Fabrication of MoSe2 nanoribbons via an unusual morphological phase transition

被引:87
作者
Chen, Yuxuan [1 ]
Cui, Ping [2 ]
Ren, Xibiao [3 ]
Zhang, Chendong [1 ,2 ]
Jin, Chuanhong [3 ]
Zhang, Zhenyu [2 ]
Shih, Chih-Kang [1 ]
机构
[1] Univ Texas Austin, Dept Phys, Austin, TX 78712 USA
[2] Univ Sci & Technol China, Int Ctr Quantum Design Funct Mat ICQD, Hefei Natl Lab Phys Sci, Microscale & Synerget Innovat Ctr Quantum Informa, Hefei 230026, Anhui, Peoples R China
[3] Zhejiang Univ, Sch Mat Sci & Engn, State Key Lab Silicon Mat, Hangzhou 310027, Zhejiang, Peoples R China
基金
美国国家科学基金会;
关键词
GRAPHENE NANORIBBONS; VALLEY POLARIZATION; MONOLAYER MOS2; METAL; ZIGZAG; CARBON; EDGES; GAP; STABILITY; SURFACE;
D O I
10.1038/ncomms15135
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Transition metal dichalcogenides (TMDs) are a family of van der Waals layered materials exhibiting unique electronic, optical, magnetic and transport properties. Their technological potentials hinge critically on the ability to achieve controlled fabrication of desirable nanostructures, such as nanoribbons and nanodots. To date, nanodots/nanoislands have been regularly observed, while controlled fabrication of TMD nanoribbons remains challenging. Here we report a bottom-up fabrication of MoSe2 nanoribbons using molecular beam epitaxy, via an unexpected temperature-induced morphological phase transition from the nanodot to nanoribbon regime. Such nanoribbons are of zigzag nature, characterized by distinct chemical and electronic properties along the edges. The phase space for nanoribbon growth is narrowly defined by proper Se:Mo ratios, as corroborated experimentally using different Se fluxes, and supported theoretically using first-principles calculations that establish the crucial role of the morphological reconstruction of the bare Mo-terminated edge. The growth mechanism revealed should be applicable to other TMD systems.
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页数:9
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