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Computational design of a 3D magnetic particle imaging (MPI) prototype. 三维磁粒子成像(MPI)样机的计算设计。
IF 1.4 4区 物理与天体物理 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-03-06 eCollection Date: 2026-03-01 DOI: 10.1063/9.0000971
Shahriar Mostufa, Bahareh Rezaei, Kai Wu

Magnetic particle imaging (MPI) is an emerging imaging modality that exploits the magnetization response of magnetic nanoparticle tracers. While MPI offers substantially higher resolution compared to magnetic resonance imaging, its translation to human-scale applications remains limited. These challenges stem from the requirement of high-intensity electric currents to generate strong magnetic fields, as well as reduced field uniformity with increasing coil spacing. To overcome these barriers, comprehensive simulation studies are essential for guiding MPI prototype design and performance optimization. In this work, we present a finite element method (FEM)-based design of a three-dimensional (3D) MPI prototype. The system integrates electromagnetic coils for the selection, drive, and focus fields, along with a gradiometer configuration for signal reception. Each coil's geometry and magnetic field were first simulated independently to validate its ability to generate the desired magnetic field and subsequently combined into a full-system design with time-domain input excitation signals. This framework achieved 3D field-free point (FFP) scanning within a 20 mm3 field of view. The selection field provided a gradient of 4, 2, and 2 T/m in z axis, y axis, and x axis, respectively, the drive field produced 20 mT, and the focus fields generated 40 mT (z-axis) and 20 mT (y-axis), enabling controlled spatial movement of the FFP. Overall, this study establishes a complete 3D FEM simulation framework for MPI system design and lays the foundation for future optimization toward clinical-scale applications.

磁颗粒成像(MPI)是一种新兴的成像方式,利用磁性纳米颗粒示踪剂的磁化响应。虽然与磁共振成像相比,MPI提供了更高的分辨率,但其在人类尺度上的应用仍然有限。这些挑战源于对高强度电流产生强磁场的要求,以及随着线圈间距的增加而降低的场均匀性。为了克服这些障碍,全面的仿真研究对于指导MPI原型设计和性能优化至关重要。在这项工作中,我们提出了一种基于有限元法(FEM)的三维(3D) MPI原型设计。该系统集成了用于选择、驱动和聚焦场的电磁线圈,以及用于信号接收的梯度计配置。首先对每个线圈的几何形状和磁场进行独立模拟,以验证其产生所需磁场的能力,然后将其与时域输入激励信号组合成一个完整的系统设计。该框架在20mm3的视场范围内实现了3D无场点(FFP)扫描。选择场在z轴、y轴和x轴上分别提供4、2和2 T/m的梯度,驱动场产生20 mT,聚焦场产生40 mT (z轴)和20 mT (y轴),实现FFP的可控空间运动。总体而言,本研究为MPI系统设计建立了完整的三维有限元模拟框架,为未来面向临床规模应用的优化奠定了基础。
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引用次数: 0
Conductive elastomer-integrated triboelectric nanogenerator for self-powered motion sensing and injury warning 用于自供电运动传感和损伤预警的导电弹性体集成摩擦电纳米发电机
4区 物理与天体物理 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-02-01 DOI: 10.1063/5.0315439
Keren Pang, Jingying Lin, Xiaoqian Wang
Wearable motion-sensing systems are increasingly used in health assessment and sports protection, creating a demand for deformable materials that can operate without external power supplies. Here, we construct a triboelectric device based on a poly(tetramethylene ether glycol)/4,4′-dicyclohexylmethane diisocyanate elastomer (PH elastomer), in which dynamic cross-linking and ionic transport pathways endow the material with high stretchability, reliable conductivity, and structural stability. These features enable the PH film to serve directly as the ionic electrode of a self-powered triboelectric nanogenerator (TENG). Under periodic contact–separation operation, the PH-TENG delivers an open-circuit voltage (VOC) of 353.2 V, a short-circuit current (ISC) of 33.6 μA, and a maximum transferred charge (QSC) of 84.2 nC, corresponding to a maximum output power of 1.95 mW. Owing to the material’s mechanical responsiveness, the device generates distinct electrical signatures under variations in bending angle, applied pressure, and motion amplitude. These sensing responses make it possible to distinguish different types of human movements, such as walking, running, and various hand or finger actions, while also enabling the device to recognize deviations from normal motion that may signal emerging injuries. The results underscore the capability of the PH-TENG as a robust platform for self-powered motion monitoring and sports-related injury warning.
