Showing papers by "Anvar A. Zakhidov published in 2019"
TL;DR: In this article, the authors acknowledge a support from the Strategic Fund of the Australian National University (SNU) and the Welch Foundation (grant AT 16-17) for nanostructures.
Abstract: This work was supported by the Ministry of Education and Science of the Russian Federation (project 16.8939.2017/8.9 for the section on devices) and Russian Science Foundation (project 17-73-20336 for the section on nanostructures). Y.K. acknowledges a support from the Strategic Fund of the Australian National University. A.Z. also acknowledges a partial support from the Welch Foundation (grant AT 16-17).
147 citations
TL;DR: This method allows one to fabricate single-mode perovskite microlasers operating at room temperature in a broad spectral range (550-800 nm) with Q-factors up to 5500 and is important for direct writing of fully integrated coherent light sources for advanced photonic and optoelectronic circuitry.
Abstract: Halide-perovskite microlasers have demonstrated fascinating performance owing to their low-threshold lasing at room temperature and low-cost fabrication. However, being synthesized chemically, controllable fabrication of such microlasers remains challenging, and it requires template-assisted growth or complicated nanolithography. Here, we suggest and implement an approach for the fabrication of microlasers by direct laser ablation of a thin film on glass with donut-shaped femtosecond laser beams. The fabricated microlasers represent MAPbBrxIy microdisks with 760 nm thickness and diameters ranging from 2 to 9 μm that are controlled by a topological charge of the vortex beam. As a result, this method allows one to fabricate single-mode perovskite microlasers operating at room temperature in a broad spectral range (550–800 nm) with Q-factors up to 5500. High-speed fabrication and reproducibility of microdisk parameters, as well as a precise control of their location on a surface, make it possible to fabricat...
130 citations
TL;DR: A novel approach to fabricate high-quality CsPbBr3 nanolasers obtained by rapid precipitation from dimethyl sulfoxide solution sprayed onto hydrophobic substrates at ambient conditions is reported, being the fastest method to the best of the authors' knowledge.
Abstract: Inorganic cesium lead halide perovskite nanowires, generating laser emission in the broad spectral range at room temperature and low threshold, have become powerful tools for the cutting-edge applications in the optoelectronics and nanophotonics. However, to achieve high-quality nanowires with the outstanding optical properties, it was necessary to employ long-lasting and costly methods of their synthesis, as well as postsynthetic separation and transfer procedures that are not convenient for large-scale production. Here we report a novel approach to fabricate high-quality CsPbBr3 nanolasers obtained by rapid precipitation from dimethyl sulfoxide solution sprayed onto hydrophobic substrates at ambient conditions. The synthesis technique allows producing the well-separated nanowires with a broad size distribution of 2-50 μm in 5-7 min, being the fastest method to the best of our knowledge. The formation of nanowires occurs via ligand-assisted reprecipitation triggered by intermolecular proton transfer from (CH3)2CHOH to H2O in the presence of a minor amount of water. The XRD patterns confirm an orthorhombic crystal structure of the as-grown CsPbBr3 single nanowires. Scanning electron microscopy images reveal their regular shape and truncated pyramidal end facets, while high-resolution transmission electron microscopy ones demonstrate their single-crystal structure. The lifetime of excitonic emission of the nanowires is found to be 7 ns, when the samples are excited with energy below the lasing threshold, manifesting the low concentration of defect states. The measured nanolasers of different lengths exhibit pronounced stimulated emission above 13 μJ cm-2 excitation threshold with quality factor Q = 1017-6166. Their high performance is assumed to be related to their monocrystalline structure, low concentration of defect states, and improved end facet reflectivity.
62 citations
TL;DR: This work fabricates high-quality CsPbBr3-xClx perovskite thin films using a wet chemical method accompanied by a chemical vapor anion exchange procedure, which allows rigorously studying their optical and structural properties at different compositions.
