Radiation Stability Research Articles

In-situ investigation of damage evolution and mechanism in composite propellants under monochromatic X-ray irradiation

Synchrotron radiation monochromatic X-ray computed tomography (CT) is a powerful tool for in-situ characterization of the internal microstructure evolution in composite materials. However, prolonged X-ray irradiation during long-term in-situ studies may affect the structure and properties of material. While the effects of white beam irradiation have been widely investigated, the specific damage mechanisms and material sensitivity to monochromatic X-ray irradiation, particularly in composite materials like propellants, are not well understood. In this study, we identify the threshold irradiation time that triggers radiation damage in PBT propellant and observe the accumulation and worsening of damage over time, primarilyinitiated by ether bond cleavage, leading to radiation-induced decomposition and increased internal porosity. This resulted in a significant reduction in the mechanical strength of PBT propellant, particularly under prolonged exposure to synchrotron radiation. In contrast, the inert binder system HTPB propellant exhibited better radiation stability. Our study highlights the importance of considering both radiation-induced damage and material X-ray sensitivity when designing in-situ synchrotron radiation CT experiments for composite materials, and suggests that the development of dynamic experimental methods to further reduce the risk of radiation damage for high-reliability in-situ assessment of material properties, as well as the need for careful consideration of radiation effects in the design and safety evaluation of solid propellant systems working in extreme circumstance.

One facile route to prepare high‐performance radiation resistant EPDM rubber composites through graphite modification technology

AbstractModification and improvement of aging resistance in nuclear power environment for the ethylene‐propylene‐diene (EPDM) rubber has been attracting the attention of scientists. In this article, graphite modified EPDM composites (ultrafine graphite [UG]/EPDM) were prepared, and effect of graphite with sizes of 13, 2.6, and 1.3 μm on the processability, vulcanization parameters, mechanical properties, stability of radiation aging of EPDM composites were investigated, respectively. The results showed that EPDM rubber was an irradiated crosslinked polymer. The Mooney viscosity and crosslinking density of EPDM gradually increased with increasing graphite content under the effect of physical and chemical cross‐linking of graphite. The lamellar structure of graphite particles in the rubber matrix is beneficial to improvement of the mechanical properties and aging resistance of the EPDM composites and play a reinforcing role, and the sp2 hybrid structure of graphite can trap and quench free radicals, delayed the irradiation aging of EPDM. UG/EPDM composites irradiation stability was improved with increasing graphite dispersion in EPDM matrix. Under the cumulative irradiation dose of 1000 kGy, the tensile strength of blank sample and UG‐2.6 μm−10 decreased by 51.1% and 17.7%, respectively, and the hardness increased by 8.7% and 4.9%, respectively. The energy storage modulus and the corresponding glass transition temperature (Tg) of UG/EPDM composites enhanced with graphite, while the thermal stability of the composites was improved.

High-performance 4-nm-resolution X-ray tomography using burst ptychography.

Advances in science, medicine and engineering rely on breakthroughs in imaging, particularly for obtaining multiscale, three-dimensional information from functional systems such as integrated circuits or mammalian brains. Achieving this goal often requires combining electron- and photon-based approaches. Whereas electron microscopy provides nanometre resolution through serial, destructive imaging of surface layers1, ptychographic X-ray computed tomography2 offers non-destructive imaging and has recently achieved resolutions down to seven nanometres for a small volume3. Here we implement burst ptychography, which overcomes experimental instabilities and enables much higher performance, with 4-nanometre resolution at a 170-times faster acquisition rate, namely, 14,000 resolution elements per second. Another key innovation is tomographic back-propagation reconstruction4, allowing us to image samples up to ten times larger than the conventional depth of field. By combining the two innovations, we successfully imaged a state-of-the-art (seven-nanometre node) commercial integrated circuit, featuring nanostructures made of low- and high-density materials such as silicon and metals, which offer good radiation stability and contrast at the selected X-ray wavelength. These capabilities enabled a detailed study of the chip's design and manufacturing, down to the level of individual transistors. We anticipate that the combination of nanometre resolution and higher X-ray flux at next-generation X-ray sources will have a revolutionary impact in fields ranging from electronics to electrochemistry and neuroscience.

