensurface topology of the spherical quantum pendulum
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We undertook a mutually complementary analytic and computational study of the full-fledged spherical (3D) quantum rotor subject to combined orienting and aligning interactions characterized, respectively, by dimensionless parameters $eta$ and $zeta$. By making use of supersymmetric quantum mechanics (SUSY QM), we found two sets of conditions under which the problem of a spherical quantum pendulum becomes analytically solvable. These conditions coincide with the loci $zeta=frac{eta^2}{4k^2}$ of the intersections of the eigenenergy surfaces spanned by the $eta$ and $zeta$ parameters. The integer topological index $k$ is independent of the eigenstate and thus of the projection quantum number $m$. These findings have repercussions for rotational spectra and dynamics of molecules subject to combined permanent and induced dipole interactions.
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We make use of supersymmetric quantum mechanics (SUSY QM) to find three sets of conditions under which the problem of a planar quantum pendulum becomes analytically solvable. The analytic forms of the pendulums eigenfuntions make it possible to find analytic expressions for observables of interest, such as the expectation values of the angular momentum squared and of the orientation and alignment cosines as well as of the eigenenergy. Furthermore, we find that the topology of the intersections of the pendulums eigenenergy surfaces can be characterized by a single integer index whose values correspond to the sets of conditions under which the analytic solutions to the quantum pendulum problem exist.
Recently, we have theoretically proposed and experimentally demonstrated an exact and efficient quantum simulation of photosynthetic light harvesting in nuclear magnetic resonance (NMR), cf. B. X. Wang, textit{et al.} npj Quantum Inf.~textbf{4}, 52 (2018). In this paper, we apply this approach to simulate the open quantum dynamics in various photosynthetic systems with different Hamiltonians. By numerical simulations, we show that for Drude-Lorentz spectral density the dimerized geometries with strong couplings within the donor and acceptor clusters respectively exhibit significantly-improved efficiency. Based on the optimal geometry, we also demonstrate that the overall energy transfer can be further optimized when the energy gap between the donor and acceptor clusters matches the peak of the spectral density. Moreover, by exploring the quantum dynamics for different types of spectral densities, e.g. Ohmic, sub-Ohmic, and super-Ohmic spectral densities, we show that our approach can be generalized to effectively simulate open quantum dynamics for various Hamiltonians and spectral densities. Because $log_{2}N$ qubits are required for quantum simulation of an $N$-dimensional quantum system, this quantum simulation approach can greatly reduce the computational complexity compared with popular numerically-exact methods.
An anharmonic oscillator when driven with a fast, frequency chirped voltage pulse can oscillate with either small or large amplitude depending on whether the drive voltage is below or above a critical value-a well studied classical phenomenon known as autoresonance. Using a 6 GHz superconducting resonator embedded with a Josephson tunnel junction, we have studied for the first time the role of noise in this non-equilibrium system and find that the width of the threshold for capture into autoresonance decreases as the square root of T, and saturates below 150 mK due to zero point motion of the oscillator. This unique scaling results from the non-equilibrium excitation where fluctuations, both quantum and classical, only determine the initial oscillator motion and not its subsequent dynamics. We have investigated this paradigm in an electrical circuit but our findings are applicable to all out of equilibrium nonlinear oscillators.
Molecules are the most demanding quantum systems to be simulated by quantum computers because of their complexity and the emergent role of quantum nature. The recent theoretical proposal of Huh et al. (Nature Photon., 9, 615 (2015)) showed that a multi-photon network with a Gaussian input state can simulate a molecular spectroscopic process. Here, we report the first experimental demonstration of molecular vibrational spectroscopy of SO$_{2}$ with a trapped-ion system. In our realization, the molecular scattering operation is decomposed to a series of elementary quantum optical operations, which are implemented through Raman laser beams, resulting in a multimode Gaussian (Bogoliubov) transformation. The molecular spectroscopic signal is reconstructed from the collective projection measurements on phonon modes of the trapped-ion system. Our experimental demonstration would pave the way to large-scale molecular quantum simulations, which are classically intractable.
We study coherent superpositions of clockwise and anti-clockwise rotating intermediate complexes with overlapping resonances formed in bimolecular chemical reactions. Disintegration of such complexes represents an analog of famous double-slit experiment. The time for disappearance of the interference fringes is estimated from heuristic arguments related to fingerprints of chaotic dynamics of a classical counterpart of the coherently rotating complex. Validity of this estimate is confirmed numerically for the H+D$_2$ chemical reaction. Thus we demonstrate the quantum--classical transition in temporal behavior of highly excited quantum many-body systems in the absence of external noise and coupling to an environment.
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