13 research outputs found
Three-Dimensional Resolvable Plasmonic Concentric Compound Lens: Approaching the Axial Resolution from Microscale to Nanoscale
We propose the design and working
principle of a plasmonic concentric
compound lens (CCL) comprising inner circular nanoslits and outer
circular nanogrooves. Dual-wavelength operations have been achieved
for 650 and 750 nm at nanoscale and microscale focal lengths along
with their depth of focus (DOF). By tuning the arrangement of nanogrooves,
the axial resolution can be modulated and the narrowest DOF is achieved
by a design of gradually decreasing groove width. For the ultrahigh
tunability of axial resolution, DOF over 400 nm for both working wavelengths
is also achieved. We not only developed an approximate-perturbed-focus
model for explaining the performance of DOF but also found an extraordinary
way to improve the resolution. The enhanced resonance of central disk
as nannoantenna in CCL also has great influence on nanofocusing with
different deigns of outer nanogrooves. This work provides new sight
of focusing ability governed by the general optical nanogrooves. The
optimized CCL shows excellent focusing performance with a lateral
resolution down to 0.32λ (λ = 650 nm), which is the best
resolving ability achieved thus far in the near field region with
a long focal length up to 500 nm
Distributed Bragg Reflectors as Broadband and Large-Area Platforms for Light-Coupling Enhancement in 2D Transition-Metal Dichalcogenides
Two-dimensional
(2D) semiconductors, particularly the direct-gap
monolayer transition metal dichalcogenides (TMDs), are currently being
developed for various atomically thin optoelectronic devices. However,
practical applications are hindered by their low quantum efficiencies
in light emissions and absorptions. While photonic cavities and metallic
plasmonic structures can significantly enhance the light–matter
interactions in TMDs, the narrow spectral resonance and the local
hot spots considerably limit the applications when broadband and large
area are required. Here, we demonstrate that a properly designed distributed
Bragg reflector (DBR) can be an ideal platform for light-coupling
enhancement in 2D TMDs. The main idea is based on engineering the
amplitude and phase of optical reflection from the DBR to produce
optimal substrate-induced interference. We show that the photoluminescence,
Raman, and second harmonic generation signals of monolayer WSe<sub>2</sub> can be enhanced by a factor of 26, 34, and 58, respectively.
The proposed DBR substrates pave the way for developing a range of
2D optoelectronic devices for broadband and large-area applications
Second Harmonic Generation from Artificially Stacked Transition Metal Dichalcogenide Twisted Bilayers
Optical second harmonic generation (SHG) is known as a sensitive probe to the crystalline symmetry of few-layer transition metal dichalcogenides (TMDs). Layer-number dependent and polarization resolved SHG have been observed for the special case of Bernal stacked few-layer TMDs, but it remains largely unexplored for structures deviated from this ideal stacking order. Here we report on the SHG from homo- and heterostructural TMD bilayers formed by artificial stacking with an arbitrary stacking angle. The SHG from the twisted bilayers is a coherent superposition of the SH fields from the individual layers, with a phase difference depending on the stacking angle. Such an interference effect is insensitive to the constituent layered materials and thus applicable to hetero-stacked bilayers. A proof-of-concept demonstration of using the SHG to probe the domain boundary and crystal polarity of mirror twins formed in chemically grown TMDs is also presented. We show here that the SHG is an efficient, sensitive, and nondestructive characterization for the stacking orientation, crystal polarity, and domain boundary of van der Waals heterostructures made of noncentrosymmetric layered materials
Submicron Memtransistors Made from Monocrystalline Molybdenum Disulfide
Multiterminal
memtransistors made from two-dimensional (2D) materials
have garnered increasing attention in the pursuit of low-power heterosynaptic
neuromorphic circuits. However, existing 2D memtransistors tend to
necessitate high set voltages (>1 V) or feature defective channels,
posing concerns regarding material integrity and intrinsic properties.
Herein, we present a monocrystalline monolayer MoS2 memtransistor
designed for operation within submicron regimes. Under reverse drain
bias sweeps, our experiments reveal memristive behavior within the
device, further controllable through modulation of the gate terminal.
