{"title":"Electrochemical growth process of Zn-Co alloys with different crystalline structures","authors":"Vinícius X. Siqueira, Raul G.G. Souza, Edivaldo dos Santos Filho, Manoel J.M. Pires","doi":"10.1016/j.electacta.2025.145783","DOIUrl":null,"url":null,"abstract":"<div><div>This work presents a study of the nucleation and growth of Zn-Co films produced by electrochemical deposition on Cu substrates. Using potentiostatic deposition at –1.4 V (vs. Ag/AgCl), both crystalline and amorphous structures were obtained by controlling the metallic ions concentrations in the electrolyte. The deposits are crystalline when Zn ions are predominant in the solution and tend to be amorphous when Co ions are in the far majority in the solutions. The process can be classified as anomalous deposition, and it is deeply affected by the initial number of electroactive sites for nucleation, which is much larger for Zn than Co. The electrodeposition has been analyzed with both static and rotating disk electrodes. The models of Scharifker-Hills and Koutechký-Levich were used in the analysis for current-time transients, and current versus the electrode rotating velocity, respectively. The results permit the inference of multi-step mechanisms for the reduction and deposition of the ions. An alternative approach with two Scharifker-Hills curves for the current-time transients is presented. Furthermore, images from scanning electron microscopy and samples composition were evaluated throughout the deposition process.</div></div>","PeriodicalId":305,"journal":{"name":"Electrochimica Acta","volume":"518 ","pages":"Article 145783"},"PeriodicalIF":5.6000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Electrochimica Acta","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S001346862500146X","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/3 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
引用次数: 0
Abstract
This work presents a study of the nucleation and growth of Zn-Co films produced by electrochemical deposition on Cu substrates. Using potentiostatic deposition at –1.4 V (vs. Ag/AgCl), both crystalline and amorphous structures were obtained by controlling the metallic ions concentrations in the electrolyte. The deposits are crystalline when Zn ions are predominant in the solution and tend to be amorphous when Co ions are in the far majority in the solutions. The process can be classified as anomalous deposition, and it is deeply affected by the initial number of electroactive sites for nucleation, which is much larger for Zn than Co. The electrodeposition has been analyzed with both static and rotating disk electrodes. The models of Scharifker-Hills and Koutechký-Levich were used in the analysis for current-time transients, and current versus the electrode rotating velocity, respectively. The results permit the inference of multi-step mechanisms for the reduction and deposition of the ions. An alternative approach with two Scharifker-Hills curves for the current-time transients is presented. Furthermore, images from scanning electron microscopy and samples composition were evaluated throughout the deposition process.
本文研究了电化学沉积在Cu衬底上制备的Zn-Co薄膜的成核和生长。在-1.4 V (vs. Ag/AgCl)下进行恒电位沉积,通过控制电解液中金属离子的浓度,获得了结晶和非晶结构。当锌离子在溶液中占主导地位时,镀层呈结晶状;当Co离子在溶液中占绝大多数时,镀层呈无定形。该过程可归类为异常沉积,其受成核初始电活性位点数量的影响很大,其中Zn的初始电活性位点数量远大于Co的初始电活性位点数量。Scharifker-Hills模型和Koutechký-Levich模型分别用于分析电流-时间瞬态和电流与电极转速的关系。结果允许对离子还原和沉积的多步骤机制进行推断。提出了一种用两条沙里夫克-希尔斯曲线求解电流-时间瞬态的替代方法。此外,在整个沉积过程中,对扫描电子显微镜图像和样品成分进行了评估。
期刊介绍:
Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.