Lanthanum Ions Research Articles

The Structure and Optical Properties of Luminescent Terbium Terephthalate Metal–Organic Frameworks Doped with Yttrium, Gadolinium, and Lanthanum Ions

The structural features and luminescent properties of heterometallic Tb–Gd, Tb–La, and Tb–Y terephthalate metal–organic frameworks, namely (TbxM1−x)2(1,4-bdc)3∙4H2O (M = Gd, La, Y), were studied in detail in a wide concentration range (x = 0.001–1). The crystalline phase of synthesized compounds corresponds to Ln2(1,4-bdc)3·4H2O. The lifetime of 5D4 decreased with increased Tb3+ concentration, but PLQY depends non-linearly on the Tb3+ concentration. The 50% substitution of Tb3+ for Y3+, Gd3+, or La3+ ions result in the significant enhancement of photoluminescence quantum yield, up to 1.6 times. The morphology, thermal stability, and vibrational structure of the selected homo- and bi-metallic materials is reported as well.

In Vitro Study on Combined Effect of Drugs for Hyperphosphatemia on Phosphorus Adsorption Capacity.

Phosphorus binders are often used in combination to produce synergistic effects. However, the synergistic effect may be affected by the change in pH or concomitant drugs. Nonetheless, the data on the adsorption capacities of these binders when used in combination with other binders are limited. In this study, we evaluated the adsorption capacity of phosphorus binders when used in combination. Precipitated calcium carbonate (CC), ferric citrate hydrate (FC), lanthanum carbonate hydrate (LC), and sucroferric oxyhydroxide (SO) were used as phosphorus binders. SO showed high adsorption capacity in the 1st and 2nd fluid, and the adsorption capacity of SO in combination with other binders was stable. In contrast, the adsorption capacities of CC + FC and FC + LC decreased in the 1st and 2nd fluid compared with that when used alone because of the release of citrate ions that chelate calcium or lanthanum ions. These results suggest that SO is less affected by interactions with other phosphorus binders and changes in pH and may be suitable for patients receiving concomitant drugs.

Impedance Spectroscopy of Lanthanum-Doped (Pb0.75Ba0.25)(Zr0.70Ti0.30)O3 Ceramics

This study examines the effects of La3+ doping on (Pb0.75Ba0.25)(Zr0.70Ti0.30)O3(PBZT) ceramics, which were synthesized using the conventional solid-state reaction method. X-ray diffraction analysis confirmed that the PBZT structure, including PBZT doped with La3+ at concentrations x = 1 at.% and x = 2 at.%, exhibited a rhombohedral (R3c) space group, while higher doping levels of x = 3 at.% and x = 4 at.% led to a dominant cubic (Pm-3m) phase with approximately 30% of a remnant rhombohedral component. Scanning electron microscopy (SEM, JEOL JSM-7100F TTL LV, Jeol Ltd., Tokyo, Japan) and energy dispersive X-ray spectroscopy (EDS) were utilized to investigate the structure and morphology of these ceramics. The findings indicated that the chemical composition of the ceramic samples closely corresponded to the initial stoichiometry of the ceramic powder. An increase in the amount of lanthanum results in a decrease in the average grain size of the ceramics. The electrical properties were further evaluated using complex impedance spectroscopy (IS) over a range of temperatures and frequencies, as well as temperature dependence of DC conductivity. The similarity in the changes in activation energy for DC conductivity and grain boundary conductivity, caused by lanthanum ion modification, allows for the conclusion that grain boundaries are the primary microstructural element responsible for conductivity in these materials.

Enhanced Tumor Immunotherapy by Triple Amplification Effects of Nanomedicine on the STING Signaling Pathway in Dendritic Cells.

Insufficient activation of stimulator of interferon genes (STING) signaling pathway in tumor-associated dendritic cells limits the efficiency of tumor immunotherapy. Herein, the "three-in-one" IAHA-LaP/siPTPN6 NPs containing lanthanum ions (La3+), cGAMP, and PTPN6 siRNA are developed for triple amplification of the STING pathway. In vitro results demonstrate that La3+ significantly promotes cGAMP-mediated activation of the STING pathway by enhancing the phosphorylation of STING, TBK1, IRF3, and NF-κB p65. Moreover, the IAHA-LaP/siPTPN6 NPs further significantly enhance the phosphorylation of STING and NF-κB p65 and augment K63-linked ubiquitination of STING protein via siPTPN6-mediated downregulation of SHP-1 protein. Furthermore, NPs improve the secretion of IFNβ (2.4-fold), IL-6 (1.5-fold), and TNF-α (1.4-fold), thereby promoting DCs maturation compared to the mixture of La3+ and cGAMP. In vivo results show that the IAHA-LaP/siPTPN6 NPs remarkably inhibit primary tumor growth by increasing the percentage of mature DCs in tumor-draining lymph nodes, polarizing M2/M1 phenotype in TME, and promoting the infiltration of CD8+T cells into tumors. Moreover, these NPs dramatically prevent the growth of distal tumor by inducing systemic anti-tumor immunity and generating a long-term anti-tumor memory for protection against tumor recurrence in mice bearing bilateral B16F10. These IAHA-LaP/siPTPN6 NPs may offer a promising platform for robust anti-tumor immune responses.

