near-IR Spectral Range Research Articles

(Invited) Ultrafast Excited Electron Relaxation in Triply Fused Ni(II) Porphyrin-Nanographene Conjugates for Energy Conversion

Porphyrins are appealing building blocks for solar energy applications, although their photosensitization capability is limited by their large optical energy gap, resulting in a mismatch in absorption for efficient harvesting of the solar spectrum. Porphyrin π-extension by edge-fusing with nanographenes can be employed to narrow their optical energy gap, enabling the development of porphyrin-based panchromatic dyes with an optimized energy onset for solar energy conversion in dye-sensitized solar fuel and solar cell configurations. Metalloporphyrin-nanographene conjugates based on open-shell transition metals, such as Ni(II), exhibit panchromatic absporption covering the entire visible and part of the near-IR spectral range. Dispite this interesting property, they exhibit fast excited-state electronic relaxation across the Ni d levels, which hampers harnessing photoexcited electrons to trigger photophysical or photochemical reactions. In this work, we shed light into the underlying mechanism behind fast non-radiative relaxation in these systems. Variable temperature transient absorption and global fit analysis are combined with time-dependent density functional theory to produce a picture of the relevant excited states and underlying relaxation pathways in the conjugates. At room temperature, photoexcitation to the lowest S1* energy level is followed by vibrational cooling in 1-2 ps, and intersystem crossing in > 10 ps, setting a short temporal window wherein a small fraction of relaxed singlets decay to the ground state. Following intersystem crossing and triplet internal conversion, triplets relax rapidly to the ground state (S0) in few tens of picoseconds. By performing measurements at low temperature, we provide evidences for the interplay of a lowest terminal triplet level with > 1 ns lifetime which acts as a bottleneck, and a sloped conical intersection to S0* which is thermally accessible at room temperature from the former energy level. The overall triplet decay is dictated by the contributions that fall along these two photophysical branches. This observation bears significance in understanding how nanographene functionalization leads to a profound effect, opening avenues for potential applications in Optoelectronics and related fields.[1] Garcia-Orrit, S., Vega-Mayoral, V., Chen, Q., Serra, G., Paternò, G. M., Cánovas, E., Narita, A., Müllen, K., Tommasini, M., Cabanillas-González, J., Nanographene-Based Decoration as a Panchromatic Antenna for Metalloporphyrin Conjugates. Small 2023, 19, 2301596.[2] Garcia-Orrit, S. et al., in preparation Figure 1

Multi-wavelength and broadband plasmonic switching with V-shaped plasmonic nanostructures on a VO2 coated plasmonic substrate

In this paper, periodic arrays of identical V-shaped gold nanostructures and variable V-shaped gold nanostructures are designed on top of a gold-coated silicon dioxide (SiO2) substrate with a thin spacer layer of vanadium dioxide (VO2) to realize multi-wavelength and broadband plasmonic switches, respectively. The periodic array of identical V-shaped nanostructures (IVNSs) with small inter-particle separation leads to coupled interactions of the elementary plasmons of a V-shaped nanostructure (VNS), resulting in a hybridized plasmon response with two longitudinal plasmonic modes in the reflectance spectra of the proposed switches when the incident light is polarized in the x-direction. The x-direction is oriented along the axis that joins the V-junctions of all VNSs in one unit cell of the periodic array. On exposure to temperature, electric field, or optical stimulus, the VO2 layer transforms from its monoclinic semiconducting state to its rutile metallic state, leading to an overall change in the reflectance spectra obtained from the proposed nanostructures and resulting in an efficient multi-wavelength switching action. Finite difference time domain modelling is employed to demonstrate that an extinction ratio (ER) >12 dB at two wavelengths can be achieved by employing the proposed switches based on periodic arrays of IVNSs. Further, plasmonic switches based on variable V-shaped nanostructures—i.e. multiple VNSs with variable arm lengths in one unit cell of a periodic array—are proposed for broadband switching. In the broadband operation mode, we report an ER >5 dB over an operational wavelength range >1400 nm in the near-IR spectral range spanning over all optical communication bands, i.e. the O, E, S, C, L and U bands. Further, it is also demonstrated that the wavelength of operation for these switches can be tuned by varying the geometrical parameters of the proposed switches. These switches have the potential to be employed in communication networks where ultrasmall and ultrafast switches with multi-wavelength operation or switching over a wide operational bandwidth are inevitably required.

