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1.
Data Storage: Developing Biotemplated Data Storage: Room Temperature Biomineralization of L10 CoPt Magnetic Nanoparticles (Adv. Funct. Mater. 29/2015)
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Johanna M. Galloway Jennifer E. Talbot Kevin Critchley Jim J. Miles Jonathan P. Bramble 《Advanced functional materials》2015,25(29):4744-4744
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Xingsen Gao Lifeng Liu Balaji Birajdar Michael Ziese Woo Lee Marin Alexe Dietrich Hesse 《Advanced functional materials》2009,19(21):3450-3455
A novel nanopatterning method using pulsed laser deposition through an ultrathin anodic aluminium oxide (AAO) membrane mask is proposed to synthesize well‐ordered nanodot arrays of magnetic CoFe2O4 that feature a wide range of applications like sensors, drug delivery, and data storage. This technique allows the adjustment of the array dimension from ~35 to ~300 nm in diameter and ~65 to ~500 nm in inter‐dot distance. The dot density can be as high as 0.21 Terabit in.?2. The microstructure of the nanodots is characterized by SEM, TEM, and XRD and their magnetic properties are confirmed by well‐defined magnetic force microscopy contrasts and by hysteresis loops recorded by a superconducting quantum interference device. Moreover, the high stability of the AAO mask enables the epitaxial growth of nanodots at a temperature as high as 550 °C. The epitaxial dots demonstrate unique complex magnetic domains such as bubble and stripe domains, which are switchable by external magnetic fields. This patterning method creates opportunities for studying novel physics in oxide nanomagnets and may find applications in spintronic devices. 相似文献
3.
Zhen Li Pei Wei Yi Qiao Sun Hao Lei Hong Li Zhao Zhong Hua Zhu Sean C. Smith Min Bo Lan Gao Qing Lu 《Advanced functional materials》2012,22(11):2387-2393
Monodispersed water‐soluble and biocompatible ultrasmall magnetic iron oxide nanoparticles (UMIONs, D = 3.3 ± 0.5 nm) generated from a high‐temperature coprecipitation route are successfully used as efficient positive and negative dual contrast agents of magnetic resonance imaging (MRI). Their longitudinal relaxivity at 4.7 T (r1 = 8.3 mM?1 s?1) is larger than that of clinically used T1‐positive agent Gd‐DTPA (r1 = 4.8 mM?1 s?1), and three times that of commercial contrast agent SHU‐555C (r1 = 2.9 mM?1 s?1). The transversal relaxivity (r2 = 35.1 mM?1 s?1) is six times that of Gd‐DTPA (r2 = 5.3 mM?1 s?1), half of SHU‐555C (r2 = 69 mM?1 s?1). The in vivo results show that the liver signal from T1‐weighted MRI is positively enhanced 26%, and then negatively decreased 20% after injection of the iron oxide nanoparticles, which is stronger than those obtained from Gd‐DTPA (<10%) using the same dosage. The kidney signal is positively enhanced up to 35%, similar to that obtained from Gd‐DTPA. Under T2‐weighted conditions, the liver signal is negatively enhanced ?70%, which is significantly higher than that from Gd‐DTPA (?6%). These results demonstrate the great potential of the UMIONs in dual contrast agents, especially as an alternative to Gd‐based positive contrast agents, which have risks of inducing side effects in patients. 相似文献
4.
Jos J. M. Lenders Harshal R. Zope Ayana Yamagishi Paul H. H. Bomans Atsushi Arakaki Alexander Kros Gijsbertus de With Nico A. J. M. Sommerdijk 《Advanced functional materials》2015,25(5):711-719
Control over magnetite (Fe3O4) formation is difficult to achieve in synthetic systems without using non‐aqueous media and high temperatures. In contrast, Nature employs often intrinsically disordered proteins to tightly tailor the size, shape, purity, and organization of the nanocrystals to optimize their magnetic properties. Inspired by such “flexible polyelectrolytes,” here random copolypeptides having different amino acid compositions are used as control agents in the bioinspired coprecipitation of magnetite through a ferrihydrite precursor, following a recently developed mineralization protocol. Importantly, the copolypeptide library is designed such that the amino acid composition can be optimized to simultaneously direct the size of the nanoparticles as well as their dispersibility in aqueous media in a one‐pot manner. Acidic amino acids are demonstrated to regulate the crystal size by delaying nucleation and reducing growth. Their relative content thus can be balanced to tune between the superparamagnetic and ferrimagnetic regimes, and high contents of negatively charged amino acids result in colloidal stabilization of superparamagnetic nanoparticles at high pH. Conversely, with positively charged lysine‐rich copolypeptides ferrimagnetic crystals are obtained which are stabilized at neutral pH and self‐organize in chains, as visualized by cryo‐transmission electron microscopy. Altogether, the presented findings give important insights for the future development of additive‐mediated nanomaterial syntheses. 相似文献
5.
