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Fe3O4
Materials · 2024 ·Vol. 17 ·期 2 ·509 · IF 3.1

Study on Magnetic and Plasmonic Properties of Fe3O4-PEI-Au and Fe3O4-PEI-Ag Nanoparticles

Shuya Ning,Shuo Wang,Zhihui Liu,Naming Zhang,Bin Yang,Fanghui Zhang

Magnetic–plasmonic nanoparticles (NPs) have attracted great interest in many fields because they can exhibit more physical and chemical properties than individual magnetic or plasmonic NPs. In this work, we synthesized Au- or Ag-decorated Fe3O4nanoparticles coated with PEI (Fe3O4-PEI-M (M = Au or Ag) NPs) using a simple method. The influences of the plasmonic metal NPs’ (Au or Ag) coating density on the magnetic and plasmonic properties of the Fe3O4-PEI-M (M = Au or Ag) NPs were investigated, and the density of the plasmonic metal NPs coated on the Fe3O4NPs surfaces could be adjusted by controlling the polyethyleneimine (PEI) concentration. It showed that the Fe3O4-PEI-M (M = Au or Ag) NPs exhibited both magnetic and plasmonic properties. When the PEI concentration increased from 5 to 35 mg/mL, the coating density of the Au or Ag NPs on the Fe3O4NPs surfaces increased, the corresponding magnetic intensity became weaker, and the plasmonic intensity was stronger. At the same time, the plasmonic resonance peak of the Fe3O4-PEI-M (M = Au or Ag) NPs was red shifted. Therefore, there was an optimal coverage of the plasmonic metal NPs on the Fe3O4NPs surfaces to balance the magnetic and plasmonic properties when the PEI concentration was between 15 and 25 mg/mL. This result can guide the application of the Fe3O4-M (M = Au or Ag) NPs in the biomedical field.

研究领域: 纳米材料科学 · 生物医学工程
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Chinese Physics B · 2018 ·Vol. 27 ·期 2 ·027805 · IF 1.321

Magnetic field aligned orderly arrangement of Fe3O4 nanoparticles in CS/PVA/Fe3O4 membranes*

Meng Du,Xing-Zhong Cao,Rui Xia,Zhong-Po Zhou,Shuo-Xue Jin,Bao-Yi Wang

The CS/PVA/Fe3O4 nanocomposite membranes with chainlike arrangement of Fe3O4 nanoparticles are prepared by a magnetic-field-assisted solution casting method. The aim of this work is to investigate the relationship between the microstructure of the magnetic anisotropic CS/PVA/Fe3O4 membrane and the evolved macroscopic physicochemical property. With the same doping content, the relative crystallinity of CS/PVA/Fe3O4-M is lower than that of CS/PVA/Fe3O4. The Fourier transform infrared spectroscopy (FT-TR) measurements indicate that there is no chemical bonding between polymer molecule and Fe3O4 nanoparticle. The Fe3O4 nanoparticles in CS/PVA/Fe3O4 and CS/PVA/Fe3O4-M are wrapped by the chains of CS/PVA, which is also confirmed by scanning electron microscopy (SEM) and x-ray diffraction (XRD) analysis. The saturation magnetization value of CS/PVA/Fe3O4-M obviously increases compared with that of non-magnetic aligned membrane, meanwhile the transmittance decreases in the UV-visible region. The o-Ps lifetime distribution provides information about the free-volume nanoholes present in the amorphous region. It is suggested that the microstructure of CS/PVA/Fe3O4 membrane can be modified in its curing process under a magnetic field, which could affect the magnetic properties and the transmittance of nanocomposite membrane. In brief, a full understanding of the relationship between the microstructure and the macroscopic property of CS/PVA/Fe3O4 nanocomposite plays a vital role in exploring and designing the novel multifunctional materials.

