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null (Ed.)(Bi 1/2 Na 1/2 )TiO 3 (BNT) based ceramics have been the hot topic for a few years because of their multiple functions, from the piezoelectric properties to more recently the electrostatic energy storage performance. However, some basic issues are still unclear, preventing their wide application in real devices. One of them is the underlying conduction mechanism, the interplay of electronic and ionic carriers as a mixed ionic case and the subsequent quantification. This paper deals with the most basic compositions, which are the typical ones from the (1 − x )(Bi 1/2 Na 1/2 )TiO 3 – x BaTiO 3 (BNT– x BT) phase diagram. The conductivity is primarily investigated by impedance spectroscopy, while different equivalent circuits are applied to different conduction mechanisms. A transition from predominantly ionic to predominantly electronic conduction is revealed to occur with the increase in BaTiO 3 concentration. The mixed ionic–electronic conduction in the composition near the morphotropic phase boundary, namely BNT–7%BT, is identified and then quantified. To verify our interpretation of impedance results, dc degradation is, for the first time, conducted in this family of materials, from which the electronic and ionic conductions can be easily separated by accessing the mean time to failure. The successful combination of the two methods enables us to have an overview of how the oxygen vacancy dynamics in the BNT– x BT system depends upon the phase nature or the domain structure.more » « less
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Abstract C(1)‐vinylation of [
closo ‐1‐CB9H10]−(A ) and [closo ‐1‐CB11H12]−(B ) with 4‐benzyloxystyryl iodide followed by hydrogenation of the double bond and reductive deprotection of the phenol functionality led to C(1)‐(4‐hydroxyphenethyl) derivatives. The phenol functionality was protected as the acetate. The esters were then treated with PhI(OAc)2and the resulting isomers were separated kinetically (for derivatives of anionA ) or by chromatography (for derivatives of anionB ) giving the difunctionalized building blocks in overall yields of 9 % and 50 %, respectively. A similar series of reactions was performed starting with anionsA andB and 4‐methoxystyryl bromide and iodide. Significant differences in the reactivity of derivatives of the two carborane anions were rationalized with DFT computational results. Application of the difunctionalized carboranes as building blocks was demonstrated through preparation of two ionic liquid crystals. The extensive synthetic work is accompanied by single crystal XRD analysis of six derivatives.
