Impurity Ions Research Articles

Exploring the electro-optical properties of nematic liquid crystal through incorporation of ZnCuGaS2 core/shell quantum dots

ABSTRACT The current study focuses on elucidating the interaction mechanisms between ZnCuGaS2 quantum dots (QDs) and nematic liquid crystals (NLCs) (5CB), intending to comprehend how this interaction leads to the alteration of electro-optical properties of the host material. Various concentrations of QDs were incorporated into NLCs and investigated to examine their emission and transmittance characteristics. Remarkably, an enhancement (~68%) in photoluminescence was observed for the concentration of 0.04 wt. %, adding an intriguing aspect to the findings. A notable decrease in the threshold voltage, from 1.5 V (in pure NLC) to 0.5 V, was observed for the optimised concentration (0.04 wt. %) calculated using transmittance-voltage measurement. This sample exhibited a noteworthy improvement in optical transmission, showing an increase by 2.7 times compared to pure NLC. Fundamentally, the introduction of QDs leads to a reduction in light leakage centres and ionic impurities, consequently enhancing radiative recombination. Moreover, the memory effect of the sample was evident in the capacitance-voltage data, revealing that the NLC with QDs significantly increased the capacitance value from 290 pF to 466 pF when compared to the pure NLC. The objective of the present research is to examine the impact of QDs on NLC concerning key parameters such as mentioned above.

5CB molecular dynamics on TiO2-coated planar aligned ITO electrodes

ABSTRACT 5CB liquid crystal (LC) is a well-studied material for a variety of applications due to its orientational ordering and viscosity. LCs mostly suffer from ionic impurities which can be filtered using metal oxide nanoparticles. Beyond this conventional role of TiO2 nanoparticles (NPs) in ionic impurity filtration in LCs, we have employed a new methodology to improve the planar orientation of 5CB molecules by depositing a thin layer of NPs on either side of the ITO electrode. The 5CB LC exhibits a typical birefringent schlieren texture; however, the presence of TiO2 layer alters the molecular orientation. On the TiO2 surface, the 5CB LC molecules showed schlieren defect points characterised by both twofold (s = ± 1/2) and fourfold (s = ± 1) brush-like structures. The change in texture and lowering of dielectric permittivity might be attributed to the change in the pretilt angle of 5CB molecules owing to the mutual interactions between 5CB and TiO2 layer. Remarkably, the 5CB LC within the TiO2-coated cell attains the isotropic phase at lower temperature as compared to the cells coated with polyimide SE-130. The underlying mechanism for coarsening kinetics in the 5CB is elucidated using the Lifshitz-Slyozov-Wagner (LSW) theory.

Impact of multifold magnetic structure on spectroscopy analysis in Heliotron J based on EMC3‐EIRENE simulation

AbstractThe distribution pattern of the connection length in the divertor region of Heliotron J was calculated by the field line tracing method. A multifold layer structure, characterized by the range of connection length, was revealed to interpret the response of the transport of the lower‐charged impurity ions to the divertor structure. Impurity transport simulated by the EMC3‐EIRENE code shows that lower‐charged impurity ions tend to concentrate in the first multifold layer. This result is consistent with the line‐integral extreme ultraviolet spectroscopy measurement, which implies that the impurity's response to the divertor topological structure needs to be considered in interpreting the spectroscopy result.

Phase behavior of sodium and potassium salts in their aqueous solutions: Experiment and computational thermodynamics

AbstractWith the rapid development of the semiconductor industry, the demand for ultraclean and high‐purity electronic chemicals, especially ultrapure water as a general solvent for cleaning semiconductor chips, has increased dramatically. The distillation process is a good choice for large‐scale production of ultrapure water that can be used to clean semiconductor chips, but there is a lack of basic thermodynamic theory for removing ionic impurities. In this work, the temperature and vapor–liquid phase composition of sodium and potassium salts aqueous solutions at vapor–liquid equilibrium (VLE) were investigated by experiments. The microstructure of each inorganic salt aqueous solution was explored by molecular dynamics simulation and quantum chemical calculation, and the interaction between each ion and water molecule was analyzed. A volatilization mechanism of inorganic salts was proposed, and it was found that the volatilization of inorganic salts in an aqueous solution was affected by the strength of interaction between the dissociated anions and cations and water molecules. Finally, the conductor‐like screening model segment activity coefficient (COSMO‐SAC) model predicted the VLE values of inorganic salt aqueous solutions. The prediction at low concentrations (xs < 0.06) was in good agreement with the experimental data.

