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1D hollow In2O3@ZnFe2O4 core-shell heterostructure for enhanced ppb-level acetone detection 一维空心In2O3@ZnFe2O4核壳异质结构增强ppb水平丙酮检测
IF 6.2 2区 材料科学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2025-12-13 DOI: 10.1016/j.jallcom.2025.185587
Tiantian Cao, Qiaolin Li, Gang Chen, Hongtao Guan, Chengjun Dong
Sensitive and selective acetone detection is critical for environmental monitoring and disease diagnostics, yet current sensors suffer from high operating temperatures and insufficient sensitivity. This study innovatively proposes an electrostatic self-assembly strategy to uniformly anchor small ZnFe2O4 nanoparticles (around 20 nm) onto MOF-derived one-dimensional (1D) hollow In2O3 nanotubes, leading to the successful construction of an In2O3@ZnFe2O4 core-shell heterostructure. The sensor based on In2O3@ZnFe2O4-7.5 exhibits a high response of 278 to 200 ppm acetone at 200 °C, a low detection limit of 50 ppb with response of 1.85, good stability and moisture resistance. It is believed that the excellent sensing performance mainly originated in the formation of n-n heterojunction interfaces to enhance interfacial charge transfer and the effective suppression of ZnFe2O4 aggregation. Thus, this work provides a facile strategy for the fabrication of heterojunction for gas sensors.
灵敏和选择性的丙酮检测对于环境监测和疾病诊断至关重要,但目前的传感器工作温度高,灵敏度不足。本研究创新性地提出了一种静电自组装策略,将小的ZnFe2O4纳米颗粒(约20 nm)均匀地锚定在mof衍生的一维(1D)空心In2O3纳米管上,从而成功构建了In2O3@ZnFe2O4核壳异质结构。基于In2O3@ZnFe2O4-7.5的传感器在200°C下具有278 ~ 200 ppm丙酮的高响应,低检测限为50 ppb,响应为1.85,具有良好的稳定性和防潮性。优异的传感性能主要来源于形成n-n异质结界面以增强界面电荷转移和有效抑制ZnFe2O4聚集。因此,这项工作为气体传感器异质结的制造提供了一种简便的策略。
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引用次数: 0
Mechanistic Insights into Cryo-Deformation and Cooling Medium Induced Strengthening in AA7075-TaC Composites AA7075-TaC复合材料低温变形和冷却介质诱导强化的机理研究
IF 6.2 2区 材料科学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2025-12-13 DOI: 10.1016/j.jallcom.2025.185531
John Samson Khalkho, Dagarapu Benny Karunakar
The superior strength of 7075 aluminium alloys is predominantly derived from precipitation hardening. Heat treatment governs the evolution of these precipitates and when coupled with cryo-deformation offers a viable pathway to further enhance both strength and ductility. This investigation first involves developing AA7075 composites reinforced with 1, 3, 5, and 7wt.% TaC through stir casting. Following this, the study explores the impact of cryo-forging on the AA7075/5wt.% TaC composite, applying different cooling methods i.e. furnace cooling (FC), air cooling (AC), and water quenching (WQ) to optimize mechanical performance. The microstructural evolution of the processed samples was examined using FESEM-EDX, XRD, EBSD, and HRTEM, and correlated with microhardness and tensile properties. Results indicate progressive grain refinement from FC to WQ conditions, with an average grain size of 59µm, alongside increased precipitation, with an average particle size of 88nm. Among all conditions, the cryo-forged (WQ) sample exhibited the highest microhardness (197 Hv), yield strength (521MPa), and ultimate tensile strength (565MPa), while the cryo-forged (FC) condition provided superior elongation (18.7%). The enhancement in strength was primarily attributed to dislocation and precipitation strengthening, whereas improved ductility was linked to reduced grain boundary area and lower dislocation density. This study introduces a novel processing route that combines cryo-forging of TaC-reinforced AA7075 with controlled cooling to achieve substantial microstructural refinement and strength enhancement. The integrated approach yields approximately a 1.4-times increase in hardness, a 2.7-times increase in yield strength, a 2.2-times increase in UTS, and an eight-times improvement in elongation compared to the unprocessed AA7075/5wt.% TaC composite.
