Cobalt-doped cerium oxide nanoparticles: Enhanced photocatalytic activity under UV and visible light irradiation

Abstract

CeO2 nanoparticles (NPs) were synthesized by coprecipitation using cerium(III) nitrate hexahydrate as the precursor and ethanol as the solvent. Different concentration of cobalt-doped cerium oxide NPs (3mol % and 6mol %) were prepared by adding various concentrations of cobalt chloride to cerium nitrate. The as-synthesized NPs were characterized through X-ray diffraction (XRD) measurements, ultraviolet (UV)–visible spectroscopy, Photoluminescence (PL) spectroscopy, and transmission electron microscopy (TEM). XRD results reveal that the as-prepared CeO2 NPs had a face-centered cubic structure with crystallite size in the range of 5–8nm. TEM analyses showed that the CeO2 NPs and Co-doped CeO2 NPs had a homogenous size distribution (sizes were within 5–12nm). Band-edge absorption of CeO2 NPs redshifted upon increasing the Co concentration as compared to undoped CeO2 NPs. PL spectra reveal a peak shift of CeO2 emission upon cobalt doping, which were due to an increase in oxygen defects localized between the Ce4f and O2p energy levels (i.e., via formation of Ce3+ states). Photocatalytic degradation of methylene blue in aqueous solution under UV and visible (sunlight) irradiation in the presence of pure CeO2 NPs and of Co-doped CeO2 NPs was investigated. The efficiency of photocatalytic degradation of CeO2 NPs increased with the Co concentration both under UV irradiation and under visible light. Co-doped CeO2 NPs (6mol%) showed degradation efficiencies of 98% and 89% at 420min of exposure to UV irradiation and to visible light, respectively.