Electronic state evolution of oxygen-doped monolayer WSe2 assisted by femtosecond laser irradiation

被引:3
|
作者
Wang, Lei [1 ]
Wang, Dan [2 ]
Luo, Yang [1 ,3 ]
Xu, Chen-Yu [1 ]
Cui, Lin [1 ]
Li, Xian-Bin [1 ]
Sun, Hong-Bo [4 ]
机构
[1] Jilin Univ, Coll Elect Sci & Engn, State Key Lab Integrated Optoelect, 2699 Qianjin St, Changchun 130012, Peoples R China
[2] Yale Univ, Dept Mech Engn & Mat Sci, New Haven, CT 06511 USA
[3] Chinese Acad Sci, Changchun Inst Opt, Fine Mech & Phys, Changchun 130033, Peoples R China
[4] Tsinghua Univ, Dept Precis Instrument, State Key Lab Precis Measurement Technol & Instrum, Beijing 100084, Peoples R China
基金
中国博士后科学基金;
关键词
CHARGE-TRANSFER;
D O I
10.1039/d2cp04495a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Electronic states are significantly correlated with chemical compositions, and the information related to these factors is especially crucial for the manipulation of the properties of matter. However, this key information is usually verified by after-validation methods, which could not be obtained during material processing, for example, in the field of femtosecond laser direct writing inside materials. Here, critical evolution stages of electronic states for monolayer tungsten diselenide (WSe2) around the modification threshold (at a Mott density of similar to 10(13) cm(-2)) are observed by broadband femtosecond transient absorption spectroscopy, which is associated with the intense femtosecond-laser-assisted oxygen-doping mechanism. First-principles calculations and control experiments on graphene-covered monolayer WSe2 further confirm this modification mechanism. Our findings reveal a photochemical reaction for monolayer WSe2 under the Mott density condition and provide an electronic state criterion to in situ monitor the degrees of modification in monolayer transition metal dichalcogenides during the femtosecond laser modification.
引用
收藏
页码:2043 / 2049
页数:7
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