Vitali Nagirnyi
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Research Interests
Vitali Nagirnyi has a total of 421 co-authors. Here are the top co-authors by number of shared publications:
- Marco Kirm
Institute of Physics, University of Tartu, W. Ostwald Str. 1, 50411 Tartu, Estonia
52 shared publications - Aleksandr Lushchik
Institute of Physics, University of Tartu, W. Ostwald Str. 1, 50411 Tartu, Estonia
30 shared publications S. Zazubovich
Institute of Physics, Riia Street 142, EE‐2400 Tartu, Estonia
28 shared publicationsA. Kotlov
16 shared publications- Dmitry A. Spassky
Institute of Physics, University of Tartu, W. Ostwald Str. 1, 50411, Tartu, Estonia
15 shared publications E. Feldbach
15 shared publications
Latest Publications
- Open Access
- 11 September 2026
- Published by Royal Society of Chemistry (RSC) in Journal of Materials Chemistry C
- Vol. 14 (34) , 15522-15530
The electronic structure of K 2 SiF 6 from GW calculations and photoelectron spectroscopy
An investigation of the electronic structure of K 2 SiF 6 based on GW theory and photoelectron spectroscopy reveals that Auger–Meitner decay of K 3p holes is energetically forbidden in this material.
- 11 September 2026
- Published by Royal Society of Chemistry (RSC) in Journal of Materials Chemistry C
- Vol. 14 (34) , 15522-15530
Open AccessThe electronic structure of K 2 SiF 6 from GW calculations and photoelectron spectroscopy
An investigation of the electronic structure of K 2 SiF 6 based on GW theory and photoelectron spectroscopy reveals that Auger–Meitner decay of K 3p holes is energetically forbidden in this material.
- Open Access
- 9 April 2026
- Published by Royal Society of Chemistry (RSC) in Journal of Materials Chemistry C
- Vol. 14 (22) , 9526-9536
Molten salt–assisted screen printing of highly textured Zn 2 SiO 4 films with enhanced deep UV emission
Scalable synthesis route to highly textured Zn 2 SiO 4 films enabling sustainable deep UV emitters.
- 9 April 2026
- Published by Royal Society of Chemistry (RSC) in Journal of Materials Chemistry C
- Vol. 14 (22) , 9526-9536
Open AccessMolten salt–assisted screen printing of highly textured Zn 2 SiO 4 films with enhanced deep UV emission
Scalable synthesis route to highly textured Zn 2 SiO 4 films enabling sustainable deep UV emitters.
- Open Access
- 1 December 2025
- Published by AIP Publishing in Review of Scientific Instruments
- Vol. 96 (12)
The time-resolved luminescence end station for studies of ultrafast relaxation processes under pulsed femtosecond X-rays at the FemtoMAX beamline
We present the time-resolved luminescence end station developed at the FemtoMAX beamline at the MAX IV Laboratory for the studies of ultrafast energy relaxation and emission properties. The instrument consists of a temperature-controlled vacuum chamber sample environment, in which the UV–visible luminescence is collected from the point of interaction of ultrashort x-ray pulses with luminescent material and directed to a monochromator equipped with an ultrafast MCP-PMT detector operating in a photon-counting mode. The instrumental response function of the setup, determined by the duration of x-ray pulses (50 fs), optical path, and fast MCP-PMT response, was measured to 32 ps (FWHM) within the spectral range of 200–700 nm. In this paper, we present the results obtained under different operational conditions on the basis of three well-known scintillating samples, demonstrating that this instrument development for the scintillator community has established the foundation for ultrafast luminescence studies at FemtoMAX.
- 1 December 2025
- Published by AIP Publishing in Review of Scientific Instruments
- Vol. 96 (12)
Open AccessThe time-resolved luminescence end station for studies of ultrafast relaxation processes under pulsed femtosecond X-rays at the FemtoMAX beamline
We present the time-resolved luminescence end station developed at the FemtoMAX beamline at the MAX IV Laboratory for the studies of ultrafast energy relaxation and emission properties. The instrument consists of a temperature-controlled vacuum chamber sample environment, in which the UV–visible luminescence is collected from the point of interaction of ultrashort x-ray pulses with luminescent material and directed to a monochromator equipped with an ultrafast MCP-PMT detector operating in a photon-counting mode. The instrumental response function of the setup, determined by the duration of x-ray pulses (50 fs), optical path, and fast MCP-PMT response, was measured to 32 ps (FWHM) within the spectral range of 200–700 nm. In this paper, we present the results obtained under different operational conditions on the basis of three well-known scintillating samples, demonstrating that this instrument development for the scintillator community has established the foundation for ultrafast luminescence studies at FemtoMAX.
