Transition Metal Oxides for Electrochemical Energy Storage


Book Description

Transition Metal Oxides for Electrochemical Energy Storage Explore this authoritative handbook on transition metal oxides for energy storage Metal oxides have become one of the most important classes of materials in energy storage and conversion. They continue to have tremendous potential for research into new materials and devices in a wide variety of fields. Transition Metal Oxides for Electrochemical Energy Storage delivers an insightful, concise, and focused exploration of the science and applications of metal oxides in intercalation-based batteries, solid electrolytes for ionic conduction, pseudocapacitive charge storage, transport and 3D architectures and interfacial phenomena and defects. The book serves as a one-stop reference for materials researchers seeking foundational and applied knowledge of the titled material classes. Transition Metal Oxides offers readers in-depth information covering electrochemistry, morphology, and both in situ and in operando characterization. It also provides novel approaches to transition metal oxide-enabled energy storage, like interface engineering and three-dimensional nanoarchitectures. Readers will also benefit from the inclusion of: A thorough introduction to the landscape and solid-state chemistry of transition metal oxides for energy storage An exploration of electrochemical energy storage mechanisms in transition metal oxides, including intercalation, pseudocapacitance, and conversion Practical discussions of the electrochemistry of transition metal oxides, including oxide/electrolyte interfaces and energy storage in aqueous electrolytes An examination of the characterization of transition metal oxides for energy storage Perfect for materials scientists, electrochemists, inorganic chemists, and applied physicists, Transition Metal Oxides for Electrochemical Energy Storage will also earn a place in the libraries of engineers in power technology and professions working in the electrotechnical industry seeking a one-stop reference on transition metal oxides for energy storage.




Metal Oxides


Book Description

The chemistry of metals has traditionally been more understood than that of its oxides. As catalytic applications continue to grow in a variety of disciplines, Metal Oxides: Chemistry and Applications offers a timely account of transition-metal oxides (TMO), one of the most important classes of metal oxides, in the context of catalysis. The




Metal Oxide-Based Photocatalysis


Book Description

Metal Oxide-Based Photocatalysis: Fundamentals and Prospects for Application explains the principles and fundamentals of metal oxide-based photocatalysis and the requirements necessary for their use in photocatalysis. It also discusses preparation methods for photocatalysis, and the advantages, disadvantages and achievements of the most important metal oxides (TiO2, ZnO, Fe2O3, Ta2O3, CuO, NiO, Cr2O3, RuO2, etc.). The book concludes with the most important photocatalytic applications and an overview of the future. Applications are organized by potential needs and solutions, addressing such areas as water treatment, hydrogen production, air treatment, chemical synthesis, and applications in medicine and construction. Provides coverage of applications, presenting needs and solutions Covers essential applications, such as water treatment, hydrogen production, air depollution, medical applications, and much more Includes the characterization of the most important metal oxides used in heterogeneous photocatalysis




Synthesis and Characterization of Transition Metal Oxide Catalysts for Environmental and Energy Storage Applications


Book Description

Nowadays, environmental concerns and the global energy crisis have become two of our greatest challenges. The main purpose of this dissertation research is to design highly active mesoporous materials that can efficiently catalyze environmental and energy related reactions. Surface properties can be easily tuned by thermal treatment and cation doping, resulting in improved catalytic activities. Synthesis and characterization of the materials, catalytic activities for carbon monoxide oxidation, oxygen reduction and oxygen evolution reactions, and mechanistic studies are covered in this thesis. The first part describes the synthesis of mesoporous cobalt oxides through an inverse micelle route for low temperature carbon monoxide oxidation applications. The prepared material showed much better activity and stability compared with commercial cobalt oxide due to its nanoparticle nature and porous structure. The catalytic performance under both dry and moisture rich conditions were tested. Detailed characterization of the materials suggested that high surface areas and the presence of surface oxygen vacancies were critical for enhanced activities. In real systems, structured catalysts such as monolithic substrates coated with a layer of active material are used instead of powder form catalysts. To evaluate the potential of our catalysts to be used in practical catalytic devices, mesoporous metal oxides (MnOx, Co3O4, CeO2) were coated on cordierite substrate by dip coating and in-situ growth and were used as low temperature diesel oxidation catalysts. The resulting materials showed promising catalytic performance. The effect of particle size, loading amount and Cu doping on the catalytic performance are discussed in detail. In the last part, mesoporous cobalt oxides were used as bifunctional catalysts for oxygen reduction and oxygen evolution reactions. If a catalyst can catalyze both reactions, it will have great potential in the application of rechargeable metal air batteries. Ni and Mn doping were introduced into the cobalt oxide material to increase the conductivity and active site population. The Ni incorporated cobalt oxide exhibited the best activity, which can be considered as a potential substituent for precious metal catalysts (Pt, Ir, Ru). Furthermore, the intrinsic structure-property relationships of the materials were established.













Synthesis and Characterization of Metal Doped Titanium Dioxide, Transition Metal Phosphides, Sulfides and Thiophosphates for Photocatalysis and Energy Applications


Book Description

This thesis covers synthetic investigations, characterization, and applications of transition metal doped titanium dioxide materials and transition metal phosphide/sulfide structures. Both areas are useful in heterogeneous catalysis, battery energy storage, and in semiconductor light to energy conversion. Two main synthesis routes have been investigated: 1) rapid solid state metathesis (SSM) of transition metal oxides, phosphides, sulfides, and thiophosphates, and 2) sealed ampoule routes of transition metal phosphides and thiophosphates. SSM reactions tend to yield kinetically controlled multiphase products while sealed ampoule routes gave more thermodynamically favorable single phase materials. Approximately 10 mol% of many first row transition metals (M = Cr, Mn, Fe, Co, Ni, Cu) were targeted for doping into TiO2, using MClx, and sodium peroxide in SSM reactions, targeting an ideal mixed phase of M0.1Ti0.9O2. X-ray diffraction showed rutile TiO2 forms and no separate dopant metal phases were seen until subsequent 1000 °C annealing in air. EDS, ICP, and XPS analysis showed slightly lower than the targeted M:Ti ratios however, the manganese sample had more than the ideal 10 mol % of dopant. DRS data showed estimated bandgap energies of the doped samples within 1.33-2.55 eV. Magnetic susceptibility showed small paramagnetic responses from all samples that increase upon annealing. SEM showed that the doped SSM-TiO2 samples were mixtures of aggregates and blocky particles. The synthesized doped titanias were tested for methylene blue and methyl orange photodegradation under UV and visible light and for H2 generation from water reduction under UV light. The doped titania samples absorb significant amounts of methylene blue dye in the dark with the manganese doped TiO2 sample being the most absorbent. Degradation of methylene blue under UV illumination was observed, however, only modest degradation under visible light was observed.