Homogeneous Doping Research Articles

Quantum yield and thermal sensitivity of SrGd2O4:Yb, Tm up-conversion nanoparticles

Luminescence thermometry is an effective method for temperature measurements using the remote operating mode. In this work, a series of Tm3+ (1 at%) and Yb3+ (2, 4, and 6 at%) ions doped SrGd2O4 up-conversion (UC) nanoparticles were synthesized by the modified sol-gel method, and fully characterized toward optimization of their composition and optical characteristic. Crystallization of single-phase nanoparticles with homogeneous doping was confirmed by XRPD, TEM/HRTEM, and STEM/EDS analysis in all samples, independently of their stoichiometry. The UC emissions recorded under 976 nm excitation revealed typical Tm3+ transitions, showing that the optimal sensitizer doping concentration is 4 at%. For this sample, a lifetime of 342 μs, and a total quantum yield of 1.12 % were determined at room temperature for the emission observed in the Vis part of up-conversion spectra. The temperature-dependent emission spectra, measured from 263 to 363 K, implied its excellent temperature-sensing capabilities. The luminescent intensity ratio (LIR) was employed for blue I479/485 and IR I795/807 Tm3+ emissions. The absolute and relative temperature sensitivity continuously decreases with the increase of the temperature, showing the values of 4.05x10−3 K-1 and 0.41 % K−1 (for blue) and 3.8x10−3 K-1 and 0.31 % K−1 (for IR) at the temperature of 300 K. The results indicate that SrGd2O4 doped with 4 % Yb3+ and 1 % Tm3+ may be employed for reliable temperature measurement over an investigated temperature range.

Promoting homogeneous tungsten doping in LiNiO2 through a grain boundary phase induced by excessive lithium

LiNiO2 (LNO) is one of the most promising cathode materials for lithium-ion batteries. Tungsten element in enhancing the stability of LNO has been researched extensively. However, the understanding of the specific doping process and existing form of W is still not perfect. This study proposes a lithium-induced grain boundary phase W doping mechanism. The results demonstrate that the introduced W atoms first react with the lithium source to generate a Li-W-O phase at the grain boundary of primary particles. With the increase of lithium ratio, W atoms gradually diffuse from the grain boundary phase to the interior layered structure to achieve W doping. The feasibility of grain boundary phase doping is verified by first principles calculation. Furthermore, it is found that the Li2WO4 grain boundary phase is an excellent lithium ion conductor, which can protect the cathode surface and improve the rate performance. The doped W can alleviate the harmful H2↔H3 phase transition, thereby inhibiting the generation of microcracks, and improving the electrochemical performance. Consequently, the 0.3wt% W-doped sample provides a significant improved capacity retention of 88.5% compared with the pristine LNO (80.7%) after 100 cycles at 2.8-4.3 V under 1 C.

Gradient Doping Enables an Extraordinary Efficiency in Thermoelectric PbTe1-xIx.

The conversion efficiency of thermoelectric generators that have to be operated under a temperature difference (ΔT) is mainly determined by material's dimensionless figure of merit (zT). However, maximization of zT at each temperature requires an optimization of carrier concentration (nopt) which strongly depends on the temperature and band parameters. Commonly utilized strategy of chemical doping usually enables a homogeneous carrier concentration throughout the material, leading the maximal zT to be achievable only within a narrow temperature range. In this work, a gradiently doping is successfully realized in PbTe1-xIx using a vertical gradient solidification technique, enabling a spatial gradient in carrier concentration that correspondingly optimizes zT at each portion of the material under its operating temperature. Such a gradient doping results in an extraordinary device efficiency of ≈14% at a ΔT of ≈500K, corresponding to a ≈40% improvement as compared to that of homogeneous doping. Since directional solidification technique commonly enables gradient dopant concentrations in semiconductors, the resultant gradient carrier concentration is illustrated here as an effective approach for advancing thermoelectrics.

