Mg 0.8 Zn 0.2 O microspheres: preparation, characterization and application for degrading organic dyes

Photocatalytic degradation of organic pollutants in wastewater is one of the most promising strategies for environmental remediation, and photocatalysts as the prerequisite have received considerable attention. Herein we reported highly efficient, nontoxic, and inexpensive Mg 0.8 Zn 0.2 O microspheres with a diameter of around 36 μm prepared through reaction between CO 3 2− , Mg 2+ and Zn 2+ for degrading organic dyes. The molar ratio between Mg 2+ and Zn 2+ was found to play a crucial role in determining the morphology and photocatalytic performance of the resulting product. According to time-dependent experiments, the plausible formation mechanism for the spherical-like Mg 0.8 Zn 0.2 O composite was proposed, in which irregular agglomerates composed of fine powders were first formed followed by their transformation into rod-like structures. Due to their thermal instability, the rod-like particles underwent further self-assembly and became a more stable spherical-like product with ZnCO 3 embedded in the space between Mg 5 (CO 3 ) 4 (OH) 2 ·4H 2 O sheets. After investigating the photocatalytic performance, the results demonstrated that the developed Mg 0.8 Zn 0.2 O composite was not only superior to other state-of-the-art catalysts such as P25 TiO 2 and g-C 3 N 4 in degrading organic dyes upon irradiation under either UV light or visible light, but also was an amphoteric photocatalyst more favorable for degrading organic dyes in both strongly acidic (pH 2–4) and strongly alkaline (pH 12) solutions. Moreover, its catalytic efficiency remained as high as 98.3% after six cycles. These features made the developed Mg 0.8 Zn 0.2 O composite promising in practical utilization for treatment of organic dyes. Further experiments including photoluminescence, adsorption and photoelectrochemical measurements accounted for the underlying photocatalytic mechanism of the Mg 0.8 Zn 0.2 O composite for degradation of organic dyes.