Self-assembly and embedding of nanoparticles by in situ reduced graphene for preparation of a 3D graphene/nanoparticle aerogel

A 3D graphene architecture can be prepared via an in situ self-assembly of graphene prepared by a mild chemical reduction. Fe(3) O(4) nanoparticles are homogeneously dispersed into graphene oxide (GO) aqueous suspension and a 3D magnetic graphene/Fe(3) O(4) aerogel is prepared during the reduction of GO to graphene. This provides a general method to prepare 3D graphene/nanoparticle composites for a wide range of applications including catalysis and energy conversion.     

Supraparamagnetic, conductive, and processable multifunctional graphene nanosheets coated with high-density Fe3O4 nanoparticles

The amazing properties of graphene are triggering extensive interests of both scientists and engineers, whereas how to fully utilize the unique attributes of graphene to construct novel graphene-based composites with tailor-made, integrated functions remains to be a challenge. Here, we report a facile approach to multifunctional iron oxide nanoparticle-attached graphene nanosheets (graphene@Fe(3)O(4)) which show the integrated properties of strong supraparamagnetism, electrical conductivity, highly chemical reactivity, good solubility, and excellent processability. The synthesis method is efficient, scalable, green, and controllable and has the feature of reduction of graphene oxide and formation of Fe(3)O(4) nanoparticles in one step. When the feed ratios are adjusted, the average diameter of Fe(3)O(4) nanoparticles (1.2-6.3 nm), the coverage density of Fe(3)O(4) nanoparticles on graphene nanosheets (5.3-57.9%), and the saturated magnetization of graphene@Fe(3)O(4) (0.5-44.1 emu/g) can be controlled readily. Because of the good solubility of the as-prepared graphene@Fe(3)O(4), highly flexible and multifunctional films composed of polyurethane and a high content of graphene@Fe(3)O(4) (up to 60 wt %) were fabricated by the solution-processing technique. The graphene@Fe(3)O(4) hybrid sheets showed electrical conductivity of 0.7 S/m and can be aligned into a layered-stacking pattern in an external magnetic field. The versatile graphene@Fe(3)O(4) nanosheets hold great promise in a wide range of fields, including magnetic resonance imaging, electromagnetic interference shielding, microwave absorbing, and so forth.     

An efficientfficient,controllable and facile two-step synthesis strategy: Fe<Subscript>3</Subscript>O<Subscript>4</Subscript>@RGO composites with various Fe<Subscript>3</Subscript>O<Subscript>4</Subscript> nanoparticles and their supercapacitance properties

An efficient,controllable,and facile two-step synthetic strategy to prepare graphene-based nanocomposites is proposed.A series of Fe3O4-decorated reduced graphene oxide (Fe3O4@RGO) nanocomposites incorporating Fe3O4 nanocrystals of various sizes were prepared by an ethanothermal method using graphene oxide (GO) and monodisperse Fe3O4 nanocrystals with diameters ranging from 4 to 10 nm.The morphologies and microstructures of the as-prepared composites were characterized by X-ray diffraction,Raman spectroscopy,nitrogen adsorption measurements,and transmission electron microscopy.The results show that GO can be reduced to graphene during the ethanothermal process,and that the Fe3O4 nanocrystals are well dispersed on the graphene sheets generated in the process.The analysis of the electrochemical properties of the Fe3O4@RGO materials shows that nanocomposites prepared with Fe3O4 nanocrystals of different sizes exhibit different electrochemical performances.Among all samples,Fe3O4@RGO prepared with Fe3O4 nanocrystals of 6 nm diameter possessed the highest specific capacitance of 481 F/g at 1 A/g,highlighting the excellent capability of this material.This work illustrates a promising route to develop graphene-based nanocomposite materials with a wide range of potential applications.     

Magnetic Fe3O4-Reduced Graphene Oxide Nanocomposites-Based Electrochemical Biosensing

Nano-Micro Letters - An electrochemical biosensing platform was developed based on glucose oxidase (GOx)/Fe3O4- reduced graphene oxide (Fe3O4-RGO) nanosheets loaded on the magnetic glassy carbon...     