7075铝合金的优异强度主要来源于沉淀硬化。热处理控制了这些析出物的演变,当与低温变形相结合时,为进一步提高强度和延展性提供了可行的途径。本研究首先涉及开发1、3、5和7wt增强的AA7075复合材料。% TaC通过搅拌铸造。随后,研究探讨了低温锻造对AA7075/5wt的影响。% TaC复合材料,采用不同的冷却方法,即炉冷却(FC),风冷(AC)和水淬(WQ),以优化机械性能。利用FESEM-EDX、XRD、EBSD和HRTEM分析了加工样品的显微组织演变,并与显微硬度和拉伸性能进行了相关分析。结果表明,从FC到WQ条件下,晶粒逐渐细化,平均晶粒尺寸为59µm,同时析出量增加,平均粒径为88nm。其中,冷锻(WQ)试样具有最高的显微硬度(197 Hv)、屈服强度(521MPa)和极限抗拉强度(565MPa),而冷锻(FC)试样具有较好的伸长率(18.7%)。强度的提高主要是由于位错和析出强化,而延展性的提高与晶界面积的减少和位错密度的降低有关。本研究提出了一种新的工艺路线,将tac增强的AA7075低温锻造与控制冷却相结合,以实现大量的组织细化和强度提高。与未加工的AA7075/5wt相比,综合方法的硬度提高了1.4倍,屈服强度提高了2.7倍,UTS提高了2.2倍,伸长率提高了8倍。% TaC复合材料。
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引用次数: 0
Improvement of the strength and water-oxygen corrosion resistance of SiC reticulated porous ceramics via residual compressive stress 利用残余压应力提高碳化硅网状多孔陶瓷的强度和耐水氧腐蚀性能
IF 6.2 2区 材料科学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2025-12-13 DOI: 10.1016/j.jallcom.2025.185600
Zhe Wu, Xiong Liang, Yawei Li, Jian Tie, Qinghu Wang, Liping Pan, Shaobai Sang
The preparation of high-performance SiC reticulated porous ceramics (SRPC) is critical to ensuring the long-term service of SiC porous media burners. Aiming to synergistically improve the strength and oxidation resistance of the SRPC with multi-layered struts, residual stress was intentionally induced within the anti-oxidation layer by adjusting the coefficient of thermal expansion (CTE). The SRPC was prepared via SiC slurry coating and vacuum infiltration of alumina composite slurry, followed by spraying of LaAlO3 slurry, whose struts included SiC skeleton, transition layers and infrared radiation coating. Results showed that the residual compressive stress generated within anti-oxidation layer when the andalusite was introduced, resulting in an enhanced strength and water-oxygen corrosion resistance. The anti-oxidation layer with ZrO2 addition was peeling off due to the formed residual tensile stress. After 10hours of water-oxygen corrosion, the compression strength of the SRPC coated with LaAlO3 coating did not decrease, which was related to the formation of rod-like whiskers in the coating. This study provides valuable guidance for the preparation of medium materials utilized in high-temperature porous medium combustion.
高性能碳化硅网状多孔陶瓷的制备是保证碳化硅多孔介质燃烧器长期使用的关键。为了协同提高多层支板SRPC的强度和抗氧化性能,通过调节热膨胀系数(CTE)在抗氧化层内有意诱导残余应力。采用SiC浆料包覆和氧化铝复合浆料真空浸润制备SRPC,然后喷涂LaAlO3浆料,LaAlO3浆料的支柱包括SiC骨架、过渡层和红外辐射涂层。结果表明:加入红柱石后,抗氧化层内产生残余压应力,提高了材料的强度和抗水氧腐蚀能力;加入ZrO2后的抗氧化层由于形成残余拉伸应力而剥落。经水氧腐蚀10h后,包覆LaAlO3涂层的SRPC抗压强度没有下降,这与涂层中棒状晶须的形成有关。该研究为高温多孔介质燃烧介质材料的制备提供了有价值的指导。
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引用次数: 0
Lowering melting temperatures of high zinc slag derived from co-smelting of primary ores and secondary resources: regulation method and mechanisms 降低原矿与二次资源共熔炼高锌渣熔炼温度的调控方法与机理
IF 6.2 2区 材料科学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2025-12-13 DOI: 10.1016/j.jallcom.2025.185594
Jiawei Lu, Liyuan Chai, Xiaobo Min, Yong Ke, Yun Li, Yunyan Wang, Xin Wang, Yiming Liu, Cong Peng
The synergistic and enhanced bath smelting of primary ores with secondary resources is a key strategy to address the paradox of resource scarcity and recycling of secondary resources in zinc metallurgy. However, due to the high melting temperature of high zinc slags (Zn > 25%), bath smelting below 1250 °C has not yet been practically implemented. This study proposes a new approach for reducing the melting temperature of high zinc slags by tailoring slag composition and co-smelting secondary resources to promote synergistic melting. The melting properties and regulation mechanisms of high zinc slags were systematically investigated through FactSage thermodynamic calculations, in-situ observation using an ash fusion temperatures auto detecting system, and quenching experiments. The results reveal that CaO/SiO₂ and FeO/SiO₂ mass ratio are the primary factors influencing the melting temperature. Excessively high or low CaO/SiO₂ and FeO/SiO₂ promote the formation of high melting point phases such as zincite, spinel, willemite and melilite, thereby increasing the melting temperature. Components from secondary resources, such as B₂O₃, Na₂O and Cu₂O, can significantly reduce the content of high melting point phase in the melting process, and reduce the melting temperature, while MgO, Cr₂O₃, etc., have the opposite effect. The melting temperature of co-smelting high zinc slag with 15% sludge and 4% borax was reduced over 125 °C. In industrial pilot-scale trial exceeding 20 tons, the flow temperature of high zinc slag containing 27.08% zinc was 1118 °C. This study establishes technical foundations for low-energy and clean co-smelting of secondary resources with primary ores.
