perovskite and titanium-dioxide

The energy conversion efficiency (ECE) (η), current density (

Topics: Calcium Compounds; Oxides; Solar Energy; Titanium

A range of solution-processed organic and hybrid organic-inorganic solar cells, such as dye-sensitized and bulk heterojunction organic solar cells have been intensely developed recently. TiO

Topics: Adsorption; Calcium Compounds; Density Functional Theory; Electric Power Supplies; Electronics; Electrons; Nanostructures; Optics and Photonics; Oxides; Solar Energy; Sunlight; Titanium

Sorption of chemical substances to nanoparticles (NPs) in the aqueous phase strongly influences NP physicochemisty, and investigations of these complex interactions can provide important insights into the environmental fate of NPs. The objective of the present study was to use differences in copper (Cu) bioavailability to investigate aqueous-phase sorption with NPs that had different physicochemical characteristics (silicon [Si], perovskite, and titanium dioxide NPs [TiO

Topics: Adsorption; Animals; Biological Availability; Calcium Compounds; Chlorella vulgaris; Copper; Gene Expression Regulation; Larva; Metallothionein; Nanoparticles; Oxides; Surface Properties; Titanium; Water; Water Pollutants, Chemical; Zebrafish

Nano-structured hydrogen titanate and sodium hydrogen titanate layers were formed when Ti metal was treated with H

Topics: Biocompatible Materials; Calcium; Hot Temperature; Hydrogen Peroxide; Sodium Hydroxide; Titanium

This work reports the first synthesis and characterization of a ferroelectric perovskite oxide-based heterostructure as well as its application for photoelectrochemical (PEC) bioanalytical purposes. Specifically, exemplified by [KNbO

Topics: Calcium Compounds; Electrochemical Techniques; Ferrous Compounds; Microscopy, Electron, Scanning; Microscopy, Electron, Transmission; Nanotubes; Oxides; Photochemical Processes; Spectrum Analysis, Raman; Titanium; X-Ray Diffraction

High quality electron-transport layer (ETL) with superior optical and electrical properties is an essential part in high efficient perovskite solar cells (PSCs). In this work, SiW

Topics: Calcium Compounds; Electric Conductivity; Microscopy, Electron, Scanning; Oxides; Silicon; Spectroscopy, Fourier Transform Infrared; Thermogravimetry; Titanium; Tungsten; X-Ray Diffraction

It is commonly believed that excess PbI

Topics: Calcium Compounds; Iodides; Lead; Methylamines; Oxides; Titanium

Incorporating appropriate plasmonic nanostructures into photovoltaic (PV) systems is of great utility for enhancing photon absorption and thus improving device performance. Herein, the successful integration of plasmonic gold nanostars (AuNSs) into mesoporous TiO

Topics: Calcium Compounds; Electric Power Supplies; Electrodes; Gold; Models, Molecular; Molecular Conformation; Nanostructures; Oxides; Porosity; Solar Energy; Titanium

Device scale-up and long-term stability constitute two major hurdles that the emerging perovskite solar technology will have to overcome before commercialization. Here, a comparative study was performed between ZnO and TiO2 electron-selective layers, two materials that allow the low-temperature processing of perovskite solar cells on polymer substrates. Although the use of TiO2 is well established on glass substrates, ZnO was chosen because it can be readily printed at low temperature and offers the potential for the large-scale roll-to-roll manufacturing of flexible photovoltaics at a low cost. However, a rapid degradation of CH3 NH3 PbI3 was observed if it was deposited on ZnO, therefore, the influence of the perovskite film preparation conditions on its morphology and degradation kinetics was investigated. This study showed that CH3 NH3 PbI3 could withstand a higher temperature on TiO2 than ZnO and that TiO2-based perovskite devices were more stable than their ZnO analogues.

Topics: Calcium Compounds; Electric Power Supplies; Microscopy, Electron, Scanning; Oxides; Polymers; Solar Energy; Titanium; X-Ray Diffraction; Zinc Oxide

[70]Fullerene is presented as an efficient alternative electron-selective contact (ESC) for regular-architecture perovskite solar cells (PSCs). A smart and simple, well-described solution processing protocol for the preparation of [70]- and [60]fullerene-based solar cells, namely the fullerene saturation approach (FSA), allowed us to obtain similar power conversion efficiencies for both fullerene materials (i.e., 10.4 and 11.4 % for [70]- and [60]fullerene-based devices, respectively). Importantly, despite the low electron mobility and significant visible-light absorption of [70]fullerene, the presented protocol allows the employment of [70]fullerene as an efficient ESC. The [70]fullerene film thickness and its solubility in the perovskite processing solutions are crucial parameters, which can be controlled by the use of this simple solution processing protocol. The damage to the [70]fullerene film through dissolution during the perovskite deposition is avoided through the saturation of the perovskite processing solution with [70]fullerene. Additionally, this fullerene-saturation strategy improves the performance of the perovskite film significantly and enhances the power conversion efficiency of solar cells based on different ESCs (i.e., [60]fullerene, [70]fullerene, and TiO2 ). Therefore, this universal solution processing protocol widens the opportunities for the further development of PSCs.

