电解质
电解
化学
反应机理
镍
乙醇
无机化学
核化学
催化作用
物理化学
有机化学
电极
作者
Junjie Zhang,Ting‐an Zhang,Sen Feng
标识
DOI:10.1016/j.ijhydene.2020.09.253
摘要
α-Ni(OH)2 was electrodeposited from NiCl2 solution by membrane electrolysis method. Various ethanol contents and concentration electrolytes were used to investigate the relevant mechanism. XRD and CV results demonstrated a preferentially conducted side reaction of Ni2+ to Ni. Ethanol was proved to be effective to poison this reaction. Linear relationships of the product mass and electrodeposition time for electrodepositions in 0.1 M NiCl2 solutions indicated an ignored output of Ni. A four-step mechanism for Ni(OH)2 electrodeposition from the side reaction priority system was proposed. XRD and FT-IR results suggested β-Ni(OH)2 and α-Ni(OH)2 were certain to be synthesized in 0.05–0.1 and 0.2–1.0 M NiCl2 solution. β-Ni(OH)2 formed in these low concentration electrolytes was proved to be prevented by circulating the cathodic electrolyte. Analyses suggested β-Ni(OH)2 formed in the present cases might be either converted from α-Ni(OH)2 under high alkaline digestion or synthesized originally due to the proper ratio of Ni2+ and OH−.
科研通智能强力驱动
Strongly Powered by AbleSci AI