Abstract: All-inorganic lead halide perovskites of various compositions have emerged as a prospective family of materials for light-emitting devices and photonic applications. However, a comprehensive study of their structural and electronic properties is still missing. Moreover, thin film fabrication of these perovskites comprising heterohalide anions by wet chemistry approaches also remains challenging. Here we fabricate high-quality CsPbBr3-xClx perovskite thin films using a wet chemical method accompanied by a chemical vapor anion exchange procedure, which allows rigorously studying their optical and structural properties at different compositions. Namely, we present both the numerical and experimental studies of the electronic properties of all-inorganic mixed-halide perovskites, showing their optical absorption, excitonic photoluminescence and exciton binding energy, phase, chemical composition, and band structure and the band gap evolution with a gradual change in x in CsPbBr3-xClx. The results reveal that as Cl ions substitute for Br ones in the perovskite crystal lattice the room-temperature phase does not change its orthorhombic symmetry, whereas the energy of the direct electronic transition from the valence to conduction band at the Γ-point increases nonlinearly. By using the experimentally derived nonlinear dependence it is easy to accurately predict the band gap for any CsPbBr3-xClx perovskite thin film consisting of grains with sizes beyond the quantum confinement regime.
57 citations
TL;DR: In this paper, the perovskite light-emitting diodes (PeLEDs) have drawn considerable attention for their favorable optoelectronic properties, and they have been used in a variety of applications.
Abstract: Perovskite light-emitting diodes (PeLEDs) have drawn considerable attention for their favorable optoelectronic properties. Perovskite light-emitting electrochemical cells (PeLECs)—devices that util...
44 citations
TL;DR: Experimental and theoretical results for MAPbBr3 nanoparticles of various sizes show that for particle radii comparable with the Bohr radius of the exciton, the blue-shift of the photoluminescence, scattering, and absorption cross-section peaks related to quantum confinement should be dominating due to the weakness of Mie resonances for such small sizes.
Abstract: Halide perovskite nanoparticles have demonstrated pronounced quantum confinement properties for nanometer-scale sizes and strong Mie resonances for 102 nm sizes. Here we studied the intermediate sizes where the nonlocal response of the exciton affects the spectral properties of Mie modes. The mechanism of this effect is associated with the fact that excitons in nanoparticles have an additional kinetic energy that is proportional to k2, where k is the wavenumber. Therefore, they possess higher energy than in the case of static excitons. The obtained experimental and theoretical results for MAPbBr3 nanoparticles of various sizes (2–200 nm) show that for particle radii comparable with the Bohr radius of the exciton (a few nanometers in perovskites), the blue-shift of the photoluminescence, scattering, and absorption cross-section peaks related to quantum confinement should be dominating due to the weakness of Mie resonances for such small sizes. On the other hand, for larger sizes (more than 50–100 nm), the influence of Mie modes increases, and the blue shift remains despite the fact that the effect of quantum confinement becomes much weaker.
41 citations
TL;DR: In this paper, a dual functional device based on mixed halide perovskite CH3NH3PbBr2I can be switched from solar cells to LED with low threshold voltage.
23 citations
TL;DR: In this article, the authors studied the temperature-tunable reconfiguration of photonic modes in periodically nanostructured perovskite (MAPbI3) film probed by enhanced photoluminescence.
22 citations
TL;DR: A wide range of AgNW/MWNT hybrid TCEs with optimized optoelectronic properties can be achieved depending of the requirements needed depending on the initial transparency of the MWNT aerogels.
Abstract: Flexible, free-standing transparent conducting electrodes (TCEs) with simultaneously tunable transmittances up to 98% and sheet resistances down to 11 Ω/sq were prepared by a facile spray-coating method of silver nanowires (AgNWs) onto dry-spun multiwall carbon nanotube (MWNT) aerogels. Counterintuitively, the transmittance of the hybrid electrodes can be increased as the mass density of AgNWs within the MWNT aerogels increases; however, the final achievable transmittance depends on the initial transparency of the MWNT aerogels. Simultaneously, a strong decrease in sheet resistance is obtained when AgNWs form a percolated network along the MWNT aerogel. Additionally, anisotropic reduction in sheet resistance and polarized transmittance of AgNW/MWNT aerogels is achieved with this method. The final AgNW/MWNT hybrid TCEs transmittance and sheet resistance can be fine-tuned by spray-coating mechanisms or by choosing initial MWNT aerogel density. Thus, a wide range of AgNW/MWNT hybrid TCEs with optimized optoelectronic properties can be achieved depending of the requirements needed. Finally, the free-standing AgNW/MWNT hybrid TCEs can be laminated onto a wide range of substrates without the need of a bonding aid.