Femtosecond laser activation of the photochemistry of bismuth and associated three-dimensional sub-micron fluorescence patterning

Localized sub-micrometer-scale visible and near-IR fluorescence structures have been achieved in three-dimension (3D) thanks to femtosecond laser-activated photochemistry of Bismuth in a Bismuth-doped phosphate glass. These structures exhibit high fluorescence contrast with good spatial resolution with spectral emission in the red and near-IR ranges. These fluorescence properties arise from femtosecond laser-induced multi-photon absorption and the creation of free electrons, which activates local redox reactions of Bi3+ that allow for the dose-dependent formation of low valence Bismuth ions such as Bi2+ and Bi+. These new species promote not only new selective fluorescence emission properties in the VIS and near-IR spectral range but also co-localized positive refractive index changes. The thermal treatment of 3D patterns evidences the possibility of Bismuth cluster formation with good thermal stability up to the glass temperature transition. These observations open the way for laser-inscribed photonic integrated circuits for potential laser amplification devices in the second telecommunication windows around 1.3 μm.

Distribution of atmospheric aerosols during the 2007 Mars dust storm (MY 28): Solar infrared occultation observations by SPICAM

Solar occultation measurements by the SPICAM IR on Mars-Express have been used to study aerosol vertical distribution during the 2007 global dust storm (GDS) of Mars Year 28. Measurements in the near-IR spectral range from 1 to 1.7 μm provide information about aerosol optical properties, extinction coefficient, particle size and number density. The observations were performed at Ls = 254–302° of MY28 and latitudes from 65°S to 65°N. Within the SPICAM spectral range we could not distinguish between absorption due to dust or water ice. The particle size distribution and its parameters, the effective radius reff and variance νeff, are retrieved assuming either mineral dust or water ice refraction indices. Before the MY 28 GDS at Ls < 265° the aerosol was detected from 20 to 60 km with dust particle size ∼0.75 μm below 50 km and decreasing with altitude above. The detached layers, presumably consisting of water ice, were observed at ∼60 km in the Southern hemisphere and 45 km in the Northern and Southern hemispheres with opacity <0.02 and 0.01–0.15, respectively. The effective radius varied from 0.2 to 1.6 μm with number density from 0.4 to 50 cm−3. With the development of the GDS dust reached to 80 km and higher, while reff tended to increase with altitude up to 0.9–1 μm at 70–75 km. The dust number density decreased from 2 to 4 cm−3 at 40 km to 0.1 cm−3 at 70–80 km. The dependence of the effective variance on altitude and season has been studied. Before the beginning GDS νeff varied below 50–60 km from 0.2 to 0.4 in the Southern hemisphere to 0.4–0.6 in the Northern hemisphere. During the GDS, the wider distribution propagated higher, with νeff ∼ 0.5 up to 70 km in the southern hemisphere. In high latitudes of both hemispheres at Ls = 268–275° optically thin water ice high altitude clouds were detected at 80–90 km with reff < 0.5 μm and number density 10–100 cm−3.

On the Theoretical Basis of the Thermal Mechanism of Local Oxygenation of Biological Tissue under the Influence of Low-intensity Radiation in the Near-IR Range

Possible thermal mechanisms of photodynamic effects on biological tissues of low-intensity quasimonochromatic optical radiation in the near-IR spectral range are analyzed with the aim of developing a method of local non-invasive oxygenation.

Nanopatterned Back-Reflector with Engineered Near-Field/Far-Field Light Scattering for Enhanced Light Trapping in Silicon-Based Multijunction Solar Cells.

Multijunction solar cells provide a path to overcome the efficiency limits of standard silicon solar cells by harvesting a broader range of the solar spectrum more efficiently. However, Si-based multijunction architectures are hindered by incomplete harvesting in the near-infrared (near-IR) spectral range as Si subcells have weak absorption close to the band gap. Here, we introduce an integrated near-field/far-field light trapping scheme to enhance the efficiency of silicon-based multijunction solar cells in the near-IR range. To achieve this, we design a nanopatterned diffractive silver back-reflector featuring a scattering matrix that optimizes trapping of multiply scattered light into a range of diffraction angles. We minimize reflection to the zeroth order and parasitic plasmonic absorption in silver by engineering destructive interference in the patterned back-contact. Numerical and experimental assessment of the optimal design on the performance of single-junction Si TOPCon solar cells highlights an improved external quantum efficiency over a planar back-reflector (+1.52 mA/cm2). Nanopatterned metagrating back-reflectors are fabricated on GaInP/GaInAsP//Si two-terminal triple-junction solar cells via substrate conformal imprint lithography and characterized optically and electronically, demonstrating a power conversion efficiency improvement of +0.9%abs over the planar reference. Overall, our work demonstrates the potential of nanophotonic light trapping for enhancing the efficiency of silicon-based multijunction solar cells, paving the way for more efficient and sustainable solar energy technologies.

