Magnetic Substrate Research Articles

Optimization of Magnetic Biochar Preparation Process, Based on Methylene Blue Adsorption.

The search for low-cost and effective adsorbents for the removal of organic dyes from contaminated water is urgently needed. The substantial amount of waste mushroom cultivation substrates generated in practical production can serve as an ideal material for the preparation of adsorbents. In this study, we investigated the main control parameters affecting the performance of magnetic mushroom substrate biochar and optimized the process of preparing biochar by using the Plackett-Burman and central composite design methods. Various analytical techniques including SEM, EDX, BET, and VSM were used to characterize the biochar. The results indicate that the carbonization temperature had the most significant impact on the yield and adsorption performance of biochar. Under the conditions of a carbonization temperature of 600 °C, a carbonization retention time of 1 h, and an impregnation ratio of 0.1, the yield and methylene blue adsorption value of magnetic biochar were 42.54% and 2297.04 μg/g, respectively, with a specific surface area of 37.17 m2/g. This biochar effectively removed methylene blue from the solution, demonstrating a high economic efficiency for wastewater treatment and pollution control. Furthermore, the adsorption-desorption cycle studies revealed its excellent stability and reusability. Additionally, based on the response surface methodology, a three-dimensional surface model of the adsorption performance of magnetic biochar under different carbonization conditions was established, providing a theoretical basis for the preparation of magnetic biochar from agricultural wastes.

High adsorption separation capacity magnetic MOF-based substrate Fe3O4@ZIF-67@Ag for sensitive and recyclable SERS detection of malachite green in aquaculture

High adsorption separation capacity magnetic MOF-based substrate Fe3O4@ZIF-67@Ag for sensitive and recyclable SERS detection of malachite green in aquaculture

Magnetic Monopole-Like Behavior in Superparamagnetic Nanoparticle Coated With Chiral Molecules.

Superparamagnetic iron oxide nanoparticles (SPIONs) have attracted wide attention due to their promising applications in biomedicine, chemical catalysis, and magnetic memory devices. In this work, the force is measured between a single SPION coated with chiral molecules and a ferromagnetic substrate by atomic force microscopy (AFM), with the substrate magnetized either toward or away from the approaching AFM tip. The force between the coated SPION and the magnetic substrate depends on the handedness of the molecules adsorbed on the SPION and on the direction of the magnetization of the substrate. By inserting nm-scale spacing layers between the coated SPION and the magnetic substrate it is shown that the SPION has a short-range magnetic monopole-like magnetic field. A theoretical framework for the nature of this field is provided.

Utilizing a synergistic strategy that combines electromagnetic and chemical enhancement to analyze the SERS effect of the Fe3O4@GO@Ag on PAHs detection

A comprehensive understanding of the enhancement mechanism of the substrate material is crucial to ensure the repeatability and functionality of SERS detection technology. Therefore, this study introduces a theoretical analysis method that integrates electromagnetic and chemical enhancement to achieve a comprehensive understanding of the SERS effect on the magnetic composite substrate. The visual model is employed in this study to comprehensively analyze and illustrate the electric field enhancement and optical effects of composite substrate materials. The study also elucidated the adsorption and charge transfer between the substrate material and target molecules. Based on this theory, Fe3O4@GO@Ag material was prepared and used to detect hydrophobic organic molecules such as polycyclic aromatic hydrocarbons (PAHs), with a concentration as low as 0.5 nM. This study comprehensively analyzed the SERS enhancement effect of the composite substrate for the first time, and prepared a magnetic composite substrate material for the detection of hydrophobic organic molecules, opening up a new avenue for theoretical guidance and experimental exploration in SERS detection and analysis.