可穿戴式运动传感系统越来越多地用于健康评估和运动保护,这就产生了对可变形材料的需求,这种材料可以在没有外部电源的情况下工作。在这里,我们构建了一个基于聚(四亚甲基醚乙二醇)/4,4 ' -双环己基甲烷二异氰酸酯弹性体(PH弹性体)的摩擦电装置,其中动态交联和离子传输途径赋予材料高拉伸性,可靠的导电性和结构稳定性。这些特性使PH膜可以直接用作自供电摩擦电纳米发电机(TENG)的离子电极。在周期性触点分离工作下,PH-TENG的开路电压(VOC)为353.2 V,短路电流(ISC)为33.6 μA,最大转移电荷(QSC)为84.2 nC,最大输出功率为1.95 mW。由于材料的机械响应性,该装置在弯曲角度、施加压力和运动幅度的变化下产生不同的电信号。这些感应反应使得区分不同类型的人类运动成为可能,例如走路、跑步和各种手或手指的动作,同时也使设备能够识别可能出现损伤的正常运动偏差。结果强调了PH-TENG作为自供电运动监测和运动相关损伤预警的强大平台的能力。
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引用次数: 0
Coaxial capacitor (COCA) coil for stretchable arrays in ultrahigh-field MRI. 用于超高场MRI可拉伸阵列的同轴电容器(COCA)线圈。
IF 1.4 4区 物理与天体物理 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2026-01-28 eCollection Date: 2026-01-01 DOI: 10.1063/5.0304790
Ming Lu, Pingping Li, Jason E Moore, Xiaoyu Jiang, John C Gore, Xinqiang Yan

Stretchable RF coils offer the potential to improve MRI performance by conforming closely to patient anatomy, regardless of patient size, thereby enhancing both signal-to-noise ratio (SNR) and patient comfort. In this work, we investigate a stretchable receive array design based on the coaxial capacitor (COCA) coil for 7 T MRI, constructed primarily from ultra-flexible Litz wire stitched onto elastic fabric substrates. The COCA coil eliminates the need for lumped capacitors and maintains stable decoupling performance under transverse stretching, provided that the overlapped area and the coil area change proportionally as the coil is stretched. Bench tests and phantom imaging experiments demonstrate that elliptical COCA coils (in the non-stretched state) maintain consistent decoupling characteristics across stretch ratios up to ×1.3 and outperform fixed arrays in SNR across varying phantom sizes. The proposed design shows strong potential for integration into wearable coil arrays, enabling improved imaging quality and adaptability for diverse patient anatomies.

可拉伸射频线圈通过密切符合患者解剖结构,从而提高MRI性能的潜力,无论患者大小如何,从而提高信噪比(SNR)和患者舒适度。在这项工作中,我们研究了一种基于同轴电容器(COCA)线圈的可拉伸接收阵列设计,该阵列主要由缝在弹性织物基板上的超柔性Litz线构成。COCA线圈消除了对集总电容器的需求,并在横向拉伸下保持稳定的去耦性能,前提是重叠面积和线圈面积随线圈拉伸成比例变化。台式测试和模体成像实验表明,椭圆COCA线圈(在非拉伸状态下)在拉伸比高达×1.3的范围内保持一致的去耦特性,并且在不同模体尺寸下的信噪比优于固定阵列。所提出的设计显示了集成到可穿戴线圈阵列的强大潜力,从而提高了成像质量和对不同患者解剖结构的适应性。
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引用次数: 0
One-step redox precipitation engineering Pt–Mn solid solutions in hollow MnO2 for ultralow-temperature CH4 oxidation 一步氧化还原沉淀工程Pt-Mn固溶体在空心二氧化锰中进行超低温CH4氧化
4区 物理与天体物理 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2025-12-01 DOI: 10.1063/5.0309944
Fang Xiang-hong, Ruikun Zhang, Zeng Xiaoyi
A HRP (hydrolysis-driven redox precipitation) strategy is developed to synthesize Pt-MnOx hollow-sphere/nanorod composites with tunable Mn/Pt ratios (2–13), enabling one-step construction of Pt–Mn solid solutions while circumventing phase separation in conventional co-precipitation. The optimized HRP-4Mn1Pt catalyst (Mn/Pt = 5) delivers an ultrahigh specific surface area (276.2 m2/g) and exceptional low-temperature methane oxidation activity (T50 = 325 °C, T90 = 334 °C at 30 000 ml g−1 h−1), representing a 15%–20% improvement in catalytic efficiency over conventional Pt/MnO2 catalysts [Li et al., Colloids Surf. A 665, 131248 (2023) and Liang et al., Mol. Catal. 547, 113380 (2023)], maintaining stability for 48 h. Our investigation into the reaction mechanism shows that adding Pt2+ distorts the MnO2 crystal structure. This distortion creates more gaps for oxygen (oxygen vacancies) and makes the catalyst easier to reduce, as shown by a peak at 228 °C in our H2-TPR measurements. This enhanced ability to transport oxygen is key to the catalyst’s high performance.
