Structure, spectral, electrical, and second harmonic generation studies of Fe3+ doped MnS single crystals

Chithrakshi Prathap, Aashis S. Roy, Raghavendra Sagar
{"title":"Structure, spectral, electrical, and second harmonic generation studies of Fe3+ doped MnS single crystals","authors":"Chithrakshi Prathap, Aashis S. Roy, Raghavendra Sagar","doi":"10.1080/23312009.2016.1269599","DOIUrl":null,"url":null,"abstract":"Abstract In this present work, we report the growth, optical, and electrical studies of inorganic single crystals of manganese sulfate and FeCl3-doped manganese sulfate grown by slow evaporation technique. Crystal structure and lattice parameters of the grown crystals were determined using powder X-ray diffraction and the studies confirm the formation of orthorhombic structure. The UV–vis spectroscopic measurement illustrates the grown crystals with good optical transparency in the visible region and less absorbance. Optical constants such as the band gap, refractive index, extinction coefficient, optical and electrical conductance reveals the good optical response of the material. The Fourier transform infrared spectroscopic analysis infers that there is a small change in the peak position and transmittance in the case of MnS:Fe3+ crystal which ensures the incorporation of Fe3+ ion to the host crystal. Second harmonic generation efficiency tested by Kurtz and Perry method showed the improvement in relative conversion efficiency compared with potassium dihydrogen phosphate.","PeriodicalId":10640,"journal":{"name":"Cogent Chemistry","volume":"2 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2016-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/23312009.2016.1269599","citationCount":"5","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cogent Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/23312009.2016.1269599","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5

Abstract

Abstract In this present work, we report the growth, optical, and electrical studies of inorganic single crystals of manganese sulfate and FeCl3-doped manganese sulfate grown by slow evaporation technique. Crystal structure and lattice parameters of the grown crystals were determined using powder X-ray diffraction and the studies confirm the formation of orthorhombic structure. The UV–vis spectroscopic measurement illustrates the grown crystals with good optical transparency in the visible region and less absorbance. Optical constants such as the band gap, refractive index, extinction coefficient, optical and electrical conductance reveals the good optical response of the material. The Fourier transform infrared spectroscopic analysis infers that there is a small change in the peak position and transmittance in the case of MnS:Fe3+ crystal which ensures the incorporation of Fe3+ ion to the host crystal. Second harmonic generation efficiency tested by Kurtz and Perry method showed the improvement in relative conversion efficiency compared with potassium dihydrogen phosphate.
Fe3+掺杂MnS单晶的结构、光谱、电学和二次谐波生成研究
摘要在本研究中,我们报道了用慢蒸发技术生长硫酸锰和fecl3掺杂硫酸锰的无机单晶的生长、光学和电学研究。用粉末x射线衍射测定了生长晶体的晶体结构和晶格参数,证实了其形成正交结构。紫外-可见光谱测量表明,生长的晶体在可见光区具有良好的光学透明度和较低的吸光度。光学常数如带隙、折射率、消光系数、光导和电导等揭示了材料良好的光学响应。傅里叶变换红外光谱分析表明,MnS:Fe3+晶体的峰值位置和透射率变化不大,这保证了Fe3+离子与基体晶体的结合。Kurtz和Perry法测试的二次谐波产生效率表明,与磷酸二氢钾相比,其相对转化效率有所提高。
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
Cogent Chemistry
Cogent Chemistry CHEMISTRY, MULTIDISCIPLINARY-
自引率
0.00%
发文量
0
×
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