Time-resolved Correlation Spectroscopy Research Articles

Heralded preparation of spin qubits in droplet-etched GaAs quantum dots using quasiresonant excitation

We present a first comprehensive study on deterministic spin preparation employing excited state resonances of droplet etched GaAs quantum dots. This achievement facilitates future investigations of spin qubit based quantum memories using the GaAs quantum dot material platform. By observation of excitation spectra for a range of fundamental excitonic transitions the properties of different quantum dot energy levels, i.e. shells, are revealed. The innovative use of polarization resolved excitation and detection in quasi-resonant excitation spectroscopy facilitates determination of $85$ $\%$ maximum spin preparation fidelity - irrespective of the relative orientations of lab and quantum dot polarization eigenbases. Additionally, the characteristic non-radiative decay time is investigated as a function of ground state, excitation resonance and excitation power level, yielding decay times as low as $29$ ps for s-p-shell exited state transitions. Finally, by time resolved correlation spectroscopy it is demonstrated that the employed excitation scheme has a significant impact on the electronic environment of quantum dot transitions thereby influencing its charge and coherence.

Syneresis and delayed detachment in agar plates.

Biogels made of crosslinked polymers such as proteins or polysaccharides behave as porous soft solids and store large amounts of solvent. These gels undergo spontaneous aging, called syneresis, which consists of the shrinkage of the gel matrix and the progressive expulsion of solvent. As a result, a biogel originally casted in a container often loses contact with the container sidewalls, and the detachment time is difficult to anticipate a priori, since it may occur over variable time spans (from hours to days). Here we report on syneresis phenomena in agar plates, which consist of Petri dishes filled with a gel mainly composed of agar. Direct observations and speckle pattern correlation analysis allow us to rationalize the delayed detachment of the gel from the sidewall of the Petri dish. The detachment time t* is surprisingly not controlled by the mass loss as one would intuitively expect. Instead, t* is strongly correlated to the gel minimum thickness emin measured along the sidewall of the plate, and increases as a robust function of emin, independently of the prior mass-loss history. Time-resolved correlation spectroscopy atypically applied to such weakly diffusive media gives access to the local thinning rate of the gel. This technique also allows us to detect the gel micro-displacements that are triggered by water evaporation prior to the detachment, and even to anticipate the latter from a few hours. Our work provides observables to predict the detachment time of agar gels in dishes, and highlights the relevance of speckle pattern correlation analysis for the quantitative investigation of the syneresis dynamics in biopolymer gels.

Foam generation and sample composition optimization for the FOAM-C experiment of the ISS

End of 2009 and early 2010 a sealed cell, for foam generation and observation, has been designed and manufactured at Astrium Friedrichshafen facilities. With the use of this cell, different sample compositions of "wet foams" have been optimized for mixtures of chemicals such as water, dodecanol, pluronic, aethoxisclerol, glycerol, CTAB, SDS, as well as glass beads. This development is performed in the frame of the breadboarding development activities of the Experiment Container FOAM-C for operation in the ISS Fluid Science Laboratory (ISS). The sample cell supports multiple observation methods such as: Diffusing-Wave and Diffuse Transmission Spectrometry, Time Resolved Correlation Spectroscopy [1] and microscope observation, all of these methods are applied in the cell with a relatively small experiment volume <3cm3. These units, will be on orbit replaceable sets, that will allow multiple sample compositions processing (in the range of >40).

Noise in laser speckle correlation and imaging techniques

We study the noise of the intensity variance and of the intensity correlation and structure functions measured in light scattering from a random medium in the case when these quantities are obtained by averaging over a finite number N of pixels of a digital camera. We show that the noise scales as 1/N in all cases and that it is sensitive to correlations of signals corresponding to adjacent pixels as well as to the effective time averaging (due to the finite integration time) and spatial averaging (due to the finite pixel size). Our results provide a guide to estimation of noise levels in such applications as multi-speckle dynamic light scattering, time-resolved correlation spectroscopy, speckle visibility spectroscopy, laser speckle imaging etc.

Theory of n-fold time-resolved correlation spectroscopy and its application to resonance fluorescence radiation

Extending the concept of the time-dependent physical spectrum introduced by Eberly and Wodkiewicz (1977) the authors present a formula for the n-fold time-resolved correlation spectrum depending on n time and n frequency arguments. The corresponding measuring device consists of n coupled photodetectors with frequency resolving equipment in front of each. As an application the authors consider the resonance fluorescence radiation of a two-level atom irradiated monochromatically. Under certain conditions the authors derive a simple expression for the n-fold detection probability of photons at time ti (i=1, . . ., n) with frequencies belonging to the central peak or to one of the sidebands of the fluorescence triplet.

Theory of time-resolved correlation spectroscopy and its application to resonance fluorescence radiation

Extending the concept of the time-dependent physical spectrum introduced by Eberly and Wodkiewicz (1977) the authors present a formula for the n-fold time-resolved correlation spectrum depending on n time and n frequency arguments. The corresponding measuring device consists of n coupled photodetectors with frequency resolving equipment in front of each. As an application the authors consider the resonance fluorescence radiation of a two-level atom irradiated monochromatically. Under certain conditions the authors derive a simple expression for the n-fold detection probability of photons at time ti (i=1, . . ., n) with frequencies belonging to the central peak or to one of the sidebands of the fluorescence triplet.