Electrically induced 2D half-metallic antiferromagnets and spin field effect transistors

自旋电子学 凝聚态物理 自旋极化 自旋晶体管 电子 自旋(空气动力学) 反铁磁性 铁磁性 电场 带隙 材料科学 密度泛函理论 物理 自旋霍尔效应 量子力学 热力学
作者
Shijing Gong,Cheng Gong,Yuyun Sun,Wen‐Yi Tong,Chun‐Gang Duan,Junhao Chu,Xiang Zhang
出处
期刊:Proceedings of the National Academy of Sciences of the United States of America [National Academy of Sciences]
卷期号:115 (34): 8511-8516 被引量:256
标识
DOI:10.1073/pnas.1715465115
摘要

Engineering the electronic band structure of material systems enables the unprecedented exploration of new physical properties that are absent in natural or as-synthetic materials. Half metallicity, an intriguing physical property arising from the metallic nature of electrons with singular spin polarization and insulating for oppositely polarized electrons, holds a great potential for a 100% spin-polarized current for high-efficiency spintronics. Conventionally synthesized thin films hardly sustain half metallicity inherited from their 3D counterparts. A fundamental challenge, in systems of reduced dimensions, is the almost inevitable spin-mixed edge or surface states in proximity to the Fermi level. Here, we predict electric field-induced half metallicity in bilayer A-type antiferromagnetic van der Waals crystals (i.e., intralayer ferromagnetism and interlayer antiferromagnetism), by employing density functional theory calculations on vanadium diselenide. Electric fields lift energy levels of the constituent layers in opposite directions, leading to the gradual closure of the gap of singular spin-polarized states and the opening of the gap of the others. We show that a vertical electrical field is a generic and effective way to achieve half metallicity in A-type antiferromagnetic bilayers and realize the spin field effect transistor. The electric field-induced half metallicity represents an appealing route to realize 2D half metals and opens opportunities for nanoscale highly efficient antiferromagnetic spintronics for information processing and storage.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
小马甲的应助被科研通管家采纳,获得30
刚刚
Akim的应助被科研通管家采纳,获得10
刚刚
英俊的铭的应助被科研通管家采纳,获得10
刚刚
上官若男的应助被科研通管家采纳,获得10
刚刚
刚刚
华仔的应助被科研通管家采纳,获得10
刚刚
刚刚
1秒前
1秒前
3秒前
tjc完成签到 ,获得积分10
4秒前
zsj发布了新的文献求助10
4秒前
5秒前
桂柏发布了新的文献求助10
5秒前
Dddd完成签到,获得积分10
6秒前
6秒前
7秒前
jianglei发布了新的文献求助10
9秒前
所所的应助被刻苦的晓槐采纳,获得10
9秒前
rx123完成签到,获得积分10
9秒前
zzz完成签到,获得积分10
11秒前
桐桐的应助被柚子采纳,获得10
11秒前
dddd完成签到 ,获得积分10
11秒前
烟花的应助被了了采纳,获得10
13秒前
徐柯完成签到 ,获得积分10
13秒前
小蘑菇的应助被大宝剑2号采纳,获得10
13秒前
77顺利毕业完成签到,获得积分20
13秒前
魏伯安发布了新的文献求助10
15秒前
17秒前
寒冷的饼干完成签到 ,获得积分10
18秒前
20秒前
20秒前
CipherSage的应助被xixijoy采纳,获得10
21秒前
21秒前
NexusExplorer的应助被伊莎贝拉采纳,获得10
23秒前
Hello的应助被爱迟到的板栗采纳,获得20
24秒前
24秒前
木易学苑发布了新的文献求助30
24秒前
耍酷饼干发布了新的文献求助10
24秒前
夜话风陵杜完成签到 ,获得积分0
26秒前
高分求助中
(应助此贴封号)通过应助OA文献获取积分 10000
Rosenblum, Global Change Biology 800
Computational Chemical Reaction Engineering: Modeling, Simulation, and Design with MATLAB 600
Organizational Behavior 510
Management and the Arts 510
A Will for the Machine: Computerization, Automation, and the Arts in South Africa 400
Decentring Leadership 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 计算机科学 工程类 纳米技术 内科学 物理 有机化学 化学工程 生物化学 复合材料 光电子学 细胞生物学 心理学 量子力学 催化作用 物理化学 电极
热门帖子
关注 科研通微信公众号,转发送积分 7809172
求助须知:如何正确求助?哪些是违规求助? 9341483
关于积分的说明 20506758
捐赠科研通 7401682
什么是DOI,文献DOI怎么找? 3329025
关于科研通互助平台的介绍 2475812
邀请新用户注册赠送积分活动 2347588