Rigid Supramolecular Aramid Nanotubes as Catalyst Supports
Abstract
Abstract Solution‐phase heterogeneous catalysts benefit from nanoscale dimensions, which maximize specific surface area and enhance catalytic activity. However, the ease of recovering such nanocatalysts depends on the design of the support materials, which are often particle‐like. Rigid 1D nanomaterials are proposed as supports that can enhance separability while offering high volumetric specific surface area for greater catalyst loading and activity. Here, aramid amphiphiles (AAs) are designed to spontaneously self‐assemble in water into high‐aspect‐ratio supramolecular nanotubes with tunable surface chemistry. These AA nanotubes exhibit high persistence lengths ( P = 750 ± 340 µm) and mechanical stiffnesses (3 N/m). Incorporating surface thiol groups enables immobilization of catalytic gold nanoparticles. The resulting AA nanotube‐gold nanoparticle complexes exhibit high catalytic activity, efficient recoverability via simple microfiltration, and sustained reusability over ten reaction cycles. This study demonstrates the utility of molecular self‐assembled 1D nanomaterials as versatile scaffolds for the reuse and recovery of nanoscale catalysts.
Article Details
Authors (11)
Yukio Cho
Stanford University , , , ,
Kiera Y. Tai
Department of Materials Science and Engineering Massachusetts Institute of Technology Cambridge Massachusetts 02139 USA
Guillaume Lamour
Université Evry Paris-Saclay, Cergy Paris Université, CNRS, Laboratoire Analyse et Modélisation pour la Biologie et l’Environnement
Ty Christoff‐Tempesta
Department of Materials Science and Engineering Massachusetts Institute of Technology Cambridge Massachusetts 02139 USA
Debaditya Bose Sinha
Department of Chemistry and Biochemistry University of California San Diego La Jolla California 92093 USA
Yu‐Jin Choi
Department of Materials Science and Engineering Massachusetts Institute of Technology Cambridge Massachusetts 02139 USA
Rebecca Meacham
Department of Materials Science and Engineering Massachusetts Institute of Technology Cambridge Massachusetts 02139 USA
Dechen T. Rota
Department of Materials Science and Engineering Massachusetts Institute of Technology Cambridge Massachusetts 02139 USA
Siyu Wu
Xiaobing Zuo
X-ray Science Division
Julia H. Ortony
Department of Materials Science and Engineering Massachusetts Institute of Technology Cambridge Massachusetts 02139 USA