This controllability facilitates the consistent manifestation of multistate
memory effects. Notably, the memtransistor behavior becomes more significant
as the channel length diminishes, particularly with channel lengths
below 1.6 μm, showcasing an increase in the switching ratio
alongside a decrease in the set voltage with the decreasing channel
length. Our optimized memtransistor demonstrates the ability to exhibit
individual resistance states spanning 5 orders of magnitude, with
switching drain voltages of approximately 0.05 V. To elucidate these
findings, we investigate hot carrier effects and their interplay with
oxide traps within the HfO2 dielectric. This work highlights
the importance of memtransisor behavior in highly scaled 2D transistors,
particularly those featuring low contact resistances. This understanding
holds the potential to tailor memory characteristics essential for
the development of energy-efficient neuromorphic devices
Hysteresis-Free Contact Doping for High-Performance Two-Dimensional Electronics
Contact doping is considered crucial for reducing the
contact resistance
of two-dimensional (2D) transistors. However, a process for achieving
robust contact doping for 2D electronics is lacking. Here, we developed
a two-step doping method for effectively doping 2D materials through
a defect-repairing process. The method achieves strong and hysteresis-free
doping and is suitable for use with the most widely used transition-metal
dichalcogenides. Through our method, we achieved a record-high sheet
conductance (0.16 mS·sq–1 without gating) of
monolayer MoS2 and a high mobility and carrier concentration
(4.1 × 1013 cm–2). We employed our
robust method for the successful contact doping of a monolayer MoS2 Au-contact device, obtaining a contact resistance as low
as 1.2 kΩ·μm. Our method represents an effective
means of fabricating high-performance 2D transistors
Investigations on Diamond Nanostructuring of Different Morphologies by the Reactive-Ion Etching Process and Their Potential Applications
We report the systematic studies
on the fabrication of aligned, uniform, and highly dense diamond nanostructures
from diamond films of various granular structures. Self-assembled
Au nanodots are used as a mask in the self-biased reactive-ion etching
(RIE) process, using an O<sub>2</sub>/CF<sub>4</sub> process plasma.
The morphology of diamond nanostructures is a close function of the
initial phase composition of diamond. Cone-shaped and tip-shaped diamond
nanostructures result for microcrystalline diamond (MCD) and nanocrystalline
diamond (NCD) films, whereas pillarlike and grasslike diamond nanostructures
are obtained for Ar-plasma-based and N<sub>2</sub>-plasma-based ultrananocrystalline
diamond (UNCD) films, respectively. While the nitrogen-incorporated
UNCD (N-UNCD) nanograss shows the most-superior electron-field-emission
properties, the NCD nanotips exhibit the best photoluminescence properties,
viz, different applications need different morphology of diamond nanostructures
to optimize the respective characteristics. The optimum diamond nanostructure
can be achieved by proper choice of granular structure of the initial
diamond film. The etching mechanism is explained by in situ observation
of optical emission spectrum of RIE plasma. The preferential etching
of sp<sup>2</sup>-bonded carbon contained in the diamond films is
the prime factor, which forms the unique diamond nanostructures from
each type of diamond films. However, the excited oxygen atoms (O*)
are the main etching species of diamond film
Spectroscopic Signatures for Interlayer Coupling in MoS<sub>2</sub>–WSe<sub>2</sub> van der Waals Stacking
Stacking of MoS<sub>2</sub> and WSe<sub>2</sub> monolayers is conducted by transferring triangular MoS<sub>2</sub> monolayers on top of WSe<sub>2</sub> monolayers, all grown by chemical vapor deposition (CVD). Raman spectroscopy and photoluminescence (PL) studies reveal that these mechanically stacked monolayers are not closely coupled, but after a thermal treatment at 300 °C, it is possible to produce van der Waals solids consisting of two interacting transition metal dichalcogenide (TMD) monolayers. The layer-number sensitive Raman out-of-plane mode A<sup>2</sup><sub>1g</sub> for WSe<sub>2</sub> (309 cm<sup>–1</sup>) is found sensitive to the coupling between two TMD monolayers. The presence of interlayer excitonic emissions and the changes in other intrinsic Raman modes such as E″ for MoS<sub>2</sub> at 286 cm<sup>–1</sup> and A<sup>2</sup><sub>1g</sub> for MoS<sub>2</sub> at around 463 cm<sup>–1</sup> confirm the enhancement of the interlayer coupling
