Layered metal chalcogenides Structures

Although there are numerous families of lamellar solids, only a handful of them exhibit the kind of versatile intercalation chemistry that forms the basis of this book. In arriving at the content of this volume, the editors have accurately identified six classes of versatile layered compounds that are at the forefront of materials intercalation chemistry, namely, smectite clays, zirconium phosphates and phos-phonates, layered double hydroxides (known informally as hydrotalcites or anionic clays ), layered manganese oxides, layered metal chalcogenides, and lamellar alkali silicates and silicic acids. Graphite and carbon nanotubes have not been included, in part because this specialty area of intercalation chemistry is limited to one or two molecular layers of comparatively small guest species that are capable of undergoing electron transfCT reactions with the host structure. 

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Wertheim, G. K., F. J. DiSalvo, and D. N. E. Buchanan (1973). Valence bands of layer structure transition metal chalcogenides. Solid State Comm. 13, 1228. 

The practical use of these calculations is limited, however, because the kinetics of a reaction can play an important role. This becomes quite obvious for layer compounds such as M0S2. The kinetics may be controlled by adsorption, surface chemistry, surface structure and crystal orientation. According to Fig. 8.15, pEdecomp is close to the conduction band, i.e. M0S2 is rather easily oxidized. In the case of a flat basal surface, it has been observed with several transition metal chalcogenides that the photocurrent onset at n-electrodes occurs with high overvoltages accompanied by a shift of Gfb.(see Section 5.3). Since this is caused by an accumulation of holes at the surface the hole transfer is kinetically inhibited. 

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