中文版 | English
题名

Nonlinear electronic and ultrafast optical signatures in chemical vapor-deposited ultrathin PtS2 ribbons

作者
通讯作者Jiang,Shaolong; Su,Fuhai; Zhang,Yanfeng; Lin,Junhao
共同第一作者Yang,Jin
发表日期
2022-02-24
DOI
发表期刊
ISSN
1998-0124
EISSN
1998-0000
卷号15页码:4366-4373
摘要

The emerging two-dimensional (2D) platinum disulfide (PtS) has driven increasing attentions due to its high electron mobility, good air-stability, and strong interlayer interaction which leads to a widely tunable electronic structure. However, a detailed study on its covalent-like layer-dependent properties remains infant. Herein, we demonstrate the successful production of ultrathin 1T-PtS ribbons with thickness centralized almost at monolayer 1L–4L and large domain size up to 210 µm on Au foils using chemical vapor deposition (CVD) technique, which enables macro- and microscopic study of its extraordinary layer-dependent features with precise control of the number of layers. Using electron energy loss spectroscopy (EELS) and optical pump-probe spectroscopy (OPPS), we reveal that both the electron and ultrafast optical absorption signals of the as-grown 2D PtS show strong nonlinear layer-dependent responses which manifest discriminated transition in 1L–4L PtS ribbons. The layer-dependent nonlinear response of 2D PtS can be well interpreted in the frame of calculated electron and phonon structures. These achievements offer a platform for successfully fabricating large-sized ultrathin 2D PtS and facilitating our knowledge about its electronic and optoelectronic properties.[Figure not available: see fulltext.]

关键词
相关链接[Scopus记录]
收录类别
SCI ; EI
语种
英语
学校署名
第一 ; 通讯
WOS记录号
WOS:000760740600005
EI入藏号
20220911708875
EI主题词
Chemical Vapor Deposition ; Electron Energy Loss Spectroscopy ; Electron Scattering ; Electronic Structure ; Electrons ; Energy Dissipation ; Light Absorption ; Nonlinear Optics ; Optical Pumping ; Platinum Compounds ; Probes
EI分类号
Energy Losses (Industrial And Residential):525.4 ; Light/Optics:741.1 ; Nonlinear Optics:741.1.1 ; Chemical Reactions:802.2
Scopus记录号
2-s2.0-85125132385
来源库
Scopus
引用统计
被引频次[WOS]:6
成果类型期刊论文
条目标识符http://sustech.caswiz.com/handle/2SGJ60CL/327890
专题理学院_物理系
量子科学与工程研究院
作者单位
1.Shenzhen Key Laboratory of Advanced Quantum Functional Materials and Devices and Department of Physics,Southern University of Science and Technology,Shenzhen,518055,China
2.Key Laboratory of Materials Physics,Institute of Solid State Physics,HFIPS,Chinese Academy of Sciences,Hefei,230031,China
3.University of Science and Technology of China,Hefei,230026,China
4.Great Bay Area Research Institute,Aerospace Information Research Institute (AIR) of Chinese Academy of Science (CAS),Guangzhou,510700,China
5.Shenzhen Institute for Quantum Science and Engineering and Department of Physics,Southern University of Science and Technology,Shenzhen,518055,China
6.Shenzhen Branch,Hefei National Laboratory,International Quantum Academy,Shenzhen,Futian District,518048,China
7.School of Materials Science and Engineering,Peking University,Beijing,100871,China
第一作者单位物理系
通讯作者单位物理系
第一作者的第一单位物理系
推荐引用方式
GB/T 7714
Jiang,Shaolong,Yang,Jin,Zhu,Liang,et al. Nonlinear electronic and ultrafast optical signatures in chemical vapor-deposited ultrathin PtS2 ribbons[J]. Nano Research,2022,15:4366-4373.
APA
Jiang,Shaolong.,Yang,Jin.,Zhu,Liang.,Xie,Jiafeng.,Guo,Weiteng.,...&Lin,Junhao.(2022).Nonlinear electronic and ultrafast optical signatures in chemical vapor-deposited ultrathin PtS2 ribbons.Nano Research,15,4366-4373.
MLA
Jiang,Shaolong,et al."Nonlinear electronic and ultrafast optical signatures in chemical vapor-deposited ultrathin PtS2 ribbons".Nano Research 15(2022):4366-4373.
条目包含的文件
文件名称/大小 文献类型 版本类型 开放类型 使用许可 操作
2022-Nano Res.-Nonli(2958KB)----限制开放--
个性服务
原文链接
推荐该条目
保存到收藏夹
查看访问统计
导出为Endnote文件
导出为Excel格式
导出为Csv格式
Altmetrics Score
谷歌学术
谷歌学术中相似的文章
[Jiang,Shaolong]的文章
[Yang,Jin]的文章
[Zhu,Liang]的文章
百度学术
百度学术中相似的文章
[Jiang,Shaolong]的文章
[Yang,Jin]的文章
[Zhu,Liang]的文章
必应学术
必应学术中相似的文章
[Jiang,Shaolong]的文章
[Yang,Jin]的文章
[Zhu,Liang]的文章
相关权益政策
暂无数据
收藏/分享
所有评论 (0)
[发表评论/异议/意见]
暂无评论

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。