原生矿与二次资源协同强化浴炼是解决锌冶炼资源短缺与二次资源循环利用矛盾的关键策略。但由于高锌渣(Zn > 25%)熔炼温度高,1250 ℃以下的熔炼尚未实际实施。本研究提出了一种降低高锌渣熔炼温度的新方法,即通过调整渣成分和共熔炼二次资源来促进协同熔炼。通过FactSage热力学计算、灰熔温度自动检测系统的现场观测和淬火实验,系统地研究了高锌渣的熔化性能和调节机理。结果表明,CaO/SiO 2和FeO/SiO 2质量比是影响熔点温度的主要因素。过高或过低的CaO/SiO₂和FeO/SiO₂都促进了高熔点相的形成,如锌辉石、尖晶石、钨辉石和千英石,从而提高了熔点温度。来自二次资源的组分,如B₂O₃、Na₂O、Cu₂O,在熔融过程中可以显著降低高熔点相的含量,降低熔融温度,而MgO、Cr₂O₃等则有相反的作用。以15%污泥和4%硼砂共熔炼高锌渣,熔点降低到125℃以上。在20吨以上的工业中试中,含锌27.08%的高锌渣的流动温度为1118℃。本研究为低能耗、清洁的二次资源与原矿共熔炼奠定了技术基础。
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引用次数: 0
DFT and Judd–Ofelt Analysis of a Novel Red-Emitting Eu3+ Doped KSrB₅O₉ Phosphor for Photonic Applications 用于光子应用的新型Eu3+掺杂KSrB₅O₉荧光粉的DFT和judd - felt分析
IF 6.2 2区 材料科学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2025-12-13 DOI: 10.1016/j.jallcom.2025.185578
Rohit Raina, Mohan L. Verma, Nabaparna Chakraborty, Kamni, Pankaj Biswas
A novel red emitting Eu3+ doped KSrB5O9 phosphors were successfully prepared using combustion method. The powder X-ray diffraction (pXRD) confirmed the single-phase monoclinic structure of prepared phosphors. The substitution of Eu3+ ions at Sr2+ sites create a charge imbalance, which is compensated by the creation of Sr2+ vacancies. Elemental composition and the oxidation states of the constituent elements present in the prepared phosphor was confirmed by X-ray photoelectron spectroscopy (XPS) and energy dispersive X-ray spectroscopy (EDX). Under excitation wavelength of 392nm, prepared phosphor samples exhibit a strong emission band centred at 618nm corresponding to hypersensitive transition 5D07F2. At 5mol % concentration of Eu3+ maximum luminescence intensity is observed. The photometric studies of the 5mol % Eu3+ doped KSrB5O9 phosphor indicates that the emission is in red region with outstanding colour purity of 99%. Tauc’s equation was used to determine the optical bandgap of prepared phosphor samples. The optical indirect and direct band gap for 5mol % Eu3+ doped KSrB5O9 phosphor was found to be 3.79eV and 4.49eV respectively. The band structure and partial density of states for undoped KSrB5O9 were investigated using density functional theory (DFT) analysis. The Judd-Ofelt intensity parameters calculated using PL emission spectra indicate covalent bonding character between Eu3+ ion and its surrounding ligands, as well as lack of symmetry around the Eu3+ ion site. Other radiative properties such as branching ratio exceeding 50% and high stimulated emission cross section were also estimated using JO parameters. All these observations indicate that the prepared phosphor is promising candidate for red emission, making it well-suited for use in photonic applications like lasers, displays and imaging.
