LaTiO2N/Bi2S3 Z-scheme nano heterostructures modified by rGO with high interfacial contact for rapid photocatalytic degradation of tetracycline

被引:37
作者
Sharma, Sunil Kumar [1 ]
Kumar, Amit [1 ,2 ]
Sharma, Gaurav [1 ,2 ]
Stadler, Florian J. [2 ]
Naushad, Mu [3 ]
Ghfar, Ayman A. [3 ]
Ahamad, Tansir [3 ]
机构
[1] Shoolini Univ, Sch Chem, Solan 173229, Himachal Prades, India
[2] Shenzhen Univ, Coll Mat Sci & Engn, Guangdong Res Ctr Interfacial Engn Funct Mat, Shenzhen Key Lab Polymer Sci & Technol,Nanshan Di, Shenzhen 518055, Peoples R China
[3] King Saud Univ, Coll Sci, Dept Chem, Bldg 5, Riyadh 11451, Saudi Arabia
关键词
Z-scheme; Heterojunction; Photocatalytic; Tetracycline; Water treatment; LaTiO2N; ADSORPTIVE REMOVAL; METHYLENE-BLUE; LIGHT; WATER; HETEROJUNCTION; ANTIBIOTICS; FABRICATION; COMPOSITE; HYBRID; NANOPARTICLES;
D O I
10.1016/j.molliq.2020.113300
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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.
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页数:12
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