A Dual-Cation Exchange Membrane Electrolyzer for Continuous H2 Production from Seawater.

Direct seawater splitting (DSS) offers an aspirational route toward green hydrogen (H2) production but remains challenging when operating in a practically continuous manner, mainly due to the difficulty in establishing the water supply-consumption balance under the interference from impurity ions. A DSS system is reported for continuous ampere-level H2 production by coupling a dual-cation exchange membrane (CEM) three-compartment architecture with a circulatory electrolyte design. Monovalent-selective CEMs decouple the transmembrane water migration from interferences of Mg2+, Ca2+, and Cl- ions while maintaining ionic neutrality during electrolysis; the self-loop concentrated alkaline electrolyte ensures the constant gradient of water chemical potential, allowing a specific water supply-consumption balance relationship in a seawater-electrolyte-H2 sequence to be built among an expanded current range. Even paired with commercialized Ni foams, this electrolyzer (model size: 2 × 2 cm2) continuously produces H2 from flowing seawater with a rate of 7.5 mL min-1 at an industrially relevant current of 1.0 A over 100 h. More importantly, the energy consumption can be further reduced by coupling more efficient NiMo/NiFe foams (≈6.2 kWh Nm-3 H2 at 1.0 A), demonstrating the potential to further optimize the continuous DSS electrolyzer for practical applications.

Mechanism of electrical performance deterioration in a-Si:H TFTs caused by source/drain Decap treatment

During the fabrication process of the display industry, the Decap treatment is usually employed as a means to reuse semiconductor materials of thin film transistors (TFTs), but the influence and mechanism of Decap process on the properties of the decapped samples is unknown. To elucidate this occurrence, the electrical characteristics of the channel layer, as well as the microstructure and components at the interface between the Source/Drain (S/D) and the channel layer were examined. It reveals that the infiltration of impurity ion (O and Mo) has significant impact on the deterioration of device performance for a-Si:H TFTs with a Mo/Al/Mo stacked S/D electrode structure. More specifically, oxygen's intrusion leads to the formation of SiOX and the alterations of the surface energy levels and charge distribution of Si, thus introduces an interface trap states between channel layer and S/D electrodes to scatter and capture of interface carriers. And Mo's intrusion may induce the come into being of MoSi or MoP chemical states, causing the decrease of the doping efficiency of phosphorus and the reduction of carrier concentration (from 5.52 × 1016 cm−3 to 4.44 × 1016 cm−3) of a-Si:H channel layer. The combined effect of these two factors results in the decline of electrical performance of S/D decapped a-Si:H TFTs.

Development of a 50kV hydrogen-helium mixed ion beam implanter.

Ion implanters have extensively been employed to simulate the irradiation effects of neutrons on relevant nuclear materials. In this study, a 50kV hydrogen-helium mixed ion beam implanter was developed to generate H2+ and He+ ion beams, with a beam current of 20 µA, while keeping the impurity ion content below 2%. The ions are generated by an antenna-type 2.45GHz electron cyclotron resonance ion source, and the hydrogen-to-helium ion beam ratio was controlled using two gas mass flow controllers to ensure long time stability of the beam current. As a result, the H2+/He+ ratio, beam size, and homogeneity of the beam spot can be maintained at a stable level. The beam line consisted of four Wien filters, a movable dual-slit plate, and an accelerator tube. The experimental results demonstrated successful transport of more than 20 µA of H2+ and He+ ion beams onto the target, with a beam axis deviation of less than 0.5mm.

Deep purification of copper from zinc sulfate solution using controllable aging FeS nanoparticles through slow-release sulfide precipitation

