Rigid Supramolecular Aramid Nanotubes as Catalyst Supports

Y Yukio Cho (Stanford University , , , ,) K Kiera Y. Tai (Department of Materials Science and Engineering Massachusetts Institute of Technology Cambridge Massachusetts 02139 USA) G Guillaume Lamour (Université Evry Paris-Saclay, Cergy Paris Université, CNRS, Laboratoire Analyse et Modélisation pour la Biologie et l’Environnement) T Ty Christoff‐Tempesta (Department of Materials Science and Engineering Massachusetts Institute of Technology Cambridge Massachusetts 02139 USA) D Debaditya Bose Sinha (Department of Chemistry and Biochemistry University of California San Diego La Jolla California 92093 USA) Y Yu‐Jin Choi (Department of Materials Science and Engineering Massachusetts Institute of Technology Cambridge Massachusetts 02139 USA) R Rebecca Meacham (Department of Materials Science and Engineering Massachusetts Institute of Technology Cambridge Massachusetts 02139 USA) D Dechen T. Rota (Department of Materials Science and Engineering Massachusetts Institute of Technology Cambridge Massachusetts 02139 USA) S Siyu Wu X Xiaobing Zuo (X-ray Science Division) J Julia H. Ortony (Department of Materials Science and Engineering Massachusetts Institute of Technology Cambridge Massachusetts 02139 USA)

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

Volume / Issue Vol. 38, Issue 6
Published January 01, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (11)

Y

Yukio Cho

Stanford University , , , ,

K

Kiera Y. Tai

Department of Materials Science and Engineering Massachusetts Institute of Technology Cambridge Massachusetts 02139 USA

G

Guillaume Lamour

Université Evry Paris-Saclay, Cergy Paris Université, CNRS, Laboratoire Analyse et Modélisation pour la Biologie et l’Environnement

T

Ty Christoff‐Tempesta

Department of Materials Science and Engineering Massachusetts Institute of Technology Cambridge Massachusetts 02139 USA

D

Debaditya Bose Sinha

Department of Chemistry and Biochemistry University of California San Diego La Jolla California 92093 USA

Y

Yu‐Jin Choi

Department of Materials Science and Engineering Massachusetts Institute of Technology Cambridge Massachusetts 02139 USA

R

Rebecca Meacham

Department of Materials Science and Engineering Massachusetts Institute of Technology Cambridge Massachusetts 02139 USA

D

Dechen T. Rota

Department of Materials Science and Engineering Massachusetts Institute of Technology Cambridge Massachusetts 02139 USA

S

Siyu Wu

X

Xiaobing Zuo

X-ray Science Division

J

Julia H. Ortony

Department of Materials Science and Engineering Massachusetts Institute of Technology Cambridge Massachusetts 02139 USA