Polar Alternating Cations Intercalated Hybrid Perovskite with Iodine‐Substituted Spacers Toward Efficient Passive X‐Ray Detection

Abstract2D hybrid perovskites, with their high X‐ray absorption and extended carrier transport, present excellent promise for efficient direct X‐ray detection. However, most of the current devices require external bias voltage, which results in the need for significant energy consumption and severe ion migration, therefore, it is urgent to develop new types of materials for achieving efficient passive X‐ray detection. Herein, two novel chiral polar alternating cations intercalation (ACI)‐type hybrid perovskite materials, named (R/S‐PPA)(IEA)PbBr4 (1‐R/S, (R/S)‐PPA = R/S‐1‐phenylpropylamine; IEA = iodoethylamine), are constructed by integrating the chiral aromatic spacer R/S‐PPA and the iodine‐substituted spacer IEA. Various intermolecular interactions, such as I···I, C─H···I, π···π interactions, are introduced due to the introduction of I‐substituted chain amines, which effectively suppresses ion migration and thus lead to improved operational stability. The device constructed along the polar axis displays superior X‐ray detection performance, such as relatively high sensitivity and an ultra‐low limit of detection (LoD) of 3.0 nGy s−1, making it the first chiral ACI‐type perovskite material for realizing efficient passive X‐ray detection. Furthermore, 1‐R also presents low dark current drift and exceptional irradiation stability. This work provides new thought for using novel ACI‐type polar perovskite for high‐performance passive direct X‐ray detection.

High-performance oxygen terminated synthetic single crystal diamond detector for high gamma dose rate measurement

A high-performance oxygen terminated synthetic single crystal diamond (SCD) detector (4.5 × 4.5 × 0.5 mm3) is presented. The SCD detector exhibits an extremely low leakage current value of 0.29 pA/mm2 with an electric field of 0.3 V/μm. The charge collection spectrum measured with a238Pu source (5.48 MeV α-particles) irradiation shows that the electron and hole charge collection efficiency (CCE) reach as high as 99.1% and 98.9%, with an energy resolution as low as 2.87% and 2.53%, respectively, compared to Si detector. The SCD detector shows excellent radiation hardness and stability under 60Co γ-ray irradiation with a dose rate of 12.737 kGy/h at 150 V bias and is able to withstand a cumulative dose of up to at least 9.3 kGy. The detector output in current mode is linearly related to the dynamic dose rate (0.409 Gy/h-12.737 kGy/h). Similarly, the counting rate of the detector in counting mode exhibits a strong linear variation within the range of 2.6 mGy/h-1269.36 Gy/h. Our results fully indicate that our fabricated SCD detector can be potentially applied to harsh γ irradiation scenarios, which is of guiding significance on real-time dose monitoring.

ZBS glass synthesized containing both Eu3+-Eu2+ CsPbBr3 quantum dots with multi-color luminescence for white LEDs

In this article, zinc-borosilicate silicon（ZBS） glass containing europium (Eu) ions and CsPbBr3 quantum dots (QDs) (ZEQ) was synthesized via melting crystallization route. The composition and luminescent properties are investigated by X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD) and photoluminescence (PL) spectra. The XRD and XPS results imply that Eu 3+, Eu 2+ ions and CsPbBr3 QDs are coexisted in ZBS glass. The dual-mode emission from cyan to orange-red can be achieved by adjusting the melting temperature. Besides, the ZEQ has good water resistance, outstanding light irradiation and excellent heating-cooling cycle stability. Moreover, based on the ZEQ, the light-emitting diodes (LEDs) are designed to obtain the white light with the correlated color temperature (CCT) of 5255 K, the Coherent Infrared Energy (CIE) color coordinate of (0.337 0.313), the NSCT color gamut of 116 % and 87 % of Rec.2020. Thus, this article provides a novel material ZEQ, which is tunable luminescence and ultra-stable. The strategy provides the route that the luminescence of Eu ions and QDs can be observed at the same time, solving the difficulty of the rare earth ions entering into the QDs lattice. Moreover, the ZEQ is expected to be used as the light source for solid-state lighting and also provides valuable research results for future exploration of functional glass containing both rare-earth ions and QDs materials.

