Inorganic Research Articles

In Ukrainian

Blood loss is one of the main causes of death, especially in war and natural disasters. At the beginning of the full-scale Russian-Ukrainian war we established the laboratory and later the industrial production of a powdered topical hemostatic composition based on nanosilica which is intended for providing first pre-medical aid. The composition contains nanosized silica A-300 and sodium alginate as two active ingredients in a mass ratio of 4:1. The aim of the work was to develop the optimal technological process for the production of a hemostatic composition and carry out physico-chemical and medical-biological studies of semi-finished products and the final product. Bulk density measurements, optical microscopy, IR spectroscopy method and microbiological research were used to study the initial materials, intermediate products as well as the final product. The effectiveness of the hemostatic effect of the composition was checked on the model of parenchymal bleeding from the liver of a rat, using the time to stop bleeding (min) as a criterion. As a result of the research, a two-stage method of manufacturing the composition is proposed: at the first stage, certain parts of the initial materials are treated in a ball mill, obtaining the semi-finished product "A-300/sodium alginate"; at the second stage, this semi-finished product is mixed with nanosilica and sodium alginate, obtaining the final product. It is shown that the bulk density serves as a useful technological parameter to control of which helps to produce a structurally homogeneous final product. In the IR spectra of the semi-finished product and the finished product, only the absorption bands of silica and sodium alginate are observed, that is, foreign substances are not formed during technological process. The microbiological purity of the composition meets the pharmacopoeial requirements for drugs of this category. An experimental study of the topical hemostatic effect of the composition revealed its significant advantage compared to the inorganic hemostatic substance kaolin, which acts according to a similar adsorption mechanism.

Gaining Insights into the Interplay between Optical and Magnetic Properties in Photoexcited Coordination Compounds.

We describe early and recent advances in the fascinating field of combined magnetic and optical properties of inorganic coordination compounds and in particular of 3d-4f single molecule magnets. We cover various applied techniques which allow for the correlation of results obtained in the frequency and time domain in order to highlight the specific properties of these compounds and the future challenges towards multidimensional spectroscopic tools. An important point is to understand the details of the interplay of magnetic and optical properties through performing time-resolved studies in the presence of external fields especially magnetic ones. This will enable further exploration of this fundamental interactions i. e. the two components of electromagnetic radiation influencing optical properties.

EuSi7P10: An Inorganic Supramolecular Nonlinear Optical Crystal Exhibiting Strong Second-Harmonic Generation Response.

Inorganic supramolecular compounds are the emergent class of infrared (IR) nonlinear optical (NLO) materials. However, the reported inorganic supramolecular IR NLO pnictides are still scarce. In this work, a new inorganic supramolecular IR NLO phosphide, EuSi7P10, has been synthesized using the metal salt flux method. The structure of EuSi7P10 features an anionic host framework containing the oriented [Si7P16] dual-T2 supertetrahedra with the guest Eu2+ cations filling in the intervals. Additionally, EuSi7P10 exhibits strong phase-matched (PM) second-harmonic generation (SHG) (4.0 × AgGaS2), large birefringence (0.087 @2050 nm), and wide infrared transparency. This study highlights the potential of inorganic supramolecular pnictides for exploring high-performance IR NLO crystals.

Enhanced low-temperature resistance of lithium-ion batteries based on methyl propionate-fluorinated ethylene carbonate electrolyte

Low temperature has been a major challenge for lithium-ion batteries to maintain satisfied electrochemical performance, as it leads to poor rechargeability and low capacity retention. Traditional carbonate solvents, vinyl carbonate and dimethyl carbonate are indispensable components of commercial electrolytes. However, the higher melting point of these carbonate solvents causes their electrical conductivity to be easily reduced when temperatures drop below zero, limiting their ability to facilitate lithium ion transport. In this work, we demonstrate that the use of methyl propionate (MP) carboxylate and fluorocarbonate vinyl (FEC) electrolytes can overcome the limitations of low temperature cycling. Compared with carbonate electrolyte, MP has the characteristics of low melting point, low viscosity and low binding energy with Li+, which is crucial to improve the low temperature performance of the battery, while FEC is an effective component to inhibit the side reaction between MP and lithium metal. The carefully formulated MP-based electrolyte can generate a solid electrolyte interface with low resistance and rich in inorganic substances, which is conducive to the smooth diffusion of Li+, allowing the battery to successfully cycle at a high rate of 0.5 C at −20 °C, and giving it a reversible capacity retention rate of 65.3% at −40 oC. This work designs a promising advanced electrolyte and holds the potential to overcome limitations of lithium-ion batteries in harsh conditions.

