首页 > 最新文献

Nuclear Materials and Energy最新文献

英文 中文
Understanding the oxidation of pure tungsten in air and its impact on the lifecycle of a fusion power plant 了解纯钨在空气中的氧化及其对核聚变电厂生命周期的影响
IF 2.7 2区 物理与天体物理 Q1 NUCLEAR SCIENCE & TECHNOLOGY Pub Date : 2025-09-18 DOI: 10.1016/j.nme.2025.101988
Rongrui Li , Guillermo Álvarez , Ayla Ipakchi , Livia Cupertino-Malheiros , Mark R. Gilbert , Emilio Martínez-Pañeda , Eric Prestat
The oxidation of pure W and the sublimation of W oxide have been investigated to assess their impact on the lifecycle of a fusion power plant. Pure W has been oxidised at temperatures between 400 and 1050 °C and for durations ranging between 1 and 70 h. The formation of voids and cracks has been observed at temperatures above 600 °C, leading to the formation of dust or oxide spalling, which could be problematic in maintenance and waste-handling scenarios of a fusion power plant. Preferential oxidation taking place at the edge of the specimen was characterised, and its impact is discussed in relation to component design. Characterisation using electron microscopy and Raman spectroscopy revealed that the oxide scale is formed of three main layers: the inner layer is 30–50 nm thick WO2 oxide, the middle layer is a 10–20 μm thick of WO2.72 and the outer layer is formed of WO2.9/WO3 phases — whose thickness varies according to the total thickness of the oxide scale. The observed microstructure is discussed in relation to the parabolic-to-linear kinetics and its potential impact on tritium permeation and detritiation efficiency.
研究了纯W的氧化和W氧化物的升华,以评估它们对核聚变电厂生命周期的影响。纯W在400至1050°C的温度下氧化,持续时间在1至70小时之间。在600°C以上的温度下观察到空洞和裂纹的形成,导致灰尘或氧化物剥落的形成,这可能会在核聚变发电厂的维护和废物处理场景中产生问题。优先氧化发生在试样的边缘进行了表征,并讨论了其影响有关的组件设计。利用电子显微镜和拉曼光谱对氧化层进行了表征,发现氧化层主要由三层组成:内层为30 ~ 50 nm厚的WO2氧化物,中间层为10 ~ 20 μm厚的WO2.72,外层为WO2.9/WO3相,其厚度根据氧化层的总厚度而变化。讨论了观察到的微观结构与抛物线-线性动力学的关系及其对氚渗透和除氚效率的潜在影响。
{"title":"Understanding the oxidation of pure tungsten in air and its impact on the lifecycle of a fusion power plant","authors":"Rongrui Li ,&nbsp;Guillermo Álvarez ,&nbsp;Ayla Ipakchi ,&nbsp;Livia Cupertino-Malheiros ,&nbsp;Mark R. Gilbert ,&nbsp;Emilio Martínez-Pañeda ,&nbsp;Eric Prestat","doi":"10.1016/j.nme.2025.101988","DOIUrl":"10.1016/j.nme.2025.101988","url":null,"abstract":"<div><div>The oxidation of pure W and the sublimation of W oxide have been investigated to assess their impact on the lifecycle of a fusion power plant. Pure W has been oxidised at temperatures between 400 and 1050 °C and for durations ranging between 1 and 70 h. The formation of voids and cracks has been observed at temperatures above 600 °C, leading to the formation of dust or oxide spalling, which could be problematic in maintenance and waste-handling scenarios of a fusion power plant. Preferential oxidation taking place at the edge of the specimen was characterised, and its impact is discussed in relation to component design. Characterisation using electron microscopy and Raman spectroscopy revealed that the oxide scale is formed of three main layers: the inner layer is 30–50 nm thick WO<span><math><msub><mrow></mrow><mrow><mn>2</mn></mrow></msub></math></span> oxide, the middle layer is a 10–20 <span><math><mi>μ</mi></math></span>m thick of WO<sub>2.72</sub> and the outer layer is formed of WO<sub>2.9</sub>/WO<span><math><msub><mrow></mrow><mrow><mn>3</mn></mrow></msub></math></span> phases — whose thickness varies according to the total thickness of the oxide scale. The observed microstructure is discussed in relation to the parabolic-to-linear kinetics and its potential impact on tritium permeation and detritiation efficiency.</div></div>","PeriodicalId":56004,"journal":{"name":"Nuclear Materials and Energy","volume":"45 ","pages":"Article 101988"},"PeriodicalIF":2.7,"publicationDate":"2025-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145221713","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Stability of oxide phases in W–Cr–Y SMART alloys W-Cr-Y SMART合金氧化相的稳定性
IF 2.7 2区 物理与天体物理 Q1 NUCLEAR SCIENCE & TECHNOLOGY Pub Date : 2025-09-17 DOI: 10.1016/j.nme.2025.101987
Ryan D. Kerr , Duc Nguyen-Manh , Mark R. Gilbert , Samuel T. Murphy
The addition of Cr and Y into tungsten can dramatically increase the oxidation resistance of the first wall of a future fusion reactor, thereby reducing the risk of formation of volatile WO3 and the release of radioactive material. Experimental observations suggest that in these SMART alloys, yttrium facilitates the formation of a self-passivating layer of Cr2O3 at the metal surface, however, how exactly the Y does this remains unclear. Therefore, this work explores the phase stability of compounds consisting of W–Y–Cr–O and solution energies for the different components in tungsten using density functional theory. The simulations suggest that there is a substantial thermodynamic driving force for the formation of Y2O3, especially from yttrium and oxygen solvated in bulk tungsten. These observations suggest that the role of the yttrium may be to remove the oxygen that may inhibit Cr diffusion to the surface from the tungsten grains. This observation is in accordance with experimental studies showing that the oxidation resistance in the alloy occurs when the oxygen–yttrium ratio in the alloy is close to the stoichiometric ratio for Y2O3.
