Nickel Research Articles

Spin-Orbit Torque Booster in an Antiferromagnet via Facilitating a Global Antiferromagnetic Order: A Route toward an Energy-Efficient Memory.

Spin transport and the associated spin torque effects in antiferromagnets (AFMs) are scientifically interesting but have remained elusive due to the varied observations of spin transport in AFMs. This study revisits the role of a global Néel order in nickel oxide (NiO) facilitated through a spin-orbit torque (SOT) and examines the enhanced SOT efficiency in a heavy metal (W)/AFM (NiO)/ferromagnet (FM, CoFeB) trilayer with varying NiO thicknesses ranging from 1 to 5 nm. At the as-grown state, the Néel order of NiO is randomly oriented due to the polycrystalline nature of the film structure, leading to increased spin absorption and blocking spin transport from the adjacent W layer. When the spin current amplitude exceeds a threshold value, SOT enables reorientation of the Néel order in NiO to an equilibrium state, forming a global Néel order aligned with the applied current. This long-range Néel order reduces spin absorption and enhances spin transport through NiO, hence boosting the SOT efficiency in the adjacent CoFeB layer. X-ray magnetic linear dichroism spectroscopy and rewritable Néel order reorientation experiments in a device with orthogonal geometry confirmed the strong correlation between the global Néel order facilitation and the boosted SOT efficiency, which is enhanced larger than 4-fold for both damping- and field-like torques in the trilayer with 5 nm NiO. This study not only reveals the strong correlation between globally facilitated Néel order and spin transport in NiO but also offers a promising manner to promote AFM-based SOT devices toward energy-efficient computing technology.

Research on heavy metal enrichment and transportation in tea plant-soil systems of different varieties.

This study aimed to investigate heavy metal enrichment in different tea plant varieties and their distribution within different plant parts and to clarify the behavioral characteristics of heavy metals in the tea tree-soil system and their influencing factors. In this study, soil samples were collected from the root zones of 13 tea tree varieties in Guizhou, which had been planted for 10years. The aim was to compare the physicochemical properties of tea plantation soils under soil-forming matrixes and consistent management. Additionally, the study investigated the enrichment and transportation patterns of Cd, Cr, Cu, Pb, Zn, and Ni in the tea tree-soil systems of different tea tree varieties. The results showed that the planting of tea trees decreased the soil pH by 0.5; soil nutrients decreased; soil Pb, Cr, Ni, Cu, and Zn contents in the root zone increased; and Cd content decreased. Heavy metals were mainly enriched in the roots, and Zn, Cu, Ni, and other elements related to the protein and enzyme synthesis of tea trees could be mostly transported to the stems and leaves. There were significant differences in the enrichment and transportation of heavy metals among the different tea tree varieties. Under consistent soil-forming parent material, soil pH, organic matter, nutrients, and other indices only had a significant effect on heavy metal enrichment in the tea tree roots. Therefore, in areas with high background soil heavy metal contents, the construction of tea plantations should be based on regional soil environmental conditions to choose tea tree varieties with low heavy metal enrichment capacities to avoid the risk of high background soil heavy metals on the safe production of tea for consumers.

Synthesis, characterization and dielectric properties evaluation of NiO-Co3O4 nanocomposite

AbstractNanosized materials are increasingly being recognized as inherent components in the development of energy storage devices and other state-of-the-art dielectric applications. In this work, nickel oxide (NiO), cobalt oxide (Co3O4) and NiO–Co3O4 nanocomposites in different compositions (10%, 20%, 30% and 40%) were successfully synthesized through hydrothermal method, optimizing concentrations of the precursors, and X-ray diffraction confirmed single-phase polycrystalline NiO and Co3O4. SEM images showed that distinct morphologies for each material and FTIR spectra reveal Ni–O and Co–O. UV–visible analysis shows a plasmon peak at 307 nm for NiO and excition absorption at 282 nm for Co3O4. NiO–Co3O4 nanocomposites displayed band gaps ranging from 2.37 eV to 2.67 eV. Dielectric properties showed a decrease in εʹ with frequency, attributed to Maxwell–Wagner and hopping models. AC conductivity increased with frequency due to Co3O4 content and oxygen vacancies. The study suggests potential applications in supercapacitors, spintronics, high-frequency devices and ultra-high dielectric materials.

Flexible Non-Enzymatic Glucose Sensors: One-Step Green Synthesis of NiO Nanoporous Films via an Electro-Exploding Wire Technique.