Innovative perspective for the cleaning of historical iron heritage: novel bio-organogel for the combined removal of undesired organic coatings and corrosion

An innovative green organogel was designed to simultaneously tackle inorganic compounds (i.e., iron corrosion) and organic substances (i.e., acrylic coatings) as undesired materials possibly present on the surface of altered indoor metal artworks. Poly-3-hydroxybutyrate (PHB), ethyl lactate (EL), and deferoxamine B (DFO) were employed in the formulation as thickening agent, organic solvent, and complexing agent, respectively, aiming to propose a sustainable and less harmful chemical cleaning method for metal care. The components were selected because they are bio-sourced, renewable, biodegradable, and non- or low-toxic materials. A multi-modal protocol of analysis was carried out to characterise the newly designed PHB-EL-DFO organogel. The cleaning performance of the novel formulation was assessed on mild steel mock-ups presenting both corrosion and organic coating to be removed. The conducted multi-analytical approach verified that the PHB-EL-DFO gel was able to tackle the two undesired materials simultaneously in an adjustable and easy-to-use way thanks to a modular application.

Critical Review of Cu-Based Hole Transport Materials for Perovskite Solar Cells: From Theoretical Insights to Experimental Validation.

Despite the remarkable efficiency of perovskite solar cells (PSCs), long-term stability remains the primary barrier to their commercialization. The prospect of enhancing stability by substituting organic transport layers with suitable inorganic compounds, particularly Cu-based inorganic hole-transport materials (HTMs), holds promise due to their high valence band maximum (VBM) aligning with perovskite characteristics. This review assesses the advantages and disadvantages of these five types of Cu-based HTMs. Although Cu-based binary oxides and chalcogenides face narrow bandgap issues, the "chemical modulation of the valence band" (CMVB) strategy has successfully broadened the bandgap for Cu-based ternary oxides and chalcogenides. However, Cu-based ternary oxides encounter challenges with low mobility, and Cu-based ternary chalcogenides face mismatches in VBM alignment with perovskites. Cu-based binary halides, especially CuI, exhibit excellent properties such as wider bandgap, high mobility, and defect tolerance, but their stability remains a concern. These limitations of single anion compounds are insightfully discussed, offering solutions from the perspective of practical application. Future research can focus on Cu-based composite anion compounds, which merge the advantages of single anion compounds. Additionally, mixed-cation chalcogenides such as CuxM1-xS enable the customization of HTM properties by selecting and adjusting the proportions of cation M.

Cyclotriphosphazene: A Versatile Building Block for Diverse Functional Materials.

Cyclotriphosphazene (CP) is a cyclic inorganic compound with the chemical formula (NPCl2)3. This unique molecule consists of a six-membered ring composed of alternating nitrogen and phosphorus atoms, each bonded to two chlorine atoms. CP exhibits remarkable versatility and significance in the realm of materials chemistry due to its easy functionalization via facile nucleophilic substitution reactions in mild conditions as well as intriguing properties of resultant final CP-based molecules or polymers. CP has been served as an important building block for numerous functional materials. This review provides a general and broad overview of the synthesis of CP-based small molecules through nucleophilic substitution of hexachlorocyclotriphosphazene (HCCP), and their applications, including flame retardants, liquid crystals (LC), chemosensors, electronics, biomedical materials, and lubricants, have been summarized and discussed. It would be expected that this review would offer a timely summary of various CP-based materials and hence give an insight into further exploration of CP-based molecules in the future.

Survey of Recent Trends of IB-IVB Metals and Their Compounds in Cancer Treatment

Metals from IB to IVB groups of the periodic table, because of their flexible oxidation states, natures of coordinated bioligands, and geometries upon complexation, display various properties and efficiency of metal-based cytotoxic drugs. Recent decades have witnessed remarkable progress in the synthesis and therapeutic application of numerous inorganic compounds in cancer investigations. The main potential therapeutic agents, such as the complexes of platinum group metals possessing antineoplastic activity have been broadly described previously in the literature and are beyond the space of this analysis. The key objective of the present study is to analyze the possible activity of IB-IVB group metals their coordination compounds against the cancer cell types. The increasing number of anticancer drug candidates among these metals proves this field offers a remarkably variation of novel opportunities for the synthesis of advanced new pharmaceutics with diverse and specific modes of action. Furthermore, the review provides forthcoming insights into prospective clinical scenarios for approaching treatment applications. That is why this field of research deserves more attention. It is expected that this review can serve as a guiding framework for future investigations in cancer chemotherapy.