在钨中加入Cr和Y可以显著提高未来聚变反应堆第一壁的抗氧化性,从而降低挥发性WO3形成和放射性物质释放的风险。实验观察表明,在这些SMART合金中,钇促进了金属表面Cr2O3自钝化层的形成,然而,Y究竟如何做到这一点尚不清楚。因此,本研究利用密度泛函理论探讨了W-Y-Cr-O组成的化合物的相稳定性和钨中不同组分的溶液能量。模拟结果表明,Y2O3的形成有重要的热力学驱动力,特别是在钨体中由钇和氧溶剂化而成。这些观察结果表明,钇的作用可能是去除可能抑制铬从钨晶向表面扩散的氧。这一观察结果与实验研究一致,表明当合金中的氧钇比接近Y2O3的化学计量比时,合金中的抗氧化性就会发生。
{"title":"Stability of oxide phases in W–Cr–Y SMART alloys","authors":"Ryan D. Kerr ,&nbsp;Duc Nguyen-Manh ,&nbsp;Mark R. Gilbert ,&nbsp;Samuel T. Murphy","doi":"10.1016/j.nme.2025.101987","DOIUrl":"10.1016/j.nme.2025.101987","url":null,"abstract":"<div><div>The addition of Cr and Y into tungsten can dramatically increase the oxidation resistance of the first wall of a future fusion reactor, thereby reducing the risk of formation of volatile WO<span><math><msub><mrow></mrow><mrow><mn>3</mn></mrow></msub></math></span> and the release of radioactive material. Experimental observations suggest that in these SMART alloys, yttrium facilitates the formation of a self-passivating layer of Cr<sub>2</sub>O<sub>3</sub> at the metal surface, however, how exactly the Y does this remains unclear. Therefore, this work explores the phase stability of compounds consisting of W–Y–Cr–O and solution energies for the different components in tungsten using density functional theory. The simulations suggest that there is a substantial thermodynamic driving force for the formation of Y<span><math><msub><mrow></mrow><mrow><mn>2</mn></mrow></msub></math></span>O<span><math><msub><mrow></mrow><mrow><mn>3</mn></mrow></msub></math></span>, especially from yttrium and oxygen solvated in bulk tungsten. These observations suggest that the role of the yttrium may be to remove the oxygen that may inhibit Cr diffusion to the surface from the tungsten grains. This observation is in accordance with experimental studies showing that the oxidation resistance in the alloy occurs when the oxygen–yttrium ratio in the alloy is close to the stoichiometric ratio for Y<span><math><msub><mrow></mrow><mrow><mn>2</mn></mrow></msub></math></span>O<span><math><msub><mrow></mrow><mrow><mn>3</mn></mrow></msub></math></span>.</div></div>","PeriodicalId":56004,"journal":{"name":"Nuclear Materials and Energy","volume":"45 ","pages":"Article 101987"},"PeriodicalIF":2.7,"publicationDate":"2025-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145107771","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Study on the corrosion behavior of static liquid Pb-16.7Li on the structural material CLF-1 steel 静态液体Pb-16.7Li对结构材料CLF-1钢的腐蚀行为研究
IF 2.7 2区 物理与天体物理 Q1 NUCLEAR SCIENCE & TECHNOLOGY Pub Date : 2025-09-14 DOI: 10.1016/j.nme.2025.101989
Haowen Deng , Shouxi Gu , Qiang Qi , Guang-nan Luo
In liquid Pb-Li tritium breeding blanket, the compatibility between liquid Pb-Li and Reduced-activation-ferritic-martensitic (RAFM) steel structure material is crucial for the successful application of the RAFM steel. Corrosion experiments on CLF-1 steel in static Pb-Li at 550 ℃ were conducted for up to 1200 h to figure out the corrosion behavior and mechanism. After exposure, a subset of specimens was cleaned by mixed acid dissolution, while the remaining samples were cold-mounted in resin for cross-sectional observation. X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), Energy Dispersive Spectroscopy (EDS), Time-of-Flight Secondary Ion Mass Spectrometry (ToF-SIMS) and Electron Backscatter Diffraction (EBSD) measurements were employed to characterize the corrosion behavior and reveal the corrosion mechanism. With increasing exposure time, corrosion initiates at grain boundaries and spreads laterally, producing boundary ditches, hollows, protrusions, and ultimately pebble‑like grains. It is proposed that corrosion occurs through the dissolution of Fe and Cr, facilitated by the diffusion of Li into the grain boundaries and grains, as well as the penetration and adsorption of Pb.
在液态Pb-Li氚孕育毯中,液态Pb-Li与还原活化铁素体-马氏体(RAFM)钢结构材料的相容性是RAFM钢能否成功应用的关键。对CLF-1钢在550℃的静态铅酸锂中进行了长达1200 h的腐蚀实验,研究了其腐蚀行为和机理。暴露后,将一部分样品用混合酸溶解清洗,其余样品用树脂冷装进行截面观察。采用x射线衍射(XRD)、扫描电子显微镜(SEM)、能量色散光谱(EDS)、飞行时间二次离子质谱(ToF-SIMS)和电子背散射衍射(EBSD)等测量方法对腐蚀行为进行了表征,揭示了腐蚀机理。随着暴露时间的增加,腐蚀从晶界开始并向横向扩散,形成晶界沟槽、空洞、突起,最终形成卵石状晶粒。提出腐蚀发生在Fe和Cr的溶解,Li扩散到晶界和晶粒中,以及Pb的渗透和吸附。
{"title":"Study on the corrosion behavior of static liquid Pb-16.7Li on the structural material CLF-1 steel","authors":"Haowen Deng ,&nbsp;Shouxi Gu ,&nbsp;Qiang Qi ,&nbsp;Guang-nan Luo","doi":"10.1016/j.nme.2025.101989","DOIUrl":"10.1016/j.nme.2025.101989","url":null,"abstract":"<div><div>In liquid Pb-Li tritium breeding blanket, the compatibility between liquid Pb-Li and Reduced-activation-ferritic-martensitic (RAFM) steel structure material is crucial for the successful application of the RAFM steel. Corrosion experiments on CLF-1 steel in static Pb-Li at 550 ℃ were conducted for up to 1200 h to figure out the corrosion behavior and mechanism. After exposure, a subset of specimens was cleaned by mixed acid dissolution, while the remaining samples were cold-mounted in resin for cross-sectional observation. X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), Energy Dispersive Spectroscopy (EDS), Time-of-Flight Secondary Ion Mass Spectrometry (ToF-SIMS) and Electron Backscatter Diffraction (EBSD) measurements were employed to characterize the corrosion behavior and reveal the corrosion mechanism. With increasing exposure time, corrosion initiates at grain boundaries and spreads laterally, producing boundary ditches, hollows, protrusions, and ultimately pebble‑like grains. It is proposed that corrosion occurs through the dissolution of Fe and Cr, facilitated by the diffusion of Li into the grain boundaries and grains, as well as the penetration and adsorption of Pb.</div></div>","PeriodicalId":56004,"journal":{"name":"Nuclear Materials and Energy","volume":"45 ","pages":"Article 101989"},"PeriodicalIF":2.7,"publicationDate":"2025-09-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145107770","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Efficiency evaluation of fuel retention diagnostic in first wall by LID-QMS: Based on LIBS 基于LIBS的LID-QMS首壁燃料滞留诊断效率评价
