Research output: Contribution to journal › Article › peer-review
Pulsed glow discharge enables direct mass spectrometric measurement of fluorine in crystal materials – Fluorine quantification and depth profiling in fluorine doped potassium titanyl phosphate. / Bodnar, Victoria; Ganeev, Alexander; Gubal, Anna; Solovyev, Nikolay; Glumov, Oleg ; Yakobson, Viktor; Murin, Igor.
In: Spectrochimica Acta, Part B: Atomic Spectroscopy, Vol. 145, No. 145, 07.2018, p. 20-28.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Pulsed glow discharge enables direct mass spectrometric measurement of fluorine in crystal materials – Fluorine quantification and depth profiling in fluorine doped potassium titanyl phosphate
AU - Bodnar, Victoria
AU - Ganeev, Alexander
AU - Gubal, Anna
AU - Solovyev, Nikolay
AU - Glumov, Oleg
AU - Yakobson, Viktor
AU - Murin, Igor
N1 - Funding Information: The research has been supported by a grant from the Russian Science Foundation (grant No. 17-73-20089 ). The Authors are grateful to St. Petersburg State University Research Park (St. Petersburg State University, St. Petersburg, Russia): Interdisciplinary Resource Centers for Nanotechnology, Chemical Analysis and Materials and “Geomodel”, for providing access to their facilities.
PY - 2018/7
Y1 - 2018/7
N2 - A pulsed direct current glow discharge time-of-flight mass spectrometry (GD TOF MS) method for the quantification of fluorine in insoluble crystal materials with fluorine doped potassium titanyl phosphate (KTP) KTiOPO4:KF as an example has been proposed. The following parameters were optimized: repelling pulse delay, discharge duration, discharge voltage, and pressure in the discharge cell. Effective ionization of fluorine in the space between sampler and skimmer under short repelling pulse delay, related to the high-energy electron impact at the discharge front, has been demonstrated. A combination of instrumental and mathematical correction approaches was used to cope for the interferences of 38Ar2+ and 1H3 16O + on 19F+. To maintain surface conductivity in the dielectric KTP crystals and insure its effective sputtering in combined hollow cathode cell, silver suspension applied by the dip-coating method was employed. Fluorine quantification was performed using relative sensitivity factors. The analysis of a reference material and scanning electron microscope-energy dispersive X-ray spectroscopy was used for validation. Fluorine limit of detection by pulsed direct current GD TOF MS was 0.01 mass%. Real sample analysis showed that fluorine seems to be inhomogeneously distributed in the crystals. That is why depth profiling of F, K, O, and P was performed to evaluate the crystals' non-stoichiometry. The approaches designed allow for fluorine quantification in insoluble dielectric materials with minimal sample preparation and destructivity as well as performing depth profiling to assess crystal non-stoichiometry.
AB - A pulsed direct current glow discharge time-of-flight mass spectrometry (GD TOF MS) method for the quantification of fluorine in insoluble crystal materials with fluorine doped potassium titanyl phosphate (KTP) KTiOPO4:KF as an example has been proposed. The following parameters were optimized: repelling pulse delay, discharge duration, discharge voltage, and pressure in the discharge cell. Effective ionization of fluorine in the space between sampler and skimmer under short repelling pulse delay, related to the high-energy electron impact at the discharge front, has been demonstrated. A combination of instrumental and mathematical correction approaches was used to cope for the interferences of 38Ar2+ and 1H3 16O + on 19F+. To maintain surface conductivity in the dielectric KTP crystals and insure its effective sputtering in combined hollow cathode cell, silver suspension applied by the dip-coating method was employed. Fluorine quantification was performed using relative sensitivity factors. The analysis of a reference material and scanning electron microscope-energy dispersive X-ray spectroscopy was used for validation. Fluorine limit of detection by pulsed direct current GD TOF MS was 0.01 mass%. Real sample analysis showed that fluorine seems to be inhomogeneously distributed in the crystals. That is why depth profiling of F, K, O, and P was performed to evaluate the crystals' non-stoichiometry. The approaches designed allow for fluorine quantification in insoluble dielectric materials with minimal sample preparation and destructivity as well as performing depth profiling to assess crystal non-stoichiometry.
KW - FluorinePulsed glow dischargeTime-of-flight mass spectrometryPotassium titanyl phosphate (KTP)Nonlinear optical materials
KW - Fluorine
KW - Nonlinear optical materials
KW - Potassium titanyl phosphate (KTP)
KW - Pulsed glow discharge
KW - Time-of-flight mass spectrometry
KW - SECONDARY CATHODE
KW - LASER
KW - TIME
KW - KTIOPO4
KW - TRACE-ELEMENTS
KW - MOLECULAR ABSORPTION SPECTROMETRY
KW - NONLINEAR-OPTICAL PROPERTIES
KW - GROWTH
KW - SAMPLES
KW - EMISSION
UR - http://www.scopus.com/inward/record.url?scp=85045570283&partnerID=8YFLogxK
UR - http://www.mendeley.com/research/pulsed-glow-discharge-enables-direct-mass-spectrometric-measurement-fluorine-crystal-materials-fluor
U2 - https://doi.org/10.1016/j.sab.2018.04.002
DO - https://doi.org/10.1016/j.sab.2018.04.002
M3 - Article
AN - SCOPUS:85045570283
VL - 145
SP - 20
EP - 28
JO - SPECTROCHIMICA ACTA PART B-ATOMIC SPECTROSCOPY
JF - SPECTROCHIMICA ACTA PART B-ATOMIC SPECTROSCOPY
SN - 0584-8547
IS - 145
ER -
ID: 23825346