Exploring the growth and oxidation of 2D-TaS2 on Cu(111).

材料科学 扫描隧道显微镜 化学工程 X射线光电子能谱 结晶学 化学物理 氧化物 单层 过渡金属 外延
作者
Afjal Khan Pathan,Aakash Gupta,Mihai E. Vaida
出处
期刊:Nanotechnology [IOP Publishing]
卷期号:32 (50): 505605-
标识
DOI:10.1088/1361-6528/ac244e
摘要

In this work, the growth and stability towards O2 exposure of two dimensional (2D) TaS2 on a Cu(111) substrate is investigated. Large area (~1cm2) crystalline 2D-TaS2 films with a metallic character are prepared on a single crystal Cu(111) substrate via a multistep approach based on physical vapor deposition. Analytical techniques such as Auger electron spectroscopy, low energy electron diffraction, and photoemission spectroscopy are used to characterize the composition, crystallinity, and electronic structure of the surface. At coverages below one monolayer equivalent (ML), misoriented TaS2 domains are formed, which are rotated up to ±13^o relative to the Cu(111) crystallographic directions. The TaS2 domains misorientation decreases as the film thickness approaches 1 ML, at which the crystallographic directions of TaS2 and Cu(111) are aligned. The TaS2 film is found to grow epitaxially on Cu(111). As revealed by low energy electron diffraction in conjunction with an atomic model simulation, the (3 × 3) unit cells of TaS2 match the (4 × 4) supercell of Cu(111). Furthermore, the exposure of TaS2 to O2, does not lead to the formation of a robust tantalum oxide film, only minor amounts of stable oxides being detected on the surface. Instead, the exposure of TaS2 films to O2 leads predominantly to a reduction of the film thickness, evidenced by a decrease in the content of both Ta and S atoms of the film. This is attributed to the formation of oxide species that are unstable and mainly desorb from the surface below room temperature. Temperature programmed desorption spectroscopy confirms the formation of SO2, which desorbs form the surface between 100 K and 500 K. These results provide new insights into the oxidative degradation of 2D-TaS2 on Cu(111).

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
kelaier发布了新的文献求助10
刚刚
NexusExplorer应助jiajia采纳,获得10
2秒前
sunny完成签到,获得积分10
3秒前
阿蒙蒙完成签到 ,获得积分10
6秒前
顾年完成签到,获得积分10
6秒前
9秒前
顾矜应助qiu采纳,获得10
9秒前
PP关闭了PP文献求助
10秒前
小王完成签到,获得积分10
11秒前
11秒前
赘婿应助csx采纳,获得10
11秒前
可乐完成签到,获得积分10
12秒前
377发布了新的文献求助10
12秒前
14秒前
14秒前
Lucas应助科研通管家采纳,获得10
15秒前
Hello应助科研通管家采纳,获得10
15秒前
上官若男应助科研通管家采纳,获得10
16秒前
思源应助汪哈七采纳,获得10
16秒前
Owen应助科研通管家采纳,获得10
16秒前
所所应助科研通管家采纳,获得10
16秒前
17秒前
浮游应助科研通管家采纳,获得10
17秒前
小蘑菇应助科研通管家采纳,获得10
17秒前
星辰大海应助科研通管家采纳,获得10
17秒前
17秒前
17秒前
molihuakai应助科研通管家采纳,获得30
18秒前
18秒前
领导范儿应助科研通管家采纳,获得10
18秒前
充电宝应助12121采纳,获得10
19秒前
jiajia发布了新的文献求助10
19秒前
19秒前
21秒前
核桃发布了新的文献求助100
23秒前
王清水发布了新的文献求助10
23秒前
iitj应助纯真冷安采纳,获得10
24秒前
kelaier发布了新的文献求助10
25秒前
26秒前
星晴完成签到,获得积分10
27秒前
高分求助中
液晶指向矢仿真分析数据集 8888
Invited Discussant 63O and 64O 1000
Dr. Dirk Wiechmann on Lingual Orthodontics: Part I 888
Ideology and Meaning-Making under the Putin Regime 750
化工技术经济第五版电子版 500
Petrology and Plate Tectonics 500
Writing Systems 500
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 计算机科学 化学工程 生物化学 物理 内科学 复合材料 催化作用 光电子学 物理化学 电极 细胞生物学 基因 遗传学
热门帖子
关注 科研通微信公众号,转发送积分 6879704
求助须知:如何正确求助?哪些是违规求助? 8579632
关于积分的说明 18229159
捐赠科研通 6262045
什么是DOI,文献DOI怎么找? 3054751
关于科研通互助平台的介绍 2064564
邀请新用户注册赠送积分活动 2032443