Pub Date : 2024-05-21DOI: 10.3390/magnetochemistry10060038
D. Starichenko, V. Vorobeva, M. Gruzdev, U. Chervonova, Nataliya G. Bichan, Aleksander V. Korolev, Ivan V. Yatsyk
The branched complexes of Schiff bases with various iron(III) salts, named G2-[L2Fe]+A− (A− is NO3−, Cl−, PF6−), were synthesized using the condensation reaction between carbazole derivatives of salicylic aldehyde and N’-ethylethylenediamine and characterized by various spectroscopic methods (GPC, IR, 1H NMR, UV/Vis). The studies revealed that the coordination of the two ligand molecules to metal occurs through the nitrogen ions and oxygen atom of azomethine to form a homoleptic system. All the synthesized coordination compounds were examined for their thermal, optical, and magnetic features. Static magnetic measurements showed that only G2-[L2Fe]Cl was in a single-phase HS state, whereas the Fe(III) ions of G2-[L2Fe]NO3 and G2-[L2Fe]PF6 at room temperatures were in mixed low-spin (LS, S = 1/2) and high-spin (HS, S = 5/2) states: 58.9% LS/41.1% HS for G2-[L2Fe]NO3, 56.1% LS and 43.9% HS for G2-[L2Fe]PF6. All G2-[L2Fe]+A− complexes demonstrate antiferromagnetic exchange interactions between neighboring Fe(III) ions. The ground spin state at 2.0 K revealed a Brillouin contribution from non-interacting LS ions and a proportion of the HS Fe(III) ions not participating in AFM interactions: 57%, 18%, and 16% for G2-[L2Fe]Cl, G2-[L2Fe]NO3 and G2-[L2Fe]PF6, respectively. EPR measurements confirmed the presence of magnetically active HS and LS states of Fe(III) ions and made it possible to distinguish two HS types-with strong low-symmetry (I-type) and weak, distorted octahedral environments (II-type). It was shown that G2-[L2Fe]+A− complexes are magnetically inhomogeneous and consist of two magnetic sub-lattices: AFM-correlated chains in layers from the I-type HS Fe(III) centers and dynamic short-range AFM ordered LS/II-type HS Fe(III) centers in the paramagnetic phase located between the layers.
{"title":"New Branched Iron(III) Complexes in Fluorescent Environment Created by Carbazole Moieties: Synthesis and Structure, Static Magnetic and Resonance Properties","authors":"D. Starichenko, V. Vorobeva, M. Gruzdev, U. Chervonova, Nataliya G. Bichan, Aleksander V. Korolev, Ivan V. Yatsyk","doi":"10.3390/magnetochemistry10060038","DOIUrl":"https://doi.org/10.3390/magnetochemistry10060038","url":null,"abstract":"The branched complexes of Schiff bases with various iron(III) salts, named G2-[L2Fe]+A− (A− is NO3−, Cl−, PF6−), were synthesized using the condensation reaction between carbazole derivatives of salicylic aldehyde and N’-ethylethylenediamine and characterized by various spectroscopic methods (GPC, IR, 1H NMR, UV/Vis). The studies revealed that the coordination of the two ligand molecules to metal occurs through the nitrogen ions and oxygen atom of azomethine to form a homoleptic system. All the synthesized coordination compounds were examined for their thermal, optical, and magnetic features. Static magnetic measurements showed that only G2-[L2Fe]Cl was in a single-phase HS state, whereas the Fe(III) ions of G2-[L2Fe]NO3 and G2-[L2Fe]PF6 at room temperatures were in mixed low-spin (LS, S = 1/2) and high-spin (HS, S = 5/2) states: 58.9% LS/41.1% HS for G2-[L2Fe]NO3, 56.1% LS and 43.9% HS for G2-[L2Fe]PF6. All G2-[L2Fe]+A− complexes demonstrate antiferromagnetic exchange interactions between neighboring Fe(III) ions. The ground spin state at 2.0 K revealed a Brillouin contribution from non-interacting LS ions and a proportion of the HS Fe(III) ions not participating in AFM interactions: 57%, 18%, and 16% for G2-[L2Fe]Cl, G2-[L2Fe]NO3 and G2-[L2Fe]PF6, respectively. EPR measurements confirmed the presence of magnetically active HS and LS states of Fe(III) ions and made it possible to distinguish two HS types-with strong low-symmetry (I-type) and weak, distorted octahedral environments (II-type). It was shown that G2-[L2Fe]+A− complexes are magnetically inhomogeneous and consist of two magnetic sub-lattices: AFM-correlated chains in layers from the I-type HS Fe(III) centers and dynamic short-range AFM ordered LS/II-type HS Fe(III) centers in the paramagnetic phase located between the layers.","PeriodicalId":18194,"journal":{"name":"Magnetochemistry","volume":null,"pages":null},"PeriodicalIF":2.7,"publicationDate":"2024-05-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141116539","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-05-19DOI: 10.3390/magnetochemistry10050036
