High-resolution Transmission Electron Microscopy Observations Research Articles

Nanomineralogy of thorite in the supergiant Huayangchuan uranium ore deposit: Revealing a new geochemical behavior of actinide in environment

Thorium (Th) is a naturally occurring radioactive element found in the environment, and recent advancements have been made in identifying and characterizing Th-bearing nanoparticles (NPs). However, the main focus is still on synthesized Th-bearing NPs and knowledge about natural Th-bearing NPs remains limited. Here, high-resolution transmission electron microscopy (HRTEM) observations of thorite from the Huayangchuan uranium ore deposit in Shaanxi Province, Central China, have revealed the nanoscale mineral characteristics of thorite. In this study, thorite NPs ranging from 5–10 nm in size were identified within the uranium ore. A combination of transmission electron microscopy-energy dispersive spectroscopy (TEM-EDS) elemental mapping and corresponding HRTEM images alongside Selected Area Electron Diffraction (SAED) and Fast Fourier Transform (FFT) patterns revealed a complex nanoscale structure in the thorite NPs, consisting of both amorphous and crystalline nanodomains with abundant defects. These nanostructures are associated with a metamictization mechanism in micrometer-sized thorite. Our findings indicate that the metamictization process can generate numerous thorite nanoparticles. Given the high penetrability and mobility of these NPs, the metamictization of thorite poses new challenges for the long-term stability of radioactive substances and the storage containers for radioactive waste. Furthermore, considering the likelihood of environmental release and the chemical toxicity, radioactivity, and nanotoxicity of natural Th-bearing NPs, increased attention should be given to the presence of natural thorite NPs in the ore deposit.

Emerging 2D nanoscale metal oxide sensor: semiconducting CeO2nano-sheets for enhanced formaldehyde vapor sensing.

Herein, we fabricated nanoscale 2D CeO2sheet structure to develop a stable resistive gas sensor for detection of low concentration (ppm) level formaldehyde vapors. The fabricated CeO2nanosheets (NSs) showed an optical band gap of 3.53 eV and cubic fluorite crystal structure with enriched defect states. The formation of 2D NSs with well crystalline phases is clearly observed from high-resolution transmission electron microscope (HRTEM) images. The NSs have been shown tremendous blue-green emission related to large oxygen defects. A VOC sensing device based on fabricated two-dimensional NSs has been developed for the sensing of different VOCs. The device showed better sensing for formaldehyde compared with other VOCs (2-propanol, methanol, ethanol, and toluene). The response was found to be 4.35, with the response and recovery time of 71 s and 310 s, respectively. The device showed an increment of the recovery time (71 s to 100 s) with the decrement of the formaldehyde ppm (100 ppm to 20 ppm). Theoretical fittings provided the detection limit of formaldehyde ≈8.86 ± 0.45 ppm with sensitivity of 0.56 ± 0.05 ppm-1. The sensor device showed good reproducibility with excellent stability over the study period of 135 d, with a deviation of 1.8% for 100 ppm formaldehyde. The average size of the NSs (≈24 nm) calculated from HRTEM observation showed lower value than the calculated Debye length (≈44 nm) of the charge accumulation during VOCs sensing. Different defect states, interstitial and surface states in the CeO2NSs as observed from the Raman spectrum and emission spectrum are responsible for the formaldehyde sensing. This work offers an insight into 2D semiconductor-based oxide material for highly sensitive and stable formaldehyde sensors.

Uncovering all possible dislocation locks in face-centered cubic materials

Dislocation reactions and locks play an important role in the plastic deformation and mechanical behavior of crystalline materials. Various types of dislocation locks in face-centered cubic (FCC) materials have been reported in the literature pertaining to material-specific molecular-dynamic simulations and high-resolution transmission electron microscopy observations. However, it is unknown how many dislocation locks are possible, and how immobile all the dislocation locks are, with respect to each other. Here we present a discrete mathematics-based approach to reveal all possible dislocation locks in the FCC crystal structure. Totally eight types of dislocation locks are uncovered, resulting from all possible reactions of mobile/glissile (namely, perfect and Shockley partial) dislocations with (a) non-coplanar Burgers vectors which reside on two slip planes intersecting at both obtuse and acute angles and (b) coplanar Burgers vectors. We redefine the degree of dislocation lock immobility based on misorientations between non-close-packed lock planes and close-packed {111} slip planes. The subsequently derived sequences for the dislocation lock immobility and formation tendency are rationalized by the reported experimental and dislocation-dynamics simulation results.

