Acidic groups-containing metal phosphonates exhibit a wide range of proton
conductivity depending on the water content and functionality. Moreover, this property can
be enhanced by appropriate post-synthesis chemical and/or thermal treatments [1,2].
In this work, focus is laid on properties derived from the combination of lanthanide ions
with the amino-sulfophosphonate ligand (H2O3PCH2)2-N-(CH2)2-SO3H. Highthrough-put
screening was used to reach the optimal synthesis conditions under hydrothermal
conditions at 140 ºC. Isolated polycrystalline solids, Ln[(O3PCH2)2-NH-(CH2)2-SO3H]·2H2O
(Ln= La, Pr, Sm, Eu, Gd, Tb and Er), crystallize in the monoclinic (La and Er) and
orthorhombic (Pr, Sm, Eu, Gd and Tb) systems with unit cell volume of ~1200 and 2548 Å3
respectively. Their crystal structures, solved ab initio from X-ray powder diffraction data,
correspond to different layered frameworks depending on the lanthanide cation size. Thus,
compounds with orthorhombic symmetry show free acidic sulfonic pointing to the interlayer
space, while La- and Er- derivatives display layered structures where both phosphonate
and sulfonated groups are coordinated to the metal, leaving free P-OH groups. As
consequence of this structural variability, different H-bond networks and proton transfer
pathways are generated. Preliminary proton conductivity measurements have been carried
out between 25 and 80 ºC at 70-95 % relative humidity. The sample exhibits conductivities
near to 3.10-3 S.cm-1 and activation energies characteristics of a Grotthuss-type
mechanism of proton transfer.Proyectos de investigación del ministerio MICINN, Españam(MAT2016-77648-R),
Proyectos de la Junta de Andalucía (P12-FQM-1656),
Universidad de Málaga. Campus de Excelencia Internacional Andalucía Tech