Removal of methylene blue from aqueous solution by a solvothermal-synthesized graphene/magnetite composite

In this study, we have demonstrated a facile one-step solvothermal method for the synthesis of the graphene nanosheet (GNS)/magnetite (Fe(3)O(4)) composite. During the solvothermal treatment, in situ conversion of FeCl(3) to Fe(3)O(4) and simultaneous reduction of graphene oxide (GO) into graphene in ethylene glycol solution were achieved. Electron microscopy study suggests the Fe(3)O(4) spheres with a size of about 200 nm are uniformly distributed and firmly anchored on the wrinkled graphene layers with a high density. The resulting GNS/Fe(3)O(4) composite shows extraordinary adsorption capacity and fast adsorption rates for removal of organic dye, methylene blue (MB), in water. The adsorption kinetics, isotherms and thermodynamics were investigated in detail to reveal that the kinetics and equilibrium adsorptions are well-described by pseudo-second-order kinetic and Langmuir isotherm model, respectively. The thermodynamic parameters reveal that the adsorption process is spontaneous and endothermic in nature. This study shows that the as-prepared GNS/Fe(3)O(4) composite could be utilized as an efficient, magnetically separable adsorbent for the environmental cleanup.     

Composites of aminodextran-coated Fe3O4 nanoparticles and graphene oxide for cellular magnetic resonance imaging

Formation of composites of dextran-coated Fe(3)O(4) nanoparticles (NPs) and graphene oxide (Fe(3)O(4)-GO) and their application as T(2)-weighted contrast agent for efficient cellular magnetic resonance imaging (MRI) are reported. Aminodextran (AMD) was first synthesized by coupling reaction of carboxymethyldextran with butanediamine, which was then chemically conjugated to meso-2,3-dimercaptosuccinnic acid-modified Fe(3)O(4) NPs. Next, the AMD-coated Fe(3)O(4) NPs were anchored onto GO sheets via formation of amide bond in the presence of 1-ethyl-3-(3-dimethyaminopropyl) carbodiimide (EDC). It is found that the Fe(3)O(4)-GO composites possess good physiological stability and low cytotoxicity. Prussian Blue staining analysis indicates that the Fe(3)O(4)-GO nanocomposites can be internalized efficiently by HeLa cells, depending on the concentration of the composites incubated with the cells. Furthermore, compared with the isolated Fe(3)O(4) NPs, the Fe(3)O(4)-GO composites show significantly enhanced cellular MRI, being capable of detecting cells at the iron concentration of 5 μg mL(-1) with cell density of 2 × 10(5) cells mL(-1), and at the iron concentration of 20 μg mL(-1) with cell density of 1000 cells mL(-1).     

Fe_3O_4-ODA/GO/PANI复合材料的制备及其电容性能

在当今能源紧缺的情况下,超级电容器由于具有功率密度高、充放电时间短、循环寿命长等优点而被广泛应用于工业自动化控制、电力、国防以及新能源汽车等众多领域。本文以十八胺修饰的四氧化三铁纳米粒子(Fe_3O_4-ODA),氧化石墨烯(GO)以及苯胺单体为原料,通过原位聚合成功制备了Fe_3O_4-ODA/GO/PANI三元复合电极材料,其比电容高达516F/g,远高于二元复合材料GO/PANI和Fe_3O_4-ODA/PANI的比电容(分别为224F/g和345F/g)。并且,在1000次循环充放电之后,其容量仍可维持86.5%。此外,利用扫描电子显微镜(SEM)、透射电子显微镜(TEM)、X射线粉末衍射(XRD)和傅立叶变换红外光谱仪(FT-IR)等手段对该复合材料的形貌和结构进行了表征。     

Graphene-encapsulated hollow Fe₃O₄ nanoparticle aggregates as a high-performance anode material for lithium ion batteries

Graphene-encapsulated ordered aggregates of Fe(3)O(4) nanoparticles with nearly spherical geometry and hollow interior were synthesized by a simple self-assembly process. The open interior structure adapts well to the volume change in repetitive Li(+) insertion and extraction reactions; and the encapsulating graphene connects the Fe(3)O(4) nanoparticles electrically. The structure and morphology of the graphene-Fe(3)O(4) composite were confirmed by X-ray diffraction, scanning electron microscopy, and high-resolution transmission microscopy. The electrochemical performance of the composite for reversible Li(+) storage was evaluated by cyclic voltammetry and constant current charging and discharging. The results showed a high and nearly unvarying specific capacity for 50 cycles. Furthermore, even after 90 cycles of charge and discharge at different current densities, about 92% of the initial capacity at 100 mA g(-1) was still recoverable, indicating excellent cycle stability. The graphene-Fe(3)O(4) composite is therefore a capable Li(+) host with high capacity that can be cycled at high rates with good cycle life. The unique combination of graphene encapsulation and a hollow porous structure definitely contributed to this versatile electrochemical performance.     