Hierarchical magneto-colorimetric labels for immediate lateral flow immunoassay of chlorothalonil residues

Quantitative detection of pesticide residues in food and environmental samples using an improved lateral flow immunoassay (LFIA) is of considerable importance for real-time analysis. This paper proposes a highly sensitive LFIA platform based on a hierarchical magneto-colorimetric compact. This compact serves as both the target magnetic enrichment substrate and a photosensitive label. Initially, a large porous dendritic silica template is prepared and doped with superparamagnetic ferric oxide nanoparticles (Fe3O4 NPs) and colloidal gold nanoparticles (AuNPs) at high densities within its vertical channels. The sequential assembly of central–radial channels allow for the three-dimensional integration of these two components, enabling independent control of their discrete functions without mutual interference. Following alkyl organosilicon encapsulation and silica sealing, the composite spheres are then applied in LFIA to detect chlorothalonil residues. Fe3O4 NPs enhance the binding efficiency to target analytes, while AuNPs amplify the signal, leveraging their high loading densities and robust optical properties. The developed LFIA platform exhibited a detection limit of 0.34 ng/mL for chlorothalonil and a linear range of 0.0085–824 ng/mL. The recoveries varied between 85.1 % and 103.1 %, and the relative standard deviations were 1.25%–8.84 %. This LFIA approach demonstrates high sensitivity, specificity, reproducibility and flexible detection modes, making it highly suitable for the on-site monitoring of pesticide residues.

Self-assembled magnetic particles on hard magnetic materials substrate for simple and rapid SERS detection of organic dye

In this paper, a detection strategy based on Surface-enhanced Raman Scattering (SERS) was proposed to quickly and simply separate target molecules from samples. Fe3O4@SiO2@Ag (FSA) magnetic particles modified with flower-like silver nanosheets were employed for efficient enrichment of target molecules, followed by their self-assembly onto the NdFeB substrate surface in fluid medium. The SERS sensitivity was indirectly adjusted by changing the reaction time to control the morphology of flower-like silver nanosheets on the surface of magnetic particles. SERS experiment showed that the substrate prepared by this detection strategy had high sensitivity, Rhodamine 6G (R6G) could be detected at the concentration of 10−8M and Methylene Blue (MB) could be detected at the concentration of 10−7M, the calculated enhancement factor was 1.34 × 105. In addition, the uniformity of the substrate was evaluated by SERS mapping using 10-6 M R6G, the RSD value of 8.89% was obtained. This detection strategy provides a new idea for simple and rapid SERS detection of organic dye.

Application of Gap Mode Ultrasensitive P-GERTs in SERS-Based Rapid Detection

In surface-enhanced Raman scattering (SERS) detection research, the shape, structure, surface modification, and material selection of nanoparticles can significantly impact the SERS intensity. Petal-like gap-enhanced Raman tags (P-GERTs) possess numerous sharp tips and edges, which generate localized electric field enhancements, further amplifying the electric field enhancement effect on neighboring molecules and enhancing the SERS signal. Additionally, the surface of P-GERTs can be modified with functional molecules, enabling their application in the detection of disease biomarkers. Using COVID-19 as an example, the performance of P-GERTs in disease biomarker detection was validated, demonstrating that the signal intensity of this probe can reach 55 times that of regular gold nanoparticles and 36.7 times that of smooth shell gap-enhanced Raman tags (S-GERTs). Furthermore, in combination with magnetically retrievable magnetic bead substrates, the N-protein antigen was specifically detected in a one-step process. N-protein was detected within 15 min using a portable Raman spectrometer. The limit of detection (LOD) for the standard sample was 4.28 pg/mL, and the LOD for the actual throat swab sample system was 25.4 pg/mL. This workflow can be extended to the detection of other biomarkers, making it widely applicable.

Magnetic Substrates for Tissue Engineering—A Review

Tissue engineering is based on combining cells with suitable scaffolds and growth factors. Recently, bone tissue engineering has been especially investigated deeply due to a large number of bone-related diseases. One approach to improve scaffolds is based on using piezoelectric materials as a way to influence the growing bone tissue by mechanical stress. Another method to stimulate tissue growth is by applying an external magnetic field to composites of magnetostrictive and piezoelectric materials, as well as the possibility to prepare oriented surfaces by orienting embedded magnetic fibers or nanoparticles. In addition, magnetic scaffolds without other special properties have also been reported to show improved properties for bone tissue and other tissue engineering. Here, we provide an overview of recent research on magnetic scaffolds for tissue engineering, differentiating between bone and other tissue engineering. We show the advantages of magnetic scaffolds, especially related to cell guidance and differentiation, and report recent progress in the production and application of such magnetic substrates for different areas of tissue engineering.

