Enhanced proton conductivity by guest molecule exchange in an acylamide-functionalized metal–organic framework

Abstract

Metal–organic frameworks (MOFs) as types of proton conductive materials have attracted much attention. Here, an acylamide-functionalized 3D MOF, [Ni₃(TPBTC)₂(stp)₂(H₂O)₄]·2DMA·32H₂O, has been successfully constructed via combining Ni(NO₃)₂, TPBTC (TPBTC = benzene-1,3,5-tricarboxylic acid tris-pyridin-4-ylamide) and 2-H₂stp (2-H₂stp = 2-sulfoterephthalic acid monosodium salt) under solvothermal conditions. Single-crystal X-ray diffraction revealed that there are uncoordinated guest DMA molecules in the pores of the compound. On removal of guest DMA molecules, the proton conductivity of the compound increased to 2.25 × 10⁻³ S cm⁻¹ at 80 °C and 98% RH which is about 110 times that of the original material. It is hoped that this work can provide essential insight for designing and obtaining improved crystalline-state proton conducting materials by considering the influences of guest molecules on proton conduction properties of porous materials.