Sub‐10 nm Lanthanide‐Doped Lu6O5F8 Nanoscintillators for Real‐Time High‐Resolution Dynamic 3D X‐Ray Imaging

AbstractLanthanide‐doped fluoride nanoscintillators (NSs) have emerged as promising candidates for X‐ray imaging. However, strong afterglow, long lifetime, and poor irradiation stability pose key challenges for real‐time dynamic X‐ray imaging. In this study, the sub‐10 nm Lu6O5F8:Tb NSs with tunable morphologies are prepared via incorporating Li+/Na+ ions. The X‐ray excited optical luminescence (XEOL) intensity of the Lu6O5F8:15Tb/10Li NSs is stronger than that of NaLuF4:15 Tb NSs with a similar particle size while its afterglow is only ≈2.7% compared to that of NaLuF4:15 Tb NSs. Utilizing the Lu6O5F8:15 Tb/10Li NSs‐integrated film as a scintillator screen, a high resolution of ≈21.6 lp/mm is achieved. Even at a low dose of 0.23 µGy, the fringe detail in the electron device is clearly observed in the X‐ray image. The afterglow intensity of the Lu6O5F8:10Eu/10Li NSs decays to 0.7% at 40 µs, which is better than that of CsI:Tl (3.6%@40 µs). Moreover, the Lu6O5F8:10Eu/10Li NSs with a lifetime of 1.65 µs are verified for use in dynamic 3D X‐ray imaging. These findings represent a significant advancement in the development of new NSs for high‐performance dynamic X‐ray imaging.

Ultrahigh-efficiency X-ray energy dissipation enabled by the integration of core–shell photon nanotraps and hierarchical natural leather

The widespread application of high-energy X-ray radiation has prompted improvements in the performance of radiation-protection materials. Currently, achieving enhanced X-ray shielding efficiency and minimized surficial photon scattering remains challenging when using traditional strategies. In this study, an ultrahigh-efficiency X-ray energy absorption strategy and mechanism are proposed by integrating Bi@Gd core–shell photon nanotraps into the hierarchical fibrous network of natural leather (Bi@Gd/NL), and the surficial-energy-transfer energy-attenuation mechanism of the traditional strategy was successfully transformed into internal-energy-dissipation. The proposed strategy could induce high-energy photons into a porous structure composed of hierarchical microfibers and nanofibers to reduce surface-scattered secondary radiation, and the well-assembled high-atomic-number core–shell nanotraps can trap photons within the structure and facilitate collisions and subsequent internal energy dissipation to improve the shielding capabilities. Our analysis shows that Bi@Gd/NL with 1.40 mmol cm−3 Bi and 0.11 mmol cm−3 Gd exhibits superior shielding performance against X-rays, comparable to that of a 0.25-mm Pb plate. More than 99.95 % photon energy is dissipated within the nanotraps, and the surficial scattering of photon is considerably lower than that of materials fabricated using the traditional strategy, indicating that the ionizing radiation hazards are successfully suppressed. Simultaneously, the developed materials demonstrate exceptional wearability, with a density of only 1/10 that of Pb, as well as outstanding flexibility, physiomechanical strength, and irradiation stability. This proposed strategy and mechanism provide important guidance and insights on the development of novel absorption-type shielding materials for protecting ionizing radiation-related individuals and environments.

Swift Au+9 ion irradiation-induced defects and alloy complexity effect on the mechanical hardness of NiCoCrFePd HEA and NiCoCrFe MEA

The outstanding radiation damage stability of an NiCoCrFePd high entropy alloy (HEA) as compared to conventional alloys poses the question for the mechanism of an ion–matter interaction. The positron annihilation lifetime spectroscopic and TEM (transmission electron microscopic) measurements are implemented to trace different kinds of defects produced by 120 MeV Au+9 ion irradiation and their evolution as a function of ion fluence. The variation of lifetimes and corresponding intensities with the ion fluence indicates the formation of dislocation-type defects at a lower ion fluence and vacancy clusters at a higher ion fluence caused by coalescence or agglomeration of dislocation defects. Formation of different types of defects in turn modulates the strain development inside the crystal. Additionally, the HR-TEM investigation of NiCoCrFePd HEA also exhibits the formation of dislocation and vacancy clusters with the average size of vacancy clusters increases from ∼2.9 ± 0.1 to ∼3.8 ± 0.1 nm with the increases in the ion fluence. Surprisingly, the average defect cluster size in NiCoCrFePd HEA is suppressed compared to NiCoCrFe MEA, thereby showing the enhanced radiation stability on Pd incorporation due to the high defect recombination caused by reduced thermal conductivity and high lattice distortion. Nano-indentation measurement shows that the radiation hardening behavior of the NiCoCrFePd HEA responded slowly owing to its damage suppression property as compared to the NiCoCrFe MEA. Additionally, softening behavior also appeared at an early fluence in NiCoCrFe MEA compared to the NiCoCrFePd HEA signifying its excellent resistance to defect accumulation.