Investigations of high-Performance Ultrasonic Transducers based on PMN-PT Single Crystals

Ultrasonic transducers for NDE applications are commonly based on Lead Zirconate Titanate or PZT, an inorganic compound and ceramic perovskite material. Until now the advantages of PMN-PT are used in medical applications, but are not implemented in NDE. Lead Magnesium Niobate-Lead Titanate (PMN-PT) is well known for its high sensitivity and broad frequency spectrum. While conventional PZT materials have an electromechanical coupling factor K33 (a measure of the conversion between electrical and acoustic energy) of about 0.72, PMN-PT materials reach peak values of more than 0.93. For applications with low signal amplitudes, high electronic noise and small transducer elements, the performance of ultrasonic probes can be significantly enhanced by using Lead Magnesium Niobate-Lead Titanate (PMN-PT) instead of PZT. This single-crystal material offers significantly better piezo parameters and leads to a higher sensitivity and larger bandwidth. There is a better depth resolution possible with this transducers as practical tests have shown. Similar to PZT it can also be fabricated in 1-3 piezo- composite technology. In a cooperation between Fraunhofer IKTS, iBULe Photonics, and IFU Diagnostic Systems, PMN-PT ultrasonic transducers are developed and optimized. The performance of phased array probes and single element transducers was measured by a so called PCUS® pro electronic front end from Fraunhofer and compared with equivalent PZT-based probes. As a result various single element and phased array transducers with im-proved performances are available for NDT of typical aerospace materials and applications. These test setups were used to weigh up the advantages and disadvantages, such as achievable precision or costs, for the implementation of a PMN-PT-based UT matrix probe. Based on this, a wiring variant adapted to the PMN-PT was developed and optimised for the matrix setups by pre- assembling the matching layers. The most favourable setup turned out to be bonding the PMN- PT composites to the prefabricated matching layers together with a rigid-flexible PCB frame. This enabled direct wire bonding of 64 matrix elements to the matching PCB pads on the rigid frame.

Phase transition, structural and magnetic parameters of vanadium-substituted Bi0.9Sm0.1FeO3 multiferroic ceramics

ABSTRACT The inorganic multiferroic compounds Bi0.9Sm0.1Fe1 − x V x O3 (x = 0.0, 0.015, 0.03, and 0.045) were prepared by the solid-state reaction method. X-ray diffraction analysis confirmed the rhombohedral perovskite-like structure with minor traces of the impurity phases Bi2Fe4O9 and Bi25FeO40. The lattice parameters a and c, and the volume of the hexagonal unit cell were extracted from the X-ray diffraction data and found to increase as the V5+ content is increased. The average crystallite size was estimated to be in the range 380–415 Å. Fourier transform infrared spectroscopy confirmed the rhombohedral perovskite-like structure via the vibration bands of the octahedral FeO6 group observed between 410 and 570 cm−1. A differential scanning calorimeter was used to record the thermal scans which revealed that the compounds have undergone crystalline phase transitions at temperatures in the range 300–320°C. A 4.5% V + 5 substitution has shifted the transition peak by 20°C. The magnetic hysteresis loops taken at room temperature with a vibrating sample magnetometer revealed the ordinary ferromagnetic behavior. The V5+ substitution enhanced the remanent magnetization, but the magnetic coercivity was found to fluctuate around an average value of about 1000 Oe. The compound Bi0.9Sm0.1Fe0.955V0.045O3 exhibited the maximum remanent magnetization.

Long-term subsoiling and tillage rotation increase carbon storage in soil aggregates and the abundance of autotrophs

