Gallium oxide (Ga2O3) is emerging as a viable candidate for certain classes of power electronics, solar blind UV photodetectors, solar cells, and sensors with capabilities beyond existing technologies due to its large bandgap. It is usually reported that there are five different polymorphs of Ga2O3, namely, the monoclinic (β-Ga2O3), rhombohedral (α), defective spinel (γ), cubic (δ), or orthorhombic (e) structures. Of these, the β-polymorph is the stable form under normal conditions and has been the most widely studied and utilized. Since melt growth techniques can be used to grow bulk crystals of β-GaO3, the cost of producing larger area, uniform substrates is potentially lower compared to the vapor growth techniques used to manufacture bulk crystals of GaN and SiC. The performance of technologically important high voltage rectifiers and enhancement-mode Metal-Oxide Field Effect Transistors benefit from the larger critical electric field of β-Ga2O3 relative to either SiC or GaN. However, the absence of clear demonstrations of p-type doping in Ga2O3, which may be a fundamental issue resulting from the band structure, makes it very difficult to simultaneously achieve low turn-on voltages and ultra-high breakdown. The purpose of this review is to summarize recent advances in the growth, processing, and device performance of the most widely studied polymorph, β-Ga2O3. The role of defects and impurities on the transport and optical properties of bulk, epitaxial, and nanostructures material, the difficulty in p-type doping, and the development of processing techniques like etching, contact formation, dielectrics for gate formation, and passivation are discussed. Areas where continued development is needed to fully exploit the properties of Ga2O3 are identified.

A review of Ga2O3 materials, processing, and devices

Ammonia-borane and related compounds as dihydrogen sources.

Hydrogen storage for transportation applications requires high volumetric and gravimetric storage capacity. B-N compounds are well suited as storage materials due to their light weight and propensity for bearing multiple protic (N-H) and hydridic (B-H) hydrogens. This critical review briefly covers the various methods of hydrogen storage, and then concentrates on chemical hydrogen storage using B-N compounds. The simplest B-N compound, ammonia borane (H3NBH3), which has a potential 19.6 wt% hydrogen storage capacity, will be emphasised (127 references).

B–N compounds for chemical hydrogen storage

The recent developments and trends in combustion science towards the synthesis of nanomaterials are discussed. Different modifications made to conventional combustion approaches for preparation of nanomaterials are critically analyzed. Special attention is paid to various applications of combustion synthesized nanosized products.

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Combustion synthesis and nanomaterials

In the search for future energy supplies, the application of hydrogen as an energy carrier is seen as a prospective issue. However, the implementation of a hydrogen economy is suffering from several unsolved problems. Particularly challenging is the storage of appropriate amounts of hydrogen. In this context one of the promising hydrogen storage techniques relies on liquid-phase chemical hydrogen storage materials, in particular, aqueous sodium borohydride, ammonia borane, hydrazine, hydrazine borane and formic acid. The use of these materials in hydrogen storage provides high gravimetric and volumetric hydrogen densities, low potential risk, and low capital investment because it is largely compatible with the current transport infrastructure. In this review, we survey the research progresses in hydrogen generation from these liquid-phase chemical hydrogen storage materials and their regeneration.

Liquid-phase chemical hydrogen storage materials

Coal gasification is a promising option for the future use of coal. Similarly to gasification in industrial reactors, underground coal gasification (UCG) produces syngas, which can be used for power generation or for the production of liquid hydrocarbon fuels and other valuable chemical products. As compared with conventional mining and surface gasification, UCG promises lower capital/operating costs and also has other advantages, such as no human labor underground. In addition, UCG has the potential to be linked with carbon capture and sequestration. The increasing demand for energy, depletion of oil and gas resources, and threat of global climate change lead to growing interest in UCG throughout the world. In this article, we review the current status of this technology, focusing on recent developments in various countries.

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Underground Coal Gasification: A Brief Review of Current Status

Magnesium is known to be a perspective fuel for engines which could use CO2 from the atmospheres of Mars and Venus as an oxidizer. Combustion of magnesium samples introduced into a high temperature CO2/CO mixture is experimentally studied. Measurements of the burning time as well as visual observations and spectral analysis of the flame show that the sharp transition from vapor-phase to heterogeneous combustion occurs with increasing CO content in the atmosphere. Study of the condensed products and thermodynamic analysis of magnesium particle combustion in CO, and CO indicate that the gas-phase reaction Mg + CO2 = MgO + CO and the heterogeneous reaction Mg + CO = MgO + C occur during combustion in C02 whereas during combustion in CO the heterogeneous reaction occurs only. Competition of the gas phase reaction, the heterogeneous reaction and the metal evaporation is the reason for the sharp transition from one to another regime.

Evgeny Shafirovich

Papers

Underground Coal Gasification: A Brief Review of Current Status

Combustion of Magnesium Particles in CO2/CO Mixtures

Combustion of novel chemical mixtures for hydrogen generation

Ignition mechanism of nickel-coated aluminum particles

Noncatalytic hydrothermolysis of ammonia borane