Wearable Photoferroelectric Perovskite X‐Ray Detectors

AbstractHigh‐sensitivity wearable radiation detectors are essential for personnel protection in radiation environments such as defense, nuclear facilities, and medical fields. Traditional detectors using bulk crystals lack flexibility, and emerging perovskite films suffer from lead toxicity and poor charge transport. Herein, lead‐free photoferroelectric hybrid metal halide perovskite flexible membranes for wearable detectors are presented, offering superior X‐ray response with sensitivities up to 7872 ± 517 µC Gyair−1 cm−2 at 50 V bias and 394 ± 67 µC Gyair−1 cm−2 in a self‐driven mode, detection limit of lower than 77 nGyair s−1, and excellent imaging capabilities. This exceptional performance is attributed to the spontaneous polarization that promotes efficient charge transport. Additionally, they show remarkable radiation stability, long‐term air stability, mechanical fatigue resistance, and water stability. They also exhibit efficient energy response under the Compton effect and meet the angle response requirements of the International Electrotechnical Commission standard for direct‐reading personal dose equivalent meters, paving the way for their integration into flexible, wearable dosimeters. These advancements have the potential to drive the realization of the next generation of flexible wearable radiation detectors.

Evolution of Microstructure During Stress Relieving Heat Treatment of 1S Aluminium

Aluminium and its alloys are extensively used in nuclear research reactors due to its low neutron absorption coefficient, good heat transfer properties, excellent corrosion and oxidation resistance in air and water environment combined with desirable mechanical properties along with considerable radiation stability. The thin walled tubes are normally manufactured through port hole die extrusion route and used in 'O' tempered condition. The thin tubes in 'O' tempered condition are undergone canning operation which may alter the microstructural features to some extent which may affect mechanical properties. The paper describes the extent to which microstructural and subsequently mechanical properties are altered due to the simulated canning process and further requirements of stress relieving heat treatment to restore the microstructural features and mechanical properties. The following studies are carried out with 1S aluminum tube in 'O' tempered state, simulated canning condition and stress relieved at different temperature, - hardness measurement, X ray line profile analysis for dislocation density measurement, tensile properties measurement using ring tensile testing, electron back scattered diffraction (EBSD) analysis for recrystallization fraction determination and changes in texture components. It is found that the canning operation changes dislocation density, micro-strain, coherent domain size which are well reflected in hardness and ring tensile testing. Subsequent stress relieving at 350°C for 2 hrs. leads to improvement of mechanical properties appreciably.

Remarkable enhancement in radio-cesium uptake from acidic feeds into an extraction chromatography resin containing a calix[4]arene-mono-crown-6 ligand

An extraction chromatography resin, prepared by the impregnation of bis-octyloxy-calix[4]arene-mono-crown-6 (BOCMC)onto an acrylic ester based polymeric support material, gave excellent uptake data for the removal of radio-cesium (Cs-137) from nitric acid feed solutions. The weight distribution coefficient (Kd) value of >300 obtained during the present study at 3 M HNO3 was the highest reported so far while using a calix-crown-6 based extraction chromatographic resin material. Analogous resin reported previously has yielded a Kd value <100 at comparable feed conditions. The sorbed metal ions could be efficiently desorbed with de-ionized water. Kinetic modeling of the uptake data indicated that both the film and the intra-particle diffusion mechanism are simultaneously operating in the sorption of Cs+ion onto the BOCMC resin. The metal ion sorption data were fitted to the sorption isotherm models and did not conform to the chemisorptions of physisorption models and indicated a pi-pi interaction between the benzene rings of the calix-crown-6 ligand and the Cs+ ion. The reusability of the resins was quite satisfactory after 5 cycles and the radiation stability of the resin material was very good upto an absorbed dose of 500 kGy. The results of column studies were quite encouraging with 15 mL (9 bed volumes) as the breakthrough volume while the elution was complete in about 12 bed volumes of de-ionized water.

A Thermo-Responsive MOFs for X-Ray Scintillator.

