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Enhanced Visible-Light Photocatalytic Activity of Ag QDs Anchored on CeO2 Nanosheets with a Carbon Coating

机译:碳涂层固定在CeO2纳米片上的Ag QD的可见光光催化活性增强

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摘要

Ag quantum dots (QDs) anchored on CeO nanosheets with a carbon coating (Ag/CeO @C) (composites) were prepared via an in situ reduction approach for the photocatalytic degradation of Cr(VI) and tetracycline hydrochloride (TCH) in the visible-light region. The photocatalytic activity of Ag/CeO @C was greatly affected by carbon content, Ag-doping content, Cr(VI) concentration, pH value, and inorganic ions. Enhanced photocatalytic activity was obtained by Ag/CeO @C (compared to CeO and CeO @C), of which 3-Ag/CeO @C-2 with an Ag-doping content of 5.41% presented the best removal efficiency and the most superior stability after five cycles. O and OH radicals were crucial for the photocatalytic capacity of 3-Ag/CeO @C-2. The combined effect of the surface plasma resonance (SPR) of Ag QDs, an electron trapper of carbon shells, and the redox activity of the Ce(III)/Ce(IV) coupling induced efficient charge transfer and separation, suppressing the recombination of electron–hole pairs.
机译:通过原位还原方法制备了可见光降解Cr(VI)和盐酸四环素(TCH)的银量子点(QD),该量子点固定在具有碳涂层(复合物)的CeO纳米片上。 -轻区域。 Ag / CeO @C的光催化活性受碳含量,Ag掺杂含量,Cr(VI)浓度,pH值和无机离子的影响很大。 Ag / CeO @ C(与CeO和CeO @ C相比)获得了增强的光催化活性,其中Ag掺杂含量为5.41%的3-Ag / CeO @ C-2表现出最好的去除效率和最优异的五个周期后的稳定性。 O和OH自由基对于3-Ag / CeO @ C-2的光催化能力至关重要。 Ag量子点的表面等离子体共振(SPR),碳壳的电子俘获器和Ce(III)/ Ce(IV)耦合的氧化还原活性的组合效应诱导了有效的电荷转移和分离,从而抑制了电子的重组-孔对。

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