H. Roussel et al., Cationic order and structure of [Zn-Cr-Cl] and [Cu-Cr-Cl] layered double hydroxides: A XRD and EXAPS study, J PHYS CH B, 104(25), 2000, pp. 5915-5923
X-ray diffraction (XRD) and extended X-ray absorption fine structure (EXAFS
) were used to evidence a cationic order within sheets of the layered doubl
e hydroxides (LDH) [Zn-Cr-Cl] and [Cu-Cr-Cl]. The [Zn-Cr-Cl] LDH is well ko
wn for its ability to be synthesized only with the ratio Zn/Cr = 2, whateve
r the proportion of di- and trivalent cations in the starting solutions; it
would thus be a good candidate for showing cationic order. The XRD diagram
s were identical and were indexed in the R-3m space group, no superstructur
e being observed. So, the cations, (Zn, Cr) and (Cu,Cr) for [Zn-Cr-Cl] and
[Cu-Cr-Cl], respectively, are distributed statistically on the same site in
the structural model obtained by Rietveld refinement from the XRD diagrams
. The interlamellar species (Cl and O of water) show a relative disordered
state. Local description of the arrangement around cations by EXAFS at cati
ons K edge concludes unambiguously for [Cu-Cr-Cl] to a cation ordering; str
ong evidence of similar ordering has been obtained for [Zn-Cr-Cl]. We have
also shown that this technique is only sensible to the species of a same sh
eet. EXAFS simulations performed at Cr and Cu K edge on the [Cu-Cr-Cl] LDH
also show a corrugation in its sheets because of the Jahn-Teller distortion
in Cu2+ octahedra, which is opposite to the [Zn-Cr-Cl] sheets presenting a
relative flatness.