Search Results (10)

This study focuses on the structural and electrochemical behavior of the compound ZnLaFeO₄ as a negative electrode material for nickel–metal hydride (Ni-MH) batteries. The material was synthesized by a sol–gel hydrothermal method to assess the influence of lanthanum doping on the ZnFe₂O₄ spinel structure. X-ray diffraction revealed the formation of a dominant LaFeO₃ perovskite phase, with ZnFe₂O₄ and La₂O₃ as secondary phases. SEM analysis showed agglomerated grains with an irregular morphology. Electrochemical characterization at room temperature and a discharge rate of C/10 (full charge in 10 h) revealed a maximum discharge capacity of 106 mAhg⁻¹. Although La³⁺ doping modified the microstructure and slowed the activation process, the electrode exhibited stable cycling with moderate polarization behavior. The decrease in capacity during cycling is due mainly to higher internal resistance. These results highlight the potential and limitations of La-doped spinel ferrites as alternative negative electrodes for Ni-MH systems. Full article

Perovskite-type structures have unique crystal architecture and chemical composition, which make them highly attractive for the design of solar cells. For instance, perovskite-based solar cells have been shown to perform better than silicon cells, capable of adsorbing a wide range of light wavelengths, and they can be relatively easily manufactured at a low cost. Importantly, the perovskite-based structures can also adsorb a significant amount of hydrogen atoms into their own structure; therefore, perovskite holds promise in the solid-state storage of hydrogen. It is widely expected by the scientific community that the controlled adsorption/desorption of the hydrogen atoms into/from perovskite-based structures can help to overcome the main hydrogen storage issues such as a low volumetric density and the safety concerns (i.e., the hydrogen embrittlement affects strongly the mechanical properties of metals and, as such, the storage or transport of the gaseous hydrogen in the vessels is, especially for large vessel volumes, challenging). The purpose of this review is to provide an updated overview of the recent results and studies focusing on the perovskite materials used for both solar cells and hydrogen storage applications. Particular attention is given to (i) the preparation and the achievable efficiency and stability of the perovskite solar cells and (ii) the structural, thermodynamic, and storage properties of perovskite hydrides and oxides. We show that the perovskite materials can not only reach the efficiency above current Si-based solar cells but also, due to good stability and reasonable price, can be preferable in the solid-state storage of hydrogen. Then, the future trends and directions in the research and application of perovskite in both solar cells and hydrogen storage are also highlighted. Full article

The cubic oxyhydride perovskite BaTiO_3−xH_x, where the well-known ferroelectric oxide BaTiO₃ is partially hydridized, exhibits a variety of functions such as being a catalyst and precursor for the synthesis of mixed-anion compounds by utilizing the labile nature of hydride anions. In this study, we present a hexagonal version, BaTi(O_3−xH_x) (x < 0.6) with the 6H-type structure, synthesized by a topochemical reaction using hydride reduction, unlike reported hexagonal oxyhydrides obtained under high pressure. The conversion of cubic BaTiO₃ (150 nm) to the hexagonal phase by heat treatment at low temperature (950~1025 °C) using a Mg getter allows the introduction of large oxygen defects (BaTiO_3−x; x − 0.28) while preventing the crystal growth of hexagonal BaTiO₃, which has been accessible at high temperatures of ~1500 °C, contributing to the increase of the hydrogen content. Hydride anions in 6H-BaTiO_3−xH_x preferentially occupy face-sharing sites, as do other oxyhydrides. Full article

Recently, perovskite-type oxides have attracted researchers as new materials for solid hydrogen storage. This paper presents the performances of perovskite-type oxide LaCrO₃ dedicated for hydrogen solid storage using both numerical and experimental methods. Ab initio calculations have been used here with the aim to investigate the electronic, mechanical and elastic properties of LaCrO₃H_x (x = 0, 6) for hydrogen storage applications. Cell parameters, crystal structures and mechanical properties are determined. Additionally, the cohesive energy indicates the stability of the hydride. Furthermore, the mechanical properties showed that both compounds (before and after hydrogenation) are stable. The microstructure and storage capacity at different temperatures of these compounds have been studied. We have shown that storage capacities are around 4 wt%. The properties obtained from this type of hydride showed that it can be used for future applications. XRD analysis was conducted in order to study the structural properties of the compound. Besides morphological, thermogravimetric analysis was also conducted on the perovskite-type oxide. Finally, a comparison of these materials with other hydrides used for hydrogen storage was carried out. Full article

The formation and hydrogen sorption properties of the NaMgH₃ perovskite/type hydride have been examined. Samples were mechanically ball milled under argon for 2, 5 and 15 h; then characterized by X-ray diffraction (XRD), differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA) coupled with a mass spectrometer (MS). Lattice parameters and cell volume of the main NaMgH₃ phase increase as a function of milling. Dehydrogenation proceeded in two-step reactions for the NaMgH₃. The maximum amount of released hydrogen was achieved for the 2 h milled NaMgH₃ hydride accounting for 5.8 wt.% of H₂ from 287 °C to 408 °C. Decomposed NaMgH₃ samples were reversibly hydrogenated under 10 bar H₂ at ~200 °C. Full article