- Top Cited PapersOpen Access
- 17 September 2025
- Published by International Union of Crystallography (IUCr) in Journal of Synchrotron Radiation
- Vol. 32 (6) , 1539-1548
The P66 time-resolved VUV spectroscopy beamline at PETRA III storage ring of DESY
The paper presents a comprehensive description of the construction features of the P66 beamline at the PETRA III storage ring as well as the experimental possibilities offered by this unique facility to the research community. The beamline is dedicated to time-resolved photoluminescence spectroscopy experiments that require high flux, high energy resolution and pulsed excitation at ultrahigh vacuum conditions. The excitation photon energies available at the beamline cover the range from 3.7 to 40 eV with two Al- and Pt-coated diffraction gratings in normal incidence geometry. Two secondary monochromators equipped with several detectors are used to register the photoluminescence signal in the spectral range from 115 to 1200 nm. The pulsed nature of the synchrotron radiation at PETRA III allows the accumulation of luminescence decay kinetics within a time interval of 192 ns (timing mode) or 16 ns (brightness mode) with a time resolution of 130 ps. Time-resolved luminescence spectroscopy studies are performed using the method of time-correlated single photon counting. The paper also reviews recent advances, as well as the most common and important scientific cases of experimental research conducted at the beamline. Plans for the future development of the beamline, along with the expansion of experimental capabilities and the implementation of additional applications of the facility, are discussed.
- 17 September 2025
- Published by International Union of Crystallography (IUCr) in Journal of Synchrotron Radiation
- Vol. 32 (6) , 1539-1548
Top Cited PapersOpen AccessThe P66 time-resolved VUV spectroscopy beamline at PETRA III storage ring of DESY
The paper presents a comprehensive description of the construction features of the P66 beamline at the PETRA III storage ring as well as the experimental possibilities offered by this unique facility to the research community. The beamline is dedicated to time-resolved photoluminescence spectroscopy experiments that require high flux, high energy resolution and pulsed excitation at ultrahigh vacuum conditions. The excitation photon energies available at the beamline cover the range from 3.7 to 40 eV with two Al- and Pt-coated diffraction gratings in normal incidence geometry. Two secondary monochromators equipped with several detectors are used to register the photoluminescence signal in the spectral range from 115 to 1200 nm. The pulsed nature of the synchrotron radiation at PETRA III allows the accumulation of luminescence decay kinetics within a time interval of 192 ns (timing mode) or 16 ns (brightness mode) with a time resolution of 130 ps. Time-resolved luminescence spectroscopy studies are performed using the method of time-correlated single photon counting. The paper also reviews recent advances, as well as the most common and important scientific cases of experimental research conducted at the beamline. Plans for the future development of the beamline, along with the expansion of experimental capabilities and the implementation of additional applications of the facility, are discussed.