研究领域: 材料科学 · 物理化学
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CATALYSIS LETTERS · 2019 ·Vol. 150 ·期 3 ·815-825 · IF 2.372

Fe3O4@Cu/C and Fe3O4@CuO Composites Derived from Magnetic Metal–Organic Frameworks Fe3O4@HKUST-1 with Improved Peroxidase-Like Catalytic Activity

Huang Yan-Feng,Zhang Lu,Ma Li,Li Ying,Zhong Chongli

Abstract Fe 3 O 4 @Cu/C and Fe 3 O 4 @CuO composites were achieved using nanoparticle-encapsulated MOFs Fe 3 O 4 @HKUST-1 as both a precursor and a self-sacrificing template. Fe 3 O 4 @HKUST-1 was thermally converted into magnetic Fe 3 O 4 @Cu/C and Fe 3 O 4 @CuO composites in different atmosphere (N 2 and air). The resulting composites not only kept superparamagnetic characteristics, but also exhibited improved peroxidase-like catalytic activity and high stability when compared to the precursor Fe 3 O 4 @HKUST-1. The morphology, crystal structure, magnetic and porous properties of Fe 3 O 4 @Cu/C and Fe 3 O 4 @CuO composites were characterized, and the kinetics parameters and the influence factors on the peroxidase-mimicking activity such as temperature, pH and H 2 O 2 concentration were evaluated. On account of the excellent peroxidase-like activity, the as-prepared Fe 3 O 4 @Cu/C and Fe 3 O 4 @CuO composites were successfully used for the catalytic removal of methylene blue (MB) dye with H 2 O 2 oxidant. This work provides an effective way to fabricate highly reactive MOFs-derived biomimetic catalysts, which have potential applications in bioassays and pollutant degradation. Graphic Abstract Fe 3 O 4 @Cu/C and Fe 3 O 4 @CuO composites were achieved using Fe 3 O 4 nanoparticle-encapsulated HKUST-1 as self-sacrificial templates and demonstrated excellent peroxidase-like activity.

研究领域: 材料科学 · 催化化学 · 环境科学
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RARE METAL MATERIALS AND ENGINEERING · 2014 · IF 0.153

Fabrication of Magnetic Fe3O4 Nanotubes by Electrospinning

Cao Xingxing,Zhang Xuebin,Shao Hao,Feng Yi

Ferroferric oxide nanotubes were prepared by calcining and reducing the composite nanofiber precursors fabricated by electrospinning. Influences of the electrospun parameters (PVA concentration of solution, applied voltage and collector distance) on the preparation of the composite nanofiber precursors were discussed. The structural properties of the obtained nanotubes were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The formation mechanism of the Fe 3 O 4 nanotubes was investigated through the nonequilibrium heat-treatment procedure. Furthermore, the magnetic property of Fe 3 O 4 was measured using a vibrating sample magnetometer. Results reveal that the tubes show a uniform and continuous morphology, whose outer and inner diameters are about 100 nm and 50 nm, respectively. Fe 3 O 4 possesses saturation magnetization ( M s ) of 54.2 A·m 2 /kg, coercivity ( H c ) of 215×79.6 A/m and remanent magnetization ( M r ) of 12.8 A·m 2 /kg, respectively.

研究领域: 材料科学 · 纳米技术
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Batteries-Basel · 2023 ·Vol. 9 ·期 6 ·326 · IF 4

Construction of Fe3O4@Fe2P Heterostructures as Electrode Materials for Supercapacitors

Congcong Lu,Chengyu Tu,Yu Yang,Yunping Ma,Maiyong Zhu

Considering their high abundance in the earth, iron-based materials have occasionally been regarded as promising electrode materials for supercapacitors. However, monometallic iron-based electrodes still demonstrate an insufficient specific capacitance value in comparison to monometallic Mn-, Ni-, and Co-based compounds and their combined materials. Herein, an enhanced iron-based heterostructure of Fe3O4@Fe2P was prepared via the in situ phosphorization of Fe3O4. Compared to pristine Fe3O4, the Fe3O4@Fe2P heterostructure showed a capacity enhancement in KOH aqueous solution. The improved electrochemical performance can be attributed to both the core shell structure, which favors buffering the collapse of the electrode, and the synergistic effect between the two iron compounds, which may provide abundant interfaces and additional electrochemically active sites. Moreover, the assembled asymmetric supercapacitor device using the Fe3O4@Fe2P heterostructure as the positive electrode and activated carbon as the negative electrode delivers a high energy density of 13.47 Wh kg−1, a high power density of 424.98 W kg−1, and an acceptable capacitance retention of 78.5% after 5000 cycles. These results clarify that monometallic Fe based materials can deliver a potential practical application. In addition, the construction method for the heterostructure developed here, in which different anion species are combined, may represent a promising strategy for designing high-performance electrodes.Keywords:Fe3O4;Fe2P;supercapacitor