In this study, we successfully synthesized nickel oxide (NiO) nanoparticles (NPs), i.e., samples NiO 24V, NiO 36V, and NiO 48V, via an environmentally friendly one-step electro-exploding wire technique by employing three distinct voltage levels of 24, 36, and 48 V, respectively. Sample NiO 48V showed the most rugged surface and smallest particle size, which helped to enhance electrocatalytic properties. The highest Ni3+ content of sample NiO 48V contributed to the increasing redox current and rendering highly enhanced chemical reactions and thereby improving their electrochemical properties and electrocatalytic performance in the glucose oxidation processes in alkaline (0.1 M NaOH, pH = 13) media. The NiO 48V electrode showcased an excellent linear detection range spanning from 0.1 to 1 mM, featuring a remarkable sensitivity of 1202 μA mM-1 cm-2 and an exceptionally low limit of detection (LOD) value of 0.25 μM. Remarkably, NiO NPs exhibited exceptional long-term stability, commendable reproducibility, favorable repeatability, and outstanding selectivity. This study also highlights the excellent operational performance of the NiO 48V electrode in real-world samples, such as commercially available beverages and human urine, highlighting the practical nature of these nonenzymatic sensors in real-life scenarios for the food industries, clinical diagnostics, and biotechnology applications.

Uji Analisis Nikel Ore/Ni (Sampel Cek) Menggunakan Metode Press Pellet Berdasarkan Variasi Suhu Pengeringan, Waktu Pengeringan, dan Berat Sampel Timbangan Press

The purpose of the study was to determine the changes in nickel levels as a result of the analysis on the variation in temperature and drying time as well as the weight of press pellet scale samples from one of the same sample types. This research method is in the form of an experiment with a factorial research design from analysis parameters in the form of MC percentage and nickel ore content of Ni element. The results of the analysis showed that drying at 105°C and 125°C achieved a constant MC during a heating time of 5 to 6 hours. Meanwhile, at a temperature of 145-185 degrees Celsius with an interval of 2-6 hours, the MC level has experienced a constant weight of 44.44%. At the same temperature treatment, which is 105oC, different constant times are obtained. This is influenced by the difference in weight between the two samples, namely in the AP/5 and AP/6 range of 0.360 grams, while AP ORI weighs 1.8 kg. The results of the Epsilon 4 reading showed that the variation in drying temperature at 105°C to 185°C and drying time of 3-6 hours affected the nickel ore content in the range of 1.50% to 1.53%, close to the standard value of nickel 1.50%. The lower the temperature and drying time, the humidity level of the sample increases, causing the nickel ore content to decrease, while the higher the temperature and drying time increases the risk of nickel decomposition. The optimum temperature and drying time is 165°C for 2-4 hours. The press sample weight is between 8-14 grams resulting in a stable nickel content at 1.47%-1.50%, with an optimum weight of 10-14 grams for optimal sample thickness and density.

Impact of metal deposition on the optical and interface properties of NiO: growth and characterization of NiO/metal thin bilayer films

Abstract Since transparent conductive oxides (TCOs) provide electrical conductivity together with optical transparency, they have found wide applications in optoelectronic devices and photovoltaics. Among the TCOs, nickel oxide (NiO) is challenging due to its inherent trade-off between transparency and electrical conductivity. To address this challenge, one effective approach is to deposit a metal layer onto NiO thin films. In this work, NiO, NiO/Au, NiO/Ag, and NiO/Cu thin films are prepared by sputtering and thermal evaporation techniques on glass substrates and fully characterized finding the proper film for optoelectronic applications. The electrical and optical properties of the fabricated films are examined by four-point probe measurements and optical spectrometry. According to the obtained results, the NiO/Au, NiO/Ag, and NiO/Cu bilayers show sheet resistance of 200, 338, and 925 Ω sq−1 respectively while their optical bandgaps vary from 3.2 to 3.76 eV. These findings provide valuable insights into the performance of these films, making them potentially viable choices for various optoelectronic applications.

Balanced d-Band Model: A Framework for Balancing Redox Reactions in Lithium-Sulfur Batteries.

