Published October 2018 | Version v1
Journal article

Solution combustion synthesis and characterization of phosphorus doped TiO2–CeO2 nanocomposite for photocatalytic applications

  • 1. Department of Physics, Vikrama Simhapuri University P.G. Centre, Kavali 524201 (India)

Description

Highlights: • Phosphorus doped TiO2-CeO2 nanocomposite was synthesized by solution combustion method. • XRD analysis reveals the retarded phase transition by increased thermal stability. • FE-SEM image shows the porous structure with uniform pore distribution. • The absorption edge of the P/TiO2-CeO2 nanocomposite exhibits redshift. • XPS studies indicate that the phosphorus enters substitutionally into Ce4+/Ti4+ site. - Abstract: Phosphorus doped TiO2-CeO2 nanocomposite (P-TiO2-CeO2) was synthesized by solution combustion method. The prepared sample has been heated at different temperatures and characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), UV–vis absorption spectra, X-ray photoelectron spctroscopy (XPS). XRD analysis reveals the retarded phase transition by increased thermal stability due to phosphorus doping. FE-SEM shows the porous structure of the sample. The absorption edge of the P/TiO2-CeO2 nanocomposite exhibits redshift with increasing heating temperature with its value around 2.93 eV, 2.90 eV and 2.89 eV at 400 °C, 500 °C and 600 °C respectively. From the observed P2p XPS peak, it is confirmed that the doped phosphorus enters substitutionally into Ce4+/Ti4+ site, which can play an important role in the photocatalytic activity of the sample. The binding energy of Ti 2p XPS peak increases slightly from 458.5 eV to 458.8 eV due to interaction between titanium and cerium.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.mseb.2018.12.001

Additional details

Identifiers

DOI
10.1016/j.mseb.2018.12.001;
PII
S0921510718300862;

Publishing Information

Journal Title
Materials Science and Engineering. B, Solid-State Materials for Advanced Technology
Journal Volume
236-237
Journal Page Range
p. 43-47
ISSN
0921-5107
CODEN
MSBTEK

Optional Information

Copyright
Copyright (c) 2017 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.