{"title":"Nanocarbon-assisted chemical etching of Ge(100) in H2O2","authors":"Junhuan Li, Seiya Yamamoto, Kouji Inagaki, Kenta Arima","doi":"10.1016/j.elecom.2024.107735","DOIUrl":null,"url":null,"abstract":"<div><p>We utilized graphene oxide (GO) flakes as a starting material to conduct nanocarbon (NC)-assisted chemical etching of Ge(1<!--> <!-->0<!--> <!-->0) surfaces in H<sub>2</sub>O<sub>2</sub> solutions. Upon initial etching in H<sub>2</sub>O<sub>2</sub>, a pitted morphology formed beneath the loaded nanocarbon. The etch pits exhibited a tendency to expand, with edges assuming square-like shapes in H<sub>2</sub>O<sub>2</sub> solutions. This phenomenon is reminiscent of an inverted pyramidal structure observed during enhanced etching of a Ge surface loaded with metallic particles, exposing (1<!--> <!-->1<!--> <!-->1) microfacets. As the etching progressed, noticeable lateral etching occurred on the Ge surface. Consequently, the small pits merged to form larger hollows, potentially exceeding the size of the initial GO flake. These etching properties were analyzed based on electrochemical reactions there, or the injection of holes created by the enhanced reduction of H<sub>2</sub>O<sub>2</sub> molecules on nanocarbons, which were compared to those observed when using O<sub>2</sub>-dissolved water as an etchant. Additionally, we provide guidelines for achieving more homogeneous and deeper etch structures using a loaded nanocarbon catalyst in H<sub>2</sub>O<sub>2</sub>.</p></div>","PeriodicalId":304,"journal":{"name":"Electrochemistry Communications","volume":"163 ","pages":"Article 107735"},"PeriodicalIF":4.7000,"publicationDate":"2024-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S138824812400078X/pdfft?md5=f80b8d5dfda141a399ad1e76350de614&pid=1-s2.0-S138824812400078X-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Electrochemistry Communications","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S138824812400078X","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
引用次数: 0
Abstract
We utilized graphene oxide (GO) flakes as a starting material to conduct nanocarbon (NC)-assisted chemical etching of Ge(1 0 0) surfaces in H2O2 solutions. Upon initial etching in H2O2, a pitted morphology formed beneath the loaded nanocarbon. The etch pits exhibited a tendency to expand, with edges assuming square-like shapes in H2O2 solutions. This phenomenon is reminiscent of an inverted pyramidal structure observed during enhanced etching of a Ge surface loaded with metallic particles, exposing (1 1 1) microfacets. As the etching progressed, noticeable lateral etching occurred on the Ge surface. Consequently, the small pits merged to form larger hollows, potentially exceeding the size of the initial GO flake. These etching properties were analyzed based on electrochemical reactions there, or the injection of holes created by the enhanced reduction of H2O2 molecules on nanocarbons, which were compared to those observed when using O2-dissolved water as an etchant. Additionally, we provide guidelines for achieving more homogeneous and deeper etch structures using a loaded nanocarbon catalyst in H2O2.
期刊介绍:
Electrochemistry Communications is an open access journal providing fast dissemination of short communications, full communications and mini reviews covering the whole field of electrochemistry which merit urgent publication. Short communications are limited to a maximum of 20,000 characters (including spaces) while full communications and mini reviews are limited to 25,000 characters (including spaces). Supplementary information is permitted for full communications and mini reviews but not for short communications. We aim to be the fastest journal in electrochemistry for these types of papers.