Towards Sustainable Viscose-to-Viscose Production: Strategies for Recycling of Viscose Fibres

The potential for using discarded viscose textiles to produce high-quality viscose fibres is limited by the low molecular weight of the cellulose and its continued reduction in the recycling process. Herein, we present a straightforward approach of reprocessing discarded viscose textiles while achieving high-quality recycled viscose fibres. Discarded viscose textile was defibrated and centrifuged, and the resulting fibres were reprocessed under industrially relevant conditions. The produced viscose dope was fluid and resulted in viscose fibres with properties comparable to fibres made from commercial wood cellulose pulp (titer ~2 dtex; dry elongation ~16%, dry tenacity ~15 cN/tex). To explore the potential for a more environmentally friendly production process, the steeping step was performed twice (double-steeping), thereby producing a more homogeneous viscose dope. Through double-steeping, the consumption of carbon disulfide (CS2) could be reduced by 30.5%. The double-steeping method shows to be a suitable approach to reprocess discarded viscose textiles while reducing the environmental impact of the viscose process associated with the use of CS2. Our work demonstrates that discarded viscose textile has the potential to be part of a circular textile value chain.

Ultralow 1/f noise in epigraphene devices

We report the lowest recorded levels of 1/f noise for graphene-based devices, at the level of SV/V2=SI/I2=4.4×10−16 (1/Hz), measured at f = 10 Hz (SV/V2=SI/I2 < 10−16 1/Hz for f > 100 Hz) in large-area epitaxial graphene on silicon carbide (epigraphene) Hall sensors. This performance is made possible through the combination of high material quality, low contact resistance achieved by edge contact fabrication process, homogeneous doping, and stable passivation of the graphene layer. Our study explores the nature of 1/f noise as a function of carrier density and device geometry and includes data from Hall sensors with device area range spanning over six orders of magnitude, with characteristic device length ranging from L = 1 μm to 1 mm. In optimized graphene Hall sensors, we demonstrate arrays to be a viable route to improve further the magnetic field detection: a simple parallel connection of two devices displays record-high magnetic field sensitivity at room temperature, with minimum detectable magnetic field levels down to Bmin = 9.5 nT/√Hz. The remarkable low levels of 1/f noise observed in epigraphene devices hold immense capacity for the design and fabrication of scalable epigraphene-based sensors with exceptional performance.

Structure and Luminescent Properties of Double‐Doped LiNbO3:Zn:Mg Crystals

The correlation between photoluminescence in the near‐IR region and point defect centers in the LiNbO3 crystals co‐doped with Zn and Mg both by homogeneous and direct methods has been studied. X‐ray diffraction (XRD) analysis shows that the LiNbO3:Zn:Mg (4.68:0.9 mol%) crystal obtained by homogeneous doping has the least number of intrinsic defects compared to the others. It has been established that ZnLi defects stimulate photoluminescence (PL) in the near‐IR region of the luminescence spectrum in the LiNbO3:Zn:Mg crystals obtained by homogeneous doping. The LiNbO3:Zn:Mg (4.68:0.90 mol%) crystal has the maximum PL intensity and the LiNbO3:Zn:Mg (3.83:0.97 mol%) crystal has the minimum. Both crystals are doped homogeneously. Such defects as niobium vacancies (VNb) and niobium in the empty octahedron (Nboct) are suggested as luminescence quenchers in the co‐doped crystals.

Preparation of Fe7S8/C composite by one-step hydrothermal method for fast efficient lithium storage with long cycle life

High-capacity metal sulfide electrode materials for lithium storage have received extensive attention for the booming battery technology. However, metal sulfide electrodes have poor reaction kinetics in the light of capacity delivery and rate performance. To increase Li-ion storage, an easy one-pot hydrothermal method was presented to prepare a Fe7S8/C composite for lithium-ion batteries anode. The homogeneous doping of nitrogen in the carbon layer is beneficial to the rapid and uniform growth of Fe7S8 nanoparticles. The Fe7S8/C composite provides a strong honeycomb network with stable interfacial bonds by the strong chemical bonds between Fe7S8 and C, which can ease mechanical tension to ensure the stability of the structure during cycling. So the Fe7S8/C composite material has long-term stability (466.8 mAh g−1 at 2C after 2000 cycles). The impressive electrochemical behaviors can be ascribed to enhanced reaction kinetics, where unique carbon network matrix plays a dual role of conductive substrate and channels for electron and ion transport, respectively.

