{"title":"Electrodeposition of aluminum from AlCl3-triethylamine hydrochloride ionic liquid","authors":"Xue Yang, Aimin Liu, Xin Zhang, Pingping Guan, Yubao Liu, Haitao Huang, Zhongning Shi","doi":"10.1007/s11581-024-05989-1","DOIUrl":null,"url":null,"abstract":"<div><p>Aluminum chloride and triethylamine hydrochloride were employed in the synthesis of an AlCl<sub>3</sub>-Et<sub>3</sub>NHCl electrolyte. An aluminum sheet was utilized as the anode for the electrodeposition of metallic aluminum onto a copper substrate. This study aimed to investigate the effects of deposition potential on the morphology of the aluminum coating, the deposition mechanism, and the changes in Al(III) complex ions during the electrodeposition process. The results indicated that a deposition potential of − 0.3 V (vs. Al) produced aluminum coatings that were uniformly dense and securely adhered to the substrate. When electrodeposition occurred at − 0.5 V (vs. Al), the substrate surface exhibited aluminum nanowires with an approximate diameter of 367 nm. XRD analysis indicated a more pronounced (200) preferred orientation in the aluminum layer deposited at more negative potentials. Raman spectroscopy analysis detected the presence of AlCl<sub>4</sub><sup>−</sup> and Al<sub>2</sub>Cl<sub>7</sub><sup>−</sup> anions in the AlCl<sub>3</sub>-Et<sub>3</sub>NHCl system before electrodeposition, followed by the formation of Al<sub>3</sub>Cl<sub>10</sub><sup>−</sup> complex ions in the system under potentiostatic control.</p></div>","PeriodicalId":599,"journal":{"name":"Ionics","volume":"31 2","pages":"1655 - 1665"},"PeriodicalIF":2.6000,"publicationDate":"2024-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ionics","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s11581-024-05989-1","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Aluminum chloride and triethylamine hydrochloride were employed in the synthesis of an AlCl3-Et3NHCl electrolyte. An aluminum sheet was utilized as the anode for the electrodeposition of metallic aluminum onto a copper substrate. This study aimed to investigate the effects of deposition potential on the morphology of the aluminum coating, the deposition mechanism, and the changes in Al(III) complex ions during the electrodeposition process. The results indicated that a deposition potential of − 0.3 V (vs. Al) produced aluminum coatings that were uniformly dense and securely adhered to the substrate. When electrodeposition occurred at − 0.5 V (vs. Al), the substrate surface exhibited aluminum nanowires with an approximate diameter of 367 nm. XRD analysis indicated a more pronounced (200) preferred orientation in the aluminum layer deposited at more negative potentials. Raman spectroscopy analysis detected the presence of AlCl4− and Al2Cl7− anions in the AlCl3-Et3NHCl system before electrodeposition, followed by the formation of Al3Cl10− complex ions in the system under potentiostatic control.
采用氯化铝和盐酸三乙胺合成了一种AlCl3-Et3NHCl电解质。利用铝板作为阳极,在铜衬底上电沉积金属铝。本研究旨在探讨电沉积电位对铝镀层形貌的影响、沉积机理以及电沉积过程中Al(III)络合离子的变化。结果表明:在−0.3 V (vs. Al)的沉积电位下,铝镀层致密均匀,牢固地粘附在基体上;当电沉积在−0.5 V (vs. Al)下时,衬底表面呈现出直径约为367nm的铝纳米线。XRD分析表明,负电位下沉积的铝层具有更明显的(200)择优取向。拉曼光谱分析检测到电沉积前AlCl3-Et3NHCl体系中存在AlCl4−和Al2Cl7−阴离子,然后在恒电位控制下形成Al3Cl10−络合物离子。
期刊介绍:
Ionics is publishing original results in the fields of science and technology of ionic motion. This includes theoretical, experimental and practical work on electrolytes, electrode, ionic/electronic interfaces, ionic transport aspects of corrosion, galvanic cells, e.g. for thermodynamic and kinetic studies, batteries, fuel cells, sensors and electrochromics. Fast solid ionic conductors are presently providing new opportunities in view of several advantages, in addition to conventional liquid electrolytes.