...
首页> 外文期刊>Applied Surface Science >Enhanced catalyst activity by decorating of Au on Ag@Cu_2O nanoshell
【24h】

Enhanced catalyst activity by decorating of Au on Ag@Cu_2O nanoshell

机译:通过在Ag @ Cu_2O纳米壳上修饰Au来增强催化剂活性

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Graphical abstractDisplay OmittedHighlightsAu-decorated Ag@Cu2O heterostructures via a simple galvanic replacement method were designed.We can easily control the density of the Au NPs on Ag@Cu2O by changing the concentration of the Au precursor.Ag@Cu2O-Au nanomaterials with high absorption exhibited significantly enhanced catalytic activity for 4-NP.AbstractWe successfully synthesized Au-decorated Ag@Cu2O heterostructures via a simple galvanic replacement method. As the Au precursor concentration increased, the density of the Au nanoparticles (NPs) on the Ag@Cu2O surface increased, which changed the catalytic activity of the Ag@Cu2O-Au structure. The combination of Au, Ag, and Cu2O exhibited excellent catalytic properties, which can further effect on the catalyst activity of the Ag@Cu2O-Au structure. In addition, the proposed Ag@Cu2O-Au nanocomposite was used to transform the organic, toxic pollutant, 4-nitrophenol (4-NP), into its nontoxic and medicinally important amino derivative via a catalytic reduction to optimize the material performance. The proposed Au-decorated Ag@Cu2O exhibited excellent catalytic activity, and the catalytic reduction time greatly decreased (5 min). Thus, three novel properties of Ag@Cu2O-Au, i.e., charge redistribution and transfer, adsorption, and catalytic reduction of organic pollutants, were ascertained for water remediation. The proposed catalytic properties have potential applications for photocatalysis and localized surface plasmon resonance (LSPR)- and peroxidase-like catalysis.
机译: 图形摘要 < ce:simple-para>省略显示 突出显示 Au装饰的Ag通过简单的电置换方法设计了@Cu 2 O异质结构。 我们可以轻松控制d通过改变Au前体的浓度,对Ag @ Cu 2 O上的Au NP的敏感性。 Ag @ Cu 2 高吸收率的O-Au纳米材料对4-NP的催化活性显着增强。 摘要 < ce:abstract-sec id =“ abst0015” view =“ all”> 我们成功合成了装饰有金的Ag @ Cu 2 O异质结构,采用简单的电置换方法。随着Au前体浓度的增加,Ag @ Cu 2 O表面上Au纳米颗粒(NPs)的密度增加,从而改变了Ag的催化活性。 @Cu 2 O-Au结构。 Au,Ag和Cu 2 O的组合具有优异的催化性能,可进一步影响Ag @ Cu 2 O-Au结构。此外,使用拟议的Ag @ Cu 2 O-Au纳米复合材料将有机有毒污染物4-硝基苯酚(4-NP)转化为其通过催化还原来优化材料性能的无毒且具有医学重要性的氨基衍生物。提出的Au修饰的Ag @ Cu 2 O表现出优异的催化活性,催化还原时间大大减少(5分钟)。因此,确定了Ag @ Cu 2 O-Au的三种新颖性质,即水的有机污染物的电荷再分配和转移,吸附以及催化还原。补救措施。拟议的催化性质在光催化和局部表面等离子体共振(LSPR)和过氧化物酶样催化方面具有潜在的应用。

著录项

  • 来源
    《Applied Surface Science》 |2018年第30期|72-78|共7页
  • 作者单位

    Key Laboratory of Functional Materials Physics and Chemistry, Ministry of Education, College of Physics, Jilin Normal University,Key Laboratory of Preparation and Applications of Environmental Friendly Materials, Ministry of Education, College of Chemistry, Jilin Normal University;

    Key Laboratory of Functional Materials Physics and Chemistry, Ministry of Education, College of Physics, Jilin Normal University;

    Key Laboratory of Functional Materials Physics and Chemistry, Ministry of Education, College of Physics, Jilin Normal University;

    Key Laboratory of Functional Materials Physics and Chemistry, Ministry of Education, College of Physics, Jilin Normal University;

    Key Laboratory of Functional Materials Physics and Chemistry, Ministry of Education, College of Physics, Jilin Normal University;

    Key Laboratory of Functional Materials Physics and Chemistry, Ministry of Education, College of Physics, Jilin Normal University;

    Key Laboratory of Functional Materials Physics and Chemistry, Ministry of Education, College of Physics, Jilin Normal University;

    Key Laboratory of Functional Materials Physics and Chemistry, Ministry of Education, College of Physics, Jilin Normal University;

    Department of Chemistry, Institute for Molecular Science and Fusion Technology, Kangwon National University;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Heterostructures; Ag@Cu2O-Au; Catalytic; 4-Nitrophenol;

    机译:异质结构;Ag @ Cu2O-Au;催化;4-硝基苯酚;

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