首页> 外文期刊>Research on Chemical Intermediates >Fabrication of noble-metal-free NiS2/g-C3N4 hybrid photocatalysts with visible light-responsive photocatalytic activities
【24h】

Fabrication of noble-metal-free NiS2/g-C3N4 hybrid photocatalysts with visible light-responsive photocatalytic activities

机译:具有可见光响应光催化活性的无贵金属NiS2 / g-C3N4杂化光催化剂的制备

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Nanocomposites of NiS2 with graphitic carbon nitride (NiS2/g-C3N4) have been successfully synthesized by means of a facile hydrothermal method. The photocatalytic activities of as-prepared samples were evaluated by monitoring the photodecomposition of rhodamine B under visible light irradiation. The experimental results indicated that visible light-driven NiS2/g-C3N4 composites exhibited an enhanced photocatalytic activity compared to that of pure NiS2, due to the fast generation, separation and transportation of the photogenerated carriers resulting from the addition of NiS2 nanoparticles (NPs). Interestingly, different amounts of NiS2 deposition can affect the photocatalytic activities of the NiS2/g-C3N4 composites. A suitable loading amount of NiS2 NPs presents the best photodegradation performance. The photocatalytic reaction mechanism for the improved photocatalytic performance of NiS2/g-C3N4 catalyst was proposed which was supported by PL, PEC, EIS and active species trapping results. A promising strategy presented here provides a facile route towards the development of economical, noble metal-free composites as photocatalysts for the applications in environmental remediation.
机译:NiS2与石墨碳氮化物(NiS2 / g-C3N4)的纳米复合材料已通过简便的水热方法成功合成。通过在可见光照射下监测若丹明B的光解作用来评估所制备样品的光催化活性。实验结果表明,可见光驱动的NiS2 / g-C3N4复合材料与纯NiS2相比具有增强的光催化活性,这是由于添加NiS2纳米颗粒(NPs)导致光生载流子的快速生成,分离和运输。有趣的是,不同数量的NiS2沉积会影响NiS2 / g-C3N4复合材料的光催化活性。 NiS2 NPs的合适负载量具有最佳的光降解性能。提出了改善NiS2 / g-C3N4催化剂光催化性能的光催化反应机理,该机理得到PL,PEC,EIS和活性物种捕获结果的支持。本文提出的一种有前途的策略为开发经济,无贵金属的复合材料作为光催化剂提供了一条可行的途径,以用于环境修复。

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