Abstract

Inorganic nanotubes with unique and well-defined porous structures show promising applications in diverse functional materials. However, it remains a challenge to fabricate inorganic nanotubes with precise length controllability. Herein, we report the synthesis of block copolymers consisting of a crystalline π-conjugated oligo(p-phenylenevinylene) (OPV) block, a hydrophilic poly(2-vinylpyridine) (P2VP) segment and a photo-cleavable o-nitrobenzyl (ONB) junction. By taking advantage of crystallinity of OPV segment, self-seeding approach of living crystallization-driven self-assembly was employed to generate uniform fiber-like micelles composed of an OPV core and a P2VP corona. The P2VP corona was then used to host the formation of silica, titania and Pt(0)-embedded silica shell. After the photo-cleavable OBN junctions were broken under light irradiation, the OPV core can be removed in a good solvent for OPV segments to give silica, titania and Pt(0)-embedded silica nanotubes. Significantly, the Pt(0)-embedded silica nanotubes exhibited much higher catalytic activity toward the reduction of p-nitroaniline than Pt(0)-embedded silica nanofibers with the same Pt content, probably owing to the presence of porous channel for nanotubes. This work opens a new avenue to fabricate inorganic nanotubes of controlled length.

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