Topics: Calcium Compounds; Electric Power Supplies; Electron Transport; Fullerenes; Oxides; Solar Energy; Titanium

Synroc (Synthetic Rock) consists of four main titanate phases: peroveskite (CaTiO3), zirconolite (CaZrTi2O7), hollandite (BaAl2Ti6O16) and rutile (TiO2). Nano-polycrystalline synroc powders were made by a synthesis combustion process. The combustion process, an externally initiated reaction is self-sustained owing to the exothermic reaction. A significant volume of gas is evolved during the combustion reaction and leads to loosely agglomerated powders. This exothermic reaction provides necessary heat to further carry the reaction in forward direction to produce nanocrystalline powders as the final product. Glycine is used as a fuel, being oxidized by nitrate ions. It is inexpensive, has high energy efficiency, fast heating rates, short reaction times and high compositional homogeneity. In this study, combustion synthesis of nano-sized synroc-B powder is introduced. The fabrication of synroc-B powder result of observation XRD were prepared for polycrystalline (perovskite, zirconolite, hollandite, rutile) structures. The characterization of the synthesized powders is conducted by using XRD, SEM/EDS and TEM.

Topics: Calcium Compounds; Ceramics; Glycine; Nanoparticles; Oxides; Radioactive Waste; Titanium

We examined different encapsulation strategies for perovskite solar cells by testing the device stability under continuous illumination, elevated temperature (85 °C) and ambient humidity of 65 %. The effects of the use of different epoxies, protective layers and the presence of desiccant were investigated. The best stability (retention of ∼80 % of initial efficiency on average after 48 h) was obtained for devices protected by a SiO

Topics: Calcium Compounds; Capsules; Drug Stability; Electric Power Supplies; Humidity; Oxides; Solar Energy; Titanium; Zinc Oxide

Selective and effective enrichment of phosphopeptides from complex samples is essential in phosphoproteome study by mass spectrometry (MS). In this work, we compared perovskites (MgTiO3, CaTiO3, SrTiO3, BaTiO3 and CaZrO3) with metal oxides (ZrO2 and TiO2) in their capability for the selective enrichment of phosphopeptides. It was found here that perovskites exhibited higher selectivity towards phosphopeptides than commonly used ZrO2 and TiO2, even though they all have high affinity to phosphopeptides. As for perovskites, CaTiO3 exhibited better selectivity for enrichment of phosphopeptides than SrTiO3, MgTiO3, BaTiO3 and CaZrO3, which might be ascribed to their crystal structures and electrophilic abilities. Moreover, to further confirm the performance of CaTiO3, CaTiO3 and TiO2 were applied to the enrichment of phosphopeptides from tryptic digest of proteins of human Jurkat-T cell lysate, respectively. The results showed CaTiO3 has much higher selectivity than TiO2 in the enrichment of phosphopeptides from the complex biological sample. Taken together, here we show that CaTiO3 is an excellent material for the highly selective enrichment of phosphopeptides and it could be potentially used in the large-scale phosphoproteome study.

Topics: Calcium Compounds; Humans; Jurkat Cells; Mass Spectrometry; Oxides; Phosphopeptides; Strontium; Titanium; Zirconium

Red mud is a worldwide environmental problem, and many authorities are trying to find an economic solution for its beneficial application or/and safe disposal. Ceramic production is one of the potential waste-to-resource strategies for using red mud as a raw material. Before implementing such a strategy, an unambiguous understanding of the reaction behavior of red mud under thermal conditions is essential. In this study, the phase compositions and transformation processes were revealed for the Pingguo red mud (PRM) heat-treated at different sintering temperatures. Hematite, perovskite, andradite, cancrinite, kaolinite, diaspore, gibbsite and calcite phases were observed in the samples. However, unlike those red mud samples from the other regions, no TiO2 (rutile or anatase) or quartz were observed. Titanium was found to exist mainly in perovskite and andradite while the iron mainly existed in hematite and andradite. A new silico-ferrite of calcium and aluminum (SFCA) phase was found in samples treated at temperatures above 1100°C, and two possible formation pathways for SFCA were suggested. This is the first SFCA phase to be reported in thermally treated red mud, and this finding may turn PRM waste into a material resource for the iron-making industry. Titanium was found to be enriched in the perovskite phase after 1200°C thermal treatment, and this observation indicated a potential strategy for the recovery of titanium from PRM. In addition to noting these various resource recovery opportunities, this is also the first study to quantitatively summarize the reaction details of PRM phase transformations at various temperatures.

