Natural Slow-Roll Inflation

It is shown that the non-perturbative dynamics of a phase change to the non-trivial phase of $\lambda\varphi^4$-theory in the early universe can give rise to slow-rollover inflation without recourse to unnaturally small couplings.Comment: 14 LaTex pages (3 figures available on request), UNITUE-THEP-15-199

Nonuniversality of the dispersion interaction: analytic benchmarks for van der Waals energy functionals

We highlight the non-universality of the asymptotic behavior of dispersion forces, such that a sum of inverse sixth power contributions is often inadequate. We analytically evaluate the cross-correlation energy Ec between two pi-conjugated layers separated by a large distance D within the electromagnetically non-retarded Random Phase Approximation, via a tight-binding model. For two perfect semimetallic graphene sheets at T=0K we find Ec = C D^{-3}, in contrast to the "insulating" D^{-4} dependence predicted by currently accepted approximations. We also treat the case where one graphene layer is replaced by a thin metal, a model relevant to the exfoliation of graphite. Our general considerations also apply to nanotubes, nanowires and layered metals.Comment: 4 pages, 0 fig

Binding energy and dephasing of biexcitons in In0.18Ga0.82As/GaAs single quantum wells

Biexciton binding energies and biexciton dephasing in In0.18Ga0.82As/GaAs single quantum wells have been measured by time-integrated and spectrally resolved four-wave mixing. The biexciton binding energy increases from 1.5 to 2.6 meV for well widths increasing from 1 to 4 nm. The ratio between exciton and biexciton binding energy changes from 0.23 to 0.3 with increasing inhomogeneous broadening, corresponding to increasing well width. From the temperature dependence of the exciton and biexciton four-wave mixing signal decay, we have deduced the acoustic-phonon scattering of the exciton-biexciton transition. It is found to be comparable to that of the exciton transition, indicating that the deformation potential interactions for the exciton and the exciton-biexciton transitions are comparable

Robustness of energy landscape control for spin networks under decoherence

Quantum spin networks form a generic system to describe a range of quantum devices for quantum information processing and sensing applications. Understanding how to control them is essential to achieve devices with practical functionalities. Energy landscape shaping is a novel control paradigm to achieve selective transfer of excitations in a spin network with surprisingly strong robustness towards uncertainties in the Hamiltonians. Here we study the effect of decoherence, specifically generic pure dephasing, on the robustness of these controllers. Results indicate that while the effectiveness of the controllers is reduced by decoherence, certain controllers remain sufficiently effective, indicating potential to find highly effective controllers without exact knowledge of the decoherence processes.Comment: 6 pages, 6 figure

Coherence dynamics and quantum-to-classical crossover in an exciton-cavity system in the quantum strong coupling regime

Interaction between light and matter generates optical nonlinearities, which are particularly pronounced in the quantum strong coupling regime. When a single bosonic mode couples to a single fermionic mode, a Jaynes-Cummings (JC) ladder is formed, which we realize here using cavity photons and quantum dot excitons. We measure and model the coherent anharmonic response of this strongly coupled exciton-cavity system at resonance. Injecting two photons into the cavity, we demonstrate a root 2 larger polariton splitting with respect to the vacuum Rabi splitting. This is achieved using coherent nonlinear spectroscopy, specifically four-wave mixing, where the coherence between the ground state and the first (second) rung of the JC ladder can be interrogated for positive (negative) delays. With increasing excitation intensity and thus rising average number of injected photons, we observe spectral signatures of the quantum-to-classical crossover of the strong coupling regime.Peer reviewe

LICOR-Liquid Columns' Resonances

The aim of the experiment LICOR was the investigation of the axial resonances oi cylindrical liquid columns supported by equal circular coaxiaJ disks. In preparation ot the D-2 experiment a •heoreiical model has been developed, which exactly describes the small amplitude oscillations of finite cylindrical columns between coaxial circular disks. In addition, in terrestrial experiments the resonance frequencies of small liquid columns with up to 5 mm in diameter have been determined and investigations with density-matched liquids (silicon oil in a waierlmethanol mixture) have been performed. For the D-2 experiment LICOR the front disk and the rear disk lor use in the AFPM have been constructed and equipped with pressure sensors and the necessary electronics. The pressure exerted by the oscillating liquid column on trie supporting disks vsas as low as 10 Pa. Since the data downlink of the Materials Research Laboratory was just one signal oer second and channel, it was necessary to determine amplitude and phase of the pressure already in the LICOR disks. The D-2 experiment has been successfully performed. It has fully confirmed the theoretical models and remarkably supplements the experiments on small liquid columns and on density-matched columns

Long Exciton Dephasing Time and Coherent Phonon Coupling in CsPbBr2_{2}Cl Perovskite Nanocrystals

Fully-inorganic cesium lead halide perovskite nanocrystals (NCs) have shown to exhibit outstanding optical properties such as wide spectral tunability, high quantum yield, high oscillator strength as well as blinking-free single photon emission and low spectral diffusion. Here, we report measurements of the coherent and incoherent exciton dynamics on the 100 fs to 10 ns timescale, determining dephasing and density decay rates in these NCs. The experiments are performed on CsPbBr$_{2}$Cl NCs using transient resonant three-pulse four-wave mixing (FWM) in heterodyne detection at temperatures ranging from 5 K to 50 K. We found a low-temperature exciton dephasing time of 24.5$\pm$1.0 ps, inferred from the decay of the photon-echo amplitude at 5 K, corresponding to a homogeneous linewidth (FWHM) of 54$\pm$5 {\mu}eV. Furthermore, oscillations in the photon-echo signal on a picosecond timescale are observed and attributed to coherent coupling of the exciton to a quantized phonon mode with 3.45 meV energy

Chemically-specific dual/differential CARS micro-spectroscopy of saturated and unsaturated lipid droplets

We have investigated the ability of dual-frequency Coherent Antistokes Raman Scattering (D-CARS) micro-spectroscopy, based on femtosecond pulses (100 fs or 5 fs) spectrally focussed by glass dispersion, to distinguish the chemical composition of micron-sized lipid droplets consisting of different triglycerides types (poly-unsaturated glyceryl trilinolenate, mono-unsaturated glyceryl trioleate and saturated glyceryl tricaprylate and glyceryl tristearate) in a rapid and label-free way. A systematic comparison of Raman spectra with CARS and D-CARS spectra was used to identify D-CARS spectral signatures which distinguish the disordered poly-unsaturated lipids from the more ordered saturated ones both in the CH-stretch vibration region and in the fingerprint region, without the need for lengthy CARS multiplex acquisition and analysis. D-CARS images of the lipid droplets at few selected wavenumbers clearly resolved the lipid composition differences, and exemplify the potential of this technique for label-free chemically selective rapid imaging of cytosolic lipid droplets in living cell