Enhanced aqueous phosphorus removal and mechanism by water spinach (Ipomoea aquatica Forsk) pretreated with lanthanum nitrate.

Excess nutrients such as phosphate (PO43-) entering surface waters promote eutrophication, and phosphorous (P) removal is important to clear the water. Phytoremediation efforts have been used to improve water quality by varieties of P removal plants, such as water spinach (Ipomoea aquatica Forsk). Water spinach can reduce both internal and external resources of phosphorus from waterbody. The ion of lanthanum (La), one rare earth element (REE), is an immobilization substance for aqueous phosphate and also a fertilizer for plants. Therefore, lanthanum nitrate La (NO3)3 was used further to improve the phytoextraction of P from the polluted water. This study investigated the effects of La on the aqueous P removal by two genotypes of water spinach, green stem large leaves (GSLL) and green stem willow leaves (GSWL). The low concentration La (NO3)3 helped the plant to remove more phosphorous from eutrophic water, but La at high concentration lowered the removal of P. Under La (NO3)3 treatments, the optimum concentration for maximum P removal in GSLL is 3mg/L, and for GSWL, it is 10mg/L and P removal rates were enhanced to 95% and 96%, respectively. When the concentration of La (NO3)3 is 100mg/L, the removal percentage of P was only 10% for both genotypes. The very high concentration of La will impose toxicity and even cause the death of the water spinach and produce secondary pollution; for example, under some specific circumstances, the bond between lanthanum and nitrates dissociates into lanthanum ions (La3⁺) and nitrate ions (NO₃⁻). If the concentration is high, then it accumulates in the aquatic water organisms and plants and causes toxicity in their bodies. If humans eat up these plants and fish, it causes toxic effects in humans. The La (NO3)3 positively affects different parameters of plants. La (NO3)3 increases the growth, pigments, enzyme activity, and malondialdehyde (MDA) of plants which were also discussed in this study. The biological mechanism should be responsible for the enhanced aqueous phosphorus removal by water spinach using lanthanum nitrate.

Enhanced phosphate removal from aqueous environments using three-dimensional La-doped carboxylic carbon nanotubes/alginate: Performance and mechanisms

The excessive amounts of phosphorus (P) discharged and usage have caused eutrophication and algal blooms, which seriously jeopardize the environment even the human health. In this study, carbon nanotubes (CNTs) served as carriers to develop a lanthanum-based sodium alginate hydrogel (La-CNT-COOH/SA) aimed at efficiently removing phosphate from wastewater. Characterization results confirmed successful deposition of La(OH)3 nanoparticles onto CNT-COOH. The optimal adsorption efficiency of La-CNT-COOH/SA hydrogels occurred at pH 4, with a maximum adsorption capacity of 54.4 mg/g under an initial phosphate concentration of 60 mg/L. Batch experiments demonstrated that La-CNT-COOH/SA performed well across a favorable pH range and exhibited high tolerance to common coexisting ions during phosphate adsorption. Adsorption isotherms indicated a dominance of both physical and chemical mechanisms in phosphate removal by La-CNT-COOH/SA. At elevated phosphate concentrations, the adsorption process followed quasi-second-order kinetics, primarily driven by chemical adsorption. Multi-instrument characterization emphasized that the substantial loading of La(OH)3 on CNT-COOH significantly contributed to adsorption, alongside crosslinked lanthanum ions on sodium alginate and abundant hydroxyl groups. Mechanisms of adsorption by La-CNT-COOH/SA encompassed electrostatic interactions, surface precipitation, and in-sphere complexation (La-O-P). These findings on fabrication, properties, and adsorption mechanisms of the phosphate-removal hydrogel lay a theoretical foundation for applying biomass-based materials in large-scale remediation practices.

