| 1. |
- Chernenk, Kirill, et al.
(författare)
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Performance and characterization of the FinEstBeAMS beamline at the MAX IV Laboratory
- 2021
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Ingår i: Journal of Synchrotron Radiation. - 0909-0495. ; 28, s. 1620-1630
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Tidskriftsartikel (refereegranskat)abstract
- FinEstBeAMS (Finnish-Estonian Beamline for Atmospheric and Materials Sciences) is a multidisciplinary beamline constructed at the 1.5 GeV storage ring of the MAX IV synchrotron facility in Lund, Sweden. The beamline covers an extremely wide photon energy range, 4.5-1300 eV, by utilizing a single elliptically polarizing undulator as a radiation source and a single grazing-incidence plane grating monochromator to disperse the radiation. At photon energies below 70 eV the beamline operation relies on the use of optical and thin-film filters to remove higher-order components from the monochromated radiation. This paper discusses the performance of the beamline, examining such characteristics as the quality of the gratings, photon energy calibration, photon energy resolution, available photon flux, polarization quality and focal spot size.
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| 2. |
- Kappelhoff, Jan, et al.
(författare)
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Spectroscopic studies on Pr3+ doped YPO4 and LuPO4 upon vacuum ultraviolet (VUV) and synchrotron radiation excitation
- 2022
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Ingår i: Chemical Physics. - : Elsevier BV. - 0301-0104. ; 562
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Tidskriftsartikel (refereegranskat)abstract
- This work concerns the spectroscopic properties of micro- and nanoscale LuPO4:Pr3+ and microscale YPO4:Pr3+ upon excitation by VUV synchrotron radiation at a wide range of energies (5–45 eV) and two different temperatures (7 and 300 K). Both Pr3+ doped host materials show more intense UV-C emission than other Pr3+ phosphors studied earlier at FinEstBeAMS beamline under the same measurement conditions. The various relaxation processes of 5d14f1 → 4f2 interconfigurational transitions of Pr3+ and the difference between both hosts are discussed in detail.
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| 3. |
- Kooser, Kuno, et al.
(författare)
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Gas-phase endstation of electron, ion and coincidence spectroscopies for diluted samples at the FinEstBeAMS beamline of the MAX IV 1.5 GeV storage ring
- 2020
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Ingår i: Journal of Synchrotron Radiation. - 0909-0495. ; 27, s. 1080-1091
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Tidskriftsartikel (refereegranskat)abstract
- Since spring 2019 an experimental setup consisting of an electron spectrometer and an ion time-of-flight mass spectrometer for diluted samples has been available for users at the FinEstBeAMS beamline of the MAX IV Laboratory in Lund, Sweden. The setup enables users to study the interaction of atoms, molecules, (molecular) microclusters and nanoparticles with short-wavelength (vacuum ultraviolet and X-ray) synchrotron radiation and to follow the electron and nuclear dynamics induced by this interaction. Test measurements of N2 and thiophene (C4H4S) molecules have demonstrated that the setup can be used for many-particle coincidence spectroscopy. The measurements of the Ar 3p photoelectron spectra by linear horizontal and vertical polarization show that angle-resolved experiments can also be performed. The possibility to compare the electron spectroscopic results of diluted samples with solid targets in the case of Co2O3 and Fe2O3 at the Co and Fe L 2,3-absorption edges in the same experimental session is also demonstrated. Because the photon energy range of the FinEstBeAMS beamline extends from 4.4 eV up to 1000 eV, electron, ion and coincidence spectroscopy studies can be executed in a very broad photon energy range.
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| 4. |
- Pankratov, Vladimir, et al.