Harnessing a WOx-based flexible transparent memristor synapse with a hafnium oxide layer for neuromorphic computing.

Transparent memristor-based neuromorphic synapses are expected to be specialised devices for high-speed information transmission and processing. The synaptic linearity and potentiation/depression cycles are imperative issues for the application of memristors. This work explores a memristor for improving switching uniformity by introducing a thin HfOx interfacial layer as a diffusion-limiting layer sandwiched between WOx and ITO bottom electrodes. An optimized HfOx thickness not only provides the best switching properties but also shows superior synaptic properties. The optimized 15 nm thin WOx layer can retain the memristor's excellence in P/D linearity, a cycling stability of 494 epochs and image recognition up to 3 mm bending, making it suitable for flexible devices. The artificial synapse is capable of reversible short-term and long-term learning behaviors confirmed by spike-timing-dependent-plasticity (STDP) results. X-ray photoelectron spectroscopy confirms the device composition and provides the oxygen vacancy concentration at the WOx/HfOx interface to realize the switching mechanism. The thicknesses of the different layers are estimated from the high-resolution transmission electron microscopy observations. The fabricated device exhibits 92.2% transparency, as confirmed by the UV-Vis spectrum.

Oriented attachment of silver nanoparticles in DMSO by collapsing under thermal stress

Nowadays, understanding the behavior of nanoparticle agglomeration is crucial to gain insight into the fundamental physicochemical processes that govern particle interactions at the nanoscale. In this work, we are focused on the thermal collapse of silver nanoparticles (NPs) stabilized with sodium citrate in dimethyl sulfoxide (DMSO). Therefore, we investigated the parameters that influence the transition from nearly isolated particles to elongated Ag agglomerates using Dynamic Light Scattering (DLS) and Ultraviolet-Visible Spectroscopy (UV-Vis). In addition, we conducted an in-depth study of the near-particle-particle interaction within the agglomerate using High-Resolution Transmission Electron Microscopy (HRTEM) observations of the agglomerates. The HRTEM results suggest that in the elongation of the agglomerate, the oriented attachment within the initial cluster plays a crucial role in the alignment along the longitudinal axis. The aging colloid exhibits minimal agglomeration, suggesting that the driving force of the collapse phenomenon is predominantly thermodynamic rather than kinetic in nature, and that the surface chemical equilibria play a key role in the preferential orientation mechanism.

Enhancement of Li intercalation kinetics of LiFePO4 nanoparticles with mesoporous carbon

Carbon-assisted energy storage in Li-ion batteries is a crucial topic in the era of carbon neutrality. This work reports a remarkable synergistic effect between lithium iron phosphate (LiFePO4, LFP) nanoparticles and mesoporous carbon (MC) that greatly improves the rate performance and cycle performance. The rapid capacitive effect of MC helps establish a local Li+-rich environment for LFP, enhancing the Li intercalation kinetics inside LFP nanoparticles during discharge. This synergistic effect is quantificationally evaluated using a single-particle model to compare the Li intercalation extent of LFP particles under the presence and absence of MC, which is further confirmed by high-resolution transmission electron microscopy observation, in-situ X-ray diffraction characterization and electrochemical impedance spectroscopy test. In addition, the LFP/MC composite cathode exhibits a nearly 100% capacity retention after 1,000 cycles under 1C charge and 10C discharge. Overall, the addition of MC proves to be a very simple but robust method to increase the capacity, power density and cycle life of LFP-based devices.

In situ heating high-resolution TEM observation of structural recovery in metamict titanite

Besides radiation resistance, thermal recovery of radiation damage provides another critical criterion to evaluate the host phase for immobilizing high-level waste (HLW) produced by nuclear plants. Despite the increasing investigations, a comprehensive atomic-scale understanding remains elusive on thermal annealing of radiation damage in ceramics. Here, using in situ heating high-resolution transmission electron microscopy, we investigate the thermal annealing of radiation damage in natural metamict titanite (CaTiSiO5) caused by a high alpha decay dose from the incorporated U and Th during the geologic time. The recovery of the fully amorphous titanite precursor starts at 456 ℃ from the appearances of monoclinic nanoparticles 2–5 nanometers wide, and more nanoparticles form as the temperature gradually increases. At 1000 ℃, the amorphous phase recovers through epitaxial growth with titanite nanoparticles as templates. This study provides information for a unit-cell-scale understanding of the thermal stability of radiation damage in titanite-based ceramics, having significance for immobilizing HLW.

