Heavy Ion Research Articles

Microstructure evolution of CdZnTe crystals irradiated by heavy ions

Consideration of irradiation effects is important for in-orbit operation and radiation protection in aerospace applications. The configuration of irradiation defects and their impact on deteriorating the carrier transport properties of CZT crystals need to be clarified. In this study, the microdefect evolution mechanism of CdZnTe (CZT) crystals under 10 MeV Chlorine (Cl) ion irradiation at flux of 1×1010∼1×1012 n·cm-2 are investigated. The stacking faults first appear in the CZT crystal at 4.5×10-4 displacement per atom (dpa), which are categorized into slip-type, gap-type and vacancy-type. In order to hinder the further expansion of stacking fault, S-shaped stacking fault dipole appears. When the dpa reaches 4.5×10-2, the local phase transition occurs in the damage zone to form CuPt-A ordered phase with ZnTe/CdTe periodic arrangement because the fluctuation in local composition and strain caused by cascade collisions. The deterioration of electric field distribution and charge collection caused by irradiation damage layer leads to the decrease of γ-ray detection ability. The energy resolution (ER) of the CZT detector for γ-ray can be maintained at 30.6% when the ion flux accumulates to 1×1012 n·cm-2, revealing high irradiation hardness. Consequently, these findings provide a theoretical basis for the radiation damage recovery of CZT detectors, further demonstrating that CZT crystals are the most competitive new generation of room-temperature nuclear radiation detection materials, and can provide radiation protection strategies for similar compound semiconductor materials.

Constructing SDBS-intercalated MoS2 nanosheets confined and near-vertically grown on network biochar adsorbent: Insights into highly efficient co-adsorption of ciprofloxacin and lead ions

To overcome the problems of the weak adsorption ability of biochar to heavy metal ions (HMIs) and competitive adsorption between HMIs and antibiotics during co-adsorption, the adsorbent material in which 2D sodium dodecylbenzenesulfonate-intercalated molybdenum disulfide nanosheets confined and growing near-vertically on 3D network biochar (SDBS-MoS2/BC) was synthesized. The SDBS-MoS2/BC demonstrated good adsorption ability for ciprofloxacin (CIP) and lead ions (Pb2+). Notably, the adsorption capacity of SDBS-MoS2/BC for the target in the binary system remains higher than in the single system, even at elevated concentrations of the competing target (Qmax,CIP = 393.701 mg g−1, Pb2+: 100 mg/L; Qmax,Pb = 264.550 mg g−1, CIP: 100 mg/L). This may be due to the improvement in the utilization of edge/interlayer adsorption sites by the near-vertical SDBS interlayer expansion of MoS2 as a heavy metal ion anchor. Furthermore, the spatial difference between the upper edge site of near-vertical SDBS-MoS2 and the BC plane, that is, the “longitudinal steric effect”, can separate the CIP and Pb2+ adsorptions in a different horizontal plane to avoid competitive adsorption. The underlying adsorption mechanism was elucidated through a series of experiments and the analysis of characterization results. Furthermore, the load of the SDBS-MoS2/BC sponge-packed column can continuously remove contaminants from water. The rapid, anti-interference, multifunctional and reusable properties make SDBS-MoS2/BC promising for excellent environmental treatment.

Study on the new slow-release carbon source biochemistry and its improvement of SRB on the acid mine drainage treatment

The content of sulfate and heavy metals in acidic mine drainage (AMD) exceeds the standard severely, and the acidity is extremely high, causing serious harm to the environment. SRB can efficiently remove sulfates through its own metabolism. The treatment of AMD by SRB faces problems such as carbon source scarcity and heavy metal ion toxicity to SRB. In this study, corn cob and polycaprolactone were embedded to prepare a novel slow-release carbon source (PSCL), which simultaneously achieves carbon source supply and metal ion removal. Through adsorption isotherms, kinetics, thermodynamics studies, and various characterization analyses, it is known that PSCL removes Cu2+ and Zn2+ through ion exchange, physical and chemical adsorption, electrostatic attraction, and surface complexation. PSCL carbon release experiments and characterization results confirm that its surface carbon distribution is dense, the molecular weight of DOM in the leachate is small, the degree of humification is low, and it has a porous structure, making it a good carbon release material and biological attachment. The experimental results of PSCL enhanced SRB treatment of AMD showed that the removal rates of SO42−, Cu2+ and Zn2+ could be increased to 97.48%, 98.11% and 90.42%, respectively, with a effluent pH of 7.05, effectively improving the water quality of AMD. This study provides new materials and methods to address the limitations of SRB in treating actual AMD.