采用燃烧法制备了一种新型Eu3+掺杂KSrB5O9发红光荧光粉。粉末x射线衍射(pXRD)证实了所制备的荧光粉具有单相单斜结构。Eu3+离子在Sr2+位置上的取代产生电荷不平衡,这由Sr2+空位的产生来补偿。用x射线光电子能谱(XPS)和能量色散x射线能谱(EDX)测定了所制备的荧光粉的元素组成和氧化态。在392nm激发波长下,制备的荧光粉样品呈现出以618nm为中心的强发射带,对应于5D0→7F2的超敏跃迁。在Eu3+浓度为5mol %时,观察到最大的发光强度。对5mol % Eu3+掺杂的KSrB5O9荧光粉的光度研究表明,该发光体位于红色区域,颜色纯度达到99%。利用陶克方程确定了制备的荧光粉样品的光学带隙。5mol % Eu3+掺杂KSrB5O9荧光粉的光学间接带隙和直接带隙分别为3.79eV和4.49eV。利用密度泛函理论(DFT)研究了未掺杂KSrB5O9的能带结构和态偏密度。利用PL发射光谱计算的Judd-Ofelt强度参数表明Eu3+离子与其周围配体之间具有共价键特征,以及Eu3+离子位点周围缺乏对称性。其他辐射特性,如分支比超过50%和高受激辐射截面,也可以使用JO参数进行估计。所有这些观察结果表明,所制备的荧光粉是有希望的红色发射候选者,使其非常适合用于激光,显示和成像等光子应用。
{"title":"DFT and Judd–Ofelt Analysis of a Novel Red-Emitting Eu3+ Doped KSrB₅O₉ Phosphor for Photonic Applications","authors":"Rohit Raina, Mohan L. Verma, Nabaparna Chakraborty, Kamni, Pankaj Biswas","doi":"10.1016/j.jallcom.2025.185578","DOIUrl":"https://doi.org/10.1016/j.jallcom.2025.185578","url":null,"abstract":"A novel red emitting Eu<ce:sup loc=\"post\">3+</ce:sup> doped KSrB<ce:inf loc=\"post\">5</ce:inf>O<ce:inf loc=\"post\">9</ce:inf> phosphors were successfully prepared using combustion method. The powder X-ray diffraction (pXRD) confirmed the single-phase monoclinic structure of prepared phosphors. The substitution of Eu<ce:sup loc=\"post\">3+</ce:sup> ions at Sr<ce:sup loc=\"post\">2+</ce:sup> sites create a charge imbalance, which is compensated by the creation of Sr<ce:sup loc=\"post\">2+</ce:sup> vacancies. Elemental composition and the oxidation states of the constituent elements present in the prepared phosphor was confirmed by X-ray photoelectron spectroscopy (XPS) and energy dispersive X-ray spectroscopy (EDX). Under excitation wavelength of 392<ce:hsp sp=\"0.25\"></ce:hsp>nm, prepared phosphor samples exhibit a strong emission band centred at 618<ce:hsp sp=\"0.25\"></ce:hsp>nm corresponding to hypersensitive transition <ce:sup loc=\"post\">5</ce:sup>D<ce:inf loc=\"post\">0</ce:inf>→<ce:sup loc=\"post\">7</ce:sup>F<ce:inf loc=\"post\">2</ce:inf>. At 5<ce:hsp sp=\"0.25\"></ce:hsp>mol % concentration of Eu<ce:sup loc=\"post\">3+</ce:sup> maximum luminescence intensity is observed. The photometric studies of the 5<ce:hsp sp=\"0.25\"></ce:hsp>mol % Eu<ce:sup loc=\"post\">3+</ce:sup> doped KSrB<ce:inf loc=\"post\">5</ce:inf>O<ce:inf loc=\"post\">9</ce:inf> phosphor indicates that the emission is in red region with outstanding colour purity of 99%. Tauc’s equation was used to determine the optical bandgap of prepared phosphor samples. The optical indirect and direct band gap for 5<ce:hsp sp=\"0.25\"></ce:hsp>mol % Eu<ce:sup loc=\"post\">3+</ce:sup> doped KSrB<ce:inf loc=\"post\">5</ce:inf>O<ce:inf loc=\"post\">9</ce:inf> phosphor was found to be 3.79<ce:hsp sp=\"0.25\"></ce:hsp>eV and 4.49<ce:hsp sp=\"0.25\"></ce:hsp>eV respectively. The band structure and partial density of states for undoped KSrB<ce:inf loc=\"post\">5</ce:inf>O<ce:inf loc=\"post\">9</ce:inf> were investigated using density functional theory (DFT) analysis. The Judd-Ofelt intensity parameters calculated using PL emission spectra indicate covalent bonding character between Eu<ce:sup loc=\"post\">3+</ce:sup> ion and its surrounding ligands, as well as lack of symmetry around the Eu<ce:sup loc=\"post\">3+</ce:sup> ion site. Other radiative properties such as branching ratio exceeding 50% and high stimulated emission cross section were also estimated using JO parameters. All these observations indicate that the prepared phosphor is promising candidate for red emission, making it well-suited for use in photonic applications like lasers, displays and imaging.","PeriodicalId":344,"journal":{"name":"Journal of Alloys and Compounds","volume":"14 1","pages":""},"PeriodicalIF":6.2,"publicationDate":"2025-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145753521","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
