Structure, Electron Density Distribution using Maximum Entropy Method, Optical and Magnetic Characteristics of Fe Doped SnS2

Author:

Pavithra Nagarathinam1,Robert Muthanain Charles1ORCID

Affiliation:

1. PG and Research Department of Physics HKRH College Uthamapalayam, Affiliated to Madurai Kamaraj University, Madurai Theni Tamil Nadu 625533 India

Abstract

AbstractTwo dimensional layered magnetic materials like Fe‐doped SnS2 are cheap, abundant, and biocompatible, used for spintronics applications. The hydrothermal synthesized hexagonal nano disc structure of the sample is seen in the SEM images at room temperature. Pure SnS2, which is diamagnetic with magnetization 0.02067 emu/g becomes soft ferromagnetic by 2.5 % Fe doping with 0.672 emug−1 saturation magnetization and 0.222 kOe coercivity. A ultraviolet‐visible spectrometer measurement of the energy bandgap reveals a drop in energy from 2.35 to 2.2 eV, and the PL spectrum displays intense blue emission at a wavelength of 482–484 nm. Maximum entropy method (MEM), confirmed the ionic to covalent conversion upon Fe doping, due to the residual charge accumulation at the intermediate regions. The electron densities in Fe doped system in the plane (023) at Bond Critical Point of Sn─S and S─S are 0.327 and 0.354 e Å−3, respectively, with negative total energy density values confirming covalent bonding. A high electron density of 0.856 e Å−3 at the Sn─Sn region confirms interstitial charge accumulation. This introduces new intermediate energy levels in the forbidden region, reducing the energy bandgap and making the substance more semiconducting, making it useful for optical, opto‐electronic, and half‐metal applications.

Publisher

Wiley

Subject

Condensed Matter Physics,General Materials Science,General Chemistry

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3