Controllable memory window in two-dimensional hybrid van der Waals heterostructured devices

范德瓦尔斯力 异质结 材料科学 磁滞 二硫化钼 非易失性存储器 光电子学 神经形态工程学 纳米技术 带隙 凝聚态物理 化学物理 物理 计算机科学 化学 分子 机器学习 人工神经网络 有机化学 冶金
作者
Huijuan Zhao,Jingxuan Ma,Shuhan Li,Yang Yang,Zhangxia Wang,Zhongzhong Luo,Xiaohan Guo,Bing Wei Luo,Li Zhu,Lianhui Wang,Li Gao
出处
期刊:Applied Physics Letters [American Institute of Physics]
卷期号:124 (17) 被引量:3
标识
DOI:10.1063/5.0187299
摘要

Van der Waals (vdW) heterostructures based on inorganic layered materials have been demonstrated as potential candidates for a variety of electronic applications due to their flexibility in energy band engineering. However, the presence of unstable charge-trapping states in atomically thin two-dimensional (2D) materials may limit the performance of devices. Here, we aim to conduct a systematic investigation on hybrid heterostructured memory devices that consist of 2D layered organic and inorganic materials. The objective is to explore the potential of these devices in offering efficient charge-trapping states. Molybdenum disulfide (MoS2) is employed as a channel, while N, N′-Dimethyl-3,4,9,10-perylenedicarboximide (Me-PTCDI) serves as the charge-trapping layer to store charges from MoS2. The hysteresis window of these heterostructured devices can be effectively modified within a range of 13–70 V by manipulating both the thickness of the organic layer and the gate voltages. The largest hysteresis window is found in a combination of a few-layer Me-PTCDI (12.6 nm) and MoS2 (6 nm), showing a high on/off current ratio (>104) and a long retention time (104 s). Furthermore, the endurance test, which lasts for over 1000 cycles, demonstrates an exceptional level of stability and reliability. In addition, multilevel memory effects can be observed when gate pulses with different widths and amplitudes are applied. These 2D hybrid heterostructured devices have the capability to broaden the scope of material systems and present substantial potential for functional neuromorphic applications.
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
iNk应助chen采纳,获得10
刚刚
酷波er应助chen采纳,获得10
刚刚
1秒前
wyblobin发布了新的文献求助10
1秒前
彭于晏应助李锐采纳,获得10
1秒前
希望天下0贩的0应助StoneT采纳,获得10
1秒前
vv发布了新的文献求助10
2秒前
2秒前
zx完成签到,获得积分10
2秒前
3秒前
3秒前
Hello应助武丝丝采纳,获得10
3秒前
刘欢发布了新的文献求助30
3秒前
雪花飞发布了新的文献求助10
4秒前
小土狗完成签到,获得积分10
4秒前
4秒前
香蕉乐荷完成签到,获得积分10
5秒前
Yang发布了新的文献求助10
5秒前
星辰大海应助Levi采纳,获得10
5秒前
繁木发布了新的文献求助20
5秒前
5秒前
向阳花开完成签到 ,获得积分10
6秒前
搞怪藏今完成签到,获得积分10
6秒前
6秒前
6秒前
6秒前
科目三应助时光机带哥走采纳,获得10
6秒前
6秒前
6秒前
6秒前
6秒前
6秒前
6秒前
7秒前
哇咔咔完成签到,获得积分20
7秒前
8秒前
Ava应助zhengbiaoying采纳,获得10
8秒前
苗条的语海完成签到,获得积分10
8秒前
8秒前
StoneT完成签到,获得积分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
晶种分解过程与铝酸钠溶液混合强度关系的探讨 8888
Les Mantodea de Guyane Insecta, Polyneoptera 2000
Chemistry and Physics of Carbon Volume 18 800
The Organometallic Chemistry of the Transition Metals 800
Leading Academic-Practice Partnerships in Nursing and Healthcare: A Paradigm for Change 800
Signals, Systems, and Signal Processing 610
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 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6422508
求助须知:如何正确求助?哪些是违规求助? 8241324
关于积分的说明 17517690
捐赠科研通 5476557
什么是DOI,文献DOI怎么找? 2892890
邀请新用户注册赠送积分活动 1869344
关于科研通互助平台的介绍 1706751