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

被引:0
|
作者
Khan, Imran [1 ]
Khan, Salman [2 ]
Wu, Shiuan-Yau [3 ,4 ]
Liu, Linlin [1 ]
Alodhayb, Abdullah N. [5 ]
Mead, James L. [6 ]
Ali, Sharafat [7 ]
ul Hassan, Sibt [1 ]
Chen, Hsin-Tsung [3 ,4 ]
Ju, Shin-Pon [8 ]
Wang, Shiliang [1 ]
机构
[1] Cent South Univ, Sch Phys & Elect, Changsha 410083, Peoples R China
[2] Heilongjiang Univ, Key Lab Funct Inorgan Mat Chem, Minist Educ Peoples Republ China, Harbin 150080, Peoples R China
[3] Chung Yuan Christian Univ, R&D Ctr Membrane Technol, Dept Chem, Taoyuan City 320314, Taiwan
[4] Chung Yuan Christian Univ, Res Ctr Semicond Mat & Adv Opt, Taoyuan City 320314, Taiwan
[5] King Saud Univ, Coll Sci, Dept Phys & Astron, Riyadh 11451, Saudi Arabia
[6] Carl von Ossietzky Univ Oldenburg, Dept Comp Sci, Div Microrobot & Control Engn AMiR, D-26129 Oldenburg, Germany
[7] Univ Elect Sci & Technol China, Sch Phys, Chengdu 610054, Peoples R China
[8] Natl Sun Yat Sen Univ, Dept Mech & Electromech Engn, Kaohsiung 804, Taiwan
基金
中国国家自然科学基金;
关键词
multifunctional electrocatalysts; high-entropy alloyednanoparticles; compositional engineering; modulatedcrystal and electronic configuration; HER OER ORR; TOTAL-ENERGY CALCULATIONS; HYDROGEN EVOLUTION; THERMAL-STABILITY; OXYGEN; METALS; CO; CU; NANOTUBES; CATALYST; TI;
D O I
10.1021/acsami.4c02468
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
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.
引用
收藏
页码:21033 / 21052
页数:20
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