Electronic Structures of Alaninehydroximate 15-Metallacrowns-5 with Lanthanum(III), Cerium(III), and Praseodymium(III) Ions

Electronic Structures of Alaninehydroximate 15-Metallacrowns-5 with Lanthanum(III), Cerium(III), and Praseodymium(III) Ions

A comprehensive investigation on lanthanum ions doped borate-tellurite-germinate glass for radiation shielding and optical application

In the present work, a group of four glass samples that have chemical composition of [(35-x) B2O3-20TeO2-10GeO2-35MgO-xLa2O3] were x values varies from 2.5 to 10 all in mol percentage, which fabricated using ordinary melting then quenching technique. Many physical and mechanical have been measured and calculated like: density, packing density, internuclear distance (ri), oxygen packing density (OPD), oxygen molar volume (OMV), dissociation energy (Gt), packing density (Vt), Poisson ratio (σ), fractal bond connectivity (d), elastic modulus. The behavior of the La10 was examined using XRD in the range of 10–80°. The UV–visible spectrum of absorption of the La2.5, La5, La7.5, and La10 glasses were measured. Several optical parameters have been calculated and extracted including the cutoff wavelength, Urbach's energy (EU), dielectric constant (ε), refractive index (n), molar refraction (RM), reflection loss (RL), molar electron polarizability (αM), Optical transmission (T), Optical basicity (Λ), and Metallization criteria (M). Various noticeable bands vibration of boron units structural besides the modes of vibration of that effected by adding metal cations were studied using FTIR to analyze different structure groups like: BO3 triangles, BO4 pyramids, tetragonal TeO4 pyramids, and trigonal TeO3 pyramids. Using Monte Carlo simulation, the MAC of glass materials was evaluated in the current work. Various radiation shielding parameters were investigated at low and high energies.

A novel lanthanum ion-assisted fluorapatite precipitation approach for efficient fluoride removal from water

Excess amounts of fluoride ions (F-) in water/wastewater bring great hazards to human health and the environment. The traditional method such as precipitation by calcium ions does not work well for low-concentration F- removal. Herein, we developed a lanthanum ion (La3+)-assisted fluorapatite precipitation approach to treat F--containing water, aiming at high removal efficiency. Through an orthogonal experimental design and single-factor experiment, the optimized reaction conditions were obtained as the molar ratio of (Ca2++La3+): PO43-: F-=7.5: 4: 1, Ca2+: La3+ = 90: 10, and reaction pH of 9. Under such reaction conditions, F- in water (10 mg L−1) could be well controlled under 1 mg L−1, fulfilling relevant environmental standards. No remarkable F- removal efficiency loss was found in the presence of typical anions (e.g., halides, bicarbonate, sulfate). The developed F- removal approach also worked well in a wide F- concentration range (10–200 mg L−1) and reaction temperature range (5–45 °C). Further reaction mechanism study proved that the formation of LaFx(OH)3-x colloids was the key step, which could accumulate F- ions in water into colloids. The subsequently added Ca2+ and PO43- destroyed the stable colloids, and then promoted the formation of fluorapatite with simultaneous La3+ doping, which existed as precipitate and allowed the easy separation from the reaction solution. As a by-product, the as-produced La3+-doped fluorapatite was evaluated as an adsorbent for organic pollutant removal, which possessed a high adsorption capacity (763.4 mg g−1) for the model pollutant of Congo red. Considering the facile operation process, high F- removal efficiency, wide operation temperature window, and anti-inference for co-existing anions, the La3+-assisted fluorapatite precipitation approach possessed great potential for F--containing water/wastewater treatment.

Impact of lanthanum ion exchange and steaming dealumination on middle distillate production using nanosized Y zeolite catalysts in hydrocracking reactions.

In the field of hydrocracking reactions, achieving optimal middle distillate yields remains a persistent challenge with commercially available zeolite Y catalysts. This limitation is attributed to challenges related to diffusion constraints within the catalyst. In response, we present a promising solution not only to these problems but also to the challenges encountered in nanosized Y zeolites when attempting to generate acidic sites within their structure and when analyzing their performance in vacuum gas oil hydrocracking. NiMo catalysts based on nanosized Y zeolites with different crystal sizes exchanged with lanthanum, effectively address diffusion issues and significantly enhance catalyst performance compared to dealuminated nanosized and commercial Y zeolite under the same reaction conditions. The catalysts were characterized by TGA, ICP-OES, XPS, N2 physisorption, FT-IR for pyridine acidity, TEM-mapping, and the 3-methyl thiophene reaction to test the hydrogenating capacity. Surface analysis and microscopy showed greater porosity in the catalysts with smaller zeolites and different arrangements of their components. The catalysts based on steamed protonated nanosized Y zeolites with a larger size and lanthanide nanosized Y zeolite with a smaller size yielded more middle distillates. Research provides a comprehensive analysis, providing a correlation between the catalytic performance and the size of the nanosized Y zeolite.