IF 2.7 2区 物理与天体物理 Q1 NUCLEAR SCIENCE & TECHNOLOGY Pub Date : 2025-09-10 DOI: 10.1016/j.nme.2025.101986
Yiqin Wang , Qingmei Xiao , Yang Liu , Shi Ye , Feng Li , Dongye Zhao
Quantifying deuterium (D) retention in plasma-facing components (PFCs) with minimal material impact is critical for fusion reactor operation. This study employs laser-induced desorption coupled with quadrupole mass spectrometry (LID-QMS) for in situ D-retention analysis on HL-3 graphite tiles. As an auxiliary strategy, laser-induced breakdown spectroscopy (LIBS) is implemented under optimized low-fluence conditions to intermittently evaluate LID-QMS desorption efficiency during operation. Laboratory experiments demonstrate > 80 % deuterium release in the first LID pulse (laser fluence > 570 MW/m2), validated via cross-calibrated QMS measurements; LIBS provides rapid efficiency assessment by correlating D/H spectral results with QMS-resolved H, HD and D2 desorption signals. The integrated LID-QMS-LIBS framework permits: real-time optimization of LID parameters during material analysis, direct efficiency validation without destructive sampling. This methodology is currently being implemented on HL-3 tokamak for in situ wall-D monitoring, demonstrating potential to replace ex situ post-mortem analysis in future fusion devices.
在最小的材料影响下量化等离子体面组件(pfc)中的氘(D)保留对聚变反应堆运行至关重要。本研究采用激光诱导解吸结合四极杆质谱法(LID-QMS)对HL-3石墨瓦进行原位d保留分析。作为辅助策略,在优化的低通量条件下实施激光诱导击穿光谱(LIBS),以间歇评估LID-QMS在运行过程中的解吸效率。实验室实验表明,在第一个LID脉冲(激光通量>; 570mw /m2)中,80%的氘释放,通过交叉校准的QMS测量验证;LIBS通过将D/H光谱结果与qms分辨的H、HD和D2解吸信号相关联,提供快速的效率评估。集成的LID- qms - libs框架允许:在材料分析期间实时优化LID参数,直接效率验证而无需破坏性取样。该方法目前正在HL-3托卡马克上实施,用于原位wall-D监测,显示了在未来的聚变装置中取代非原位死后分析的潜力。
{"title":"Efficiency evaluation of fuel retention diagnostic in first wall by LID-QMS: Based on LIBS","authors":"Yiqin Wang ,&nbsp;Qingmei Xiao ,&nbsp;Yang Liu ,&nbsp;Shi Ye ,&nbsp;Feng Li ,&nbsp;Dongye Zhao","doi":"10.1016/j.nme.2025.101986","DOIUrl":"10.1016/j.nme.2025.101986","url":null,"abstract":"<div><div>Quantifying deuterium (D) retention in plasma-facing components (PFCs) with minimal material impact is critical for fusion reactor operation. This study employs laser-induced desorption coupled with quadrupole mass spectrometry (LID-QMS) for in situ D-retention analysis on HL-3 graphite tiles. As an auxiliary strategy, laser-induced breakdown spectroscopy (LIBS) is implemented under optimized low-fluence conditions to intermittently evaluate LID-QMS desorption efficiency during operation. Laboratory experiments demonstrate &gt; 80 % deuterium release in the first LID pulse (laser fluence &gt; 570 MW/m<sup>2</sup>), validated via cross-calibrated QMS measurements; LIBS provides rapid efficiency assessment by correlating D/H spectral results with QMS-resolved H, HD and D<sub>2</sub> desorption signals. The integrated LID-QMS-LIBS framework permits: real-time optimization of LID parameters during material analysis, direct efficiency validation without destructive sampling. This methodology is currently being implemented on HL-3 tokamak for in situ wall-D monitoring, demonstrating potential to replace ex situ post-mortem analysis in future fusion devices.</div></div>","PeriodicalId":56004,"journal":{"name":"Nuclear Materials and Energy","volume":"45 ","pages":"Article 101986"},"PeriodicalIF":2.7,"publicationDate":"2025-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145057400","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Energetics and clustering properties of boron in tungsten and molybdenum: A comparative analysis from first-principles study 硼在钨和钼中的能量学和聚类性质:第一性原理研究的比较分析
IF 2.7 2区 物理与天体物理 Q1 NUCLEAR SCIENCE & TECHNOLOGY Pub Date : 2025-09-10 DOI: 10.1016/j.nme.2025.101985
Peng Shao, Xiaowei Ma, Yunshan Xiong, Aoyu Mo, Haijun Li, Quan-Fu Han, Kun Jie Yang, Yue-Lin Liu
Using first-principles calculations, we have systematically explored the geometric structures, electronic properties, diffusion behavior, and clustering with vacancies for impurity B (boron) in tungsten (W) and molybdenum (Mo). A single B atom prefers to occupy octerhedral interstitial position (oip) rather than tetrahedral interstitial position (tip) in bulk metals. B atoms can be easily captured by vacancies, and a single B atom prefers to occupy an oip next to vacancy center with a capturing energies of −2.67 and −2.51 eV in W and Mo, respectively. As the trapping progresses, at least 6B atoms can be captured by one vacancy, which is therefore regarded as the capturing center of B atoms to form BnV clusters in both metals. For interstitial B and mono-vacancy, the most favorable diffusion pathways are oip → tip → oip and the <111> direction, respectively. At the same temperature, the diffusion coefficients of interstitial B and mono-vacancy in W are about 2–9 orders of magnitude lower than those in Mo, indicating that both interstitial B and mono-vacancy migrate much slower in W than in Mo. On the other hand, since the diffusion coefficient of interstitial B is significantly greater than that of mono-vacancy in both metals, the interstitial B migration is much easier than that of mono-vacancy. We therefore conclude that the BnV formation mechanism can be attributed to that the relatively stable vacancies capture these relatively mobile interstitial B atoms in both metals.