Managing the redox reactions of polysulfides is crucial for improving the performance of lithium-sulfur batteries (LSBs). Herein, we introduce a progressive theoretical framework: the balanced d-band model, which is based on classical d-band center theory. Specifically, by optimizing the position of the d-band center in the middle between the highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) of each sulfur species, balanced and fast oxidation and reduction reactions of the sulfur species can be achieved simultaneously. To validate this theory, we synthesized a catalyst featuring an in situ phosphorized heterostructure (NOP) based on nickel oxide (NiO), which effectively optimizes the d-band center at the middle between the HOMO and LUMO of each sulfur species. Aided by the balanced oxidation and reduction kinetics of the sulfur species, the NOP-based cell achieved a high reversible capacity, superior cycling stability, and prolonged cycle life. This study extends the conventional d-band center theory and introduces an innovative theoretical model to expand our understanding of the internal reaction mechanisms in LSBs.

Different metal-doped NiO nanoparticles for sunlight-mediated degradation of low-density polyethylene microplastic films.

Due to the widespread use and incorrect handling of plastics, we need to find a practical and effective way to eliminate plastic waste from the environment. Different metal-doped nickel oxide (DMD-NiO) nanoparticles (NPs) were synthesized using a sol-gel technique and were used to degrade low-density polyethylene (LDPE) microplastic (MP) films when exposed to sunlight. The optical and structural properties of sol-gel method synthesized materials were investigated using a variety of characterization methods (Fourier transform infrared (FT-IR), UV-vis diffuse reflectance spectroscopy (UV-vis DRS), X-ray diffractometer (XRD) analysis, X-ray photoelectron spectroscopy (XPS), high-resolution transmission electron microscopy (HR-TEM), scanning electron microscopy (SEM) with energy dispersive X-ray (EDX) analysis, and thermogravimetric analysis (TGA). Degradation study results suggest that the photocatalytic activity of DMD-NiO-LDPE nanocomposites (NCs) films was greater than that of pure LDPE and undoped NiO-LDPE films. Because of their increased optical absorption and efficient suppression of photo-produced charge carriers' recombination, the DMD-NiO NPs showed higher photocatalytic degradation of LDPE films. Thus, LDPE films with 2% wt Fe-NiO (iron-doped nickel oxide) nanomaterials showed a degradation of around 38.16% among DMD-NiO-LDPE NCs films under visible light over a short period of 30 days (240 h). The formation of carbonyl groups in the degradation product of LDPE was confirmed by Fourier transform infrared (FT-IR) analysis. When compared to the original LDPE film, the Fe-NiO-LDPE NCs films showed a significant decrease in crystallinity and carbonyl indexes, as much as 8.4% lower. The current project proposes the development of eco-friendly photocatalysts using a sol-gel technique for combating MP pollution in the environment.

Role of synthetic process parameters of nano-sized cobalt/nickel oxide in controlling their structural characteristics and electrochemical energy performance as supercapacitor electrodes

The synthesis of nano-sized bimetallic Cobalt/Nickel oxides (Ni1.5Co1.5O4) with a 1:1 Co/Ni atomic ratio has been achieved using a surfactant-free co-precipitation/hydrothermal process. The growth mechanism of Cobalt/Nickel oxides Ni1.5Co1.5O4 is elucidated by tuning the synthesis process parameters, including co-precipitation pH and hydrothermal time. The formation of Cobalt/Nickel oxides Ni1.5Co1.5O4 oxide began with the nucleation of cobalt nickel hydroxide nanoplates through the co-precipitation process, followed by dissolution-recrystallization, stacked hexagonal nano-flakes, and a flower-like microstructure. The electrochemical performances of the oxides were evaluated, with the largest surface area observed at pH 9 being the main factor for the best super-capacitive performance. As hydrothermal time increased, the structural directing growth forward, resulted in the formation of a nano-flower structure with a larger surface area. The as-prepared cobalt nickel oxide exhibited a maximum specific capacitance value of 525.5 F g-1 at a current density of 1 A g-1 and energy and power densities of 88.2 WhKg-1 and 606 WKg-1, respectively.

Preparation and Characterization of Vanadium Pentoxide and Nickel Oxide Nanoparticles and Their Use in Removing Tetracycline from Water

Preparation and Characterization of Vanadium Pentoxide and Nickel Oxide Nanoparticles and Their Use in Removing Tetracycline from Water

Methodological insights into soil elemental nickel in typical Karst areas: comprehensive analysis of geochemical characteristics, source determination, and influencing factors.

