Reuseable Monolithic Nanoporous Graphite-Supported Nanocatalysts (Fe, Au, Pt, Pd, Ni, and Rh) from Pyrolysis and Galvanic Transmetalation of Ferrocene-Based Polyamide Aerogels
Source abstract
Abstract
Polyamide aerogels with ferrocene as a monomer repeat unit were prepared in one step from ferrocene dicarboxylic acid and tris(4-isocyanatophenyl)methane. Pyrolysis at ≥800 °C yielded nanoporous carbons doped throughout with crystallites of α-Fe (about 50 nm in diameter), which in turn were shrouded in graphitic ribbons (<30 graphene layers thick). Transmetalation was carried out with aqueous solutions of Au, Pt, Pd, Rh, and Ni salts, via a path akin to galvanic corrosion, whereas graphitic ribbons separated anodes (α-Fe particles) from cathodes (defects along the ribbons). The new metallic phases formed clusters of smaller crystallites (10–20 nm in diameter) on the graphitic ribbons, leaving behind empty cage-like formations previously occupied by the Fe(0) nanoparticles. All metal-doped carbons were monolithic and over 85% porous. Catalytic activity was demonstrated with the oxidation of benzyl alcohol to benzaldehyde catalyzed with carbon-supported Au or Pt, the reduction of nitrobenzene by hydrazine to aniline catalyzed with carbon-supported Fe, and two Heck coupling reactions of iodobenzene with styrene or butyl acrylate, catalyzed with carbon-supported Pd. The distinguishing feature of those catalysts was that they could be just picked up, for example, with a pair of tweezers, and redeployed in a new reaction mixture immediately, thus bypassing less efficient recovery processes like filtration.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Nanomaterials for catalytic reactions · Supercapacitor Materials and Fabrication · Catalytic Processes in Materials Science
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, Missouri University of Science and Technology, Rolla, Missouri 65409, United States
Funding
Army Research Office
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