Large-Area Synthesis of Highly Crystalline WSe<sub>2</sub> Monolayers and Device Applications
The monolayer transition metal dichalcogenides have recently attracted much attention owing to their potential in valleytronics, flexible and low-power electronics, and optoelectronic devices. Recent reports have demonstrated the growth of large-size two-dimensional MoS<sub>2</sub> layers by the sulfurization of molybdenum oxides. However, the growth of a transition metal selenide monolayer has still been a challenge. Here we report that the introduction of hydrogen in the reaction chamber helps to activate the selenization of WO<sub>3</sub>, where large-size WSe<sub>2</sub> monolayer flakes or thin films can be successfully grown. The top-gated field-effect transistors based on WSe<sub>2</sub> monolayers using ionic gels as the dielectrics exhibit ambipolar characteristics, where the hole and electron mobility values are up to 90 and 7 cm<sup>2</sup>/Vs, respectively. These films can be transferred onto arbitrary substrates, which may inspire research efforts to explore their properties and applications. The resistor-loaded inverter based on a WSe<sub>2</sub> film, with a gain of ∼13, further demonstrates its applicability for logic-circuit integrations
Photoluminescence Enhancement and Structure Repairing of Monolayer MoSe<sub>2</sub> by Hydrohalic Acid Treatment
Atomically thin two-dimensional transition-metal
dichalcogenides
(TMDCs) have attracted much attention recently due to their unique
electronic and optical properties for future optoelectronic devices.
The chemical vapor deposition (CVD) method is able to generate TMDCs
layers with a scalable size and a controllable thickness. However,
the TMDC monolayers grown by CVD may incorporate structural defects,
and it is fundamentally important to understand the relation between
photoluminescence and structural defects. In this report, point defects
(Se vacancies) and oxidized Se defects in CVD-grown MoSe<sub>2</sub> monolayers are identified by transmission electron microscopy and
X-ray photoelectron spectroscopy. These defects can significantly
trap free charge carriers and localize excitons, leading to the smearing
of free band-to-band exciton emission. Here, we report that the simple
hydrohalic acid treatment (such as HBr) is able to efficiently suppress
the trap-state emission and promote the neutral exciton and trion
emission in defective MoSe<sub>2</sub> monolayers through the <i>p</i>-doping process, where the overall photoluminescence intensity
at room temperature can be enhanced by a factor of 30. We show that
HBr treatment is able to activate distinctive trion and free exciton
emissions even from highly defective MoSe<sub>2</sub> layers. Our
results suggest that the HBr treatment not only reduces the <i>n</i>-doping in MoSe<sub>2</sub> but also reduces the structural
defects. The results provide further insights of the control and tailoring
the exciton emission from CVD-grown monolayer TMDCs
Low-Threshold Plasmonic Lasers on a Single-Crystalline Epitaxial Silver Platform at Telecom Wavelength
We
report on the first demonstration of metal–insulator–semiconductor-type
plasmonic lasers at the telecom wavelength (∼1.3 μm)
using top-down fabricated semiconductor waveguides on single-crystalline
metallic platforms formed using epitaxially grown Ag films. The critical
role of the Ag film thickness in sustaining plasmonic lasing at the
telecom wavelength is investigated systematically. Low-threshold (0.2
MW/cm<sup>2</sup>) and continuous-wave operation of plasmonic lasing
at cryogenic temperatures can be achieved on a 150 nm Ag platform
with minimum radiation leakage into the substrate. Plasmonic lasing
occurs preferentially through higher-order surface-plasmon-polariton
modes, which exhibit a higher mode confinement factor, lower propagation
loss, and better field–gain coupling. We observed plasmonic
lasing up to ∼200 K under pulsed excitations. The plasmonic
lasers on large-area epitaxial Ag films open up a scalable platform
for on-chip integrations of plasmonics and optoelectronics at the
telecom wavelength