开发了HRP(水解驱动氧化还原沉淀)策略来合成具有可调Mn/Pt比(2-13)的Pt- mnox空心球/纳米棒复合材料,实现了Pt-Mn固溶体的一步构建,同时避免了传统共沉淀法中的相分离。优化后的HRP-4Mn1Pt催化剂(Mn/Pt = 5)具有超高的比表面积(276.2 m2/g)和优异的低温甲烷氧化活性(T50 = 325°C, T90 = 334°C, 30 000 ml g - 1 h - 1),比传统Pt/MnO2催化剂的催化效率提高了15%-20% [Li等人,Colloids Surf]。A 665, 131248(2023)和Liang et al., Mol. catalal . 547, 113380(2023)],维持了48小时的稳定性。我们对反应机理的研究表明,加入Pt2+会扭曲MnO2的晶体结构。这种变形为氧气创造了更多的空隙(氧空位),使催化剂更容易减少,正如我们在H2-TPR测量中在228°C时的峰值所示。这种增强的运输氧的能力是催化剂高性能的关键。
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引用次数: 0
Testing of silica-chitosan decorated NiFe2O4 magnetic nano-adsorbents for adsorption of Pb(II), Zn(II), and Cd(II) ions from aqueous solution 二氧化硅-壳聚糖修饰NiFe2O4磁性纳米吸附剂对水溶液中Pb(II)、Zn(II)和Cd(II)离子的吸附性能研究
4区 物理与天体物理 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2025-10-01 DOI: 10.1063/5.0291245
Tareq Kareri, Syed Murad Ali Shah, Shazia Shukrullah, Muhammad Irfan, Mohammed Jalalah, Muawia Abdelkafi Magzoub Mohamed Ali
Water contamination with toxic heavy metals such as Pb(II), Zn(II), and Cd(II) poses a serious environmental and health challenge. This study aims to develop efficient and reusable nanoadsorbents for wastewater treatment. Chitosan-functionalized NiFe2O4@SiO2 (NiFe2O4@SiO2-chitosan) core–shell nanospheres were synthesized using a co-precipitation method to produce NiFe2O4 nanoparticles, followed by silica coating and surface modification with chitosan. The functionalized nanocomposites demonstrated high adsorption capacities of 258.39 mg/g for Pb(II), 246.91 mg/g for Zn(II), and 224.21 mg/g for Cd(II). The adsorption behavior aligned with the Langmuir isotherm model, indicating monolayer coverage, while the kinetics followed a pseudo-second-order model, confirming chemisorption via coordination with the amino groups. The nanospheres also exhibited superparamagnetic behavior with a magnetization (Ms) of 12.41 emu/g, enabling rapid magnetic separation, and retained a removal efficiency of 77%–81% after five regeneration cycles. Overall, NiFe2O4@SiO2-chitosan nanocomposites demonstrate strong potential as sustainable, reusable, and magnetically separable adsorbents for the effective removal of heavy metals from wastewater.