Insights into the mechanochemical synthesis of nanostructured PbTe: The role of structural defects

Mechanochemical synthesis of nanostructured PbTe, adding isopropyl alcohol during milling, is promoted by the presence of structural defects such as edge dislocations, amorphous zones, grain boundaries, among others. High-resolution transmission electron microscopy observations revealed that the nanostructured PbTe formation is fundamentally dependent upon crystalline imperfections during the high-energy milling process. Even though defect-dependent mechanisms rule the formation of nanostructured PbTe, oriented-attachment mechanism is also traced and contributes to the PbTe formation. Hence, experimentally, isopropyl alcohol is a key parameter for the mechanochemical synthesis of nanostructured PbTe.

Pressure-induced ferroelectric and electronic transitions in two-dimensional ferroelectric semiconductor of NbOCl2 up to 41.7 GPa

NbOCl2, a representative van der Waals ferroelectric (FE) semiconductor, has become the research frontier due to its peculiar appeal in both fundamental research studies and potential applications. In the present work, the high-pressure structural, vibrational, and electrical transport properties of NbOCl2 under different hydrostatic environments were systematically investigated over a wide pressure range of 1.7–41.7 GPa using a diamond anvil cell coupled with in situ Raman spectroscopy, electrical conductivity, and high-resolution transmission electron microscopy (HRTEM) observations. Upon non-hydrostatic compression, NbOCl2 underwent a FE-to-antiferroelectric phase transition at 3.4 GPa, followed by a semiconductor-to-metal transformation at 15.7 GPa. Under hydrostatic compression, the FE transformation and metallization of NbOCl2 were postponed by ∼2.0 and ∼4.0 GPa due to the effect of helium pressure-transmitting medium. Upon decompression, the phase transition was demonstrated to be reversible under different hydrostatic environments, which was well corroborated by HRTEM analyses. In addition, the linear relations between electrical current and sinusoidal voltage with the nonlinearity factors of ∼1.0 reflect the Ohmic response of NbOCl2 before and after the FE transition. Our findings on NbOCl2 provide a guideline for exploring other layered FE materials under high pressure and establishing a design paradigm for new generations of FE-based devices.

Enhanced photocatalytic antibacterial activity of Au-coated Ni–Ti–O nanotubes for biomedical applications

Nickel-titanium (NiTi) alloy is a smart material exhibiting superelasticity, contributing to low stiffness and facilitating integration with bone structures. However, NiTi alloy's bioactivity and antibacterial activity limit its dental applications. In this study, we fabricated nickel titanium oxide (Ni–Ti–O) nanotubes with the potential for bioactivity and photocatalytic properties on the surface of NiTi alloy. Specifically, we applied a coating of gold (Au) nanoparticles to the surface of Ni–Ti–O nanotubes, in order to leverage the antibacterial activity through the photocatalytic effect under 470 nm visible light. Field-emission scanning electron microscopy (FE-SEM) and high-resolution transmission electron microscopy (HR-TEM) observations revealed that Au was deposited mainly at the top surface of Ni–Ti–O nanotubes (diameter: 12.76 ± 2.91 nm, height: 721.12 ± 50.25 nm). X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and diffuse reflectance spectroscopy (DRS) analyses revealed that the Ni–Ti–O nanotubes were NiTiO3 crystalline phases with low crystallinity. Therefore, based on the methylene blue (MB) degradation test, the photocatalytic effect was only achieved under visible light at 470 nm, facilitated by the presence of Au. The antibacterial colony forming unit test and enzymatic activity tests demonstrated that Au-coated Ni–Ti–O nanotubes displayed excellent antibacterial activity under 470 nm visible light irradiation, which was also attributed to photocatalytic effect. Consequently, the combination of Au-coated Ni–Ti–O nanotubes and visible light-based photofunctionalization holds promise for expressing antibacterial properties in dental applications.

Copper nanoparticle and point defect formation in Cu+-Na+ ion-exchanged glass using protons of 2 MeV energy.

