Co Modified Pr0.6Sm0.4Mn1O3 Perovskite Enhances the Non‐Radical Pathway for Efficient Removal of Rhodamine B

Abstract Because of its excellent catalytic activity and stability, perovskite materials are widely used in advanced oxidation processes to remove refractory organic pollutants. In this study, a series of catalysts Pr 0.6 Sm 0.4 Co x Mn 1‐x O 3 (x = 0, 0.2, 0.4, 0.5, 0.6,0.8 and 1) with limited range effect are prepared by sol–gel method with the regulation strategy of injecting active metal Co at B site in the crystal lattice of perovskite catalyst Pr 0.6 Sm 0.4 MnO 3 . Under the optimal conditions, the Pr 0.6 Sm 0.4 Co 0.8 Mn 0.2 O 3 /PMS/RhB system showed superior catalytic performance, and the removal rate of Rhodamine B (100 mg L −1 ) is close to 100% within 40 min. In addition, the Pr 0.6 Sm 0.4 Co 0.8 Mn 0.2 O 3 catalyst has a wider pH (2‐10) tolerance range and still has outstanding catalytic properties after multiple cycle tests. The quenching experiment and EPR test confirmed that a variety of active species are produced in the system, and the singlet oxygen as the leading path of a variety of active substances assisted to promote the efficient degradation of Rhodamine B in wastewater. This study provides a new reaction system and regulatory strategy of active structural sites for the design of Fenton‐like catalytic systems based on novel perovskite oxides.