In this critical review, metal oxides-based materials for electrochemical supercapacitor (ES) electrodes are reviewed in detail together with a brief review of carbon materials and conducting polymers. Their advantages, disadvantages, and performance in ES electrodes are discussed through extensive analysis of the literature, and new trends in material development are also reviewed. Two important future research directions are indicated and summarized, based on results published in the literature: the development of composite and nanostructured ES materials to overcome the major challenge posed by the low energy density of ES (476 references).

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A review of electrode materials for electrochemical supercapacitors

In recent years, tremendous research effort has been aimed at increasing the energy density of supercapacitors without sacrificing high power capability so that they reach the levels achieved in batteries and at lowering fabrication costs For this purpose, two important problems have to be solved: first, it is critical to develop ways to design high performance electrode materials for supercapacitors; second, it is necessary to achieve controllably assembled supercapacitor types (such as symmetric capacitors including double-layer and pseudo-capacitors, asymmetric capacitors, and Li-ion capacitors) The explosive growth of research in this field makes this review timely Recent progress in the research and development of high performance electrode materials and high-energy supercapacitors is summarized Several key issues for improving the energy densities of supercapacitors and some mutual relationships among various effecting parameters are reviewed, and challenges and perspectives in this exciting field are also discussed This provides fundamental insight into supercapacitors and offers an important guideline for future design of advanced next-generation supercapacitors for industrial and consumer applications

Recent Advances in Design and Fabrication of Electrochemical Supercapacitors with High Energy Densities

The state-of-the-art of polymer electrolyte membrane fuel cell (PEMFC) technology is based on perfluorosulfonic acid (PFSA) polymer membranes operating at a typical temperature of 80 °C. Some of the key issues and shortcomings of the PFSA-based PEMFC technology are briefly discussed. These include water management, CO poisoning, hydrogen, reformate and methanol as fuels, cooling, and heat recovery. As a means to solve these shortcomings, high-temperature polymer electrolyte membranes for operation above 100 °C are under active development. This treatise is devoted to a review of the area encompassing modified PFSA membranes, alternative sulfonated polymer and their composite membranes, and acid−base complex membranes. PFSA membranes have been modified by swelling with nonvolatile solvents and preparing composites with hydrophilic oxides and solid proton conductors. DMFC and H2/O2(air) cells based on modified PFSA membranes have been successfully operated at temperatures up to 120 °C under ambient pressure...

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Approaches and Recent Development of Polymer Electrolyte Membranes for Fuel Cells Operating above 100 °C

Recent developments in cathode materials for lithium ion batteries

A review of conduction phenomena in Li-ion batteries

Chromium doping as a new approach to improve the cycling performance at high temperature of 5 V LiNi0.5Mn1.5O4-based positive electrode

High-temperature cubic spinels were obtained by thermal treatment at 1100 °C of the corresponding LiCoyMn2-yO4 (0 ≤ y ≤ 1) spinels. The samples were characterized by X-ray powder diffraction, thermogravimetric analysis, electron paramagnetic resonance (EPR) spectroscopy, and electrical and electrochemical measurements. The lattice parameter of the new phases in the 0.3 0.65 the sharp increase in conductivity observed is associated with a change in electron hopping from Mn3+/Mn4+ ions to Co2+/Co3+ ones. At high temperatures, the conductivity is explained in terms of phonon-assisted polaron hopping among either Mn3+/Mn4+ or Co2+/Co3+ nearest neighbors. At low temperatures electron hopping beyond the nearest neighbors accounts for the conductivity. The electrochemical behavior of the new compound...

High temperature co-doped LiMn2O4-based spinels. Structural, electrical, and electrochemical characterization

Nanocrystalline samples of lithium manganese oxide with cubic spinel structure have been prepared by combustion of reaction mixtures containing Li(I) and Mn(II) nitrates that operate as oxidisers, and sucrose that acts as fuel. The samples were characterised by X-ray diffraction, transmission electron microscopy, thermal analysis, and impedance and electrochemical measurements. The effect of the fuel content on the purity and morphology of the products was analysed. The samples as prepared showed small amounts of Mn2O3 and Mn3O4 as impurities, depending on the amount of sucrose used in the synthesis. Annealing at 700 °C led to single-phase cubic spinels. In these phases, the smallest average particle size (ca. 30 nm) corresponded to the sample obtained with a hyperstoichiometric amount of fuel. This sample showed the Li1.05Mn1.95O4 composition
as deduced from the thermal and electrochemical data. No variation in conductivity associated with the cubic⇔orthorhombic phase transition was observed. The electrochemical behaviour as positive electrode showed good cyclability at high current densities (reversible capacity of 73 mAh g−1 at 2.46 mA cm−2).

Synthesizing nanocrystalline LiMn2O4 by a combustion route

Powders of ternary Mn–Ni–Co oxide negative temperature coefficient thermistors were synthesized by a low-temperature alternative route. The procedure allowed straightforward preparation without the addition of any binder, of highly densified Mn–Ni–Co–O semiconducting ceramics as cubic single-phase spinels, at relatively moderate temperature (≈1000 °C). A tentative cation distribution for the Mn1.5Ni0.6Co0.9O4 spinel oxide has been proposed, and its variation with temperature has also been considered. The dilatometric and X-ray powder diffraction studies carried out for Mn1.5Ni0.6Co0.9O4 showed that sintering takes place in a single stage between 900 and 1000 °C, and yields highly densified ceramic with an apparant density larger than 96% of the calculated X-ray density. Scanning electron microscopy showed different microstructures for the Mn1.5Ni0.6Co0.9O4 spinel oxide, depending on sintering conditions. The value of the sensitivity index, β=3068 K, indicates a good technological thermistor performance for this material. © 1998 Chapman & Hall

Rosa M. Rojas

Papers

Chromium doping as a new approach to improve the cycling performance at high temperature of 5 V LiNi0.5Mn1.5O4-based positive electrode

High temperature co-doped LiMn2O4-based spinels. Structural, electrical, and electrochemical characterization

Synthesizing nanocrystalline LiMn2O4 by a combustion route

Preparation and characterization of spinel-type Mn–Ni–Co–O negative temperature coefficient ceramic thermistors

Microstructural characterization of nanocrystals of ZnO and CuO obtained from basic salts