P. V. Thach, Satoshi Sumi, Kenji Tanabe, Hiroyuki Awano
Current-induced domain wall motion (CIDWM) in magnetic wires can be driven by spin transfer torque (STT) originating from transferring angular momentums of spin-polarized conducting electrons to the magnetic DW and can be driven by spin orbit torque (SOT) originating from the spin Hall effect (SHE) in a heavy metal layer and Dzyaloshinsky Moriya (DMI) generated at an interface between a heavy metal layer and a magnetic layer. In this work, we carried out a comparative study of CIDWM driven by STT and by SOT in ferrimagnetic GdFeCo wires with magnetic perpendicular anisotropy based on structures of SiN (10 nm)/GdFeCo (8 nm)/SiN (10 nm) and Pt (5 nm)/GdFeCo (8 nm)/SiN (10 nm). We found that CIDWM driven by SOT exhibited a much lower critical current density (JC), and much higher DW mobility (µDW). Our work might be useful for the realization and the development of low-power and high-speed memory devices.
{"title":"Comparison of Current Induced Domain Wall Motion Driven by Spin Transfer Torque and by Spin Orbit Torque in Ferrimagnetic GdFeCo Wires","authors":"P. V. Thach, Satoshi Sumi, Kenji Tanabe, Hiroyuki Awano","doi":"10.3390/magnetochemistry10050036","DOIUrl":"https://doi.org/10.3390/magnetochemistry10050036","url":null,"abstract":"Current-induced domain wall motion (CIDWM) in magnetic wires can be driven by spin transfer torque (STT) originating from transferring angular momentums of spin-polarized conducting electrons to the magnetic DW and can be driven by spin orbit torque (SOT) originating from the spin Hall effect (SHE) in a heavy metal layer and Dzyaloshinsky Moriya (DMI) generated at an interface between a heavy metal layer and a magnetic layer. In this work, we carried out a comparative study of CIDWM driven by STT and by SOT in ferrimagnetic GdFeCo wires with magnetic perpendicular anisotropy based on structures of SiN (10 nm)/GdFeCo (8 nm)/SiN (10 nm) and Pt (5 nm)/GdFeCo (8 nm)/SiN (10 nm). We found that CIDWM driven by SOT exhibited a much lower critical current density (JC), and much higher DW mobility (µDW). Our work might be useful for the realization and the development of low-power and high-speed memory devices.","PeriodicalId":18194,"journal":{"name":"Magnetochemistry","volume":null,"pages":null},"PeriodicalIF":2.7,"publicationDate":"2024-05-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141123750","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-05-17DOI: 10.3390/magnetochemistry10050035
P. Ziogas, A. Bourlinos, P. Chatzopoulou, G. Dimitrakopulos, A. Markou, A. Douvalis
This study introduces a novel magnetic nanohybrid material consisting of ferromagnetic (FM) bcc Fe–Co nanoparticles (NPs) grown on nanodiamond (ND) nanotemplates. A combination of wet chemistry, which produces chemical precursors and their subsequent thermal treatment under vacuum, was utilized for its development. The characterization and study of the prepared samples performed with a range of specialized experimental techniques reveal that thermal treatment of the as-prepared hybrid precursors under a range of annealing conditions leads to the development of Co-rich Fe–Co alloy NPs, with average sizes in the range of 6–10 nm, that exhibit uniform distribution on the surfaces of the ND nanotemplates and demonstrate FM behavior throughout a temperature range from 2 K to 400 K, with maximum magnetization values ranging between 18.9 and 21.1 emu/g and coercivities ranging between 112 and 881 Oe. Moreover, 57Fe Mössbauer spectroscopy reveals that apart from the predominant bcc FM Fe–Co phase, iron atoms also participate in the formation of a secondary martensitic-type Fe–Co phase. The emergence of this distinctive phase is attributed to the diffusion of carbon atoms within the Fe–Co lattices during their formation at elevated temperatures. The source of these carbon atoms is related to the unique morphological properties of the ND growth matrices, which facilitate surface sp2 formations. Apart from their diffusion within the Fe–Co NP lattice, the carbon atoms also reconstruct layered graphitic-type nanostructures enveloping the metallic alloy NPs. These non-typical nanohybrid materials, reported here for the first time in the literature, hold significant potential for use in applications related, but not limited to, biomedicine, biopharmaceutics, catalysis, and other various contemporary technological fields.