利用第一性原理计算,我们系统地探索了钨(W)和钼(Mo)中杂质B(硼)的几何结构、电子性质、扩散行为和与空位的聚类。在大块金属中,单个B原子更倾向于占据八面体间隙位置(oip)而不是四面体间隙位置(tip)。B原子容易被空位捕获,单个B原子更倾向于占据空位中心附近的oip, W和Mo的捕获能分别为- 2.67和- 2.51 eV。随着捕获过程的进行,一个空位至少可以捕获6B原子,因此该空位被认为是B原子在两种金属中形成BnV簇的捕获中心。对于间隙B和单空位,最有利的扩散路径分别是oip→tip→oip和<;111>;方向。在相同温度下,W中间隙B和单空位的扩散系数比Mo中低约2-9个数量级,说明W中间隙B和单空位的迁移速度都比Mo慢得多。另一方面,由于两种金属中间隙B的扩散系数都明显大于单空位,因此间隙B的迁移要比单空位容易得多。因此,我们得出结论,BnV的形成机制可归因于两种金属中相对稳定的空位捕获了这些相对移动的间隙B原子。
{"title":"Energetics and clustering properties of boron in tungsten and molybdenum: A comparative analysis from first-principles study","authors":"Peng Shao,&nbsp;Xiaowei Ma,&nbsp;Yunshan Xiong,&nbsp;Aoyu Mo,&nbsp;Haijun Li,&nbsp;Quan-Fu Han,&nbsp;Kun Jie Yang,&nbsp;Yue-Lin Liu","doi":"10.1016/j.nme.2025.101985","DOIUrl":"10.1016/j.nme.2025.101985","url":null,"abstract":"<div><div>Using first-principles calculations, we have systematically explored the geometric structures, electronic properties, diffusion behavior, and clustering with vacancies for impurity B (boron) in tungsten (W) and molybdenum (Mo). A single B atom prefers to occupy octerhedral interstitial position (oip) rather than tetrahedral interstitial position (tip) in bulk metals. B atoms can be easily captured by vacancies, and a single B atom prefers to occupy an oip next to vacancy center with a capturing energies of −2.67 and −2.51 eV in W and Mo, respectively. As the trapping progresses, at least 6B atoms can be captured by one vacancy, which is therefore regarded as the capturing center of B atoms to form B<sub>n</sub>V clusters in both metals. For interstitial B and mono-vacancy, the most favorable diffusion pathways are oip → tip → oip and the &lt;111&gt; direction, respectively. At the same temperature, the diffusion coefficients of interstitial B and mono-vacancy in W are about 2–9 orders of magnitude lower than those in Mo, indicating that both interstitial B and mono-vacancy migrate much slower in W than in Mo. On the other hand, since the diffusion coefficient of interstitial B is significantly greater than that of mono-vacancy in both metals, the interstitial B migration is much easier than that of mono-vacancy. We therefore conclude that the B<sub>n</sub>V formation mechanism can be attributed to that the relatively stable vacancies capture these relatively mobile interstitial B atoms in both metals.</div></div>","PeriodicalId":56004,"journal":{"name":"Nuclear Materials and Energy","volume":"45 ","pages":"Article 101985"},"PeriodicalIF":2.7,"publicationDate":"2025-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145061572","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Investigating the stability and work function effects of Ba atoms adsorption on the Mo (110) surface 研究Ba原子在Mo(110)表面吸附的稳定性和功函数效应
IF 2.7 2区 物理与天体物理 Q1 NUCLEAR SCIENCE & TECHNOLOGY Pub Date : 2025-09-09 DOI: 10.1016/j.nme.2025.101984
Yubo Ma , Wei Li , Jun Hu , Xin Zhang , Yuhong Xu , Guangjiu Lei , Shaofei Geng , Haifeng Liu , Xianqu Wang , Jie Huang , Hai Liu , Jun Cheng , Changjian Tang
This study systematically investigates the effects of the stability and work function of barium (Ba) atoms adsorption on the Mo (110) surface using first-principles density functional (DFT) theory calculations. The results demonstrate that the long-bridge site represents the most stable adsorption configuration for Ba atoms on Mo (110) surface. As the Ba coverage increases, the work function initially decreases sharply and then increases slowly, reaching a minimum value of 2.25 eV at a coverage of 4/16 θ (3.35 × 1014 cm−2), which is markedly lower than the work function of 4.85 eV for the clean Mo (110) surface. This indicates that the adsorption of Ba atoms on the Mo (110) surface substantially reduces the work function. Theoretical analysis reveals a linear correlation between work function variations and dipole moment density changes, with charge redistribution induced by Ba adsorption dominating the total dipole moment modification. These results provide the reference for the research of the Cs-free alternative materials for neutral beam injection systems in fusion research.
