Issue 38, 2014

Three-dimensional self-branching anatase TiO2 nanorods: morphology control, growth mechanism and dye-sensitized solar cell application

Abstract

Complex three-dimensional (3D) hierarchical nanostructures based on well-defined low-dimensional nanobranches of different sizes and specific exposed facets are highly desirable to obtain tunable physicochemical properties. Herein, a facile, one-step hydrothermal method is employed to construct self-branching anatase TiO2 (SBAT) 3D hierarchical nanostructures. By simply controlling the reaction time and weight ratio of F127/TBAH, SBAT nanorods can be obtained with a large percentage of exposed {010} facets. Based on X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM) and transmission electron microscopy (TEM) analysis, a growth mechanism is proposed for the formation of such self-branching 3D nanostructures, which involves the formation of the L-shaped step edges on the [103] surfaces and the alignment of the crystal facets (103) of anatase nanocrystals with the (103) face on the tips of the main anatase TiO2 nanorods. The dye-sensitized solar cell assembled with the SBAT nanorods exhibits an outstanding power conversion efficiency of 7.17%, which is superior to that of the devices based on the 1D anatase TiO2 nanorods and P25 TiO2. This high performance can be attributed to the high dye-uptake density, large size and unique self-branching 3D hierarchical nanostructures built from 1D nanobranches growing epitaxially from the main rod.

Graphical abstract: Three-dimensional self-branching anatase TiO2 nanorods: morphology control, growth mechanism and dye-sensitized solar cell application

Supplementary files

Article information

Article type
Paper
Submitted
02 Jun 2014
Accepted
05 Aug 2014
First published
05 Aug 2014

J. Mater. Chem. A, 2014,2, 16030-16038

Author version available

Three-dimensional self-branching anatase TiO2 nanorods: morphology control, growth mechanism and dye-sensitized solar cell application

W. Yang, Y. Xu, Y. Tang, C. Wang, Y. Hu, L. Huang, J. Liu, J. Luo, H. Guo, Y. Chen, W. Shi and Y. Wang, J. Mater. Chem. A, 2014, 2, 16030 DOI: 10.1039/C4TA02761B

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