Autotrophic microorganisms in soil can increase soil carbon (C) sequestration by utilising chemical energy released from inorganic compounds to fix atmospheric CO2. Therefore, the effects of tillage systems on soil C stocks and autotrophic microbial community deserves in-depth study. The effects of five tillage systems, including no tillage (NoTill), subsoiling (SubS), rotary tillage (RotTill, local general tillage), no tillage-subsoiling-no tillage (NoTill-SubS), and rotary tillage-subsoiling-rotary tillage (RotTill-SubS) were investigated within a 17-year field experiment. Their effects on soil aggregates, C content and enzyme activities were studied, and the impacts on C-fixing microbial communities were analysed using the C-fixing gene cbbL. The macroaggregate portion and RubisCO and ATPase activities were the highest under SubS, causing the aggregate-associated organic C (AOC) to be 93 % higher than that under RotTill. Under RotTill-SubS, SOC, AOC and aggregate-associated microbial biomass C (AMBC) were larger than those under RotTill. RotTill-SubS reduced the microaggregate portion, increased enzyme activities and the relative abundance of C-fixing bacteria, including Sphingomonadales, Burkholderiales, and Nitrosomonadales. The macroaggregate portion under NoTill-SubS and the relative abundance of Sphingomonadales and Burkholderiales was the highest. Correspondingly, the SOC content was the largest (29 % higher than that in RotTill), and the AOC and AMBC contents were 42 % and 31 % larger, respectively, than those in RotTill. Structural equation modelling reveals that increasing tillage or lowering AOC content can directly increase differences in autotrophic bacterial communities. The reduced aggregate stability decreases C content and increases ATPase and RubisCO activities can indirectly increase differences in bacterial community composition.

A sensitive and selective voltammetric method for the detection of pyrogallol in tomato and water samples using platinum electrode modified with alizarin red S film.

In contrast to the hyperactive platinum electrode, ARS modified platinum electrode presents a remarkable inertness toward adsorption and surface processes and lends it for further voltammetric applications. Measuring pyrogallol levels in samples is significant for assessing their antioxidant activity, which is crucial for understanding their potential health benefits and ability to combat oxidative stress. In addition, the excess consumption of pyrogallol can have significant negative effects on human health. A voltammetric sensor has been developed for the determination of pyrogallol using ARS modified platinum electrode. The electrode was prepared by electrodeposition of alizarin red S on a platinum electrode using cyclic voltammetry with a potential scan range of - 0.4 to 1.2V against an Ag/AgCl quasi reference electrode for 60 cycles as optimum number of cycles. The modified electrode was characterized by CV and SEM techniques. This modified alizarin red S platinum electrode showed remarkable electrocatalytic performance and stability, resulting in a significant increase in pyrogallol oxidation current by 11.05% compared to the pyrogallol oxidative current at the unmodified platinum electrode. A well-defined oxidation peak was observed at ~ 0.40V. The sensor exhibited a low limit of detection (LOD) of 0.28µM and a linear standard curve covering the ranges of 1.0-40µM and 0.01-10.0mM pyrogallol. Extensive studies were performed to evaluate possible interferences from various organic and inorganic compounds and yielded satisfactory results that confirm the selectivity of the developed sensor for pyrogallol determination. In addition, the ARS-Pt electrode provided consistently reliable results for the accurate detection of pyrogallol in water and tomato samples.

Rapid detection of explosives in collected dust using ion mobility spectrometry

Vapor and particulate matter from explosives can be adsorbed onto dust, enabling their detection in security and military applications. In this study, model explosive-adsorbed dust specimens were prepared using four types of dust from two inorganic substances [silica (SL) and clay (CL)] and two organic materials [sawdust (SD) and cotton fabric (CF)]. Three explosives, namely 2,4,6-trinitrotoluene (TNT), 1,3,5-trinitro-1,3,5-triazacyclohexane (RDX), and pentaerythritol tetranitrate (PETN), were investigated, along with two different collection filters of poly(tetrafluoroethylene) (PTFE) and lens cleansing paper (LCP). The dust was sprayed in a hood and collected using a cyclone collector. The explosive components present in the dust were rapidly detected using ion mobility spectrometry (IMS). The adsorption efficiencies of TNT, RDX, and PETN onto dust were 36 – 97, 45 – 76, and 37 – 90 %, respectively, and the values of the inorganic dusts were higher than those of the organic dusts. The dust collection rate ranged from 5 to 15 %, and decreased in the order of CL > CF > SL = SD. The factors influencing rapid explosive detection were the intrinsic vapor pressure of the explosive, interactions between the dust and the explosive, thermal conductivities of the dusts and collection filters, and structure of the collection filter. Due to the low vapor pressure of RDX, this explosive was detected later than TNT and PETN. In most cases, detection was more rapid when using the LCP than when using the PTFE because of the thicker and woven structure of the PTFE filter. The detection limits achieved using the LCP (0.049 – 1.17 μg) were lower than those of the PTFE (0.67 – 10.05 μg). When the PTFE was used, the detection limits for the organic dusts were lower than those for the inorganic dusts. Notably, the detection limits of the explosives adsorbed onto dust were significantly higher than those of the pure explosives.