CAS / MDL: 7440-44-0 64365-11-3
研究领域: 材料科学 · 电化学
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RSC Advances · 2020 ·Vol. 10 ·期 44 ·26142-26150 · IF 3.119

Magnetic core–shell Fe3O4@Cu2O and Fe3O4@Cu2O–Cu materials as catalysts for aerobic oxidation of benzylic alcohols assisted by TEMPO and N-methylimidazole

Binyu Xu,Samuthirarajan Senthilkumar,Wei Zhong,Zhongquan Shen,Chunxin Lu,Xiaoming Liu

In this work, core–shell Fe3O4@Cu2O and Fe3O4@Cu2O–Cu nanomaterials for aerobic oxidation of benzylic alcohols are reported with 2,2,6,6-tetramethylpiperidine-N-oxyl (TEMPO) and N-methylimidazole (NMI) as the co-catalysts. To anchor Cu2O nanoparticles around the magnetic particles under solvothermal conditions, the magnetic material Fe3O4 was modified by grafting a layer of L-lysine (L-Lys) to introduce –NH2 groups at the surface of the magnetic particles. With amine groups as the anchor, Cu(NO3)2 was used to co-precipitate the desired Cu2O by using ethylene glycol as the reducing agent. Prolonging the reaction time would lead to over-reduced forms of the magnetic materials in the presence of copper, Fe3O4@Cu2O–Cu. The nanomaterials and its precursors were fully characterized by a variety of spectroscopic techniques. In combination with both TEMPO and NMI, these materials showed excellent catalytic activities in aerobic oxidation of benzylic alcohols under ambient conditions. For most of the benzylic alcohols, the conversion into aldehydes was nearly quantitative with aldehydes as the sole product. The materials were recyclable and robust. Up to 7 repeat runs, its activity dropped less than 10%. The over-reduced materials, Fe3O4@Cu2O–Cu, exhibited slightly better performance in durability. The magnetic properties allowed easy separation after reaction by simply applying an external magnet.

研究领域: 材料科学 · 催化 · 化学工程 · 纳米技术
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Desalination and Water Treatment · 2025 · IF 1

Effect of Fe3O4 substrate preparation method for Fe3O4/Ag composite on methyl orange and 4-nitrophenol catalytic reduction

An Nang Vu,Ngoc – Hoa T. Le,Thanh- My T. Nguyen,Uyen N. Nguyen-Thai,Kim – Phung L. Nguyen,Lan Duc Vu

We present a straightforward method for creating reusable magnetic Fe 3 O 4 /Ag catalysts. Three distinct Fe 3 O 4 varieties were synthesized using different methods, and Ag nanoparticles were deposited onto the Fe 3 O 4 matrix via a hydrothermal process. The resulting Fe 3 O 4 and Fe 3 O 4 /Ag materials were characterized by XRD, XPS, FT-IR, Raman, DLS, FE-SEM, TEM, EDX, VSM, and UV-Vis spectroscopy. XRD analysis of the Fe 3 O 4 particles synthesized using the solvothermal reduction process (S2) revealed firm diffraction peaks, indicating high crystallinity. After hydrothermal treatment, S2/Ag retained a hollow spherical morphology and magnetic properties similar to Fe 3 O 4 . The synthesized Fe 3 O 4 /Ag catalytic performance was evaluated for the reduction of 4-nitrophenol (4-NP) and methyl orange (MO) dye in the presence of NaBH 4 . All catalysts effectively reduced both dyes and could be magnetically separated from the aqueous solution. The P1/Ag catalyst achieved over 95 % reduction of MO and 4-NP within 2 minutes. S2/Ag exhibited superior stability, preventing Ag leaching during the reaction. Furthermore, its high saturation magnetization allows easy magnetic extraction from the solution. These findings strongly suggest S2/Ag as a promising catalyst due to its selectivity and advantageous properties.