Topics: Calcium Compounds; Ceramics; Ferric Compounds; Hot Temperature; Iron; Kaolin; Oxides; Titanium; Waste Products; X-Ray Diffraction

Planar-structured HC(NH2 )2 PbI3 (FAPbI3 ) perovskite solar cells were prepared via a two-step deposition process. To investigate the role of interface, the perovskite morphology was intentionally modified by varying HC(NH2 )2 I concentration. Surface and grain sizes of the deposited FAPbI3 became rougher and larger as the HC(NH2 )2 I concentration decreased from 58.2 to 40.7 mM. Average photocurrent was improved but photovoltage deteriorated slightly with decreasing concentration. Consequently, the average efficiency was improved from 7.82 % to 10.70 % and the best efficiency of 12.17 % was obtained at 40.7 mM. Photoluminescence (PL) at TiO2 /FAPbI3 interface was reduced with decreasing concentration, which was, however, reversed at FAPbI3 /spiro-MeOTAD one. By correlating PL data and the photovoltaic performance, we concluded that the TiO2 /perovskite interface plays a crucial role in determining photocurrent while the perovskite/spiro-MeOTAD interface is important in governing photovoltage.

Topics: Calcium Compounds; Coordination Complexes; Diamines; Electric Power Supplies; Fluorine; Gold; Oxides; Solar Energy; Tin Compounds; Titanium

Perovskite solar cells (PSCs) are the most promising candidates as next-generation solar energy conversion systems. To design a highly efficient PSC, understanding electronic properties of mesoporous metal oxides is essential. Herein, we explore the effect of Nb doping of TiO2 on electronic structure and photovoltaic properties of PSCs. Light Nb doping (0.5 and 1.0 at %) increased the optical band gap slightly, but heavy doping (5.0 at %) distinctively decreased it. The relative Fermi level position of the conduction band is similar for the lightly Nb-doped TiO2 (NTO) and the undoped TiO2 whereas that of the heavy doped NTO decreased by as much as ∼0.3 eV. The lightly doped NTO-based PSCs exhibit 10 % higher efficiency than PSCs based on undoped TiO2 (from 12.2 % to 13.4 %) and 52 % higher than the PSCs utilizing heavy doped NTO (from 8.8 % to 13.4 %), which is attributed to fast electron injection/transport and preserved electron lifetime, verified by transient photocurrent decay and impedance studies.

Topics: Calcium Compounds; Electric Power Supplies; Electron Transport; Niobium; Oxides; Solar Energy; Titanium

We investigate zirconium (Zr) incorporation into the titanium dioxide (TiO2) electron-transporting layer used in organometal halide perovskite photovoltaics. Compared to Zr-free controls, solar cells employing electrodes containing Zr exhibit increased power conversion efficiency (PCE) and decreased hysteresis. We use transient photovoltage and photocurrent extraction to measure carrier lifetimes and densities and observe longer carrier lifetimes and higher charge densities in devices on Zr-containing electrodes at microsecond times as well as longer persistent photovoltages extending from ∼milliseconds to tens of seconds. We characterize the surface stoichiometry and change in work function and reduction potential of the TiO2 upon incorporation of Zr and discuss the charge recombination at the TiO2 interface in the context of these variables. Finally, we show that the combination of Zr-TiO2 electrode modification with device pyridine treatment leads to a cumulative improvement in performance.

Topics: Calcium Compounds; Electrodes; Oxides; Solar Energy; Titanium; Zirconium

Perovskite solar cells have attracted enormous attention in recent years due to their low cost and superior technical performance. However, the use of toxic metals, such as lead, in the perovskite dye and toxic chemicals in perovskite solar cell manufacturing causes grave concerns for its environmental performance. To understand and facilitate the sustainable development of perovskite solar cell technology from its design to manufacturing, a comprehensive environmental impact assessment has been conducted on titanium dioxide nanotube based perovskite solar cells by using an attributional life cycle assessment approach, from cradle to gate, with manufacturing data from our laboratory-scale experiments and upstream data collected from professional databases and the literature. The results indicate that the perovskite dye is the primary source of environmental impact, associated with 64.77% total embodied energy and 31.38% embodied materials consumption, contributing to more than 50% of the life cycle impact in almost all impact categories, although lead used in the perovskite dye only contributes to about 1.14% of the human toxicity potential. A comparison of perovskite solar cells with commercial silicon and cadmium-tellurium solar cells reveals that perovskite solar cells could be a promising alternative technology for future large-scale industrial applications.