Excessive levels of Nickel in the soil can compromise the security of agricultural products, posing a threat to health of human beings; therefore, the repair and treatment of Nickel exceeding the standard levels in soil are particularly critical. Although it is crucial that the potential restoration of Nickel in ensuring the security of both soil and farm produce within karst regions., few studies have been conducted on the potential restoration of large-scale Nickel-contaminated soils. In this study, the soil in Wuming, Guangxi, a typical karst area, was comprehensively studied. 12,547 surface soil samples, 134 deep soil samples and 60 soil profiles were collected systematically. The results showed that the Nickel background value of the surface soil was 34.9mg/kg, indicating strong background characteristics and high variability. Principal component analysis showed that soil Nickel was primarily derived from natural sources in the geological background and partly derived from agricultural sources. Analysis of variance showed that the Nickel content of the soil was affected by the parent rock, soil type, soil use type, and topography. In addition, the distribution of Nickel in the soil profile increased exponentially with depth. Therefore, the exponential model and multiple integrals were used to derive the formula for the Nickel potential restoration amount at different depth ranges, and the potential restoration amount of soil Nickel was calculated based on different parent material, soil, and land use types. The formula is reasonable and representative and can provide a theoretical basis for the remediation and treatment of Nickel-polluted soil in karst areas.

N/S‐codoped Nickel oxide supported on activated Montmorillonite clay as an Efficient Bifunctional Electrocatalyst for Overall Water Splitting

Developing low‐cost, highly effective, and durable electrocatalysts for complete water splitting (OER/HER) is crucial for future energy provision. Herein, we report N/S‐codoped Nickel oxide supported on activated Montmorillonite clay as an efficient bifunctional electrocatalyst for water electrolysis. The different wt% of Ni‐MMT catalysts were synthesized using an effortless one‐step solvothermal method and their phase recognition, morphology, analysis of elements, and electrochemical performance were confirmed by various characterization techniques. The optimal 10 Ni‐MMT catalyst exhibits outstanding efficiency in both HER (170 mV) and OER (365 mV) at a current density of 10 mAcm‐2 in 1M KOH. Furthermore, doping of N/S heteroatoms increases the active sites for HER/OER, facilitates charge transfer and achieves electrochemical stability of 15 h. The Ni‐MMT catalyst achieved an overall water‐splitting performance in 1M KOH, reaching 10 mAcm‐2 at a cell voltage of 1.82 V.

Effect of ultra-fine grain zone on mechanical properties of CuCrZr-Hastelloy X bimetallic structure manufactured by laser-directed energy deposition

In this study, CuCrZr-Hastelloy X bimetallic structure featuring an ultra-fine grain zone (UFGZ) near the interface were fabricated by laser-directed energy deposition (L-DED). Samples with UFGZ were obtained with 300 °C preheating, whereas samples without preheating did not contain UFGZ. The microstructures and mechanical properties of samples with and without UFGZ were compared. The formation of UFGZ was attributed to the presence of a spherical phase near the interface, which was identified as Ni (Fe, Cr, Mo). Due to the higher melting point of Hastelloy X compared to CuCrZr, Ni elements mixed into CuCrZr with the flow of the molten pool, solidified first, and served as substrates for the heterogeneous nucleation, ultimately promoting the formation of UFGZ. With 300 °C preheating, the hardness of CuCrZr near the interface increased from 115.07 HV to 148.51 HV due to the presence of UFGZ. And the hardness gap near the interface decreased from 172.58 HV to 147.19 HV, which improved the uniformity of mechanical properties. Moreover, the nanoindentation tests results that UFGZ increased the hardness of the zone near the interface from 1.42 GPa to 1.72 GPa. Tensile test results indicated that the UFGZ altered the fracture mode from brittle to ductile. Samples with UFGZ exhibited ductile fracture, while those without UFGZ exhibited brittle fracture. At room temperature, the tensile strength of samples with UFGZ increased from 298.44 MPa to 347.05 MPa. For tests conducted at 400 °C, the tensile strength increased from 165.12 MPa to 229.53 MPa. This enhancement indicated that UFGZ could improve the strength and toughness of the interface, thereby enhancing the interfacial bonding strength. This study is of great significance for improving the interfacial bonding strength of CuCrZr-Hastelloy X bimetallic structures.