本研究采用第一性原理密度泛函(DFT)理论计算,系统地研究了钡原子在Mo(110)表面吸附的稳定性和功函数的影响。结果表明,Mo(110)表面上Ba原子最稳定的吸附构型是长桥位。随着Ba覆盖率的增加,功函数先急剧减小后缓慢增大,在4/16 θ (3.35 × 1014 cm−2)覆盖率下达到最小值2.25 eV,明显低于干净Mo(110)表面的功函数4.85 eV。这表明Ba原子在Mo(110)表面的吸附大大降低了功函数。理论分析表明,功函数变化与偶极矩密度变化呈线性相关,吸附Ba引起的电荷重分布主导了总偶极矩变化。这些结果为核聚变研究中中性束注入系统的无cs替代材料的研究提供了参考。
{"title":"Investigating the stability and work function effects of Ba atoms adsorption on the Mo (110) surface","authors":"Yubo Ma ,&nbsp;Wei Li ,&nbsp;Jun Hu ,&nbsp;Xin Zhang ,&nbsp;Yuhong Xu ,&nbsp;Guangjiu Lei ,&nbsp;Shaofei Geng ,&nbsp;Haifeng Liu ,&nbsp;Xianqu Wang ,&nbsp;Jie Huang ,&nbsp;Hai Liu ,&nbsp;Jun Cheng ,&nbsp;Changjian Tang","doi":"10.1016/j.nme.2025.101984","DOIUrl":"10.1016/j.nme.2025.101984","url":null,"abstract":"<div><div>This study systematically investigates the effects of the stability and work function of barium (Ba) atoms adsorption on the Mo (110) surface using first-principles density functional (DFT) theory calculations. The results demonstrate that the long-bridge site represents the most stable adsorption configuration for Ba atoms on Mo (110) surface. As the Ba coverage increases, the work function initially decreases sharply and then increases slowly, reaching a minimum value of 2.25 eV at a coverage of 4/16 θ (3.35 × 10<sup>14</sup> cm<sup>−2</sup>), which is markedly lower than the work function of 4.85 eV for the clean Mo (110) surface. This indicates that the adsorption of Ba atoms on the Mo (110) surface substantially reduces the work function. Theoretical analysis reveals a linear correlation between work function variations and dipole moment density changes, with charge redistribution induced by Ba adsorption dominating the total dipole moment modification. These results provide the reference for the research of the Cs-free alternative materials for neutral beam injection systems in fusion research.</div></div>","PeriodicalId":56004,"journal":{"name":"Nuclear Materials and Energy","volume":"45 ","pages":"Article 101984"},"PeriodicalIF":2.7,"publicationDate":"2025-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145050308","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
High heat flux testing of wire-based laser metal deposition coated plasma-facing components 线基激光金属镀层等离子表面元件的高热流密度测试
IF 2.7 2区 物理与天体物理 Q1 NUCLEAR SCIENCE & TECHNOLOGY Pub Date : 2025-09-07 DOI: 10.1016/j.nme.2025.101983
Jannik Tweer , Thomas Derra , Daniel Dorow-Gerspach , Mauricio Gago , Sascha Gierlings , Stefan Gräfe , Gerald Pintsuk , Marius Wirtz , Christian Linsmeier , Thomas Bergs , Ghaleb Natour
The severe environment and loads acting on plasma-facing components (PFCs) of future fusion power plants cause inevitable erosion of their armor. In situ regeneration of tungsten (W) armored PFCs by local deposition of material would open up the possibility of damage healing and compensation of eroded material. The wire-based laser metal deposition (LMD-w) process fulfils the necessary requirements for use in the reactor vessel. Process development for the deposition of W on W substrate has already been carried out and it has been proven that thermal induced damage in the PFM can be healed this way. In this study, W armored PFCs were coated using LMD-w and tested under fusion–relevant thermal loads in the electron beam facility JUDITH 2. One respectively two stacked layers, each 0.65 mm in height, were applied on the top surfaces of the W double tiles with surface areas of 28 × 12 mm2 respectively, which are the characteristic dimensions for the plasma-facing surface of monoblocks. Some of the coated surfaces were also smoothed by laser remelting. In the electron beam facility JUDITH 2, the test components were exposed to steady state as well as combined steady state and transient thermal loads that are expected in the divertor area of the future DEMOnstration power plant. The coatings were tested with cyclic (200 and 1000 cycles) steady state thermal loading in the form of surface temperatures equivalent to heat fluxes on monoblock components of 10 MW m−2 (∼1000 °C) and 15 MW m−2 (∼1500 °C). To determine the performance of LMD-w layers under thermal loads that are expected during exposure to edged localized modes (ELMs), some layers were subjected to combined steady state and transient loading scenarios (0.13–0.55 GW m−2, 103 to 105 pulses of 0.48 ms, 200–700 °C base-temperature). The temperature data obtained from the HHF experiments was processed and analyzed. Profile measurements on the coated surfaces before and after the high heat flux (HHF) exposure were used to investigate the influence of thermal stress on the deposited layers. Furthermore, cross-sectional micrographs of the test components were prepared and analyzed.
未来核聚变电站的等离子体面组件(pfc)所处的恶劣环境和载荷将不可避免地导致其装甲的侵蚀。材料局部沉积原位再生将为侵蚀材料的损伤愈合和补偿提供可能。线基激光金属沉积(LMD-w)工艺满足了在反应堆容器中使用的必要要求。在W衬底上沉积W的工艺开发已经进行,并且已经证明这种方法可以修复PFM中的热损伤。在这项研究中,使用LMD-w涂层W装甲pfc,并在电子束设施JUDITH 2中进行融合相关热负荷测试。两层堆叠层,每层高度约0.65 mm,分别应用于W双瓦的顶部表面,其表面积分别为28 × 12 mm2,这是单体体面向等离子体表面的特征尺寸。一些涂层表面也被激光重熔光滑。在电子束设施JUDITH 2中,测试组件暴露于稳态以及稳态和瞬态热负荷的组合,这些负荷预计将在未来示范电厂的导流区使用。涂层在循环(200和1000循环)稳态热负荷下进行测试,其表面温度相当于10 MW m - 2(~ 1000°C)和15 MW m - 2(~ 1500°C)的单块组件的热流。为了确定LMD-w层在边缘局域模式(elm)下的热负荷下的性能,一些层经受了稳态和瞬态载荷的组合(0.13-0.55 GW m−2,103 - 105脉冲,0.48 ms, 200-700°C基温)。对HHF实验得到的温度数据进行了处理和分析。采用高热流密度(HHF)暴露前后涂层表面的剖面测量方法,研究了热应力对镀层的影响。此外,制备并分析了被试组分的截面显微图。
