A broad organic–inorganic series of hybrid metal iodide perovskites with the general formulation AMI3, where A is the methylammonium (CH3NH3+) or formamidinium (HC(NH2)2+) cation and M is Sn (1 and 2) or Pb (3 and 4) are reported. The compounds have been prepared through a variety of synthetic approaches, and the nature of the resulting materials is discussed in terms of their thermal stability and optical and electronic properties. We find that the chemical and physical properties of these materials strongly depend on the preparation method. Single crystal X-ray diffraction analysis of 1–4 classifies the compounds in the perovskite structural family. Structural phase transitions were observed and investigated by temperature-dependent single crystal X-ray diffraction in the 100–400 K range. The charge transport properties of the materials are discussed in conjunction with diffuse reflectance studies in the mid-IR region that display characteristic absorption features. Temperature-dependent studies show a ...

Semiconducting tin and lead iodide perovskites with organic cations: phase transitions, high mobilities, and near-infrared photoluminescent properties.

A ceramic fuel cell in an all solid-state energy conversion device that produces electricity by electrochemically combining fuel and oxidant gases across an ionic conducting oxide. Current ceramic fuel cells use an oxygen-ion conductor or a proton conductor as the electrolyte and operate at high temperatures (>600°C). Ceramic fuel cells, commonly referred to as solid-oxide fuel cells (SOFCs), are presently under development for a variety of power generation applications. This paper reviews the science and technology of ceramic fuel cells and discusses the critical issues posed by the development of this type of fuel cell. The emphasis is given to the discussion of component materials (especially, ZrO2 electrolyte, nickel/ZrO2 cermet anode, LaMnO3 cathode, and LaCrO3 interconnect), gas reactions at the electrodes, stack designs, and processing techniques used in the fabrication of required ceramic structures.

Ceramic Fuel Cells

Zinc oxide is a unique material that exhibits semiconducting and piezoelectric dual properties. Using a solid–vapour phase thermal sublimation technique, nanocombs, nanorings, nanohelixes/nanosprings, nanobelts, nanowires and nanocages of ZnO have been synthesized under specific growth conditions. These unique nanostructures unambiguously demonstrate that ZnO probably has the richest family of nanostructures among all materials, both in structures and in properties. The nanostructures could have novel applications in optoelectronics, sensors, transducers and biomedical sciences. This article reviews the various nanostructures of ZnO grown by the solid–vapour phase technique and their corresponding growth mechanisms. The application of ZnO nanobelts as nanosensors, nanocantilevers, field effect transistors and nanoresonators is demonstrated.

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Zinc oxide nanostructures: growth, properties and applications

Understanding the mechanism of ionic transport in organic–inorganic halide perovskites is crucial for the design of future solar cells. Here, Eames et al. undertake a combined experimental and computational study to elucidate the ion conducting species and help rationalize the unusual behaviour observed in these perovskite-based devices.

/pdf/ionic-transport-in-hybrid-lead-iodide-perovskite-solar-cells-4arch9smzt.pdf

Ionic transport in hybrid lead iodide perovskite solar cells

Recent worldwide interest in building a decentralized, hydrogen-based energy economy has refocused attention on the solid oxide fuel cell (SOFC) as a potential source of efficient, environmentally friendly, fuel-versatile electric power. Due to its high operating temperature, the SOFC offers several potential advantages over polymer-based fuel cells, including reversible electrode reactions, low internal resistance, high tolerance to typical catalyst poisons, production of high-quality waste heat for (among other uses) reformation of hydrocarbon fuels, as well as the possibility of burning hydrocarbon fuels directly. Today, SOFCs are much closer to commercial reality than they were 20 years ago, due largely to technological advances in electrode material composition, microstructure control, thin-film ceramic fabrication, and stack and system design. These advances have led to dozens of active SOFC development programs in both stationary and mobile power and contributed to commercialization or development in a number of related technologies, including gas sensors,1 solid-state electrolysis devices,2 and iontransport membranes for gas separation and partial oxidation.3 Many reviews are available which summarize the technological advances made in SOFCs over the last 15-35 yearssreaders who are primarily interested in knowing the state-of-the art in materials, design, and fabrication (including the electrodes) are encouraged to consult these reviews.4-12 This review focuses on the factors governing SOFC cathode performancesadvances we have made over † Dedicated to Brian Steele, 1929-2003. Researcher, Entrepreneur, Consensus Seeker. 4791 Chem. Rev. 2004, 104, 4791−4843

Factors Governing Oxygen Reduction in Solid Oxide Fuel Cell Cathodes

Nonstoichiometry of the perovskite-type oxides La1−xSrxCoO3−δ

Nonstoichiometry and defect structure of the perovskite-type oxides La1−xSrxFeO3−°

Diffusion of oxide ion vacancies in perovskite-type oxides

In order to elucidate the correlations between composition, structure and electrical properties of a high-Tc superconductor Ba-Y-Cu-O system, thermogravimetric measurement and chemical analysis of oxygen nonstoichiometry were made at a temperature range of 350 to 1000°C and under the oxygen partial pressure of 10-4 to 1 atm. Within a stability range of the composition Ba2YCu3O7-δ, the oxygen deficiency, δ, was found to vary approximately from zero to 0.9, with associated mean valence of copper ions varying from 2.33 to 1.73. At a possible phase boundary region of tetragonal to orthorhombic crystal structures, no sign of discontinuity in δ was observed, suggesting its phase transition was of higher than a first order.

https://iopscience.iop.org/article/10.1143/JJAP.26.L1228/pdf

Kazuo Fueki

Papers

Nonstoichiometry of the perovskite-type oxides La1−xSrxCoO3−δ

Nonstoichiometry and defect structure of the perovskite-type oxides La1−xSrxFeO3−°

Diffusion of oxide ion vacancies in perovskite-type oxides

Determination of Oxygen Nonstoichiometry in a High-Tc Superconductor Ba2YCu3O7-δ

Ionic conduction of the perovskite-type halides