David John
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
David John has a total of 102 co-authors. Here are the top co-authors by number of shared publications:
Maksym Buryi
4 shared publicationsKarol Bartosiewicz
3 shared publicationsAkira Yoshikawa
Institute for Materials Research, Tohoku University, 2-1-1 Katahira Aoba-ku, Sendai, Miyagi 9808577, Japan
2 shared publicationsGabriel Buse
2 shared publicationsJakub Volf
Institute of Physics, Academy of Sciences of the Czech Republic, Na Slovance 1999/2, 18200, Prague, Czech Republic
2 shared publicationsJan Zich
2 shared publications
Latest Publications
- Open Access
- 10 June 2026
- Published by Elsevier in Optical Materials
- Vol. 178
Ytterbium charge state and stabilization in the Ba(Ca)F2 host by electron paramagnetic resonance and infrared photoluminescence
- 10 June 2026
- Published by Elsevier in Optical Materials
- Vol. 178
Open AccessYtterbium charge state and stabilization in the Ba(Ca)F2 host by electron paramagnetic resonance and infrared photoluminescence
- Open Access
- 30 March 2026
- Published by American Chemical Society (ACS) in ChemRxiv
Ytterbium charge state and stabilization in the Ba(Ca)F2 host by electron paramagnetic resonance and infrared photoluminescence
Lanthanide-doped fluorides are promising materials for advanced photonic and quantum applications due to their wide bandgap, low phonon energy, and chemical stability. In this work, we investigate the influence of the host cation, Ba2+ versus Ca2+, on the charge state, local environment, and incorporation behavior of ytterbium (Yb) dopants in BaF2 and CaF2 single crystals at low doping levels (0.05–0.2 mol%). Using a combination of X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), electron paramagnetic resonance (EPR), transmittance, and infrared photoluminescence (IR PL), we explore how host lattice properties affect the stabilization of Yb3+ and Yb2+ ions. XRD confirmed cubic phase purity and lattice parameter stability in both hosts, while XPS revealed surface chemical composition variations associated with charge-compensating defects and trace impurities. EPR spectra indicated that BaF2 favored perturbed Yb3+ environments with increasing dopant levels, while CaF2 maintained predominantly unperturbed sites, suggesting a more favorable ionic match for Yb2+. Photothermal deflection spectroscopy (PDS) and IR PL results showed host-specific optical responses, with CaF2 exhibiting crystal-field splitting and broader local field effects. These findings highlight the critical role of host cation identity in governing Yb charge state and lattice interaction, offering valuable insights for optimizing rare-earth-doped fluoride crystals in laser, scintillator, and quantum device applications.
- 30 March 2026
- Published by American Chemical Society (ACS) in ChemRxiv
Open AccessYtterbium charge state and stabilization in the Ba(Ca)F2 host by electron paramagnetic resonance and infrared photoluminescence
Lanthanide-doped fluorides are promising materials for advanced photonic and quantum applications due to their wide bandgap, low phonon energy, and chemical stability. In this work, we investigate the influence of the host cation, Ba2+ versus Ca2+, on the charge state, local environment, and incorporation behavior of ytterbium (Yb) dopants in BaF2 and CaF2 single crystals at low doping levels (0.05–0.2 mol%). Using a combination of X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), electron paramagnetic resonance (EPR), transmittance, and infrared photoluminescence (IR PL), we explore how host lattice properties affect the stabilization of Yb3+ and Yb2+ ions. XRD confirmed cubic phase purity and lattice parameter stability in both hosts, while XPS revealed surface chemical composition variations associated with charge-compensating defects and trace impurities. EPR spectra indicated that BaF2 favored perturbed Yb3+ environments with increasing dopant levels, while CaF2 maintained predominantly unperturbed sites, suggesting a more favorable ionic match for Yb2+. Photothermal deflection spectroscopy (PDS) and IR PL results showed host-specific optical responses, with CaF2 exhibiting crystal-field splitting and broader local field effects. These findings highlight the critical role of host cation identity in governing Yb charge state and lattice interaction, offering valuable insights for optimizing rare-earth-doped fluoride crystals in laser, scintillator, and quantum device applications.
- Open Access
- 6 June 2025
- Published by Royal Society of Chemistry (RSC) in Journal of Materials Chemistry C
- Vol. 13 (27) , 13691-13712
Shaping scintillation and UV-VIS-NIR luminescence properties through synergistic lattice disordered engineering and exciton-mediated energy transfer in Pr 3+ -doped Lu 1.5 Y 1.5 Al 5− x Sc x O 12 ( x = 0.0–2.0) garnets
Substituting Sc 3+ for Al 3+ in Pr 3+ -doped Lu 1.5 Y 1.5 Al 5− x Sc x O 12 crystals enhances the Pr 3+ emission across the UV-Vis-NIR spectral range. This enhancement is attributed to an efficient Sc 3+ → Pr 3+ energy transfer and increased structural disorder.