Electrochemical activation of periodate with graphite electrodes for degradation of high concentrations of thiocyanogen (SCN−) in mineral processing tail liquid

Cyanide has been widely used in gold extraction due to its cost-effectiveness, high selectivity and recovery. Regrettably, its wide application also leads to the presence of a large amount of thiocyanogen (SCN−) in the tail liquid of mineral processing plants, which affects the quality of the effluent water, and thus poses a threat to the ecological environment and human health. This paper investigates the degradation of high concentration of SCN− in water using electrochemical oxidation/periodate (E-GP/PI) system. A degradation rate of 90.25 % of SCN− was achieved by optimising various operating parameters. The effects of organic matter and typical heavy metal ion concentrations on the degradation of SCN− were investigated, and it was found that Cu2+ was able to promote the degradation of SCN− through the formation of stable complexes with SCN−, which enhanced the degradation rate to 96.48 %. However, the presence of Octadecyltrimethylammonium bromide (OTAB) and butylxanthin hindered the degradation process, where 500 mg/L of OTAB reduced the degradation rate of SCN− to 80.88 %, while 100 mg/L of butylxanthin reduced the degradation rate to 78.66 %. On this basis, experiments were carried out using real wastewater samples and SCN− degradation efficiencies of about 90 % were obtained. Afterwards, through electron paramagnetic resonance analysis, free radical burst, ion chromatograph and other research techniques, IO3 and O2– were obtained as the main drivers of SCN− degradation and SCN− degradation pathways were elucidated. Finally, the E-GP/PI system was shown to be effective in reducing the ecotoxicity of SCN− by increasing the 24-h LC50 from 12.5 % to 48.5 % in a toxicity test with daphnia. This study provides a new idea for the green and efficient treatment of SCN− rich beneficiation tail liquid.

Functionalizing heavy metal contained incinerated sewage sludge ash in recycled glass-based alkali-activated materials for sewer environment

This study evaluates the performance of alkali-activated cement (AAC) mortars in an artificial sewage environment. The mortars, initially prepared with waste glass powder (GP) and ground granulated blast furnace slag (GGBS) in a 50:50 mass ratio, were modified by replacing 10 wt% of GGBS with incinerated sewage sludge ash (ISSA) with the goal of offering a biocidal effect. Comparisons were made with calcium aluminate cement (CAC), metakaolin (MK), and MK combined with zinc ferrite nanoparticles, each at a similar GGBS replacement level. The results showed that only incorporating CAC improved the strength development, achieving compressive and flexural strengths of 62.7 MPa and 7.4 MPa, respectively, at 28 days, while introducing ISSA or MK reduced the compressive strength to 47 MPa and flexural strength to 4.5 MPa. Although heavy metal ions from ISSA or zinc ferrite nanoparticles minimized biofilm thickness, they could not compensate for the reduced strength and increased alkalis leaching. Among all the tested mixtures, the 50GP40GGBS10CAC mixture exhibited superior biogenic acid resistance, possibly due to its Al-rich C-N-A-S-H gel phases (Ca/Si = 0.4, Na/Al = 0.8, Si/Al = 3.4) and refined pore structure (porosity = 3.4 %), making it the most microbial acid-resistant option for sewer rehabilitation.

Sulfur-containing cellulose esters for selectively anchoring gold for water catalytic decontamination

The facile preparation of sustainable sulfur-containing polymer functional materials has been obtained great attention due to their chemical reactivity and metal complexing ability. In this study, taking the solution properties advantages of the newly developed cellulose solvent system of DBU/DMSO/CO2, thiol and disulfide bond functionalized cellulose ester (TDSCE) was facilely prepared via in-situ tandem transesterification and oxidation reaction by using methyl 3-mercaptopropionate, without adding any external catalyst. The synthetic protocol was featured by that the DBU not only acted as reagent for the dissolution of cellulose, but also catalysts for the transesterification of cellulose with methyl 3-mercaptopropionate to yield cellulose 3-mercaptopropionate (Cell-MP) with maximum degrees of substitution (DS) of 0.77, and an oxidant for the partial oxidation of Cell-MP to produce a cellulose methyl 3,3′-disulfanediyldipropionate (Cell-MDSP) with maximum DS of 0.36 mixed ester, respectively. With successful introduction of thiol and disulfide bond into the cellulose backbone, the TDSCEs indicated desirable selective absorption of Au3+ from mimic heavy mental ions waste water due to the sulfur-Au chemistry with maximal adsorption capacity for Au3+ of 415.2 mg/g. The subsequent reduction of Au3+ into gold nanoparticles (Au NPs) fabricated a robust TDSCE-2@Au NPs composite catalyst with high catalytic activity for the hydrogenation treatment of water pollutes, such as 4-nitrophenol (4-NP)and azo dyes.

