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We have quantified excitonic many-body interaction energies in GaAs quantum wells using two-dimensional coherent spectroscopy. The anharmonic oscillator model for excitons is used to extract the inter- and intra-mode interaction energies from 2D spectra.
We demonstrate 2D coherent spectroscopy of CdSe/ZnS nanocrystals and measure the exciton homogeneous linewidth. The 2D spectra also reveal an off-diagonal peak that oscillates as a function of the waiting time T.
We have studied spectral diffusion of excitons in GaAs quantum wells using two-dimensional coherent spectroscopy. Localized and delocalized excitons exhibit distinct spectral diffusion characteristics. These results cannot be explained in the strong redistribution approximation.
Two-dimensional coherent spectroscopy on a series of quantum dot samples with different morphology reveals that biexciton binding is independent of the details of confinement in InAs dots, in contrast to the behavior in GaAs dots.
The frequency-frequency correlation function for excitons in a GaAs quantum well is measured using optical two-dimensional Fourier transform spectroscopy and a numerical fitting procedure. We also report frequency-frequency correlation functions for biexciton and two-exciton states.
Many-body interactions in a doped CdTe/CdMgTe quantum well are investigated using optical 2D Fourier-transform spectroscopy. The nature of coherent exciton-trion correlations is examined by analyzing lineshapes in the 2D spectra.
Multi-particle correlations are investigated in an InAs quantum dot ensemble using 2D Fourier-transform spectroscopy. Signatures of trions and a fifth-order contribution from the biexciton are observed by varying the excitation polarization and density.
Coherence decay times of and between fine-structure states is obtained from an InAs quantum dot ensemble using optical 2D Fourier-transform spectroscopy. This technique allows us to investigate properties of QDs within the ensemble.
We present an algorithmic approach for determining, in polynomial time, disulfide bonds in proteins using mass spectrometry data. The proposed technique is based on matching the set of all theoretically possible disulfide bonded structures with precursor ions derived from a tandem MS/MS experiment. For each match found, theoretical fragments from a disulfide bonded peptide structure are matched with...
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