基于Pd/Fe3O4/rGO纳米复合材料的H2O2无酶传感器

环境监测、食品工业、临床、制药等领域对过氧化氢(H_2O_2)的快速、准确检测有极大的需求,而电化学检测方法由于灵敏度高、响应快、检测限低等特点被认为是最理想的H_2O_2检测方法.本文利用电化学沉积的方法将Pd纳米颗粒沉积到四氧化三铁/石墨烯(Fe_3O_4/rGO)纳米复合材料修饰的玻碳电极表面,形成基于新型磁性纳米复合材料的H_2O_2无酶传感器;并采用循环伏安和计时安培电流等方法对修饰电极的电化学性能进行了表征.结果表明:制备的Pd/Fe_3O_4/r GO/GCE对H_2O_2的催化还原显示出较好的电催化活性,Pd纳米颗粒和Fe_3O_4/rGO在催化H_2O_2还原的过程中表现出了良好的协同作用.测定H_2O_2的线性范围为0.05~1 m M和1~2.6 m M两段,最低检测限达到3.918μM(S/N=3).并且该传感器具有较高的灵敏度和较好的重现性和抗干扰性,具有一定的实际应用价值.     

Optically stimulated luminescence from Al2O3:C irradiated with relativistic heavy ions.

Optically stimulated luminescence (OSL) from Al2O3:C (ALOC) irradiated with selected heavy ions (4He, 12C, 40Ar, and 56Fe) was examined for discussion on the effectiveness of ALOC for space radiation protection dosimetry. The OSL efficiency on the absorbed dose basis was almost unity for He (LETinfinity x H2O: 2.2 keV x microm(-1)) and decreased with increasing LET for C (14 keV x microm(-1)), Ar (91 keV x microm(-1)), and Fe (198 keV x microm(-1)); a notable reduction greater than 60%, was observed for Fe ions. The linearity in dose response and the angular independence for the heavy ions were fairly good (+/- <15%) Although further experimental studies are clearly necessary, these results suggest that small ALOC chips can be a part of an integrating dosimetry system in future space missions.     

Functional microspheres of graphene quantum dots

Graphene-quantum-dot microspheres (GQDSs) have been prepared by assembly of graphene quantum dots (GQDs) via a water-in-oil (W/O) emulsion technique without the addition of any surfactants. Although made of quantum-sized graphene dots, the as-formed GQDSs are solid and remain intact after slight ultrasonication. The versatile W/O emulsion method allows the in?situ intercalation of functional nanocomponents into the GQDSs for specific applications. As exemplified by the Fe(3)O(4)-containing GQDSs, Fe(3)O(4)-GQDSs exhibit a large magnetic response. Furthermore, the embedded Fe(3)O(4) nanoparticles in GQDSs can act as the catalysts for the growth of carbon nanotubes (CNTs), which opens the opportunities for fabricating new complex structures of CNTs surrounding GQDSs by simple chemical vapor deposition.     

Photocatalytic reduction of Cr(VI) on the new hetero-system CuAl2O4/TiO2

A magnetic adsorbent, amine-functionalized silica magnetite (NH(2)/SiO(2)/Fe(3)O(4)), has been synthesized to behave as an anionic or cationic adsorbent by adjusting the pH value of the aqueous solution to make amino groups protonic or neutral. NH(2)/SiO(2)/Fe(3)O(4) were used to adsorb copper ions (metal cation) and Reactive Black 5 (RB5, anionic dye) in an aqueous solution in a batch system, and the maximum adsorption were found to occur at pH 5.5 and 3.0, respectively. The adsorption equilibrium data were all fitted the Langmuir isotherm equation reasonably well, with a maximum adsorption capacity of 10.41 mg g(-1) for copper ions and of 217 m g g(-1) for RB5. A pseudo-second-order model also could best describe the adsorption kinetics, and the derived activation energy for copper ions and RB5 were 26.92 kJ mol(-1) and 12.06 kJ mol(-1), respectively. The optimum conditions to desorb cationic and anionic adsorbates from NH(2)/SiO(2)/Fe(3)O(4) were provided by a solution with 0.1M HNO(3) for copper ions and with 0.05 M NaOH for RB5.     