Synthesis of carbon nanotube–iron oxide and silver nanocomposites as photocatalyst in removing carcinogenic aromatic dyes

Abstract In this research, a three-component composite was synthesized by using carbon nanotube as the background phase. Iron oxide phase with high magnetization and low coercivity (with particle size of 200 nm) has been coated on the carbon nanotubes. Then, the silver nanoparticles were coated on a conductive and magnetized substrate by an ultrasonic method. Semiconductor photocatalys is a favorable route for the degradation of organic pollutants. Ultraviolet–visible spectrophotometry has been used to investigate the photocatalytic properties of synthesized nanocomposite and control of their dye degradation on methyl blue, methyl orange and methyl red. The obtained nanocomposite is easily collected due to its magnetic property and does not pose a risk to environmental waters. The dye degradation degree has been compared for the produced nanocomposite. The experimental results confirmed that methyl red shows the greatest amount of degradation within 1 h, which was about 90 %, methyl orange shows about 80 %, and methyl blue shows the lowest degradation, around 60 %.

Magnetic anisotropy and GGG substrate stray field in YIG films down to millikelvin temperatures

Quantum magnonics investigates the quantum-mechanical properties of magnons, such as quantum coherence or entanglement for solid-state quantum information technologies at the nanoscale. The most promising material for quantum magnonics is the ferrimagnetic yttrium iron garnet (YIG), which hosts magnons with the longest lifetimes. YIG films of the highest quality are grown on a paramagnetic gadolinium gallium garnet (GGG) substrate. The literature has reported that ferromagnetic resonance (FMR) frequencies of YIG/GGG decrease at temperatures below 50 K despite the increase in YIG magnetization. We investigated a 97 nm-thick YIG film grown on 500 μm-thick GGG substrate through a series of experiments conducted at temperatures as low as 30 mK, and using both analytical and numerical methods. Our findings suggest that the primary factor contributing to the FMR frequency shift is the stray magnetic field created by the partially magnetized GGG substrate. This stray field is antiparallel to the applied external field and is highly inhomogeneous, reaching up to 40 mT in the center of the sample. At temperatures below 500 mK, the GGG field exhibits a saturation that cannot be described by the standard Brillouin function for a paramagnet. Including the calculated GGG field in the analysis of the FMR frequency versus temperature dependence allowed the determination of the cubic and uniaxial anisotropies. We find that the total crystallographic anisotropy increases more than three times with the decrease in temperature down to 2 K. Our findings enable accurate predictions of the YIG/GGG magnetic systems behavior at low and ultralow millikelvin temperatures, crucial for developing quantum magnonic devices.

Spin Resolved Zero-Line Modes in Minimally Twisted Bilayer Graphene from Exchange Field and Gate Voltage

Abstract The reliance on spin-orbit coupling or strong magnetic fields has always posed significant challenges for the mass production and even laboratory realization of most topological materials. Valley-based topological zero-line modes have attracted widespread attention due to their substantial advantage of being initially realizable with just an external electric field. However, the uncontrollable nature of electrode alignment and precise fabrication has greatly hindered the advancement in this field. By utilizing minimally twisted bilayer graphene and introducing exchange fields from magnetic substrates, we successfully realize a spin-resolved, electrode-free topological zero-line mode. Further integration of electrodes that do not require alignment considerations significantly enhances the tunability of the system’s band structure. Our approach offers a promising new support for the dazzling potential of topological zero-line mode in the realm of low-energy-consumption electronics.

