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负载于TiO@N掺杂多孔碳上的金-银纳米颗粒:通过等离子体光催化在可见光下增强环丙沙星的降解

AuAg Nanoparticles Grafted on TiO@N-Doped Porous Carbon: Improved Depletion of Ciprofloxacin under Visible Light through Plasmonic Photocatalysis.

作者信息

Jiménez-Salcedo Marta, Monge Miguel, Tena María Teresa

机构信息

Department of Chemistry, University of La Rioja, C/Madre de Dios 53, E-26006 Logroño, Spain.

Centro de Investigación en Síntesis Químicas (CISQ), University of La Rioja, C/Madre de Dios 53, E-26006 Logroño, Spain.

出版信息

Nanomaterials (Basel). 2022 Jul 22;12(15):2524. doi: 10.3390/nano12152524.

Abstract

TiO2 nanoparticles (NPs) were modified to obtain photocatalysts with different composition sophistication and displaying improved visible light activity. All of them were evaluated in the photodegradation of ciprofloxacin. The band gap of TiO2 NPs was successfully tailored by the formation of an N-doped porous carbon (NPC)-TiO2 nanohybrid through the pyrolysis of melamine at 600 °C, leading to a slight red-shift of the absorption band edge for nanohybrid NPC-TiO2 1. In addition, the in-situ formation and grafting of plasmonic AuAg NPs at the surface of NPC sheets and in close contact with TiO2 NPs leads to AuAg-NPC-TiO2 nanohybrids 2−3. These nanohybrids showed superior photocatalytic performance for the degradation of ciprofloxacin under visible light irradiation, compared to pristine P25 TiO2 NPs or to AuAg-PVP-TiO2 nanohybrid 4 in which polyvinylpyrrolidone stabilized AuAg NPs were directly grafted to TiO2 NPs. The materials were characterized by transmission electron microscope (TEM), High Angle Annular Dark Field—Scanning Transmission Electron Microscopy—Energy Dispersive X-ray Spectroscopy HAADF-STEM-EDS, X-ray photoelectron spectroscopy and solid UV-vis spectroscopy. Moreover, the active species involved in the photodegradation of ciprofloxacin using AuAg-NCS-TiO2 nanohybrids were evaluated by trapping experiments to propose a mechanism for the degradation.

摘要

对二氧化钛纳米颗粒(NPs)进行改性,以获得具有不同组成复杂度且可见光活性有所提高的光催化剂。对所有这些光催化剂进行了环丙沙星光降解性能评估。通过在600℃下热解三聚氰胺形成氮掺杂多孔碳(NPC)-TiO2纳米杂化物,成功地调整了TiO2 NPs的带隙,导致纳米杂化物NPC-TiO2 1的吸收带边缘出现轻微红移。此外,在NPC片表面原位形成并接枝等离子体AuAg NPs,并使其与TiO2 NPs紧密接触,得到AuAg-NPC-TiO2纳米杂化物2-3。与原始的P25 TiO2 NPs或聚乙烯吡咯烷酮稳定的AuAg NPs直接接枝到TiO2 NPs上的AuAg-PVP-TiO2纳米杂化物4相比,这些纳米杂化物在可见光照射下对环丙沙星的降解表现出优异的光催化性能。通过透射电子显微镜(TEM)、高角度环形暗场-扫描透射电子显微镜-能量色散X射线光谱(HAADF-STEM-EDS)、X射线光电子能谱和固体紫外-可见光谱对材料进行了表征。此外,通过捕获实验评估了使用AuAg-NCS-TiO2纳米杂化物进行环丙沙星光降解过程中涉及的活性物种,以提出降解机理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f250/9329855/6c5c2eab657f/nanomaterials-12-02524-sch001.jpg

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