Thickness-dependent structural stability and transition in molybdenum disulfide under hydrostatic pressure

2020 ◽  
Vol 29 (8) ◽  
pp. 086403
Author(s):  
Jiansheng Dong ◽  
Gang Ouyang
2011 ◽  
Vol 31 (1) ◽  
pp. 186-190 ◽  
Author(s):  
Shujie You ◽  
Mattias Mases ◽  
Ilya Dobryden ◽  
Alexander A. Green ◽  
Mark C. Hersam ◽  
...  

ACS Nano ◽  
2016 ◽  
Vol 10 (1) ◽  
pp. 1619-1624 ◽  
Author(s):  
Xiuming Dou ◽  
Kun Ding ◽  
Desheng Jiang ◽  
Xiaofeng Fan ◽  
Baoquan Sun

ACS Nano ◽  
2014 ◽  
Vol 8 (7) ◽  
pp. 7458-7464 ◽  
Author(s):  
Xiuming Dou ◽  
Kun Ding ◽  
Desheng Jiang ◽  
Baoquan Sun

2019 ◽  
Vol 1867 (2) ◽  
pp. 107-113 ◽  
Author(s):  
Liina Kangur ◽  
Kõu Timpmann ◽  
Dominik Zeller ◽  
Patrick Masson ◽  
Judith Peters ◽  
...  

Nanomaterials ◽  
2020 ◽  
Vol 10 (11) ◽  
pp. 2154
Author(s):  
Xiangyu Dai ◽  
Zhengfang Qian ◽  
Qiaolu Lin ◽  
Le Chen ◽  
Renheng Wang ◽  
...  

In this paper, the band-gap tunability of three monolayer semiconductors under hydrostatic pressure was intensively investigated based on first-principle simulations with a focus on monolayer antimony (Sb) as a semiconductor nanomaterial. As the benchmark study, monolayer black phosphorus (BP) and monolayer molybdenum disulfide (MoS2) were also investigated for comparison. Our calculations showed that the band-gap tunability of the monolayer Sb was much more sensitive to hydrostatic pressure than that of the monolayer BP and MoS2. Furthermore, the monolayer Sb was predicted to change from an indirect band-gap semiconductor to a conductor and to transform into a double-layer nanostructure above a critical pressure value ranging from 3 to 5 GPa. This finding opens an opportunity for nanoelectronic, flexible electronics and optoelectronic devices as well as sensors with the capabilities of deep band-gap tunability and semiconductor-to-metal transition by applying mechanical pressure.


RSC Advances ◽  
2014 ◽  
Vol 4 (87) ◽  
pp. 46780-46786 ◽  
Author(s):  
Xiaoli Huang ◽  
Defang Duan ◽  
Fangfei Li ◽  
Yanping Huang ◽  
Lu Wang ◽  
...  

Author(s):  
Chenkai Li ◽  
Yaoyao Liu ◽  
Qishuo Yang ◽  
Qunfei Zheng ◽  
Zhipeng Yan ◽  
...  

2011 ◽  
Vol 184 (4) ◽  
pp. 786-789 ◽  
Author(s):  
Shouxin Cui ◽  
Wenxia Feng ◽  
Haiquan Hu ◽  
Guiqing Zhang ◽  
Zengtao Lv ◽  
...  

Author(s):  
T. Kizuka ◽  
N. Tanaka

Structure and stability of atomic clusters have been studied by time-resolved high-resolution electron microscopy (TRHREM). Typical examples are observations of structural fluctuation in gold (Au) clusters supported on silicon oxide films, graphtized carbon films and magnesium oxide (MgO) films. All the observations have been performed on the clusters consisted of single metal element. Structural stability of ceramics clusters, such as metal-oxide, metal-nitride and metal-carbide clusters, has not been observed by TRHREM although the clusters show anomalous structural and functional properties concerning to solid state physics and materials science.In the present study, the behavior of ceramic, magnesium oxide (MgO) clusters is for the first time observed by TRHREM at 1/60 s time resolution and at atomic resolution down to 0.2 nm.MgO and gold were subsequently deposited on sodium chloride (001) substrates. The specimens, single crystalline MgO films on which Au particles were dispersed were separated in distilled water and observed by using a 200-kV high-resolution electron microscope (JEOL, JEM2010) equipped with a high sensitive TV camera and a video tape recorder system.


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