21 citations
TL;DR: In this paper, the perovskite nanostructures not only improve absorption of the incident laser pulses, but also lead to a non-symmetric near field distribution.
Abstract: Abstract Lead halide perovskites were known to be a prospective family of materials for terahertz (THz) generation. On the other hand, perovskite nanostructures, nanoantennas, and metasurfaces allow tailoring perovskites optical characteristics, resulting in more efficient interaction with incident or emitted light. Moreover, the perovskites are robust materials against formation of defects caused by mechanical deformations and can be efficiently nanostructured by various high throughput methods. In this work, we have enhanced THz emission from MAPbI3 perovskite upon femtosecond laser irradiation using nanoimprint lithography. The formed nanostructures not only improve absorption of the incident laser pulses, but also lead to a non-symmetric near-field distribution. As a result, we have enhanced the efficiency of THz emission from the nanostructured perovskite by 3.5 times as compared with a smooth perovskite film. Our results paved the way for a new application of large-scale perovskite nanostructuring, making halide perovskites competitive with more expensive conventional semiconductors for THz generation.
16 citations
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TL;DR: In this article, the first single-particle all-dielectric monolithic nanolaser driven by Mie resonances in visible and near-IR frequency range was demonstrated.
Abstract: All-dielectric subwavelength structures utilizing Mie resonances provide a novel paradigm in nanophotonics for controlling and manipulating light. So far, only spontaneous emission enhancement was demonstrated with single dielectric nanoantennas, whereas stimulated emission was achieved only in large lattices supporting collective modes. Here, we demonstrate the first single-particle all-dielectric monolithic nanolaser driven by Mie resonances in visible and near-IR frequency range. We employ halide perovskite CsPbBr$_3$ as both gain and resonator material that provides high optical gain (up to $\sim 10^4$ cm$^{-1}$) and allows simple chemical synthesis of nanocubes with nearly epitaxial quality. Our smallest non-plasmonic Mie-resonant single-mode nanolaser with the size of 420 nm operates at room temperatures and wavelength 535 nm with linewidth $\sim 3.5$ meV. These novel lasing nanoantennas can pave the way to multifunctional photonic designs for active control of light at the nanoscale.
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TL;DR: In this article, a spray-coating method of silver nanowires (AgNWs) onto dry-spun multi-wall carbon nanotube (MWNT) aerogels was used to obtain flexible, free-standing transparent conducting electrodes (TCEs) with simultaneously tunable transmittances up to 98% and sheet resistances down to 11 ε/sq.
Abstract: Flexible, free-standing transparent conducting electrodes (TCEs) with simultaneously tunable transmittances up to 98% and sheet resistances down to 11 {\Omega}/sq were prepared by a facile spray-coating method of silver nanowires (AgNWs) onto dry-spun multiwall carbon nanotube (MWNT) aerogels. Counterintuitively, the transmittance of the hybrid electrodes can be increased as the mass density of AgNWs within the MWNT aerogels increase, however, the final achievable transmittance depends on the initial transparency of the MWNT aerogels. At the same time, a strong decrease in sheet resistance is obtained when AgNWs form a percolated network along the MWNT aerogel. Additionally, anisotropic reduction in sheet resistance and polarized transmittance of AgNWs/MWNTs aerogel is achieved with this method. The final AgNWs/MWNTs hybrid TCEs transmittance and sheet resistance can be fine-tuned by spray-coating mechanisms or by the choice of initial MWNT aerogel density. Thus, a wide range of AgNWs/MWNTs hybrid TCEs with optimized optoelectronic properties can be achieved depending of the requirements needed. Finally, the free-standing AgNWs/MWNTs hybrid TCEs can be laminated onto a wide range of substrates without the need of a bonding aid.
