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Identification of the Mechanism of Electrocatalytic Ozone Generation on Ni/Sb-SnO2

Christensen, PA; Attidekou, PS; Egdell, RG; Maneelok, S; Manning, DAC; Palgrave, R; (2017) Identification of the Mechanism of Electrocatalytic Ozone Generation on Ni/Sb-SnO2. The Journal of Physical Chemistry C , 121 (2) pp. 1188-1199. 10.1021/acs.jpcc.6b10521. Green open access

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Abstract

This paper reports a systematic study of the codoping of SnO2with Sb and Ni to identify the mechanism responsible for the electrocatalytic generation of ozone on Ni/Sb-SnO2. On the basis of interpretation of a combination of X-ray diffraction, BET surface area measurements (N2), and thermal analysis, the formation of ozone appears to take place on particle surfaces of composite Sb-SnO2grains and is controlled by diffusion of OH along internal crystallite surfaces within the grain. Sb-doped SnO2is inactive with respect to ozone evolution in the absence of Ni, demonstrating a synergic interaction between nickel and antimony. From X-ray photoelectron spectroscopy (XPS) investigations, Sb(V) ions substitute for Sn(IV) in the lattice with a preference for centrosymmetric coordination sites, while the Sb(III) ions occur at grain surfaces or boundaries. Ni was not detected by XPS, being located in the subsurface region at concentrations below the detection limit of the instrument. In addition to identification of a possible mechanism for ozone formation, the study resulted in the production of active nanopowders which will allow the fabrication of high-surface-area anodes with the potential to exceed the space-time yields of β-PbO2anodes, permitting the application the Ni/Sb-SnO2anodes in the treatment of real waters.

Type: Article
Title: Identification of the Mechanism of Electrocatalytic Ozone Generation on Ni/Sb-SnO2
Open access status: An open access version is available from UCL Discovery
DOI: 10.1021/acs.jpcc.6b10521
Publisher version: http://dx.doi.org/10.1021/acs.jpcc.6b10521
Language: English
Additional information: This version is the author accepted manuscript. For information on re-use, please refer to the publisher’s terms and conditions.
UCL classification: UCL
UCL > Provost and Vice Provost Offices > UCL BEAMS
UCL > Provost and Vice Provost Offices > UCL BEAMS > Faculty of Maths and Physical Sciences
UCL > Provost and Vice Provost Offices > UCL BEAMS > Faculty of Maths and Physical Sciences > Dept of Chemistry
URI: https://discovery.ucl.ac.uk/id/eprint/10060306
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