文摘
Heterogeneous catalysis performed in wall-coated reactors and electrocatalysis require homogeneous catalytic coatings with high surface area and good accessibility of the active sites. Conventional coating methods necessitate the use of binder components that often block pores and active sites, which limits catalytic efficiency, and utilization of expensive active metals. We report an approach for the direct and binder-free synthesis of chemically, mechanically, and thermally stable catalytic coatings based on ordered mesoporous carbon films employed as catalyst support. The synthesis relies on the codeposition of a structure-directing agent and small clusters of polymeric carbon precursors along with ionic metal species on a substrate. A sequence of thermal treatments converts the polymer into partly graphitized carbon, decomposes the structure-directing agent, and converts the metal precursor into highly active nanoparticles. Syntheses and catalytic applications are exemplarily demonstrated for palladium on carbon, a system widely used in heterogeneous catalysis and electrocatalysis. The obtained catalysts provide significantly higher space–time yields in the selective gas-phase hydrogenation of butadiene than all reported Pd/C catalysts while at the same time retaining isothermal reactor conditions. Moreover, when they were tested in the electrocatalytic hydrogen evolution reaction (HER), the catalysts outperformed reported Pd/C catalysts by a factor of 3, which underlines the benefits of the developed binder-free catalyst system.