Spin-Dependent ππ^{*} Gap in Graphene on a Magnetic Substrate.

We present a detailed analysis of the electronic properties of graphene/Eu/Ni(111). By using angle- and spin-resolved photoemission spectroscopy and abinitio calculations, we show that the intercalation of Eu in the graphene/Ni(111) interface gives rise to a gapped freestanding dispersion of the ππ^{*} Dirac cones at the K[over ¯] point with an additional lifting of the spin degeneracy due to the mixing of graphene and Eu states. The interaction with the magnetic substrate results in a large spin-dependent gap in the Dirac cones with a topological nature characterized by a large Berry curvature and a spin-polarized Van Hove singularity, whose closeness to the Fermi level gives rise to a polaronic band.

An ultra-wideband magnetic composite metamaterial microwave absorber embedded with multilayered graphene FSS

Nowadays, it is still challenging to develop high-efficiency broadband microwave absorption materials for electronic equipment and communication facilities. Herein, an ultra-wideband metamaterial microwave absorber (MMA) composed of CoNi@CNH/epoxy composite absorption substrates and the multilayered graphene frequency selective surface (FSS) is designed and fabricated. Thanks to the effective synergies of the multilayered graphene FSS with impressive tunable frequency features and magnetic absorption substrates with distinguished broadband absorption capacity, the obtained MMA showcases an effective absorption bandwidth from 4.5 GHz to 18 GHz. Meanwhile, an equivalent circuit model is proposed to explain its physical absorption mechanism. The designed MMA exhibits the insensitivity to both polarization modes and oblique incidences, and a significant radar cross-section reduction. The experimental results of the as-fabricated sample match well with the simulation values. Furthermore, the as-designed MMA possesses a simple fabrication process and an ultralight feature of 2.7 kg/m2. All these excellent properties make this MMA a high application prospect in both military stealth and civil fields.

Hypersensitive detection of CYFRA21-1 by SERS dual antibody sandwich method

PurposeAs an important reference index for the early diagnosis of non-small cell lung cancer (NSCLC), CYFRA21-1 still lacks the detection of low equipment cost, wide linear range and high sensitivity. Surface-enhanced Raman scattering (SERS) is a vibration spectrum technology based on the surface plasma of precious metal nanoparticles, which has been effectively applied to the detection of tumor markers. The combination of SERS technology and sensors has great potential in the ultrasensitive detection of tumor markers. The purpose of this study was to develop a sensitive method using SERS to quantitatively detect CYFRA21-1 for early diagnosis of NSCLC. MethodsA double-antibody sandwich immunoassay based on SERS was designed and tested to implement the ultrasensitive detection of CYFRA21-1 in the serum of NSCLC patients. ResultsGold @Ag nanorods (Au @Ag NRs) with higher Raman signals were prepared and used as probes, while magnetic graphene oxide was used as a magnetic substrate. The immunized probe, immune substrate and CYFRA21-1 standard substance in the buffer system formed a double-antibody sandwich structure. The standard curve displayed a liner range from 1pg mL−1 to 10 ng mL−1, and the detection limit (LOD) is 0.8943pg mL−1. The Raman intensity exhibited a wide linear relationship with the logarithm of CYFRA21-1 concentration. ConclusionOur study successfully established a double-antibody sandwich immunoassay based on SERS. This method demonstrated high specificity and sensitivity for detecting CYFRA21-1 protein content in serum. It has the potential to be applied for early detection of lung cancer biomarkers.

