首页> 外文期刊>Applied Catalysis, B. Environmental: An International Journal Devoted to Catalytic Science and Its Applications >Novel 3D core-shell structured CQDs/Ag3PO4@Benzoxazine tetrapods for enhancement of visible-light photocatalytic activity and anti-photocorrosion
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Novel 3D core-shell structured CQDs/Ag3PO4@Benzoxazine tetrapods for enhancement of visible-light photocatalytic activity and anti-photocorrosion

机译:新型3D核心壳结构CQDS / AG3PO4 @苯并恶嗪Tetrapods提高可见光光催化活性和抗光腐蚀

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摘要

To improve the visible-light photocatalytic activity and anti-photocorrosion of Ag3PO4, novel 3D core-shell CQDs/Ag3PO4@benzoxazine tetrapods with more exposure of {110} facets of Ag3PO4 has been successfully synthesized for the first time by electrochemical oxidation, chemical precipitation and molecular self-assembly reaction. In CQDs/Ag3PO4@benzoxazine tetrapods, CQDs could not only induce more photocarrier generation from high-energy facets of Ag3PO4 tetrapods but also accelerate the electrons transfer from conduction band of Ag3PO4 tetrapods to the bottom of conduction band of CQDs. Furthermore, silver amine complex could act as a bridge for the photo-electrons flowing from core to shell, which is beneficial to the subsequent free radical chain reaction. In addition, the 3D core-shell structure decreased the solubility of Ag3PO4. UV-vis DRS, indicating that the band gap of CQDs(0.38%)/Ag3PO4 @benzoxazine (1.65 eV) was far less than that of Ag3PO4 tetrapods (2.0 eV) and traditional Ag3PO4 (2.45 eV). Moreover, the photocurrent tests showed that CQDs(0.38%)/Ag3PO4@benzoxazine had perfect drift ability of generated photocarriers. Accordingly, the CQDs(0.38%)/Ag3PO4@benzoxazine tetrapods exhibited excellent visible-light photocatalytic activity and anti-photocorrosion performance. More than 93% of Methylorange and rhodamine B could be photodegraded within 16 min and 10 min over CQDs(0.38%)/Ag3PO4@benzoxazine tetrapods, respectively. Even after 9 cycles, CQDs(0.38%)/Ag3PO4@benzoxazine could still remain 95% removal rate of sulfamethoxazole (SMX) with 10 min. Through recycling catalytic experiments and photodegradation pathway explore of SMX, the CQDs(0.38%)/Ag3PO4@ benzoxazine composite suggest its great mineralization capability on sulfonamide antibiotics. The free radicals trapping experiments demonstrated that the holes photoinduced were the main active oxidizing species which played the dominant role in the photocatalytic process. Thus, CQDs(0.38%)/Ag3PO4@benzoxazine is a promising visible-light responses catalyst for photodegradation of organic pollutants in the environmental protection.
机译:为了改善Ag3PO4的可见光光催化活性和抗光腐蚀,通过电化学氧化,化学沉淀首次成功地合成了GEDOS-AG3PO4的新型3D核 - 壳CQDS / AG3PO4 / AG3PO4 / AG3PO4 @苯并恶嗪TETRAPODS的{110}小件。和分子自组装反应。在CQDS / AG3PO4 @苯并恶嗪Tetrapods中,CQD不能仅诱导来自Ag3PO4 Tetrapods的高能谱的更高的光载体产生,但也加速了从Ag3Po4 TetraPod的导通带的电子转移到CQD的传导带的底部。此外,银胺络合物可以作为从芯流到壳体流动的光电的桥梁,这对随后的自由基链反应有益。此外,3D核 - 壳结构降低了Ag3PO4的溶解度。 UV-VIS DRS,表明CQDS的带隙(0.38%)/ Ag3PO4 @苯并恶嗪(1.65eV)远低于Ag3PO4四抗(2.0eV)和传统Ag3PO4(2.45eV)的差距。此外,光电流测试显示CQDS(0.38%)/ Ag3PO4苯并恶嗪具有完全的产生光载体的漂移能力。因此,CQDS(0.38%)/ Ag3PO4(0.38%)/ Ag3PO4苯并恶嗪Tetrapods表现出优异的可见光光催化活性和抗光腐蚀性能。超过93%的甲基橙色和罗丹明B可以在16分钟内光降解,分别在CQDS(0.38%)/ Ag3PO4 @苯并恶嗪Tetrapods上10分钟。即使在9个循环后,CQDS(0.38%)/ Ag3PO4仍然可以仍然仍然保​​持95%的磺胺甲氧唑(SMX)的去除率10分钟。通过再循环催化实验和光降解途径SMX,CQDS(0.38%)/ Ag3PO4苯并恶嗪复合材料表明其对磺酰胺抗生素的良好的矿化能力。自由基捕获实验表明,光致孔的孔是在光催化过程中起主要作用的主要活性氧化物质。因此,CQDS(0.38%)/ Ag3PO4苯并恶嗪是一种有希望的可见光反应催化剂,用于在环保中的有机污染物的光降解。

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