A nanoflower structure rare-earth La3+ doping Sn3O4 with highly catalytic active interfaces as a sulfur host facilitates the conversion kinetics of polysulfides in high-performance lithium-sulfur batteries

Lithium-sulfur batteries are considered a favourable contender for next-generation energy storage systems owing to their high energy density (2600 Wh·kg−1). However, the severe "shuttle effect" of polysulfides and the slow redox kinetics involving phase transitions have seriously limited the commercialization of lithium-sulfur batteries. On this basis, in this paper, a type of nanoflower structure rare-earth lanthanum ion (La3+) doping Sn3O4 with a large number of catalytic active interfaces is designed via a facile one-step hydrothermal method. When serves as a capture centre to immobilize polysulfides, it exhibits a strong chemical adsorption capacity. Moreover, due to the unique 4 f electron configuration of the rare-earth elements, nanoflower structure La3+ doping Sn3O4 (La@Sn3O4) as sulfur-wrapped matrix has a strong catalytic activity, which can effectively accelerate the conversion process of polysulfides. At the same time, the catalytic mechanism of La@Sn3O4/S composite cathode material targeting the solid to liquid phase transformation of polysulfides is effectively revealed via in-situ Raman spectroscopy test and the initial discharge capacity can reach 1429.6 mAh·g−1 at a current density of 0.1 C, and the capacity retention rate is 76.5 % after 130 cycles.

How Fe-La-CS microspheres have selective adsorption capacity for As(V) over a wide pH range: Coupling molecular scale interpretation with experiments

In this study, an Fe-La-CS adsorbent with a reticulated structure was prepared by an in situ method, which was able to adsorb arsenate efficiently over a wide pH range of 3–11. The incorporation of iron and lanthanum ions broadened the tolerant pH range of the adsorbent compared with chitosan beads (CS). Arsenic was mainly present in the pH range of 3–9 as two forms, H2AsO4− and HAsO42−. Calculations using the density-functional theory (DFT) showed that in the Ligand interactions and electrostatic interactions dominate in the pH range, with surface precipitation, and hydrogen bonding interactions playing a facilitating role. The background ions mainly compete with arsenic adsorption for electrostatic interaction sites. However, due to the different valence states of the background ions, the competition intensity is different. Such as low valence state representative ions Na+, K+ competitiveness is weak, and arsenic competition adsorption first occupy different adsorption sites, therefore, from the quantum chemistry and molecular dynamics point of view of Na+, K+ on arsenic adsorption almost no effect. Cl−, SO42− will have some influence on arsenic adsorption because of the same charge with arsenic, but the charged amount is smaller than arsenic and the molecular structure is different from that of arsenic, so the influence is not very big. In summary, the material design of Fe-La-CS adsorbent has great potential and theoretical significance for selective purification of heavy metal wastewater at wide pH.

Thermodynamics of the Complexation of Cerium(III) and Lanthanum(III) Ions with Glycine and Ethylenediaminedisuccinic Acid in Aqueous Solutions

Thermodynamics of the Complexation of Cerium(III) and Lanthanum(III) Ions with Glycine and Ethylenediaminedisuccinic Acid in Aqueous Solutions

The Structure and Optical Properties of Luminescent Europium Terephthalate Antenna Metal-Organic Frameworks Doped by Yttrium, Gadolinium, and Lanthanum Ions.

New heterometallic antenna terephthalate MOFs, namely, (EuxM1-x)2bdc3·4H2O (M = Y, La, Gd) (x = 0.001-1), were synthesized by a one-step method from aqueous solutions. The resulting compounds are isomorphic to each other; the crystalline phase corresponds to Ln2bdc3∙4H2O. Upon 300 nm excitation to the singlet excited state of terephthalate ions, all compounds exhibit a bright red emission corresponding to the of 5D0-7FJ (J = 0-4) f-f transitions of Eu3+ ions. The Eu(III) concentration dependence of the photophysical properties was carefully studied. We revealed that Gd-doping results in photoluminescence enhancement due to the heavy atom effect. To quantitatively compare the antenna effect among different compounds, we proposed the new approach, where the quantum yield of the 5D0 formation is used to characterize the efficiency of energy transfer from the ligand antenna to the Eu3+ emitter.