Molecular Weight-Dependent Physiochemical Behaviors of Calcium Carbonate Chains.

The regulation of physiochemical behaviors by changing molecular weights is an important cornerstone of polymer physics. However, similar correlations between molecular weights and properties have not been discovered in inorganic ionic compounds. In this work, we prepared a calcium carbonate specimen with a semiflexible chain topology analogous to those of polymers. The molecular weights of the calcium carbonate chains, which ranged from 3400 to 54 100 Da, were directly correlated to their physiochemical behaviors, including gel point, zero shear viscosity, and plateau modulus. The calcium carbonate chains showed similar polymeric characteristics, including shear thinning, thixotropy, entropic elasticity, and viscoelasticity. These features agreed with recent theories and formulas in polymer physics textbooks. On the basis of this understanding, the mechanical properties of calcium carbonate-based gels could be altered by changing their molecular weights. This study could represent a fusion of inorganic chemistry and polymer physics with similar molecular weight-dependent behaviors and material properties, establishing an alternative pathway for designing future inorganic materials.

Inorganic fillers tailored Li+ solvation sheath for stable lithium metal batteries

Ionogel electrolytes based on gel scaffolds and ionic liquids (ILs) have garnered widespread attention for their processing compatibility, non-flammability, and exceptional thermal/electrochemical properties. While there have been many studies demonstrating the effectiveness of the bisalt approach in stabilizing lithium metal anode, the precise impact of skeleton-constrained dual-anion ionogels on interface modulation remains somewhat obscured and deserves further attention. Herein, we formulate a Li6.4La3Zr1.4Ta0.6O12 (LLZTO)-incorporated dual-anion ionogel to reveal the solvation chemistry in the presence of LLZTO and detail the Li+ transport mechanism and effect on the interfacial chemistries of Li-metal. The impact of inorganic substances on the solvation structure in IL-based solid electrolytes and their role in forming the SEI layer on lithium metal was unveiled. To be specific, the introduction of fillers exert a selective modulating influence on the anions species in the Li+-solvated shell and fine-tunes the local Li+ environment, thereby fostering a more robust interfacial layer. Modified ion environment in ionogels enables a preferable shift from vehicular to structural Li+ transport, whereby a high Li ion conductivity (1.24×10−3 S/cm) and high Li ion transference number of 0.42 is achieved. The synergistic solvent coordination and adjustment of the electrode-electrolyte interface enable the LiFePO4|PIL-10|Li cells to cycle steadily with capacity retention of 95.4 % after 500 cycles at 1C and 25 °C. The strategy of promoting transport mechanisms holds promise for designing the next-generation solid-state lithium metal batteries with high energy density.

Recent progress in MXenes-based lithium-sulfur batteries

Lithium-sulfur batteries (LSBs) are considered as the potent candidates for next-generation energy storage systems due to their high theoretical energy density. However, some inherent problems, including sulfur insulation, shuttle effect caused by lithium polysulfides, and lithium dendrites, hinder their practical application. Various materials have been studied to address the aforementioned issues. A class of two-dimensional inorganic compounds (MXenes), such as transition metal carbides, nitrides, and carbon nitrides, have recently emerged. In this review, we summarize the characteristics and commonly used preparation methods of MXenes and outline the latest development of MXenes and their composites in LSBs. When utilized as sulfur carriers, modified layers of separators, hosts for lithium metal anodes, and electrolyte additives in LSBs, the diversity of structure, excellent conductivity, and high mechanical strength of MXenes and their composites highlight the competitive advantages. This review provides some ideas for the future development of MXenes in LSBs.

In Situ Characterizations of the Dynamics of Cathode Electrolyte Interfaces at Different Current Densities.

