11 research outputs found
Shape Approaches for Enhancing Plasmon Propagation in Graphene
Graphene
plasmonics is a promising alternative for on-chip high
speed communication that integrates optics and electronics, where
the strong confinement of the electromagnetic energy at subwavelength
scale and the tunability of the plasmon frequency via an external
gate voltage are key advantages. The main drawback of graphene plasmons
is their rather short decay and propagation length, which is due to
intrinsic losses and substrate-related defects. Toward plasmonic devices,
noble metal antennas represent a viable approach for plasmon launching
in graphene waveguides, with the challenge of efficient coupling and
plasmon propagation that are feasible for on chip communication. Here
we discuss and analyze, using numerical simulations, different designs
of metal antennas and their coupling to graphene plasmons (GP), as
well as graphene based nanopatterned waveguides that can lead to a
more efficient GP propagation. A Yagi-Uda antenna leads to stronger
coupling to GPs and allows for directive propagation as compared to
a simple dipole antenna. This is especially advantageous to launch
plasmons in graphene nanowire waveguides, where propagation up to
3 μm and frequency and phase control can be achieved. In tapered
graphene waveguides, the constructive interference of the plasmon
reflection at the edges can lead to strong plasmon signals up to 8
μm distant from the launching dipole antenna. Nanostructuring
of rectangular waveguides into asymmetric chains of truncated triangles
greatly enhances directionality of GP propagation and conserves phase
information. A comparison of the propagation length and electric near-field
strength of these different approaches is presented, and confronted
with the efficiency of GP launching by light scattering on scanning
near field optical microscopy (SNOM) tips
Keratin-Graphene Nanocomposite: Transformation of Waste Wool in Electronic Devices
Electronic
devices, designed to be long lasting, are commonly made
with rigid, nondegradable materials. These, together with the presence
of rare and toxic elements, create significant issues for their waste
management. The production of electronic devices, made with biodegradable
materials that are sourced from waste streams of the agricultural
sector, will create the premises for circular economy systems in the
electronics sector that will increase their sustainability. Here,
this new approach has been demonstrated by using keratin, the protein
extracted from waste wool clips, combined with graphene to produce
protein-based electronic materials. Resistors plane capacitors and
inductors were fabricated, characterized, and then assembled together
to obtain analogue electrical circuits such as high-pass filters or
resonators. Morphological structures, electrical characteristics,
thermal stability, and mechanical properties were fully investigated.
Finally, a water-based ink of keratin and graphene was used to functionalize
cellulose to obtain flexible electrodes with remarkable sheet resistances
(≈10 Ω/sq); ohmic I–V curves were obtained, and
the electrical conductivity after folding/unfolding cycles was measured.
All the processing and fabrication methods used water as the only
solvent. The described approach produced easily disposable electronics
materials with a reduced fingerprint on the environment, demonstrating
that keratin from wool waste is an excellent candidate for the creation
of circular economy systems in the electronics sector. The proposed
valorization of waste materials for electronics applications is named
“wastetronics”
Supplementary document for Strongly Enhanced Sensitivities of CMOS compatible Plasmonic Titanium Nitride Nanohole Arrays for Refractive Index Sensing under Oblique Incidence - 6319542.pdf
Supplemental Documen
Vibrational Properties in Highly Strained Hexagonal Boron Nitride Bubbles
Hexagonal boron nitride
(hBN) is widely used as a protective layer
for few-atom-thick crystals and heterostructures (HSs), and it hosts
quantum emitters working up to room temperature. In both instances,
strain is expected to play an important role, either as an unavoidable
presence in the HS fabrication or as a tool to tune the quantum emitter
electronic properties. Addressing the role of strain and exploiting
its tuning potentiality require the development of efficient methods
to control it and of reliable tools to quantify it. Here we present
a technique based on hydrogen irradiation to induce the formation
of wrinkles and bubbles in hBN, resulting in remarkably high strains
of ∼2%. By combining infrared (IR) near-field scanning optical
microscopy and micro-Raman measurements with numerical calculations,
we characterize the response to strain for both IR-active and Raman-active
modes, revealing the potential of the vibrational properties of hBN
as highly sensitive strain probes
Metastable CdTe@HgTe Core@Shell Nanostructures Obtained by Partial Cation Exchange Evolve into Sintered CdTe Films Upon Annealing
Partial
Hg2+ → Cd2+ cation exchange
(CE) reactions were exploited to transform colloidal CdTe nanocrystals
(NCs, 4–6 nm in size) into CdTe@HgTe core@shell nanostructures.
