NEXAFS at nitrogen K-edge and titanium L-edge using a laser-plasma soft x-ray source based on a double-stream gas puff target

We present a possibility of reaching higher energy absorption edges of organic materials, beyond the carbon K-edge, in the near edge X-ray absorption fine structure (NEXAFS) spectroscopy technique using a compact laser-produced plasma soft X-ray (SXR) source based on a double-stream gas puff target....

Full description

Saved in:
Bibliographic Details
Published inAPL photonics Vol. 4; no. 3; pp. 30807 - 030807-7
Main Authors Wachulak, Przemysław, Duda, Martin, Bartnik, Andrzej, Węgrzyński, Łukasz, Fok, Tomasz, Fiedorowicz, Henryk
Format Journal Article
LanguageEnglish
Published AIP Publishing LLC 01.03.2019
Online AccessGet full text
ISSN2378-0967
2378-0967
DOI10.1063/1.5085810

Cover

More Information
Summary:We present a possibility of reaching higher energy absorption edges of organic materials, beyond the carbon K-edge, in the near edge X-ray absorption fine structure (NEXAFS) spectroscopy technique using a compact laser-produced plasma soft X-ray (SXR) source based on a double-stream gas puff target. The source was optimized for emission in the SXR spectral range from 1.5 to 5 nm wavelength using the krypton/helium target. The emission spectrum of the source and the absorption spectrum of the investigated sample were measured simultaneously by means of a grazing incidence spectrometer, equipped with a single, large aperture diffractive element. Based on both spectra, the optical density was computed for the silicon nitride membranes in a transmission mode, to reveal the NEXAFS features near the nitrogen K-edge. Moreover, due to spectral narrowing of the SXR emission by the use of titanium filter, reaching the titanium L-edge was also possible. Multiple SXR pulse data were compared to single SXR pulse (single-shot) data as well as to the numerical simulations. In this paper, the detailed information about the source, spectroscopy system, and the results of NEXAFS measurements is presented and discussed.
ISSN:2378-0967
2378-0967
DOI:10.1063/1.5085810