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Romana Kucerkova

Publications and source records attributed to Romana Kucerkova.

5 recordsLinked to original sources

Optimized Photoemission from Organic Molecules in 2D Layered Halide Perovskites

In recent years, hybrid organic-inorganic metal halides have been at the forefront of materials research. Typically, the functional (e.g., optoelectronic) properties of hybrid halides are derived from the inorganic structural part, whereas the organic structural units can add extra advantages in terms of stability, rigidity, and processability. Here, we report the design, synthesis, and characterization of two new hybrid materials in which the outstanding photophysical properties originate from the organic structural part. The new compounds, (C15H16N)2CdCl4 and ((Br)C15H15N)2CdCl4, have 2D layered Ruddlesden-Poppertype perovskite structures. These hybrids are blue-white light emitters just like their corresponding pure organic salts, but with much improved emission efficiencies. Optical spectroscopy and density functional theory (DFT) studies confirm that photoemission comes from the trans-stilbene organic cations. The photoluminescence quantum yield (PLQY) values of these new materials are among the highest known, 50.83 % and 26.60 % for (C15H16N)2CdCl4 and ((Br)C15H15N)2CdCl4, respectively. This is up to a 5-fold increase as compared to the light emission efficiency of the precursor salt C15H16NCl (PLQY of 10.33 %). Alongside their outstanding optical properties, their environmental and thermal stability allow their consideration for potential practical applications such as radiation detection. This work shows that hybrid metal halides can be compositionally and structurally engineered to have highly efficient photoemission originating from the organic components for fast scintillation applications.

cond-mat.mtrl-sci↗

Bridgman method grown $Cs_2Li_3I_5$: an inter-alkali metal scintillator with high lithium content

In this study, we report on the growth of ternary caesium lithium iodide ($Cs_2Li_3I_5$, CLI) bulk crystals, both undoped and doped with thallium (Tl) and indium (In), using the miniaturised vertical Bridgman method (mVB). X-ray Powder Diffraction (XRPD) confirmed the presence of the ternary CLI phase in all three crystals, with CLI : In appearing homogeneous structure-wise throughout the entire ingot. Measurements of radioluminescence (RL), photoluminescence emission (PL), photoluminescence excitation (PLE) spectra, and photoluminescence decay kinetics (PL decay) demonstrated that the primary luminescence centers originate from the matrix itself. When doped with thallium, the efficiency of the luminescence was significantly increased. Furthermore, CLI : Tl and CLI : In crystals exhibited emission spectra similar to those of their doped caesium iodide counterparts, CsI : Tl and CsI : In, respectively. The main component of the PL decay was 523 ns, 557 ns, and 554 ns for the undoped, Tl+-doped, and In+-doped crystals, respectively. It is worthy of note that only CLI : Tl exhibited a single exponential decay. Differential Scanning Calorimetry (DSC) measurements revealed two endothermic peaks corresponding to the eutectic and liquidus temperature for CLI and CLI : In, indicating that this ternary compound has a congruent melting behaviour. Finally, the melting point of CLI was estimated to be approximately 220 °C.

cond-mat.mtrl-sci↗

Ultraviolet cross-luminescence in ternary chlorides of alkali and alkaline-earth metals

After the discovery of a cross-luminescence (CL) in BaF2 in 1982, a large number of CL scintillators were investigated. However, no CL scintillator superior to BaF2 has been discovered, and the research of CL scintillators has subsided. Recent technological development in medical imaging and high-energy physics created a new demand for ultra-fast scintillators further supported by the development of UV-sensitive semiconductor photodetectors. As a consequence, renewed interest in CL scintillators appeared. To satisfy the requirements of fast timing applications high photo-detection efficiency, e. i. a good spectral match between the scintillator and photodetector must be achieved. Cesium-based ternary chlorides could provide a red-shift (~1.5 eV) of CL towards the sensitive region of the photodetector (PMT or SiPM) while keeping light output and timing characteristics comparable to BaF2.

physics.ins-det↗

Growth and Spectroscopic Properties of Pr$^{3+}$ Doped Lu$_2$S$_3$ SingleCrystals

For the first time Lu$_2$S$_3$ (undoped and Pr-doped) single crystals were successfully grown from melt using micro-pulling-down (mPD) technique. Customization of halide mPD apparatus allowed us to grow rod-shaped (Ø2 mm and length around 20 mm) crystals of Lu$_2$S$_3$ with high melting temperature (~1750 $^\circ$C). X-ray powder diffraction revealed that the grown crystals exhibit the ε-Lu$_2$S$_3$ crystal structure ($α$-Al$_2$O$_3$ type, space group R-3c). Optical and scintillation properties of both the undoped and Pr$^{3+}$ doped Lu$_2$S$_3$ were investigated. Fast 5d-4f Pr$^{3+}$ luminescence was observed in both photoluminescence and radioluminescence spectra. The presented technology is an effective tool for the exploration of a large family of high-melting sulfides. Such materials show promise for application as scintillators, active laser media, and optoelectronic components.

cond-mat.mtrl-sci↗

Temperature dependence and quenching characteristics of (La, Gd)$_2$Si$_2$O$_7$ scintillators at various Ce concentrations

We investigated the thermal stability of scintillation and the luminescence performances of (La, Gd)${}_{2}$Si${}_{2}$O${}_{7}$ single crystals at various Ce concentrations. We prepared (La${}_{0.25-x}$, Ce${}_{x}$, Gd${}_{0.75}$)${}_{2}$Si${}_{2}$O${}_{7}$ (x = 0.0001, 0.001, 0.005, 0.01, 0.02, 0.05, and 0.1; unit: molar concentration) single crystals by the Czochralski and micro-pulling-down methods. With increasing Ce concentration, the photoluminescence emission and photoluminescence excitation spectral bands shifted to low energies and the activation energy $\mathrm{Δ}E$ for thermal quenching decreased. For Ce $\mathrm{<}$ 0.5 at.% samples, the photoluminescence emission background value calculated in the exponential approximation started to increase at temperatures greater than 320 K, which is probably because of Ce${}^{3+}$ 5$\textit{d}$ excited-state ionization. However, the effect was weaker for the Ce $\ge $ 0.5% samples, which may indicate a comparatively larger contribution from other nonradiative relaxations. Thus the main reason for the thermal quenching of the Ce${}^{3+}$ emission in (La, Gd)${}_{2}$Si${}_{2}$O${}_{7}$ is the combination of the 5$\textit{d}$1 excited-state ionization and nonradiative relaxation via thermally excited crossover from the 5$\textit{d}$ excited state to the 4$\textit{f}$ ground state. The temperature dependence of the scintillation light yield was similar irrespective of the Ce concentration, with Ce 1.0% exhibiting the best performance within the temperature range 300 K to 450 K.

cond-mat.mtrl-sci↗