iron disilicide
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Nanomaterials ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 849
Author(s):  
Liwei D. Geng ◽  
Sahil Dhoka ◽  
Ilan Goldfarb ◽  
Ranjit Pati ◽  
Yongmei M. Jin

Magnetism has recently been observed in nominally nonmagnetic iron disilicide in the form of epitaxial γ-FeSi2 nanostructures on Si(111) substrate. To explore the origin of the magnetism in γ-FeSi2/Si(111) nanostructures, we performed a systematic first-principles study based on density functional theory. Several possible factors, such as epitaxial strain, free surface, interface, and edge, were examined. The calculations show that among these factors, only the edge can lead to the magnetism in γ-FeSi2/Si(111) nanostructures. It is shown that magnetism exhibits a strong dependency on the local atomic structure of the edge. Furthermore, magnetism can be enhanced by creating multiple-step edges. In addition, the results also reveal that edge orientation can have a significant effect on magnetism. These findings, thus, provide insights into a strategy to tune the magnetic properties of γ-FeSi2/Si(111) nanostructures through controlling the structure, population, and orientation of the edges.



2021 ◽  
Vol 3 (2) ◽  
pp. 890-897
Author(s):  
Antoine Micallef ◽  
Christian Stiewe ◽  
Gregor Oppitz ◽  
Eckhard Müller


2020 ◽  
Vol 709 ◽  
pp. 138248
Author(s):  
Peerasil Charoenyuenyao ◽  
Nathaporn Promros ◽  
Rawiwan Chaleawpong ◽  
Nattakorn Borwornpornmetee ◽  
Pattarapol Sittisart ◽  
...  




2020 ◽  
Vol 20 (1) ◽  
pp. 433-441
Author(s):  
Rawiwan Chaleawpong ◽  
Nathaporn Promros ◽  
Peerasil Charoenyuenyao ◽  
Kenji Hanada ◽  
Li Chen ◽  
...  


Author(s):  
Maria М. Kuzminykh ◽  
Viktoria V. Panteleeva ◽  
Anatoliy B. Shein

The kinetics of hydrogen evolution reaction on FeSi2-electrode in 0.5 M H2SO4 solution has been studied using methods of polarization and impedance measurements. With the help of diagnostic criteria for the hydrogen evolution reaction mechanisms based on the analysis of the dependence of the parameters of the equivalent electric circuit on overvoltage, it was established that the reaction of hydrogen evolution on iron disilicide in the sulfuric acid solution proceeds along the discharge - electrochemical desorption route, where desorption is the rate-determining stage. Both stages are irreversible, the transfer coefficients α of the stages are equal, simultaneously the hydrogen absorption reaction by the electrode material proceeds in the kinetic mode (in the whole investigated range of potentials). It was found that the adsorption of atomic hydrogen is described by the equation of the Langmuir isotherm. The influence of thin oxide film on the hydrogen evolution kinetics is noted. The influence of various methods of modifying of the surface of FeSi2-electrode on the kinetics and mechanism of the cathodic process has been studied. It was found that the modification of the disilicide surface by hydrogenation at a current density of i = 30 mA/cm2, an anodic etching in 0.5 M H2SO4 at the potential E = 0.4 V relative to the standard hydrogen electrode, an anodic etching in 1.0 M NaOH at the potential E = 0.1 V, chemical etching in 5.0 M NaOH at 70 °C reduce the overvoltage of hydrogen evolution, but the mechanism of the cathodic process does not change as a result of the electrode modification. Reduction of the overvoltage of hydrogen evolution on iron disilicide is due to the action of two factors: the development of the surface and the change in the composition of the surface layer of the electrode. It has been concluded that FeSi2 in the sulfuric acid solution is a promising electrode material that exhibits activity in the electrolytic hydrogen evolution reaction.



Author(s):  
Maria M. Kuzminykh ◽  
Victoria V. Panteleeva ◽  
Anatoliy B. Shein

The kinetics of hydrogen evolution reaction on FeSi2-electrode in 1.0 M NaOH solution has been studied using methods of polarization and impedance measurements. With the help of diagnostic criteria for the hydrogen evolution reaction mechanisms based on the analysis of the dependence of the parameters of the equivalent electric circuit on overvoltage, it was established that the reaction of hydrogen evolution on iron disilicide in the alkaline electrolyte proceeds along the discharge - electrochemical desorption route, where desorption is the rate-determining stage. Both stages are irreversible, the transfer coefficients of the stages are equal (α1 = α2 = α), simultaneously the hydrogen absorption reaction by the electrode material proceeds in the diffusion mode (in the whole investigated range of potentials). It was found that the adsorption of atomic hydrogen is described by the equation of the Langmuir isotherm. The influence of various methods of modifying of the surface of FeSi2-electrode on the kinetics and mechanism of the cathodic process has been studied. It was found that the modification of the disilicide surface by hydrogenation at a current density of i = 30 mA/cm2, an anodic etching in 0.5 M H2SO4 at the potential E = 0.4 V relative to the standard hydrogen electrode, an anodic etching in 1.0 M NaOH at the potential E = 0.1 V, chemical etching in 5.0 M NaOH at 70 °C reduce the overvoltage of hydrogen evolution, but the mechanism of the cathodic process does not change as a result of the modification. Reduction of the overvoltage of hydrogen evolution on iron disilicide is due to the action of two factors: the development of the surface and the change in the composition of the surface layer of the electrode. It has been concluded that FeSi2 in the alkaline electrolyte is a promising electrode material that exhibits activity in the electrolytic hydrogen evolution reaction.



Materials ◽  
2018 ◽  
Vol 11 (12) ◽  
pp. 2384 ◽  
Author(s):  
Wei-Jie Huang ◽  
Yu-Yang Chen ◽  
Hsiu-Ming Hsu ◽  
Kuo-Chang Lu

In this paper, we report the synthesis of iron silicide and β-iron disilicide nanowires with chemical vapor deposition; remarkably, the latter has drawn much attention but has seldom been achieved. We also propose the formation mechanisms for the two phases. To investigate the effects of the growth parameters on compositions and morphologies of the iron silicide nanowires, we changed and studied the reaction time, substrate temperature, position of samples, and pressure. The reaction concentration was found to be altered by all of the parameters; thus, we observed different nanowires in terms of morphologies and compositions with scanning electron microscopy. To confirm the growth direction and crystal structure of the nanowires, we conducted x-ray diffraction and high-resolution transmission electron microscopy studies. With the potential of being utilized as circuit elements in electronic devices for Schottky barriers, ohmic contacts, and interconnection among silicon-based transistors, the silicide work at nanoscale is beneficial for nanoelectronics. Understanding the effects of these growth parameters facilitates the control of nanowire growth with better quality.



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