- 15 July 2025
- Published by Elsevier in Optical Materials
- Vol. 167
Phase dependent luminescence properties of Pr3+ doped BaLu2F8–BaLuF5 materials
- 15 July 2025
- Published by Elsevier in Optical Materials
- Vol. 167
Phase dependent luminescence properties of Pr3+ doped BaLu2F8–BaLuF5 materials
- 13 May 2025
- Published by Elsevier in Ceramics International
- Vol. 51 (21) , 34922-34931
Elucidating reaction mechanism by molten salt of potential rare-earth-free Zn2SiO4 UV-B emitter: Insights into morphology and emission features
- 13 May 2025
- Published by Elsevier in Ceramics International
- Vol. 51 (21) , 34922-34931
Elucidating reaction mechanism by molten salt of potential rare-earth-free Zn2SiO4 UV-B emitter: Insights into morphology and emission features
- 12 May 2025
- Published by Elsevier in Materials Research Bulletin
- Vol. 191
Crystal structure controlled energy transfer to Tb3+ in KTb(MoO4)2 and K5Tb(MoO4)4 crystals
- 12 May 2025
- Published by Elsevier in Materials Research Bulletin
- Vol. 191
Crystal structure controlled energy transfer to Tb3+ in KTb(MoO4)2 and K5Tb(MoO4)4 crystals
- Open Access
- 8 May 2025
- Published by American Chemical Society (ACS) in ACS Omega
- Vol. 10 (19) , 19817-19831
Correlating Structural Disorder and Pr3+ Emission Dynamics in Lu3Al2.5–xScxGa2.5O12 Crystals: A Comprehensive Structure–Property Investigation
This study explored the influence of Sc3+ ions incorporation on the structural, vibrational, luminescent, and scintillation properties of Pr3+-doped Lu3(Al, Sc)2.5Ga2.5O12 garnet crystals. Addressing the limited research on Sc-admixed and Pr3+ doped garnet systems, this work successfully demonstrated the crystallization of garnet crystals from the melt, overcoming the substantial atomic mismatch between Sc and Al while preserving the thermodynamic stability of the garnet phase. Importantly, Sc-admixing enhanced atomic homogeneity and allowed for increased doping concentrations of Pr3+ ions, which is crucial for tailoring the functional properties of advanced optical materials. The trap depths ranged from 1.63 eV (deep traps) to 0.22 eV (shallow traps) across all samples, with frequency factors predominantly between 1 × 107 and 1 × 1011 s–1, consistent with first-order thermoluminescent kinetics. From a materials design perspective, Sc3+ ions substitution induced beneficial host lattice disorder, enhancing the emission intensity of 4f15d11 → 4f2 interconfigurational and 4f2 → 4f2 intraconfigurational transitions. This effect highlighted the potential of Sc as a promising substituent for enhancing the luminescence intensity of rare earth elements. Synchrotron radiation experiments provided insights into the impact of Sc on band gap energy and energy transfer efficiency toward Pr3+ ions offering new opportunities for engineering scintillators and phosphors with tunable optical properties.
- 8 May 2025
- Published by American Chemical Society (ACS) in ACS Omega
- Vol. 10 (19) , 19817-19831
Open AccessCorrelating Structural Disorder and Pr3+ Emission Dynamics in Lu3Al2.5–xScxGa2.5O12 Crystals: A Comprehensive Structure–Property Investigation
This study explored the influence of Sc3+ ions incorporation on the structural, vibrational, luminescent, and scintillation properties of Pr3+-doped Lu3(Al, Sc)2.5Ga2.5O12 garnet crystals. Addressing the limited research on Sc-admixed and Pr3+ doped garnet systems, this work successfully demonstrated the crystallization of garnet crystals from the melt, overcoming the substantial atomic mismatch between Sc and Al while preserving the thermodynamic stability of the garnet phase. Importantly, Sc-admixing enhanced atomic homogeneity and allowed for increased doping concentrations of Pr3+ ions, which is crucial for tailoring the functional properties of advanced optical materials. The trap depths ranged from 1.63 eV (deep traps) to 0.22 eV (shallow traps) across all samples, with frequency factors predominantly between 1 × 107 and 1 × 1011 s–1, consistent with first-order thermoluminescent kinetics. From a materials design perspective, Sc3+ ions substitution induced beneficial host lattice disorder, enhancing the emission intensity of 4f15d11 → 4f2 interconfigurational and 4f2 → 4f2 intraconfigurational transitions. This effect highlighted the potential of Sc as a promising substituent for enhancing the luminescence intensity of rare earth elements. Synchrotron radiation experiments provided insights into the impact of Sc on band gap energy and energy transfer efficiency toward Pr3+ ions offering new opportunities for engineering scintillators and phosphors with tunable optical properties.
