Cathodes interaction with electrolyte

Chemical stability and relatively low interactions with electrolyte. With YSZ electrodes, many La-based compounds form the insulating La2Zr20 . With ceria-based electrolytes, this issue is not a concern and other cathode materials are considered (e.g. (La,Sr)(Co,Fe)03 or LSCF). 

Interaction of Carbon Cathode Blocks with Electrolyte During Startup and in Service Wear. Infiltration... 

However, reliable information about dependence of the functional properties of complex nickelates on their chemical composition and structure is still absent, while any straightforward and accelerated design of cathode materials is to be based upon reliable (and independent upon their interaction with electrolyte) characterization of the ability of then-surface sites to catalyze the oxygen reduction as well as of oxygen mobility in the bulk. Several lanthanum-nickel-iron mixed oxides with perovskite structure have demonstrated promising performance as cathodes for IT SOFC with traditional YSZ and GDC electrolytes [111-112]. However, studies of the behavior of electrode materials in contact with ATLS electrolytes or that of ATLS-based composites are veiy scarce [113]. 

Metalliding. MetaUiding, a General Electric Company process (9), is a high temperature electrolytic technique in which an anode and a cathode are suspended in a molten fluoride salt bath. As a direct current is passed from the anode to the cathode, the anode material diffuses into the surface of the cathode, which produces a uniform, pore-free alloy rather than the typical plate usually associated with electrolytic processes. The process is called metalliding because it encompasses the interaction, mostly in the soHd state, of many metals and metalloids ranging from beryUium to uranium. It is operated at 500—1200°C in an inert atmosphere and a metal vessel the coulombic yields are usually quantitative, and processing times are short controUed... 

These primary electrochemical steps may take place at values of potential below the eqnilibrinm potential of the basic reaction. Thns, in a solntion not yet satnrated with dissolved hydrogen, hydrogen molecnles can form even at potentials more positive than the eqnilibrinm potential of the hydrogen electrode at 1 atm of hydrogen pressnre. Becanse of their energy of chemical interaction with the snbstrate, metal adatoms can be prodnced cathodically even at potentials more positive than the eqnilibrinm potential of a given metal-electrolyte system. This process is called the underpotential deposition of metals. 

Electrolyte The challenges for electrolyte developments are non-catalytic in nature. However, because anode and cathode development activities have to consider compatibility and interaction with the electrolyte, the most important issues are mentioned here. First, the oxygen ion conductivity of the electrolyte should... 

Electrolyte Structure Ohmic losses contribute about 65 mV loss at the beginning of life and may increase to as much as 145 mV by 40,000 hours (15). The majority of the voltage loss is in the electrolyte and the cathode components. The electrolyte offers the highest potential for reduction because 70% of the total cell ohmic loss occurs there. FCE investigated increasing the porosity of the electrolyte 5% to reduce the matrix resistance by 15%, and change the melt to Li/Na from Li/K to reduce the matrix resistivity by 40%. Work is continuing on the interaction of the electrolyte with the cathode components. At the present time, an electrolyte loss of 25% of the initial inventory can be projected with a low surface area cathode current collector and with the proper selection of material. 

Another issue closely related with the anodic stability of electrolytes is the interaction between electrolyte components and the commonly used cathode substrate A1 in lithium ion cells. 

MacNeil and Dahn, whether the LiBOB-based electrolytes are safer against thermal runaway would still depend on their interaction with the cathode materials. 

The free-radicals are generated by discharge of proton, peroxides and easily reducible compounds at the cathode according to Eq. (1—4). The radial-anion of monomer is obtained by both direct and indirect electron transfer process [Eq. (5—6)]. The indirect process means that the active oxidizing species is formed from the electrolytes by electrode reaction, followed by interaction with the monomer. An unstable monomer like a,a -2-trichloro-p-xylene is formed and polymerizes instantaneously [Eq. (7)]. The regeneration of ferrous ion from the pool of used up ferric ion in a redox system is electrolytically successful [Eq. (8)] and an... 

The oxide redox energy levels for all elements except gold are cathodic to the redox level of the H2O/O2 couple. Gold, however, is an impractical component for compound semiconductors. All other compound semiconductors employed as electrolysis photoanodes will undergo surface oxidation in aqueous electrolytes to produce a surface oxide film which normally constitutes the stable surface of the photoelectrode. Our proposed mechanism indicates that the proton induced oxide dissolution reaction arises from product ir ion interactions with the oxide anion (0=). 

Electrolytically initiated polymerization may either depend on a direct electron transfer between electrode and monomer, or on the formation of an intermediate which interacts with a monomer molecule in a fast chemical step, thus creating a chain initiator. As an example of the former type of process, the formation of a living polymer from the cathodic polymerization of a -methylstyrene by electrolysis in sodium tetraethylaluminate - tetrahydrofuran may be cited 639 whereas a typical case of the latter type is the anodic polymerization of vinyl monomers by electrolyzing them together with sodium acetate in aqueous solution 63 7,640) Here it is assumed that acetate ion is discharged to form an acetoxy or methyl radical which attacks the monomer molecule in a fast chemical step. 

Electrodialysis can be performed with two main cell types multi-membrane cells for dilution-concentration and water dissociation applications, and electrolysis (or electro-electrodialysis [EED]) cells for oxidoreduction reactions. In multimembrane cells, only the membrane transport phenomena intervene, while electrochemical reactions occurring at the electrodes do not interact with the separation process the electrodes are simple electrical terminals immersed in electrolytes allowing the current transfer. The electrolysis cell operates with only one membrane that separates two solutions circulating in each electrode compartment. This application is based on electrode redox reactions, which are electrolysis specific properties. The anode induces oxidations, and reductions occur at the cathode [4]. 

The main problem arose with respect to the negative electrode. Complications typical for galvanic practice appear under its charge, that is, under cathodic deposition of lithium. As pointed out in Chapter 11, the surface of lithium in aprotic electrolytes is covered by a passive film (SEI) because of the chemical interaction with the components of electrolyte the organic solvent and anions. This film has the properties of solid electrolyte with conductivity by lithium ions. The film is sufficiently thin (its thickness does not exceed several nanometers) and it protects lithium safely from... 

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