- 6 June 2025
- Published by Royal Society of Chemistry (RSC) in Journal of Materials Chemistry C
- Vol. 13 (27) , 13691-13712
Open AccessShaping scintillation and UV-VIS-NIR luminescence properties through synergistic lattice disordered engineering and exciton-mediated energy transfer in Pr 3+ -doped Lu 1.5 Y 1.5 Al 5− x Sc x O 12 ( x = 0.0–2.0) garnets
Substituting Sc 3+ for Al 3+ in Pr 3+ -doped Lu 1.5 Y 1.5 Al 5− x Sc x O 12 crystals enhances the Pr 3+ emission across the UV-Vis-NIR spectral range. This enhancement is attributed to an efficient Sc 3+ → Pr 3+ energy transfer and increased structural disorder.
- Open Access
- 1 January 2025
- Published by TANGER Ltd.
- Vol. 2024, 33-40
comparison of Lu3Al5O12:Ce(Er) bulk and nano single crystals
- 1 January 2025
- Published by TANGER Ltd.
- Vol. 2024, 33-40
Open Accesscomparison of Lu3Al5O12:Ce(Er) bulk and nano single crystals
- 20 May 2024
- Published by Elsevier in Applied Materials Today
- Vol. 38
On the potential of Transparent Rare-Earth-Free ZnAl2O4 Ceramics targeted at the UV-C to UV-B emission
- 20 May 2024
- Published by Elsevier in Applied Materials Today
- Vol. 38
On the potential of Transparent Rare-Earth-Free ZnAl2O4 Ceramics targeted at the UV-C to UV-B emission
- Open Access
- 25 September 2023
- Published by Institute of Archaeology of the CAS - Prague, v.v.i. in Archeologické rozhledy
- Vol. 75 (1) , 40-67
Možnosti a limity radiouhlíkového datování se zaměřením na netypické archeologické vzorky
Radiocarbon dating is an established method that helps to determine the absolute age of archaeological finds. This topical review presents the basic principles of the radiocarbon method, conventions for selecting samples from archaeological contexts, how to handle samples before sending them to the radiocarbon laboratory, laboratory methods for sample preparation, the AMS measurement procedure, and the cali bration of results. Factors that limit the results of radiocarbon dating, particularly radiocarbon plateaux and the reservoir effect, are explained along with the ways how to recognise and eliminate their influence. The main aim of the paper is to critically evaluate the application of radiocarbon dating to less common archaeological samples (lipids preserved in the pores of pottery, charred bone, dental calculus, iron objects and iron slags, mortar, pollen and phytolith concentrates extracted from sediments or soils). Their dating opens new possibilities for the chronological determination of past natural and cultural processes or events. radiocarbon dating-lipids-charred bones-dental calculus-iron-mortar-pollen and phytolith con centrates
- 25 September 2023
- Published by Institute of Archaeology of the CAS - Prague, v.v.i. in Archeologické rozhledy
- Vol. 75 (1) , 40-67
Open AccessMožnosti a limity radiouhlíkového datování se zaměřením na netypické archeologické vzorky
Radiocarbon dating is an established method that helps to determine the absolute age of archaeological finds. This topical review presents the basic principles of the radiocarbon method, conventions for selecting samples from archaeological contexts, how to handle samples before sending them to the radiocarbon laboratory, laboratory methods for sample preparation, the AMS measurement procedure, and the cali bration of results. Factors that limit the results of radiocarbon dating, particularly radiocarbon plateaux and the reservoir effect, are explained along with the ways how to recognise and eliminate their influence. The main aim of the paper is to critically evaluate the application of radiocarbon dating to less common archaeological samples (lipids preserved in the pores of pottery, charred bone, dental calculus, iron objects and iron slags, mortar, pollen and phytolith concentrates extracted from sediments or soils). Their dating opens new possibilities for the chronological determination of past natural and cultural processes or events. radiocarbon dating-lipids-charred bones-dental calculus-iron-mortar-pollen and phytolith con centrates
- Open Access
Influence of Golden Nanoparticles on the Incorporation of Eu2+ into BaI2 and Defect Concentration
Conjugated BaI2:Eu (5 at.%) nanocrystalline particles were synthesized, decorated with golden nanoparticles (GNP). GNP demonstrated some hydrophilic effect, leading to the BaI2·H2O phase creation. The Eu2+ luminescence intensity was reduced according to the GNP content. This was due to the decreased number of Eu2+ ions in the BaI2, most probably, arising from the Au substitution for Ba competing with Eu. Moreover, the decay time of luminescence was decreased upon GNP content. This was explained by the moderation of negative charge in the GNP, leading to the repulsion with an electron in the excited Eu2+.
Open AccessInfluence of Golden Nanoparticles on the Incorporation of Eu2+ into BaI2 and Defect Concentration
Conjugated BaI2:Eu (5 at.%) nanocrystalline particles were synthesized, decorated with golden nanoparticles (GNP). GNP demonstrated some hydrophilic effect, leading to the BaI2·H2O phase creation. The Eu2+ luminescence intensity was reduced according to the GNP content. This was due to the decreased number of Eu2+ ions in the BaI2, most probably, arising from the Au substitution for Ba competing with Eu. Moreover, the decay time of luminescence was decreased upon GNP content. This was explained by the moderation of negative charge in the GNP, leading to the repulsion with an electron in the excited Eu2+.