The purification of impurity ions within zinc hydrometallurgical solutions significantly impacts the subsequent quality of zinc electrodeposition. Traditional methods for copper removal from zinc solutions suffer from issues like limited reactivity, high consumption, and elevated costs. To address these challenges, controllable aging of FeS nanoparticles was designed, employing temperature variations to facilitate comprehensive copper removal from neutral zinc leachates. The aging process imparts a crystalline structure to the FeS nanoparticles, enabling the slow release of sulfide ions. A temperature of 60°C is regarded as the optimal aging temperature, at which the resultant FeS nanoparticles exhibit an optimal sustained-release performance during the aging process. Temperature has been found to be a crucial factor influencing the sustained-release performance of FeS. Once the reaction temperature surpasses 60°C, the utilization efficiency of S ions in the sustained-release agent can reach over 95%, with a maximum of 98.5%. Under optimal conditions featuring a reaction temperature of 60°C, a reaction duration of 30 minutes, and a solution pH maintained at 1, the dosage aged FeS at the S/Cu (II) ratio of 1.2 times, nearly 100% copper removal rate can be achieved. The maximum removal rate for cadmium does not exceed 2.5%, and the residual copper concentration in the zinc leachate is below 0.2 mg/L. The precipitate obtained is high-purity copper sulfide residue, which contains virtually no zinc. Slow-release sulfidation can maximize the utilization efficiency of sulfide ions in the solution, reduce the occurrence of competing reactions, and minimize the intermixing of products. It offers advantages such as high selectivity and deep purification.

Impurity Ions Mn2+ and Fe3+ as Paired Spin Labels for the Study of Structural Transformations in Phyllosilicates by the ESR Method

Impurity Ions Mn2+ and Fe3+ as Paired Spin Labels for the Study of Structural Transformations in Phyllosilicates by the ESR Method

Low metal content and hierarchically porous structure of “Fabaceae-Plants” derived activated carbon for high-performance supercapacitors

Plants with naturally ordered tissues and unique cell structures have become good precursors as activated carbon (AC) electrodes for supercapacitors. The various inherent plants derived ergastic substances induce numerous impurities in ACs, seriously impeding electrochemical performance. Aiming at elevating electrochemical activities, we herein, select suitable “Fabaceae-Plants” precursors via pre-leaching and carbonization-KOH activation for purer AC supercapacitor electrodes. The inherent parenchyma tissues and intrinsic low metal ion properties ensure “Fabaceae-Plants” derived ACs have large specific surface areas (SSA) (> 3000 m2 g−1) and low self-discharge rates. After ethanol reflux, most ergastic substances were removed, leading to a lower metal ion content that meets the standard procedure in Chinese GB/T 37386-2019 codes and higher mesopore volumes due to the better KOH activation effect. The mung bean sprouts-based activated carbon (AC) prepared by ethanol reflux exhibits higher capacitance (370 F g−1 at 0.5 A g−1), excellent rate performance (81.8 % from 0.5 to 50 A g−1), and an impressively low open circuit voltage attenuation rate (19.9 mV h−1). These characteristics are attributed to the synergistic effect of low metal ion impurities and higher mesopore volumes. Hence, the “Fabaceae-Plants” derived ACs are potential materials for clean energy storage and conversion systems, and the pre-leaching strategy may propose a strategy for high value-added utilization of biomass.

Unraveling the coordination behavior and transformation mechanism of Cr3+ in Fe–Cr redox flow battery electrolytes

Currently, the iron chromium redox flow battery (ICRFB) has become a research hotspot in the energy storage field owing to its low cost and easily-scaled-up. However, the activity of electrolyte is still ambiguous due to its complicated solution environment. Herein, we performed a pioneering investigation on the coordination behavior and transformation mechanism of Cr3+ in electrolyte and prediction of impurity ions impact through quantum chemistry computations. Based on the structure and symmetry of electrostatic potential distribution, the activity of different Cr3+ complex ions is confirmed as [Cr(H2O)5Cl]2+ > [Cr(H2O)4Cl2]+ > [Cr(H2O)6]3+. The transformation mechanism between [Cr(H2O)6]3+ and [Cr(H2O)5Cl]2+ is revealed. We find the metal impurity ions (especially Mg2+) can exacerbate the electrolyte deactivation by reducing the transformation energy barrier from [Cr(H2O)5Cl]2+ (24.38 kcal mol−1) to [Cr(H2O)6]3+ (16.23 kcal mol−1). The solvent radial distribution and mean square displacement in different solvent environments are discussed and we conclude that the coordination configuration limits the diffusivity of Cr3+. This work provides new insights into the activity of electrolyte, laying a fundamental sense for the electrolyte in ICRFB.