Preparation of strontium hexaferrite based materials by solution combustion: the effect of charges arising in precursors and an external magnetic field

The formation of electric charges during the synthesis of complex oxide materials based on strontium hexaferrite SrFe12O19, including doped with lanthanum and cobalt ions, via the combustion of nitrate-organic precursors has been established. Precursors included polyvinyl alcohol or glycine as organic component. The intensity of charge generation was lower for precursors containing a larger amount of organic component. Data on the magnetic characteristics of the samples were obtained: magnetization, coercive force. The influence of an external magnetic field during the synthesis of hexaferrites significantly affected the coercive force of the samples and allowed to increase its values due to the formation of extended ensembles of nanoparticles. At the same time, such an effect on samples with a relatively low level of charge generation during precursor combustion was more effective. The relationship between the factors influencing the formation of extended aggregates is analyzed. The Sr0.8La0.2Fe11.8Co0.2O19 samples had the maximum coercive force. One of the techniques for increasing the coercive force is a two-stage thermomagnetic treatment, including a low-temperature stage. The formation of branched extended structures at the macro- and micro-levels was found during the combustion of glycine-containing precursors.

Photocatalytic Degradation of Paracetamol and Antibacterial Activity of La-Modified TiO2 Obtained by Non-Hydrolytic Sol–Gel Route

The current study aims to synthesize and analyze both pure and La-doped TiO2, and evaluate the photocatalytic and antibacterial activity of as-prepared samples. Doped and undoped samples were prepared by the non-hydrolytic sol–gel method from titanium(IV) chloride, benzyl alcohol, and lanthanum(III) nitrate followed by thermal treatment. Lanthanum content in synthesized samples was 0.4, 1, and 5 mol%. The resulting nanopowders’ structure and morphology were described using XRD, IR, and UV–Vis analysis. The average particle sizes of pure and doped TiO2 were about 6–15 nm and anatase was found to be a dominant crystalline phase in the samples. It was observed that particle sizes decreased on increasing La content. The photocatalytic activity of the pure and La-doped sol–gel powders was estimated in the decomposition of paracetamol in distilled water using ultraviolet light illumination. Doping with lanthanum ions has been shown to increase the photocatalytic properties on the degradation of paracetamol. Furthermore, the annealed catalysts (pure and La3+ doped) showed increased photocatalytic activity and degradation of the analgesic in comparison with non-annealed materials. In both cases, the highest photocatalytic efficiency is observed at the optimal La3+ (1 mol%) concentration. The antimicrobial activity of 1 mol% La/TiO2 was tested against a reference strain E. coli in the presence of ultraviolet light and in dark conditions. The number of viable bacterial cells was determined by a spread plate method, and kill curves were performed. The results showed that photoactivated 1 mol% La/TiO2 exhibited a strong bactericidal effect, and in concentration, 1 mg/mL efficiently killed bacteria at an initial cell density of about 105 colony forming units in 1 mL within 15 min.

Direct Catalytic Conversion of Carbon Dioxide to Liquid Hydrocarbons over Cobalt Catalyst Supported on Lanthanum(III) Ion‐Doped Cerium(IV) Oxide

AbstractDirect CO2 conversion to liquid hydrocarbons (HCs) in a single process was achieved using cobalt (Co) catalysts supported on lanthanum ion (La3+)‐doped cerium oxide (CeO2) under a gas stream of H2/CO2/N2=3/1/1. The yield of liquid HCs was the highest for 30 mol% of La3+‐doped CeO2, which was because extrinsic oxygen vacancy formed by doping La3+ could act as an effective reaction site for reverse water gas shift reaction. However, the excess La3+ addition afforded surface covering lanthanum carbonates, resulting in depression of the catalytic performance. On the other hand, bare CeO2 lead to an increase in the selectivity of undesirable methane, which arose from reduction of CO2 to CO proceeding by intrinsic oxygen vacancy generated by only Ce3+, and weaker CO2 capture ability of intrinsic oxygen vacancy than extrinsic one, resulting in the proceeding of Sabatier reaction on Co catalyst. The rational design of reaction sites presented in this study will contribute to sustainability.