PdRux/CdS: A Visible-Light-Driven Water Splitting Photocatalyst Based on Strain Engineering and Interface Modulation PdRux/CdS:一种基于应变工程和界面调制的可见光水分解光催化剂
IF 6.2 2区 材料科学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2025-12-13 DOI: 10.1016/j.jallcom.2025.185596
Liuying Xiong, Yangbo Ma, Miao Fa, Yihui Zhang, Xiying Li, Shuaishuai Zhou, Wei Chen, Liqun Mao
CdS, as one of the representative narrow-bandgap semiconductor photocatalyst for hydrogen production from water splitting, suffers from rapid recombination of photogenerated charge carriers, which limits its practical applications. To address this issue, metal alloy/CdS system with tunable surface stain was proposed. In this study, PdRux cubic nanoalloys (~10nm) were synthesized and deposited on 2D-CdS. Comprehensive characterizations, including XRD, TEM, XPS, TRPL, ESR, photoelectrochemical measurements, and density functional theory (DFT) calculations, were employed to systematically investigate the charge transfer behavior and the strain-induced electronic structure modulation. The PdRux nanoalloys exhibits a high work function, leading to interfacial Schottky barrier formation, effectively minimizing charge carrier recombination. Additionally, strain effects shift the d-band center of Pd downward by 0.019eV, optimizing the hydrogen adsorption free energy (ΔGH*) to +0.14eV, thereby reducing the hydrogen evolution reaction barrier. The optimized 2.0% PdRu0.02/CdS achieved an outstanding hydrogen evolution rate of 84.64mmol·g-1·h-1 under visible light (λ > 420nm), representing a 665% improvement over pristine CdS. This study provides both experimental and theoretical insights for designing highly efficient and stable alloy/semiconductor photocatalytic systems, offering a promising strategy for advancing solar-driven hydrogen production.
CdS作为具有代表性的水裂解制氢窄带隙半导体光催化剂之一,其光生载流子的复合速度较快,限制了其实际应用。为了解决这一问题,提出了具有可调表面染色的金属合金/CdS体系。本研究合成了PdRux立方纳米合金(~10nm),并将其沉积在2d - cd上。采用XRD、TEM、XPS、TRPL、ESR、光电化学测量和密度泛函理论(DFT)计算等综合表征方法,系统地研究了该材料的电荷转移行为和应变诱导的电子结构调制。PdRux纳米合金具有较高的功函数,可形成界面肖特基势垒,有效地减少载流子复合。此外,应变效应使Pd的d带中心下移0.019eV,使氢吸附自由能(ΔGH*)优化至+0.14eV,从而降低析氢反应势垒。优化后的2.0% PdRu0.02/CdS在可见光(λ > 420nm)下的析氢速率为84.64mmol·g-1·h-1,比原始CdS提高了665%。该研究为设计高效稳定的合金/半导体光催化系统提供了实验和理论见解,为推进太阳能驱动制氢提供了有前途的策略。
{"title":"PdRux/CdS: A Visible-Light-Driven Water Splitting Photocatalyst Based on Strain Engineering and Interface Modulation","authors":"Liuying Xiong, Yangbo Ma, Miao Fa, Yihui Zhang, Xiying Li, Shuaishuai Zhou, Wei Chen, Liqun Mao","doi":"10.1016/j.jallcom.2025.185596","DOIUrl":"https://doi.org/10.1016/j.jallcom.2025.185596","url":null,"abstract":"CdS, as one of the representative narrow-bandgap semiconductor photocatalyst for hydrogen production from water splitting, suffers from rapid recombination of photogenerated charge carriers, which limits its practical applications. To address this issue, metal alloy/CdS system with tunable surface stain was proposed. In this study, PdRu<ce:inf loc=\"post\"><ce:italic>x</ce:italic></ce:inf> cubic nanoalloys (~10<ce:hsp sp=\"0.25\"></ce:hsp>nm) were synthesized and deposited on 2D-CdS. Comprehensive characterizations, including XRD, TEM, XPS, TRPL, ESR, photoelectrochemical measurements, and density functional theory (DFT) calculations, were employed to systematically investigate the charge transfer behavior and the strain-induced electronic structure modulation. The PdRu<ce:inf loc=\"post\"><ce:italic>x</ce:italic></ce:inf> nanoalloys exhibits a high work function, leading to interfacial Schottky barrier formation, effectively minimizing charge carrier recombination. Additionally, strain effects shift the d-band center of Pd downward by 0.019<ce:hsp sp=\"0.25\"></ce:hsp>eV, optimizing the hydrogen adsorption free energy (ΔG<ce:inf loc=\"post\">H*</ce:inf>) to +0.14<ce:hsp sp=\"0.25\"></ce:hsp>eV, thereby reducing the hydrogen evolution reaction barrier. The optimized 2.0% PdRu<ce:inf loc=\"post\">0.02</ce:inf>/CdS achieved an outstanding hydrogen evolution rate of 84.64<ce:hsp sp=\"0.25\"></ce:hsp>mmol·g<ce:sup loc=\"post\">-1</ce:sup>·h<ce:sup loc=\"post\">-1</ce:sup> under visible light (λ &gt; 420<ce:hsp sp=\"0.25\"></ce:hsp>nm), representing a 665% improvement over pristine CdS. This study provides both experimental and theoretical insights for designing highly efficient and stable alloy/semiconductor photocatalytic systems, offering a promising strategy for advancing solar-driven hydrogen production.","PeriodicalId":344,"journal":{"name":"Journal of Alloys and Compounds","volume":"154 1","pages":""},"PeriodicalIF":6.2,"publicationDate":"2025-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145753499","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Mechanical response of gradient nanostructured Zr-1.5Hf-0.15O under tensile deformation: experimental and CPFEM modeling study 梯度纳米结构Zr-1.5Hf-0.15O在拉伸变形下的力学响应:实验和CPFEM模型研究
IF 6.2 2区 材料科学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2025-12-13 DOI: 10.1016/j.jallcom.2025.185581
Jinping Wang, Conghui Zhang, Kangkai Song, Shuaiyang Liu, Wenguang Zhu, Ruixuan Tian
A gradient nanostructure (GNS) was fabricated on Zr-1.5Hf-0.15 O by the ultrasonic surface rolling process (USRP). The strengthening mechanisms and microstructural evolution of the GNS were systematically investigated by combining experimental characterization and the crystal plasticity finite element method (CPFEM). A graded structural layer approximately 350 μm thick was formed on the Zr-1.5Hf-0.15 O surface, as revealed by microstructural analysis following USRP treatment. The yield strength of GNS Zr-1.5Hf-0.15 O (GNS-Zr) increased by 16.7% compared to the coarse-grained Zr-1.5Hf-0.15 O (CG-Zr), with a concurrent uniform elongation of ~26.4%. The contribution of grain refinement strengthening, dislocation strengthening and twinning-induced strengthening to the overall strength in GNS-Zr was quantified by using the mixing principle. Notably, the CPFEM results effectively captured the stress-strain behavior of both the GNS and CG structures. Compared to the CG structure, the surface layer of the GNS structure exhibits higher microscopic stress, while its core region demonstrates greater plastic strain. Furthermore, the CPFEM results indicated that multiple deformation modes were activated in the GNS-Zr, which not only coordinates the deformation but also provides higher strain hardening. Finally, the effect of the slip system on texture evolution was explored by combining the in-grain misorientation axis (IGMA) and CPFEM. The results showed that the (0001) basal texture remains stable after tension due to the activation of considerable prismatic slips.
采用超声表面轧制法(USRP)在Zr-1.5Hf-0.15 O表面制备了梯度纳米结构(GNS)。采用实验表征和晶体塑性有限元相结合的方法,系统研究了GNS的强化机理和微观组织演变。经USRP处理后,在Zr-1.5Hf-0.15 O表面形成了约350 μm厚的渐变组织层。GNS Zr-1.5Hf-0.15 O (GNS- zr)的屈服强度比粗晶Zr-1.5Hf-0.15 O (CG-Zr)提高了16.7%,同时均匀伸长率为~26.4%。采用混合原理量化了GNS-Zr中晶粒细化强化、位错强化和孪晶强化对整体强度的贡献。值得注意的是,CPFEM结果有效地捕获了GNS和CG结构的应力-应变行为。与CG结构相比,GNS结构的表层表现出更高的微观应力,而其核心区域表现出更大的塑性应变。此外,CPFEM结果表明,GNS-Zr中激活了多种变形模式,不仅协调了变形,而且提供了更高的应变硬化。最后,结合晶内取向轴(IGMA)和CPFEM,探讨滑移系统对织构演化的影响。结果表明,(0001)基底织构在拉伸后仍保持稳定,这是由于大量棱柱滑移的激活。
