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Lithium-electrode potential

In view of the ionisation energies the electrode potentials for lithium and beryllium might be expected to be higher than for sodium and magnesium. In fact... [Pg.134]

The electrode potential of lithium is -3.01 V vs. NHE, which is the lowest value among all the metals. Lithium has the lowest density (0.54gcnrf3) and the lowest electrochemical equivalent (0.259 g Ah-1) of all solids. As a result of these... [Pg.32]

There are some other matters that should be considered when comparing metallic lithium alloys with the lithium-carbons. The specific volume of some of the metallic alloys can be considerably lower than that of the carbonaceous materials. As will be seen later, it is possible by selection among the metallic materials to find good kinetics and electrode potentials that are sufficiently far from that of pure lithium for there to be a much lower possibility of the potentially dangerous forma-... [Pg.362]

This thermodynamically based methodology provides predictions of the lithium capacities in addition to the electrode potentials of the various three-phase equilibria under conditions of complete equilibrium. This information is included as the last column in Table 2, in terms of the number of moles of lithium per kilogram total alloy weight. [Pg.364]

Equation (40) relates the lifetime of potential-dependent PMC transients to stationary PMC signals and thus interfacial rate constants [compare (18)]. In order to verify such a correlation and see whether the interfacial recombination rates can be controlled in the accumulation region via the applied electrode potentials, experiments with silicon/polymer junctions were performed.38 The selected polymer, poly(epichlorhydrine-co-ethylenoxide-co-allyl-glycylether, or technically (Hydrine-T), to which lithium perchlorate or potassium iodide were added as salt, should not chemically interact with silicon, but can provide a solid electrolyte contact able to polarize the silicon/electrode interface. [Pg.497]

For any type of nonaqueous electrolyte (nonaqueous solutions, melts, solid electrolytes) we can select suitable reference electrodes, measure the potentials of other electrodes, and set up tables of electrode potentials. The order of the reactions (electrodes) as a rule does not strongly differ between the different media. A strong reducing agent such as lithium will have a more negative potential than a weaker reducing agent such as copper, both in water and in other media. [Pg.50]

The intercalation compounds of lithium with graphite are very different in their behavior from intercalation compounds with oxides or halcogenides. Intercalation processes in the former compounds occur in the potential region from 0 to 0.4 V vs. the potential of the lithium electrode. Thus, the thermodynamic activity of lithium in these compounds is close to that for metallic lithium. For this reason, lithium intercalation compounds of graphite can be used as negative electrodes in batteries rather than the difficultly of handling metallic lithium, which is difficult to handle. [Pg.446]

The Li-Ion system was developed to eliminate problems of lithium metal deposition. On charge, lithium metal electrodes deposit moss-like or dendrite-like metallic lithium on the surface of the metal anode. Once such metallic lithium is deposited, the battery is vulnerable to internal shorting, which may cause dangerous thermal run away. The use of carbonaceous material as the anode active material can completely prevent such dangerous phenomenon. Carbon materials can intercalate lithium into their structure (up to LiCe). The intercalation reaction is very reversible and the intercalated carbons have a potential about 50mV from the lithium metal potential. As a result, no lithium metal is found in the Li-Ion cell. The electrochemical reactions at the surface insert the lithium atoms formed at the electrode surface directly into the carbon anode matrix (Li insertion). There is no lithium metal, only lithium ions in the cell (this is the reason why Li-Ion batteries are named). Therefore, carbonaceous material is the key material for Li-Ion batteries. Carbonaceous anode materials are the key to their ever-increasing capacity. No other proposed anode material has proven to perform as well. The carbon materials have demonstrated lower initial irreversible capacities, higher cycle-ability and faster mobility of Li in the solid phase. [Pg.179]

Lithium electrodes, 3 408 standard potential, 3 413t Lithium fluoride, 15 138-139 Lithium fluoroborate, 4 153 manufacture, 4 155 physical properties of, 4 152t thermodynamic properties of, 4 154t uses of, 4 157... [Pg.531]

Recently, our laboratory produced a foldable, bendable, and cutable postage-stamp-sized battery (Fig. 12.2). The device looks like a simple sheet of black paper, but it could spell a revolution in implantable battery technology (Pushparaj et al., 2007). The paper battery, a one-piece-integrated device is made of cellulose with CNT and lithium electrodes. The device is flexible, rechargeable, and has the ability to function over a wide range of temperatures giving it a wide variety of potential biomedical applications. As a biomaterial, this paper battery may be useful as a pacemaker because it could easily be inserted under a patient s skin. [Pg.287]

Table 4 lists selected electrochemical stability data for various lithium salt anions that are commonly used in lithium-based electrolytes, with the measurement approaches indicated. Although it has been known that the reduction of anions does occur, sometimes at high potentials, the corresponding processes are usually sluggish and a definite potential for such reductions is often hard to determine. The reduction of solvents, occurring simultaneously with that of anions on the electrode, further complicates the interpretation efforts. For this reason, only the anodic stability of salt anions is of interest, while the cathodic limit of the salt in most cases is set by the reduction of its cation (i.e., lithium deposition potential). [Pg.84]

Compare the chemical activity of the studied alkali metals. What does it depend on Why does lithium head the electrochemical series of the metals Find the values of the standard electrode potentials of the alkali metals (see Appendix 1, Table 21). [Pg.181]

The properties of lithium metal were described in Chapter 4, where particular note was made of its high specific capacity and electrode potential. However, because of its highly electropositive nature, it is thermodynamically unstable in contact with a wide variety of reducible materials. In particular, lithium reacts with components of most electrolytes to form a passivating layer. Film formation of this type ensures long shelf life for primary lithium cells, but causes severe problems when the electrode is cycled in a secondary cell. [Pg.202]

The use of lithium amalgam electrodes allows better control of electrode potential than the potassium amalgam electrode. Separations of Sm from Gd, Eu from Sm, Sm from Eu and of Yb from heavy rare earths have been successfully carried out by Onstott [135—137]. [Pg.102]


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