Fe/Li Co-doped CuO: enhanced photosensing and conductivity correlated with structural modifications

IF 2.8 4区 工程技术 Q2 ENGINEERING, ELECTRICAL & ELECTRONIC
Prashant Kumar Mishra, Rachit Dobhal, Somaditya Sen
{"title":"Fe/Li Co-doped CuO: enhanced photosensing and conductivity correlated with structural modifications","authors":"Prashant Kumar Mishra,&nbsp;Rachit Dobhal,&nbsp;Somaditya Sen","doi":"10.1007/s10854-024-13463-x","DOIUrl":null,"url":null,"abstract":"<div><p>The photocatalytic and electronic properties of sol–gel-prepared divalent Fe<sup>3+</sup> and Li<sup>+</sup> co-doped monoclinic (c2/c) Cu<sub>0.945</sub>Fe<sub>0.055-x</sub>Li<sub>x</sub>O powders were investigated. O-ions are in excess in Fe-rich samples, whereas O-vacancies (Vo) are prevalent in Li-rich samples due to the valence state differences between Fe<sup>3+</sup> and Li<sup>+</sup> ions. The bandgap remained largely unaffected, but lattice disorder increased with higher Li content. The electrical conductivity (<i>σ</i>) increased with increasing Li content. While the <i>p</i>-type nature decreased with increasing Li content, the electron mobility decreased with increasing Li content. The photocatalytic decomposition of harmful methylene blue (MB) dye was maximum for Cu<sub>0.945</sub>Fe<sub>0.0275</sub>Li<sub>0.0275</sub>O. For both Cu<sub>0.945</sub>Fe<sub>0.055</sub>O and Cu<sub>0.945</sub>Li<sub>0.055</sub>O, the degradation was lesser due to other physical processes, e.g., changes in the photocurrent. Light detection was faster in Fe-rich samples compared to pure and Li-rich samples. An attempt was made to form a heterojunction of ZnO/Cu<sub>0.945</sub>Fe<sub>0.014</sub>Li<sub>0.041</sub>O that exhibited significantly faster response times than their bulk counterparts for both pure and Li-rich samples. These findings highlight the potential of Cu<sub>0.945</sub>Fe<sub>0.055-x</sub>Li<sub>x</sub>O samples and heterojunction configurations for enhanced photocatalytic and sensing applications.</p></div>","PeriodicalId":646,"journal":{"name":"Journal of Materials Science: Materials in Electronics","volume":null,"pages":null},"PeriodicalIF":2.8000,"publicationDate":"2024-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Materials Science: Materials in Electronics","FirstCategoryId":"5","ListUrlMain":"https://link.springer.com/article/10.1007/s10854-024-13463-x","RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENGINEERING, ELECTRICAL & ELECTRONIC","Score":null,"Total":0}
引用次数: 0

Abstract

The photocatalytic and electronic properties of sol–gel-prepared divalent Fe3+ and Li+ co-doped monoclinic (c2/c) Cu0.945Fe0.055-xLixO powders were investigated. O-ions are in excess in Fe-rich samples, whereas O-vacancies (Vo) are prevalent in Li-rich samples due to the valence state differences between Fe3+ and Li+ ions. The bandgap remained largely unaffected, but lattice disorder increased with higher Li content. The electrical conductivity (σ) increased with increasing Li content. While the p-type nature decreased with increasing Li content, the electron mobility decreased with increasing Li content. The photocatalytic decomposition of harmful methylene blue (MB) dye was maximum for Cu0.945Fe0.0275Li0.0275O. For both Cu0.945Fe0.055O and Cu0.945Li0.055O, the degradation was lesser due to other physical processes, e.g., changes in the photocurrent. Light detection was faster in Fe-rich samples compared to pure and Li-rich samples. An attempt was made to form a heterojunction of ZnO/Cu0.945Fe0.014Li0.041O that exhibited significantly faster response times than their bulk counterparts for both pure and Li-rich samples. These findings highlight the potential of Cu0.945Fe0.055-xLixO samples and heterojunction configurations for enhanced photocatalytic and sensing applications.

Abstract Image

铁/锂共掺杂铜氧化物:增强的光传感和导电性与结构修饰有关
研究了溶胶-凝胶法制备的二价 Fe3+ 和 Li+ 共掺杂单斜(c2/c)Cu0.945Fe0.055-xLixO 粉末的光催化和电子特性。由于 Fe3+ 和 Li+ 离子之间的价态差异,富含铁的样品中 O 离子过剩,而富含锂的样品中则普遍存在 O 空位(Vo)。带隙基本不受影响,但晶格无序度随着锂含量的增加而增加。电导率(σ)随着锂含量的增加而增加。虽然 p 型性质随着锂含量的增加而降低,但电子迁移率却随着锂含量的增加而降低。Cu0.945Fe0.0275Li0.0275O 对有害亚甲基蓝(MB)染料的光催化分解作用最大。对于 Cu0.945Fe0.055O 和 Cu0.945Li0.055O,由于其他物理过程(如光电流变化)的影响,降解程度较低。与纯样品和富锂样品相比,富铁样品的光检测速度更快。在尝试形成 ZnO/Cu0.945Fe0.014Li0.041O 异质结后,纯样品和富锂样品的响应时间都明显快于块状样品。这些发现凸显了 Cu0.945Fe0.055-xLixO 样品和异质结配置在增强光催化和传感应用方面的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Materials Science: Materials in Electronics
Journal of Materials Science: Materials in Electronics 工程技术-材料科学:综合
CiteScore
5.00
自引率
7.10%
发文量
1931
审稿时长
2 months
期刊介绍: The Journal of Materials Science: Materials in Electronics is an established refereed companion to the Journal of Materials Science. It publishes papers on materials and their applications in modern electronics, covering the ground between fundamental science, such as semiconductor physics, and work concerned specifically with applications. It explores the growth and preparation of new materials, as well as their processing, fabrication, bonding and encapsulation, together with the reliability, failure analysis, quality assurance and characterization related to the whole range of applications in electronics. The Journal presents papers in newly developing fields such as low dimensional structures and devices, optoelectronics including III-V compounds, glasses and linear/non-linear crystal materials and lasers, high Tc superconductors, conducting polymers, thick film materials and new contact technologies, as well as the established electronics device and circuit materials.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信