11 research outputs found

    Shape Approaches for Enhancing Plasmon Propagation in Graphene

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    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

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    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”

    Vibrational Properties in Highly Strained Hexagonal Boron Nitride Bubbles

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    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

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    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

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    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

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    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 CaF2_{2} and Si/SiO2_{2} 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 10410^{4}, 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

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    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

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    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
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