There are several applications for irradiating materials with protons that could provide alternative methodologies to synthesize and induce the formation of new compounds of different size scales. In this study, we explored the effects of proton irradiation oncommercial glass silicate that was previously subjected to a Cu+-Na+ ion exchange (IE) treatment at 600 °C for a duration of 60 min. The ion-exchanged glass samples were irradiated with protons (p+) of 2 MeV energy at doses in the range of thousands of grays (3.3 × 103, 7.9 × 103 Gy) and hundreds of thousands of grays (3.6 × 105 Gy). Significant changes in the optical and structural properties were observed post the radiation treatment. The UV-Visible absorption spectra of the irradiated samples revealed the appearance of overlapping absorption bands, which could be deconvoluted into three Gaussian-shaped bands peaking at 566, 620 and 680 nm. These three bands could be attributed to the surface plasmon resonance (SPR) of copper nanoparticles, non-bridging oxygen hole centers (NBOHCs) and self-trapped hole (STH) defects, respectively. Prominent photoluminescence (PL) was observed in the Cu-exchanged and irradiated samples, mainly induced by the presence of both Cu+ and Cu2O. Increasing the irradiation dose led to an increase in the PL intensity due to the conversion of Cu2+ ions into Cu+. This result was confirmed by electron paramagnetic resonance (EPR) spectroscopy that shows a decrease in the Cu2+ signal when increasing the dose of proton exposure. Transmission electron microscopy (TEM) and high-resolution TEM (TEM and HRTEM) observations confirmed the presence of copper nanoparticles (CuNPs) in the doped and p+ irradiated Cu-exchanged glass silicate samples. These CuNPs were found to be crystalline with an average size of 12.39 nm.

Graphene-like materials supported on sepiolite clay synthesized at relatively low temperature

The preparation of solids with graphitic structure usually requires synthesis procedures using very high temperatures. In this work, a comparative study involving different experimental strategies of synthesis at relatively low temperature was carried out to obtain graphene-like materials supported on microporous sepiolite (SEP) clay. The final objective was the optimization of the development of new clay-graphitic nanostructured materials to achieve porous solids while saving energy and time during the preparation stages. The pyrolysis of sucrose (SUC), used as carbon precursor, was accomplished by microwave (MW) pyrolysis or tube furnace (TF) pyrolysis at 200 or 500 °C followed by a hydrothermal carbonization (HTC) step. The resulting carbon-clay nanoarchitectures were characterized by Raman and Infrared spectroscopy, X-ray diffraction, elemental analysis, electron microscopy, and nitrogen adsorption-desorption isotherms. The MW200 and TF200 treatments caramelized SUC and the post-HTC step was fundamental to obtain porous carbonaceous materials. The TF500 pyrolysis produced predominantly crystalline carbon, while the MW500 pyrolysis formed an amorphous material. Moreover, the high-resolution transmission electron microscopy observations of TF500 sample revealed a crystalline material with a d-spacing of 0.33 nm, matching the graphitic lattice. All the treatment conditions performed at 500 °C i.e., MW or TF followed or not by HTC, resulted in mesoporous carbons with a specific surface area above 200 m2 g−1. The MW pyrolysis saved 100 min of the reaction time in comparison to TF pyrolysis to obtain the carbonaceous porous materials.

A phenomenological model for predicting the size of soot primary particles emitted from an aero-engine combustor

Soot particles emitted from aero-engines are harmful to airport local air quality, and the adverse impact from soot particles is closely related to particle morphology, microstructure and chemical properties. To understand those properties of aviation soot particles, combustion experiments using conventional aviation fuel RP-3 were conducted on a Rich-Burn/Quick-Quench/Lean-Burn (RQL) aero-engine combustor. The soot emissions from the RQL combustor were analyzed via a high resolution transmission electron microscope (HRTEM), and the size distributions of primary particles at different power levels were determined based on the HRTEM images. Since the primary particle size is strongly related to the power level and follows an S-shaped curve, a phenomenological model with low-computational complexity and general applicability was established. Furthermore, the model was validated by using previously published experimental data of a CFM56–2C1 aero-engine burning four different fuels, including sustainable aviation fuels (SAF), demonstrating the influence of fuel properties on primary particle sizes at different power levels.Novelty and Significance Statement: In this paper, combustion experiments were conducted on an RQL combustor burning RP-3 fuel. Based on the HRTEM observation, the log-normal size distributions of primary particles at different power levels were determined. Furthermore, based on the fact that the relationship between primary particle size and power level followed an S-shaped curve, a phenomenological model linking primary particle size and combustor power was proposed and validated.