Crystallization and activator reduction simultaneously for calcium sulfide nanophosphors and evaluation of red-light compensation - Environmental reliability

Calcium sulfide nanophosphors (CaS:Eu2+) with red emissions were synthesized by hydrothermal-derived 250 nm carbon-sphere templates to induce a reduction atmosphere to activate an activator valence transition and crystallize (Ca,Eu)S simultaneously at 800 °C without extra sulfur atmosphere. The cationic concentration z = [Ca2++Eu2+] and ionic ratio y = [S2−]/[Ca2++Eu2+] were controlled in an innovative chemical solution reflux process to synthesize a sulfide nanophosphor precursor on carbon-sphere template. The particle size and crystallinity of the prepared nanophosphors increased with the “y” value increase. The photoluminescence (PL) intensity of the 652 nm emission excited by 450 nm increased to y = 1 and kept nearly constant to y = 20. High PL intensity was achieved by 0.025CaS-1 and 0.025CaS-10 samples with individually sphere-like nanoparticles, enough crystallinity and homogeneous Eu doping as well as fully reduced Eu2+ in the nanophosphors. The CaS:Eu2+ nanoparticles prepared by carbon-sphere templates showed thermal quenching with temperature. The Eu2+-doped CaS emitted 652 nm red light by 450 nm but not by 380 nm excitation that was only for CaS host at 555 nm emission. The prepared 0.025CaS-10 paste of only 7 wt% was individually coated on a blue-light LED and commercially available YAG-LED. The red emission intensity was enhanced and broadened by the prepared sulfide nanophosphor compared to a commercially available red LED. The CRI value for R9 increased to higher than 90, and the measured Ra was higher than 95 for the prepared sulfide nanophosphor-coated commercial WLED. The prepared sulfide nanophosphors could keep the red-light brightness over six months' exposure at rainy marina to show the environmental reliability.

Orbital-selective metal skin induced by alkali-metal-dosing Mott-insulating Ca2RuO4

Doped Mott insulators are the starting point for interesting physics such as high temperature superconductivity and quantum spin liquids. For multi-band Mott insulators, orbital selective ground states have been envisioned. However, orbital selective metals and Mott insulators have been difficult to realize experimentally. Here we demonstrate by photoemission spectroscopy how Ca2RuO4, upon alkali-metal surface doping, develops a single-band metal skin. Our dynamical mean field theory calculations reveal that homogeneous electron doping of Ca2RuO4 results in a multi-band metal. All together, our results provide evidence for an orbital-selective Mott insulator breakdown, which is unachievable via simple electron doping. Supported by a cluster model and cluster perturbation theory calculations, we demonstrate a type of skin metal-insulator transition induced by surface dopants that orbital-selectively hybridize with the bulk Mott state and in turn produce coherent in-gap states.

Multi-Scale Engineered 2D Carbon Polyhedron Array with Enhanced Electrocatalytic Performance.

Electrocatalyst engineering from the atomic to macroscopic level of electrocatalysts is one of the most powerful routes to boost the performance of electrochemical devices. However, multi-scale structure engineering mainly focuses on the range of atomic-to-particle scale such as hierarchical porosity engineering, while catalyst engineering at the macroscopic level, such as the arrangement configuration of nanoparticles, is often overlooked. Here, a 2D carbon polyhedron array with a multi-scale engineered structure via facile chemical etching, ice-templating induced self-assembly, and high-temperature pyrolysis processes is reported. Controlled phytic acid etching of the carbon precursor introduces homogeneous atomic phosphorous and nitrogen doping, as well as a well-defined mesoporous structure. Subsequent ice-templated self-assembly triggers the formation of a 2D particle array superstructure. The atomic-level doping gives rise to high intrinsic activity, while the well-engineered porous structure and particle arrangement addresses the mass transport limitations at the microscopic particle level and macroscopic electrode level. As a result, the as-prepared electrocatalyst delivers outstanding performance toward oxygen reduction reaction in both acidic and alkaline media, which is better than recently reported state-of-the-art metal-free electrocatalysts. Molecular dynamics simulation together with extensive characterizations indicate that the performance enhancement originates from multi-scale structural synergy.

Molten-salt mediated homogenous Mo-doped CoP for enhanced anion exchange membrane water electrolysis

Membrane electrode water electrolyzer is the most promising industrial large-scale hydrogen production energy equipment, which is used to promote the conversion of old and new energy and the realization of low carbon goals. However, there is still a lack of efficient and robust alkaline HER electrocatalysts for tightly assembled, bubble-dense and high-current density anion exchange membrane (AEM) electrolyzers. Herein, we developed an effective salt-melting homogenization synthesis strategy for the preparation of cobalt foam (CF)-supported uniform Mo-doped chrysanthemum-like CoP electrodes (M-Mo-CoP/CF). Alkaline AEM electrolytic cells driven by M-Mo-CoP/CF have ideal water splitting properties (1000 mA/cm−2 at 1.80 Vcell) and high current tolerance. In addition, detailed experimental and theoretical calculation results show that the M-Mo-CoP/CF prepared by this strategy has excellent metal-like conductivity and optimized H* adsorption free energy. In conclusion, this work strongly confirms the application potential of salt-melting assisted homogeneous doping strategy in the preparation of high-performance hydrogen evolution catalytic materials.

