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Lithium battery performances

Lithium-Ion Cells. Lithium-ion cells and the newer alternative, lithium-ion-polymer, can usually run much longer on a charge than comparable-size Nicad and nickel-metal hydride batteries. Usually is the keyword here since it depends on the battery s application. If the product using the battery requires low levels of sustained current, the lithium battery will perform very well however, for high-power technology, lithium cells do not perform as well as Nicad or nickel-metal hydride batteries. [Pg.120]

An Li-Al Alloy was investigated for use as a negative electrode material for lithium secondary batteries. Figure 41 shows the cycle performance of a Li-Al electrode at 6% depth of discharge (DOD). The Li-Al alloy was prepared by an electrochemical method. The life of this electrode was only 250 cycles, and the Li-Al alloy was not adequate as a negative material for a practical lithium battery. [Pg.42]

Carbon dioxide has been proposed as an additive to improve the performance of lithium batteries [60]. Aurbach et al. [61] studied the film formed on lithium in electrolytes saturated with C02, and using in situ FTIR found that Li2C03 is a major surface species. This means that the formation of a stable Li2C03 film on the lithium surface may improve cyclability [62], Osaka and co-workers [63] also studied the dependence of the lithium efficiency on the plating substrate in LiC104-PC. The addition of C02 resulted in an increase in the efficiency when the substrate was Ni or Ti, but no effect was observed with Ag or Cu substrates. [Pg.349]

It is now well established that in lithium batteries (including lithium-ion batteries) containing either liquid or polymer electrolytes, the anode is always covered by a passivating layer called the SEI. However, the chemical and electrochemical formation reactions and properties of this layer are as yet not well understood. In this section we discuss the electrode surface and SEI characterizations, film formation reactions (chemical and electrochemical), and other phenomena taking place at the lithium or lithium-alloy anode, and at the Li. C6 anode/electrolyte interface in both liquid and polymer-electrolyte batteries. We focus on the lithium anode but the theoretical considerations are common to all alkali-metal anodes. We address also the initial electrochemical formation steps of the SEI, the role of the solvated-electron rate constant in the selection of SEI-building materials (precursors), and the correlation between SEI properties and battery quality and performance. [Pg.420]

Currently, there is great interest in the application of solid electrolytes for high-performance secondary lithium batteries... [Pg.525]

ELECTROCHEMICAL PERFORMANCE OF Ni/Cu-METALLIZED CARBON-COATED GRAPHITES FOR LITHIUM BATTERIES... [Pg.369]

Carbon-coating is an effective way to improve the performance of electrode materials for lithium batteries, particularly with graphites [11-14], It is also known to aid in the surface conductivity for LiFeP04 as a cathode material [27], There are many ways to coat powders with carbon, but in this study, we have chosen to decompose a hydrocarbon vapor of propylene in a nitrogen carrier gas at a moderate temperature of 700 °C. Criteria for using this process include a material that is stable at this temperature and under a reducing environment. [Pg.377]

Yang S, Cui G, Pang S, Cao Q, Kolb U, Feng X, Amier J, Mullen K. Fabrication of cobalt and cobalt oxide/graphene composites Towards high-performance anode materials for lithium batteries, ChemSusChem 2010, 3, 236-239. [Pg.292]

The benefit of a hybrid phase for the intercalation-deintercalation of mobile species such as Li+ cations is well illustrated by the study of conductive polymers such as polyaniline or polypyrrole intercalated into a V2O5 framework as potential electrode materials in lithium batteries [34]. For PANI/V2O5, an oxidative post-treatment performed under an oxygen atmosphere allowed the authors to compare the conductivity attributed to the polymer, as in absence of reduced cations, there was no electronic hopping between ions, and the conductive state was due only to the... [Pg.127]

Intercalation of species into the CNT structure has also been performed. For instance, the intercalation of lithium in CNTs [93,94] is one attractive topic due to the potential applications in electrochemical energy storage in lithium batteries. Edge-plane defects turn out to be very important for such processes [95]. [Pg.135]

However, certain restrictions on battery performance arise from these state-of-the-art electrolytes, for which these two indispensable components are mainly responsible (1) a low-temperature limit (—20 °C) set by EC due to the high melting point and the high liquidus temperature it confers upon the solvent mixture, and (2) a high-temperature limit (50 °C) set by LiPEe due to its reactivity with solvents. As a result, the commercialized lithium ion batteries can... [Pg.76]

Hying, C. Separion separators for lithium batteries—safety performance. Presented at Batteries 2004, 6th Ed. Paris, June 2-4, 2004. [Pg.221]

Although much of the V NMR has been performed on model systems or catalytic materials containing vanadium, 29 >30 compounds such as V2O5 or VOPO4 are used in both the catalysis and lithium battery fields, and many of the results can be used to help elucidate the structures of vanadium-containing cathode materials. V NMR spectra are sensitive to changes in the vanadium coordination number and distortions of the vanadium local environments from regular tetrahedra or octahedra. >33 5>V isotropic chemical shifts of between —400 and —800 ppm are seen for vanadium oxides, and unfortunately, unlike... [Pg.268]

Because of the importance of high-performance secondary batteries, the techniques of the secondary lithium batteries are still making rapid progresses. Lithium polymer secondary batteries, having gel-polymer electrolytes, are advantageous in that the rigid metal container is not essential. Thus, all-plastic thin lithium secondary batteries are now available. [Pg.315]


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See also in sourсe #XX -- [ Pg.75 , Pg.76 , Pg.77 ]




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