Width-dependent Photoluminescence and Anisotropic Raman Spectroscopy from Monolayer MoS$_2$ Nanoribbons
Single layers of transition metal dichalcogenides such as MoS$_2$ are direct bandgap semiconductors with optical and electronic properties distinct from multilayers due to strong vertical confinement. Despite the fundamental monolayer limit of thickness, the electronic structure of isolated layers c...
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Main Authors | , , , |
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Format | Journal Article |
Language | English |
Published |
12.09.2017
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Subjects | |
Online Access | Get full text |
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Summary: | Single layers of transition metal dichalcogenides such as MoS$_2$ are direct
bandgap semiconductors with optical and electronic properties distinct from
multilayers due to strong vertical confinement. Despite the fundamental
monolayer limit of thickness, the electronic structure of isolated layers can
be further tailored with lateral degrees of freedom in nanostructures such as
quantum dots or nanoribbons. Although one-dimensionally confined monolayer
semiconductors are predicted to have interesting size- and edge-dependent
properties useful for spintronics applications, experiments on the
opto-electronic features of monolayer transition metal dichalcogenide
nanoribbons is limited. We use nanolithography to create monolayer MoS$_2$
nanoribbons with lateral sizes down to 20 nm. The Raman spectra show
polarization anisotropy and size-dependent intensity. The nanoribbons prepared
with this technique show reduced susceptibility to edge defects and emit
photoluminescence with size-dependent energy that can be understood from a
phenomenological model. Fabrication of monolayer nanoribbons with strong
exciton emission can facilitate exploration of low-dimensional opto-electronic
devices with controllable properties. |
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DOI: | 10.48550/arxiv.1709.04001 |