Surface Engineering of Ni-Rich Cathodes Enables Homogeneous Doping of High-Valence Mo Ions for Li-Ion Batteries

Surface Engineering of Ni-Rich Cathodes Enables Homogeneous Doping of High-Valence Mo Ions for Li-Ion Batteries

Long-term stability of molecular doped epigraphene quantum Hall standards: single elements and large arrays (R K/236 ≈ 109 Ω)

In this work we investigate the long-term stability of epitaxial graphene (epigraphene) quantum Hall resistance standards, including single devices and an array device composed of 236 elements providing R K/236 ≈ 109 Ω, with R K the von Klitzing constant. All devices utilize the established technique of chemical doping via molecular dopants to achieve homogenous doping and control over carrier density. However, optimal storage conditions and the long-term stability of molecular dopants for metrological applications have not been widely studied. In this work we aim to identify simple storage techniques that use readily available and cost-effective materials which provide long-term stability for devices without the need for advanced laboratory equipment. The devices are stored in glass bottles with four different environments: ambient, oxygen absorber, silica gel desiccant, and oxygen absorber/desiccant mixture. We have tracked the carrier densities, mobilities, and quantization accuracies of eight different epigraphene quantum Hall chips for over two years. We observe the highest stability (i.e. lowest change in carrier density) for samples stored in oxygen absorber/desiccant mixture, with a relative change in carrier density below 0.01% per day and no discernable degradation of quantization accuracy at the part-per-billion level. This storage technique yields a comparable stability to the currently established best storage method of inert nitrogen atmosphere, but it is much easier to realize in practice. It is possible to further optimize the mixture of oxygen absorber/desiccant for even greater stability performance in the future. We foresee that this technique can allow for simple and stable long-term storage of polymer-encapsulated molecular doped epigraphene quantum Hall standards, removing another barrier for their wide-spread use in practical metrology.

Keplerate polyoxomolybdate nanoball mediated controllable preparation of metal-doped molybdenum disulfide for electrocatalytic hydrogen evolution in acidic and alkaline media

Rationally designed novel cost-effective hydrogen evolution reaction (HER) electrocatalysts with controlled surface composition and advanced structural superiority is extremely critical to optimize the HER performance. Polyoxometalates (POMs) with structural diversity and adjustable element compositions represent a promising precursor for rational design and preparation of HER electrocatalysts. Herein, a series of transition metal-doped MoS2 materials with different surface engineered structures (Fe, Cr, V doping and S vacancies) (M-MoS2/CC, M = Fe, Cr and V) were fabricated by a simple hydrothermal-vulcanization strategy using Keplerate polyoxomolybdate nanoball ({Mo72Fe30}, {Mo72Cr30}, {Mo72V30}, {Mo132}) as precursors. The enlarged interlayer spacing as well as the integration of homogeneous transition metal doping and abundant sulfur vacancies endows prepared M-MoS2/CC with superior HER electrocatalytic performance and excellent long-term working stability in both acidic and alkaline media. The optimized Fe-MoS2/CC afford current densities of 10 and 50 mA/cm2 at overpotentials of 188/272 mV and 194/394 mV in 0.5 mol/L H2SO4 and 1.0 mol/L KOH aqueous solution, respectively, outperforming most of reported typical transition metal sulfide-based catalysts. This work represents an important breakthrough for POMs-mediated highly efficient transition metal sulfide-based HER electrocatalysts with wide range pH activity and may provide new options for the rational design of promising HER electrocatalysts and beyond.

