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Large-Scale Fabrication of Hollow Pt3Al Nanoboxes and Their Electrocatalytic Performance for Hydrogen Evolution Reaction

机译:中空PT3AL纳米氧化的大规模制造及其对氢气进化反应的电催化性能

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摘要

Hollow structuring and alloying have been known to be effective methods to improve physicochemical properties and create new functionalities of nanomaterials. However, it is technically difficult to fabricate hollow alloyed intermetallic compound nanostructures, which are emerging as promising electrocatalysts for water splitting, in a controllable and scalable manner using current wet chemical routes. Here, we report a simple method allowing for large-scale fabrication of hollow Pt_(3)Al nanoparticles using a melt-spinning and subsequent self-templating etching route. We demonstrate that upon etching, both microstructure and phase composition changed, leading to the transformation of Al-rich PtAl_(6) intermetallic compound ribbons to interconnected hollow nanoparticles of Pt-rich Pt_(3)Al with sizes varying from 4 to 22 nm. The electrochemical measurement shows that the hollow Pt_(3)Al intermetallic nanoparticles have better electrocatalytic activity and catalytic stability than commercial Pt/C catalysts for the hydrogen evolution reaction in alkali media, showing that the hollow Pt_(3)Al nanobox can be used as potential cathode catalysts for water splitting. The facile melt-spinning and self-templating etching route can be readily extended to fabricate other noble-metal-based alloy hollow nanostructures on a large scale for various applications.
机译:已知中空结构化和合金化是改善物理化学性质的有效方法,并产生纳米材料的新功能。然而,在技术上难以制造中空合金金属间化合物纳米结构,其作为具有电流湿化学途径可控和可扩展的方式的用于水分裂的有前途的电催化剂。在这里,我们报告了一种简单的方法,允许使用熔融纺丝和随后的自模塑料蚀刻途径进行大规模制造中空PT_(3)纳米颗粒的大规模制造。我们证明,在蚀刻时,两种微观结构和相位组成都改变,导致富含铝的Ptal_(6)金属间化合物带的转化为富含4-22nm的尺寸的富含Pt的Pt_(3)Al的中空纳米颗粒。电化学测量表明,中空Pt_(3)Al金属间纳米颗粒具有比碱介质中的氢进化反应的商业Pt / C催化剂更好的电催化活性和催化稳定性,显示中空Pt_(3)Al Nanobox可以用作用于水分裂的潜在阴极催化剂。容易熔融纺丝和自模板蚀刻途径可以容易地延伸以制造其他贵金属基合金中空纳米结构,用于各种应用。

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