先进制备石墨烯集成高熵合金@碳纳米复合材料,作为卓越的多功能电催化剂

IF 8.2 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY
Imran Khan, Salman Khan, Shiuan-Yau Wu, Linlin Liu, Abdullah N. Alodhayb, James L. Mead, Sharafat Ali, Sibt ul Hassan, Hsin-Tsung Chen, Shin-Pon Ju and Shiliang Wang*, 
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引用次数: 0

摘要

高熵材料表现出无与伦比的反应性和可调的电化学性能,使它们处于电催化水分解的前沿。它们的各种界面和元素都是有目的地在纳米尺度上设计的,这对提高它们的电化学特性至关重要。在内部有高熵合金(HEA) (HEA@C)的石墨烯包覆纳米颗粒(NPs)中观察到的特殊催化效率是几种金属成分共同作用的结果。然而,提高催化效率仍然是一项非常困难的任务,特别是当涉及到通过高效的合成技术获得对组成和结构的精确控制时。HEA@C NPs卓越的反应性和适应性电化学特性使它们在慢氧析氧(SOE)活动中表现更好。本研究中提出的新型多层石墨烯增强HEA CoNiFeCuV@C NPs电催化剂是碳基的,透射电子显微镜(TEM)研究证实了其有效性。该电催化剂大大提高了析氧反应(OER)、析氢反应(HER)和氧还原反应(ORR)的效率。核壳HEA CoNiFeCuV@C NPs对HER、OER和ORR具有显著的电催化性能,尽管其高应力晶格存在结构缺陷。这些催化剂在0.1 M HClO4中,在10 mA cm-2的中等电流密度下达到0.87 V的半波电位,HER和OER起始电位分别为20和259 mV。使用循环伏安法扫描,该研究通过检查激活前后材料的形态,化学状态和元素组成来深入研究材料的演变。除了引入新的电催化剂外,本研究还大大提高了我们对多组分金属间高熵合金的刻意合成的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Advanced Fabrication of Graphene-Integrated High-Entropy Alloy@Carbon Nanocomposites as Superior Multifunctional Electrocatalysts

Advanced Fabrication of Graphene-Integrated High-Entropy Alloy@Carbon Nanocomposites as Superior Multifunctional Electrocatalysts

High entropy materials exhibit unparalleled reactivity and tunable electrochemical properties, putting them at the forefront of advances in electrocatalysis for water splitting. Their various interfaces and elements are purposefully engineered at the nanoscale, which is essential to enhancing their electrochemical characteristics. The exceptional catalytic efficiency observed in graphene-coated nanoparticles (NPs) with an inner high-entropy alloy (HEA) (HEA@C) is a result of the combined action of several metallic constituents. However, increasing catalytic efficiency is still a very difficult task, particularly when it comes to obtaining precise control over the composition and structure via efficient synthesis techniques. HEA@C NPs exceptional reactivity and adaptable electrochemical characteristics allow them to perform better in slow oxygen evolution (SOE) activities. The novel multilayer graphene-enhanced HEA CoNiFeCuV@C NPs electrocatalyst presented in this work is carbon-based, and transmission electron microscopy (TEM) investigations verify its efficacy. The efficiency of the oxygen evolution reaction (OER), hydrogen evolution reaction (HER), and oxygen reduction reaction (ORR) is greatly increased by this electrocatalyst. The electrocatalytic performance of the core–shell HEA CoNiFeCuV@C NPs is remarkable for HER, OER, and ORR, even though its highly stressed lattice has structural flaws. These catalysts reach a half-wave potential of 0.87 V in 0.1 M HClO4 at a moderate current density of 10 mA cm–2, with HER and OER onset potentials of 20 and 259 mV, respectively. Using cyclic voltammetry scans, the study delves deeper into the material’s evolution by examining its morphology, chemical state, and elemental makeup both before and after activation. In addition to introducing novel electrocatalysts, this study significantly enhances our understanding of the deliberate synthesis of multicomponent intermetallic high-entropy alloys.

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来源期刊
ACS Applied Materials & Interfaces
ACS Applied Materials & Interfaces 工程技术-材料科学:综合
CiteScore
16.00
自引率
6.30%
发文量
4978
审稿时长
1.8 months
期刊介绍: ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.
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