Author Affiliations
Abstract
1 Institute of Electronic Structure and Laser (IESL), Foundation for Research and Technology (FORTH), N. Plastira 100, Vassilika Vouton, Heraklion 70013, Greece
2 Department of Physics, University of Crete, Heraklion 71003, Greece
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We present a novel approach for tailoring the laser induced surface topography upon femtosecond (fs) pulsed laser irradiation. The method employs spatially controlled double fs laser pulses to actively regulate the hydrodynamic microfluidic motion of the melted layer that gives rise to the structures formation. The pulse train used, in particular, consists of a previously unexplored spatiotemporal intensity combination including one pulse with Gaussian and another with periodically modulated intensity distribution created by Direct Laser Interference Patterning (DLIP). The interpulse delay is appropriately chosen to reveal the contribution of the microfluidic melt flow, while it is found that the sequence of the Gaussian and DLIP pulses remarkably influences the surface profile attained. Results also demonstrate that both the spatial intensity of the double pulse and the effective number of pulses per irradiation spot can further be modulated to control the formation of complex surface morphologies. The underlying physical processes behind the complex patterns’ generation were interpreted in terms of a multiscale model combining electron excitation with melt hydrodynamics. We believe that this work can constitute a significant step forward towards producing laser induced surface structures on demand by tailoring the melt microfluidic phenomena.
laser-matter interaction direct laser interference patterning surface functionalization laser micro/nano fabrication Opto-Electronic Advances
2022, 5(3): 210052
Author Affiliations
Abstract
1 Institute of Electronic Structure and Laser (IESL), Foundation for Research and Technology-Hellas (FORTH), Herakleio 70013, Greece
2 Electrical and Computer Engineering Department, Hellenic Mediterranean University, Herakleio 71004, Greece
3 Department of Materials Science and Technology, University of Crete, Herakleio 70013, Greece
4 Department of Physics, University of Crete, Herakleio 70013, Greece
Despite that organic-inorganic lead halide perovskites have attracted enormous scientific attention for energy conversion applications over the recent years, the influence of temperature and the type of the employed hole transport layer (HTL) on the charge carrier dynamics and recombination processes in perovskite photovoltaic devices is still largely unexplored. In particular, significant knowledge is missing on how these crucial parameters for radiative and non-radiative recombinations, as well as for efficient charge extraction vary among different perovskite crystalline phases that are induced by temperature variation. Herein, we perform micro photoluminescence (μPL) and ultrafast time resolved transient absorption spectroscopy (TAS) in Glass/Perovskite and two different Glass/ITO/HTL/Perovskite configurations at temperatures below room temperature, in order to probe the charge carrier dynamics of different perovskite crystalline phases, while considering also the effect of the employed HTL polymer. Namely, CH3NH3PbI3 films were deposited on Glass, PEDOT:PSS and PTAA polymers, and the developed Glass/CH3NH3PbI3 and Glass/ITO/HTL/CH3NH3PbI3 architectures were studied from 85 K up to 215 K in order to explore the charge extraction dynamics of the CH3NH3PbI3 orthorhombic and tetragonal crystalline phases. It is observed an unusual blueshift of the bandgap with temperature and the dual emission at temperature below of 100 K and also, that the charge carrier dynamics, as expressed by hole injection times and free carrier recombination rates, are strongly depended on the actual pervoskite crystal phase, as well as, from the selected hole transport material.Despite that organic-inorganic lead halide perovskites have attracted enormous scientific attention for energy conversion applications over the recent years, the influence of temperature and the type of the employed hole transport layer (HTL) on the charge carrier dynamics and recombination processes in perovskite photovoltaic devices is still largely unexplored. In particular, significant knowledge is missing on how these crucial parameters for radiative and non-radiative recombinations, as well as for efficient charge extraction vary among different perovskite crystalline phases that are induced by temperature variation. Herein, we perform micro photoluminescence (μPL) and ultrafast time resolved transient absorption spectroscopy (TAS) in Glass/Perovskite and two different Glass/ITO/HTL/Perovskite configurations at temperatures below room temperature, in order to probe the charge carrier dynamics of different perovskite crystalline phases, while considering also the effect of the employed HTL polymer. Namely, CH3NH3PbI3 films were deposited on Glass, PEDOT:PSS and PTAA polymers, and the developed Glass/CH3NH3PbI3 and Glass/ITO/HTL/CH3NH3PbI3 architectures were studied from 85 K up to 215 K in order to explore the charge extraction dynamics of the CH3NH3PbI3 orthorhombic and tetragonal crystalline phases. It is observed an unusual blueshift of the bandgap with temperature and the dual emission at temperature below of 100 K and also, that the charge carrier dynamics, as expressed by hole injection times and free carrier recombination rates, are strongly depended on the actual pervoskite crystal phase, as well as, from the selected hole transport material.