{"title":"Novel Hybrid Ferromagnetic Fe–Co/Nanodiamond Nanostructures: Influence of Carbon on Their Structural and Magnetic Properties","authors":"P. Ziogas, A. Bourlinos, P. Chatzopoulou, G. Dimitrakopulos, A. Markou, A. Douvalis","doi":"10.3390/magnetochemistry10050035","DOIUrl":"https://doi.org/10.3390/magnetochemistry10050035","url":null,"abstract":"This study introduces a novel magnetic nanohybrid material consisting of ferromagnetic (FM) bcc Fe–Co nanoparticles (NPs) grown on nanodiamond (ND) nanotemplates. A combination of wet chemistry, which produces chemical precursors and their subsequent thermal treatment under vacuum, was utilized for its development. The characterization and study of the prepared samples performed with a range of specialized experimental techniques reveal that thermal treatment of the as-prepared hybrid precursors under a range of annealing conditions leads to the development of Co-rich Fe–Co alloy NPs, with average sizes in the range of 6–10 nm, that exhibit uniform distribution on the surfaces of the ND nanotemplates and demonstrate FM behavior throughout a temperature range from 2 K to 400 K, with maximum magnetization values ranging between 18.9 and 21.1 emu/g and coercivities ranging between 112 and 881 Oe. Moreover, 57Fe Mössbauer spectroscopy reveals that apart from the predominant bcc FM Fe–Co phase, iron atoms also participate in the formation of a secondary martensitic-type Fe–Co phase. The emergence of this distinctive phase is attributed to the diffusion of carbon atoms within the Fe–Co lattices during their formation at elevated temperatures. The source of these carbon atoms is related to the unique morphological properties of the ND growth matrices, which facilitate surface sp2 formations. Apart from their diffusion within the Fe–Co NP lattice, the carbon atoms also reconstruct layered graphitic-type nanostructures enveloping the metallic alloy NPs. These non-typical nanohybrid materials, reported here for the first time in the literature, hold significant potential for use in applications related, but not limited to, biomedicine, biopharmaceutics, catalysis, and other various contemporary technological fields.","PeriodicalId":18194,"journal":{"name":"Magnetochemistry","volume":null,"pages":null},"PeriodicalIF":2.7,"publicationDate":"2024-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140963242","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-05-15DOI: 10.3390/magnetochemistry10050034
Han Zhou, Zaitian Cheng, Zhiqiang Ai, Xinyao Li, Lin Hu, Fapei Zhang
The development of novel synthesis and assembly strategies is critical to achieving a ferromagnetic organic semiconductor with high Curie temperature. In this study, we report a high magnetic field (HMF)-modified solvothermal approach for the reduction in neutral perylene diimide (PDI) into the dianion species to prepare the PDI magnets comprising radical anions after subsequent oxidation processes. The PDI materials, assembled from the dianion solution by an HMF-modified reduction, exhibit a smaller crystallite size and an enlarged distance of the π-π stacking in the PDI aggregates. Furthermore, the PDI magnets obtained from the process under a 9T field reveal weakened ferromagnetism and the rapid degradation of electrical conductivity compared to those prepared without a magnetic field. Based on spectral and structural characterizations, such performance deterioration originates from the enhanced instability of the radical anions exposed to air, as well as the decreased crystallinity for the radical PDIs synthesized from the HMF-modified reduction process. This work demonstrates that magnetic fields offer an effective way in the material synthesis process to manipulate the structure and magnetic properties of the radical-based organic magnets.