Microwave-enhanced synthesis of magnetic porous covalent triazine-based framework composites for fast separation of organic dye from aqueous solution

A novel type of magnetic porous carbonaceous polymeric material, CTF/Fe(2)O(3) composite (CTF = covalent triazine-based framework), has been synthesized by a facile microwave-enhanced high-temperature ionothermal method. By selecting ZnCl(2) as a reaction medium and the Lewis acid catalyst, and choosing FeCl(3)·6H(2)O as an iron oxide precursor, a series of CTF/Fe(2)O(3) composites with different γ-Fe(2)O(3) contents has been prepared in 60 min. The resulting samples were characterized by the X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), vibration sample magnetometer (VSM), and N(2) sorption-desorption isotherms. The obtained CTF/Fe(2)O(3) composites exhibit high surface areas (930-1149 m(2) g(-1)), and their saturation magnetizations at 300 K vary from 1.1 to 5.9 emu g(-1), depending respectively on different Fe(2)O(3) contents (6.43-12.43 wt%) in the CTF/Fe(2)O(3) composites. The CTF/Fe(2)O(3) composites were applied to remove organic dye from aqueous solution by selecting methyl orange as a model molecule, and both high adsorption capacity (291 mg g(-1), corresponding to 0.889 mmol g(-1)) and fast adsorption kinetics (k(ads) = 4.31 m(2) mg(-1) min(-1)) were observed.     

Synthesis of surface imprinted polymers based on wrinkled flower-like magnetic graphene microspheres with favorable recognition ability for BSA

Nowadays,the employing of molecular imprinting technique in the analysis and separation of proteins from complex biological samples has been widely favored by researchers.To enrich the types of surface protein imprinted materials and expand the application fields of graphene materials,novel surface molecular imprinted polymers (MIPs) based on magnetic graphene microspheres Fe304@rGO@MIPs are first synthesized in this paper.Fe304@rGO@MIPs are prepared by oxidative self-polymerization of dopamine on the surface of magnetic graphene (Fe304@rGO) composite microspheres.Bovine serum albumin (BSA) is selected as protein template.Fe3O4@rGO microspheres with wrinkled flower-like structure are obtained by compounding Fe3O4 and graphene oxide in an appropriate ratio via the method of high-temperature reduction self-assembly.The microspheres exhibit promising dispersibility,high external surface area,rich pore structure,and sufficient magnetic properties.These advantages not only prevent the agglomeration of imprinted microspheres in the aqueous phase,which is conducive to contact and static adsorption,but also increase the amount of protein imprinting.Additionally,sufficient magnetic properties ensure fast and effective separation of the adsorbents.While the adsorption capacity is increased,the separation procedure becomes simple.The binding capacity of Fe304@rGO@MIPs for BSA can reach 317.58 mg/g within 60 min,and the imprinting factor (IF) is 4.24.More importantly,Fe3O4@rGO@MIPs can specifically recognize the target BSA from the mixed proteins and the actual sample.There is no significant decrease in the adsorption amount,IF,and magnetic properties after eight runs.It is promising to be used in the separation of proteins from the actual biological samples.     

Facile synthesis of monodisperse ultrasmall Fe3O4 nanoparticles on graphene nanosheets with excellent microwave absorption performance

Journal of Materials Science: Materials in Electronics - The monodispersed ultrasmall Fe3O4 nanoparticles (NPs) have been anchored on reduced graphene oxide (rGO) nanosheets through a one-step...     

E36钢的海水腐蚀模拟试验研究

青岛海域投样初期的24 h内,电联接长尺试样上的阴阳极交错出现,并非潮差区为阴极,海水全浸区为阳极,与公认的氧浓差电池引起潮差区钢样受阴极保护之说不相符.在试验室内用人造海水和3%NaCl溶液模拟潮差区钢样的腐蚀环境,对干湿交替试样与全浸试样间的电偶电流进行了研究,探讨了潮差区钢样受阴极保护的原因.结果表明:潮差区试样表面锈层由FeOOH和Fe_3O_4组成,海水全浸区试样表面锈层由FeOOH组成,这种锈层结构的差异直接产生了试样间的腐蚀电位差,使潮差区的钢样受到了阴极保护,最终导致长尺试样在潮差区的腐蚀速率降低.     

Enhanced cycling performance of nanocrystalline Fe3O4/C as anode material for lithium-ion batteries

Fe3O4-carbon composite was prepared by the sol-gel method. The crystal structure, morphology, and phases present in the product were investigated by X-ray diffraction and by scanning electron microscopy (SEM) combined with energy dispersive X-ray spectroscopy and field-emission SEM. Electrochemical characterization was performed using constant current charge-discharge testing and electrochemical impedance spectroscopy. The Fe3O4/C electrode has high initial columbic efficiency (87%) and outstanding cycling performance (775.3 mAh g(-1) after 90 cycles at a current density of 100 mA g(-1)).     

