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首页> 外文期刊>Separation and Purification Technology >Investigation of visible-light-driven photocatalytic tetracycline degradation via carbon dots modified porous ZnSnO3 cubes: Mechanism and degradation pathway
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Investigation of visible-light-driven photocatalytic tetracycline degradation via carbon dots modified porous ZnSnO3 cubes: Mechanism and degradation pathway

机译:通过碳点改性多孔ZnSNO3立方体调查可见光光催化四环素降解:机理和降解途径

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It is highly desired to enhance the photocatalytic activity of ZnSnO3 owing to its potential application prospects in the photocatalytic degradation of antibiotics in water, such as the low cost, non-toxicity, simple preparation, although ZnSnO3 possesses wide band gap (similar to 3.2 eV). Herein, a novel carbon dots (CDs) modified porous ZnSnO3 cubic photocatalyst was designed and synthesized using a simple precipitation-calcination method, which was to utilize the up-conversion photoluminescence performance and the ability of electronic transfer of CDs, further broadening the visible light absorption range of the photocatalyst and accelerating the separation of the electron-hole pairs. The experimental results indicate that with the optimal CDs loading (3 wt%), the CDs modified ZnSnO3 exhibits 21 times higher degradation kinetic towards tetracycline (TC) than pure ZnSnO3. The enhanced photocatalytic activity of CDs-ZnSnO3 composites may be attributed to the increased absorption of visible light as well as the improved separation of interface charge carrier. The possible mechanism of antibiotic photodegradation in the CDs-ZnSnO3 composite photocatalytic system was proposed by active species capture experiment and electron spin resonance (ESR) technique. Furthermore, the possible photodegradation pathway of TC was proposed on the basis of the intermediates detected by liquid chromatography-mass spectrometry (LC-MS) technology. This work provides a feasible strategy for effectively applying ZnSnO3-based photocatalyst to photocatalytic degradation of antibiotics.
机译:由于其在水中抗生素的光催化降解的潜在应用前景,因此强烈希望增强ZnSNO3的光催化活性,例如低成本,无毒性,简单的制备,尽管ZnSNO3具有宽带隙(类似于3.2eV )。在此,使用简单的沉淀煅烧方法设计和合成了一种新型碳点(CDS)改性多孔ZnSO3立方光催化剂,该方法是利用上转化的光致发光性能和CD的电子转移能力,进一步展现可见光光催化剂的吸收范围并加速电子孔对的分离。实验结果表明,随着最佳CDS载荷(3wt%),Cds改性ZnSNO3表现出比纯ZnSNO3的四环素(TC)更高的降解动力学。 CDS-ZnSNO3复合材料的增强的光催化活性可归因于可见光的吸收增加以及接口电荷载体的改进分离。通过活性物种捕获实验和电子自旋共振(ESR)技术提出了CDS-ZnSNO3复合光催化系统中抗生素光降解的可能机制。此外,基于通过液相色谱 - 质谱(LC-MS)技术检测的中间体提出了TC的可能光降解途径。这项工作提供了可行的策略,可有效地将ZnSNO3的光催化剂应用于抗生素的光催化降解。

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