Quasi-Fourier-transform limited, scannable, high energy titanium-sapphire laser source for high resolution spectroscopy

2007 ◽  
Vol 78 (3) ◽  
pp. 033102 ◽  
Author(s):  
Patrick Dupré ◽  
Terry A. Miller
2022 ◽  
Vol 61 (01) ◽  
Author(s):  
Pornapa Artsang ◽  
Christophe Buisset ◽  
Panomsak Meemon ◽  
Pakakaew Rittipruk ◽  
Sirinrat Sithajan ◽  
...  

1998 ◽  
Vol 5 (3) ◽  
pp. 208-214 ◽  
Author(s):  
Y. Sakurai

The advent of synchrotron radiation sources for well polarized and high-energy X-rays offers new opportunities for exploiting Compton scattering spectroscopy as a tool for investigating the electronic and magnetic structures of materials. Recent high-resolution Compton scattering experiments show the unique capability for the study of Fermiology-related issues and electron–electron correlation effects. Intense, high-energy and circularly polarized X-ray sources have improved magnetic Compton scattering spectroscopy from the point of statistical accuracy and momentum resolution. As a next advance, a high-energy inelastic scattering beamline dedicated to Compton scattering spectroscopies is being constructed at SPring-8. The light source is an elliptic multipole wiggler with a periodic length of 12 cm. The beamline includes two experimental stations: one is for high-resolution spectroscopy using 100–150 keV X-rays and the other is for magnetic Compton scattering experiments using circularly polarized 300 keV X-rays. The use of such high-energy X-rays makes it possible to carry out experiments efficiently on samples including heavier elements, such as high-T c superconductors and 4f and 5f magnetic materials.


2008 ◽  
Vol 86 (1) ◽  
pp. 241-244 ◽  
Author(s):  
D B Thorn ◽  
G V Brown ◽  
J H.T. Clementson ◽  
H Chen ◽  
M Chen ◽  
...  

We present a measurement of the K-shell spectrum of He-like through Be-like praseodymium ions trapped in the Livermore SuperEBIT electron beam ion trap using a bismuth absorber pixel on the XRS/EBIT microcalorimeter. This measurement is the first of its kind where the n = 2 to n = 1 transitions of the various charge states are spectroscopically resolved. The measured transition energies are compared with theoretical calculations from several atomic codes.PACS Nos.: 32.30.–r, 32.30.Rj, 39.30.+w


1991 ◽  
Vol 69 (3-4) ◽  
pp. 427-431 ◽  
Author(s):  
D. J. S. Beckett ◽  
M. K. Nissen ◽  
M. L. W. Thewalt

The identification of substitutional shallow donors in GaAs by optical techniques has been problematic because of the extremely small chemical shifts of these effective-masslike impurities. Photoluminescence has been successfully applied in identifying donors in high-purity epitaxial material through the painstaking use of high-resolution spectroscopy, high-magnetic fields, and resonant excitation. Relatively little work has been done in bulk GaAs, where the broadened transitions hinder the resolution of different species. Recently we demonstrated that the high resolution and high-signal throughput obtained with Fourier transform photoluminescence (FTPL) gives superior results for epitaxial material. In this report we show that the advantages of FTPL can also be applied to reliable donor identification in bulk GaAs.


2013 ◽  
Vol 91 (11) ◽  
pp. 963-965 ◽  
Author(s):  
D. Golebiowski ◽  
M. Herman ◽  
O. Lyulin

Near-infrared absorption spectra of a carbon dioxide sample enriched with oxygen-17 were recorded in the spectral range 1.2–1.25 μm. A high-resolution continuous scan Fourier transform interferometer fitted with a femto OPO/Idler laser source and cavity-enhanced absorption was used. The optimal root mean squared noise equivalent absorption was 1.2 × 10−10 cm−1Hz–1/2 per spectral element, corresponding to αmin = 10−8 cm−1. Two cold bands in 17O12C18O and one hot band in 16O12C17O were newly identified and rotationally analyzed. More lines than previously published (Lyulin et al. J. Quant. Spectrosc. Radiat. Transfer, 113, 2167 (2012)), were assigned in the observed bands of 12C17O2 and 16O12C17O. New upper state rotational constants were obtained from a band-by-band analysis.


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