Enhanced Activation of Peroxymonosulfate via Sulfate Radicals and Singlet Oxygen by SrCoxMn1−xO3 Perovskites for the Degradation of Rhodamine B

催化作用 罗丹明B 单线态氧 化学 激进的 降级(电信) 钙钛矿(结构) 氧气 无机化学 光化学 硫酸盐 光催化 有机化学 计算机科学 电信
作者
Ping Shao,Xi-Ping Yin,Chenyu Yu,Shuai Han,Baohuai Zhao,Kezhi Li,Xiang Li,Zhenyu Yang,Yuan Zhang,Qinzhi Shi,Jing Ren,Haiqiang Hu,Kai Cui,Tengfei Li,Jun Jiang
出处
期刊:Processes [Multidisciplinary Digital Publishing Institute]
卷期号:11 (4): 1279-1279
标识
DOI:10.3390/pr11041279
摘要

Perovskite is of burgeoning interest in catalysis, principally due to such material having high thermal stability, modifiable variability, ferromagnetism, and excellent catalytic performance in peroxomonosulfate (PMS) activation. In this study, the SrCoxMn1−xO3 perovskites with different Mn doping were synthesized by a facile sol-gel method for peroxymonosulfate (PMS) activation to degrade Rhodamine B. The obtained SrCo0.5Mn0.5O3 perovskite exhibited the best catalytic efficiency, as Rhodamine B (40 mg/L) was removed completely within 30 min. In the system of SrCo0.5Mn0.5O3–PMS, several reactive species were produced, among which sulfate radicals and the singlet oxygen mainly contributed to Rhodamine B degradation. The relatively high catalytic performance could be attributed to the coupled redox cycle between Mn and Co, and the abundant oxygen vacancies. Moreover, the SrCo0.5Mn0.5O3 catalyst showed excellent stability and reusability, maintaining a high catalytic activity after several cycling tests. This study demonstrated that the Mn doping of SrCoO3 could not only enhance the B-site activation in SrCo0.5Mn0.5O3 but also enrich the oxygen vacancies, thus improving the efficiency of PMS activation.
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