Issue 41, 2013

Single crystalline brookite titanium dioxide nanorod arrays rooted on ceramic monoliths: a hybrid nanocatalyst support with ultra-high surface area and thermal stability

Abstract

In this study, a cost-effective solution synthesis of commercial scale single crystalline titanium dioxide (TiO2) nanorod arrays has been successfully achieved on the inner walls of cordierite monoliths, which may provide a new class of nanostructured hybrid support for catalysis and energy applications. The morphological evolution has been observed from dandelion TiO2 nanorod clusters to vertically aligned nanorod arrays while increasing the solution treatment time. A heterogeneous nucleation–dissolution–crystallization mechanism is proposed for the growth of the brookite structured TiO2 nanorod arrays on the inner walls of honeycomb monoliths. The brookite structured TiO2 nanorod arrays have a high surface area up to ~250 m2 g−1, with an overall specific surface area in the hybrid nanostructured monolith increasing by 1.8 and 2.5 times after TiO2 nanorods coating for 4 h and 24 h, respectively. The thermal stability tests using differential scanning calorimetry (DSC), thermogravimetric analysis (TGA) and hydrothermal stability tests under boiling water for 24 h suggest that the TiO2 nanorods coated hybrid monoliths are very stable. An as-prepared 9-cm-long TiO2 nanorod-array monolithic device was demonstrated as a continuous flow fixed-bed absorbent with efficient performance in Rhodamine B removal from aqueous solution.

Graphical abstract: Single crystalline brookite titanium dioxide nanorod arrays rooted on ceramic monoliths: a hybrid nanocatalyst support with ultra-high surface area and thermal stability

Article information

Article type
Paper
Submitted
22 Apr 2013
Accepted
19 Aug 2013
First published
19 Aug 2013

CrystEngComm, 2013,15, 8345-8352

Single crystalline brookite titanium dioxide nanorod arrays rooted on ceramic monoliths: a hybrid nanocatalyst support with ultra-high surface area and thermal stability

Y. Guo, G. Liu, Z. Ren, A. Piyadasa and P. Gao, CrystEngComm, 2013, 15, 8345 DOI: 10.1039/C3CE40705E

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