TEM characterization of defects in κ-(In x Ga1−x )2O3 thin film grown on (001) FZ-grown ε-GaFeO3 substrate by mist CVD

We have characterized defects in κ-(In x Ga1–x )2O3 thin films grown on (001) FZ-grown ε-GaFeO3 substrates by mist CVD using TEM. We found two types of defects: dislocation half-loops and microdefects. The half-loops are U-shaped and lie on the (100) plane. From contrast experiment, their Burgers vector was determined to be parallel to 〈010〉. While the microdefects were observed just above the interface between the κ-(In x Ga1–x )2O3 film and the ε-GaFeO3 substrate. They are 5–15 nm in size and accompany strong strain field. From (010) high-resolution transmission electron microscopic observation, it has been found that they are planar defects lying on the (001) plane. From these results, generation mechanisms of these defects are discussed.

Plasma-activated high-strength non-isothermal anodic bonding for efficient fabrication of the micro atomic vapor cells

Microfabricated alkali metal vapor cells are the core components for miniaturizing quantum devices, such as atomic clocks, atomic gyroscopes, and atomic magnetometers. Alkali metals are prone to thermal migration at the bonding interface during the sealing of the vapor cell, which leads to bonding failure. In this study, a non-isothermal anodic bonding process based on plasma activation was developed to achieve high-strength bonding at low temperatures using the temperature gradient to keep the alkali metal away from the bonding interface. This procedure eliminates interference from the alkali metal and significantly increases the success rate of anodic bonding of vapor cells. Simulation results for the temperature field and the residual stresses during anodic bonding demonstrate that the procedure is theoretically feasible. The effect of plasma treatment on the contact angle and roughness of the bonding surface revealed a mechanism for improving the bond strength. In addition, the construction of an integrated processing platform made it possible to perform non-isothermal anode bonding, injection of alkali metal, filling of inert gases, and recovery and recycling of noble gases. The high strength and good hermeticity of the bonding interface were demonstrated by the bond strength, cross-sectional high-resolution transmission electron microscopy observations, and leakage rate tests. Finally, the absorption spectrum and free-induction decay signal of the fabricated vapor cell were measured.

Pressure-Driven Structural and Electronic Transitions in a Two-Dimensional Janus WSSe Crystal.

In this work, we presented the first report on the high-pressure structural stability and electrical transport characteristics in WSSe under different hydrostatic environments through Raman spectroscopy, electrical conductivity, and high-resolution transmission electron microscopy (HRTEM) coupled with first-principles theoretical calculations. For nonhydrostatic conditions, WSSe endured a phase transition at 15.2 GPa, followed by a semiconductor-to-metal crossover at 25.3 GPa. Furthermore, the bandgap closure was accounted for the metallization of WSSe as derived from theoretical calculations. Under hydrostatic conditions, ∼ 2.0 GPa pressure hysteresis was detected for the emergence of phase transition and metallization in WSSe because of the feeble deviatoric stress. Upon depressurization, the reversibility of the phase transition was substantiated by those of microscopic HRTEM observations under different hydrostatic environments. Our high-pressure investigation on WSSe advances the insightful understanding of the crystalline structure and electronic properties for the Janus transition-metal dichalcogenide (TMD) family and boosts prospective developments in functional devices.

3D nanostructure prediction of porous carbons via gas adsorption

Structural characterization of porous carbon materials is critical for the evaluation of their synthesis procedures and performance. Throughout the last decades, many methods have been employed to determine porosity properties from gas adsorption such as surface area, pore size distribution (PSD) and real density. However, gas adsorption models use 1D structures of carbon nanopores, although adsorption and separation properties of nanoporous carbons are governed by 3D pore parameters. Estimating the 3D nanostructure of nanoporous carbons using gas adsorption would accelerate progress in research and implementation of nanoporous carbons. We report here a promising 3D pore nanostructural characterization from gas adsorption. Using atomistic simulations, we have generated a database of realistic 3D porous carbon structures spanning a wide range of pore sizes and geometries. After calculating their gas adsorption isotherms, we employed a numerical procedure to find the relative contribution for each of the structures to the adsorption isotherm of a nanoporous carbon sample. These contributions allowed us to estimate the surface area and pore size distribution of carbon materials; moreover (and perhaps more importantly!), we will show that the plausible 3D pore structures correlate very well with the local carbon structure as experimentally determined by high-resolution TEM observations and can successfully predict adsorption of different molecules. This is a powerful procedure that can be extended to other materials, and with enough computer power, to larger pore sizes.

