Jinmyeong Seo , Jungjoon Park , Haneul Han , Soojin Kim , Soobin Park , Sanghwa Yoon , Bongyoung Yoo
{"title":"Electrochemical pathway-controlled growth of tellurium nanostructures on a nonconductive substrate","authors":"Jinmyeong Seo , Jungjoon Park , Haneul Han , Soojin Kim , Soobin Park , Sanghwa Yoon , Bongyoung Yoo","doi":"10.1016/j.electacta.2025.147390","DOIUrl":null,"url":null,"abstract":"<div><div>This study demonstrates that the morphology and spatial distribution of tellurium (Te) nanostructures can be precisely controlled on electrically insulating substrates (SiO₂) by systematically tuning the electrochemical reaction pathway of HTeO<sub>2</sub><sup>+</sup>. By varying only two key parameters, the precursor concentration and applied potential, the relative contribution of each step, including the overpotential deposition, H<sub>2</sub>Te formation, and chemical reduction, was modulated. This enabled the fabrication of diverse nanostructures, including nano-dots, nano-rods, and feather-like morphologies, under different electrochemical conditions. Notably, Te formation was achieved solely via the chemical pathway on insulating SiO₂ without the need for external electron transport, providing the first unambiguous experimental validation of EC-driven formation and growth on electrically insulating substrate. This strategy successfully circumvents the limitations of conventional electroplating techniques, which are generally restricted to conductive substrates, and offers a template-free platform for the site- and shape-selective growth of Te nanostructures. These findings present a promising route toward applications in Te-based sensors, thermoelectric devices, and bio-functional nanomaterials.</div></div>","PeriodicalId":305,"journal":{"name":"Electrochimica Acta","volume":"541 ","pages":"Article 147390"},"PeriodicalIF":5.6000,"publicationDate":"2025-09-15","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/S0013468625017475","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
引用次数: 0
Abstract
This study demonstrates that the morphology and spatial distribution of tellurium (Te) nanostructures can be precisely controlled on electrically insulating substrates (SiO₂) by systematically tuning the electrochemical reaction pathway of HTeO2+. By varying only two key parameters, the precursor concentration and applied potential, the relative contribution of each step, including the overpotential deposition, H2Te formation, and chemical reduction, was modulated. This enabled the fabrication of diverse nanostructures, including nano-dots, nano-rods, and feather-like morphologies, under different electrochemical conditions. Notably, Te formation was achieved solely via the chemical pathway on insulating SiO₂ without the need for external electron transport, providing the first unambiguous experimental validation of EC-driven formation and growth on electrically insulating substrate. This strategy successfully circumvents the limitations of conventional electroplating techniques, which are generally restricted to conductive substrates, and offers a template-free platform for the site- and shape-selective growth of Te nanostructures. These findings present a promising route toward applications in Te-based sensors, thermoelectric devices, and bio-functional nanomaterials.
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.