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首页> 外文期刊>Nanotechnology >Graphene oxide-grafted plasmonic Au@Ag nanoalloys with improved synergistic effects for promoting hot carrier-driven photocatalysis under visible light irradiation
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Graphene oxide-grafted plasmonic Au@Ag nanoalloys with improved synergistic effects for promoting hot carrier-driven photocatalysis under visible light irradiation

机译:石墨烯氧化物移植等离子体Au @ Ag纳米合金,具有改进的协同效应,用于在可见光照射下促进热载波驱动的光催化分析

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摘要

Plasmonic metallic nanostructure with unique hot carrier-driven photocatalysis has recently emerged as a promising photocatalyst. Herein, we show that the plasmonic photocatalysis can be significantly promoted by supporting bimetallic Au@Ag nanoalloys (NAs) on graphene oxide (GO). The obtained Au-3@Ag-1/GO (molar ratio of Au to Ag similar to 3:1) with improved synergistic effects provides a remarkable higher visible-light (>400 nm) photocatalytic activity for a complete degradation (99.36%) of tetracycline hydrochloride (TCH) molecules within 70 min, while about 61.74% or 62.38% via monometallic Au/GO or Ag/GO. The optimum photocatalytic performance is attributed to the production of high yield hot carriers on NAs with enhanced localized surface plasmon resonance property and the pronounced photoinduced electron-transfer ability of modified GO support by overgrowth of NAs. These findings enable the optimal Au-3@Ag-1/GO to become an appealing high-performance photocatalyst for promoting diverse photochemical reactions.
机译:等离子体金属纳米结构具有独特的热载流子驱动光催化性能,是一种很有前途的光催化剂。在此,我们表明,支持双金属材料可以显著促进等离子体光催化Au@Ag氧化石墨烯(GO)上的纳米合金(NAs)。获得的Au-3@Ag-1/GO(Au/Ag的摩尔比类似于3:1)具有更好的协同效应,可在70分钟内完全降解(99.36%)盐酸四环素(TCH)分子,提供显著更高的可见光(>400 nm)光催化活性,而通过单金属Au/GO或Ag/GO约61.74%或62.38%。最佳光催化性能归因于在NAs上产生高产量的热载流子,具有增强的局域表面等离子体共振特性,以及通过NAs的过度生长得到的改性GO载体的显著光诱导电子转移能力。这些发现使最佳Au成为可能-3@Ag-1/GO将成为一种具有吸引力的高性能光催化剂,用于促进多种光化学反应。

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