Colloidal 2D Lead Chalcogenide Nanocrystals: Synthetic Strategies, Optical Properties, and Applications.

Lead chalcogenide nanocrystals (NCs) are an emerging class of photoactive materials that have become a versatile tool for fabricating new generation photonics devices operating in the near-IR spectral range. NCs are presented in a wide variety of forms and sizes, each of which has its own unique features. Here, we discuss colloidal lead chalcogenide NCs in which one dimension is much smaller than the others, i.e., two-dimensional (2D) NCs. The purpose of this review is to present a complete picture of today's progress on such materials. The topic is quite complicated, as a variety of synthetic approaches result in NCs with different thicknesses and lateral sizes, which dramatically change the NCs photophysical properties. The recent advances highlighted in this review demonstrate lead chalcogenide 2D NCs as promising materials for breakthrough developments. We summarized and organized the known data, including theoretical works, to highlight the most important 2D NC features and give the basis for their interpretation.

Electron density and temperature in a diffuse nanosecond pulse discharge in air at atmospheric pressure

This work presents the first experimental results on the electron properties of a nanosecond diffuse fast ionisation wave generated in synthetic dry air at atmospheric pressure under very strong overvoltage. Both density and mean temperature of electrons are investigated by incoherent Thomson scattering. The electron density is also derived from the Stark broadening of oxygen lines resolved by optical emission spectroscopy. The extreme voltages applied question some common hypothesis of the diagnostics implemented. The solutions adopted and the remaining limitations are discussed in the paper. Each diagnostic covers a specific region of interest within the discharge and they show good agreement in conditions where they overlap. It is shown that most of the volume of the pin-to-plane discharge is quite representative of a quasi-steady state glow discharge dominated by the emission of the first and second positive systems of nitrogen. Once its propagation completed within the first two nanoseconds and until the end of the 10 ns pulse, it is characterized by rather homogeneous properties close to the axis. The electron density is of the order of 1015 cm−3 and the mean temperature is about 3 eV within the whole air gap. About 6 ns after the start of the discharge from the pin, a sub-millimetric region of strong ionization develops at the pin, which is consistent with the observation of a continuum of emission spreading from the UV to the near-IR spectral range. Within this part of the discharge, the electron density reaches values greater than 1017 cm−3 with an ionization degree higher than 1%. The radiative recombination of nitrogen ions N2 + and the three-body recombination of N+ with a large number of electrons could help to explain the continuum.

Improving the Efficiency of Organic Solar Cells via the Molecular Engineering of Simple Fused Non-Fullerene Acceptors

The development of novel non-fullerene small-molecule acceptors (NFAs) with a simple chemical structure for high-performance organic solar cells (OSCs) remains an urgent research challenge to enable their upscaling and commercialization. In this work, we report on the synthesis and comprehensive investigation of two new acceptor molecules (BTPT-OD and BTPT-4F-OD), which have one of the simplest fused structures among the Y series of NFAs, along with the medium energy bandgap (1.85 eV–1.94 eV) and strong absorption in the visible and near-IR spectral range (700–950 nm). The novel NFAs have high thermal stability, good solubility combined with a high degree of crystallinity, and deep-lying levels of the lowest unoccupied molecular orbital (up to −3.94 eV). The BTPT-OD with indan-1-one-3-dicyanvinyl terminal acceptor group is superior to its counterpart BTPT-4F-OD with 5,6-difluorindan-1-one-3-dicyanvinyl group both in the number of synthetic steps and in the photovoltaic performance in OSCs. PM6:BTPT-OD systems exhibit superior photovoltaic performance due to the higher charge mobility and degree of photoresponsiveness, faster carrier extraction, and longer carrier lifetime. As a result, BTPT-OD has almost two times higher photovoltaic performance with PM6 as a donor material due to the higher JSC and FF than BTPT-4F-OD systems. The results obtained indicate that further development of OSCs can be well achieved through a rational molecular design.

Zero-Background Small-Molecule Sensors for Near-IR Fluorescent Imaging of Biomacromolecular Targets in Cells.

