Members of the PbFCI-Type Family: Possible Candidates for Room-Temperature Photochemical Hole Burning

We report on crystal growth and about physico-chemical studies on SryBa1-yFClxBr1-x (y = 0, 0.5, and 1) compounds doped with Sm. Persistent spectral hole burning at 300 K is further reported on Sr0.5Ba0.5FCl0.5Br0.5:Sm single crystals

Graphene functionalised by laser ablated V2O5 as highly sensitive NH3 sensor

Graphene has been recognized as a promising gas sensing material. The response of graphene-based sensors can be radically improved by introducing defects in graphene using, e. g., metal or metal oxide nanoparticles. We have functionalised CVD grown, single layer graphene by applying pulsed laser deposition (PLD) of V2O5 which resulted in a thin V2O5 layer on graphene with average thickness of ~0.6 nm. According to Raman analysis, PLD process also induced defects in graphene. Compared to unmodified graphene, the obtained chemiresistive sensor showed considerable improvement of sensing ammonia at room temperature. In addition, also the response time, sensitivity and reversibility were essentially enhanced due to graphene functionalisation by laser deposited V2O5. This can be explained by increased surface density of gas adsorption sites introduced by high energy atoms in laser ablation plasma and formation of nanophase boundaries between deposited V2O5 and graphene.Comment: 22 pages, 6 figure

Structure-Dependent CO 2

Rare earth oxycarbonates are potential candidate materials for constructing simple and low-cost chemiresistive sensors for monitoring carbon dioxide (CO2) gas in the living and working environment for personal comfort and health reasons. Also, measurement of CO2 concentrations is needed in many industrial processes. Specifically, sol-gel made nanoparticles of Nd and La oxycarbonates have been studied previously as novel CO2 gas sensor materials. In this paper, pulsed laser deposition of La oxycarbonate (La2O2CO3) thin films was studied and structural properties of obtained thin films were characterized. Also, CO2 gas sensing ability of synthesized films was evaluated. The films deposited under CO2 partial pressure in various conditions were all Raman amorphous. In situ or ex situ annealing procedure at high CO2 partial pressure was needed for obtaining crystalline La2O2CO3 films, whereby hexagonal and monoclinic polymorphs were obtained in ex situ and in situ processes, respectively. Sensor structure, made using in situ process, was sensitive to CO2 gas and showed relatively fast response and recovery characteristics

Semiquantitative Classification of Two Oxidizing Gases with Graphene-Based Gas Sensors

Miniature and low-power gas sensing elements are urgently needed for a portable electronic nose, especially for outdoor pollution monitoring. Hereby we prepared chemiresistive sensors based on wide-area graphene (grown by chemical vapor deposition) placed on Si/Si3N4 substrates with interdigitated electrodes and built-in microheaters. Graphene of each sensor was individually functionalized with ultrathin oxide coating (CuO-MnO2, In2O3 or Sc2O3) by pulsed laser deposition. Over the course of 72 h, the heated sensors were exposed to randomly generated concentration cycles of 30 ppb NO2, 30 ppb O3, 60 ppb NO2, 60 ppb O3 and 30 ppb NO2 + 30 ppb O3 in synthetic air (21% O2, 50% relative humidity). While O3 completely dominated the response of sensors with CuO-MnO2 coating, the other sensors had comparable sensitivity to NO2 as well. Various response features (amplitude, response rate, and recovery rate) were considered as machine learning inputs. Using just the response amplitudes of two complementary sensors allowed us to distinguish these five gas environments with an accuracy of ~ 85%. Misclassification was mostly due to an overlap in the case of the 30 ppb O3, and 30 ppb O3 + 30 ppb NO2 responses, and was largely caused by the temporal drift of these responses. The addition of recovery rates to machine learning input variables enabled us to very clearly distinguish different gases and increase the overall accuracy to ~94%

Phase stability and oxygen-sensitive photoluminescence of ZrO2:Eu,Nb nanopowders

This work was supported by institutional research funding ( IUT34-27 and IUT2-14 ) of the Estonian Ministry of Education and Research .We studied structure and oxygen-sensitive photoluminescence (PL) of ZrO2:Eu,Nb nanocrystalline powders synthesized via a sol-gel route and heat-treated up to 1200 °C. The material containing only 2 at% Eu3+ was predominantly monoclinic, whereas 8 at% of Eu3+ stabilized tetragonal phase. Comparable amount of niobium co-doping effectively suppressed the formation of tetragonal phase. PL of Eu3+ ions was observed under direct excitation at 395 nm. PL decay kinetics showed that the luminescence was partially quenched, depending on doping concentrations and ambient atmosphere. At 300 °C, the PL intensity of all samples systematically responded (with up to 70% change) to changing oxygen content in the O2/N2 mixture at atmospheric pressure. At low doping levels, the dominant factor controlling the PL intensity was an energy transfer from excited PL centers to randomly distributed defects in the ZrO2 lattice. We argue that the charge transfer between the defects and adsorbed oxygen molecules alters the ability of the defects to quench Eu3+ luminescence. At high doping levels, another type of sensor response was observed, where some Eu3+ emitters are effectively switched on or off by the change of ambient gas. A remarkable feature of the studied material is a reversing of the sensor response with the variation of the Nb concentration.Estonian Ministry of Education and Research IUT34-27 and IUT2-14; Institute of Solid State Physics, University of Latvia as the Center of Excellence has received funding from the European Union’s Horizon 2020 Framework Programme H2020-WIDESPREAD-01-2016-2017-TeamingPhase2 under grant agreement No. 739508, project CAMART

Room temperature persistent spectral hole burning in Sm-dopedSrFCl1/2Br1/2 mixed crystals

Two-photon persistent hole burning is observed at T = 296 K in 5D1–7F0 and 5D0–7F0 transitions of Sm2+ ions in substitutionally disordered SrFCl1/2 single crystals, showing the ratio of inhomogeneous to homogeneous linewidth of 20 ÷ 25. The minimum hole widths of 3.5 cm-1 and 2.6 cm-1, respectively, were determined for these transitions. In fact, the applicability of persistent spectral hole burning, known as a low-temperature high-resolution spectroscopic method and a potential basis for the use of a new–spectral–dimension in optical data storage and processing, is demonstrated for the first time at room temperature in inorganic materials

f-f and f-d transition interference in Sm2+:SrFCl

The 5D3(4f6)-7F0(4f6) transition of Sm2+ in SrFCl is found to be anomalously strong and it exhibits an asymmetric line shape, which is interpreted in terms of resonant interaction between the 5D3 excited state and the vibronic levels of a low-lying 4f55d electronic state. The electronic coupling strength is estimated to be of the order of 100 cm-1. The symmetry species of interacting levels are identified, and the possibility of an E×(b1+b2) type of Jahn-Teller effect in the 4f55d state is discussed

High-temperature spectral hole burning on Sm-doped single crystal materials of PbFCl family

Basic properties relevant to spectral hole burning (homogeneous and inhomogeneous spectral broadening, hole burning and filling mechanisms) are investigated in MeIyMeII1 − yFXIxXII1 − x: Sm2+ (Me = Ca,Sr,Ba; X = Cl,Br,I) single crystals. The relations between the spectral characteristics of 5D0,1-7F0 transitions and the material structure are described. Hole stability is investigated up to 430 K and is shown to be determined by ionic diffusion