Abbott Andrew P, Harris Robert C, Hsieh Yi-Ting, Ryder Karl S, Sun I-Wen
Chemistry Department, University of Leicester, Leicester, LE1 7RH, UK.
Phys Chem Chem Phys. 2014 Jul 28;16(28):14675-81. doi: 10.1039/c4cp01508h.
The electrodeposition of aluminium is demonstrated using a eutectic mixture of aluminium chloride and urea. The mixture is shown to be conducting through the formation of both cationic (AlCl2·urean) and anionic (AlCl4(-)) species and electrodeposition is achieved through the cationic species. The use of a biphasic system with the ionic liquid and a protective hydrocarbon layer allows metal deposition to be carried out in an environment with ambient moisture without the need for a glove box. A direct comparison is made between the AlCl3:urea and imidazolium chloride:AlCl3 systems and the differences in speciation and mass transport manifest themselves in different deposit morphologies. Brighteners which work in the chloroaluminate system such as toluene and LiCl are shown to be ineffective in the urea based system and the reasons for these differences are ascribed to the mechanism of the anodic reaction which is rate limiting.
使用氯化铝和尿素的低共熔混合物演示了铝的电沉积过程。该混合物通过形成阳离子([AlCl₂·尿素⁺])和阴离子(AlCl₄⁻)物种而具有导电性,并且通过阳离子物种实现电沉积。使用离子液体和保护性烃层的双相系统可使金属沉积在有环境湿度的环境中进行,而无需手套箱。对AlCl₃:尿素体系和氯化咪唑鎓:AlCl₃体系进行了直接比较,物种形成和传质的差异在不同的沉积物形态中表现出来。在氯铝酸盐体系中起作用的增亮剂,如甲苯和LiCl,在基于尿素的体系中无效,这些差异的原因归因于作为速率限制的阳极反应机理。