Issue 97, 2015

Interface reacted ZnFe2O4 on α-Fe2O3 nanoarrays for largely improved photoelectrochemical activity

Abstract

ZnFe2O4/α-Fe2O3 heterojunctions were successfully synthesized by depositing ZnO films on α-Fe2O3 nanorods through the atomic layer deposition technique, followed by annealing in air. The as-fabricated heterostructures showed a significant enhancement in photoelectrochemical (PEC) performance when compared to the bare α-Fe2O3, with photocurrent density increasing from 0.03 mA cm−2 for pristine α-Fe2O3 to 0.29 mA cm−2. The increased photocurrent for the ZnFe2O4/α-Fe2O3 heterojunction was ascribed to the enhanced charge carrier density and the efficient separation of electron–hole pairs at the ZnFe2O4/α-Fe2O3 interface. The significant performance enhancement suggests that the rational design and construction of the heterostructures with suitable band alignment as photoelectrodes are promising to achieve highly efficient PEC water splitting.

Graphical abstract: Interface reacted ZnFe2O4 on α-Fe2O3 nanoarrays for largely improved photoelectrochemical activity

Supplementary files

Article information

Article type
Paper
Submitted
04 Aug 2015
Accepted
07 Sep 2015
First published
07 Sep 2015

RSC Adv., 2015,5, 79440-79446

Interface reacted ZnFe2O4 on α-Fe2O3 nanoarrays for largely improved photoelectrochemical activity

Q. Liu, F. Cao, F. Wu, W. Tian and L. Li, RSC Adv., 2015, 5, 79440 DOI: 10.1039/C5RA15596G

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements