De-intercalation

Further, tungsten oxysulfide films, WOyS, have shown promising behavior as positive electrodes in microbatteries, unlike WS2 that is not suitable as cathode in lithium cells. Using amorphous thin films of WO1.05S2 and WO1.35S2.2 in the cell Li/LiAsFe, 1 M ethyl-methyl sulfone (EMS)/W03,Sz, Martin-Litas et al. [80] obtained current densities up to 37 xA cm between 1.6 and 3 V. In these cathode materials, 0.6 and 0.8 lithium per formula unit, respectively, could be intercalated and de-intercalated reversibly. 

It should be noted here, that not only the (chemical and morphological) composition of the protective layers at the basal plane surfaces and prismatic surfaces is different, but that these layers also have completely different functions. At the prismatic surfaces, lithium ion transport into/ffom the graphite structure takes place by intercalation/de-intercalation. Here the formed protective layers of electrolyte decomposition products have to act as SEI, i.e., as transport medium for lithium cations. Those protective layers, which have been formed on/at the basal plane surfaces, where no lithium ion transport into/from the graphite structure takes place, have no SEI function. However, these non-SEI layers still protect these anode sites from further reduction reactions with the electrolyte. 

Figure 17. The basal plane and prismatic surfaces of graphite have different functions with respect to lithium intercalation and de-intercalation (= charge, discharge, self-discharge, etc.). As a consequence, only the electrolyte decomposition product layers at the prismatic surfaces have SEIfunction. Any processes related with electrolyte decomposition product layers at the basal plane surfaces (= non-SEI layers) therefore can not be directly related to electrochemical data such as charge, discharge, self-discharge, etc. The situation is even more complex as the SEI composition and morphology at the basal and prismatic surface...

Properties Charge (intercalation) at OV, mAh/g De-intercalation at 2V, mAh/g Irreversible capacity, %... 

Figure 3. Voltage dependence of the HF semi circle radius during Li de-intercalation (a) and re-intercalation (b) into graphite.

Figure 5 displays the composition dependence of during intercalation and de intercalation. This curve seems to feature four distinguishable domains. 

Figure 5. Composition dependence of the average graphene interlayer spacing during the lithium intercalation and de-intercalation.

SWNTs, the stability of the (C, PF ) ionic compound should be lower than in flat graphite layers. Therefore, during the electrochemical intercalation a chemical de-intercalation (decomposition) may take place, which explains the low faradaic yield of the anodic intercalation. 

Fig. 7.8 Potential-capacity curve for a graphite electrode, determined during the first intercalaLion/de-intercalation cycle...

The electrochemical discharge-charge process of the battery is based on the intercalation/de-intercalation of lithium molybdenum disulphide ... 

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