研究领域: 材料科学 · 环境化学
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CHEMOSPHERE · 2024 · IF 8.1

Enhanced uranium removal from aqueous solution by core–shell Fe0@Fe3O4: Insight into the synergistic effect of Fe0 and Fe3O4

Shizong Wang,Jun Hu,Jianlong Wang

In this study, Fe 0 @Fe 3 O 4 was synthesized and used to remove U(VI) from groundwater. Different experimental conditions and cycling experiments were used to investigate the performance of Fe 0 @Fe 3 O 4 in the U(VI) removal, and the XRD, TEM, XPS and XANES techniques were employed to characterize the Fe 0 @Fe 3 O 4 . The results showed that the U(VI) removal efficiency of Fe 0 @Fe 3 O 4 was 48.5 mg/g that was higher than the sum of removal efficiency of Fe 0 and Fe 3 O 4 . The uranium on the surface of Fe 0 @Fe 3 O 4 mainly existed as U(IV), followed by U(VI) and U(V). The Fe 0 content decreased after reaction, while the Fe 3 O 4 content increased. Based on the results of experiments and characterization, the enhanced removal efficiency of Fe 0 @Fe 3 O 4 was attributed to the synergistic effect of Fe 0 and Fe 3 O 4 in which Fe 3 O 4 accelerated the Fe 0 corrosion that promoted the progressively formation of Fe(II) that promoted the reduction of adsorbed U(VI) to U(IV) and incorporated U(VI) to U(V). The performance of Fe 0 @Fe 3 O 4 at near-neutrality condition was better than at acidic and alkalic conditions. The chloride ions, sulfate ions and nitrate ions showed minor effect on the Fe 0 @Fe 3 O 4 performance, while carbonate ions exhibited significant inhibition. The metal cations showed different effect on the Fe 0 @Fe 3 O 4 performance. The removal efficiency of Fe 0 @Fe 3 O 4 decreased with the number of cycling experiment. Ionizing radiation could regenerate the used Fe 0 @Fe 3 O 4 . This study provides insight into the U(VI) removal by Fe 0 @Fe 3 O 4 in aqueous solution.

研究领域: 环境科学 · 材料科学
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Nanomaterials · 2023 ·Vol. 13 ·期 4 ·707 · IF 5.3

Facile Synthesis of Hollow Fe3O4-rGO Nanocomposites for the Electrochemical Detection of Acetaminophen

Lazhen Shen,Jinlong Dong,Bin Wen,Xiangping Wen,Jianhui Li

Acetaminophen (AC) is one of the most popular pharmacologically active substances used as an analgesic and antipyretic drug. Herein, a new type of hollow Fe3O4-rGO/GCE electrode was prepared for electrochemical detection of AC through a three-step approach involving a solvothermal method for the synthesis of hollow Fe3O4and the chemical reduction of graphene oxide (GO) for reduced graphene oxide (rGO) and Fe3O4-rGO nanocomposites modified on the glassy carbon electrode (GCE) surface. The as-prepared Fe3O4-rGO nanocomposites were characterized using a transmission electron microscope (TEM), X-ray diffraction (XRD), and a magnetic measurement system (SQUID-VSM). The magnetic Fe3O4-rGO/GCE electrodes were employed for the electrochemical detection of AC using cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and square wave voltammetry (SWV) and exhibited an ultra-high selectivity and accuracy, a low detection limit of 0.11 µmol/L with a wider linear range from 5 × 10−7to 10−4mol/L, and high recovery between 100.52% and 101.43%. The obtained Fe3O4-rGO-modified GCE displays great practical significance for the detection of AC in drug analysis.Keywords:acetaminophen;electrochemical detection;hollow Fe3O4nanoparticles;magnetic Fe3O4-rGO/GCE electrode

