Issue 2, 2014

Self-assembly of aligned rutile@anatase TiO2 nanorod@CdS quantum dots ternary core–shell heterostructure: cascade electron transfer by interfacial design

Abstract

A novel self-assembly approach based on electrostatic interactions has been developed for the synthesis of a rutile@anatase TiO2 nanorod (NR)@CdS quantum dots (QDs) ternary core–shell heterostructure, in which an in situ formed monodisperse anatase TiO2 layer was intimately sandwiched between rutile TiO2 NRs and CdS QDs. It has been demonstrated that the well-defined bilayer interface significantly improves the photocatalytic performance of the ternary heterostructure (i.e. rutile@anatase TiO2 NR@CdS QDs), owing predominantly to the appropriate band alignment of the constituent semiconductors, thus facilitating photogenerated electron–hole separation and charge collection under simulated solar light irradiation.

Graphical abstract: Self-assembly of aligned rutile@anatase TiO2 nanorod@CdS quantum dots ternary core–shell heterostructure: cascade electron transfer by interfacial design

Supplementary files

Article information

Article type
Communication
Submitted
29 Aug 2013
Accepted
02 Oct 2013
First published
02 Oct 2013

Mater. Horiz., 2014,1, 259-263

Self-assembly of aligned rutile@anatase TiO2 nanorod@CdS quantum dots ternary core–shell heterostructure: cascade electron transfer by interfacial design

F. Xiao, J. Miao and B. Liu, Mater. Horiz., 2014, 1, 259 DOI: 10.1039/C3MH00097D

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