Daniel Loof, Oliver Thüringer, Dr. Marco Schowalter, Dr. Christoph Mahr, Anmona Shabnam Pranti, Prof. Dr. Walter Lang, Prof. Dr. Andreas Rosenauer, Dr. Volkmar Zielasek, Dr. Sebastian Kunz, and Prof. Dr. Marcus Bäumer
Abstract Porous networks of Pt nanoparticles interlinked by bifunctional organic ligands have shown high potential as catalysts in micro‐machined hydrogen gas sensors. By varying the ligand among p‐phenylenediamine, benzidine, 4,4‘‘‐diamino‐p‐terphenyl, 1,5‐diaminonaphthalene, and trans‐1,4‐diaminocyclohexane, new variants of such networks were synthesized. Inter‐particle distances within the networks, determined via transmission electron microscopy tomography, varied from 0.8 to 1.4 nm in accordance with the nominal length of the respective ligand. While stable structures with intact and coordinatively bonded diamines were formed with all ligands, aromatic diamines showed superior thermal stability. The networks exhibited mesoporous structures depending on ligand and synthesis strategy and performed well as catalysts in hydrogen gas microsensors. They demonstrate the possibility of deliberately tuning micro‐ and mesoporosity and thereby transport properties and steric demands by choice of the right ligand also for other applications in heterogeneous catalysis.