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Register a new userEngineering Purcell factor anisotropy for dark and bright excitons in two dimensional semiconductors
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Tightly bound dark excitons in atomically thin semiconductors can be used for various optoelectronic applications including light storage and quantum communication. Their optical accessibility is however limited due to their out-of-plane transition dipole moment. We thus propose to strengthen the coupling of dark excitons in two dimensional materials with out-of-plane resonant modes of a cavity at room temperature, by engineering the anisotropy in the Purcell factor. A silica micro-disk characterised by high confinement of light in small modal volume, high Q-factor and free spectral range is used to couple to the excitons in monolayer transition metal dichalcogenides. We show numerically that the tapering of sidewalls of the micro-disk is an extremely versatile route for achieving the selective coupling of whispering gallery modes to light emitted from out-of-plane dipoles to the detriment of that from in-plane ones for four representative monolayer transition metal dichalcogenides.
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Electrical contact resistance to two-dimensional (2D) semiconductors such as monolayer MoS_{2} is a key bottleneck in scaling the 2D field effect transistors (FETs). The 2D semiconductor in contact with three-dimensional metal creates unique current crowding that leads to increased contact resistance. We developed a model to separate the contribution of the current crowding from the intrinsic contact resistivity. We show that current crowding can be alleviated by doping and contact patterning. Using Landauer-Buttiker formalism, we show that van der Waals (vdW) gap at the interface will ultimately limit the electrical contact resistance. We compare our models with experimental data for doped and undoped MoS_{2} FETs. Even with heavy charge-transfer doping of > 2x10^{13} cm^{-2}, we show that the state-of-the-art contact resistance is 100 times larger than the ballistic limit. Our study highlights the need to develop efficient interface to achieve contact resistance of < 10 {Omega}.{mu}m, which will be ideal for extremely scaled devices.
Scattering processes in an optical microcavity are investigated for the case of silicon nanocrystals embedded in an ultra-high Q toroid microcavity. Using a novel measurement technique based on the observable mode-splitting, we demonstrate that light scattering is highly preferential: more than 99.8% of the scattered photon flux is scattered into the original doubly-degenerate cavity modes. The large capture efficiency is attributed to an increased scattering rate into the cavity mode, due to the enhancement of the optical density of states over the free space value and has the same origin as the Purcell effect in spontaneous emission. The experimentally determined Purcell factor amounts to 883.
A fascinating photonic platform with a small device scale, fast operating speed, as well as low energy consumption is two-dimensional (2D) materials, thanks to their in-plane crystalline structures and out-of-plane quantum confinement. The key to further advancement in this research field is the ability to modify the optical properties of the 2D materials. The modifications typically come from the materials themselves, for example, altering their chemical compositions. This article reviews a comparably less explored but promising means, through engineering the photonic surroundings. Rather than modifying materials themselves, this means manipulates the dielectric and metallic environments, both uniform and nanostructured, that directly interact with the materials. For 2D materials that are only one or a few atoms thick, the interaction with the environment can be remarkably efficient. This review summarizes the three degrees of freedom of this interaction: weak coupling, strong coupling, and multi-functionality. Also, it reviews a relatively timing concept of engineering that directly applied to the 2D materials by patterning. Benefiting from the burgeoning development of nanophotonics, the engineering of photonic environments provides a versatile and creative methodology of reshaping light-matter interaction in 2D materials.
Defect induced trap states are essential in determining the performance of semiconductor photodetectors. The de-trap time of carriers from a deep trap could be prolonged by several orders of magnitude as compared to shallow trap, resulting in additional decay/response time of the device. Here, we demonstrate that the trap states in two-dimensional ReS2 could be efficiently modulated by defect engineering through molecule decoration. The deep traps that greatly prolong the response time could be mostly filled by Protoporphyrin (H2PP) molecules. At the same time, carrier recombination and shallow traps would in-turn play dominant roles in determining the decay time of the device, which can be several orders of magnitude faster than the as-prepared device. Moreover, the specific detectivity of the device is enhanced (as high as ~1.89 x 10^13 Jones) due to the significant reduction of dark current through charge transfer between ReS2 and molecules. Defect engineering of trap states therefore provides a solution to achieve photodetectors with both high responsivity and fast response.
Plasmonic waveguides are an essential element of nanoscale coherent sources, including nanolasers and four-wave mixing (FWM) devices. Here we report how the design of the plasmonic waveguide needs to be guided by the ultimate application. This contrasts with traditional approaches in which the waveguide is considered in isolation. We find that hybrid plasmonic waveguides, with a nonlinear material sandwiched between the metal substrate and a high-index layer, are best suited for FWM applications, whereas metallic wedges are preferred in nanolasers. We also find that in plasmonic nanolasers high-index buffer layers perform better than more traditional low-index buffers.
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