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首页> 外文期刊>Journal of Molecular Liquids >LaTiO2N/Bi2S3 Z-scheme nano heterostructures modified by rGO with high interfacial contact for rapid photocatalytic degradation of tetracycline
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LaTiO2N/Bi2S3 Z-scheme nano heterostructures modified by rGO with high interfacial contact for rapid photocatalytic degradation of tetracycline

机译:Latio2N / BI2S3 Z-Schement通过RGO改性的纳米异质结构,具有高界面接触,用于快速光催化降解四环素

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Rationally fabricated Z-scheme hetero-junctions with intimate interfacial contact have proven to accelerate the photocatalytic degradation of noxious pollutants by effectively suppressing the recombination and promoting charges transfer rate. Herein, we report fabrication of reduced graphene oxide (RGO) modified LaTiO2N/Bi2S3 heterojunction photocatalyst by sovothermal route. The microstructure analysis, structure determination, electronic and optical analysis of as prepared photocatalysts was done by using multiple techniques. The Z-scheme LaTiO2N/Bi2S3@RGO (LBR) photocatalyst shows remarkable performance for photo-degradation of tetracycline (TC) under visible light. 96.4% TC was eliminated within 90 min under visible light with similar to 100% removal in 60 min under full spectrum irradiation. In addition the heterojunction shows 80.2% TC removal under natural sunlight irradiation. The TC degradation with LBR heterojunction is similar to 9 times faster than bare Bi2S3. The Z-scheme transfer follows the route as Bi2S3 -> RGO -> LaTiO2N and provides a swift path for movement of electrons from CB of LaTiO2N to VB of Bi2S3. The possible degradation route of TC has also been proposed based on quenching experiments and identification of degradation intermediates by Liquid chromatography-mass spectrometry (LC-MS). The quenching experiments reveal that center dot O-2(-) radicals are the main active species involved followed by center dot OH radicals which has been explained by thermodynamic feasibility of their production from the junction arrangement. The mechanism has been explained by Z-scheme transfer by comparing to the conventional type-II junction. The enhancement in photocatalytic activity is primarily attributed to Z-scheme charge transfer between LaTiO2N and Bi2S3 facilitated by reduced graphene oxide sheet via strong interfacial contact maintaining high potential for redox conversions. The recycling experiments reveal the stability and reusability of the LBR hybrid photocatalyst with ability to perform under sunlight. The novel nitrides-phosphide based junction with improved properties for visible and solar photocatalytic activity provides future prospects in forming superior hetero-structures for environmental remediation. (C) 2020 Elsevier B.V. All rights reserved.
机译:理性制造的Z方案Z样方具有紧密界面接触的异质连接,已经证明通过有效地抑制重组和促进电荷转移率来加速有毒污染物的光催化降解。在此,我们通过Sovothermal途径报告制备石墨烯氧化物(RGO)改性的Latio2N / Bi2S3异质结光催化剂的制备。通过使用多种技术进行作为制备的光催化剂的微结构分析,结构测定,电子和光学分析。 Z-Scheme Latio2N / Bi2S3 @ rgo(LBR)光催化剂显示出在可见光下的四环素(TC)的光降解的显着性能。在可见光下在90分钟内除去96.4%Tc,在全谱辐射下60分钟内以100%除去。此外,异质结显示在自然阳光照射下的80.2%TC去除。具有LBR异质结的TC降解类似于比裸BI2S3快9倍。 Z形方案传递遵循途径为Bi2S3 - > Rgo - > Latio2N,并提供来自Latio2N的CB的电子从BI2S3的VB移动的SWIFT路径。还基于淬火实验和通过液相色谱 - 质谱(LC-MS)的降解中间体的鉴定,提出了TC的可能降解途径。淬火实验表明,中心点O-2( - )基团是所涉及的主要活性物质,其次是中心点OH基团,其已经通过从结装置生产的热力学可行性来解释。通过与常规II型结进行比较,通过Z方案转移来解释该机制。光催化活性的增强主要归因于通过氧化石墨烯氧化物片通过强的界面接触而促进的Latio2N和BI2S3之间的Z方案电荷转移,其保持高电位的氧化还原转化率。再循环实验揭示了LBR杂交光催化剂在阳光下进行的能力的稳定性和可重用性。具有改进的可见性和太阳能光催化活动性能的新型氮化酯基结提供了形成卓越的环境修复的杂结构的未来前景。 (c)2020 Elsevier B.v.保留所有权利。

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