journal article·2015

Bi-phasic titanium dioxide nanoparticles doped with nitrogen and neodymium for enhanced photocatalysis

Virginia Gomez, Joseph C. Bear, Paul D. McNaughter, James D. McGettrick, Trystan Watson, Cecile Charbonneau, Paul O'Brien, Andrew R. Barron, Charles W. Dunnill

Nanoscale· Volume 7· Issue 42
Publisher page

Abstract

Bi-phasic or multi-phasic composite nanoparticles for use in photocatalysis have been produced by a new synthetic approach. Sol-gel methods are used to deposit multiple layers of active material onto soluble substrates. In this work, a layer of rutile (TiO2) was deposited onto sodium chloride pellets followed by an annealing step and a layer of anatase. After dissolving the substrate, bi-phasic nanoparticles containing half anatase and half rutile TiO2; with "Janus-like" characteristics are obtained. Nitrogen and neodymium doping of the materials were observed to enhance the photocatalytic properties both under UV and white light irradiation. The unique advantage of this synthetic method is the ability to systematically dope separate sides of the nanoparticles. Nitrogen doping was found to be most effective on the anatase side of the nanoparticle while neodymium was found to be most effective on the rutile side. Rhodamine B dye was effectively photodegraded by co-doped particles under white light.
Source: openalex_inverted_index · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: TiO2 Photocatalysis and Solar Cells · Advanced Photocatalysis Techniques · Copper-based nanomaterials and applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Energy Safety Research Institute (ESRI)

College of Engineering

Swansea University

Fabian Way Swansea, UK

School of Chemistry

University of Manchester

Manchester, UK

SPECIFIC

Baglan Bay Innovation and Knowledge Centre

Port Talbot, UK

School of Materials

Department of Chemistry and Department of Materials Science and Nanoengineering

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