{"title":"High heat flux testing of wire-based laser metal deposition coated plasma-facing components","authors":"Jannik Tweer ,&nbsp;Thomas Derra ,&nbsp;Daniel Dorow-Gerspach ,&nbsp;Mauricio Gago ,&nbsp;Sascha Gierlings ,&nbsp;Stefan Gräfe ,&nbsp;Gerald Pintsuk ,&nbsp;Marius Wirtz ,&nbsp;Christian Linsmeier ,&nbsp;Thomas Bergs ,&nbsp;Ghaleb Natour","doi":"10.1016/j.nme.2025.101983","DOIUrl":"10.1016/j.nme.2025.101983","url":null,"abstract":"<div><div>The severe environment and loads acting on plasma-facing components (PFCs) of future fusion power plants cause inevitable erosion of their armor. In situ regeneration of tungsten (W) armored PFCs by local deposition of material would open up the possibility of damage healing and compensation of eroded material. The wire-based laser metal deposition (LMD-w) process fulfils the necessary requirements for use in the reactor vessel. Process development for the deposition of W on W substrate has already been carried out and it has been proven that thermal induced damage in the PFM can be healed this way. In this study, W armored PFCs were coated using LMD-w and tested under fusion–relevant thermal loads in the electron beam facility JUDITH 2. One respectively two stacked layers, each <strong>∼</strong>0.65 mm in height, were applied on the top surfaces of the W double tiles with surface areas of 28 × 12 mm<sup>2</sup> respectively, which are the characteristic dimensions for the plasma-facing surface of monoblocks. Some of the coated surfaces were also smoothed by laser remelting. In the electron beam facility JUDITH 2, the test components were exposed to steady state as well as combined steady state and transient thermal loads that are expected in the divertor area of the future DEMOnstration power plant. The coatings were tested with cyclic (200 and 1000 cycles) steady state thermal loading in the form of surface temperatures equivalent to heat fluxes on monoblock components of 10 MW m<sup>−2</sup> (∼1000 °C) and 15 MW m<sup>−2</sup> (∼1500 °C). To determine the performance of LMD-w layers under thermal loads that are expected during exposure to edged localized modes (ELMs), some layers were subjected to combined steady state and transient loading scenarios (0.13–0.55 GW m<sup>−2</sup>, 10<sup>3</sup> to 10<sup>5</sup> pulses of 0.48 ms, 200–700 °C base-temperature). The temperature data obtained from the HHF experiments was processed and analyzed. Profile measurements on the coated surfaces before and after the high heat flux (HHF) exposure were used to investigate the influence of thermal stress on the deposited layers. Furthermore, cross-sectional micrographs of the test components were prepared and analyzed.</div></div>","PeriodicalId":56004,"journal":{"name":"Nuclear Materials and Energy","volume":"45 ","pages":"Article 101983"},"PeriodicalIF":2.7,"publicationDate":"2025-09-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145050311","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Recrystallization, cracking, and erosion of dispersoid-strengthened tungsten materials during exposure to divertor plasmas 分散增强钨材料暴露于分流等离子体时的再结晶、开裂和侵蚀
IF 2.7 2区 物理与天体物理 Q1 NUCLEAR SCIENCE & TECHNOLOGY Pub Date : 2025-09-05 DOI: 10.1016/j.nme.2025.101982
R.D. Kolasinski , J.D. Coburn , D.D. Truong , J.G. Watkins , T. Abrams , Z.Z. Fang , R. Hood , R.E. Nygren , A.W. Leonard , J. Ren , D.L. Rudakov , J. Sugar , C. Tsui , H.Q. Wang , J.A. Whaley , I. Bykov , A. Cruz , F. Glass , J. Herfindal , C. Lasnier , W. York
In this study, we investigated the effects of combined intense particle and heat flux exposure on advanced tungsten plasma-facing materials within the DIII-D fusion facility. Our test matrix included two types of dispersoid-strengthened tungsten (containing either 100 nm diameter TiO2 or Ni particles), along with high-purity polycrystalline tungsten as a reference. This experiment relied on a sample geometry angled at 15° relative to the divertor surface, thereby allowing the surfaces to intercept steady-state perpendicular heat fluxes (q) ranging from 10.1 to 19.6 MW/m2. During each shot, the samples were exposed to 42 Hz edge-localized modes (ELMs), allowing us to test the material response to transient heating. We correlated the exposure conditions with extensive post-test surface composition analysis and microscopy to determine how the plasma modified each surface. The angled specimens closest to the strike point received the highest combined heat and particle flux and melted midway through the experiment. EBSD analysis revealed they were completely recrystallized throughout, with an average grain size >100 µm. On the other hand, the specimens that received a lower steady state heat flux survived with more superficial surface damage. Whereas the high-purity polycrystalline tungsten exhibited a higher surface roughness, the dispersoid-strengthened material exhibited more extensive shallow inter-granular cracking. In addition, the surface was depleted of dispersoids following plasma exposure, possibly because of evaporation and/or sputtering. The results described here provide insights into the performance of these materials in a fusion environment which can guide further optimization for use in long-pulse devices.