{"title":"Tuning Structure and Properties of a Ferromagnetic Organic Semiconductor via a Magnetic Field-Modified Reduction Process","authors":"Han Zhou, Zaitian Cheng, Zhiqiang Ai, Xinyao Li, Lin Hu, Fapei Zhang","doi":"10.3390/magnetochemistry10050034","DOIUrl":"https://doi.org/10.3390/magnetochemistry10050034","url":null,"abstract":"The development of novel synthesis and assembly strategies is critical to achieving a ferromagnetic organic semiconductor with high Curie temperature. In this study, we report a high magnetic field (HMF)-modified solvothermal approach for the reduction in neutral perylene diimide (PDI) into the dianion species to prepare the PDI magnets comprising radical anions after subsequent oxidation processes. The PDI materials, assembled from the dianion solution by an HMF-modified reduction, exhibit a smaller crystallite size and an enlarged distance of the π-π stacking in the PDI aggregates. Furthermore, the PDI magnets obtained from the process under a 9T field reveal weakened ferromagnetism and the rapid degradation of electrical conductivity compared to those prepared without a magnetic field. Based on spectral and structural characterizations, such performance deterioration originates from the enhanced instability of the radical anions exposed to air, as well as the decreased crystallinity for the radical PDIs synthesized from the HMF-modified reduction process. This work demonstrates that magnetic fields offer an effective way in the material synthesis process to manipulate the structure and magnetic properties of the radical-based organic magnets.","PeriodicalId":18194,"journal":{"name":"Magnetochemistry","volume":null,"pages":null},"PeriodicalIF":2.7,"publicationDate":"2024-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140975242","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-04-24DOI: 10.3390/magnetochemistry10050032
H. Sakiyama, Rin Kimura, Haruto Oomiya, R. Mitsuhashi, Sho Fujii, K. Kanaizuka, M. Muddassir, Yuga Tamaki, E. Asato, Makoto Handa
Octahedral nickel(II) complexes are among the simplest systems that exhibit zero-field splitting by having two unpaired electrons. For the purpose of clarifying the relationship between structure and zero-field splitting in a low-symmetric system, distorted octahedral nickel(II) complexes were prepared with a tetradentate ligand, 2-[bis(2-methoxyethyl)aminomethyl]-4-nitrophenolate(1−) [(onp)−]. The complex [Ni(onp)(dmso)(H2O)][BPh4]·2dmso (1) (dmso = dimethyl sulfoxide) was characterized as a bulk sample by IR, elemental analysis, mass spectrometry, electronic spectra, and magnetic properties. The powder electronic spectral data were analyzed based on the angular overlap model to conclude that the spectra were typical of D4-symmetric octahedral coordination geometry with a weak axial ligand field. Simultaneous analysis of the temperature-dependent susceptibility and field-dependent magnetization data yielded the positive axial zero-field splitting parameter D (H = guβSuHu + D[Sz2 − S(S + 1)/3]), which was consistent with the weak axial ligand field. Single-crystal X-ray analysis revealed the crystal structures of [Ni(onp)(dmso)(H2O)][BPh4]·dmso (2) and [Ni(onp)(dmf)2][BPh4] (3) (dmf = N,N-dimethylformamide). The density functional theory (DFT) computations based on the crystal structures indicated the D4-symmetric octahedral coordination geometries with weak axial ligand fields. This study also showed the importance of considering g-anisotropy in magnetic analysis, even if g-anisotropy is small.