Thermo-responsive smart materials have aroused extensive interest due to the particular significance of temperature sensing. Although various photoluminescent materials are explored in thermal detection, it is not applicable enough in X-ray radiation environment where the accuracy and reliability will be influenced. Here, a strategy is proposed by introducing the concept of radio-luminescent functional building units (RBUs) to construct thermo-responsive lanthanide metal-organic frameworks (Ln-MOFs) scintillators for self-calibrating thermometry. The rational designs of RBUs (including organic ligand and Tb3+/Eu3+) with appropriate energy levels lead to high-performance radio-luminescence. Ln-MOFs scintillators exhibit perfect linear response to X-ray, presenting low dose rate detection limit (min ≈156.1 nGyairs-1). Self-calibrating detection based on ratiometric XEL intensities is achieved with good absolute and relative sensitivities of 6.74 and 8.1%K-1, respectively. High relative light yield (max ≈39000 photons MeV-1), imaging spatial resolution (max ≈18 lpmm-1), irradiation stability (intensity ≈100% at 368 K in total dose up to 215 Gyair), and giant color transformation visualization benefit the applications, especially the in situ thermo-responsive X-ray imaging. Such strategy provides a promising way to develop the novel smart photonic materials with excellent scintillator performances.

Comparing 3D printing techniques (SLA vs. FDM) for their use in radionuclide metrology

This paper presents a comparative analysis, in which we evaluate the parameters of SLA and FDM printing technologies, for the production of radioactive standard sources in the SARPAGAN geometry, frequently encountered in radionuclide metrology. Aspects such as material compatibility, dimensional accuracy, radiation stability and the influence of 3D printing technology on the reliability of the final product will be addressed. Furthermore, the results obtained by gamma-ray spectrometry on a sample of 99mTc, using the standard SARPAGAN geometry, in comparison with the two 3D printed SARPAGAN geometries (SLA and FDM), were analyzed to evaluate how both the material and the technique printing of the geometry influences the results.

MgGa2O4-based thermal control coating: An ultra-low solar absorption coating with high irradiation stability

In this study, the viability of MgGa2O4 as a pigment for thermal control coatings is discussed. Notably, the MgGa2O4 based coating exhibited excellent initial optical properties and irradiation stability. After irradiation with 40 keV proton at a dose of 1.4 × 1014 P/cm2, the optical performance of the coating remained essentially unchanged, while the solar absorption of the coating is still maintained below 0.10 after irradiation with 40 keV electron at a dose of 1.6 × 1016 e/cm2. Further, the mechanism of the optical changes induced by electron irradiation was elucidated through experimental and computational methods. In MgGa2O4 lattice, two different types of oxygen vacancies and a transition process of them were found. This process was accompanied by the leakage of some oxygen atoms from the lattice, leading to an increased number of color centers and the change in optical properties. Despite the solar absorption raised after electron irradiation, the MgGa2O4 based thermal control coating showed minimal change and low end-of-irradiation-life values, which suggests that they have excellent stability and promising applications.

Effect of Gamma Irradiation on Electrophysical Parameters of Silicon Solar Cells Doped with Nickel

The results of the studies of changes in the electro-physical parameters (Voc – no-load voltage, Isc – short-circuit current density; τ – lifetime of nonequilibrium charge carriers) of photocells made on plates of monocrystalline silicon of the p-type conductivity with the specific resistance ρ 0.5 Ohm cm, doped with nickel, under irradiation with γ-quanta from 60Co source are presented. It is shown that the efficiency of the solar energy conversion in nickel-doped photovoltaic cells remains higher than in standard cells up to irradiation doses of 108 rad. It was established that with increasing diffusion temperature of nickel atoms radiation stability of electrophysical parameters of photovoltaic cells also increases. A decrease in the concentration of recombination-active radiation defects is due to the getterization by nickel atoms of technological (background) impurities and the action of nickel clusters as effluents for radiation-induced vacancies.