研究领域: 分析化学 · 纳米材料 · 电化学 · 药物分析
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Materials · 2021 ·Vol. 15 ·期 1 ·115 · IF 3.623

Fabrication of PDMS@Fe3O4/MS Composite Materials and Its Application for Oil-Water Separation

Jiaqi Wang,Zhenzhong Fan,Qingwang Liu,Qilei Tong,Biao Wang

The discharge of oily wastewater and oil spills at sea are the current difficulties in water pollution control. This problem often leads to terrible disasters. Therefore, the effective realization of oil-water separation is a very challenging problem. Superhydrophobic sponge is a promising oil-absorbing material. In this article, we reported a superhydrophobic sponge with nano-Fe3O4for oil-water separation. The addition of nano-Fe3O4allows the sponge to be recycled under the action of magnetic force. The sponge has the advantages of low cost, simple preparation and efficient oil-water separation. This kind of sponge is very worthy of promotion for the treatment of oily wastewater and marine oil spill accidents.

研究领域: 材料科学 · 环境科学
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PROCESS SAFETY AND ENVIRONMENTAL PROTECTION · 2025 · IF 7.8

Enhanced removal of gatifloxacin by Fe3O4@bacteria: Performance and mechanism

Jianfu Man,Xinran Wang,Wenpeng Jia,Yongzheng Tang,Yongrui Pi

A novel magnetic biobased material, synthesized from nano Fe 3 O 4 and degrading-bacteria, was developed for the effective removal of gatifloxacin (GAT). Investigations into various parameters influencing the adsorption process revealed that the optimal adsorption capacity of 56.63 mg/g for GAT was achieved under mildly acidic conditions. Furthermore, the adsorption capacity of GAT increased with temperature, specifically within the range of 20 °C to 30 °C, while a decrease was noted at lower concentrations of NaCl. The adsorption kinetics of GAT onto Fe 3 O 4 @bacteria were best described by the pseudo-second-order (PSO) kinetic model and the Langmuir isotherm model. Thermodynamic evaluations confirmed that the adsorption process was both endothermic and spontaneous. The primary mechanisms driving the adsorption of GAT included pore filling, π-π conjugation, hydrogen bonding, and electrostatic interactions. Therefore, Fe 3 O 4 @bacteria was established as an effective and environmentally sustainable adsorbent for the removal of GAT.

研究领域: 环境科学 · 微生物学
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CLAYS AND CLAY MINERALS · 2019 ·Vol. 67 ·期 4 ·275-282 · IF 1.835

Synthesis of Magnetic Fe3O4 Nanorings for BSA Protein Adsorption

Liu Xiaonan,Zhang Youkui,Bian Liang,Li Jinshan

The adsorption of bovine serum albumin (BSA) protein is important for protein research but remains a great challenge. Here, the hydrothermal method and calcination in a hydrogen-argon mixed atmosphere were used to obtain ordered mono-crystalline magnetic Fe 3 O 4 nanorings with controllable size and uniform structure, which were applied to the adsorption of BSA protein. The results showed that the magnetic Fe 3 O 4 nanorings prepared have the advantages of good crystallinity, controllable morphology, and excellent magnetic response. The Fe 3 O 4 nanorings had an outer diameter of ~160–180 nm, inner diameter of ~80–110 nm, and height of 70 to ~110 nm. The amount of BSA adsorbed by magnetic Fe 3 O 4 nanorings increased with increasing protein concentration; when the concentration of BSA was ~2.75 mg·mL -1 the adsorption amount approached saturation. When the pH value of the solution was ~5, the Fe 3 O 4 nanorings absorption of BSA was greatest. With increasing adsorption time, the amount adsorbed increased gradually. Adsorption equilibrium was reached after 3 h. According to the formula, the saturated adsorption capacity of BSA per gram of magnetic Fe 3 O 4 nanorings was 325.2 mg. .

CAS / MDL: 6104-58-1
研究领域: 生物化学 · 材料科学
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