Preparation and Identification of Magnetic Iron Nanoparticle based on a Natural Hydrogel and its Performance in Targeted Drug Delivery

Billions of dollars are spent annually in the world to treat and investigate problems caused by drug side effects. According to the estimates of health researchers, about 40%of people who take medicine suffer from side effects. In this way, the necessity of using a targeted system in order to deliver medicine to the desired place without damaging healthy tissues is felt more than ever. In recent years, targeted drug delivery systems based on nanoparticles have received much attention. Meanwhile, the use of natural polymers is more suitable for various purposes in drug delivery systems in terms of indicating greater biological compatibility with the body and being non-toxic.In this research, the natural hydrogel extracted from the seeds of the Plantago ovata, which is loaded on the bed of magnetic iron nanoparticles, was used to entrap the drugmefenamic acid. In order to achieve this goal, at the beginning, magnetic iron nanoparticles were prepared by co-precipitation method using iron (II) and iron (III) oxides, and then a coating of silica was created on its surface, then the hydrocolloid of Plantago ovata was extracted from its seed, in order to connect the magnetite nanoparticles and the polymer extracted from the Plantago ovata, the surface of both components was modified by vinyl-functional groups. Next, radical polymerization under heat was used to connect the particles and trap the drug, after that the release of the drug from the polymer capsule was checked by UV-Vis device. Before examining the drug release, the resulting product was identified by FT-IR, XRD, VSM, DLS, TGA, SEM analysis. Therefore, the obtained results indicated that the natural polymer was correctly loaded on the desired magnetic substrate and the drug mefenamic acid was trapped inside the hydrogel networks and polymer capsule. Therefore, the drug can be directed in a controlled and targeted manner by the magnetic field, and the release of the drug was done well and at an acceptable speed.

Construction of selectively enhanced MOF-SERS sensor and highly sensitive detection of hCE1 in HepG2 cells

In this paper, a surface-enhanced Raman scattering (SERS) magnetic immunosensor for human carboxylesterase 1 (hCE1) assay was developed using a sandwich structure consisting of a magnetic support substrate, a SERS tag, and a target. The objective was to investigate the correlation between changes in hCE1 levels and liver injury. The utilization of Co-MOF-74@Au@methylene blue (MB) magnetic support substrate facilitated the expedient separation of biological samples while uniformly distributing the AuNPs, thereby enhancing the SERS intensity and improving the reproducibility. The introduction of Co-MOF-74 metal–organic frameworks (MOFs), endowed with its own selective SERS-enhancing properties, into the Co-MOF-74@Au@MB SERS tag further enhances the SERS sensing capability. The proposed SERS sensor exhibited good linearity over the concentration range of hCE1 from 10−2 to 102 μg·mL−1, with a correlation coefficient (R2) of 0.990 and a limit of detection (LOD) of 8.3 ng·mL−1. This demonstrates the potential of this strategy for the detection of trace proteins or enzymes in complex biological samples. In the meantime, the selective SERS enhancement mechanism of MOFs on Raman reporter molecules was preliminarily explored. This provides a new idea for the development of SERS substrates and SERS assays.

Defect controlled spin state transitions in FePc adsorbed CrI3

Our study employs first principles to explore the impact of spin on iron phthalocyanine (molecule) upon adsorption onto defect-functionalized CrI3. We focus on three stable vacancy defects commonly found in CrI3, created by the removal of ‘-Cr-’, ‘-I-’ and ‘-CrI3-’ units from the pristine CrI3 lattice, analyzing their electronic and magnetic characteristics in both FM and AFM scenarios. Notably, these defects predominantly affect the electronic structure near the Fermi level. The adsorption of FePc, on defect-functionalized CrI3, exhibits reduced stability compared to the pristine substrate. FePc demonstrates two stable spin states, a 2 μB low spin state and a 4 μB high spin state. We present two spin-control mechanisms when FePc adsorbs onto these defect-functionalized substrates. We name these — substrate-induced and molecular spin vector-induced control. The former involves manipulating the magnetic order of the substrate (FM/AFM), leading to molecular spin state transitions. The latter mechanism involves modifying the spin orientation on the molecular Fe atom relative to the substrate’s spin (parallel/antiparallel), resulting in molecular spin state transitions. This research proposes novel effective methods to control the spin states of magnetic metal complexes during adsorption onto magnetic substrates, offering potential applications in molecular electronics and spintronics.