Spectroscopic studies on natural fluorapatites irradiated with 10 MeV electrons

Fluorapatites are one of the candidate matrices for hosting the nuclear waste from molten salt reactors. To assess their radiation stability and long-term performance, natural analogue study approach was undertaken. Naturally occurring fluorapatites containing with carbonate substitutions were irradiated with 10 MeV electron beam radiation for doses 20 MGy. X-ray diffraction, Raman and Fourier Transform infrared spectroscopy show no evidence of structural degradation or phosphate condensation. However, a change in the intensity of ν3 Phosphate Raman bands was observed indicating that the phosphate tetrahedra is affected by the electron beam consistent with the displacement cross-section calculations for each constituent element. Overall, the study confirmed that fluorapatite possess good structural stability against electron radiation upto 20 MGy.

Synthesis of dual functional Zn(II) MOF for colorimetric detection of norfloxacin and photocatalytic degradation of ornidzole drugs in aqueous medium

Pharmaceuticals widespread use of antibiotics endangers humans and animals. Antibiotic residues in groundwater, rivers, lakes, and other surfaces pose serious health risks. Therefore, the synthesis of high-performance sensors and catalyst materials for the selective and ultra-sensitive detection and removal of antibiotics from water is crucial for community health and environmental quality. This study created [Zn(Cei)] (1) flower-like colourless crystals using bis(2-carboxyethyl) isocyanurate (H2Cei) a simple room-temperature process and tested their photoluminescence sensing and photocatalytic destruction of antibiotics. Physicochemical characterisation of produced (1) was done using analytical and spectroscopic methods. The photoluminescent characteristics of (1) demonstrated that it is very sensitive and selectively detects NFX and NFT in aqueous solution at 0.323 and 0.590 ppm, respectively. However, [Zn(Cei)] (1) showed excellent photocatalytic activity against ODZ and CMP with degradation efficiency of 90.15% and 86.09% within 120 min under UV irradiation, respectively, and good stability by monitoring photocatalyst reusability.

Enhancing mechanical property, thermal conductivity, and radiation stability of fluorine rubber through incorporation of hexagonal boron nitride nanosheets

AbstractFluorine rubber (FKM) stands as a pivotal sealing material extensively employed in aerospace and nuclear industries. However, its efficacy will be seriously affected by ionizing radiation. Enhancing its radiation resistance becomes imperative to uphold the stability and safety of associated equipment. This study introduced hexagonal boron nitride (h‐BN) into the FKM as radioprotective fillers through mechanical blending. The interfacial interaction between matrix and h‐BN, the mechanical performances, thermal properties, and radiation stability of composites were systematically examined. Noteworthy findings highlight the presence of robust interaction forces between h‐BN and the matrix, leading to increased crosslink density and improved mechanical properties. The tensile strength of composite with 10 phr fillers (BN/FKM‐10) increased by 30% compared to that of pure FKM. Simultaneously, the introduction of h‐BN greatly enhanced thermal conductivity and radiation stability. The absorbed dose required to achieve a 50% reduction in elongation at break of BN/FKM‐10 surpassed that of FKM by 1.69 times. These results underscore the potential of incorporating h‐BN to simultaneously enhance the mechanical performance, thermal property, and radiation resistance of fluorine rubber.Highlights The chemical interaction force between h‐BN and FKM was confirmed. FKM composites tensile strength was enhanced by h‐BN as an additive crosslinker. The incorporation of h‐BN improves FKM composites thermal conductivity. The radiation resistance of FKM composites has been improved with h‐BN.

Anomalous exchange bias behavior of NiFe/NiO bilayers induced by high-energy Xe+ ion irradiation

The alteration of the microstructure and magnetic performance of an exchange bias system, induced by ion irradiation, adversely affects the practical application of spintronic/storage devices in extreme environments. Here, we report systematically the correlation between static and dynamic magnetism and microstructure changes in NiFe/NiO exchange-biased bilayers after high-energy Xe+ ion irradiation. The effect of cascade collision induced by irradiation on exchange bias is studied through Monte Carlo simulations. It is distinguished from the traditional modification caused by keV-level ion irradiation. At low doses, the transition from amorphous to recrystallization occurs in the NiFe layer and the anomalous exchange bias behavior is induced. A step-like structure appears in the magnetic hysteresis loop and the step gradually shifts downward as the dose increases. At high doses, the exchange bias effect is suppressed due to the disordered antiferromagnetic moment caused by heat accumulation during cascade collision, which significantly decreases the thermal stability of the sample by 5–6 times. In addition, the non-monotonic evolution of high-frequency magnetic properties is observed with increasing irradiation doses. This work provides important foundational data for designing future spintronic/memory devices to enhance radiation tolerance and stability.