Influence of tin doping on the liquefied petroleum gas and humidity sensing properties of NiO nanoparticles

This research deals with study of enhanced liquefied petroleum gas (LPG) and humidity sensing properties of Sn-doped NiO pellets synthesized by chemical precipitation route. XRD, FTIR, SEM, and UV–Vis studies were employed to understand the effect of Sn doping on the structural, morphological, and optical properties of the NiO nanoparticles. XRD results revealed that doping of tin in NiO had a significant impact on the crystallite size, peak intensity, strain, lattice parameter, etc. The calculated crystallite size of pure and 3 mol% doped NiO was 33.2 nm and 13.3 nm, respectively. SEM micrographs revealed that the structure of the samples was irregular spheres and non-homogeneous. The dependence of LPG sensing properties on the structural and surface morphological properties has also been studied. The maximum response of 30.46% to 2.0 vol% of LPG was observed at room temperature (300 K). The same sample also shows high humidity sensing response of 87.11% towards 90% RH. Graphic abstract

Sodium-Ion Conductivity and Humidity-Sensing Properties of Na2O-MoO3-P2O5 Glass-Ceramics

A series of glass-ceramics were prepared by heat-treatments of 40Na2O-30MoO3-30P2O5 (in mol%) glass in a temperature range from 380 (Tg) to 490 °C (Tc) and for 1–24 h. The prepared glass-ceramics contain from 2 to 25 wt.% of crystalline NaMoO2PO4. The sodium-ion conductivity in these materials decreases up to one order of magnitude with an increase in the degree of crystallization due to the immobilization of sodium ions in crystalline NaMoO2PO4. The transport of sodium ions in these materials occurs primarily through the dominant continuous glassy phase, and it is weakly affected by the sporadically distributed crystalline grains. However, the prepared glass-ceramics exhibit high proton conductivity in a humid atmosphere and remarkable humidity-sensing properties; this could be related to crystalline NaMoO2PO4, which provides sites for water adsorption. The glass-ceramic prepared at 450 °C for 24 h shows the best humidity-sensing performance among all samples, showing an increase in proton conductivity for more than seven orders of magnitude with the increase in relative humidity from 0% to 95%. Under a highly humid atmosphere (95% relative humidity and 25 °C), the proton conductivity of this glass-ceramic reaches 5.2 × 10−3 (Ω cm)−1. Moreover, the electrical response of these materials on the change in the relative humidity is linear and reversible in the entire range of the relative humidity, which indicates that they are novel promising candidates for application as humidity sensors.

Humidity sensing properties of spray deposited Fe doped TiO2 thin film

In the present work, ferrite (Fe) doped TiO2 thin films with different volume percentage (vol%) were synthesized using a spray pyrolysis technique. The effect of Fe doping on structural properties such as crystallite size, texture coefficient, microstrain, dislocation densities etc. were evaluated from the X ray diffratometry (XRD) data. XRD data revealed a polycrystalline anatase TiO2 phase for sample synthesized up to 2 vol% and mixed anatase and rutile crystalline phase for sample synthesized at 4 vol% Fe doped TiO2. The crystalline size was observed to decrease with increase in Fe dopant vol% and also other structural parameters changes with Fe dopant percentage. In the present work, electrical resistance was observed to decrease with a rise in Fe dopant vol% and temperature of the sample. Thermal properties like temperature coefficient of resistance and activation energy also showed strong correlation with Fe dopant vol%. Humidity sensing properties of the synthesized sample altered with a change in Fe dopant vol%. In the present paper, maximum sensitivity of about 88.7% for the sample synthesized with 2 vol% Fe doped TiO2 and also the lowest response and recovery time of about 52 and 3 s were reported for the same sample.

Electrical and Humidity-Sensing Properties of EuCl2, Eu2O3 and EuCl2/Eu2O3 Blend Films

Impedance-type humidity sensors based on EuCl2, Eu2O3 and EuCl2/Eu2O3 blend films were fabricated. The electrical properties of the pure EuCl2 and Eu2O3 films and EuCl2/Eu2O3 blend film that was blended with different amounts of EuCl2 were investigated as functions of relative humidity. The influences of the EuCl2 to the humidity-sensing properties (sensitivity and linearity) of the EuCl2/Eu2O3 blend film were thus elucidated. The impedance-type humidity sensor that was made of a 7 wt% EuCl2/Eu2O3 blend film exhibited the highest sensitivity, best linearity, a small hysteresis, a fast response time, a small temperature coefficient and long-term stability. The complex impedance plots were used to elucidate the role of ions in the humidity-sensing behavior of the EuCl2/Eu2O3 blend film.

Humidity-Sensing Properties of an 1D Antiferromagnetic Oxalate-Bridged Coordination Polymer of Iron(III) and Its Temperature-Induced Structural Flexibility

A novel one-dimensional (1D) oxalate-bridged coordination polymer of iron(III), {[NH(CH3)(C2H5)2][FeCl2(C2O4)]}n (1), exhibits remarkable humidity-sensing properties and very high proton conductivity at room temperature (2.70 × 10−4 (Ω·cm)−1 at 298 K under 93% relative humidity), in addition to the independent antiferromagnetic spin chains of iron(III) ions bridged by oxalate groups (J = −7.58(9) cm−1). Moreover, the time-dependent measurements show that 1 could maintain a stable proton conductivity for at least 12 h. Charge transport and magnetic properties were investigated by impedance spectroscopy and magnetization measurements, respectively. Compound 1 consists of infinite anionic zig-zag chains [FeCl2(C2O4)]nn− and interposed diethylmethylammonium cations (C2H5)2(CH3)NH+, which act as hydrogen bond donors toward carbonyl oxygen atoms. Extraordinarily, the studied coordination polymer exhibits two reversible phase transitions: from the high-temperature phase HT to the mid-temperature phase MT at T ~213 K and from the mid-temperature phase MT to the low-temperature phase LT at T ~120 K, as revealed by in situ powder and single-crystal X-ray diffraction. All three polymorphs show large linear thermal expansion coefficients.