八面体镍（II）配合物是最简单的体系之一，它们通过拥有两个未成对电子而表现出零场分裂。为了阐明低对称体系中结构与零场分裂之间的关系，研究人员用四价配体 2-[双（2-甲氧基乙基）氨基甲基]-4-硝基苯酚（1-）[(onp)-]制备了变形八面体镍（II）配合物。复合物[Ni(onp)(dmso)(H2O)][BPh4]-2dmso (1)（dmso = 二甲基亚砜）作为块状样品，通过红外光谱、元素分析、质谱分析、电子光谱和磁性能进行了表征。根据角度重叠模型对粉末电子能谱数据进行了分析，得出的结论是该能谱是典型的 D4 对称八面体配位几何，具有微弱的轴向配位场。同时分析了随温度变化的电感和随磁场变化的磁化数据，得出了正的轴向零场分裂参数 D（H = guβSuHu + D[Sz2 - S(S+1)/3]），这与弱轴向配体场一致。单晶 X 射线分析揭示了[Ni(onp)(dmso)(H2O)][BPh4]-dmso（2）和[Ni(onp)(dmf)2][BPh4]（3）（dmf = N,N-二甲基甲酰胺）的晶体结构。基于晶体结构的密度泛函理论（DFT）计算表明，[Ni(onp)(dmf)2][BPh4]具有弱轴向配体场的 D4 对称八面体配位几何结构。这项研究还表明了在磁性分析中考虑 g 各向异性的重要性，即使 g 各向异性很小。
{"title":"Relationship between Structure and Zero-Field Splitting of Octahedral Nickel(II) Complexes with a Low-Symmetric Tetradentate Ligand","authors":"H. Sakiyama, Rin Kimura, Haruto Oomiya, R. Mitsuhashi, Sho Fujii, K. Kanaizuka, M. Muddassir, Yuga Tamaki, E. Asato, Makoto Handa","doi":"10.3390/magnetochemistry10050032","DOIUrl":"https://doi.org/10.3390/magnetochemistry10050032","url":null,"abstract":"Octahedral nickel(II) complexes are among the simplest systems that exhibit zero-field splitting by having two unpaired electrons. For the purpose of clarifying the relationship between structure and zero-field splitting in a low-symmetric system, distorted octahedral nickel(II) complexes were prepared with a tetradentate ligand, 2-[bis(2-methoxyethyl)aminomethyl]-4-nitrophenolate(1−) [(onp)−]. The complex [Ni(onp)(dmso)(H2O)][BPh4]·2dmso (1) (dmso = dimethyl sulfoxide) was characterized as a bulk sample by IR, elemental analysis, mass spectrometry, electronic spectra, and magnetic properties. The powder electronic spectral data were analyzed based on the angular overlap model to conclude that the spectra were typical of D4-symmetric octahedral coordination geometry with a weak axial ligand field. Simultaneous analysis of the temperature-dependent susceptibility and field-dependent magnetization data yielded the positive axial zero-field splitting parameter D (H = guβSuHu + D[Sz2 − S(S + 1)/3]), which was consistent with the weak axial ligand field. Single-crystal X-ray analysis revealed the crystal structures of [Ni(onp)(dmso)(H2O)][BPh4]·dmso (2) and [Ni(onp)(dmf)2][BPh4] (3) (dmf = N,N-dimethylformamide). The density functional theory (DFT) computations based on the crystal structures indicated the D4-symmetric octahedral coordination geometries with weak axial ligand fields. This study also showed the importance of considering g-anisotropy in magnetic analysis, even if g-anisotropy is small.","PeriodicalId":18194,"journal":{"name":"Magnetochemistry","volume":null,"pages":null},"PeriodicalIF":2.7,"publicationDate":"2024-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140660337","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
In this study, a novel green tea/Mg-functionalized magnetic nano-adsorbent, denoted as GTE-MgO-Fe3O4 NPs, was developed and applied to the extraction of Methylene Blue (MB) from water-based solutions. The GTE-MgO-Fe3O4 NPs were synthesized by incorporating green tea extracts (GTE) and Mg species onto the surface of Fe3O4 nanoparticles using a hydrothermal method. Characterization analyses corroborated the successful functionalization of the Fe3O4 surface with GTE and Mg species, resulting in a superparamagnetic adsorbent equipped with abundant surface functional groups, which promoted MB adsorption and facilitated magnetic separation. Batch experiments revealed that different operating parameters had an impact on the adsorption behavior, such as adsorbent dosage, pH, coexisting ions, contact time, the initial MB concentration, and temperature. The investigations of adsorption kinetics and isotherms emphasized that the MB adsorption onto GTE-MgO-Fe3O4 NPs was an exothermic process dominated by chemisorption. The experimental adsorption capacity of GTE-MgO-Fe3O4 NPs for MB surpassed 174.93 mg g−1, markedly superior to the performance of numerous other adsorbents. Ultimately, the utilized GTE-MgO-Fe3O4 NPs could be effectively regenerated through acid pickling, retaining over 76% of its original adsorption capacity after six adsorption–desorption cycles, which suggested that GTE-MgO-Fe3O4 NPs was a suitable adsorbent for eliminating MB from effluent.
