Growth of MoS2 nanosheets on M@N-doped carbon particles (M = Co, Fe or CoFe Alloy) as an efficient electrocatalyst toward hydrogen evolution reaction

被引:79
作者
Shah, Sayyar Ali [1 ]
Xu, Li [1 ]
Sayyar, Rani [1 ]
Bian, Ting [1 ]
Liu, Zeyu [1 ]
Yuan, Aihua [1 ]
Shen, Xiaoping [2 ]
Khan, Iltaf [3 ]
Tahir, Asif Ali [3 ]
Ullah, Habib [4 ]
机构
[1] Jiangsu Univ Sci & Technol, Sch Environm & Chem Engn, Zhenjiang 212003, Jiangsu, Peoples R China
[2] Jiangsu Univ, Sch Chem & Chem Engn, Zhenjiang 212013, Jiangsu, Peoples R China
[3] Heilongjiang Univ, Sch Chem & Mat Sci, Key Lab Funct Inorgan Mat Chem, Harbin 150080, Peoples R China
[4] Univ Exeter, Environm & Sustainabil Inst, Penryn Campus, Penryn TR10 9FE, Cornwall, England
关键词
Electrocatalyst; Hydrogen evolution reaction; Molybdenum disulfide; N-doped carbon encapsulated metal particles; Density functional theory; ACTIVE EDGE SITES; HYBRID CATALYSTS; CHARGE-TRANSFER; PHOSPHIDE; GENERATION; CLOTH;
D O I
10.1016/j.cej.2021.132126
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The design and synthesis of a highly active noble metal-free electrocatalyst for hydrogen evolution reaction (HER) from water splitting are crucial for renewable energy technologies. Herein, we report the growth of molybdenum disulfide (MoS2) on N-doped carbon encapsulated metal particles (M@NDC@MoS2, where M = Co, Fe or CoFe alloy) as a highly active electrocatalyst for HER. The hierarchical MoS2 nanosheets are grown on M@NDC using the hydrothermal method. Our results show that CoFe@NDC@MoS2 hybrid spheres exhibit excellent HER performance with an overpotential of 64 mV at a current density of 10 mA cm-2 and a small Tafel slope of 45 mV dec-1. In addition, CoFe@NDC@MoS2 hybrid spheres have good long-term stability and durability in acidic conditions. Besides, density functional theory (DFT) simulations of the proposed catalysts are performed and suggest that the superior catalytic activity of CoFe@NDC@MoS2 is due to the optimal electron transfer from CoFe@NDC nanoparticles to MoS2 nanosheets. This electron transfer facilitates H+ interaction and adsorption, leading to a decreased Gibbs free energy (Delta GH* approximate to 0.08 eV) and local work function on the surface, which consequently enhances the HER performance.
引用
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页数:9
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