金属间化合物
电解
材料科学
非阻塞I/O
循环伏安法
电化学
氧化物
扫描电子显微镜
阳极
无机化学
分析化学(期刊)
冶金
电极
化学
催化作用
物理化学
复合材料
色谱法
合金
电解质
生物化学
作者
Mohd. Sufiyan Khan,Anwesha Mukherjee,L. Shakila,V. Arunkumar,R. Kumaresan
标识
DOI:10.1149/1945-7111/acf8fc
摘要
The aim of the present study was to prepare ZrFe 2 and ZrFe 1.8 Ni 0.2 intermetallic compounds by FFC Cambridge process. The intermetallic compounds were prepared directly from the mixed oxide precursors, namely ZrO 2 -Fe 2 O 3 and ZrO 2 -Fe 2 O 3 -NiO, respectively. Electrochemical de-oxidation experiments were carried out with mixed oxide pellet cathode and HD graphite anode by applying a constant cell voltage of 3.1 V in CaCl 2 melt at 900 o C. The electrochemical behaviour of oxides was studied by cyclic voltammetry using metallic cavity electrodes (MCEs). The electrolysis was carried out for different durations of time to understand the mechanistic pathway of reduction of ZrO 2 -Fe 2 O 3 . The electro-reduced products were characterized by X-ray diffraction (XRD) technique, scanning electron microscope (SEM) and energy dispersive X-ray spectroscopy (EDS). The reduction intermediates involved Fe, CaZrO 3 , calcia stabilised zirconia (CSZ), Fe 23 Zr 6 , Zr 6 Fe 3 O and Zr 2 Fe. Single cubic C15 phase of ZrFe 2 was obtained in 48 h electrolysis product. ZrFe 1.8 Ni 0.2 was also electrochemically synthesized from its oxide precursors viz. ZrO 2 , Fe 2 O 3 and NiO. Apart from ZrFe 1.8 Ni 0.2 phase, the electro-reduced products had a Zr 2 Ni phase even after 72 h of electrolysis.
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