In this review, we describe different families of metastable materials, some of them with relevant technological applications, which can be stabilized at moderate pressures 2–3.5 GPa in a piston-cylinder press. The synthesis of some of these systems had been previously reported under higher hydrostatic pressures (6–10 GPa), but can be accessed under milder conditions in combination with reactive precursors prepared by soft-chemistry techniques. These systems include perovskites with transition metals in unusual oxidation states (e.g., RNiO₃ with Ni³⁺, R = rare earths); double perovskites such as RCu₃Mn₄O₁₂ with Jahn–Teller Cu²⁺ ions at A sites, pyrochlores derived from Tl₂Mn₂O₇ with colossal magnetoresistance, pnictide skutterudites M_xCo₄Sb₁₂ (M = La, Yb, Ce, Sr, K) with thermoelectric properties, or metal hydrides Mg₂MH_x (M = Fe, Co, Ni) and AMgH₃ (A: alkali metals) with applications in hydrogen storage. The availability of substantial amounts of sample (0.5–1.5 g) allows a complete characterization of the properties of interest, including magnetic, transport, thermoelectric properties and so on, and the structural characterization by neutron or synchrotron X-ray diffraction techniques. Full article

SrVO₂H, obtained by a topochemical reaction of SrVO₃ perovskite using CaH₂, is an anion-ordered phase with hydride anions exclusively at the apical site. In this study, we conducted a CaH₂ reduction of SrVO₃ thin films epitaxially grown on KTaO₃ (KTO) substrates. When reacted at 530 °C for 12 h, we observed an intermediate phase characterized by a smaller tetragonality of c/a = 0.96 (vs. c/a = 0.93 for SrVO₂H), while a longer reaction of 24 h resulted in the known phase of SrVO₂H. This fact suggests that the intermediate phase is a metastable state stabilized by applying tensile strain from the KTO substrate (1.4%). In addition, secondary ion mass spectrometry (SIMS) revealed that the intermediate phase has a hydrogen content close to that of SrVO₂H, suggesting a partially disordered anion arrangement. Such kinetic trapping of an intermediate state by biaxial epitaxial strain not only helps to acquire a new state of matter but also advances our understanding of topochemical reaction processes in extended solids. Full article

NaMgH₃ perovskite hydride and NaMgH₃–carbon nanomaterials (NH-CM) composites were prepared via the reactive ball-milling method. To investigate the catalytic effect of CM on the dehydriding kinetic properties of NaMgH₃ hydride, multiwall carbon nanotubes (MWCNTs) and graphene oxide (GO) were used as catalytic additives. It was found that dehydriding temperatures and activation energies (ΔE₁ and ΔE₂) for two dehydrogenation steps of NaMgH₃ hydride can be greatly reduced with a 5 wt. % CM addition. The NH–2.5M–2.5G composite presents better dehydriding kinetics, a lower dehydriding temperature, and a higher hydrogen-desorbed amount (3.64 wt. %, 638 K). ΔE₁ and ΔE₂ can be reduced by about 67 kJ/mol and 30 kJ/mol, respectively. The results suggest that the combination of MWCNTs and GO is a better catalyst as compared to MWCNTs or GO alone. Full article

Inorganic-organic hydride perovskites bring the hope for fabricating low-cost and large-scale solar cells. At the beginning of the research, two open questions were raised: the hysteresis effect and the role of chloride. The presence of chloride significantly improves the crystallization and charge transfer property of the perovskite. However, though the long held debate over of the existence of chloride in the perovskite seems to have now come to a conclusion, no prior work has been carried out focusing on the role of chloride on the electronic performance and the crystallization of the perovskite. Furthermore, current reports on the crystal structure of the perovskite are rather confusing. This article analyzes the role of chloride in CH₃NH₃PbI_3-xCl_x on the crystal orientation and provides a new explanation about the (110)-oriented growth of CH₃NH₃PbI₃ and CH₃NH₃PbI_3-xCl_x. Full article

A novel metal borohydride ammonia-borane complex Ca(BH₄)₂·NH₃BH₃ is characterized as the decomposition product of the recently reported perovskite-type metal borohydride NH₄Ca(BH₄)₃, suggesting that ammonium-based metal borohydrides release hydrogen gas via ammonia-borane-complexes. For the first time the concept of proton-hydride interactions to promote hydrogen release is applied to a cation-anion pair in a complex metal hydride. NH₄Ca(BH₄)₃ is prepared mechanochemically from Ca(BH₄)₂ and NH₄Cl as well as NH₄BH₄ following two different protocols, where the synthesis procedures are modified in the latter to solvent-based ball-milling using diethyl ether to maximize the phase yield in chlorine-free samples. During decomposition of NH₄Ca(BH₄)₃ pure H₂ is released, prior to the decomposition of the complex to its constituents. As opposed to a previously reported adduct between Ca(BH₄)₂ and NH₃BH₃, the present complex is described as NH₃BH₃-stuffed α-Ca(BH₄)₂. Full article