Solar-light-driven ternary MgO/TiO2/g-C3N4 heterojunction photocatalyst with surface defects for dinitrobenzene pollutant reduction

Abstract

Defect engineering and heterojunction are promising strategies to improve the photocatalytic performance of particular catalyst through effective charge carrier separation and transport. Herein, we developed Z-scheme MgO/TiO2/g-C3N4 ternary heterojunction photocatalyst with surface defects and effective charge separation for reduction of recalcitrant dinitrobenzene isomers under simulated solar light irradiation. Mott-Schottky (MS) plot analysis and electron spin resonance (ESR) radical trapping experiment suggested the formation of Z-scheme heterojunction at the interface of TiO2/g-C3N4, which played a crucial role in the electron-hole separation. Incorporating MgO into the structure further enhances charge separation via Ti3+ and oxygen vacancy (OV) defects formation at the TiO2/MgO interface as confirmed by electron paramagnetic resonance (EPR) and X-ray photoelectron spectroscopy (XPS) analyses. Besides, the surface basicity of MgO enhanced conversion of dinitrobenzene (DNB) isomers through formation of nitrophenylhydroxylamine intermediate which can easily be reduced to phenylenediamines (PDAs). As confirmed by high performance liquid chromatography (HPLC) analysis, excellent selectivity for PDAs (95–98%) was achieved in 90 min with ternary MgO/TiO2/g-C3N4 composite compared to the binary MgO/TiO2 and TiO2/g-C3N4. A possible reaction pathway and photocatalytic reduction mechanism were proposed and elucidated. This work demonstrated an effective strategy to reduce recalcitrant dinitrobenzene isomers using efficient, low-cost, and environmental benign photocatalyst with a facile identification of reaction intermediates.