Physical chemistry of the TiN/Hf0.5Zr0.5O2 interface

退火(玻璃) X射线光电子能谱 铁电性 肖特基势垒 空位缺陷 兴奋剂 电极 材料科学 化学 纳米技术 光电子学 物理化学 冶金 结晶学 化学工程 复合材料 电介质 二极管 工程类
作者
Wassim Hamouda,A. Pancotti,C. Lubin,Ludovic Tortech,Claudia Richter,Thomas Mikolajick,Uwe Schroeder,N. Barrett
出处
期刊:Journal of Applied Physics [American Institute of Physics]
卷期号:127 (6) 被引量:162
标识
DOI:10.1063/1.5128502
摘要

Ferroelectric hafnia-based thin films are promising candidates for emerging high-density embedded nonvolatile memory technologies, thanks to their compatibility with silicon technology and the possibility of 3D integration. The electrode–ferroelectric interface and the crystallization annealing temperature may play an important role in such memory cells. The top interface in a TiN/Hf0.5Zr0.5O2/TiN metal–ferroelectric–metal stack annealed at different temperatures was investigated with X-ray photoelectron spectroscopy. The uniformity and continuity of the 2 nm TiN top electrode was verified by photoemission electron microscopy and conductive atomic force microscopy. Partial oxidation of the electrode at the interface is identified. Hf is reduced near the top interface due to oxygen scavenging by the top electrode. The oxygen vacancy (VO) profile showed a maximum at the top interface (0.71%) and a sharp decrease into the film, giving rise to an internal field. Annealing at higher temperatures did not affect the VO concentration at the top interface but causes the generation of additional VO in the film, leading to a decrease of the Schottky Barrier Height for electrons. The interface chemistry and n-type film doping are believed to be at the origin of several phenomena, including wake-up, imprint, and fatigue. Our results give insights into the physical chemistry of the top interface with the accumulation of defective charges acting as electronic traps, causing a local imprint effect. This may explain the wake-up behavior as well and also can be a possible reason of the weaker endurance observed in these systems when increasing the annealing temperature.
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
Eeee发布了新的文献求助10
1秒前
2秒前
li完成签到 ,获得积分10
3秒前
乐乐乐发布了新的文献求助10
6秒前
Orange应助Eeee采纳,获得10
6秒前
轻松的万天完成签到 ,获得积分10
8秒前
8秒前
天天快乐应助David采纳,获得10
11秒前
了晨发布了新的文献求助10
11秒前
无极微光应助puhong zhang采纳,获得20
12秒前
bkagyin应助小费采纳,获得20
12秒前
科研通AI6.4应助小费采纳,获得20
12秒前
科研通AI6.1应助小费采纳,获得20
12秒前
13秒前
贪玩的秋柔应助阿方采纳,获得10
14秒前
艾辉完成签到,获得积分10
15秒前
康宁应助ww采纳,获得10
15秒前
YangZhang完成签到,获得积分20
18秒前
英俊的铭应助CLK123456采纳,获得10
18秒前
善学以致用应助彦成采纳,获得10
18秒前
lvdou发布了新的文献求助10
19秒前
19秒前
烟花应助xwlXWL采纳,获得10
19秒前
20秒前
21秒前
蓝天发布了新的文献求助10
23秒前
24秒前
25秒前
淡定的太清完成签到,获得积分10
27秒前
jeonghan完成签到 ,获得积分10
28秒前
David发布了新的文献求助10
28秒前
Leo发布了新的文献求助10
28秒前
puhong zhang完成签到,获得积分10
28秒前
痛米完成签到 ,获得积分10
31秒前
32秒前
whm应助xiaolizi采纳,获得30
32秒前
32秒前
puhong zhang发布了新的文献求助20
32秒前
球球尧伞耳完成签到,获得积分10
33秒前
乐乐乐完成签到 ,获得积分10
36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
PowerCascade: A Synthetic Dataset for Cascading Failure Analysis in Power Systems 2000
Picture this! Including first nations fiction picture books in school library collections 1000
Signals, Systems, and Signal Processing 610
Unlocking Chemical Thinking: Reimagining Chemistry Teaching and Learning 555
Photodetectors: From Ultraviolet to Infrared 500
信任代码:AI 时代的传播重构 450
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 6357450
求助须知:如何正确求助?哪些是违规求助? 8172117
关于积分的说明 17206929
捐赠科研通 5413121
什么是DOI,文献DOI怎么找? 2864930
邀请新用户注册赠送积分活动 1842401
关于科研通互助平台的介绍 1690526