Synthesis of covalently bonded reduced graphene oxide-Fe3O4 nanocomposites for efficient electromagnetic wave absorption

High-performance electromagnetic (EM) wave absorbers,covalently bonded reduced graphene oxide-Fe3O4 nanocomposites (rGO-Fe3O4),are synthesized via hydrothermal reaction,amidation reaction and reduction process.The microstructure,surface element composition and morphology of rGO-Fe3O4 nanocomposites are characterized and corresponding EM wave absorption properties are analyzed in great detail.It demonstrates that Fe3O4 nanoparticles are successfully covalently grafted onto graphene by amide bonds.When the mass ratio of rGO and Fe3O4 is 2∶1 (sample S2),the absorber exhibits the excellent EM wave absorption performance that the maximum reflection loss (RL) reaches up to-48.6 dB at 14.4 GHz,while the effective absorption bandwidth (RL＜-10 dB) is 6.32 GHz (11.68-18.0 GHz) with a matching thickness of 2.1 mm.Furthermore,radar cross section (RCS) simulation calculation is also adopted to evaluate the ability of absorbers to scatter EM waves,which proves again that the absorption performance of absorber S2 is optimal.The outstanding EM wave absorption performance is attributed to the synergistic effect between dielectric and magnetic loss,good attenuation ability and excellent impedance matching.Moreover,covalent bonds considered to be carrier channels can facilitate electron migration,adjust EM parameters and then enhance EM wave absorption performance.This work provides a possible method for preparing efficient EM wave absorbers.     

Fe(3)O(4) nanobelts: one-pot and template-free synthesis, magnetic property, and application for lithium storage

We report on the synthesis of Fe(3)O(4) nanobelts with good magnetic properties and lithium storage performances by using a one-pot and template-free hydrothermal method with Na(2)CO(3) and FeCl(2) as the reactants. By controlling the amount of Na(2)CO(3), we obtained pure Fe(3)O(4) nanobelts with widths of 0.1-2?μm, thicknesses of about 10 nm and lengths of 20-30?μm, showing a high aspect ratio. XRD and SAED patterns of the obtained sample demonstrated that the Fe(3)O(4) nanobelts were well crystallized. Nitrogen adsorption/desorption measurements showed that Fe(3)O(4) nanobelts manifested a BET surface area of 25.04?m(2)?g(-1). Further experiments demonstrated that the amount of Na(2)CO(3) played an important role in controlling both the morphologies and crystal structures of the products. The formation mechanism of Fe(3)O(4) nanobelts was also studied. More importantly, we found that the Fe(3)O(4) nanobelts showed magnetic properties with a magnetic saturation value of 77.0?emu?g(-1) and lithium storage performances with a high initial discharge capacity of 1090?mAh?g(-1) at a current rate of 500?mA?g(-1), and a reversible capacity of 404?mAh?g(-1) retained after 60 charge/discharge cycles. These results suggest that the Fe(3)O(4) nanobelts might be promising for magnetic and lithium battery applications.     

Humic acid coated Fe3O4 magnetic nanoparticles as highly efficient Fenton-like catalyst for complete mineralization of sulfathiazole

Humic acid coated Fe(3)O(4) magnetic nanoparticles (Fe(3)O(4)/HA) were prepared for the removal of sulfathiazole from aqueous media. Fe(3)O(4)/HA exhibited high activity to produce hydroxyl (OH) radicals through catalytic decomposition of H(2)O(2). The degradation of sulfathiazole was strongly temperature-dependent and favored in acidic solution. The catalytic rate was increased with Fe(3)O(4)/HA dosage and H(2)O(2) concentration. When 3 g L(-1) of Fe(3)O(4)/HA and 0.39 M of H(2)O(2) were introduced to the aqueous solution, most sulfathiazole was degraded within 1h, and >90% of total organic carbon (TOC) were removed in the reaction period (6h). The major final products were identified as environmentally friendly ions or inorganic molecules (SO(4)(2-), CO(2), and N(2)). The corresponding degradation rate (k) of sulfathiazole and TOC was 0.034 and 0.0048 min(-1), respectively. However, when 3 g L(-1) of bare Fe(3)O(4) were used as catalyst, only 54% of TOC was eliminated, and SO(4)(2-) was not detected within 6h. The corresponding degradation rate for sulfathiazole and TOC was 0.01 and 0.0016 min(-1), respectively. The high catalytic ability of Fe(3)O(4)/HA may be caused by the electron transfer among the complexed Fe(II)-HA or Fe(III)-HA, leading to rapid regeneration of Fe(II) species and production of OH radicals.