{"title":"Mechanical response of gradient nanostructured Zr-1.5Hf-0.15O under tensile deformation: experimental and CPFEM modeling study","authors":"Jinping Wang, Conghui Zhang, Kangkai Song, Shuaiyang Liu, Wenguang Zhu, Ruixuan Tian","doi":"10.1016/j.jallcom.2025.185581","DOIUrl":"https://doi.org/10.1016/j.jallcom.2025.185581","url":null,"abstract":"A gradient nanostructure (GNS) was fabricated on Zr-1.5Hf-0.15<!-- --> <!-- -->O by the ultrasonic surface rolling process (USRP). The strengthening mechanisms and microstructural evolution of the GNS were systematically investigated by combining experimental characterization and the crystal plasticity finite element method (CPFEM). A graded structural layer approximately 350 μm thick was formed on the Zr-1.5Hf-0.15<!-- --> <!-- -->O surface, as revealed by microstructural analysis following USRP treatment. The yield strength of GNS Zr-1.5Hf-0.15<!-- --> <!-- -->O (GNS-Zr) increased by 16.7% compared to the coarse-grained Zr-1.5Hf-0.15<!-- --> <!-- -->O (CG-Zr), with a concurrent uniform elongation of ~26.4%. The contribution of grain refinement strengthening, dislocation strengthening and twinning-induced strengthening to the overall strength in GNS-Zr was quantified by using the mixing principle. Notably, the CPFEM results effectively captured the stress-strain behavior of both the GNS and CG structures. Compared to the CG structure, the surface layer of the GNS structure exhibits higher microscopic stress, while its core region demonstrates greater plastic strain. Furthermore, the CPFEM results indicated that multiple deformation modes were activated in the GNS-Zr, which not only coordinates the deformation but also provides higher strain hardening. Finally, the effect of the slip system on texture evolution was explored by combining the in-grain misorientation axis (IGMA) and CPFEM. The results showed that the (0001) basal texture remains stable after tension due to the activation of considerable prismatic slips.","PeriodicalId":344,"journal":{"name":"Journal of Alloys and Compounds","volume":"14 1","pages":""},"PeriodicalIF":6.2,"publicationDate":"2025-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145732239","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Deformation Mechanism, Crack Behavior and Microstructural Evolution of 2195 Al-Li alloy at High-Temperature 2195 Al-Li合金高温变形机理、裂纹行为及显微组织演变
IF 6.2 2区 材料科学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2025-12-13 DOI: 10.1016/j.jallcom.2025.185548
Lichong Ye, Jin Zhang, Chen Shi, Chunnan Zhu, Dongfeng Shi, Guoqing Wang
{"title":"Deformation Mechanism, Crack Behavior and Microstructural Evolution of 2195 Al-Li alloy at High-Temperature","authors":"Lichong Ye, Jin Zhang, Chen Shi, Chunnan Zhu, Dongfeng Shi, Guoqing Wang","doi":"10.1016/j.jallcom.2025.185548","DOIUrl":"https://doi.org/10.1016/j.jallcom.2025.185548","url":null,"abstract":"","PeriodicalId":344,"journal":{"name":"Journal of Alloys and Compounds","volume":"59 1","pages":""},"PeriodicalIF":6.2,"publicationDate":"2025-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145730790","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Intermetallic phase formation in non-equiatomic high-entropy alloy FeMnNiAlCrSiC and FeMnNiAlTiSiC nanoparticles synthesized using laser ablation and processing: The synergistic role of Silicon, Chromium, and Titanium 非等原子高熵合金FeMnNiAlCrSiC和FeMnNiAlTiSiC纳米颗粒的金属间相形成:硅、铬和钛的协同作用
IF 6.2 2区 材料科学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2025-12-13 DOI: 10.1016/j.jallcom.2025.185580
Bibek Kumar Singh, Yagnesh Shadangi, Harsh Jain, R. Sai Prasad Goud, N.K. Mukhopadhyay, A.P. Pathak, Venugopal Rao Soma, Somendra Nath Chakraborty, Archana Tiwari, A. Tripathi