含铅(II)、锌(II)和镉(II)等有毒重金属的水污染构成了严重的环境和健康挑战。本研究旨在开发高效、可重复使用的纳米吸附剂用于废水处理。采用共沉淀法合成了壳聚糖功能化的NiFe2O4@SiO2 (NiFe2O4@SiO2-chitosan)核壳纳米球,制备了NiFe2O4纳米粒子,然后进行二氧化硅包覆和壳聚糖表面改性。功能化纳米复合材料对Pb(II)、Zn(II)和Cd(II)的吸附量分别为258.39 mg/g、246.91 mg/g和224.21 mg/g。吸附行为符合Langmuir等温线模型,表明单层覆盖,而动力学遵循伪二阶模型,证实通过与氨基配位进行化学吸附。纳米微球还表现出超顺磁性,磁化强度(Ms)为12.41 emu/g,实现了快速磁分离,并在5次再生循环后保持了77%-81%的去除率。总体而言,NiFe2O4@SiO2-chitosan纳米复合材料作为可持续、可重复使用和可磁分离的吸附剂,在有效去除废水中的重金属方面表现出强大的潜力。
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引用次数: 0
Structure and mechanical properties of high-entropy carbide (Ti0.2Zr0.2Nb0.2Ta0.2Cr0.2)C: Effect of sintering method 高熵碳化物(Ti0.2Zr0.2Nb0.2Ta0.2Cr0.2)C的组织与力学性能:烧结方法的影响
4区 物理与天体物理 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2025-09-01 DOI: 10.1063/5.0283206
Wenjie Guo, Jin You, Yanrong Li, Yilong Pan, Tian Cui
High-entropy carbide ceramics (HECCs) have attracted increasing attention for extreme-environmental applications due to their unique multi-elemental compositions and outstanding mechanical properties. While most existing studies focus on IVB and VB transition metals synthesized via spark plasma sintering (SPS), group VIB elements, such as Cr, have been comparatively less studied. In this study, a Cr-containing HECC, (Ti0.2Zr0.2Nb0.2Ta0.2Cr0.2)C, was synthesized via both high temperature and high pressure (HTHP) sintering and SPS. Comparative analysis revealed that HTHP processing at 5 GPa and 1600 °C produced ultrafine grains (∼0.41 μm), moderate density (94.2%), and enhanced fracture toughness (5.05 ± 0.37 MPa m1/2). In contrast, SPS at 1800 °C yielded near-theoretical density (99.4%) and higher nanohardness (34.15 ± 0.51 GPa) but resulted in significant grain coarsening (∼6.24 μm) and reduced fracture toughness (∼3.5 MPa m1/2). These findings highlight the distinct structure–property relationships governed by the sintering route and provide insights into tailoring HECC performance for demanding service conditions.
高熵碳化物陶瓷(HECCs)由于其独特的多元素组成和优异的力学性能,在极端环境应用中受到越来越多的关注。现有的研究大多集中在火花等离子烧结(SPS)合成的IVB和VB过渡金属上,而对VIB族元素如Cr的研究相对较少。本研究通过高温高压(HTHP)烧结和SPS合成了一种含cr的HECC (Ti0.2Zr0.2Nb0.2Ta0.2Cr0.2)C。对比分析表明,在5 GPa和1600°C高温高温下处理后的合金可获得超细晶粒(~ 0.41 μm)、中等密度(94.2%)和增强的断裂韧性(5.05±0.37 MPa m1/2)。相比之下,在1800°C时,SPS产生了接近理论的密度(99.4%)和更高的纳米硬度(34.15±0.51 GPa),但导致明显的晶粒粗化(~ 6.24 μm)和断裂韧性降低(~ 3.5 MPa m1/2)。这些发现强调了由烧结路线决定的独特结构-性能关系,并为根据苛刻的使用条件定制HECC性能提供了见解。
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引用次数: 0
Shape transitions of red blood cell under oscillatory flows in microchannels. 微通道内振荡流动下红细胞的形状转变。
IF 1.4 4区 物理与天体物理 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2025-08-11 eCollection Date: 2025-08-01 DOI: 10.1063/5.0278720
Lahcen Akerkouch, Trung Bao Le

This paper aims to examine the ability to control a model of red blood cell (RBC) dynamics and the associated extracellular flow patterns in microfluidic channels via oscillatory flows. Our computational approach employs a hybrid continuum-particle coupling, in which the cell membrane and cytosol fluid are modeled using the dissipative particle dynamics method. The blood plasma is modeled as an incompressible fluid via the immersed boundary method. This coupling is novel because it provides an accurate description of RBC dynamics while the extracellular flow patterns around the RBCs are also captured in detail. Our coupling methodology is validated with available experimental and computational data in the literature and shows excellent agreement. We explore the controlling regimes by varying the shape of the oscillatory flow waveform at the channel inlet. Our simulation results show that a host of RBC morphological dynamics emerges depending on the channel geometry, the incoming flow waveform, and the RBC initial location. Complex dynamics of RBC are induced by the flow waveform. Our results show that the RBC shape is strongly dependent on its initial location. Our results suggest that the controlling of oscillatory flows can be used to induce specific morphological shapes of RBCs and the surrounding fluid patterns in bio-engineering applications.