- 22 January 2025
- Published by Elsevier in Ceramics International
- Vol. 51 (12) , 15646-15653
A fluorozirconate compound TlZrF5 synthesised by a facile hydrothermal method and its characterization
- 22 January 2025
- Published by Elsevier in Ceramics International
- Vol. 51 (12) , 15646-15653
A fluorozirconate compound TlZrF5 synthesised by a facile hydrothermal method and its characterization
- 21 July 2023
- Published by American Physical Society (APS) in Physical Review Applied
- Vol. 20 (1) , 014047
Energy-Transfer Processes in Nonstoichiometric and Stoichiometric , , , , and -Codoped :YAG Transparent Ceramics: Toward High-Power and Warm-White Laser Diodes and LEDsTransparent light-converting (YAG:) ceramics have become promising materials for advanced light-emitting diode and laser-driven white-light-generation technology. However, their functionality is highly dependent on factors such as structural quality, uniformity of dopant distribution, the presence of defects, and the cost of fabrication. The emission of YAG: ceramics remains thermally stable when high-power-density laser excitation is uniformly spread over the entire surface area of the ceramics due to light-scattering processes. The creation of light-scattering centers that can provide homogeneous white light in ceramics is crucial. One of the drawbacks of YAG: as a material for converting ultraviolet emission into white light is the lack of a red component, which results in cold light and a low color rendering index. Therefore, the codoping of YAG: with red-emitting ions (, , , , and ) was carried out and slight nonstoichiometry was induced in the present study to improve the photoconversion parameters. The phase purity of the studied ceramics was analyzed using powder x-ray diffraction and SEM combined with energy-dispersive spectroscopy (EDS). EDS studies revealed that nonstoichiometric ceramics contained phase inclusions that acted as light-scattering centers. Optical transmittance and absorption spectra measurements revealed the presence of light-scattering centers imposed by phase inclusions and nanodefects related to perturbations of the local lattice structure by dopants. EDS mapping and photoluminescence analysis showed the formation of -, ( is a transition metal) pairs and the availability of energy transfer between the pair-forming ions. Intrinsic thermal quenching of luminescence started above 400 K. The nonstoichiometric YAG: sample showed luminescence stability up to 650 K with a luminous efficacy of 198 lm/W. The photoconversion parameters of the transparent ceramic packaged with a blue light-emitting diode or a laser diode were compared. It was shown that the color temperature of ceramic emissions could be controlled by the spectral width of the excitation beam. Thermally stimulated luminescence was applied to investigate the deep trapping centers imposed by the codopants. A detailed EPR study revealed the presence of , , and centers.- 21 July 2023
- Published by American Physical Society (APS) in Physical Review Applied
- Vol. 20 (1) , 014047
Energy-Transfer Processes in Nonstoichiometric and Stoichiometric , , , , and -Codoped :YAG Transparent Ceramics: Toward High-Power and Warm-White Laser Diodes and LEDsTransparent light-converting (YAG:) ceramics have become promising materials for advanced light-emitting diode and laser-driven white-light-generation technology. However, their functionality is highly dependent on factors such as structural quality, uniformity of dopant distribution, the presence of defects, and the cost of fabrication. The emission of YAG: ceramics remains thermally stable when high-power-density laser excitation is uniformly spread over the entire surface area of the ceramics due to light-scattering processes. The creation of light-scattering centers that can provide homogeneous white light in ceramics is crucial. One of the drawbacks of YAG: as a material for converting ultraviolet emission into white light is the lack of a red component, which results in cold light and a low color rendering index. Therefore, the codoping of YAG: with red-emitting ions (, , , , and ) was carried out and slight nonstoichiometry was induced in the present study to improve the photoconversion parameters. The phase purity of the studied ceramics was analyzed using powder x-ray diffraction and SEM combined with energy-dispersive spectroscopy (EDS). EDS studies revealed that nonstoichiometric ceramics contained phase inclusions that acted as light-scattering centers. Optical transmittance and absorption spectra measurements revealed the presence of light-scattering centers imposed by phase inclusions and nanodefects related to perturbations of the local lattice structure by dopants. EDS mapping and photoluminescence analysis showed the formation of -, ( is a transition metal) pairs and the availability of energy transfer between the pair-forming ions. Intrinsic thermal quenching of luminescence started above 400 K. The nonstoichiometric YAG: sample showed luminescence stability up to 650 K with a luminous efficacy of 198 lm/W. The photoconversion parameters of the transparent ceramic packaged with a blue light-emitting diode or a laser diode were compared. It was shown that the color temperature of ceramic emissions could be controlled by the spectral width of the excitation beam. Thermally stimulated luminescence was applied to investigate the deep trapping centers imposed by the codopants. A detailed EPR study revealed the presence of , , and centers.