光催化
盐酸四环素
材料科学
电子顺磁共振
纳米颗粒
光化学
表面等离子共振
介电谱
吸附
光致发光
甲醛
核化学
电化学
催化作用
纳米技术
四环素
化学
电极
有机化学
抗生素
生物化学
光电子学
物理
核磁共振
物理化学
作者
Shuqing Zhang,Dongmei Han,Zhihua Wang,Fubo Gu
出处
期刊:Small
[Wiley]
日期:2024-04-30
被引量:2
标识
DOI:10.1002/smll.202309656
摘要
Abstract Bi/CeO 2 (BC‐ x ) photocatalysts are successfully prepared by solvothermal loading Bi nanoparticles and Bi‐doped CeO 2 derived by Ce‐MOF (Ce‐BTC). Formaldehyde gas (HCHO) and tetracycline hydrochloride (HTC) are used to evaluate the photocatalytic activity of the synthesized Bi/CeO 2 . For BC‐1000 photocatalyst, the degradation of HTC by 420 nm < λ < 780 nm light reaches 91.89% for 90 min, and HCHO by 350 nm < λ < 780 nm light reaches 94.66% for 120 min. The photocatalytic cycle experiments prove that BC‐1000 has good cyclic stability and repeatability. The results of photoluminescence spectra, fluorescence lifetime, photocurrent response, and electrochemical impedance spectroscopy showed that the SPR (Surface Plasmon Resonance) effect of Bi nanoparticles acted as a bridge and promoted electron transfer and enhanced the response‐ability of Bi/CeO 2 to visible light. Bi‐doping produced more oxygen vacancies to provide adsorption sites for adsorbing oxygen and generated more ·O 2 − thus promoting photocatalytic reactions. The mechanism of photocatalytic degradation is analyzed in detail utilizing active free radical capture experiments and electron paramagnetic resonance (EPR) characterization. The experimental results indicate that ·O 2 − and h + active free radicals significantly promote the degradation of pollutants.
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