{"title":"Chemical Pressure-Induced enhancement of electrochemical performance in Ni1-X CuxTe2 (X = 0 and 0.10) layered compounds","authors":"Rajkumar Sokkalingam , Manikandan Krishnan , Jesman Sthevan Kovil Pitchai , Sivakumar Periyasamy , Arjun Kumar Bojarajan , Arumugam Sonachalam , Sambasivam Sangaraju","doi":"10.1016/j.elecom.2025.107872","DOIUrl":null,"url":null,"abstract":"<div><div>This article employed the self-flux technique to successfully generate single crystalline Ni<sub>1-X</sub>Cu<sub>X</sub>Te<sub>2</sub> (X = 0 and 0.10) for electrochemical applications. The X-ray powder diffraction (XRPD) patterns revealed that both compounds have a CdI<sub>2</sub>-type trigonal structure with a <em>P</em>3<em>m</em>1 space group. The field emission scanning electron microscope (FESEM) images depicted the layered structure of these compounds. The elemental composition was analyzed via X-ray photoelectron spectroscopy (XPS). The electrochemical measuring results demonstrated that the Ni<sub>1-X</sub>Cu<sub>X</sub>Te<sub>2</sub> (X = 0 and 0.10) composite electrodes exhibit improved electrocatalytic activity, with 360 and 544 F/g capacitances, respectively. This enhancement in electrochemical performance is attributed to the addition of Cu doping and the presence of many flaws. Furthermore, Ni<sub>1-X</sub>Cu<sub>X</sub>Te<sub>2</sub> (X = 0 and 0.10) electrodes exhibited high electrochemical stability in supercapacitors (SCs). These findings suggest that the Ni<sub>1-X</sub>Cu<sub>X</sub>Te<sub>2</sub> (X = 0 and 0.10) compounds are promising candidates for SCs with increased capacitance and stability. The combination of structural properties, Cu doping, and defect-induced enhancement led to better electrochemical performance.</div></div>","PeriodicalId":304,"journal":{"name":"Electrochemistry Communications","volume":"171 ","pages":"Article 107872"},"PeriodicalIF":4.7000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Electrochemistry Communications","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1388248125000116","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
This article employed the self-flux technique to successfully generate single crystalline Ni1-XCuXTe2 (X = 0 and 0.10) for electrochemical applications. The X-ray powder diffraction (XRPD) patterns revealed that both compounds have a CdI2-type trigonal structure with a P3m1 space group. The field emission scanning electron microscope (FESEM) images depicted the layered structure of these compounds. The elemental composition was analyzed via X-ray photoelectron spectroscopy (XPS). The electrochemical measuring results demonstrated that the Ni1-XCuXTe2 (X = 0 and 0.10) composite electrodes exhibit improved electrocatalytic activity, with 360 and 544 F/g capacitances, respectively. This enhancement in electrochemical performance is attributed to the addition of Cu doping and the presence of many flaws. Furthermore, Ni1-XCuXTe2 (X = 0 and 0.10) electrodes exhibited high electrochemical stability in supercapacitors (SCs). These findings suggest that the Ni1-XCuXTe2 (X = 0 and 0.10) compounds are promising candidates for SCs with increased capacitance and stability. The combination of structural properties, Cu doping, and defect-induced enhancement led to better electrochemical performance.
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.