Topics: Calcium Compounds; Coloring Agents; Conservation of Natural Resources; Electric Power Supplies; Electrodes; Oxides; Solar Energy; Titanium

Perovskite solar cells with power conversion efficiencies exceeding 16% at AM 1.5 G one sun illumination are developed using the black polymorph of formamidnium lead iodide, HC(NH2)2 PbI3 . Compared with CH3 NH3 PbI3 , HC(NH2 )2 PbI3 extends its absoprtion to 840 nm and shows no phase transition between 296 and 423 K. Moreover, a solar cell based on HC(NH2 )2 PbI3 exhibits photostability and little I-V hysteresis.

Topics: Absorption, Physicochemical; Amidines; Calcium Compounds; Cellulose; Electric Power Supplies; Iodides; Lead; Oxides; Solar Energy; Titanium

This work reports on an investigation into interfacial charge transfer in CH3NH3PbI3 perovskite solar cells by using anatase TiO2 nanocuboids enclosed by active {100} and {001} facets. The devices show 6.0 and 8.0% power conversion efficiency with and without hole-transport material. Transient photovoltage/photocurrent decay and charge extraction, as well as impedance spectroscopy measurements, reveal that carbon materials are effective counter electrodes in perovskite solar cells. The photogenerated charges are observed to be stored in mesoporous TiO2 film under illumination and in the CH3NH3PbI3 layer in the dark. The use of 2,2',7,7'-tetrakis(N,N-di-p-methoxyphenylamine)-9,9-spirobifluorene (spiro-MeOTAD) as a hole-transport material accelerates interfacial charge recombination between the photogenerated electrons and holes.

Topics: Calcium Compounds; Carbon; Electric Power Supplies; Iodides; Lead; Light; Nanostructures; Oxides; Quaternary Ammonium Compounds; Solar Energy; Titanium

The lattice dynamics of La(1/2)Na(1/2)TiO(3) single crystal have been investigated by far-infrared and Raman scattering spectroscopy. Far-IR reflectivity spectra revealed Slater, Last and Axe modes near 140, 190 and 555 cm(-1), respectively. The frequency of the Slater mode decreases by about 10% on cooling, which is enough to account for the observed increase of the low-frequency permittivity. The results allowed us to discuss the reasons for the suppressed ferroelectricity of the material. Temperature evolution of the Raman scattering intensity of an oxygen octahedra bending mode near 455 cm(-1) suggests a second-order phase transition towards the perovskite aristotype phase near 870 K.

Topics: Calcium Compounds; Lanthanum; Models, Molecular; Molecular Structure; Oxides; Phase Transition; Sodium; Spectrophotometry, Infrared; Spectrum Analysis, Raman; Temperature; Thermodynamics; Titanium

Lead-free (1-x)Ba(Zr₀.₁₅Ti₀.₈₅)O₃-x(K₀.₅Na₀.₅)NbO₃ ; x=0-0.05) (BZT-KNN) perovskite ceramics, a materials with potential applications for energy storage, are investigated. The samples are prepared by a solid-state reaction method. Powder X-ray diffraction (XRD) and scanning electron microscopy (SEM) are used to study the microstructure of the samples. Their dielectric properties and impedance spectra are reported as functions of temperature and frequency. The addition of 1 mol % (K₀.₅Na₀.₅)NbO₃ to Ba(Zr₀.₁₅Ti₀.₈₅)O₃ improves the dielectric constant and enhances its diffuseness in a wide temperature range. The small amount of (K₀.₅Na₀.₅)NbO₃ is found to markedly affect the microstructure of the Ba(Zr₀.₁₅Ti₀.₈₅)O₃ ceramic (grain size and other characteristics) without changing the phase or crystal symmetry. In addition, we report that fine substructures in the grains, so-called sheet structures, are responsible for the dielectric properties (both diffuseness and dielectric constant) of (1-x)Ba(Zr₀.₁₅Ti₀.₈₅)O₃-x(K₀.₅Na₀.₅)NbO₃ (x=0-0.03; especially x=0.01) ceramics.