Influence of Doping Technology on the Stoichiometry and Features of the Localization of B3+ Cations in LiNbO3:B Single Crystals

We have established that relatively simple calculations of the Coulomb interaction in the lattice of doped lithium niobate (LN, LiNbO3) can confirm the physical properties of real crystals. We have developed a method for the double adjustment of real XRD data for calculations of Coulomb interaction in a LN cluster. The study considers two crystals doped with boron (LN:B); LN:B(1) has been grown from a charge with 0.02 mol% B2O3, boron has been introduced by homogeneous doping, LN:B(2) has been grown from a charge with 0.547 mol% B2O3, and boron has been introduced by direct solid-state doping. XRD and Rietveld method data have been obtained for these crystals. The obtained data have been used to build a model of the LN cluster; the cluster in the calculations consists of six oxygen octahedra of the LN structure. The cluster configuration has been chosen in such a way that the structure contains two tetrahedral voids. We have studied 10 variants of filling a cluster with intrinsic cations (Li, Nb), defects, and vacancies. There are 10 of them because, in addition to the basic cations in their positions, defects are present in the structure. In terms of the defects used (NbLi, NbV), we have used only those that Rietveld found for these exact LN:B crystals, and the vacancy in the niobium octahedron (VNb) compensates for these defects, according to the models known for LN. The energy of the Coulomb interaction between the cluster structure of a real crystal and the boron cation localized in it in different positions has been calculated for each of the configurations. Calculations have demonstrated that B is more likely to be embedded near a defect than in a regular structure. This means that boron positively influences the local substructure of doped LN crystals, not only structures the melt during crystal growth. Calculations have shown that the type and location of structural defects affect the position of boron in the structure of a LN crystal. Calculations have also shown that LN:B(1) has a more stable structure, including optical damage resistance. The photoinduced light scattering (PILS) patterns and conoscopic patterns confirm this conclusion for the studied LN:B crystals. The information obtained in this study may be useful for interpreting the defective structure of LN crystals co-doped with boron and metals (Mg, Zn, etc.). This will supplement the knowledge available in the literature regarding models that describe the structure of complexly doped LN crystals.

CDs Regulated Sulfur-Based Flexible Electrode with Range pH Values for Efficient and Durable Hydrogen Evolution Reaction.

How to mildly structure a high intrinsic activity and stable catalytic electrode to realize long-term catalytic water splitting to produce hydrogen at a wide range of pH values at industrial high current is a challenge. Herein, this work creatively proposes to prepare industrial-grade catalytic electrodes with high efficiency and stability at high current density through carbon quantum dots (CDs) modification nickel sulfide on hydrophilic flexible filter paper via one-step mild chemical plating (denoted as CDs-Ni3 S2 @HFP). The intrinsic activity and surface area, electron transfer ability, and corrosion resistance of Ni3 S2 material are increased due to the regulation, homogenous, and high concentration doping of CDs. The overpotential of the flexible catalytic electrode is only 30, 35, and 87mV in 1m KOH, simulated seawater (1m KOH + 0.5m NaCl), and neutral electrolyte (0.5m PBS) at a current density of 10mA cm-2 . More attractively, the CDs-Ni3 S2 @HFP electrode achieves over 500h of efficient and stable catalysis at industrial high current density (500mA cm-2 ). Due to the advantages of mild, universal, and large-area preparation of catalytic materials, this work provides technical support for flexible catalytic electrodes in efficient catalysis toward water splitting, energy storage, and device preparation.

Structure, Optical Properties and Physicochemical Features of LiNbO3:Mg,B Crystals Grown in a Single Technological Cycle: An Optical Material for Converting Laser Radiation.

Two series of LiNbO3:Mg:B crystals have been grown and studied. Two doping methods-have been used. The crystals-have been co-doped with Mg and a non-metallic dopant, B. The physicochemical features of the growth-have been considered for LiNbO3:Mg:B crystals obtained from a boron-doped melt. The charge-has been prepared using different technologies: homogeneous (HG) and solid-phase (SP) doping. The same two methods have been used to grow single-doped LiNbO3:Mg crystals. A control near-stoichiometric (NSLN) crystal-has been grown via the HTTSSG (high-temperature top-seeded solution growth) method from a congruent melt (Li/Nb ≈ 0.946) with 5.5 wt% K2O. The characteristics of the LiNbO3:Mg:B crystals-have been compared with those of the LiNbO3:Mg and NSLN crystals. Physicochemical and structural reasons have been established for the differences in the distribution coefficients of magnesium (KD) during the growth of the HG- and SP-doped LiNbO3:B:Mg and LiNbO3:Mg crystals. The optical characteristics of the LiNbO3:B:Mg crystals-have been studied via optical spectroscopy, laser conoscopy and photoinduced light scattering (PILS). The influence of boron on the microstructure, compositional and optical uniformities and optical damage resistance of the LiNbO3:Mg:B crystals-has been estimated. Optimal technological approaches to growing optically uniform LiNbO3:B:Mg crystals have been determined. LiNbO3:Mg:B crystals have been shown to have a significant advantage over the commercially used LiNbO3:Mg crystals since large LiNbO3:Mg:B crystals can be grown without stripes. Such stripes usually appear perpendicular to the growth axis. In addition, the photorefractive effect is suppressed in LiNbO3:Mg:B crystals at lower magnesium concentrations ([Mg] ≈ 2.5 mol%) than in LiNbO3:Mg ([Mg] ≈ 5.5 mol%).

