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溴代氯铝酸离子液体的微波合成及电沉积铝应用 被引量:1

Microwave synthesis of bromo-chloroaluminate ionic liquid and its application in aluminium electrodeposition
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摘要 采用新型微波合成方法制备溴代氯铝酸离子液体,测试其物理化学性能,并将其作为电解质应用于铝的电沉积。通过测定循环伏安曲线、计时电流曲线以及极化曲线探讨铝在2AlCl3/[EMIM]Br离子液体中的电沉积机理。室温下在铜基体上进行铝的恒电位沉积,沉积层形貌以及结构特性分别用SEM、XRD进行表征。结果表明:溴代氯铝酸离子液体的新型微波合成与普通微波合成相比,大大缩短了反应时间,提高了产品性能;铝的电沉积为准可逆的动力学行为,沉积过程非单纯的扩散控制而是复杂的动力学限制步骤;铝在不同电位下的沉积层大致分为3种典型形貌,并对各种形貌产生的原因及特征进行分析。 A new microwave synthesis method was proposed to prepare bromo-chloroaluminate ionic liquid. The physical and chemical characteristics of this ionic liquid were tested and the ionic liquid was used as the electrolyte in aluminium electrodeposition. Electrochemical techniques of cyclicvoltammetry, chronoamperometry and polarization curve (tafel) were used to investigate the mechanism of aluminium electrodeposition from 2A1CIa/[EMIM]Br ionic liquid. Constant potential electrodepositon of aluminium was conducted on the copper substrates at room temperature and the qualitative analysis of the deposits was performed using SEM and XRD, respectively. The results indicate that the reaction time of the new microwave synthesis of bromo-cbloroaluminate is drastically reduced, comparing with that of the conventional methods, and the properties of chloroaluminate ionic liquid are improved. Alurninium electrodeposition from this ionic liquid is not a simple linear diffusion controlled process, but a quasi-reversible process with complex kinetic limitations. The aluminium deposits obtained at different potentials are mainly about three typical morphologies and the reason for the three typical morphologies and their characteristics are analyzed.
出处 《中国有色金属学报》 EI CAS CSCD 北大核心 2012年第6期1812-1820,共9页 The Chinese Journal of Nonferrous Metals
基金 国家自然科学基金资助项目(51054003 50374045) 山东省自然科学基金资助项目(Y2007F60 ZR2011BL005) 山东省高等学校科技计划资助项目(J09LB59) 山东省中青年科学家科研奖励基金资助项目(BS2009NJ007) 淄博市科学技术发展计划资助项目(2008)
关键词 微波合成 电沉积 活化极化 浓差极化 microwave synthesis electrodeposition activation polarization concentration polarization
作者简介 通信作者:于先进,教授,博士,电话:18253376831,E-mail:hgxyzlp@sdut.edu.cn
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