High sedimentation efficiency and enhanced rare earth recovery in the impurity removal process of rare earth leachate by flocculation system

The main impurity ion in rare earth (RE) leachate are aluminum ions, which can be effectively removed by precipitation in the form of aluminum hydroxides. The flocculent colloidal precipitation formed by aluminum ions has a loose structure and high liquid content, resulting in lower sedimentation efficiency and higher RE loss. The addition of flocculants in the impurity removal process of RE leachate is expected to solve this problem. The cationic polyacrylamide flocculant (CPAM) was screened as the flocculant to accelerate the sedimentation of the impurity removal process as well as to effectively improve the recovery of RE. The effects of CPAM concentration, dosage, stirring rate and stirring time on the flocculation process was investigated. The optimal flocculation effect could be obtained under conditions of dosage of 0.5 mL, concentration of 0.1%, stirring speed of 700 r/min and stirring time of 2 min. Under this condition, RE recovery efficiency was 97%, Al removal efficiency was 96%, and the sedimentation time of the flocs was 20 min. Compared with absence of flocculants in this process, Al removal efficiency remained almost unchanged, while RE recovery efficiency and the sedimentation time of flocs increased by 4% and shortened by 40 min, respectively. The flocculation mechanism was discussed by the theory of two-dimensional fractal dimension, and it was found that the flocculation was mainly based on the combined effect of bridge flocculation and electrical neutralization.

Reactive Carbon Capture Enables CO2 Electrolysis with Liquid Feedstocks.

ConspectusThe electrochemical reduction of carbon dioxide (CO2RR) is a promising strategy for mitigating global CO2 emissions while simultaneously yielding valuable chemicals and fuels, such as CO, HCOO-, and C2H4. This approach becomes especially appealing when integrated with surplus renewable electricity, as the ensuing production of fuels could facilitate the closure of the carbon cycle. Despite these advantages, the realization of industrial-scale electrolyzers fed with CO2 will be challenged by the substantial energy inputs required to isolate, pressurize, and purify CO2 prior to electrolysis.To address these challenges, we devised an electrolyzer capable of directly converting reactive carbon solutions (e.g., a bicarbonate-rich eluent that exits a carbon capture unit) into higher value products. This "reactive carbon electrolyzer" operates by reacting (bi)carbonate with acid generated within the electrolyzer to produce CO2 in situ, thereby facilitating CO2RR at the cathode. This approach eliminates the need for expensive CO2 recovery and compression steps, as the electrolyzer can then then coupled directly to the CO2 capture unit.This Account outlines our endeavors in developing this type of electrolyzer, focusing on the design and implementation of materials for electrocatalytic (bi)carbonate conversion. We highlight the necessity for a permeable cathode that allows the efficient transport of (bi)carbonate ions while maintaining a sufficiently high catalytic surface area. We address the importance of the supporting electrolyte, detailing how (bi)carbonate concentration, counter cations, and ionic impurities impact selectivity for products formed in the electrolyzer. We also catalog state-of-the-art performance metrics for reactive carbon electrolyzers (i.e., Faradaic efficiency, full cell voltage, CO2 utilization efficiency) and outline strategies to bridge the gap between these values and those required for commercial operation Collectively, these findings contribute to the ongoing efforts to realize industrial-scale electrochemical reactors for CO2 conversion, bringing us closer to a sustainable and closed-loop carbon cycle.

First-principle study on the structure and stability of LiNi1/3Co1/3Mn1/3O2 doped with metal cations of different valences

To minimize resource and energy consumption during the impurity removal process in industrial battery preparation and waste battery recycling, we conducted a preliminary study on the differential purification of impurity ions: Na+, Mg2+, Al3+. Utilizing the first-principle calculation, we assessed the impact of ions doping LiNi1/3Co1/3Mn1/3O2 on three factors that influence cycle stability: phase stability, structural changes during cycling, and oxygen vacancy formation. The results indicate that Na-doped exhibits a tendency for phase separation and increases structural changes during cycling, making it unsuitable for retention in the final products. On the other hand, Mg-doped and Al-doped demonstrate excellent phase stability, reduce structural changes during cycling due to the preferential oxidation of Co3+, and inhibit oxygen release. From a cycle stability perspective, they are suitable for inclusion in the final products.

