Pub Date : 2026-03-06eCollection Date: 2026-03-01DOI: 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.
{"title":"Computational design of a 3D magnetic particle imaging (MPI) prototype.","authors":"Shahriar Mostufa, Bahareh Rezaei, Kai Wu","doi":"10.1063/9.0000971","DOIUrl":"10.1063/9.0000971","url":null,"abstract":"<p><p>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 mm<sup>3</sup> 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.</p>","PeriodicalId":7619,"journal":{"name":"AIP Advances","volume":"16 3","pages":"035003"},"PeriodicalIF":1.4,"publicationDate":"2026-03-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12967246/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147375818","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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.
{"title":"Conductive elastomer-integrated triboelectric nanogenerator for self-powered motion sensing and injury warning","authors":"Keren Pang, Jingying Lin, Xiaoqian Wang","doi":"10.1063/5.0315439","DOIUrl":"https://doi.org/10.1063/5.0315439","url":null,"abstract":"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.","PeriodicalId":7619,"journal":{"name":"AIP Advances","volume":"16 2","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147381481","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-28eCollection Date: 2026-01-01DOI: 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.
{"title":"Coaxial capacitor (COCA) coil for stretchable arrays in ultrahigh-field MRI.","authors":"Ming Lu, Pingping Li, Jason E Moore, Xiaoyu Jiang, John C Gore, Xinqiang Yan","doi":"10.1063/5.0304790","DOIUrl":"10.1063/5.0304790","url":null,"abstract":"<p><p>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.</p>","PeriodicalId":7619,"journal":{"name":"AIP Advances","volume":"16 1","pages":"015129"},"PeriodicalIF":1.4,"publicationDate":"2026-01-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12854774/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146103543","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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。
{"title":"One-step redox precipitation engineering Pt–Mn solid solutions in hollow MnO2 for ultralow-temperature CH4 oxidation","authors":"Fang Xiang-hong, Ruikun Zhang, Zeng Xiaoyi","doi":"10.1063/5.0309944","DOIUrl":"https://doi.org/10.1063/5.0309944","url":null,"abstract":"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.","PeriodicalId":7619,"journal":{"name":"AIP Advances","volume":"15 12","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147333039","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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.
{"title":"Testing of silica-chitosan decorated NiFe2O4 magnetic nano-adsorbents for adsorption of Pb(II), Zn(II), and Cd(II) ions from aqueous solution","authors":"Tareq Kareri, Syed Murad Ali Shah, Shazia Shukrullah, Muhammad Irfan, Mohammed Jalalah, Muawia Abdelkafi Magzoub Mohamed Ali","doi":"10.1063/5.0291245","DOIUrl":"https://doi.org/10.1063/5.0291245","url":null,"abstract":"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.","PeriodicalId":7619,"journal":{"name":"AIP Advances","volume":"15 10","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147331815","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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.
{"title":"Structure and mechanical properties of high-entropy carbide (Ti0.2Zr0.2Nb0.2Ta0.2Cr0.2)C: Effect of sintering method","authors":"Wenjie Guo, Jin You, Yanrong Li, Yilong Pan, Tian Cui","doi":"10.1063/5.0283206","DOIUrl":"https://doi.org/10.1063/5.0283206","url":null,"abstract":"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.","PeriodicalId":7619,"journal":{"name":"AIP Advances","volume":"15 9","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.aip.org/aip/adv/article-pdf/doi/10.1063/5.0283206/20678780/095003_1_5.0283206.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147331376","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-08-11eCollection Date: 2025-08-01DOI: 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.
{"title":"Shape transitions of red blood cell under oscillatory flows in microchannels.","authors":"Lahcen Akerkouch, Trung Bao Le","doi":"10.1063/5.0278720","DOIUrl":"10.1063/5.0278720","url":null,"abstract":"<p><p>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.</p>","PeriodicalId":7619,"journal":{"name":"AIP Advances","volume":"15 8","pages":"085010"},"PeriodicalIF":1.4,"publicationDate":"2025-08-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12342962/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144844016","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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。
{"title":"Synthesis of silicon nanowire anode materials from forsterite by molten salt electrolysis","authors":"Shuanlao Dong, Zefang Li, Jie Gao, Yi Sun, Yun Gao, Yanan Zhou, Zhanbin Qin, Ran Tian","doi":"10.1063/5.0256216","DOIUrl":"https://doi.org/10.1063/5.0256216","url":null,"abstract":"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.","PeriodicalId":7619,"journal":{"name":"AIP Advances","volume":"15 7","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147332415","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-06-06eCollection Date: 2025-06-01DOI: 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.
{"title":"Using high speed visualization to identify variations in the formation and distribution of plasmonic microbubbles.","authors":"Mohammad Amer Allaf, Koji Okamoto, Takuto Owa","doi":"10.1063/5.0272623","DOIUrl":"10.1063/5.0272623","url":null,"abstract":"<p><p>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 <i>μ</i>m) within 50 <i>μ</i>s. 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.</p>","PeriodicalId":7619,"journal":{"name":"AIP Advances","volume":"15 6","pages":"065109"},"PeriodicalIF":1.4,"publicationDate":"2025-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12145202/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144245789","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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.
{"title":"Au@Pd nanorods with a suitable shell thickness of titanium dioxide can improve its catalytic performances","authors":"Yu‐Chun Cheng, Tian‐Song Deng","doi":"10.1063/5.0270975","DOIUrl":"https://doi.org/10.1063/5.0270975","url":null,"abstract":"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.","PeriodicalId":7619,"journal":{"name":"AIP Advances","volume":"15 6","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147333482","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}