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Electrochemistry of Related Materials

In the above-studied systems, the aluminosilicate framework merely acts as a porous, electrochemically inert support embedding the redox-active guests. In contrast to this, the presence of electroactive atoms in the composition of the aluminosilicates renders the solid electroactive. This applies to the case of titanium [Pg.82]

It should be noted that thermal treatments applied to aluminosilicates can vary significantly with their properties. For instance, silica calcination at temperatures ca. 900°C produces condensation of neighboring silanol groups to form silanoxy bridges (Hozumi et al., 2000 Naono et al., 2000). This process can be schematized as  [Pg.83]

From the electrochemical point of view, an important class of materials is that constituted by aluminosilicates incorporating cobalt, iron, etc., centers. In the case of Fe-based zeolites with Mobil Five structure (FeZSM-5) materials, different forms of iron can coexist. These include isolated ions either in framework positions (isomorphously substituting silicon centers), isolated ions in cationic positions in zeolite channels, binuclear and oligonuclear iron complexes in extra-framework positions, iron oxide nanoparticles (size 2 nm), and large iron oxide particles (FcjOj) in a wide distribution (up to 25 nm in size) located in the surface of the zeolite crystal (Perez-Ramirez et al., 2002). The electrochemistry of such materials will be reviewed in Chapter 8. [Pg.83]


See other pages where Electrochemistry of Related Materials is mentioned: [Pg.82]    [Pg.753]    [Pg.779]   


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