在这项研究中,我们研究了在DIII-D聚变设施中,强粒子和热通量联合暴露对先进钨等离子体表面材料的影响。我们的测试基质包括两种分散体增强钨(含有100nm直径的TiO2或Ni颗粒),以及作为参考的高纯度多晶钨。该实验依赖于相对于分流器表面的15°角度的样本几何形状,从而允许表面拦截稳态垂直热通量(q⊥),范围从10.1到19.6 MW/m2。在每次拍摄过程中,样品暴露在42 Hz的边缘局部化模式(elm)下,使我们能够测试材料对瞬态加热的响应。我们将暴露条件与广泛的测试后表面成分分析和显微镜相关联,以确定等离子体如何修饰每个表面。最接近撞击点的倾斜试样获得最高的热和粒子通量,并在实验过程中熔化。EBSD分析显示,它们完全再结晶,平均晶粒尺寸为100µm。另一方面,接受较低稳态热通量的试样存活,表面损伤较多。高纯度多晶钨的表面粗糙度较高,而分散体增强材料则表现出更广泛的浅晶间裂纹。此外,等离子体暴露后,表面的分散体被耗尽,可能是由于蒸发和/或溅射。本文描述的结果为这些材料在聚变环境中的性能提供了见解,可以指导在长脉冲器件中使用的进一步优化。
{"title":"Recrystallization, cracking, and erosion of dispersoid-strengthened tungsten materials during exposure to divertor plasmas","authors":"R.D. Kolasinski ,&nbsp;J.D. Coburn ,&nbsp;D.D. Truong ,&nbsp;J.G. Watkins ,&nbsp;T. Abrams ,&nbsp;Z.Z. Fang ,&nbsp;R. Hood ,&nbsp;R.E. Nygren ,&nbsp;A.W. Leonard ,&nbsp;J. Ren ,&nbsp;D.L. Rudakov ,&nbsp;J. Sugar ,&nbsp;C. Tsui ,&nbsp;H.Q. Wang ,&nbsp;J.A. Whaley ,&nbsp;I. Bykov ,&nbsp;A. Cruz ,&nbsp;F. Glass ,&nbsp;J. Herfindal ,&nbsp;C. Lasnier ,&nbsp;W. York","doi":"10.1016/j.nme.2025.101982","DOIUrl":"10.1016/j.nme.2025.101982","url":null,"abstract":"<div><div>In this study, we investigated the effects of combined intense particle and heat flux exposure on advanced tungsten plasma-facing materials within the DIII-D fusion facility. Our test matrix included two types of dispersoid-strengthened tungsten (containing either 100 nm diameter TiO<sub>2</sub> or Ni particles), along with high-purity polycrystalline tungsten as a reference. This experiment relied on a sample geometry angled at 15° relative to the divertor surface, thereby allowing the surfaces to intercept steady-state perpendicular heat fluxes (<span><math><mrow><msub><mi>q</mi><mo>⊥</mo></msub></mrow></math></span>) ranging from 10.1 to 19.6 MW/m<sup>2</sup>. During each shot, the samples were exposed to 42 Hz edge-localized modes (ELMs), allowing us to test the material response to transient heating. We correlated the exposure conditions with extensive post-test surface composition analysis and microscopy to determine how the plasma modified each surface. The angled specimens closest to the strike point received the highest combined heat and particle flux and melted midway through the experiment. EBSD analysis revealed they were completely recrystallized throughout, with an average grain size &gt;100 µm. On the other hand, the specimens that received a lower steady state heat flux survived with more superficial surface damage. Whereas the high-purity polycrystalline tungsten exhibited a higher surface roughness, the dispersoid-strengthened material exhibited more extensive shallow inter-granular cracking. In addition, the surface was depleted of dispersoids following plasma exposure, possibly because of evaporation and/or sputtering. The results described here provide insights into the performance of these materials in a fusion environment which can guide further optimization for use in long-pulse devices.</div></div>","PeriodicalId":56004,"journal":{"name":"Nuclear Materials and Energy","volume":"45 ","pages":"Article 101982"},"PeriodicalIF":2.7,"publicationDate":"2025-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145057401","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Influence of near-surface helium on the deuterium retention and uptake in tungsten 近表面氦对钨中氘保留和吸收的影响
IF 2.7 2区 物理与天体物理 Q1 NUCLEAR SCIENCE & TECHNOLOGY Pub Date : 2025-09-05 DOI: 10.1016/j.nme.2025.101981
S. Markelj , T. Schwarz-Selinger , A. Šestan , J. Zavašnik , M. Kelemen
The effect of near-surface helium (He) on deuterium (D) retention and uptake into the bulk of tungsten (W) was investigated. To quantify the He influence on D uptake, He was implanted close to the surface with 3 keV energy at different fluences and different temperatures. 20 MeV W irradiation was performed at room temperature after He implantation to create defects within the first 2.3 µm. Samples were then exposed to a low flux, low energy (300 eV/D) D ion beam at 450  K. The defects created by W ions trap penetrating D and make it hence possible to quantify D transport into depth below the He layer using 3He nuclear reaction analysis. Elastic recoil detection analysis enabled us to measure the D and He concentration depth profiles near the surface. Results show that D gets preferentially retained where He is implanted with D concentrations up to 10 at.%. At the same time D uptake beyond the He zone is reduced by a factor of 15 compared to a He-free W sample.
研究了近表面氦(He)对氘(D)在钨(W)体中的保留和吸收的影响。为了量化He对D吸收的影响,在不同的影响和不同的温度下,以3 keV的能量在接近表面的地方注入He。He注入后在室温下进行20 MeV W辐照,在前2.3µm内形成缺陷。然后将样品暴露在450k低通量,低能量(300 eV/D)的D离子束中。W离子产生的缺陷捕获了穿透D,因此可以使用3He核反应分析来量化D向He层以下深度的输运。弹性反冲检测分析使我们能够测量地表附近的D和He浓度深度剖面。结果表明,当D浓度达到10% at.%时,He被优先保留。同时,与无He的W样品相比,He区以外的D吸收减少了15倍。
{"title":"Influence of near-surface helium on the deuterium retention and uptake in tungsten","authors":"S. Markelj ,&nbsp;T. Schwarz-Selinger ,&nbsp;A. Šestan ,&nbsp;J. Zavašnik ,&nbsp;M. Kelemen","doi":"10.1016/j.nme.2025.101981","DOIUrl":"10.1016/j.nme.2025.101981","url":null,"abstract":"<div><div>The effect of near-surface helium (He) on deuterium (D) retention and uptake into the bulk of tungsten (W) was investigated. To quantify the He influence on D uptake, He was implanted close to the surface with 3 keV energy at different fluences and different temperatures. 20 MeV W irradiation was performed at room temperature after He implantation to create defects within the first 2.3 µm. Samples were then exposed to a low flux, low energy (300 eV/D) D ion beam at 450 <!--> <!-->K. The defects created by W ions trap penetrating D and make it hence possible to quantify D transport into depth below the He layer using <sup>3</sup>He nuclear reaction analysis. Elastic recoil detection analysis enabled us to measure the D and He concentration depth profiles near the surface. Results show that D gets preferentially retained where He is implanted with D concentrations up to 10 at.%. At the same time D uptake beyond the He zone is reduced by a factor of 15 compared to a He-free W sample.</div></div>","PeriodicalId":56004,"journal":{"name":"Nuclear Materials and Energy","volume":"45 ","pages":"Article 101981"},"PeriodicalIF":2.7,"publicationDate":"2025-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145050310","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Preparing LIBS for in-situ measurements in JET tokamak: system overview and co-deposited layer thicknesses 为JET托卡马克的原位测量准备LIBS:系统概述和共沉积层厚度
IF 2.7 2区 物理与天体物理 Q1 NUCLEAR SCIENCE & TECHNOLOGY Pub Date : 2025-09-01 DOI: 10.1016/j.nme.2025.101968
Jasper Ristkok , Salvatore Almaviva , Jari Likonen , Juuso Karhunen , Indrek Jõgi , Peeter Paris , Shweta Soni , Pavel Veis , Sahithya Atikukke , Jelena Butikova , Rongxing Yi , Ionut Jepu , Pawel Gasior , Corneliu Porosnicu , Mihaela Bojan , Bianca Solomonea , Sebastijan Brezinsek
Laser-induced breakdown spectroscopy (LIBS) is a method for elemental composition analysis that has been proposed for fusion reactor safety diagnostics. A significant milestone in this development was the LIBS campaign conducted in 2024 at the Joint European Torus (JET), using a prototype LIBS enclosure, deployed with the MASCOT tele-manipulation arm. The work presented here prepared for the JET campaign by testing the LIBS enclosure.