本文旨在研究通过振荡流动控制微流体通道中红细胞(RBC)动力学模型和相关细胞外流动模式的能力。我们的计算方法采用混合连续-粒子耦合,其中细胞膜和细胞质流体使用耗散粒子动力学方法建模。采用浸入边界法将血浆建模为不可压缩流体。这种耦合是新颖的,因为它提供了红细胞动力学的准确描述,同时红细胞周围的细胞外流动模式也被详细捕获。我们的耦合方法通过文献中可用的实验和计算数据进行了验证,并显示出极好的一致性。我们通过改变通道入口的振荡流波形的形状来探索控制机制。我们的模拟结果表明,根据通道的几何形状、流入的流波形和RBC的初始位置,大量的RBC形态动态会出现。血流波形引起红细胞的复杂动力学。我们的结果表明,红细胞形状强烈依赖于其初始位置。我们的研究结果表明,在生物工程应用中,振荡流动的控制可以用来诱导红细胞的特定形态和周围的流体模式。
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引用次数: 0
Synthesis of silicon nanowire anode materials from forsterite by molten salt electrolysis 熔盐电解法合成硅纳米线负极材料
4区 物理与天体物理 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2025-07-01 DOI: 10.1063/5.0256216
Shuanlao Dong, Zefang Li, Jie Gao, Yi Sun, Yun Gao, Yanan Zhou, Zhanbin Qin, Ran Tian
Silicon nanowires, which can be used as anodes in lithium-ion batteries, were synthesized from forsterite. SiO2 obtained from acid leaching of forsterite was electrolyzed in CaCl2 molten salt, in which silicon nanowire materials were generated. A surfactant (PEG-2000) was added to obtain uniform morphology features during the preparation of silica from etching forsterite. The molten salt electrolysis process was explored, and applicable conditions were proposed. Compared to the silicon produced from commercial silica, the silicon anode materials synthesized from forsterite showed a higher initial discharge specific capacity up to 2271 mAh g−1 at a discharge current density of 100 mA g−1, indicating satisfactory electrochemical performance. This method provides a new strategy for high value-added utilization of forsterite and low-cost preparation of anode materials for lithium-ion batteries.
硅纳米线可以作为锂离子电池的阳极,是由橄榄石合成的。用CaCl2熔盐对酸浸得到的SiO2进行电解,得到硅纳米线材料。在蚀刻橄榄石制备二氧化硅的过程中,加入表面活性剂PEG-2000以获得均匀的形貌特征。对熔盐电解工艺进行了探索,并提出了适用条件。在放电电流密度为100 mA g−1的情况下,由硅辉石合成的硅负极材料的初始放电比容量高达2271 mAh g−1,电化学性能令人满意。该方法为锂离子电池正极材料的高附加值利用和低成本制备提供了新策略。
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引用次数: 0
Using high speed visualization to identify variations in the formation and distribution of plasmonic microbubbles. 利用高速可视化技术识别等离子体微泡形成和分布的变化。
IF 1.4 4区 物理与天体物理 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2025-06-06 eCollection Date: 2025-06-01 DOI: 10.1063/5.0272623
Mohammad Amer Allaf, Koji Okamoto, Takuto Owa

Plasmonic heating of gold nanoparticles (GNPs) using pulsed lasers (PLs) enables microbubble generation for imaging, diagnostics, and microfluidics. However, aggregation and photomodification cause inconsistencies (variations) in microbubble formation and distribution, particularly in pool-like environments where GNPs undergo aggregation and photomodification. This study experimentally investigates microbubble generation by heating GNPs (532 nm, nanoseconds PL) of various sizes and concentrations, using high-speed imaging (20 kfps). Results show unpredictable variations in bubble formation area (BFA), even under similar energy absorption. Large individual microbubbles were observed at relatively low energy absorption, primarily due to aggregation. Boiling on the transparent surface occurred in multiple tests, a phenomenon linked to optical pulling forces that deposited GNPs on the surface. This produced well-defined semi-circular bubbles (∼600 μm) within 50 μs. MB formation was more concentrated near the backward facing surface than along the laser beam, highlighting the role of optical pulling. Dissolved gas release influenced microbubble growth, particularly in samples prone to aggregation. In addition, prior laser pulses impacted BFA through photomodification and aggregation, sometimes reducing BFA despite higher energy absorption. This study provides new insights into the factors influencing microbubble formation and distribution in the plasmonic heating of GNPs. Understanding these mechanisms can help improve the reliability and efficiency of photothermal applications, enabling better control over plasmonic bubble generation for various scientific and technological advancements.