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TL;DR: In this paper, the authors presented an easy-to-do transparent ambipolar light emitting subpixel based on inorganic perovskite and single wall carbon nanotubes.
Abstract: Perovskite light-emitting diodes (PeLEDs) have recently attracted great research luminescence at room temperature in interest for their narrow emissions and solution processability. Remarkable progress has been achieved PeLEDs in recent years. Here we present the new configuration of ambipolar transparent perovskite light emitting device. The combination of voltage induced p-i-n formation and ionically doped carbon electrodes and allows electroluminescence in forward and reverse bias. Here we present easy-to-do transparent ambipolar light emitting subpixel based on inorganic perovskite and single wall carbon nanotubes. For this experiment PeLEDs were assembled using a glass substrate with ITO stripes as bottom electrode; spin-coated CsPbBr3/I3:PEO composite as emissive layer; single wall carbon nanotubes deposited by a simple press transfer process at room temperature. We demonstrate a concept of stacked multicolor tandem pixel. Stack of transparent light emitting units might allow fine color tuning in parallel tandem connection without segregation compared to mixed halide perovskites. This configuration conforms pixel downsizing and make to fabrication of emissive multijunction pixels in a stack.
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TL;DR: In this article, an ionically gated planar PS-PV solar cell with ultra-thick fullerene ETL with a porous CNT electron collector on top of it was demonstrated.
Abstract: We demonstrate an ionically gated planar PS-PV solar cell with ultra-thick fullerene ETL with a porous CNT electron collector on top of it. Perovskite photovoltaic devices usually have undoped electron transport layers, usually thin like C60 due to its high resistance. Metallic low work function cathodes are extremely unstable in PS-PV due to reaction with halogens I-/Br-, and it would be desirable to have stable carbon cathodes on top of thick low resistance ETL for enhancing the stability of PS-PVs. We show that gating such top CNT cathode in ionic liquid, as part of a supercapacitor charged by Vg tunes the Fermi level of CNT by EDL charging, and causes lowering of a barrier at of C60/C70 ETL. Moreover, at higher gating voltage ions further propagates into fullerene by electrochemical n-doping, which increases dramatically PV performance by raising mostly two parameters: Isc and FF, resulting in PCE efficiency raised from 3 % to 11 %. N-doping of ETL strongly enhances charge collection by ETL and CNT raising Isc and lowering series resistance and thus increasing strongly PCE. Surprisingly Voc is not sensitive in PS-PV to external Vg gating, on the contrary, to strongly enhanced Voc in ionically gated organic PV, where it is the main gating effect. This insensitivity of Voc to lowering of the work function of Vg gated CNT electrode is a clear indication that Voc in PS-PV is determined by inner p-i-n junction formation in PS itself, via accumulation of its intrinsic mobile ionic species halogens and cations and their vacancies.
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TL;DR: In this paper, a single layer perovskite light-emitting electrochemical cells (PeLEC) from CsPbBr3:PEO:LiPF6 with 0.5% wt. LiPF6 produced highly efficient (22 cd/A) and bright (~15000 cd/m2) electroluminescence.
Abstract: Perovskite light-emitting diodes (PeLEDs) have drawn considerable attention for their favorable optoelectronic properties. Perovskite light-emitting electrochemical cells (PeLECs) _ devices that utilize mobile ions _ have recently been reported but have yet to reach the performance of the best PeLEDs. We leveraged a poly(ethylene oxide) electrolyte and lithium dopant in CsPbBr3 thin films to produce PeLECs of improved brightness and efficiency. In particular, we found that a single layer PeLEC from CsPbBr3:PEO:LiPF6 with 0.5% wt. LiPF6 produced highly efficient (22 cd/A) and bright (~15000 cd/m2) electroluminescence. To understand this improved performance among PeLECs, we characterized these perovskite thin films with photoluminescence (PL) spectroscopy, scanning electron microscopy (SEM), atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS), and X-ray diffraction (XRD). These studies revealed that this optimal LiPF6 concentration improves electrical double layer formation, reduces the occurrence of voids, charge traps, and pinholes, and increases grain size and packing density.
