In this study, we first manufactured ultrathin g-C3N4 (CN) nanosheets by thermal etching and ultrasonic techniques. Then, EuVO4 (EV) nanoparticles were loaded onto CN nanosheets to form EuVO4/g-C3N4 heterojunctions (EVCs). The ultrathin and porous structure of the EVCs increased the specific surface area and reaction active sites. The formation of the heterostructure extended visible light absorption and accelerated the separation of charge carriers. These two factors were advantageous to promote the synergistic effect of adsorption and photocatalysis, and ultimately enhanced the adsorption capability and photocatalytic removal efficiency of methylene blue (MB). EVC-2 (2 wt% of EV) exhibited the highest adsorption and photocatalytic performance. Almost 100% of MB was eliminated via the adsorption-photocatalysis synergistic process over EVC-2. The MB adsorption capability of EVC-2 was 6.2 times that of CN, and the zero-orderreaction rate constant was 5 times that of CN. The MB adsorption on EVC-2 followed the pseudo second-order kinetics model and the adsorption isotherm data complied with the Langmuir isotherm model. The photocatalytic degradation data of MB on EVC-2 obeyed the zero-order kinetics equation in 0-10 min and abided by the first-order kinetics equation for10-30 min. This study provided a promising EVC heterojunctions with superior synergetic effect of adsorption and photocatalysis for the potential application in wastewater treatment.
Keywords: EuVO4/g-C3N4 heterojunction; Langmuir isotherm; adsorption; methylene blue; photocatalysis.