铈
光催化
电子顺磁共振
氧气
激进的
光降解
材料科学
无机化学
核化学
吸附
化学
乙二醇
光化学
催化作用
物理化学
有机化学
物理
核磁共振
作者
Ting Li,Shanyu Quan,Xuefeng Shi,Cong Liu,Linmei Yang
标识
DOI:10.1002/slct.202000951
摘要
Abstract The photocatalysts Bi 2 O 3 :Ce 3+ /Ce 4+ (cerium content 0.2, 0.5, 0.8, and 1.1 wt. %) were prepared via one‐pot ethylene glycol‐assisted solvothermal method. The prepared x Ce‐Bi 2 O 3 (x =0.5, 0.8, 1.1) samples present δ‐Bi 2 O 3 phase with space group of Fm‐3 m at room temperature, which indicates that the high‐temperature cubic phase could be stabilized via Ce doping in Bi 2 O 3 lattices. Moreover, the addition of Ce 3+ /Ce 4+ could change the amount of oxygen vacancies (OVs) and adsorbed oxygen on the surface of photocatalysts. The existence of oxygen vacancies and adsorbed oxygen facilitated the generation of superoxide radicals () and hydroxide radicals (), which were the dominant reactive oxygen species for phenol degradation. The photocatalyst containing 0.8 wt. % cerium presented the highest photoactivity than the other synthesized samples. A photodegradation mechanism is proposed based on scavenger and electron spin resonance studies.
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