过电位
塔菲尔方程
铁磁性
材料科学
反铁磁性
掺杂剂
兴奋剂
过渡金属
纳米晶
催化作用
顺磁性
无机化学
电化学
凝聚态物理
纳米技术
化学
物理化学
电极
光电子学
物理
生物化学
作者
Luis M. Martinez,J. A. Delgado,C. L. Saiz,Adrian Cosio,Yanyu Wu,D. Villagrán,Kinjal Gandha,C. Karthik,Ikenna C. Nlebedim,Srinivasa Rao Singamaneni
摘要
In this paper, the magnetic and electrocatalytic properties of hydrothermally grown transition metal doped (10% of Co, Ni, Fe, and Mn) 2H-MoS2 nanocrystals (NCs) with a particle size 25–30 nm are reported. The pristine 2H-MoS2 NCs showed a mixture of canted anti-ferromagnetic and ferromagnetic behavior. While Co, Ni, and Fe doped MoS2 NCs revealed room temperature ferromagnetism, Mn doped MoS2 NCs showed room temperature paramagnetism, predominantly. The ground state of all the materials is found to be canted-antiferromagnetic phase. To study electrocatalytic performance for hydrogen evolution reaction, polarization curves were measured for undoped and the doped MoS2 NCs. At the overpotential of η = −300 mV, the current densities, listed from greatest to least, are FeMoS2, CoMoS2, MoS2, NiMoS2, and MnMoS2, and the order of catalytic activity found from Tafel slopes is CoMoS2 > MoS2 > NiMoS2 > FeMoS2 > MnMoS2. The increasing number of catalytically active sites in Co doped MoS2 NCs might be responsible for their superior electrocatalytic activity. The present results show that the magnetic order-disorder behavior and catalytic activity can be modulated by choosing the suitable dopants in NCs of 2D materials.
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