光催化
复合数
可见光谱
抗菌活性
材料科学
金属
核化学
化学
铋
溶剂
光化学
细菌
复合材料
有机化学
生物
催化作用
遗传学
光电子学
作者
Yanni Li,Yujia Han,Hongxia Li,Xiaohui Niu,Weisheng Liu,Deyi Zhang,Haiyan Fan,Kunjie Wang
标识
DOI:10.1016/j.jcis.2023.09.130
摘要
A composite based on Ag and carbon quantum dot (CQDs) doped bismuth metal organic framework (CAU-17) was synthesized by a one-step thermal solvent in situ growth. The microstructure, chemical composition, morphology, photogenerated electron-hole pairs, and photocatalytic activity of the composite were characterized. The produced composite with its unique energy band structure, enhances the visible light absorption and effectively delays the recombination of the photogenerated carriers. On the other hand, the modification with CQDs increases the concentration and transport rate of photogenerated carriers mainly attributed to their superior electron transport capacity and light trapping ability. The photocatalytic antibacterial effect of CAU-17/Ag/CQDs against common Gram-positive, Gram-negative bacteria (Staphylococcus aureus, Escherichia coli) and drug-resistant bacteria (methicillin-resistant Staphylococcus aureus), as well as its inhibition against HepG2 tumor cell were investigated. The results showed that CAU-17/Ag/CQDs exhibited a photocatalytic antibacterial effect with an inactivation rate as high as 99.9 %. At the low dose (0.2 mg/mL), CAU-17/Ag/CQDs indicated a significant inhibition against bacterial growth 20 min after visible light exposure, whereas at the concentration of 0.5 mg/mL, CAU-17/Ag/CQDs completely killed all the tested bacteria. At the concentration of 0.8 mg/mL, the inhibition rate against HepG2 tumor cells reached 75 %. The excellent photocatalytic property of the as prepared composite contributed to the doping of Ag and CQDs, which fundamentally altered the morphology and energy band distribution. Such a composite can be developed into an effective photocatalytic disinfection system and applied to water purification systems, biofilm rejection, combating different antibiotic resistances, and tumor therapy.
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