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TL;DR: In this article, the authors demonstrate controllable band bending due to migration of both cation and anion ions in mixed halide perovskite devices and demonstrate that the band structure rearrangement is demonstrated in light emitting solar cells based on the perov-skite with organic cations methylammonium (MA+) and formamidinium (FA+), possessing non-zero dipole momentum of 2.29 and 0.21 Debye, respectively, and with PEDOT:PSS and C60 transport layers having a high barrier
Abstract: Ionic migration in organo-halide perovskites plays an important role in operation of perovskite based solar cells and light emitting diodes. Despite the ionic migration being a reversible process, it often leads to worsening of perovskite based device performance, hysteresis in current-voltage characteristics, and phase segregation in mixed halide perovskites being as the most harmful effect. The reason is in dynamical band structure changes, which controllable engineering would solve one of the biggest challenges for development of light-emitting solar cells. Here we demonstrate controllable band bending due to migration of both cation and anion ions in mixed halide perovskite devices. The band structure rearrangement is demonstrated in light emitting solar cells based on the perovskite with organic cations methylammonium (MA+) and formamidinium (FA+), possessing non-zero dipole momentum of 2.29 and 0.21 Debye, respectively, and with PEDOT:PSS and C60 transport layers having a high barrier of 0.8 eV for charge injection. Under applied external voltage MA+ and FA+ cations move towards the electron transport layer and form a dipole layer at the perovskite/electron transport interface, which lowers threshold voltage for electroluminescence down to 1.7 V for MAPbBr2I and 2.6 V for FAPbBr2I, whereas monohalide perovskite MAPbBr3 does not demonstrate such behavior. This ability to in-situ change the device band structure paves the way developing of dual-functional devices based on simple design. It also makes mixed halide perovskites more flexible than mono halides ones for developing different optoelectronic devices without the use of special types of work function modifying transport materials.
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TL;DR: In this article, a morphological, structural and interfacial engineering of CH3NH3PbBr3 (MAPbBBr3) thin films to improve perovskite's intrinsic stability, as well as high quality cavity design to reduce the operational power is proposed.
Abstract: Metal halide perovskites have emerged as promising gain materials for on-chip lasers in photonic integrated circuits (PICs). However, stable continuous wave (CW) lasing behavior under optical pumping at room temperature - a prerequisite for electrically pumped lasing - has not yet been demonstrated. To achieve stable CW operation, we introduce a multiplex of strategies that include morphological, structural and interfacial engineering of CH3NH3PbBr3 (MAPbBr3) thin films to improve perovskite's intrinsic stability, as well as high quality cavity design to reduce the operational power. We demonstrate for the first time, over 90-minute-long green CW lasing with 9.4W/cm2 threshold from a polycarbonate (PC)-defect-passivated, directly patterned MAPbBr3 two-dimensional photonic crystal (PhC) cavity without any substrate cooling. We also show our approach's effectiveness on the performance of MAPbBr3 under electrical excitation: we observe a seven-fold current efficiency enhancement by applying our strategies to a MAPbBr3 LED. This work paves the way to the realization of electrically pumped lasing in perovskites.
05 May 2019
TL;DR: In this paper, a direct patterning of methylammonium lead bromide (MAPbBr 3 )perovskite enabled green lasing in two-dimensional photonic crystal on the Si platform, under continuous wave pumping at room temperature.
Abstract: Direct patterning of methylammonium lead bromide (MAPbBr 3 )perovskite enabled green lasing in two-dimensional photonic crystal on the Si platform, under continuous wave pumping at room temperature for the first time. © 2019 The Author(s)