A tailored dual core-shell magnetic SERS substrate with precise shell-thickness control for trace organophosphorus pesticides residues detection

For addressing the challenges of strong affinity SERS substrate to organophosphorus pesticides (OPs), herein, a rapid water-assisted layer-by-layer heteronuclear growth method was investigated to grow uniform UiO-66 shell with controllable thickness outside the magnetic core and provide abundant defect sites for OPs adsorption. By further assembling the tailored Au@Ag, a highly sensitive SERS substrate Fe3O4-COOH@UiO-66/Au@Ag (FCUAA) was synthesized with a SERS enhancement factor of 2.11 × 107. The substrate's suitability for the actual vegetable samples (cowpeas and peppers) was confirmed under both destructive and non-destructive detection conditions, showing a strong SERS response to fenthion and triazophos, with limits of detection of 1.21 × 10-5 and 2.96 × 10-3 mg/kg in the vegetables under destructive conditions, and 0.13 and 1.39 ng/cm2 for non-destructive detection, respectively. The FCUAA substrate had high SERS performance, effective adsorption capability for OPs, and demonstrated good applicability, thus exhibiting great potential for rapid detection of trace OPs residues in the food industry.

Effective enrichment and separation of three flavonoids from Ohwia caudata (Thunberg) H. Ohashi using magnetic layered double hydroxide/ZIF-8 composites and pCEC

In this study, Fe3O4@ZnCr–layered double hydroxide/zeolitic imidazolate frameworks-8 (MLDH/ZIF-8) magnetically functionalized composites were synthesized by co-precipitation and in situ growth based on the advantages of LDHs and ZIF-8 using Fe3O4 nanoparticles as a magnetic substrate to obtain adsorbents with excellent performance. Moreover, the composite was used for the efficient enrichment of flavonoids in Chinese herbal medicines. The internal structures and surface properties were characterized by SEM, Fourier transform infrared spectroscopy, X-ray diffraction and so on. MLDH/ZIF-8 exhibited a large specific surface area and good paramagnetic properties. The MLDH/ZIF-8 magnetic composite was used as a magnetic solid-phase extraction (MSPE) adsorbent, and a MLDH/ZIF-8 MSPE–pressurized capillary electrochromatography coupling method was developed for the separation and detection of flavonoids (luteolin, kaempferol and apigenin) in a sample of the Chinese herb Ohwia caudata (Thunberg) H. Ohashi. The relevant parameters affecting the extraction efficiency were optimized to determine the ideal conditions for MSPE. 5 mg of adsorbent in sample solution at pH 6, vortex extraction for 5 min, elution with 1.5 mL of ethyl acetate for 15 min. The method showed good linearity in the concentration range of 3–50 μg mL−1 with correlation coefficients of 0.9934–0.9981, and displayed a relatively LODs of 0.07–0.09 μg mL−1. The spiked recoveries of all analytes ranged from 84.5% to 122.0% with RSDs (n=3) between 4.5% and 7.7%. This method is straightforward and efficient, with promising potential in the separation and analysis of active ingredients in various Chinese herbal medicines.

Proximity-Induced Exchange Interaction: A New Pathway for Quantum Sensing Using Spin Centers in Hexagonal Boron Nitride.

Defects in hexagonal boron nitride (hBN), a two-dimensional van der Waals material, have attracted a great deal of interest because of its potential in various quantum applications. Due to hBN's two-dimensional nature, the spin center in hBN can be engineered in the proximity of the target material, providing advantages over its three-dimensional counterparts, such as the nitrogen-vacancy center in diamond. Here we propose a novel quantum sensing protocol driven by exchange interaction between the spin center in hBN and the underlying magnetic substrate induced by the magnetic proximity effect. By first-principles calculation, we demonstrate that the induced exchange interaction dominates over the dipole-dipole interaction by orders of magnitude when in the proximity. The interaction remains antiferromagnetic across all stacking configurations between the spin center in hBN and the target van der Waals magnets. Additionally, we explored the scaling behavior of the exchange field as a function of the spatial separation between the spin center and the targets.