TiO2/银纳米线复合材料增强亚甲基蓝的光电催化降解

IF 1.7 4区 化学 Q4 CHEMISTRY, PHYSICAL
Yung-Hsiang Hsu, Shoaib Siddique, Bo-Tau Liu
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引用次数: 0

摘要

采用多元醇法制备了银纳米线,并将其用于制备透明导电薄膜。采用双层TiO2/AgNWs结构进行了亚甲基蓝(MB)的光电催化降解。虽然TiO2光催化降解MB不存在过电位问题,但施加偏置电压可显著提高催化活性。与ITO导体相比,AgNWs表现出优越的光电催化性能,这可能是由于它们增加了界面接触和TiO2基体内的快速电荷传输,有效地抑制了电子-空穴复合。外加电压通过促进电荷分离和产生额外的羟基自由基进一步提高了催化效率。活性表面积和薄片电阻受TiO2层厚度的影响,影响电子传递和电荷复合速率。阳极条件下的MB降解效率高于阴极条件,因为阳极电极有效地提取了激发态电子,增强了电荷分离。偏置电压虽然提高了TiO2/AgNWs催化剂的催化活性,但并没有改变反应顺序和残碳比例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Enhanced photoelectrocatalytic degradation of methylene blue using TiO2/silver nanowires composites

Enhanced photoelectrocatalytic degradation of methylene blue using TiO2/silver nanowires composites

Silver nanowires (AgNWs) were synthesized using the polyol method and utilized to fabricate transparent conductive films. A bilayer TiO2/AgNWs structure was employed for the photoelectrocatalytic degradation of methylene blue (MB). While TiO2 photocatalysis for MB degradation did not suffer from overpotential issues, applying a bias voltage significantly enhanced catalytic activity. Compared to ITO conductors, AgNWs demonstrated superior photoelectrocatalytic performance, likely due to their increased interfacial contact and rapid charge transport within the TiO2 matrix, effectively suppressing electron–hole recombination. The application of an external voltage further improved catalytic efficiency by promoting charge separation and generating additional hydroxyl radicals. The active surface area and sheet resistance were influenced by the thickness of the TiO2 layer, impacting electron transport and charge recombination rates. MB degradation under anodic conditions was more efficient than under cathodic conditions, as the anodic electrode effectively extracted excited electrons, enhancing charge separation. Although bias voltage improved the catalytic activity of TiO2/AgNWs catalysts, it did not change the reaction order and the ratio of residual carbon.

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来源期刊
CiteScore
3.30
自引率
5.60%
发文量
201
审稿时长
2.8 months
期刊介绍: Reaction Kinetics, Mechanisms and Catalysis is a medium for original contributions in the following fields: -kinetics of homogeneous reactions in gas, liquid and solid phase; -Homogeneous catalysis; -Heterogeneous catalysis; -Adsorption in heterogeneous catalysis; -Transport processes related to reaction kinetics and catalysis; -Preparation and study of catalysts; -Reactors and apparatus. Reaction Kinetics, Mechanisms and Catalysis was formerly published under the title Reaction Kinetics and Catalysis Letters.
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