Uncovering the role of free lanthanum (La3+) ions and La oligomer on the surface of La (oxy)hydroxide particles for phosphate removal

La (oxy)hydroxide-based materials have been recognized as promising adsorbents for aqueous phosphate (P) removal. However, comprehending the adsorption behavior of P onto La (oxy)hydroxide particles remains challenging, given the heterogeneous low-crystalline surface encompassing La oligomers and free La3+ ions. In this study, a hydrogen (H) bond capping method was developed to construct La (oxy)hydroxide oligomers (LHOs) to simulate the low-crystalline La on the surface of La (oxy)hydroxide particles. The P uptake capacity was compared among free La3+ ions, LHOs, and La nanoparticle (La-NP) with maximum capacities of 1967.3 ± 30.8 mg/g, 461.1 ± 53.7 mg/g and 62.5 ± 6.0 mg/g, respectively. The FT-IR, Raman, in situ-XRD and XPS deconvolution analyses revealed that the removal of P by free La3+ ions mainly involve the process of chemical precipitation to form LaPO4·0.5H2O. Conversely, the elimination of P by LHOs is primarily attributed to inner-sphere complexation and hydroxyl exchange effect between LaOOH and P. Based on this study, the free La3+ ions and La oligomers on the surface of La (oxy)hydroxide particles play a primary role in P adsorption. These results also suggest that the successively decreased adsorption capacity of La (oxy)hydroxide-based adsorbents in the continuously adsorption/desorption cycles might be due to the irreversible inactivation and recrystallization of free La3+ ions and La oligomers on the surface.

Molecular Dynamic Simulation of the Interaction of a Deep Eutectic Solvent Based on Tetraethylammonium Bromide with La3+ in Acidic Media

In recent years, noticeable progress has been made in the development of alternative extraction systems characterized by greater sustainability. In this context, deep eutectic solvents (DESs) have emerged as a promising alternative to the conventional solvents commonly used in metal extraction. This work focuses on investigating the extraction of lanthanum in an aqueous solution of sulfuric acid using a deep eutectic solvent, employing molecular dynamics simulations (MD). The structural characteristics of the solvent and its interactions with the components of the aqueous solution are explored. In this study, tetraethylammonium bromide (TEABr) is combined with ethylene glycol (EG) to form a DES, in which sodium cyanide (NaCN) is subsequently solubilized. According to the results obtained from the MD simulation, the primary interactions in the DESs are established through hydrogen bonds between the bromine and the hydrogens of the methyl group of tetraethylammonium at 3.5 Å, as well as between the bromine and the hydrogens of the methylene group of ethylene glycol at 3.5 Å. Similarly, the main interactions between the binary DES and sodium cyanide occur through the hydrogens of the hydroxyl group of EG and the carbon of cyanide at 1.7 Å, and between the oxygen of the hydroxyl group of EG and the sodium at 2.5 Å. In the acidic solution, the primary interaction is highlighted between the lanthanum ion and the oxygen of the bisulfate at 2.8 Å. Additionally, it is observed that the interaction between the DES and the aqueous solution occurs between the lanthanum and the oxygen of the hydroxyl group of EG, as well as between the lanthanum and the carbon of cyanide at 4.4 Å. It is important to note that, when increasing the temperature from 25 to 80 °C, the interaction distance between the lanthanum and the carbon of cyanide decreases to 2.4 Å, suggesting a possible correlation with the increase in lanthanum extraction, as experimentally observed. Overall, this study underscores the importance of considering the fundamental structural interactions of the DES with the lanthanum acid solution, providing an essential theoretical basis for future experimental investigations.

THz vs NIR laser-assisted atom probe tomography of LaB6 samples

Terahertz (THz) radiation with low-energy photons (meV) is used in a wide range of applications, such as microscopy, sensing, and spectroscopy. However, recently, high amplitude THz pulses of MV/cm have been generated and used for electron emission and ion evaporation from field emitters, opening up the possibility of using high amplitude THz pulses for material imaging by THz-assisted atom probe tomography (APT). In this work, we compare the APT analyses of lanthanum hexaboride (LaB6) samples using a femtosecond near-infrared laser with those obtained using high-amplitude single-cycle THz pulses. The atomic-scale characterization of stoichiometric LaB6 is challenging in laser-assisted APT due to the detection losses of boron ions. Here, we show that the THz radiation reduces the emission of molecular ions and multiple detection events, and it increases the charge state of the emitted ions. All these effects result in an improvement in boron detection. Furthermore, the emission dynamics of boron and lanthanum ions differ in their evaporation times when using THz radiation. This work emphasizes the ability of high-amplitude, single-cycle THz pulses to well control material analysis in APT, leading to better results on chemical composition. It also paves the way for the use of this radiation for material manipulation.