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首页> 外文期刊>Nano: brief reports and reviews >Photocatalytic Degradation Mechanism of Tetracycline by Ag@ZnO/C Core-Shell Plasmonic Photocatalyst Under Visible Light
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Photocatalytic Degradation Mechanism of Tetracycline by Ag@ZnO/C Core-Shell Plasmonic Photocatalyst Under Visible Light

机译:可见光下Ag ZnO / C芯壳等离子体光催化剂Tetracycline的光催化降解机理

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摘要

A series of hamburger-like Ag@ZnO/C core-shell plasmonic photocatalysts have been synthesized via a simple solvothermal method for degradation of tetracycline (TC) under visible light irradiation, possessing high photocatalytic activity and good stability. The presence of localized surface plasmon resonance (LSPR) in the Ag core has increased the photocatalytic activity over an extended wavelength range. The plasmon-induced resonant energy transfer (PIRET) and direct electron transfer (DET) have facilitated the excitation and separation of photogenerated e(-)/h(+) pairs, which has been further confirmed by electrochemical investigations. The presences of hydroxyl radicals (center dot OH), superoxide radicals (center dot O-2(-)) and singlet oxygen (O-2(-)) in the photocatalytic reaction system of Ag@ZnO/C photocatalyst have been demonstrated by electron spin resonance (ESR) measurements. All of the experiment results indicate that the ternary structure of Ag@ZnO/C can effectively enhance the photocatalytic activity. Furthermore, the effects of introduced Ag contents and carbon source dosage were researched by comparative photocatalytic experiments, and the potential structures of photodegradation products were studied by HPLC-MS.
机译:通过简单的溶剂热法合成了一系列汉堡包@ ZnO / C核壳等离子体光催化剂,用于在可见光照射下降解四环素(TC),具有高光催化活性和良好的稳定性。 AG核中的局部表面等离子体共振(LSPR)的存在在延伸波长范围内增加了光催化活性。等离子体诱导的谐振能量转移(PiRet)和直接电子转移(DET)促进了光生E( - )/ h(+)对的激发和分离,这已经通过电化学研究进一步证实。已经证明了AG @ ZnO / C光催化剂的光催化反应体系中的羟基自由基(中央点OH),超氧化物自由基(中央点O-2( - ))和单线氧(O-2())电子自旋共振(ESR)测量。所有实验结果表明,AG @ ZnO / C的三元结构可以有效地增强光催化活性。此外,通过对比光催化实验研究了引入的Ag含量和碳源剂量的影响,通过HPLC-MS研究了光降解产物的潜在结构。

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