{"title":"A Novel Magnetic Nano-Adsorbent Functionalized with Green Tea Extract and Magnesium Oxide to Remove Methylene Blue from Aqueous Solutions: Synthesis, Characterization, and Adsorption Behavior","authors":"Wenchao Lin, Yaoyao Huang, Shuang Liu, Wei Ding, H. Li, Huaili Zheng","doi":"10.3390/magnetochemistry10050031","DOIUrl":"https://doi.org/10.3390/magnetochemistry10050031","url":null,"abstract":"In this study, a novel green tea/Mg-functionalized magnetic nano-adsorbent, denoted as GTE-MgO-Fe3O4 NPs, was developed and applied to the extraction of Methylene Blue (MB) from water-based solutions. The GTE-MgO-Fe3O4 NPs were synthesized by incorporating green tea extracts (GTE) and Mg species onto the surface of Fe3O4 nanoparticles using a hydrothermal method. Characterization analyses corroborated the successful functionalization of the Fe3O4 surface with GTE and Mg species, resulting in a superparamagnetic adsorbent equipped with abundant surface functional groups, which promoted MB adsorption and facilitated magnetic separation. Batch experiments revealed that different operating parameters had an impact on the adsorption behavior, such as adsorbent dosage, pH, coexisting ions, contact time, the initial MB concentration, and temperature. The investigations of adsorption kinetics and isotherms emphasized that the MB adsorption onto GTE-MgO-Fe3O4 NPs was an exothermic process dominated by chemisorption. The experimental adsorption capacity of GTE-MgO-Fe3O4 NPs for MB surpassed 174.93 mg g−1, markedly superior to the performance of numerous other adsorbents. Ultimately, the utilized GTE-MgO-Fe3O4 NPs could be effectively regenerated through acid pickling, retaining over 76% of its original adsorption capacity after six adsorption–desorption cycles, which suggested that GTE-MgO-Fe3O4 NPs was a suitable adsorbent for eliminating MB from effluent.","PeriodicalId":18194,"journal":{"name":"Magnetochemistry","volume":null,"pages":null},"PeriodicalIF":2.7,"publicationDate":"2024-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140664785","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Effects of varying Mn and Ni concentrations on the structure and piezoresistive properties of CuMnNi films deposited by magnetron sputtering with a segmented target were investigated. An increase in the Ni content refines the CuNi film grains, inducing an increase in defects such as internal micropores and a decrease in film density. At the same time, the positive piezoresistive coefficient of the film changes to negative. When 17.5 at.% Ni was added, the negative piezoresistive coefficient of the CuNi film was −2.0 × 10−4 GPa−1. The doping of Ni has a weakening effect on the positive piezoresistive effect of the film. Adding Mn into Cu refines the film grains while increasing the film density. The surface roughness of the film decreases with the increase in Mn content. When the Mn content was 16.7 at.%, the piezoresistive coefficient reached the largest recorded value of 23.81 × 10−4 GPa−1, and the film exhibited excellent repeatability in multiple piezoresistive tests. After the CuMn film with 16.7 at.% Mn was annealed at 400 °C for 2 h, the film grains grew slightly and the film residual stress decreased. The optimization of the film structure can reduce the scattering of electrons during transportation. The piezoresistive coefficient of the film was further improved to 35.78 × 10−4 GPa−1.