This study reports synthesis and phase evolution of non-equiatomic high-entropy alloy (HEA) nanoparticles (NPs) using a two-step process. NPs were first syntheized via pulsed laser ablation using a picosecond laser, from two different compositions, FeMnNiAlCrSiC (HEA-Cr) and FeMnNiAlTiSiC (HEA-Ti), followed by laser-processing using a nanosecond laser. The investigation focused on phase evolution, elemental distribution, and structural transformations. Detailed analysis revealed that Si plays a crucial role in driving the intermetallic phase formation. HEA-Cr NPs exhibited a non-uniform elemental distribution, with Al being prominent towards the edges, and strong Fe-Ni and Fe-Si mixing was observed. Structural analysis confirmed the presence of BCC, B2, Fe<span><span style=""></span><span style="font-size: 90%; display: inline-block;" tabindex="0"><svg focusable="false" height="1.509ex" role="img" style="vertical-align: -0.582ex;" viewbox="0 -399.4 453.9 649.8" width="1.054ex" xmlns:xlink="http://www.w3.org/1999/xlink"><g fill="currentColor" stroke="currentColor" stroke-width="0" transform="matrix(1 0 0 -1 0 0)"><g is="true"><g is="true"></g><g is="true" transform="translate(0,-150)"><g is="true"><use transform="scale(0.707)" xlink:href="#MJMAIN-35"></use></g></g></g></g></svg></span><script type="math/mml"><math><msub is="true"><mrow is="true"></mrow><mrow is="true"><mn is="true">5</mn></mrow></msub></math></script></span>Si<span><span style=""></span><span style="font-size: 90%; display: inline-block;" tabindex="0"><svg focusable="false" height="1.509ex" role="img" style="vertical-align: -0.582ex;" viewbox="0 -399.4 453.9 649.8" width="1.054ex" xmlns:xlink="http://www.w3.org/1999/xlink"><g fill="currentColor" stroke="currentColor" stroke-width="0" transform="matrix(1 0 0 -1 0 0)"><g is="true"><g is="true"></g><g is="true" transform="translate(0,-150)"><g is="true"><use transform="scale(0.707)" xlink:href="#MJMAIN-33"></use></g></g></g></g></svg></span><script type="math/mml"><math><msub is="true"><mrow is="true"></mrow><mrow is="true"><mn is="true">3</mn></mrow></msub></math></script></span>, Cr<span><span style=""></span><span style="font-size: 90%; display: inline-block;" tabindex="0"><svg focusable="false" height="1.509ex" role="img" style="vertical-align: -0.582ex;" viewbox="0 -399.4 453.9 649.8" width="1.054ex" xmlns:xlink="http://www.w3.org/1999/xlink"><g fill="currentColor" stroke="currentColor" stroke-width="0" transform="matrix(1 0 0 -1 0 0)"><g is="true"><g is="true"></g><g is="true" transform="translate(0,-150)"><g is="true"><use transform="scale(0.707)" xlink:href="#MJMAIN-35"></use></g></g></g></g></svg></span><script type="math/mml"><math><msub is="true"><mrow is="true"></mrow><mrow is="true"><mn is="true">5</mn></mrow></msub></math></script></span>Si<span><span style=""></span><span style="font-size: 90%; display: inline-block;" tabindex="0"><svg focusable="false" height="1.509ex" role="img" style="vertical-align: -0.582ex;" view
本研究报道了非等原子高熵合金(HEA)纳米颗粒(NPs)的两步法合成和相演化。首先用皮秒激光脉冲烧蚀法合成了两种不同成分的纳米粒子,分别是FeMnNiAlCrSiC (HEA-Cr)和FeMnNiAlTiSiC (HEA-Ti),然后用纳秒激光进行激光加工。研究的重点是相演化、元素分布和结构转变。详细分析表明,Si在驱动金属间相形成中起着至关重要的作用。HEA-Cr NPs的元素分布不均匀,Al向边缘突出,Fe-Ni和Fe-Si混合强烈。结构分析证实了BCC、B2、Fe5Si3、Cr5Si3和γ-黄铜型相的存在,后处理增强了Fe5Si3和Cr5Si3的形成。在HEA-Ti体系中,用Ti代替Cr改善了元素分布的均匀性,这是由于Ti与其他组成元素具有较高的互溶性。Ti对Si的强亲和力导致Ti5Si3型相的形成。后处理后,随着ti5si3型相的形成,元素分布的均匀性进一步增强。在HEA- cr和HEA- ti体系中,后处理后的HEA NPs(固溶体和金属间相的混合物)转变为金属间HEA NPs。热力学计算证实,后处理有利于金属间HEA NPs的形成,这归因于激光诱导退火效应。这项工作强调了Si与Cr和Ti在定制相组成中的协同作用,并为HEA NPs中用于先进材料设计的激光驱动相工程提供了见解。
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引用次数: 0
Improved Compositional Homogeneity by Zone Melting Combined with Controlled Annealing: A Route to Enhanced Magnetocaloric Performance in All-d-Metal Ni-Co-Mn-Ti Heusler Alloys 区域熔化结合控制退火改善成分均匀性:提高全金属Ni-Co-Mn-Ti Heusler合金磁热性能的途径
IF 6.2 2区 材料科学 Q2 CHEMISTRY, PHYSICAL Pub Date : 2025-12-13 DOI: 10.1016/j.jallcom.2025.185588
Jie Shao, Zhixing Ye, Huan Chen, Qiuping Chen, Kongyang Yu, Jun Shen, Zhaojun Mo
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引用次数: 0
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Journal of Alloys and Compounds
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