Metal phosphonates are multifunctional solids which possess tunable properties, such as
H-bond networks, while exhibiting high chemical and thermal stability. Depending on the protonation of the ligand, different crystalline phases can be obtained.
Here, we report three different families of proton conductors based on lanthanide nitrilotrismethylphosphonates.
Compounds having cationic layers compensate by chloride or sulfate
anions were isolated: [Ln(H4NMP)(H2O)2]Cl·2H2O and Ln(H5NMP)]·SO4·4H2O [H6NMP =
nitrilotris(methylphosphonic acid)]. The crystal structure of Gd-(H5NMP)]·SO4·4H2O was
solved ab initio from synchrotron powder diffraction data (λ=0.4124 Å, beamline BL04-MSPD ALBA) and refined by the Rietveld method. Chloride containing phases show two irreversible solid state transformations take place: (1) a crystalline-to-crystalline phase transition, {Ln-H4NMP → [Ln2(H3NMP)2(H2O)4]·4.5H2O for Ln= La, Pr}, and (2) crystalline-to-amorphous
phase transition, {LnH4NMP → [Ln(H3NMP)]·1.5H2O for Ln= Gd - Ho}, both implies the loss
of HCl and structural rearrangements of the frameworks. Variations in average and local
structure have been monitored by high resolution powder diffraction and PDF analysis, upon exposure the samples at high relative humidity and temperature (95% RH and 80 ºC), in order to understand their behavior as proton conductors.Universidad de Málaga. Campus de Excelencia Internacional Andalucía Tech
