scholarly journals Polarization dependence of semiconductor exciton and biexciton contributions to phase-resolved optical two-dimensional Fourier-transform spectra

2009 ◽  
Vol 79 (16) ◽  
Author(s):  
Alan D. Bristow ◽  
Denis Karaiskaj ◽  
Xingcan Dai ◽  
Richard P. Mirin ◽  
Steven T. Cundiff
Author(s):  
Patrick F. Tekavec ◽  
Jeffrey A. Myers ◽  
Kristin L. M. Lewis ◽  
Franklin Fuller ◽  
Jennifer P. Ogilvie

2007 ◽  
Vol 126 (4) ◽  
pp. 044511 ◽  
Author(s):  
Michael K. Yetzbacher ◽  
Nadia Belabas ◽  
Katherine A. Kitney ◽  
David M. Jonas

2002 ◽  
Vol 106 (34) ◽  
pp. 7651-7654 ◽  
Author(s):  
John D. Hybl ◽  
Anchi Yu ◽  
Darcie A. Farrow ◽  
David M. Jonas

2009 ◽  
Vol 113 (47) ◽  
pp. 13287-13299 ◽  
Author(s):  
Byungmoon Cho ◽  
Michael K. Yetzbacher ◽  
Katherine A. Kitney ◽  
Eric R. Smith ◽  
David M. Jonas

Author(s):  
L. Reimer ◽  
R. Oelgeklaus

Quantitative electron energy-loss spectroscopy (EELS) needs a correction for the limited collection aperture α and a deconvolution of recorded spectra for eliminating the influence of multiple inelastic scattering. Reversely, it is of interest to calculate the influence of multiple scattering on EELS. The distribution f(w,θ,z) of scattered electrons as a function of energy loss w, scattering angle θ and reduced specimen thickness z=t/Λ (Λ=total mean-free-path) can either be recorded by angular-resolved EELS or calculated by a convolution of a normalized single-scattering function ϕ(w,θ). For rotational symmetry in angle (amorphous or polycrystalline specimens) this can be realised by the following sequence of operations :(1)where the two-dimensional distribution in angle is reduced to a one-dimensional function by a projection P, T is a two-dimensional Fourier transform in angle θ and energy loss w and the exponent -1 indicates a deprojection and inverse Fourier transform, respectively.


1985 ◽  
Vol 50 (11) ◽  
pp. 2480-2492 ◽  
Author(s):  
Soňa Přádná ◽  
Dušan Papoušek ◽  
Jyrki Kauppinen ◽  
Sergei P. Belov ◽  
Andrei F. Krupnov ◽  
...  

Fourier transform spectra of the ν2 band of PH3 have been remeasured with 0.0045 cm-1 resolution. Ground state combination differences from these data have been fitted simultaneously with the microwave and submillimeterwave data to determine the ground state spectroscopical parameters of PH3 including the parameters of the Δk = ± 3n interactions. The correlation between the latter parameters has been discussed from the point of view of the existence of two equivalent effective rotational operators which are related by a unitary transformation. The ΔJ = 0, +1, ΔK = 0 (A1 ↔ A2, E ↔ E) rotational transitions in the ν2 and ν4 states have been measured for the first time by using a microwave spectrometer and a radiofrequency spectrometer with acoustic detection.


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