Energy dependence of heavy-ion initial condition in isobar collisions

Collisions of isobar nuclei, those with the same mass number but different structure parameters, provide a new way to probe the initial condition of the heavy ion collisions. Using transport model simulation of 96Ru+96Ru and 96Zr+96Zr collisions at two energies sNN=0.2 TeV and 5.02 TeV, where 96Ru and 96Zr nuclei have significantly different deformations and radial profiles, we identify sources of eccentricities contributing independently to the final state harmonic flow vn. The efficacy for flow generation differs among these sources, and explains the modest energy dependence of the isobar ratios of vn. Additionally, a significant component of vn is found to be uncorrelated with the eccentricity, but is instead generated dynamically during system evoluation. Experimental measurement of these ratios at the LHC energy and comparison with RHIC energy can provide insight into the collision-energy dependence of the initial condition.

Collective behaviour in proton number fluctuations seen in [formula omitted] 2.4 GeV Au+Au collisions

At energies of a few GeV per nucleon, nuclear collisions exhibit phenomena more complex than the individualistic nucleon interactions observed at much higher energies. From recent results on proton number fluctuations in Au+Au collisions at sNN=2.4 GeV obtained by the HADES experiment at GSI, we suggest that measuring the multiplicity distributions heavy-ion collisions can be used to probe density fluctuations associated with correlation phenomena. Using the combinant analysis, we demonstrate that the proton multiplicity distributions can be described by a compound Poisson-binomial distribution, suggesting the formation of clusters as a possible mechanism of such proton number fluctuations.

The Theoretical Research of Two Particle Angular Correlation in PbPb Collisions

This literature review explores the significance of two-particle angular correlation in comprehending the complex dynamics of proton-heavy ion collisions in the quark gluon plasma (QGP) and the CMS detector at the LHC. We present a detailed account of the experimental setup and the findings derived from our measurements. The oneparticle distribution equation and the two-particle angular correlation functions are fundamental components for comprehensively investigating the theoretical aspects of the two-particle angular correlation. Following that, we present a concise summary of significant metrics, such as centrality, uncertainty, and Fourier coefficient, that may be determined from the available data. Additionally, we provide a concise summary of prior investigations into the two-particle angular correlation in collisions involving pp, p-Pb, or Pb-Pb at various energy levels. Specifically, we have utilized the MC model for the analysis and modeling of collision data. Various MC models are listed and evaluated using specific situations. Higher order correlations are now possible to help clarify information from proton or heavy ion collisions.

Changes in heavy metal levels in the oral fluid of young patients with and without plaque-induced gingivitis undergoing treatment with braces

Relevance. Research into the effects of nickel-titanium alloys and heavy metal ions on the development of inflammatory oral diseases is becoming increasingly significant in orthodontics. The relationship between toxic elements and inflammatory responses remains under-researched and controversial. Data on the connection between heavy metals and inflammatory reactions could influence the choice of orthodontic appliance materials and guide the subsequent management and monitoring of patients with braces. The question of the safe use of nickel-titanium alloy braces continues to be a relevant concern.Purpose. To assess the levels of heavy metals in the oral fluid of young patients with braces, both in those who developed plaque-induced gingivitis and those who did not.Materials and Methods. The study involved 50 clinically healthy patients (Groups I and II health categories) with intact teeth, including patients with compensated dental caries (isolated carious lesions – Grade I) and no periodontal diseases (PMA index <20), presenting with dental crowding and malocclusion (K07.2, K07.3). The average age of the patients was 22.1 ± 2.7 years, all of whom were undergoing treatment with metal braces. Oral fluid samples were analyzed for 12 heavy metal elements using inductively coupled plasma mass spectrometry (ICP-MS) in a laboratory setting. Additionally, lysozyme activity and oral fluid pH were measured before appliance placement and six months into orthodontic treatment.Results. Adaptation to braces in young patients is frequently complicated by the development of gingivitis and periodontitis due to impaired oral hygiene and the mechanical pressure exerted on teeth and gums, leading to elemental imbalances. Patients with gingivitis during orthodontic treatment are particularly at risk of developing such imbalances and therefore require timely correction of their mineral metabolism.

