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.