In this study, we report a general approach to the design of a new generation of small-molecule sensors that produce a zero background but are brightly fluorescent in the near-IR spectral range upon selective interaction with a biomolecular target. We developed a fluorescence turn-on/-off mechanism based on the aggregation/deaggregation of phthalocyanine chromophores. As a proof of concept, we designed, prepared, and characterized sensors for in-cell visualization of epidermal growth factor receptor (EGFR) tyrosine kinase. We established a structure/bioavailability correlation, determined conditions for the optimal sensor uptake and imaging, and demonstrated binding specificity and applications over a wide range of treatment options involving live and fixed cells. The new approach enables high-contrast imaging and requires no in-cell chemical assembly or postexposure manipulations (i.e., washes). The general design principles demonstrated in this work can be extended toward sensors and imaging agents for other biomolecular targets.

Effect of Solubilizing Group on the Antibacterial Activity of Heptamethine Cyanine Photosensitizers.

Antibiotic resistance of pathogenic bacteria dictates the development of novel treatment modalities such as antimicrobial photodynamic therapy (APDT) utilizing organic dyes termed photosensitizers that exhibit a high cytotoxicity upon light irradiation. Most of the clinically approved photosensitizers are porphyrins that are poorly excitable in the therapeutic near-IR spectral range. In contrast, cyanine dyes function well in the near-IR region, but their phototoxicity, in general, is very low. The introduction of iodine atoms in the cyanine molecules was recently demonstrated to greatly increase their phototoxicity. Herein, we synthesized a series of the new iodinated heptamethine cyanine dyes (ICy7) containing various solubilizing moieties, i.e., negatively charged carboxylic (ICy7COOH) and sulfonic (ICy7SO3H) groups, positively charged triphenylphosphonium (ICy7PPh3), triethylammonium (ICy7NEt3) and amino (ICy7NH2) groups, and neutral amide (ICy7CONHPr) group. The effect of these substituents on the photodynamic eradication of Gram-positive (S. aureus) and Gram-negative (E. coli and P. aeruginosa) pathogens was studied. Cyanine dyes containing the amide and triphenylphosphonium groups were found to be the most efficient for eradication of the investigated bacteria. These dyes are effective at low concentrations of 0.05 µM (33 J/cm2) for S. aureus, 50 µM (200 J/cm2) for E. coli, and 5 µM (100 J/cm2) for P. aeruginosa and considered, therefore, promising photosensitizers for APDT applications. The innovation of the new photosensitizers consisted of a combination of the heavy-atom effect that increases singlet oxygen generation with the solubilizing group's effect improving cell uptake, and with effective near-IR excitation. Such a combination helped to noticeably increase the APDT efficacy and should pave the way for the development of more advanced photosensitizers for clinical use.

Study on Ultrathin Silver Film Transparent Electrodes Based on Aluminum Seed Layers with Different Structures.

Ag has the lowest electrical resistivity among all metals, and at the same time, the best optical properties in the visible and near-IR spectral range; it is therefore the most widely employed material for thin-metal-film-based transparent conductors. In this work, an ultra-thin transparent silver film electrode with aluminum as seed layer was prepared by a resistive thermal evaporation technique. Using a range of electrical, optical and surface morphology techniques, it can be noted that the presence of the thin layer of aluminum changes the growth kinetics (nucleation and evolution) of the thermal evaporation of Ag, leading to silver films with smooth surface morphology and high electrical conductivity, and the threshold thickness of the silver film is reduced. It is inferred that the aluminum layer showed a good infiltration effect on the ultra-thin silver film, by analyzing the transmittance spectrum, sheet resistance and surface morphology. Moreover, the average transmittance of silver film with 10 nm is 40% in the 400–2500 nm band, whereas the sheet resistance is 13 Ωsq −1. A series of experiments show that the introduction of Al seed layer has certain effect on improving the properties of transparent conductive silver films. Then, a new method for deposition of 1 nm Al seed layer was proposed; that is, the 1 nm aluminum infiltrated layer is divided into two or more layers, and the average transmittance of silver film with 5 nm is 60% in the 400–2500 nm band, whereas the sheet resistance does not exceed 100 Ω sq−1.

Synthesis of Titanium Nitride Nanoparticles by Pulsed Laser Ablation in Different Aqueous and Organic Solutions.