Review of Deep Learning in High-Energy Heavy-Ion Collisions

The hot deconfined matter called quark–gluon plasma (QGP) can be generated in relativistic heavy-ion collisions (HICs). Its properties under high temperatures have been widely studied. Since the short-lived QGP is not directly observable, data-driven methods, including deep learning, are often used to infer the initial-state properties from the final distributions of hadrons. This paper reviews various applications of machine learning in relativistic heavy-ion collisions, explains the fundamental concepts of deep learning, and discusses how the properties of HIC data can be interpreted using efficient machine learning models.

A Rapid Sequence of Solar Energetic Particle Events Associated with a Series of Extreme-ultraviolet Jets: Solar Orbiter, STEREO-A, and Near-Earth Spacecraft Observations

A series of solar energetic electron (SEE) events was observed from 2022 November 9 to November 15 by Solar Orbiter, STEREO-A, and near-Earth spacecraft. At least 32 SEE intensity enhancements at energies >10 keV were clearly distinguishable in Solar Orbiter particle data, with 13 of them occurring on November 11. Several of these events were accompanied by ≲10 MeV proton and ≲2 MeV nucleon−1 heavy-ion intensity enhancements. By combining remote-sensing and in situ data from the three viewpoints (Solar Orbiter and STEREO-A were ∼20° and ∼15° east of Earth, respectively), we determine that the origin of this rapid succession of events was a series of brightenings and jetlike eruptions detected in extreme ultraviolet (EUV) observations from the vicinity of two active regions. We find a close association between these EUV phenomena, the occurrence of hard X-ray flares, type III radio bursts, and the release of SEEs. For the most intense events, usually associated with extended EUV jets, the distance between the site of these solar eruptions and the estimated magnetic connectivity regions of each spacecraft with the Sun did not prevent the arrival of electrons at the three locations. The capability of jets to drive coronal fronts does not necessarily imply the observation of an SEE event. Two peculiar SEE events on November 9 and 14, observed only at electron energies ≲50 keV but rich in ≲1 MeV nucleon−1 heavy ions, originated from slow-rising confined EUV emissions, for which the process resulting in energetic particle release to interplanetary space is unclear.

Determination of RBE of 450 MeV/nucleon carbon ions using the micronucleus test and survival of mice after irradiation in different regions of the Bragg curve

Purpose Determination of the value of relative biological effectiveness (RBE) of heavy charged ions in vivo is an important task for their optimal use in particle radiotherapy. The aim of this study was to determine the RBE value of a beam of carbon ions with an energy of 450 MeV/nucleon in different regions of the Bragg curve in irradiation of mice at low, medium, and high doses in comparison with X-ray radiation. Materials and methods SHK mice (n = 330) were irradiated in three regions of the Bragg curve in the dose range of 0–1.5 Gy for cytogenetic damage detection and at a dose of 6.5 Gy for determination of 30-day survival. For irradiation of mice in the Bragg peak, two widths of a spread-out Bragg peak (SOBP) were used: 10 mm (LET ∼100 keV/µm) and 30 mm (LET ∼39 keV/µm). Results The RBE value was 0.8–0.9 before the Bragg peak (LET ∼15 keV/µm) and 0.8 after the peak (LET ∼5 keV/µm), and did not depend on the determination method, despite the differences in LET values. The RBE value determined by the micronucleus test was 1.1–1.7 for the 10-mm-wide SOBP and 1.0–1.3 for the 30-mm-wide SOBP, with the highest RBE value obtained in the low-dose region upon irradiation of mice in the 10-mm-wide Bragg peak. The RBE values in the high-dose region determined by the 30-day survival test lay in the range from 1.4 to 2.6 depending on the width of the Bragg peak and the chosen criterion for calculating the value. The RBE values in the 10-mm-wide Bragg peak (LET ∼100 keV/µm) were higher than those in the 30-mm-wide Bragg peak (LET ∼39 keV/µm) at all used criteria. Conclusions The present findings suggest that there is the complex relationship between LET and organism response to accelerated charged particle radiation, and the contribution of specific factors and mechanisms must be further considered.

