Issue 8, 2017

Same titanium glycolate precursor but different products: successful synthesis of twinned anatase TiO2 nanocrystals with excellent solar photocatalytic hydrogen evolution capability

Abstract

Exploiting a synthesis protocol to tailor TiO2 with a unique morphology and crystal phase has received considerable interest in the energy and environmental fields. We here describe the use of a titanium glycolate precursor in a hydrothermal hydrolysis reaction to engineer TiO2 nanocrystals with different crystal phases and structures. Anatase TiO2 nanocrystals with twinned structures were obtained by using a lower amount of NaOH in the hydrolysis system, while brookite TiO2 nanocrystals were formed when higher amounts of NaOH were employed. The as-synthesized different TiO2 nanocrystals have a suitable bandgap to harvest photons and a more negative bottom level of the conduction band than the redox potential of H+/H2 indicating their potential as hydrogen-evolution semiconductor photocatalysts. However, the TiO2 nanotwins show promoted charge separation efficiency, and thus result in superior photocatalytic H2 generation activity compared to the anatase and brookite TiO2 nanocrystals. Our findings provide an effective and versatile solution for the fabrication of TiO2-based nanostructures with different phases and morphologies through chemical conversion of powder precursor nanoparticles, which could pave the way to the design of other functional nano-oxides with unique structures.

Graphical abstract: Same titanium glycolate precursor but different products: successful synthesis of twinned anatase TiO2 nanocrystals with excellent solar photocatalytic hydrogen evolution capability

Article information

Article type
Research Article
Submitted
21 May 2017
Accepted
19 Jun 2017
First published
20 Jun 2017

Inorg. Chem. Front., 2017,4, 1319-1329

Same titanium glycolate precursor but different products: successful synthesis of twinned anatase TiO2 nanocrystals with excellent solar photocatalytic hydrogen evolution capability

G. Cheng, Y. Wei, J. Xiong, Y. Gan, J. Zhu and F. Xu, Inorg. Chem. Front., 2017, 4, 1319 DOI: 10.1039/C7QI00278E

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