{"title":"The Piezoresistive Performance of CuMnNi Alloy Thin-Film Pressure Sensors Prepared by Magnetron Sputtering","authors":"Zhengtao Wu, Xiaotao He, Yu Cao, Qimin Wang, Yisong Lin, Liangliang Lin, Chao Liu","doi":"10.3390/magnetochemistry10050030","DOIUrl":"https://doi.org/10.3390/magnetochemistry10050030","url":null,"abstract":"Effects of varying Mn and Ni concentrations on the structure and piezoresistive properties of CuMnNi films deposited by magnetron sputtering with a segmented target were investigated. An increase in the Ni content refines the CuNi film grains, inducing an increase in defects such as internal micropores and a decrease in film density. At the same time, the positive piezoresistive coefficient of the film changes to negative. When 17.5 at.% Ni was added, the negative piezoresistive coefficient of the CuNi film was −2.0 × 10−4 GPa−1. The doping of Ni has a weakening effect on the positive piezoresistive effect of the film. Adding Mn into Cu refines the film grains while increasing the film density. The surface roughness of the film decreases with the increase in Mn content. When the Mn content was 16.7 at.%, the piezoresistive coefficient reached the largest recorded value of 23.81 × 10−4 GPa−1, and the film exhibited excellent repeatability in multiple piezoresistive tests. After the CuMn film with 16.7 at.% Mn was annealed at 400 °C for 2 h, the film grains grew slightly and the film residual stress decreased. The optimization of the film structure can reduce the scattering of electrons during transportation. The piezoresistive coefficient of the film was further improved to 35.78 × 10−4 GPa−1.","PeriodicalId":18194,"journal":{"name":"Magnetochemistry","volume":null,"pages":null},"PeriodicalIF":2.7,"publicationDate":"2024-04-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140667805","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-04-18DOI: 10.3390/magnetochemistry10040029
V. Borodin, A. Bubenchikov, M. A. Bubenchikov, Dmitry S. Kaparulin, Vyacheslav A. Ovchinnikov
Columnar phases consisting of a group of carbon toroidal molecules (C120, C192, C252, C288) are studied numerically. Each nanotorus was previously doped with an iron atom. This made it possible to use an external magnetic field as a tool for influencing both an individual molecule and a linear fragment of the columnar phase. A high-precision scheme for calculating the dynamics of large molecules with a rigid frame structure is proposed to solve the problem. The group dynamics of nanotori clusters under the influence of an external magnetic field has been studied using classical molecular dynamics methods. The influence of the molecular cluster size, temperature, magnetic moment of the molecule, and magnetic field direction on the collective behavior of iron-doped toroidal molecules with different contents of carbon atoms is analyzed. Molecular dynamics calculations showed that systems of nanotori doped with a single iron atom retain a columnar structure both in the absence and in the presence of an external magnetic field. The columnar fragment behaves as a stable linear association of molecules even at sufficiently high values of magnetic induction, performing a coordinated collective orbital rotation around a common center of mass on a nanosecond time scale.
{"title":"Numerical Analysis of the Influence of a Magnetic Field on the Group Dynamics of Iron-Doped Carbon Nanotori","authors":"V. Borodin, A. Bubenchikov, M. A. Bubenchikov, Dmitry S. Kaparulin, Vyacheslav A. Ovchinnikov","doi":"10.3390/magnetochemistry10040029","DOIUrl":"https://doi.org/10.3390/magnetochemistry10040029","url":null,"abstract":"Columnar phases consisting of a group of carbon toroidal molecules (C120, C192, C252, C288) are studied numerically. Each nanotorus was previously doped with an iron atom. This made it possible to use an external magnetic field as a tool for influencing both an individual molecule and a linear fragment of the columnar phase. A high-precision scheme for calculating the dynamics of large molecules with a rigid frame structure is proposed to solve the problem. The group dynamics of nanotori clusters under the influence of an external magnetic field has been studied using classical molecular dynamics methods. The influence of the molecular cluster size, temperature, magnetic moment of the molecule, and magnetic field direction on the collective behavior of iron-doped toroidal molecules with different contents of carbon atoms is analyzed. Molecular dynamics calculations showed that systems of nanotori doped with a single iron atom retain a columnar structure both in the absence and in the presence of an external magnetic field. The columnar fragment behaves as a stable linear association of molecules even at sufficiently high values of magnetic induction, performing a coordinated collective orbital rotation around a common center of mass on a nanosecond time scale.","PeriodicalId":18194,"journal":{"name":"Magnetochemistry","volume":null,"pages":null},"PeriodicalIF":2.7,"publicationDate":"2024-04-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140687541","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-04-16DOI: 10.3390/magnetochemistry10040028
