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首页> 外文期刊>RSC Advances >Facile room-temperature precipitation strategy for Ag2O/Bi2WO6 heterojunction with high simulated sunlight photocatalytic performance via bi-directed electron migration mechanism
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Facile room-temperature precipitation strategy for Ag2O/Bi2WO6 heterojunction with high simulated sunlight photocatalytic performance via bi-directed electron migration mechanism

机译:Ag2O / Bi2WO6异质结具有高模拟阳光光催化性能的Facile室温降水策略通过双向电子迁移机制

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摘要

A trace Ag2O modified Bi2WO6 heterojunction was facilely synthesized via a solution precipitation strategy at ambient temperature. The characterizations of composition, morphology, microstructure, UV-vis absorption, photoluminescence, BET, photocurrent and solar simulated photocatalytic behavior were systematically investigated. They showed that besides a few visible nanoparticles, most of the Ag2O phase was inconspicuously distributed on the surface of the Bi2WO6 substrate. The composite photocatalyst exhibited obviously enhanced photocatalytic activity compared with pure Ag2O and Bi2WO6 for degradation of organic contaminants. In particular, the sample of Ag-0.6 wt% presented the best photocatalytic activity with a rate constant 4.8-fold as fast as that of Bi2WO6. Photochemical and photoelectrochemical analysis indicated that the introduction of trace Ag2O effectively broadened the visible-light absorption and inhibited the photogenerated carrier recombination in Bi2WO6. Based on band structure analysis and XPS results of recycled samples, a bi-directed migration mechanism of photogenerated electrons is proposed at the heterostructure interface. The band-gap coupling effect between Ag2O and Bi2WO6 and the electronic effect of trace metallic Ag in situ photoreduced from the self-stabilized Ag2O are believed to play vital roles in the separation and migration of e(-)/h(+) pairs. The work provides some insights into the rational design of hybrid photocatalysts with high performance via multi-path photogenerated carrier migration.
机译:通过在环境温度下通过溶液沉淀策略施加痕量Ag2O改性的Bi2WO6异质结。系统地研究了组合物,形态,微观结构,UV-Vis吸收,光致发光,BET,光电流和太阳模拟光催化行为的特征。它们表明,除了几个可见的纳米颗粒之外,大部分Ag 2 O相对于Bi2WO6底物的表面不显着分布。与纯Ag2O和Bi2WO6相比,复合光催化剂显着增强了光催化活性,用于降解有机污染物。特别地,Ag-0.6wt%的样品呈现最佳的光催化活性,速率恒定为4.8倍,尽可能快地快速。光化学和光电化学分析表明,痕量Ag2O的引入有效地扩展了可见光吸收并抑制了Bi2WO6中的光生载体重组。基于带结构分析和再循环样品的XPS结果,在异质结构界面处提出了一种双向迁移机制的光发学电子。 AG2O和BI2WO6之间的带间隙耦合效果和来自自稳压Ag2O的原位的痕量金属Ag的电子效果被认为在E( - )/ h(+)对的分离和迁移中起重要作用。该作品通过多路径光发化载体迁移,对高性能的杂化光催化剂的合理设计提供了一些见解。

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  • 来源
    《RSC Advances 》 |2015年第41期| 共10页
  • 作者单位

    Tianjin Normal Univ Tianjin Key Lab Struct &

    Performance Funct Mol Key Lab Inorgan Organ Hybrid Funct Mat Chem Minist Educ Coll Chem Tianjin 300387 Peoples R China;

    Tianjin Normal Univ Tianjin Key Lab Struct &

    Performance Funct Mol Key Lab Inorgan Organ Hybrid Funct Mat Chem Minist Educ Coll Chem Tianjin 300387 Peoples R China;

    Tianjin Normal Univ Tianjin Key Lab Struct &

    Performance Funct Mol Key Lab Inorgan Organ Hybrid Funct Mat Chem Minist Educ Coll Chem Tianjin 300387 Peoples R China;

    Tianjin Normal Univ Tianjin Key Lab Struct &

    Performance Funct Mol Key Lab Inorgan Organ Hybrid Funct Mat Chem Minist Educ Coll Chem Tianjin 300387 Peoples R China;

    Tianjin Normal Univ Tianjin Key Lab Struct &

    Performance Funct Mol Key Lab Inorgan Organ Hybrid Funct Mat Chem Minist Educ Coll Chem Tianjin 300387 Peoples R China;

    Tianjin Normal Univ Tianjin Key Lab Struct &

    Performance Funct Mol Key Lab Inorgan Organ Hybrid Funct Mat Chem Minist Educ Coll Chem Tianjin 300387 Peoples R China;

    Tianjin Normal Univ Tianjin Key Lab Struct &

    Performance Funct Mol Key Lab Inorgan Organ Hybrid Funct Mat Chem Minist Educ Coll Chem Tianjin 300387 Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学 ;
  • 关键词

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