Metal phosphonate (MP)-based coordination polymers (CPs) are structurally versatile multifunctional compounds containing different acidic groups such as P-OH; SO3H, COOH, N+-H, etc. These features result in the formation of extended H-bond networks and confer a wide range of proton conduction properties to be used as components of membrane electrode assemblies (MEAs).In this work, the focus is placed on the proton conduction properties of coordination polymers derived from the combination of lanthanide ions with different multifunctional phosphonic ligands, such as phosphonotaurine (2-[bis(phosphonomethyl)amino]-ethanesulfonic acid) or nitrilo-tris (methylenephosphonic acid). High-throughput hydrothermal screening has been used to reach optimal synthesis conditions. Their crystal structures were solved ab initio from X-ray powder or single-crystal diffraction data. Proton conductivities of the MPs and Nafion-mixed membranes were determined by electrochemical impedance spectroscopy (EIS). We report the synthesis and structural features of several members of both families of MPs. The presence of the different functional groups in these ligands such us free sulfonic groups or the incorporating sulphate species into the framework of CPs, lead to a wide variety of metal ligand coordination modes and frameworks, which determine their proton conductivity properties, ranged between 10−3 and 10−2 S·cm−1 at 90 °C and 95% RH. Selected materials were studied as fillers for the preparation of Nafion-mixed membranes, and their responses in proton exchange membrane fuel cells (PEMFCs) were established under operating conditions. The structural role and orientation of the acid groups of the ligand contribute to tune the H-bonding networks and, hence, the proton transfer processes. Preliminary results indicate that these solids perform satisfactorily as fillers of Nafion-based membranes, showing power and current densities higher than those of the pristine Nafion in short times.
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