Owing to a strong photothermal response in the near-IR spectral range and very low toxicity, titanium nitride (TiN) nanoparticles (NPs) synthesized by pulsed laser ablation in liquids (PLAL) present a novel appealing object for photo-induced therapy of cancer, but the properties of these NPs still require detailed investigation. Here, we have elaborated methods of femtosecond laser ablation from the TiN target in a variety of liquid solutions, including acetonitrile, dimethylformamide, acetone, water, and H2O2, to synthesize TiN NPs and clarify the effect of liquid type on the composition and properties of the formed NPs. The ablation in all solvents led to the formation of spherical NPs with a mean size depending on the liquid type, while the composition of the NPs ranged from partly oxidized TiN to almost pure TiO2, which conditioned variations of plasmonic peak in the region of relative tissue transparency (670–700 nm). The degree of NP oxidation depended on the solvent, with much stronger oxidation for NPs prepared in aqueous solutions (especially in H2O2), while the ablation in organic solvents resulted in a partial formation of titanium carbides as by-products. The obtained results contribute to better understanding of the processes in reactive PLAL and can be used to design TiN NPs with desired properties for biomedical applications.

Interfaces Based on Laser-Structured Arrays of Carbon Nanotubes with Albumin for Electrical Stimulation of Heart Cell Growth.

Successful formation of electronic interfaces between living cells and electronic components requires both good cell viability and performance level. This paper presents a technology for the formation of nanostructured arrays of multi-walled carbon nanotubes (MWCNT) in biopolymer (albumin) layer for higher biocompatibility. The layer of liquid albumin dispersion was sprayed on synthesized MWCNT arrays by deposition system. These nanostructures were engineered using the nanosecond pulsed laser radiation mapping in the near-IR spectral range (λ = 1064 nm). It was determined that the energy density of 0.015 J/cm2 provided a sufficient structuring of MWCNT. The structuring effect occurred during the formation of C–C bonds simultaneously with the formation of a cellular structure of nanotubes in the albumin matrix. It led to a decrease in the nanotube defectiveness, which was observed during the Raman spectroscopy. In addition, laser structuring led to a more than twofold increase in the electrical conductivity of MWCNT arrays with albumin (215.8 ± 10 S/m). Successful electric stimulation of cells on the interfaces with the system based on a culture plate was performed, resulting in the enhanced cell proliferation. Overall, the MWCNT laser-structured arrays with biopolymers might be a promising material for extended biomedical applications.

Salisbury screen with lossy nonconducting materials: Way to increase spectral selectivity of absorption

We present a modified Salisbury screen design in which the thin absorbing metal layer is replaced with a layer of nonconducting lossy material. The conditions for total absorption in such a structure are explained using a simplified analytical model and rigorous numerical calculations. For the proof-of-principle experiments, germanium/silicon bilayers deposited on aluminium substrates are designed and manufactured. The structures demonstrate nearly perfect absorption in the near-IR spectral range. Compared to conventional Salisbury screens, a lossy semiconductor top layer exhibits increased spectral selectivity of absorption. The wavelength of nearly perfect absorption remains tunable by optimizing the thicknesses of the lossy and transparent layers.

Persistent near-infrared photoconductivity of ZnO nanoparticles based on plasmonic hot charge carriers

We report on the coupling of ZnO nanoparticles with plasmonic gold nanoislands in a solution-processed photodetector, which results in a clear enhancement in the optical absorption and the electrical responsivity of ZnO nanoparticles, to cover the visible and the near-IR (NIR) spectral range, well beyond its intrinsic optical absorption. This enhancement, which arises from the coupling between ZnO nanoparticles and the plasmonically mediated hot electron generation in the Au plasmonic nanoislands, results in a significant plasmonically driven photoresponse in the NIR of 2.5 × 10−5 A/W. The recorded photocurrent exhibits a persistent behavior, which is attributed to surface defect states in the ZnO nanoparticles. This study provides a route to the solution-processed, low-cost device fabrication schemes with important implications on low processing temperature optoelectronics technology to enhance the performance of photovoltaic devices over a wide solar spectrum. Additionally, this unusual behavior paves the way toward harnessing plasmonic resonances to probe and examine the surface defects of metal oxide semiconductors.

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

Αn 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.