Topics: Barium; Calcium Compounds; Carbonates; Ceramics; Electric Impedance; Electric Power Supplies; Microscopy, Electron, Scanning; Niobium; Oxides; Potassium; Powder Diffraction; Titanium; Zirconium

Plasma electrochemical oxidation (PEO) was used to prepare TiO2-based coating containing Ca and P on titanium alloy. After alkali- and then heat-treatment at 800 degrees C of the PEO coating, a CaTiO3/TiO2 composite (CTC) coating was obtained. The current results indicate that the apatite-forming ability of the CTC coating is higher than that of the PEO coating. During the simulated body fluid (SBF) incubation, Ca of the CTC coating is released into the SBF. An ionic exchange between Ca(2+) ions of the CTC coating and H(3)O(+) ions of the SBF may take place during the SBF incubation. As a result, the abundant Ti--OH groups are formed on the surface of the CTC coating. The hydroxyl functionalized surface greatly enhances the nucleation and growth of apatite, leading to the high apatite-forming ability of the CTC coating. The apatite induced by the CTC coating exhibits a porous and carbonated structure.

Topics: Alloys; Apatites; Biomimetic Materials; Biomimetics; Calcium Compounds; Coated Materials, Biocompatible; Oxidation-Reduction; Oxides; Titanium

Bioactive coatings on cp-Ti and Ti-6Al-4V were prepared by a simple chemical technique. Specimens of cp-Ti and Ti-6Al-4V were initially immersed in a 5 M NaOH solution at 60 degrees C for 24 h which resulted in the formation of a porous network structure composed of Na2Ti5O11 and TiO2. The specimens were then immersed in a Ca-rich solution either at 60 degrees C or at 36.5 degrees C for 24 h. During this treatment Na+ was released and Ti-OH groups were formed. Subsequently, TiO2 dissociated from the Ti-OH group and combined with calcium ions to form calcium titanate (CaTiO3), which was embedded in a titania gel layer during the immersion period. The specimens were then immersed in r-SBF at 36.5 degrees C for 1-30 days. After immersion in r-SBF for 3 days, HAp (hydroxyapatite) spheroids began to deposit on the substrates, and within a week the surfaces were covered. The HAp spheroids were 5 microm in size with a Ca/P ratio of 1.68 which was close to bone-like apatite (1.67). The average thicknesses of HAp layer after immersion in r-SBF for 3 days, 1 week, and 2 weeks were 3.8, 5.6, and 6.4 microm, respectively. A scratch test, used to evaluate the adhesive strength of the HAp layer, showed that the HAp layer was not scraped off until the applied load reached 26 N.

Topics: Alloys; Apatites; Calcium; Calcium Compounds; Durapatite; Ions; Materials Testing; Models, Chemical; Oxides; Sodium Hydroxide; Surface Properties; Temperature; Tensile Strength; Time Factors; Titanium

In the scope of the present contribution, perovskite SrTi(1-x)Fe(x)O(3-delta) was investigated as a model material for conductometric hydrocarbon sensing at intermediate temperatures between 350 and 450 degrees C. To explain the observations made during sensor optimization in a quantitative way, a novel sensor model was proposed. At the microscopic scale, the local gas concentration affects local conductivity of the gas sensitive material. In the case of n-type tin oxide sensors, this interaction is commonly attributed to a redox reaction between the reducing analyte gas and adsorbed oxygen. In contrast, a reduction process affecting the entire bulk was assumed to govern gas sensitivity of SrTi(1-x)Fe(x)O(3-delta) films. Although very few variables needed to be assumed or fitted, the present bulk-type model was found to represent well sensor functionality of p-type conducting SrTi(0.8)Fe(0.2)O(3-delta) films. In addition to the temperature dependence of sensor response, the hydrocarbon sensitivity, m, was predicted with good accuracy. The different sensor responses towards hydrocarbons with a different chemical reactivity and other cross-interfering species, such as NO, was explained as well as the dependence on film thickness for screen printed films.

Topics: Calcium Compounds; Carbonates; Electric Conductivity; Electrodes; Ferric Compounds; Hydrocarbons; Models, Chemical; Oxides; Particle Size; Semiconductors; Sensitivity and Specificity; Strontium; Surface Properties; Temperature; Titanium

Topics: Calcium Chloride; Calcium Compounds; Electrochemistry; Electrolysis; Oxidation-Reduction; Oxides; Particle Size; Temperature; Time Factors; Titanium