Experiments were conducted at VTT Technical Research Centre of Finland, analyzing JET wall samples from the 2011–2016 ILW1–3 fusion campaigns, primarily from the divertor. The focus was on the analysis of co-deposited layers on the plasma-facing components containing hydrogen isotopes and elements from bulk layers: Be, W, Mo, CFC, and Inconel. Measurements were performed under atmospheric pressure air with an argon flow.
Optimal experimental conditions for the use of an Echelle spectrometer in subsequent JET LIBS campaign were identified, and the depth profiles of the surface layers are presented. The LIBS depth profiles defined distinct material layers. Ablating through the co-deposited layers required 1–870 laser shots (∼0.1–90 µm) on samples from different locations, with typical variations of 10–40 % on the same sample and the largest variation spanning 15–480 shots (∼1.5–50 µm).
The LIBS, Secondary Ion Mass Spectrometry (SIMS), and optical profilometry results showed good qualitative agreement. The ablation rate was ∼30–50 nm/shot for the W layers, ∼100–140 nm/shot for bulk Be limiters, and intermediate for the co-deposited layers. The insights gained in this study supported the preparation of the JET LIBS campaign.
激光诱导击穿光谱(LIBS)是一种用于核聚变反应堆安全诊断的元素组成分析方法。这一发展的一个重要里程碑是2024年在欧洲联合环面(JET)进行的LIBS运动,使用了一个原型LIBS外壳,配备了MASCOT远程操纵臂。本文介绍的工作通过测试LIBS外壳为JET活动做了准备。实验在芬兰VTT技术研究中心进行,分析了2011-2016年ILW1-3聚变运动中的JET壁面样本,主要来自转向器。重点分析了共沉积层中含有氢同位素的面向等离子体组分和来自体层的元素:Be、W、Mo、CFC和Inconel。测量在常压下进行,空气中有氩气流动。确定了在后续JET - LIBS活动中使用梯队光谱仪的最佳实验条件,并给出了表层的深度分布。LIBS深度剖面定义了不同的材料层。通过共沉积层的烧蚀需要在不同位置的样品上进行1-870次激光照射(~ 0.1-90µm),在同一样品上的典型变化为10 - 40%,最大变化跨越15-480次(~ 1.5-50µm)。LIBS,次级离子质谱(SIMS)和光学谱分析结果显示了良好的定性一致性。W层的烧蚀速率为~ 30-50 nm/shot,大块Be限制器的烧蚀速率为~ 100-140 nm/shot,共沉积层的烧蚀速率为中间速率。在这项研究中获得的见解支持了JET LIBS活动的准备。
{"title":"Preparing LIBS for in-situ measurements in JET tokamak: system overview and co-deposited layer thicknesses","authors":"Jasper Ristkok ,&nbsp;Salvatore Almaviva ,&nbsp;Jari Likonen ,&nbsp;Juuso Karhunen ,&nbsp;Indrek Jõgi ,&nbsp;Peeter Paris ,&nbsp;Shweta Soni ,&nbsp;Pavel Veis ,&nbsp;Sahithya Atikukke ,&nbsp;Jelena Butikova ,&nbsp;Rongxing Yi ,&nbsp;Ionut Jepu ,&nbsp;Pawel Gasior ,&nbsp;Corneliu Porosnicu ,&nbsp;Mihaela Bojan ,&nbsp;Bianca Solomonea ,&nbsp;Sebastijan Brezinsek","doi":"10.1016/j.nme.2025.101968","DOIUrl":"10.1016/j.nme.2025.101968","url":null,"abstract":"<div><div>Laser-induced breakdown spectroscopy (LIBS) is a method for elemental composition analysis that has been proposed for fusion reactor safety diagnostics. A significant milestone in this development was the LIBS campaign conducted in 2024 at the Joint European Torus (JET), using a prototype LIBS enclosure, deployed with the MASCOT tele-manipulation arm. The work presented here prepared for the JET campaign by testing the LIBS enclosure.</div><div>Experiments were conducted at VTT Technical Research Centre of Finland, analyzing JET wall samples from the 2011–2016 ILW1–3 fusion campaigns, primarily from the divertor. The focus was on the analysis of co-deposited layers on the plasma-facing components containing hydrogen isotopes and elements from bulk layers: Be, W, Mo, CFC, and Inconel. Measurements were performed under atmospheric pressure air with an argon flow.</div><div>Optimal experimental conditions for the use of an Echelle spectrometer in subsequent JET LIBS campaign were identified, and the depth profiles of the surface layers are presented. The LIBS depth profiles defined distinct material layers. Ablating through the co-deposited layers required 1–870 laser shots (∼0.1–90 µm) on samples from different locations, with typical variations of 10–40 % on the same sample and the largest variation spanning 15–480 shots (∼1.5–50 µm).</div><div>The LIBS, Secondary Ion Mass Spectrometry (SIMS), and optical profilometry results showed good qualitative agreement. The ablation rate was ∼30–50 nm/shot for the W layers, ∼100–140 nm/shot for bulk Be limiters, and intermediate for the co-deposited layers. The insights gained in this study supported the preparation of the JET LIBS campaign.</div></div>","PeriodicalId":56004,"journal":{"name":"Nuclear Materials and Energy","volume":"44 ","pages":"Article 101968"},"PeriodicalIF":2.7,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145048916","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Nuclear Materials and Energy
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1