This was achieved by working under a slow CE rate, which limited the
exchange to the surface of the CdTe NCs. In such nanostructures, when
annealed at mild temperatures (as low as 200 °C), the HgTe shell
sublimated or melted and the NCs sintered together, with the concomitant
desorption of their surface ligands. At the end of this process, the
annealed samples consisted of ligand-free CdTe sintered films containing
an amount of Hg2+ that was much lower than that of the
starting CdTe@HgTe NCs. For example, the CdTe@HgTe NCs that initially
contained 10% of Hg2+, after being annealed at 200 °C
were transformed to CdTe sintered films containing only traces of
Hg2+ (less than 1%). This procedure was then used to fabricate
a proof-of-concept CdTe-based photodetector exhibiting a photoresponse
of up to 0.5 A/W and a detectivity of ca. 9 × 104 Jones
under blue light illumination. Our strategy suggests that CE protocols
might be exploited to lower the overall costs of production of CdTe
thin films employed in photovoltaic technology, which are currently
fabricated at high temperatures (above 350 °C), using post-process
ligand-stripping steps
Tailoring Photoluminescence by Strain-Engineering in Layered Perovskite Flakes
Strain
is an effective strategy to modulate the optoelectronic
properties of 2D materials, but it has been almost unexplored in layered
hybrid organic–inorganic metal halide perovskites (HOIPs) due
to their complex band structure and mechanical properties. Here, we
investigate the temperature-dependent microphotoluminescence (PL)
of 2D (C6H5CH2CH2NH3)2Cs3Pb4Br13 HOIP
subject to biaxial strain induced by a SiO2 ring platform
on which flakes are placed by viscoelastic stamping. At 80 K, we found
that a strain of <1% can change the PL emission from a single peak
(unstrained) to three well-resolved peaks. Supported by micro-Raman
spectroscopy, we show that the thermomechanically generated strain
modulates the bandgap due to changes in the octahedral tilting and
lattice expansion. Mechanical simulations demonstrate the coexistence
of tensile and compressive strain along the flake. The observed PL
peaks add an interesting feature to the rich phenomenology of photoluminescence
in 2D HOIPs, which can be exploited in tailored sensing and optoelectronic
devices
Multiband Plasmonic Sierpinski Carpet Fractal Antennas
Deterministic fractal antennas are employed to realize multimodal plasmonic devices. Such structures show strongly enhanced localized electromagnetic fields typically in the infrared range with a hierarchical spatial distribution. Realization of engineered fractal antennas operating in the optical regime would enable nanoplasmonic platforms for applications, such as energy harvesting, light sensing, and bio/chemical detection. Here, we introduce a novel plasmonic multiband metamaterial based on the Sierpinski carpet (SC) space-filling fractal, having a tunable and polarization-independent optical response, which exhibits multiple resonances from the visible to mid-infrared range. We investigate gold SCs fabricated by electron-beam lithography on CaF and Si/SiO substrates. Furthermore, we demonstrate that such resonances originate from diffraction-mediated localized surface plasmons, which can be tailored in deterministic fashion by tuning the shape, size, and position of the fractal elements. Moreover, our findings illustrate that SCs with high order of complexity present a strong and hierarchically distributed electromagnetic near-field of the plasmonic modes. Therefore, engineered plasmonic SCs provide an efficient strategy for the realization of compact active devices with a strong and broadband spectral response in the visible/mid-infrared range. We take advantage of such a technology by carrying out surface enhanced Raman spectroscopy (SERS) on Brilliant Cresyl Blue molecules deposited onto plasmonic SCs. We achieve a broadband SERS enhancement factor up to , thereby providing a proof-of-concept application for chemical diagnostics
Temperature-Driven Transformation of CsPbBr<sub>3</sub> Nanoplatelets into Mosaic Nanotiles in Solution through Self-Assembly
Two-dimensional
colloidal halide perovskite nanocrystals are promising
materials for light-emitting applications. Recent studies have focused
on nanoplatelets that are able to self-assemble and transform on solid
substrates. However, the mechanism behind the process and the atomic
arrangement of their assemblies remain unclear. Here, we present a
detailed analysis of the transformation of self-assembled
stacks of CsPbBr3 nanoplatelets in solution over a period
of a few months by using ex situ transmission electron microscopy
and surface analysis. We demonstrate that the transformation mechanism
can be understood as oriented attachment, proceeding through the following
steps: (i) desorption of the ligands from the surfaces of the
particles, causing the seamless atomic merging of nanoplatelet stacks
into nanobelts; (ii) merging of neighboring nanobelts that form more
extended nanoplates; and (iii) attachment of nanobelts and nanoplates,
forming objects with an atomic structure that resembles a mosaic made
of broken nanotiles. We reveal that aged nanobelts and nanoplates,
which are mainly stabilized by amine/ammonium ions, link through a
bilayer of CsBr, with the atomic columns of neighboring perovskite
lattices shifted by a half-unit-cell, forming Ruddlesden–Popper
planar faults. We also show, via in situ monitoring of the nanocrystal
photoluminescence combined with transmission electron microscopy analysis,
that the transformation is temperature driven and that it can take
place within tens of minutes in solution and in spin-coated films.
Understanding this process gives crucial information for the design
and fabrication of perovskite materials, where control over the type
and density of defects is desired, stimulating the development of
perovskite nanocrystal structures with tailored electronic properties
Selective Growth of GaP Crystals on CMOS-Compatible Si Nanotip Wafers by Gas Source Molecular Beam Epitaxy
Gallium phosphide (GaP) is a III–V semiconductor
with remarkable optoelectronic properties, and it has almost the same
lattice constant as silicon (Si). However, to date, the monolithic
and large-scale integration of GaP devices with silicon remains challenging.
In this study, we present a nanoheteroepitaxy approach using gas-source
molecular-beam epitaxy for selective growth of GaP islands on Si nanotips,
which were fabricated using complementary metal–oxide semiconductor
(CMOS) technology on a 200 mm n-type Si(001) wafer. Our results show
that GaP islands with sizes on the order of hundreds of nanometers
can be successfully grown on CMOS-compatible wafers. These islands
exhibit a zinc-blende phase and possess optoelectronic properties
similar to those of a high-quality epitaxial GaP layer. This result
marks a notable advancement in the seamless integration of GaP-based
devices with high scalability into Si nanotechnology and integrated
optoelectronics