Pollution risk assessment and spatial distribution of potentially hazardous elements in selenium-rich soils in the Menyuan Basin of the northeastern Tibetan Plateau

The scientific utilization of selenium (Se)-rich soils necessitates the evaluation of the contents of potentially hazardous elements (PHEs). The Menyuan Basin, a representative Se-rich region located on the northern periphery of the Qinghai–Tibet Plateau, was chosen as the research area. Pollution risk and spatial source analysis was conducted for eight PHEs (As, Cr, Cu, Pb, Zn, Cd, Ni and Hg) using 5297 topsoil samples and 480 deep-soil samples. The results show that more than 50% of the total area has a Se content >0.24 mg kg –1 . According to both single and comprehensive pollution indices, there are extremely few sampling sites with PHEs at risk of contamination. Low ecological risk was seen in 93.34% of the topsoil samples. The results show that although the overall level of surface soil pollution in the study area may be deemed negligible, on the surface or in deeper layers, the concentration centres of As, Cr, Ni, Zn, Pb and other elements show consistency, indicating that underlying parent rocks are the primary source of these elements. The findings presented in this study establish a scientific foundation for the secure development and utilization of Se-rich soils.

System analysis with life cycle assessment for NiMH battery recycling.

The nickel metal hydride (NiMH) battery technology has been designed for use in electric vehicles, solar-powered applications and power tools. These batteries contain the critical and strategic raw materials cobalt, nickel and several rare earth elements (REE). When designing a battery recycling process, there are several choices to be made regarding end-products and process chemicals. The aim of this study is to investigate and compare the environmental and economic sustainability of different recycling options for NiMH batteries by taking projected market developments into consideration and by applying life cycle assessment and life cycle costing methods. The comparative study is limited to recovery of the REEs. Two hydrometallurgical processes for recovery of the REEs from the anode material are compared with extraction of REEs from primary sources in China. The processes compared are a high-temperature sulfation roasting process and a process based on hydrochloric acid leaching followed by precipitation of REE oxalates. By comparing the different recycling approaches, the hydrochloric acid process performs best. However, the use of oxalic acid has a large impact on the overall sustainability footprint. For the sulfation roasting process, the energy, sodium hydroxide and sulphuric acid consumption contribute most to the total environmental footprint. This article is part of the discussion meeting issue 'Sustainable metals: science and systems'.

Comparative Analysis of Structural, Optical, and Electronic Properties of Nickel Oxide and Potassium‐Doped Nickel Oxide Nanocrystals

ABSTRACTMetal oxide semiconductors, known for their exceptional optical transparency, high carrier mobility, and stability, have found extensive use in emerging technologies such as optoelectronics and energy storage devices. Among all metal oxide semiconductors, nickel oxide (NiO) stands out as a highly favorable candidate due to its p‐type conductivity along with its substantial band gap (3.5–4 eV) for the broad range of applications, including gas sensors, high‐rate Lithium‐ion batteries, high‐performance supercapacitors, and photovoltaic devices. In light of these versatile applications, our current study presents a comprehensive comparative analysis of the structural and optoelectronic properties of NiO and potassium (K)‐doped NiO nanocrystals. The nanocrystals were synthesized using the co‐precipitation route and subsequently annealed at 500°C under ambient conditions. The effect of K doping on the structural and optoelectronic characteristics was systematically examined using various techniques, including x‐ray diffraction, UV–visible spectroscopy, Raman spectroscopy, and Hall effect measurements. To explore the structural characteristics, XRD measurements were performed, which confirm the FCC structure of nanocrystals. The optical property analysis suggested that the formation of the energy level can contribute to reduction of the band gap. A sharp peak at 397 cm−1 is associated with NiO bond in FTIR spectra which verifies the formation of nanocrystals. Moreover, the incorporation of K increases the intensity of the Raman peaks, which provides evidence for the higher degree of crystallinity in doped samples. These results of Raman scattering are in good agreement with XRD outcomes. In addition, the resistivity of NiO nanocrystals decreases monotonically with the increasing K concentration. The results of temperature‐dependent resistivity further demonstrate that electrons required more energy to jump from one polaron state to another in the case of x = 0.01 M and 0.03 M doped Ni0.5‐xKxO samples. The combination of a diminished band gap and enhanced conductivity makes these materials exceptionally promising for applications in optoelectronics and energy storage.

Measurement of temporal evolution of antiferromagnetic domain change in nickel oxide driven by 2TO phonon mode excitation via pump-probe experiment

The temporal evolution of antiferromagnetic domain pattern changes under resonant excitation of the second-order transverse optical phonon mode in nickel oxide was investigated using mid-infrared free electron laser (MIR-FEL) pulses and visible nanosecond probe laser pulses at room temperature. We visualized the domain patterns through magneto-optical polarized microscopy in transmission and observed their temporal variation after the phonon excitation via MIR-FEL. We evaluated the differences throughout the timeline using the structural similarity index measure technique from domain images with and without MIR-FEL irradiation. We found that the MIR-FEL irradiation induces significant structural changes in the domain patterns. The maximum difference was observed at the timing of the MIR-FEL irradiation and exponentially recovered with the time constant of 1.4 ± 0.2 ms. This rather long-time constant could be owing to the spin relaxation, whilst further investigation is needed to confirm the underlying mechanism.