Jiaqi Li, Kaixin Su, Hai-Yun Liu, Yuan Zou
The manipulation of droplets plays a vital role in biomedicine, chemistry, and hydromechanics, especially in microfluidics. Magnetic droplet manipulation has emerged as a prominent and advanced technique in comparison to other modes such as dielectric infiltration, optical radiation, and surface acoustic waves. Its notable progress is attributed to several advantages, including excellent biocompatibility, remote and non-contact control, and instantaneous response. This review provides a comprehensive overview of recent developments in magnetic droplet manipulation and its applications within the biomedical field. Firstly, the discussion involves an examination of the distinctive features associated with droplet manipulation based on both permanent magnet and electromagnet principles, along with a thorough exploration of the influencing factors impacting magnetic droplet manipulation. Additionally, an in-depth review of magnetic actuation mechanisms and various droplet manipulation methods is presented. Furthermore, the article elucidates the biomedical applications of magnetic droplet manipulation, particularly its role in diagnostic assays, drug discovery, and cell culture. Finally, the highlights and challenges of magnetic droplet manipulation in biomedical applications are described in detail.
{"title":"Recent Advances in Magnetically Actuated Droplet Manipulation for Biomedical Applications","authors":"Jiaqi Li, Kaixin Su, Hai-Yun Liu, Yuan Zou","doi":"10.3390/magnetochemistry10040028","DOIUrl":"https://doi.org/10.3390/magnetochemistry10040028","url":null,"abstract":"The manipulation of droplets plays a vital role in biomedicine, chemistry, and hydromechanics, especially in microfluidics. Magnetic droplet manipulation has emerged as a prominent and advanced technique in comparison to other modes such as dielectric infiltration, optical radiation, and surface acoustic waves. Its notable progress is attributed to several advantages, including excellent biocompatibility, remote and non-contact control, and instantaneous response. This review provides a comprehensive overview of recent developments in magnetic droplet manipulation and its applications within the biomedical field. Firstly, the discussion involves an examination of the distinctive features associated with droplet manipulation based on both permanent magnet and electromagnet principles, along with a thorough exploration of the influencing factors impacting magnetic droplet manipulation. Additionally, an in-depth review of magnetic actuation mechanisms and various droplet manipulation methods is presented. Furthermore, the article elucidates the biomedical applications of magnetic droplet manipulation, particularly its role in diagnostic assays, drug discovery, and cell culture. Finally, the highlights and challenges of magnetic droplet manipulation in biomedical applications are described in detail.","PeriodicalId":18194,"journal":{"name":"Magnetochemistry","volume":null,"pages":null},"PeriodicalIF":2.7,"publicationDate":"2024-04-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140695727","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-04-15DOI: 10.3390/magnetochemistry10040027
Bishal Gautam, Saja M. Nabat Al-Ajrash, Mohammad Jahid Hasan, Abhishek Saini, Sarah J. Watzman, E. Ureña-Benavides, Erick S. Vasquez-Guardado
In the original publication [...]
在最初的出版物中 [...]
{"title":"Correction: Gautam et al. Experimental Thermal Conductivity Studies of Agar-Based Aqueous Suspensions with Lignin Magnetic Nanocomposites. Magnetochemistry 2024, 10, 12","authors":"Bishal Gautam, Saja M. Nabat Al-Ajrash, Mohammad Jahid Hasan, Abhishek Saini, Sarah J. Watzman, E. Ureña-Benavides, Erick S. Vasquez-Guardado","doi":"10.3390/magnetochemistry10040027","DOIUrl":"https://doi.org/10.3390/magnetochemistry10040027","url":null,"abstract":"In the original publication [...]","PeriodicalId":18194,"journal":{"name":"Magnetochemistry","volume":null,"pages":null},"PeriodicalIF":2.7,"publicationDate":"2024-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140701349","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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