2 research outputs found

    Enhancing Proton Conduction in a Metal–Organic Framework by Isomorphous Ligand Replacement

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    Using the concept of isomorphous replacement applied to entire ligands, a <i>C</i><sub>3</sub>-symmetric trisulfonate ligand was substituted with a <i>C</i><sub>3</sub>-symmetric tris­(hydrogen phosphonate) ligand in a proton conducting metal–organic framework (MOF). The resulting material, PCMOF2<sup>1</sup>/<sub>2</sub>, has its proton conduction raised 1.5 orders of magnitude compared to the parent material, to 2.1 × 10<sup>–2</sup> S cm<sup>–1</sup> at 90% relative humidity and 85 °C, while maintaining the parent MOF structure

    Achieving Superprotonic Conduction in Metal–Organic Frameworks through Iterative Design Advances

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    Two complementary design strategies, isomorphous ligand replacement and heterocycle doping, have been applied to iteratively enhance the proton conductivity of a metal–organic framework, β-PCMOF2. The resulting materials, PCMOF2<sup>1</sup>/<sub>2</sub>(Pz) and PCMOF2<sup>1</sup>/<sub>2</sub>(Tz) (Pz = 1<i>H</i>-pyrazole, Tz = 1<i>H</i>-1,2,4-triazole), have their proton conduction raised almost 2 orders of magnitude compared to β-PCMOF2. The bulk conductivities of these materials are over 10<sup>–1</sup> S cm<sup>–1</sup> at 85 °C and 90% relative humidity (RH), while maintaining the parent MOF structure. A solid state synthetic route for doping 1-D channels is also presented
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