Nafion/graphite-bismuth nanoplate with a vibration unit for portable heavy metal ion detection

Contamination of natural resources, particularly water sources, by heavy metal ions, even at low concentrations, poses a significant threat to ecosystems and human health, underscoring the importance of developing sensors with point-of-use (POU) applications. To that end, a vibration-unit-equipped portable electrochemical system (vPES) capable of extremely sensitive detection of Pb2+ and Cd2+ in water is reported herein. The vibration unit enhances sensitivity by facilitating sample diffusion, and its compactness makes it suitable for point-of-use applications through mobile phone connectivity. The system also integrates Nafion and a graphite/bismuth-nanoplate-functionalized screen-printed carbon electrode to detect heavy metals efficiently. The approach implemented in this study and validated through experiments and simulations suggests that vibration-based mixing leads to 540 % and 511 % higher Pb2+ and Cd2+ detection efficiencies, respectively, than those in the absence of vibration. Additionally, the sensor exhibits the limits of detection of 0.98 and 1.65 nM for Pb2+ and Cd2+, respectively, in laboratory environments. Samples collected from the Nakdong River in Korea and real environmental specimens—freshwater, soil, and serum—validate the detection performance. Overall, this study highlights the potential of vPES as a rapid, sensitive POU sensor for heavy metal detection, thereby bolstering environmental and public health monitoring efforts.

Photoinduced Zn-Air Battery-Assisted Self-Powered Sensor Utilizing Cobalt and Sulfur Co-Doped Carbon Nitride for Portable Detection Device.

Most self-powered electrochemical sensors (SPESs) are limited by low open circuit voltage and power density, leading to a narrow detection range and low sensitivity. Herein, a photoinduced Zn-air battery-assisted SPES (ZAB-SPES) is proposed based on cobalt and sulfur co-doped carbon nitride with the cyano group (Co, S-CN). The cyano functionalization remarkably enhances visible light utilization, and the cyano moiety acts as an electron-withdrawing group to promote electron enrichment. Co and S co-doping can create a p-n homojunction within carbon nitride, enabling the efficient migration and separation of carriers, thereby significantly improving the performance of the oxygen reduction reaction. The synergistic effects endow Co, S-CN photocathode with an open circuit voltage of 1.85V and the maximum power density of 43.5µW cm-2 in the photoinduced ZAB. Employing heavy metal copper ions as the target model, the photoinduced ZAB-SPES exhibited dual-mode and sensitive detection. Furthermore, a portable detection device based on the photoinduced ZAB-SPES is designed and exhibits high linearity in the range of 5 ~ 600nM with a detection limit of 1.7nM. This work offers a portable detection method based on the photoinduced ZAB-SPES in the aquatic environment.

The Impact of Adsorption Property Modification by Crosslinkers on Graphene Oxide Membrane Separation Performance

The health risks associated with the presence of heavy metals in drinking water can be severe. To address this issue, membrane separation technology is one of the consolidated alternatives. Inorganic, porous membranes were found in applications where low energy consumption is highly desirable. The selectivity of these membranes is attained by functionalisation. Graphene oxide functionalised membrane technology is promising for removing heavy metal ions. This work summarises, discusses and presents the relationship between adsorption and overall membrane separation process performance for heavy metal ions removal from wastewater when a graphene oxide-functionalised membrane is used. The separation performance depends on the hydrophobic interactions of the membrane and the solute. The electrostatic interaction between the negatively charged membrane surface and positively charged metal ions facilitates the adsorption, leading to the rejection of these metal ions. The influences of the chemical nature of the modifiers of graphene oxide layers are highlighted.

Modeling net-charge fluctuations in heavy-ion collisions at the LHC

Abstract The analysis of Pb+Pb data for net-charge fluctuations at LHC energies
within the HYDJET++ model is presented. The strongly intensive
quantities $D$ and $\Sigma$ are used to get rid of the effects related
to volume fluctuations of the system. We employ two versions of the
HYDJET++ for the analysis. The first one is the standard or default
version, whereas the second one represents its further modification,
which takes into account explicit event-by-event conservation of the
electric net-charge of produced particles. Inclusion of the canonical
net-charge conservation in the model allows one for better description
of the experimental data obtained by the ALICE and the CMS
Collaborations. Comparison with calculations of other models is also
presented.

Synthesis of Porous Red Mud/Slag-Based Spherical Geopolymers for Efficient Methylene Blue and Ni2+ Removal from Water.

