arXiv subjects

Maria Kandyla

Publications and source records attributed to Maria Kandyla.

9 recordsLinked to original sources

arXiv2022

Broadband wavelength-selective isotype heterojunction n+-ZnO/n-Si photodetector with variable polarity

An isotype heterojunction n+-ZnO/n-Si photodetector is developed, demonstrating wavelength-selective or broadband operation, depending on the applied bias voltage. Additionally, at self-powered (zero bias) operation, it distinguishes between UV, visible, and near IR (NIR) photons by polarity control of the photocurrent. The photodetector is developed by atomic layer deposition (ALD) of ZnO on n-Si, followed by electric contact deposition and annealing. Photoluminescence measurements reveal high optical quality and improved crystallinity of annealed ZnO on silicon. Photocurrent measurements as a function of illumination wavelength and bias voltage show small negative values in the UV-visible spectral range at zero and positive bias voltage and high positive values in the NIR spectral range. For these measurements, we consider the electric contact to ZnO as the anode and the electric contact to silicon as the cathode. At negative bias voltage, the device shows broadband operation with high photocurrent values across the UV-vis-NIR.

cond-mat.mtrl-sci↗

arXiv2020

Laser-microstructured ZnO/p-Si photodetector with enhanced and broadband responsivity across the UV-Vis-NIR

We develop ZnO/p-Si photodetectors by atomic layer deposition (ALD) of ZnO thin films on laser-microstructured silicon and we investigate their electrical and optical behavior, demonstrating high sensitivity and broadband operation. Microstructured p-type silicon was obtained by ns-laser irradiation in SF6 gas, which results in the formation of quasi-ordered and uniform microspikes on the silicon surface. The irradiated silicon contains sulfur impurities, which extend its absorbance to the near infrared. A thin film of ZnO was conformally deposited on the microstructured silicon substrates by ALD. Photoluminescence measurements indicate high crystalline quality of the ZnO film after annealing. Current-voltage (I-V) measurements of the ZnO/p-Si heterodiodes in dark show a non-linear behavior with unusual high current values in reverse bias. Under illumination photocurrent is observed for reverse bias, even for wavelengths below the silicon bandgap in the case of the laser-microstructured photodetectors. Higher current values are measured for the microstructured photodetectors, compared to planar ones. Photoconductivity measurements show enhanced responsivity across the UV-Vis-NIR spectral range for the laser-microstructured devices, due to their increased surface area and light absorption.

physics.app-ph↗

arXiv2020

Functional surfaces of laser-microstructured silicon coated with thermoresponsive PS/PNIPAM polymer blends: switching reversibly between hydrophilicity and hydrophobicity

We developed functional surfaces of laser-microstructured silicon coated with blends of polystyrene (PS) and poly(N-isopropylacrylamide) (PNIPAM) and we study their switching wetting behavior between hydrophilicity and hydrophobicity. Large areas of silicon are processed with reproducible surface micromorphology and spin-coated with PS/PNIPAM blends of two blend ratios. The wetting behavior of the surfaces is modified by the combination of surface topography and surface chemistry effects. PS/PNIPAM films are casted on flat and microstructured silicon substrates with or without a native SiO2 layer. All films respond to the stimulus of temperature and films casted on microstructured silicon substrates with a native SiO2 layer show the highest thermoresponsiveness presumably because they adopt a more favorable structure. Microstructuring provides a large specific area that extends the contact of PNIPAM chains with water molecules according to the Wenzel model, and thus increasing the film thermoresponsiveness, resulting in a reversible transition from hydrophilicity to hydrophobicity upon heating. The absence of the native SiO2 layer from the silicon substrates affects the PS and PNIPAM arrangement in the films, increasing the water contact angle both below and above the lower critical solution temperature of PNIPAM and decreasing their thermoresponsiveness.

cond-mat.mtrl-sci↗

arXiv2019

Thin films of PS/PS-b-PNIPAM and PS/PNIPAM polymer blends with tunable wettability

We develop thin films of blends of polystyrene (PS) with the thermoresponsive polymer poly(N-isopropylacrylamide) (PNIPAM) (PS/PNIPAM) and its diblock copolymer polystyrene-b-poly(N-isopropylacrylamide) (PS/PS-b-PNIPAM) in different blend ratios and we study their surface morphology and thermoresponsive wetting behaviour. The blends of PS/PNIPAM and PS/PS-b-PNIPAM are spin-casted on flat silicon surfaces with various drying conditions. The surface morphology of the films depends on the blend ratio and the drying conditions. The PS/PS-b-PNIPAM films do not show an increase of their water contact angles with temperature, as it is expected by the presence of the PNIPAM block. All PS/PNIPAM films show an increase in the water contact angle above the lower critical solution temperature of PNIPAM, which depends on the ratio of PNIPAM in the blend and is insensitive to the drying conditions of the films. The difference between the wetting behaviour of PS/PS-b-PNIPAM and PS/PNIPAM films is due to the arrangement of the PNIPAM chains in the film.

physics.chem-ph↗

arXiv2019

Surface-Enhanced Raman Spectroscopy of Graphene Integrated in Plasmonic Silicon Platforms with Three-Dimensional Nanotopography