(författare)
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Progress in development of a new luminescence setup at the FinEstBeAMS beamline of the MAX IV laboratory
- 2019
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Ingår i: Radiation Measurements. - : Elsevier BV. - 1350-4487. ; 121, s. 91-98
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Tidskriftsartikel (refereegranskat)abstract
- FinEstBeAMS is a new materials science beamline at the 1.5 GeV storage ring of the MAX IV Laboratory in Lund, Sweden. It has been built based on grazing incidence monochromatization of synchrotron light, which allows to cover a remarkably wide excitation energy range from ultraviolet to soft x-rays (4.5–1450 eV). A new mobile luminescence spectroscopy end station has been commissioned with design benefitting from the advantages of a high flux elliptically polarizing undulator light source. We report on the design of the luminescence end station, its technical realization and performance achieved so far. Special attention is paid to the experimental challenges for luminescence spectroscopy under grazing incidence excitation conditions. The first luminescence results obtained demonstrate a reliable performance of the advanced setup at FinEstBeAMS.
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| 5. |
- Saaring, Juhan, et al.
(författare)
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Relaxation of electronic excitations in K2GeF6 studied by means of time-resolved luminescence spectroscopy under VUV and pulsed electron beam excitation
- 2021
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Ingår i: Journal of Alloys and Compounds. - : Elsevier BV. - 0925-8388. ; 883
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Tidskriftsartikel (refereegranskat)abstract
- Highly crystalline K2GeF6 micropowders were prepared by co-precipitation in the hydrofluoric acid-water-alcohol solution and studied by means of the cathodoluminescence and time-resolved luminescence spectroscopy under synchrotron radiation excitation at 7 K. The nature of various intrinsic emissions was revealed. The luminescence band at 510 nm detected under excitation by photons with the energy above 9 eV is related to the radiative decay of self-trapped excitons. Fast emission bands with ~400 ps decay time found in the spectral range from VUV to visible (8–2.4 eV) are assigned to the cross-luminescence transitions from K 3p hole states and intraband luminescence transitions due to the presence of the Ge 4s, 4p valence states. The creation of cation excitons was detected in the energy range 18–20 eV. Their non-radiative decay results in the formation of hole states in the Ge energy bands, which finally recombine with electrons from the above lying valence states and provide fast intraband luminescence. Important electronic band structure parameters including the energy gap width of 11 eV, cation exciton formation energy 18.1 eV and ionization energy of cation states 20.0 eV were determined from the luminescence excitation spectra.
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| 6. |
- Saaring, Juhan, et al.
(författare)
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Time-resolved luminescence spectroscopy of ultrafast emissions in BaGeF6
- 2022
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Ingår i: Journal of Luminescence. - : Elsevier BV. - 0022-2313. ; 244
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Tidskriftsartikel (refereegranskat)abstract
- Phase-pure crystalline micropowder samples of BaGeF6 were prepared and studied under excitation by tuneable synchrotron radiation and 10 keV electron beam. Time-resolved photoluminescence emission and excitation spectra and a set of single emission decay curves were recorded at 7 K for the exciting photon energy region of 4.3–45 eV. Several intrinsic emissions were revealed in BaGeF6 and their origin investigated. A single broad emission band peaking at 455 nm is assigned to be of excitonic origin due to its long decay time in the μs range and due to the presence of an intense excitation peak at 10.1 eV right in the region of the host absorption onset. The energy gap width of BaGeF6 was determined experimentally from the photoluminescence excitation spectra of the 455 nm emission to be 10.9 eV. Several emission bands, including distinct peaks at 270 and 455 nm, with the main decay component of ∼180 ps were revealed across the wavelength range of 200–500 nm. The revealed ultrafast emissions were studied by means of time-resolved photoluminescence spectroscopy and their origin was assigned to cross-luminescence resulting from radiative transitions between the Ba 5p core level and sub-bands of the valence band (Ge 4s, Ge 4p and F 2p hybridized states) and to intraband luminescence between the valence band sub-bands. Photoluminescence excitation spectra of the ultrafast emissions revealed a gently sloping onset at 17 eV, related to transitions from the Ge 4s states. It is followed by a distinct peak at 19.4 eV, which corresponds to the ionization of the Ba 5p cation states and is related to the excitation threshold of cross-luminescence.
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