Phosphate-Induced Reaction to Prepare Coal-Based P-Doped Hard Carbon with a Hierarchical Porous Structure for Improved Sodium-Ion Storage

The use of coal as a precursor for producing hard carbon is favored due to its abundance, low cost, and high carbon yield. To further optimize the sodium storage performance of hard carbon, the introduction of heteroatoms has been shown to be an effective approach. However, the inert structure in coal limits the development of heteroatom-doped coal-based hard carbon. Herein, coal-based P-doped hard carbon was synthesized using Ca3(PO4)2 to achieve homogeneous phosphorus doping and inhibit carbon microcrystal development during high-temperature carbonization. This involved a carbon dissolution reaction where Ca3(PO4)2 reacted with SiO2 and carbon in coal to form phosphorus and CO. The resulting hierarchical porous structure allowed for rapid diffusion of Na+ and resulted in a high reversible capacity of 200 mAh g−1 when used as an anode material for Na+ storage. Compared to unpretreated coal-based hard carbon, the P-doped hard carbon displayed a larger initial coulombic efficiency (64%) and proportion of plateau capacity (47%), whereas the unpretreated carbon only exhibited an initial coulombic efficiency of 43.1% and a proportion of plateau capacity of 29.8%. This work provides a green, scalable approach for effective microcrystalline regulation of hard carbon from low-cost and highly aromatic precursors.

Heterogeneous doping via charge carrier transport improves Photoelectrochemical H2O oxidative H2O2 synthesis

Photoelectrochemical (PEC) water splitting into H2O2 and H2 has attracted significant attention due to its low cost and sustainability. However, slow charge carrier transport and water oxidation kinetics limit the selectivity for H2O2 production and solar conversion efficiency. Herein, we propose a heterogeneous doping approach that combines surface gradient doping with bulk doping to improve the charge carrier transport in the photoelectrode. Inducing gradient Nb and homogeneous Mo doping into BiVO4 photoanode (G-Nb/Mo:BVO) can promote charge separation and carrier transfer, leading to the high selectivity for H2O2 generation and suppression of O2 production. Consequently, the heterogeneously doped G-Nb/Mo:BVO photoanode presents an average Faraday efficiency (FE) of over 80% for H2O2 production in a wide potential of 0.6–1.8 VRHE with the maximum FE of 83.7% at 1.2 VRHE under AM 1.5G illumination. More importantly, H2O2 production rate can reach 1.23 μmol min−1 cm−2 at 1.23 VRHE, representing the best H2O2 production rate reported for the photoelectrodes. Density functional theory calculations prove that Mo and Nb co-doping increases the reactivity of BiVO4 and improves 2e− water oxidation reaction activity and selectivity. This work demonstrates that heterogeneous doping provides a cost-effective strategy to break performance trade-offs by improving charge carrier separation and transport in light absorbers, and modulating the selectivity and activity of water oxidation reaction to generate H2O2, which can be extended to other photocatalytic reactions.

РАСЧЕТ НЕЛИНЕЙНО-ОПТИЧЕСКИХ ХАРАКТЕРИСТИК КРИСТАЛЛОВ LiNbO3:Zn:Mg, ПОЛУЧЕННЫХ ПО ТЕХНОЛОГИЯМ ПРЯМОГО И ГОМОГЕННОГО ЛЕГИРОВАНИЯ

The coefficients of the second-order nonlinear optical tensor (dij) for lithium niobate crystals doubly doped with magnesium and zinc by different methods of impurity introduction were calculated.Impurity concentrations (Zn:Mg) in crystals were 3.74:1.09 mol. % in case of direct doping, 3.83:0.97 mol. % in case of homogeneous doping. It was shown that the efficiency of radiation conversion with second harmonic generation in a homogeneously doped crystal is higher than in a crystal obtained by the direct doping method.