LiNi0.8Mn0.1Co0.1O2 with high nickel content plays a critical role in enabling lithium metal batteries (LMBs) to achieve high specific energy density, making them a prominent choice for electric vehicles (EVs). However, ensuring the long-term cycling stability of the cathode electrolyte interfaces (CEIs), particularly at fast-charge conditions, remains an unsolved challenge. The decay mechanism associated with CEIs and electrolytes in LMB at high current densities is still not fully understood. To address this issue, in situ Fourier transform infrared (FTIR) is employed to observe the dynamic process of formation/disappearance/regeneration of CEIs during charge and discharge cycles. These dynamic processes further exacerbate the instability of CEIs as current density increases, leading to rupture and dissolution of CEIs and subsequent deterioration in battery performance because of continuous electrolyte reactions. Additionally, the dynamic changes occurring within individual components of CEIs at different cycling stages and various current densities are also discussed. The results demonstrate that excellent capacity retention at small current density is attributed to enrichment of inorganic compounds (Li2CO3, LiF, etc.) and rendering better stability and smaller expansion of CEIs. The key to achieving excellent electrochemical performance at high current densities lies on protecting CEIs, mainly inorganic components.

Ultrasonic reactor set-ups and applications: A review

Sonochemistry contributes to green science as it uses less hazardous solvents and methods to carry out a reaction. In this review, different reactor designs are discussed in detail providing the necessary knowledge for implementing various processes. The main characteristics of ultrasonic batch systems are their low cost and enhanced mixing; however, they still have immense drawbacks such as their scalability. Continuous flow reactors offer enhanced production yields as the limited cognition which governs the design of these sonoreactors, renders them unusable in industry. In addition, microstructured sonoreactors show improved heat and mass transfer phenomena due to their small size but suffer though from clogging. The optimisation of various conditions of regulations, such as temperature, frequency of ultrasound, intensity of irradiation, sonication time, pressure amplitude and reactor design, it is also discussed to maximise the production rates and yields of reactions taking place in sonoreactors. The optimisation of operating parameters and the selection of the reactor system must be considered to each application’s requirements. A plethora of different applications that ultrasound waves can be implemented are in the biochemical and petrochemical engineering, the chemical synthesis of materials, the crystallisation of organic and inorganic substances, the wastewater treatment, the extraction processes and in medicine. Sonochemistry must overcome challenges that consider the scalability of processes and its embodiment into commercial applications, through extensive studies for understanding the designs and the development of computational tools to implement timesaving and efficient theoretical studies.

Thermoelectric Performance of Hybrid Inorganic/Organic Composites Based on PEDOT:PSS/Tin(II) Oxide.

PSS(poly(3,4-ethylenedioxylthiophene):poly(styrenesulfonate))-based composites often exhibit remarkable characteristics regarding high electrical conductivity and great processability, being a suitable candidate for thermoelectric (TE) applications. To increase its performance, PEDOT:PSS is commonly blended with scarce and toxic inorganic compounds based on Se, Te or Bi. In this work we propose the use of one p-type metal oxide semiconductor (MOs): tin(II) oxide (SnO), motivated by its abundance and low toxicity. Hybrid PEDOT:PSS/SnO composites were obtained by firstly blending Ethylene glycol (EG) with PEDOT:PSS and then by adding p-type SnO, previously synthesized by a chemical route. The mixture was deposited via spin-coating onto glass substrates. The Power Factor (PF) of the composites increased by a factor of 300 with the combined EG/SnO composition.

Catalytic Growth of Ionic Conductive Lithium Nitride Nanowire Array for Dendrite‐Free Lithium Metal Anode

AbstractThe development of an artificial solid‐electrolyte interphase (SEI) has been recognized as the most efficient strategy to overcome the safety concerns associated with the lithium metal anode (LMA). Inorganic‐rich SEIs on the LMA are crucial for suppressing Li dendrites. Among the prevalent SEI inorganic compounds observed for LMA, lithium nitride (Li3N) is often found in the SEIs of high‐performance LMA. Herein, the Li3N nanowire array is successfully synthesized and the catalytic base‐growth mechanism is thoroughly investigated. The fast ionic conductor Li3N nanowires act as pillars to control the nucleation and growth of lithium metal along the vertical direction of the nanowire by bottom‐up self‐lubrication, which fundamentally prevents the dendrite growth. The Li3N is characterized by abundant lithiophilic nucleation sites, which effectively reduces the local current density, and facilitates homogeneous Li+ flux. Symmetric cells utilizing the Li3N@Li anode have demonstrated excellent stability, featuring uniform deposition without dendrite formation. Additionally, high‐capacity retentions of 98% at 0.5 C after 400 cycles and impressive high‐rate performance at 31.1 mA cm−2 have been realized in high‐loading Li3N@Li||LFP cells. The universal preparation of the Li3N nanowires with various precursors and substrates is further explored, which is expected to be applied in solid‐state batteries and hydrogen storage.