z-logo
Premium
A Unique Disintegration–Reassembly Route to Mesoporous Titania Nanocrystalline Hollow Spheres with Enhanced Photocatalytic Activity
Author(s) -
Wang Xin,
Bai Licheng,
Liu Hongyan,
Yu Xuefeng,
Yin Yadong,
Gao Chuanbo
Publication year - 2018
Publication title -
advanced functional materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.069
H-Index - 322
eISSN - 1616-3028
pISSN - 1616-301X
DOI - 10.1002/adfm.201704208
Subject(s) - materials science , photocatalysis , crystallinity , mesoporous material , chemical engineering , nanoparticle , polystyrene , nanocrystalline material , polymerization , dispersity , polymer , nanotechnology , composite material , polymer chemistry , organic chemistry , catalysis , chemistry , engineering
A novel disintegration–reassembly route is reported for the synthesis of mesoporous TiO 2 nanocrystalline hollow spheres with controlled crystallinity and enhanced photocatalytic activity. In this unique synthesis strategy, it is demonstrated that sol–gel‐derived mesoporous TiO 2 colloidal spheres can be disintegrated into discrete small nanoparticles that are uniformly embedded in the polymer (polystyrene, PS) matrix by surface‐induced photocatalytic polymerization. Subsequent reassembly of these TiO 2 nanoparticles can be induced by an annealing process after further coating of a resorcinol–formaldehyde (RF) resin, which forms self‐supported hollow spheres of TiO 2 at the PS/RF interface. The abundant phenolic groups on the RF resin serve as anchoring sites for the TiO 2 nanoparticles, thus enable the reassembly of the TiO 2 nanoparticles and prevent their sintering during the thermal crystallization process. This unique disintegration–reassembly process leads to the formation of self‐supported TiO 2 hollow spheres with relatively large surface area, high crystallinity, and superior photocatalytic activity in dye degradation under UV light irradiation.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here