Near-UV-to-Near-IR Hyperbolic Photonic Dispersion in Epitaxial (Hf,Zr)N/ScN Metal/Dielectric Superlattices

Hyperbolic metamaterials (HMMs) with extreme dielectric anisotropy have shown great promise in nanophotonic applications such as superlensing, enhancement of spontaneous emission, negative refraction, and the diverging photonic density of states. Noble metal-based metal/dielectric multilayers (e.g., Au/SiO2 and Ag/TiO2) and metallic (Au and Ag) nanowires embedded inside a dielectric matrix have been traditionally used to demonstrate HMM properties and for implementations into devices. Noble metals are, however, unstable at high temperatures, complementary metal oxide semiconductor incompatible, and difficult to deposit in thin-film form due to their high surface energies that limit their potential applications. TiN has emerged as an alternative plasmonic material to Au in recent years, and epitaxial TiN/Al0.72Sc0.28N metal/semiconductor superlattices were developed that exhibit excellent HMM properties. As TiN exhibits ε-near-zero (ENZ) at ∼500 nm, TiN/Al0.72Sc0.28N HMM also operates from ∼500 nm to long-wavelength regions. However, for several energy-conversion-related applications as well as for fundamental studies, it is desirable to achieve HMM wavelengths from the near-UV to the near-IR region of the spectrum. In this article, we demonstrate hyperbolic photonic dispersion in (Hf,Zr)N/ScN, a class of metal/semiconducting superlattice metamaterial that covers the near-UV to the near-IR spectral range. Epitaxial HfN/ScN, ZrN/ScN, and Hf0.5Zr0.5N/ScN superlattices are deposited on (001) MgO substrates and characterized with synchrotron-radiation X-ray diffraction as well as high-resolution electron microscopy techniques. Superlattices grow with cube-on-cube epitaxy and with sharp interfaces. Optical characterization reveals both type-I and type-II hyperbolic photonic dispersions as well as low losses and high figures-of-merit. Along with its high-temperature thermal stability, demonstration of HMM properties in (Hf,Zr)N/ScN metal/dielectric superlattices makes them potential candidates for HMM devices.

Световоды типа кварц-кварц с малыми потерями и тонкой полимерной оболочкой для ближнего ИК-спектрального диапазона.

The issues of obtaining silica optical fibers with SiO2/SiO2-F composition (where SiO2 is a core, and SiO2-F is a light-reflecting cladding) with low optical losses for the near-IR spectral range are considered. This fiber type is widely used in various fields of science and technology, including laser medicine. The study results of the dependence of the numerical aperture and fluorine concentration in silica glass of the formed fiber preforms on the Freon (C3F8) consumption in the gas phase when using a waveguide-type microwave plasmotron at the H10 wavelength, are presented. It is showed that to increase the fluorimeters sensitivity in the near-IR spectral range as probe fibers for detecting luminescence, it is promising to use quartz-quartz fibers with the “Heraeus” glass core and the reflective SiO2-F cladding with an increased fluorine content in the glass (up to 7 wt. %). In this case, the numerical aperture of such fibers will reach values up to 0.32. For laser procedures in ophthalmology, surgery, phlebology and etc., optical fibers with a standard numerical aperture 0.20-0.24 can be used (with a fluorine concentration in the glass up to 3 wt. %).

Modelling Mie scattering in pyrolite in the laser-heated diamond anvil cell: Implications for the core-mantle boundary temperature determination

The core-mantle boundary (CMB) at ~2900 km depth and ~135 GPa is the interface between the solid silicate mantle and the liquid metallic outer core. The temperature at CMB (TCMB) is a key parameter in assessing the heat flow out of the core and is thus important for our understanding of the geodynamo and mantle convection. The upper bound on TCMB is constrained by the solidus temperature (onset of melting) of pyrolite, a chemical proxy of the mantle rock, at ~135 GPa because the lowermost mantle is predominantly solid. Previous laser-heated diamond anvil cell (LH DAC) studies reported pyrolite solidus temperatures of 3430–4180 K (± <200K) at P ~ 135 GPa (Andrault et al., 2011; Fiquet et al., 2010; Kim et al., 2020; Nomura et al., 2014). These temperatures were determined by pyrometry assuming that the optical properties of the sample are wavelength-independent in the visible to near-IR spectral range. Here we use Mie theory to show that this assumption is grossly inadequate for a polyphase sample with the grain sizes and refractive indices representative of those in a pyrolite compressed in the diamond anvil cell. We compute the wavelength-dependent light extinction coefficient of pyrolite samples and show that the previous melting studies may have underestimated pyrolite solidus temperature by up to 20–30%. This implies that the upper bound on the TCMB is of the order of ~5000 K.