To reuse red mud and slag wastes as raw materials, a green type of porous spherical red mud/slag-based geopolymer (RSG) was synthesized by utilizing suspension curing and foaming techniques. Because methylene blue (MB) and nickel ion (Ni2+) were common and difficult to treat in wastewater, the adsorption characteristics of MB and Ni2+, as well as the phase and microstructure of the porous RSG spheres prior to and after adsorption, were thoroughly investigated. The porous RSG spheres showed a stable and mesoporous structure with a BET surface area of 31.36 m2/g. The spheres achieved the maximum removal efficiencies of 99.81% (MB) and 99.01% (Ni2+) at dosages of 16 and 10 g/L, respectively. The pseudo-second-order kinetic model and the Langmuir model could match the adsorption data of these spheres, with predicted maximum adsorption capacity (Qmax) values of 19.88 mg/g for MB and 12.39 mg/g for Ni2+, respectively. After three adsorption-desorption cycles, porous RSG spheres demonstrated good recycling capability with removal efficiencies of 98.10% (MB) and 54.60% (Ni2+). The spheres were also effective in adsorbing additional dyes (methyl orange (MO), crystal violet (CV), and malachite green (MG)) and heavy metal ions (Cd2+, Pb2+, Zn2+, and Cu2+). The spheres have potential use in water treatment.

Willow catkin template synthesis of NiS@NSC hollow tubes for highly sensitive dual-function electrochemical detection of acetaminophen and Cu2.

Public health and environmental well-being have become increasingly threatened by the contamination of pharmaceuticals and heavy metal ions. This study focuses on addressing this critical issue by developing a novel electrochemical sensor for the dual-functional detection of acetaminophen (AP) and Cu2+. Utilizing willow catkins as a biomass template, a hollow tubular NiS@NSC composite was prepared by simple nickel salt impregnation combined with calcination and sulfurization.Ahighly sensitive dual-functional electrochemical sensor wasthus constructed that can detect both acetaminophen (AP) and Cu2+. By examining its electrochemical properties, the sensor achieves an impressive detection limit of 1.33 pM for AP, with a linear range of 4.00 pM ~ 0.15 mM. The sensor can also detect Cu2+, with a detection limit of 1.04 µM, and a linear range of 3.13 µM ~ 0.66 mM. The sensor also exhibits strong resistance to interference, and goodrepeatabilityand stability. In addition, the sensor has demonstrated good performance in actual sample analysis, including the detection of AP in serum and Cu2+ in wastewater. This excellent electrochemical sensing performance is mainly attributed to the synergistic effect of its unique tubular structure and highly conductive N, S co-doped carbon.Thisresults in the sensor exhibiting minimal charge transfer resistance, an extensive electrochemically active surface area, and a high density of active sites.

Enhanced NO2 Gas Sensing in Nanocrystalline MoS2 via Swift Heavy Ion Irradiation: An Experimental and DFT Study.

Nanostructured transition metal dichalcogenides (TMDs) like MoS2 hold promise for gas sensing applications due to their exceptional properties. However, limitations exist in maximizing sensor performance, such as limited active sites for gas interaction and sluggish response/recovery times. This study explores swift heavy ion (SHI) irradiation as a strategy to address these challenges in MoS2-based NO2 gas sensors. MoS2 nanoflakes were fabricated and subsequently irradiated with 120 MeV silver (Ag) ions to induce structural and morphological modifications. Characterization techniques confirmed the formation of Mo and S vacancies within the MoS2 lattice due to irradiation. Significantly, SHI irradiation resulted in a remarkable enhancement of approximately 3 times improvement in sensing response compared to pristine MoS2 sensors. Additionally, the irradiated sensors exhibit substantial improvements in both response and recovery times for NO2 detection. SHI irradiation resulted in the formation of self-affine nanostructures and increased grain fragmentation as fluence rises. This enhanced surface area is hypothesized to promote gas-sensor response. To gain deeper insights into the underlying mechanism, first-principles calculations were employed. These calculations suggest that electron transfer occurs from the MoS2 surface to the NO2 molecule during interaction. Furthermore, the irradiation-induced vacancies facilitate stronger NO2 adsorption on the MoS2 surface compared to the pristine sample. This work demonstrates the effectiveness of SHI irradiation in engineering defects within MoS2 nanoflakes, leading to significantly improved NO2 gas-sensing performance. This approach offers a promising avenue for developing next-generation TMD-based gas sensors with enhanced sensitivity, response times, and stability.