等离子体加热金纳米粒子(GNPs)使用脉冲激光(PLs)使微泡成像,诊断和微流体的产生。然而,聚集和光电化导致微泡形成和分布的不一致(变化),特别是在GNPs经历聚集和光电化的池状环境中。本研究利用高速成像技术(20 kfps),对不同尺寸和浓度的GNPs (532 nm,纳秒PL)加热后产生的微泡进行了实验研究。结果表明,即使在相同的能量吸收下,气泡形成面积(BFA)的变化也不可预测。在相对较低的能量吸收下观察到大的单个微泡,主要是由于聚集。在多次测试中,透明表面出现了沸腾现象,这种现象与光学拉力在表面沉积GNPs有关。这在50 μs内产生了定义明确的半圆形气泡(~ 600 μm)。MB的形成更集中在靠近后表面的地方,而不是沿着激光束的方向,这突出了光牵引的作用。溶解气体的释放影响微泡的生长,特别是在易于聚集的样品中。此外,先前的激光脉冲通过光电化和聚集影响BFA,有时会降低BFA,尽管能量吸收较高。本研究为GNPs等离子体加热中影响微泡形成和分布的因素提供了新的认识。了解这些机制有助于提高光热应用的可靠性和效率,从而更好地控制等离子体气泡的产生,促进各种科技进步。
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引用次数: 0
Au@Pd nanorods with a suitable shell thickness of titanium dioxide can improve its catalytic performances Au@Pd纳米棒中适当的二氧化钛壳厚可以提高其催化性能
4区 物理与天体物理 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2025-06-01 DOI: 10.1063/5.0270975
Yu‐Chun Cheng, Tian‐Song Deng
The localized surface plasmon resonances (LSPRs) in plasmonic nanoparticles have been used in accelerating photocatalytic reactions under light illumination. To improve the catalytic performances, bimetallic nanoparticles composed of a plasmonic core and a catalytic shell, where LSPR-excited hot electrons and the intrinsic catalytically active sites work synergistically, have attracted much attention. Bimetallic nanostructures are a promising material for the fabrication of a novel type of photo-enhanced nanoreactor. This work presents a photoreactor based on gold–palladium (Au@Pd) nanorods with an optimized photothermal conversion and localized surface plasmon effect. Au@Pd nanorods were fabricated via a seed-mediated growth method using the surfactant hexadecylpyridiniumbromide monohydrate, making the Au@Pd surface rough, which can provide more active sites than smooth surfaces. The photothermal conversion of Au@Pd nanorods was improved with a titanium dioxide shell. Through the titanium dioxide shell, under the same light irradiation, its efficiency in catalyzing methylene blue is at most five times that of gold nanorods and at most two times that of Au@Pd nanorods.
等离子体纳米粒子中的局部表面等离子体共振(LSPRs)已被用于加速光催化反应。为了提高催化性能,由等离子体核和催化壳层组成的双金属纳米颗粒备受关注,其中lspr激发的热电子与内在催化活性位点协同作用。双金属纳米结构是一种很有前途的新型光增强纳米反应器材料。本文提出了一种基于金钯纳米棒(Au@Pd)的光反应器,具有优化的光热转换和局部表面等离子体效应。利用表面活性剂十六烷基吡啶溴一水合物通过种子介导生长法制备Au@Pd纳米棒,使Au@Pd表面粗糙,比光滑表面提供更多的活性位点。利用二氧化钛壳提高了Au@Pd纳米棒的光热转化率。通过二氧化钛外壳,在同样的光照射下,其催化亚甲蓝的效率最多是金纳米棒的5倍,Au@Pd纳米棒的2倍。
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引用次数: 1
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