Performance and stability improvement of CVD monolayer MoS2 transistors through HfO2 dielectrics engineering

钝化 材料科学 光电子学 电介质 单层 原子层沉积 栅极电介质 电子迁移率 晶体管 阈值电压 二硫化钼 图层(电子) 纳米技术 电压 电气工程 复合材料 工程类
作者
Chunhui Huang,Zeyi Yan,Chengwei Hu,Xiong Xiong,Yanqing Wu
出处
期刊:Applied Physics Letters [American Institute of Physics]
卷期号:123 (7) 被引量:10
标识
DOI:10.1063/5.0157416
摘要

Monolayer molybdenum disulfide (MoS2) is a promising semiconductor channel material for future electronics due to its atomic thickness and high mobility. However, conventional back-gate MoS2 transistors suffer from substantial scattering caused by substrate and surface adsorbates, which impair carrier mobility and device reliability. In this work, we demonstrate an exemplary dielectric engineering approach that uses atomic-layer-deposited hafnium oxide (HfO2) as the gate dielectric and channel passivation layer to improve device performance and positive bias instability. The large-single-crystal monolayer MoS2 film was directly synthesized on SiO2/Si substrates by a low-pressure chemical vapor deposition method. MoS2 transistors with various dielectrics were fabricated and characterized for a fair comparison. The mobility increased from 4.2 to 19.9 cm2/V·s by suppressing charged impurities and phonon scattering when transferring the MoS2 channel from 100 nm SiO2 substrates to 20 nm HfO2 substrates. Passivation of another 10 nm HfO2 on the back-gate transistors further increased the mobility to 36.4 cm2/V·s with a high drive current of 107 μA/μm. Moreover, the threshold voltage shift of the passivated transistor was reduced by about 58% from 1.9 to 0.8 V under positive bias stress. This is due to the fact that channel passivation with HfO2 effectively eliminated charge trapping of adsorbed substances. These results reveal that HfO2 gate dielectric and passivation by atomic-layer deposition are effective methods to improve the performance and stability of MoS2 devices.
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
当归完成签到,获得积分10
刚刚
wuffff完成签到 ,获得积分10
刚刚
Jasper应助孙越采纳,获得10
刚刚
大聪明完成签到 ,获得积分10
刚刚
1秒前
cs完成签到,获得积分10
1秒前
akete发布了新的文献求助10
1秒前
Li_wang完成签到,获得积分10
1秒前
1秒前
Cherry完成签到,获得积分10
1秒前
eagle发布了新的文献求助10
1秒前
mm完成签到,获得积分10
1秒前
海贵完成签到,获得积分10
2秒前
3秒前
小明同学完成签到,获得积分10
3秒前
arniu2008发布了新的文献求助10
3秒前
温暖的行走完成签到,获得积分10
3秒前
3秒前
DW应助爱撒娇的天磊采纳,获得10
3秒前
3秒前
4秒前
CCH完成签到,获得积分10
4秒前
CodeCraft应助1AN采纳,获得10
4秒前
4秒前
罗嘉尔完成签到,获得积分10
4秒前
充电宝应助Manxi采纳,获得10
5秒前
5秒前
123完成签到,获得积分20
5秒前
Linda完成签到 ,获得积分10
6秒前
半山青黄完成签到,获得积分10
6秒前
可爱半山发布了新的文献求助10
6秒前
小小应助coolru采纳,获得100
6秒前
陌上发布了新的文献求助30
7秒前
CipherSage应助温柔宛采纳,获得10
7秒前
7秒前
WW关注了科研通微信公众号
7秒前
情怀应助王大伟2023采纳,获得10
7秒前
大模型应助王大伟2023采纳,获得10
8秒前
8秒前
我是老大应助王大伟2023采纳,获得10
8秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
HYDROLYSE ACIDE DE QUELQUES DIOXASPIROCYCLANES 1000
Navigating Normative Orders. Interdisciplinary Perspectives 800
1 Peter and Christ's Descent to the Dead in Its Early Christian Reception 700
Essentials of Carbohydrate Chemistry and Biochemistry, 4th Edition 600
Organizational Behavior 510
Management and the Arts 510
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7741413
求助须知:如何正确求助?哪些是违规求助? 9290023
关于积分的说明 20198572
捐赠科研通 7319745
什么是DOI,文献DOI怎么找? 3306727
关于科研通互助平台的介绍 2458937
邀请新用户注册赠送积分活动 2317134