Impact of Co-Doping on the Visible Light-Driven Photocatalytic and Photoelectrochemical Activities of Eu(OH)3.

Abstract

The microwave-assisted synthesis approach was used to synthesize Eu(OH)3 and Co-Eu(OH)3 nanorods. Various techniques were used to investigate the structural, optical, and morphological features of the Eu(OH)3 and Co-Eu(OH)3 NRs. Both Eu(OH)3 and Co-Eu(OH)3 NRs were found to be hexagonal with crystallite sizes ranging from 21 to 35 nm. FT-IR and Raman spectra confirmed the formation of Eu(OH)3 and Co-Eu(OH)3. Rod-shaped Eu(OH)3 and Co-Eu(OH)3 with average lengths and diameters ranging from 27 to 50 nm and 8 to 12 nm, respectively, were confirmed by TEM. The addition of Co was found to increase the particle size. Furthermore, with increased Co doping, the band gap energies of Co-Eu(OH)3 NRs were lowered (3.80-2.49 eV) in comparison to Eu(OH)3, and the PL intensities with Co doping were quenched, suggesting the lessening of electron/hole recombination. The effect of these altered properties of Eu(OH)3 and Co-Eu(OH)3 was observed through the photocatalytic degradation of brilliant green dye (BG) and photoelectrochemical activity. In the photocatalytic degradation of BG, 5% Co-Eu(OH)3 had the highest response. However, photoelectrochemical experiments suggested that 10% Co-Eu(OH)3 NRs showed improved activity when exposed to visible light. As a result, Co-Eu(OH)3 NRs have the potential to be a promising visible-light active material for photocatalysis.