...
首页> 外文期刊>Journal of Colloid and Interface Science >Facile synthesis of CeO2/carbonate doped Bi2O2CO3 Z-scheme heterojunction for improved visible-light photocatalytic performance: Photodegradation of tetracycline and photocatalytic mechanism
【24h】

Facile synthesis of CeO2/carbonate doped Bi2O2CO3 Z-scheme heterojunction for improved visible-light photocatalytic performance: Photodegradation of tetracycline and photocatalytic mechanism

机译:CeO2 /碳酸酯掺杂Bi2O2CO3 Z样品合成,改善可见光光催化性能的异质结:四环素和光催化机制的光降解

获取原文
获取原文并翻译 | 示例

摘要

CeO2 nanoparticles are successfully loaded on carbonate doped Bi2O2CO3 (CBOC) nanosheets by a facile hydrothermal and low-temperature calcination method. CeO2/CBOC heterojunction shows significantly enhanced photocatalytic activity, when 35 mg of CeO2/CBOC photocatalyst is added to tetracycline (TC) solution (20 mg/L, 100 mL), about 79.5% TC is degraded within 90 min under visible light irradiation, which is much higher than that of original CeO2 and CBOC. According to photoelectrochemical characterization and active radical capture experiments, the Z-scheme electron transfer mechanism is the reason for the significant enhancement of photocatalytic activity. Besides, the XPS results indicate that Ce4+/Ce3+ redox pairs are formed at the contact interface between CeO2 and CBOC, which is conducive to the transfer of photoexcited electrons and production of superoxide radicals. Additionally, the photocatalytic mechanism and possible degradation pathway of TC is proposed through free radical trapping experiments and liquid chromatography-mass (LC-MS) analysis. This study will accumulate experience for the combination of CeO2 and bismuth-based nanomaterials, and provide a feasible way to design wide band-gap bismuth-based photocatalysts, thereby achieving efficient visible light degradation of environmental pollutants. (C) 2020 Elsevier Inc. All rights reserved.
机译:通过一种简单的水热和低温煅烧方法,将CeO2纳米颗粒成功地负载在碳酸盐掺杂的Bi2O2CO3(CBOC)纳米片上。CeO2/CBOC异质结的光催化活性显著增强,当向四环素(TC)溶液(20mg/L,100mL)中加入35mg CeO2/CBOC光催化剂时,在可见光照射下90min内约有79.5%的TC被降解,远高于原始的CeO2和CBOC。根据光电化学表征和活性自由基捕获实验,Z型电子转移机制是光催化活性显著增强的原因。此外,XPS结果表明,CeO2与CBOC的接触界面上形成了Ce4+/Ce3+氧化还原对,这有利于光激发电子的转移和超氧自由基的产生。此外,通过自由基捕获实验和液相色谱-质谱(LC-MS)分析,提出了TC的光催化机理和可能的降解途径。本研究将为CeO2与铋基纳米材料的结合积累经验,为设计宽禁带铋基光催化剂提供可行的途径,从而实现环境污染物的高效可见光降解。(C) 2020爱思唯尔公司版权所有。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号