First-Principles Investigations of the Electronic Structure and Mechanical Characteristics of Nd3+-Doped YAlO3 Crystals

Near-infrared laser radiation based on Nd3+-doped yttrium ortho-aluminate (Nd:YAlO3, Nd:YAP) has garnered significant interest regarding solid-state lasers. Nevertheless, the crystal microstructures and electronic characteristics of Nd:YAP are still unclear, and the unique physical properties underlying its enormous applications require clarification. In this study, we conducted first-principles calculations at the atomic level to explore the electronic properties and mechanical characteristics of both pure YAP and Nd3+-doped YAP. The results suggest that the substitution of the Y3+ ion site with the Nd3+ impurity ion induces slight structural distortion in the YAP crystal lattice. An impurity band emerges between the original conduction band and the valence band, attributed to the 4f orbital of the Nd3+ ion, exerting a substantial influence on the narrowing of the band gap. Through an analysis of the mechanical characteristics of both pure YAP and Nd:YAP, we conclude that the incorporation of Nd3+ atoms leads to a reduction in the mechanical properties of YAP to a certain extent. Our study can serve as a foundational data source for investigations into material performance, especially for the application of Nd:YAP in solid-state laser systems.

Divertor enrichment of recycling impurity species (He, N2, Ne, Ar, Kr) in ASDEX Upgrade H-modes

Particle balance calculations are done for the seeding species N2, Ne, Ar, Kr as well as He with the aim of obtaining a realistic description of the divertor and core plasma impurity content. Experimental time traces of main plasma impurity densities are fitted by a single, time-independent parameter v z,ineff . This parameter represents the product of the impurity inward pinch in the pedestal, used for the description of gross fueling here, and the enrichment factor between the sub-divertor gas reservoir and the upstream separatrix. v z,ineff depends strongly on the first ionization energy as well as on the charge Z or mass of the impurity. The prevailing dependence of the enrichment values on the ionization energy suggests the importance of the relative impurity and deuterium ionization lengths in the divertor. Regression analysis of v z,ineff yields an expression for the impurity concentrations in the core and the divertor of ASDEX Upgrade which allows the prediction of the corresponding impurity densities and their divertor enrichment within a factor of 2 with only engineering parameters as input. A simple wall model has been introduced to take into account wall storage and release of impurities, e.g. for conditions of pre-loaded walls due to seeding in previous discharges. Wall effects are observed for all species considered, but wall storage turns out to be more important for N and He compared to Ne, Ar, Kr. Similar enrichment values are obtained for ELMy H-modes and EDA/QCE no-ELM regimes. A factor of approximately 1.4 reduction in enrichment is observed for divertor conditions for pronounced detachment with Ar and N2. The obtained analytical model for the core and sub-divertor impurity densities is well suited for integration into a discharge flight simulator or a real time state observer.

Synergistic preparation and application in PCU of α-calcium sulfate hemihydrate whiskers from phosphogypsum and electrolytic manganese residue

The α-calcium sulfate hemihydrate whiskers (α-CSHWs) were first prepared using phosphogypsum (PG) and electrolytic manganese residue (EMR) as raw materials for coating urea, demonstrating excellent controlled-release properties. The effects of different reaction conditions on α-CSHWs, achieved by optimizing the reaction time, the concentrations of NH4+, Mn2+, and other factors, were discussed. Results showed that when the EMR content was 25 wt%, the reaction temperature was 100 °C, and the reaction time was 3 h, α-CSHWs with a length-to-diameter ratio of 39 were obtained. Through experiments and density functional theory (DFT), the mechanism of α-CSHWs preparation was elucidated. The results show that the addition of EMR reduces the content of impurity ions PO43− and F− in PG while introducing NH4+ and Mn2+. Interestingly, both NH4+ and Mn2+ can reduce the nucleation time of α-CSHWs, while PO43−, Mn2+, and F− are more likely to adsorb on the (0 0 6) crystal plane of α-CSHWs, NH4+ readily adsorbs on the (4 0 0) crystal plane. The controlled-release performance of modified α-CSHWs incorporated into polyurethane-coated urea (PCU) was investigated, and it was found that the addition of Mα significantly prolonged the nutrient release period, with the period extending up to 116 days for coatings of 5wt% and above. This work not only enhances the efficiency of PG and EMR utilization but also serves as a reference for the straightforward synthesis and application of α-CSHWs.