Martensitic transformation pathways and crystallographic orientation relationships in steel

Martensite is one of the most important structures determining the ability to tailor the performance of steel and several other engineering materials. In previous studies, the face-centered cubic (FCC) to hexagonal close-packed (HCP) (or body-centered cubic (BCC)) martensitic transformation and the FCC to body-centered tetragonal (BCT) (or BCC) martensitic transformation during deformation and quenching were widely investigated; these transformations usually improve the plasticity and strength of steel, respectively. In this work, detailed transmission electron microscopy (TEM) observations and electron diffraction pattern analyses of the BCT and BCC twins are performed along the [110], [131], and [1¯53] zone axes. The transformation of BCT twins into BCC twins along the [131] zone axis is also analyzed through in situ heating during the TEM observations. The high-resolution TEM observations of mutually perpendicular BCT variants are consistent with the atomic arrangement obtained for the quenching pathway during the martensitic transformation. In addition, different orientation relationships between austenite and martensite are explained in terms of the atomic migration occurring during the deformation pathway and the quenching pathway of the martensitic transformation.

Copper bonding silicon nitride substrate using atmosphere plasma spray

Silicon nitride (Si3N4) is an excellent engineering ceramic with high strength, fracture toughness, wear resistance, and good chemical and thermal stability. Recently, the enhanced thermal conductivity enables Si3N4 to have potential application prospects in the electronic and orthopedic fields. Metal bonding with Si3N4 is often the key to these applications. Here we report a facile approach for the titanium-activated Cu bonding on Si3N4 substrates using an atmosphere plasma spray (APS) process. With X-ray diffraction (XRD) and high-resolution transmission electron microscopy (HRTEM) observation, it was shown that the interaction between the pre-bonded Ti (by APS) on Si3N4 promoted the adhesion and high bonding strength of APS Cu on Si3N4. The interfacial structure and phases were characterized, and tensile strength, electrical resistivity, thermal conductivity, and residual stress of Cu bonded Si3N4 were measured accordingly. The APS deposited Cu layer is dense, has a high purity, and is joined firmly with Ti pre-bonded Si3N4 substrate. The maximum tensile strength between Cu and Si3N4 is as high as 89.4 MPa. The Si3N4 substrate bonded with highly dense Cu demonstrates a low surface resistivity of 8.72 × 10−4 Ω∙mm, and high thermal conductivity of 98.12 W/m·K, which shows potential applications in electronic devices.

New strategy to improve the overall performance of single-crystal superalloys by designing a bimodal γ′ precipitation microstructure

Advanced single-crystal superalloys, developed to improve the high temperature capability of gas turbines, often underperform in low-temperature conditions. This limitation compromises the overall reliability of turbine blades under complex service environments. This study introduces a novel strategy to enhance the overall performance of a fourth-generation single-crystal superalloy. Rapid liquid-nitrogen quenching following the aging treatment promotes extensive nucleation of ultrafine γ′ particles (γ′γ) with an average size of ∼10 nm, precipitated under extremely low supersaturation, as evidenced by high-resolution transmission electron microscopy (HRTEM) and atom probe tomography investigations. The combination of differential scanning calorimetry analysis, density functional theory calculations, and kinetic models verifies the high stability of γ′γ particles at low-temperature conditions around 900 °C. HRTEM observations reveal Orowan bypassing and dislocation cutting of γ′γ particles, leading to additional precipitation hardening by limiting dislocation motion in the γ phase and shear of primary precipitates. Consequently, a bimodal precipitation microstructure comprising γ′γ particles and primary γ′ phase significantly reduces the strain rate of low-temperature creep and nearly doubles the creep rupture life at 800 °C/735 MPa. Simultaneously, high-temperature properties at 900 °C/392 MPa and 1100 °C/137 MPa remain comparable to those of the original microstructure as the primary γ/γ′ microstructure is minimally affected by rapid cooling. This advancement improves overall performance and redefines the importance of small precipitates, broadening microstructure design concepts for future superalloy development.