Utilizing cationic vacancies to enhance nickel-cobalt layered double hydroxides for efficient electrocatalytic urea oxidation reaction

Electrocatalytic urea oxidation reaction (UOR) is a promising approach for urea-rich wastewater splitting, which benefits for reducing energy consumption in hydrogen production accompanying environmental protection and sustainable energy development. To address the limitations posed by the self-oxidation of nickel-based catalysts on the activity of UOR, we here developed a NiCo LDH nanosheet catalyst with abundant Ni vacancies to initiate the UOR process prior to nickel oxidation. Electrochemical impedance spectroscopy and In-situ spectroscopic characterizations confirm that the UOR process primarily occurs on the surface of the catalyst, rather than being driven by nickel oxidation products. The favorable electronic structure modulation induced by Ni vacancies makes the catalyst more energetically favorable for the UOR compared to nickel self-oxidation. The catalyst exhibits excellent UOR activity, only requiring 1.27 V vs. RHE at 10 mA cm−2 and 1.34 V vs. RHE at 100 mA cm−2, with no significant decay observed after over 120 h of operation. Furthermore, it can function as a bifunctional catalyst, requiring only 1.66 V to achieve 100 mA cm−2 for the UOR||HER system. This study expands the pathway for the application of cationic vacancies in UOR.

Effect of Flash-Ni Plating Layer on Interfacial Behavior of Zn-Al-Mg Coating/DH780 Steel

The Zn-Al-Mg coated DH780 high-strength steel with a flash-Ni plating layer was used in this study. The occurrence state of Ni element at the coating/steel interface was investigated, and the relationship between Mn and Si elements and the internal oxidation at the interface was discussed. The results show that Ni existed between the Fe2Al5 layer and the steel substrate in the form of Fe(Ni) solid solution and Ni elemental substance. The mutual diffusion rate between Fe and Al was greatly reduced after flash-Ni plating, and the continuity of Fe2Al5 layer of the flash-Ni-plated steel was slightly lower than that of the Ni-free steel. Moreover, the diffusion coefficients of Mn and Si in the Ni layer were lower than those in the steel substrate, which indicated that the Ni layer significantly inhibited the diffusion of Mn and Si to the surface. The average depth of internal oxidation was reduced by 70.8% after flash-Ni plating, the average Mn, Si and O contents at the interface after flash-Ni plating were reduced by 19.6%, 6.1% and 22.7%, respectively, which indicated that the flash-Ni plating layer can isolate the steel substrate from the annealing atmosphere, inhibit the internal oxidation and interfacial enrichment of Mn and Si, especially for Mn. Therefore, the flash-Ni plating layer can improve the wettability of high-strength steel sheets during continuous annealing.

Synergistic regulation of nano-precipitates and reversed austenite in titanium-free maraging steel by low-temperature solution treatment and double aging treatment

To synergistically enhance the strength and toughness of titanium-free maraging steel, a multi-scale characterization method was used to illustrate the effects of low-temperature solution treatment and double aging treatment on the microstructure of titanium-free maraging steel in this paper. After the low-temperature solution treatment and the double aging treatment, the tensile strength of titanium-free maraging steel increased from 1954 MPa to 2160 MPa and the elongation increased by 8.95 %. By the low-temperature solution treatment, the original austenite grain size of the titanium-free maraging steel was refined to 0.69 μm. The double aging treatment promoted the diffusion of Mo and Ni elements, increased the volume fraction of ω phase, Ni3Mo nano-precipitation phase and reversed austenite, and refined the size of ω phase and Ni3Mo by 14.2 % and 7.9 %, respectively. The nanoparticles of titanium-free maraging steel mainly include the ω phase, Ni3Mo and Laves phase. The strengthening mechanism of nanoparticles was quantitatively evaluated from the shear mechanism and Orowan dislocation loop mechanism. The mechanism shows that the ω phase is the main contributor to the overall precipitation strengthening. Therefore, low-temperature solution treatment and double aging treatment provide a potential solution for achieving high strength and high toughness in maraging steel.