Spectroscopic properties and photoluminescence of the Li2B4O7:Mn,Sm glass

The Li2B4O7:Mn,Sm glass containing 1.0 mol.% MnO2 and Sm2O3 were researched by X-ray diffraction (XRD), electron paramagnetic resonance (EPR), and optical spectroscopy methods. The studied glass of high optical quality was obtained by high temperature melting technique. Parameters of the local structure (interatomic distances and coordination numbers) of Li2B4O7:Mn,Sm glass were derived from XRD data analysis. The EPR and optical spectroscopy (absorption, luminescence excitation, emission, decay kinetics) show the presence of Mn2+(3d5) and Mn3+(3d4) impurity ions in the Li2B4O7:Mn,Sm glass. By EPR spectroscopy in the studied glass were identified three types of Mn2+ centres: single Mn2+ (1) centres in the strongly distorted sites (ratio of rhombic and axial constants, |E/D| ≤ 1/3), single Mn2+ (2) centres in the sites with almost cubic symmetry (D ≅ 0, E ≅ 0) as well as Mn2+ pairs and small clusters coupled by magnetic dipolar and exchange interaction, respectively. The Mn2+ EPR spectra parameters in the Li2B4O7:Mn,Sm glass have been determined at T = 295 K. Optical absorption spectrum of the Li2B4O7:Mn,Sm glass contains a very broad intense band peaked at 467 nm belonging to the 5Eg(D) → 5T2g(D) transition of Mn3+ ions and several weak narrow lines corresponding to the 6H5/2 → 6P3/2, 6H5/2 → 6F9/2, 6F7/2, 6F5/2 transitions of Sm3+ (4f5, 6H5/2) ions. Emission spectrum of the Li2B4O7:Mn,Sm glass exhibits a broad band corresponding to the 4T1g(G) → 6A1g(S) transition of Mn2+ ions and three characteristic bands in the yellow-orange-red range belonging to the 4G5/2 → 6H5/2, 6H7/2, 6H9/2 transitions of Sm3+ ions. Photoluminescence spectra (excitation and emission) and decay kinetics of the Mn2+ and Sm3+ ions in the Li2B4O7:Mn,Sm glass are interpreted in comparison with corresponding results for Li2B4O7:Mn and Li2B4O7:Sm glasses. Energy transfer processes Sm3+→Mn2+, Mn3+, and Mn2+→Mn3+ in the studied glass are considered.

Modeling turbulent impurity transport in the SOL of DIII-D with a reduced model

A novel impurity transport model that approximates SOL turbulence as a fluctuating poloidal electric field is shown to be an acceptable replacement for the traditional approach of assigning an arbitrary radial diffusion coefficient to the impurity ions. The model is implemented in the DIVIMP impurity transport code and applied to an L-Mode tungsten divertor experiment on DIII-D. The poloidal electric field is represented as fluctuating between ±1000 V m−1 based on previous measurements. The resulting intermittent vr = E θ × BT transport causes ions to transport both into the core as well as into the far-SOL. Simultaneous agreement with estimates of the W density just inside the separatrix as well as in the far-SOL is obtained (nW ∼ 1014 m−3 and nW ∼ 1012 m−3, respectively). Prompt re-deposition of the W ions was necessary to obtain agreement (fredep ∼ 99%). We conclude that simulating impurity transport using a physics-based approximation for turbulence in the SOL, versus arbitrarily assigning diffusion coefficients, may enable better reactor scale predictions of core impurity contamination.

Correlation between impurity radiation rollover and divertor detachment with boundary impurity seeding in HL-2A

Divertor detachment has significant potential for reducing the divertor target thermal load, and impurity seeding is the primary method for achieving divertor detachment. In this study, different impurity seeding scenarios (N, Ne, and Ar) at the boundary region of HL-2A were simulated using the SOLPS-ITER code. Density scans revealed that when the divertor target electron temperature dropped below 5 eV, a rollover in impurity radiation from the core edge regions of Ar, N, and Ne occurred, and the radiation from impurities in the divertor started to increase concurrently, indicating a correlation between impurity radiation rollover and divertor detachment. Impurity radiation rollover is discovered to be primarily related to impurity transport, which is governed by thermal and friction forces.Prior to divertor detachment, the dominance of thermal forces over friction forces causes impurity ions to transport upstream. However, after detachment, friction forces dominate the impurity ions transport to the divertor region. After analyzing the density and velocity of impurity ions in different charge states, it was found that the core radiation rollover after detachment is mainly caused by high charge state impurity ions. Furthermore, the ability of the divertor to achieve particle flow rollover primarily depends on whether the decrease in plasma pressure ( P t ) exceeds the decrease in plasma temperature ( T t 1 / 2 ).