transient absorption spectroscopy μ-photoluminescence variable temperature perovskite crystalline phases hole transport layer charge carrier dynamics Opto-Electronic Science
2022, 1(4): 210005
Author Affiliations
Abstract
1 Institute of Electronic Structure and Laser, Foundation for Research and Technology-Hellas, Heraklion Crete 71110, Greece
2 Department of Materials Science and Technology, University of Crete, Heraklion Crete 71003, Greece
3 Department of Physics, University of Crete, Heraklion Crete 71003, Greece
We report the femtosecond (fs) laser fabrication of biomimetic omnidirectional iridescent metallic surfaces exhibiting efficient diffraction for practically any angle of light incidence. Such diffractive behavior is realized by means of multi-directional low-spatial-frequency, laser-induced periodic surface structures (LSFL) formed upon exploiting the cylindrical symmetry of a cylindrical vector (CV) fs field. We particularly demonstrate that the multi-directional gratings formed on stainless steel surface by a radially polarized fs beam, could mimic the omnidirectional structural coloration properties found in some natural species. Accordingly, the fabricated grating structures can spatially disperse the incident light into individual wavelength with high efficiency, exhibiting structural iridescence at all viewing angles. Analytical calculations using the grating equation reproduced the characteristic variation of the vivid colors observed as a function of incident angle. We envisage that our results will significantly contribute to the development of new photonic and light sensing devices.
laser processing structural colors radial polarisation Opto-Electronic Advances
2020, 3(5): 05190035
Author Affiliations
Abstract
1 Institute of Electronic Structure and Laser, Foundation for Research and Technology-Hellas, Heraklion Crete 71110, Greece
2 Department of Physics, University of Crete, Heraklion Crete 71003, Greece
3 Department of Materials Science and Technology, University of Crete, Heraklion Crete 71003, Greece
We use laser-scanning nonlinear imaging microscopy in atomically thin transition metal dichalcogenides (TMDs) to reveal information on the crystalline orientation distribution, within the 2D lattice. In particular, we perform polarization-resolved second-harmonic generation (PSHG) imaging in a stationary, raster-scanned chemical vapor deposition (CVD)-grown WS2 flake, in order to obtain with high precision a spatially resolved map of the orientation of its main crystallographic axis (armchair orientation). By fitting the experimental PSHG images of sub-micron resolution into a generalized nonlinear model, we are able to determine the armchair orientation for every pixel of the image of the 2D material, with further improved resolution. This pixel-wise mapping of the armchair orientation of 2D WS2 allows us to distinguish between different domains, reveal fine structure, and estimate the crystal orientation variability, which can be used as a unique crystal quality marker over large areas. The necessity and superiority of a polarization-resolved analysis over intensity-only measurements is experimentally demonstrated, while the advantages of PSHG over other techniques are analysed and discussed.
nonlinear imaging of 2D materials crystal orientation mapping crystal quality marker polarization-resolved second-harmonic generation atomically thin transition metal dichalcogenides graphene-related materials Opto-Electronic Advances
2019, 2(11): 11190026