Integrating graphene with plasmonic nanostructures results in multifunctional hybrid systems with enhanced performance for numerous applications. In this work, we take advantage of the remarkable mechanical properties of graphene to combine it with scalable 3D plasmonic nanostructured silicon substrates, which enhance the interaction of graphene with electromagnetic radiation. Large areas of femtosecond laser-structured arrays of silicon nanopillars, decorated with gold nanoparticles, are integrated with graphene, which conforms to the substrate nanotopography. We obtain Raman spectra at 488, 514, 633, and 785 nm excitation wavelengths, spanning the entire visible range. For all excitation wavelengths, the Raman signal of graphene is enhanced by 2-3 orders of magnitude, similarly to the highest enhancements measured to date, concerning surface-enhanced Raman Spectroscopy (SERS) of graphene on plasmonic substrates. Moreover, in contrast to traditional deposition and lithographic methods, the fabrication method employed here relies on single-step, maskless, cost-effective, rapid laser processing of silicon in water, amenable to large-scale fabrication. Finite-difference time-domain simulations elucidate the advantages of the 3D topography of the substrate. Conformation of graphene to the Au-decorated silicon nanopillars enables graphene to sample near fields from an increased number of nanoparticles. Due to synergistic effects with the nanopillars, different nanoparticles become more active for different wavelengths and locations on the pillars, providing broadband enhancement. Nanostructured plasmonic silicon is a promising platform for integration with graphene and other 2D materials, for next-generation applications of large-area hybrid nanomaterials in the fields of sensing, photonics, optoelectronics, and medical diagnostics.

physics.app-ph↗

arXiv2017

Real-time observation of a coherent lattice transformation into a high-symmetry phase

Excursions far from their equilibrium structures can bring crystalline solids through collective transformations including transitions into new phases that may be transient or long-lived. Direct spectroscopic observation of far-from-equilibrium rearrangements provides fundamental mechanistic insight into chemical and structural transformations, and a potential route to practical applications, including ultrafast optical control over material structure and properties. However, in many cases photoinduced transitions are irreversible or only slowly reversible, or the light fluence required exceeds material damage thresholds. This precludes conventional ultrafast spectroscopy in which optical excitation and probe pulses irradiate the sample many times, each measurement providing information about the sample response at just one probe delay time following excitation, with each measurement at a high repetition rate and with the sample fully recovering its initial state in between measurements. Using a single-shot, real-time measurement method, we were able to observe the photoinduced phase transition from the semimetallic, low-symmetry phase of crystalline bismuth into a high-symmetry phase whose existence at high electronic excitation densities was predicted based on earlier measurements at moderate excitation densities below the damage threshold. Our observations indicate that coherent lattice vibrational motion launched upon photoexcitation with an incident fluence above 10 mJ/cm2 in bulk bismuth brings the lattice structure directly into the high-symmetry configuration for tens of picoseconds, after which carrier relaxation and diffusion restore the equilibrium lattice configuration.

cond-mat.mtrl-sci↗

arXiv2016

Plasmon enhanced optical tweezers with gold-coated black silicon

Plasmonic optical tweezers are a ubiquitous tool for the precise manipulation of nanoparticles and biomolecules at low photon flux, while femtosecond-laser optical tweezers can probe the nonlinear optical properties of the trapped species with applications in biological diagnostics. In order to adopt plasmonic optical tweezers in real-world applications, it is essential to develop large-scale fabrication processes without compromising the trapping efficiency. Here, we develop a novel platform for continuous wave (CW) and femtosecond plasmonic optical tweezers, based on gold-coated black silicon. In contrast with traditional lithographic methods, the fabrication method relies on simple, single-step, maskless tabletop laser processing of silicon in water that facilitates scalability. Gold-coated black silicon supports repeatable trapping efficiencies comparable to the highest ones reported to date. From a more fundamental aspect, a plasmon-mediated efficiency enhancement is a resonant effect, and therefore, dependent on the wavelength of the trapping beam. Surprisingly, a wavelength characterization of plasmon-enhanced trapping efficiencies has evaded the literature. Here, we exploit the repeatability of the recorded trapping efficiency, offered by the gold-coated black silicon platform, and perform a wavelength-dependent characterization of the trapping process, revealing the resonant character of the trapping efficiency maxima. Gold-coated black silicon is a promising platform for large-scale parallel trapping applications that will broaden the range of optical manipulation in nanoengineering, biology, and the study of collective biophotonic effects.

physics.optics↗

arXiv2015

Near-field enhanced optical tweezers utilizing femtosecond-laser nanostructured substrates

We present experimental evidence of plasmonic-enhanced optical tweezers, of polystyrene beads in deionized water in the vicinity of metal-coated nanostructures. The optical tweezers operate with a continuous wave (CW) near-infrared laser. We employ a Cu/Au bilayer that significantly improves dissipation of heat generated by the trapping laser beam and avoid de-trapping from heat convection currents. We investigate the improvement of the optical trapping force, the effective trapping quality factor, and observe an exponential distance dependence of the trapping force from the nanostructures, expected from the evanescent plasmon field.

physics.optics↗

arXiv2013

Nanocomposite NiO:Au hydrogen sensors with high sensitivity and low operating temperature

We present results on the development of nanocomposite NiO:Au thin-film hydrogen sensors, which are able to detect hydrogen concentrations as low as 2 ppm in air, operating at low temperatures in the range 125-150C. Thin NiO films were sputter-deposited on oxidized silicon substrates. The structural, morphological, and nanomechanical properties of the films were investigated with respect to post-deposition annealing. Au nanoparticles were added on the NiO surface via pulsed laser deposition and the films were tested as hydrogen sensors before and after Au deposition. The performance of the NiO films as hydrogen sensors improved significantly in the presence of Au nanoparticles on the surface. The detection limit (lowest detectable hydrogen concentration) decreased by two orders of magnitude, while the response time also decreased by a factor of three.

cond-mat.mtrl-sci↗