Issue 19, 2013

Co–Ni layered double hydroxides for water oxidation in neutral electrolyte

Abstract

The electrochemical properties of Co–Ni layered double hydroxides (LDHs) as efficient electrocatalysts for water oxidation were investigated in potassium phosphate electrolyte under neutral pH condition. The Co–Ni LDHs with a core–shell structure were fabricated using a facile route from a Co–Ni hydroxide precursor with iodine as a topotactic oxidizer. The unique core–shell morphology is likely due to the enrichment of Co(III) hydroxide in the inner core indicated by selected area electron diffraction and energy-dispersive spectroscopy. Through a self-assembling process at the organic/inorganic interface and dip-coating, the Co–Ni LDHs were deposited onto FTO glass substrates to prepare composite electrodes. Low over-potential and high current density was achieved in the oxygen evolution reaction. The excellent electrocatalytic activity of Co–Ni LDHs may be attributed to more accessible Co active sites and rapid movement of interlayer ions within their layered structure.

Graphical abstract: Co–Ni layered double hydroxides for water oxidation in neutral electrolyte

Supplementary files

Article information

Article type
Paper
Submitted
16 Jan 2013
Accepted
17 Mar 2013
First published
18 Mar 2013

Phys. Chem. Chem. Phys., 2013,15, 7363-7369

Co–Ni layered double hydroxides for water oxidation in neutral electrolyte

Y. Zhang, B. Cui, C. Zhao, H. Lin and J. Li, Phys. Chem. Chem. Phys., 2013, 15, 7363 DOI: 10.1039/C3CP50202C

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