André Müller Sara E. C. Dale Miles A. Engbarth Simon J. Bending Laurence M. Peter Andreas Knittel Hans Fangohr 《Advanced functional materials》2011,21(10):1874-1880
Three dimensional ferromagnet–superconductor core–shell structures are realized by electrocrystallisation and their magnetic properties investigated. We observe fully re‐entrant core superconductivity in increasing fields that survives well above the bulk critical field due to compensation effects. The net measured magnetization of optimized structures could be switched from absolute para(ferro‐)magnetic to diamagnetic by tuning the external magnetic field. Micromagnetic simulations of the structures are in good qualitative agreement with our results. 相似文献
6.
Xiao Yang Zhenhua Li Hong Xiao Ning Wang Yanpu Li Xinyuan Xu Zhijun Chen Hong Tan Jianshu Li 《Advanced functional materials》2018,28(32)
A simple and universal method for manufacturing a mineralization coating on various surfaces is developed using a biofilm‐based material obtained from engineered curli nanofibers. The amyloid protein (CsgA) is the main proteinaceous component in the Escherichia coli (E. coli) biofilm, which can withstand detergents in the harsh environment. The peptide sequence DDDEEK is bioinspired from salivary acquired pellicles in the dental plaque biofilm, having a strong ability to absorb mineral ions and induce the formation of biominerals. The bioinspired coating is successfully secreted by the engineered E. coli, which is transformed with a recombinant plasmid for expression with T7 promoter (PET), namely PET‐22b‐CsgA‐DDDEEK plasmid. The uniform coating can bear shear force and stay on virtually any type of material surface for at least one month. Moreover, the coated slices had a good mineralization performance and better stability than hydroxyapatite (HA)‐spray slices. Furthermore, MG63 cells on the bioactive HA layer induced by the coating possess a better growth capacity than those on the commercial product Matrigel. The animal experiment results suggest that the coated Ti6Al4V screws with induced HA present better osteogenicity and osseointegration than HA‐sprayed screws after 12 weeks, as well as no extra immunogenicity. Thus, the coating is highly promising for biomedical applications. 相似文献
7.
Yuan Jiang Haofei Gong Maciej Grzywa Dirk Volkmer Laurie Gower Helmut Cölfen 《Advanced functional materials》2013,23(12):1547-1555
An easy design route via simple evaporation is reported for macroscopic mosaic thin films comprising the quaternary system of dl ‐lysine·HCl, poly(acrylic acid), water, and EtOH. By depositing droplets of the quaternary dispersions onto hydrophilic cover slips, the formation of macroscopic crack‐free mosaic mesocrystal thin films are produced. The formation follows a multistage crystallization process, which includes the formation of a polymer‐induced liquid‐precursor (PILP) phase, the formation of spherulitic thin films, and the recrystallization of mosaic mesocrystal thin films. A slow cooling rate is noted to be beneficial for the mesocrystal thin films, enabling the films to be crack‐free and to display low surface roughness at the nanoscale. 相似文献
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Anitha Ethirajan Ulrich Ziener Andrey Chuvilin Ute Kaiser Helmut Cölfen Katharina Landfester 《Advanced functional materials》2008,18(15):2221-2227
Here, we report a novel biomimetic strategy to synthesize hydroxyapatite (HAP) inside of crosslinked gelatin nanoparticles, which serve as a nanoenvironment for crystal growth in the aqueous phase. The synthesis of gelatin nanoparticles with the inverse miniemulsion technique is very intriguing because of the flexibility offered by the technique in tailoring the properties of the gelatin nanoparticles. It can be shown that the nanoenvironment promotes a different growth environment for the crystal because of the confinement inside the particle. The formation of HAP inside the particles follows Ostwald's rule of stages. At first an amorphous phase is formed, which itself has a great potential to be used as a resorbable bone substitute. This further transforms into single crystalline HAP via an octacalcium phosphate intermediate. The solution‐mediated transformation into the HAP phase without any calcination step is studied in detail using transmission electron microscopy (TEM) and X‐ray diffraction (XRD) measurements. 相似文献
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Kai Li Dan Ding Da Huo Kan‐Yi Pu Ngo Nguyen Phuong Thao Yong Hu Zhi Li Bin Liu 《Advanced functional materials》2012,22(15):3107-3115
A facile strategy is developed to synthesize dual‐modal fluorescent‐magnetic nanoparticles (NPs) with surface folic acid by co‐encapsulation of a far‐red/near‐infrared (FR/NIR)‐emissive conjugated polymer (PFVBT) and lipid‐coated iron oxides (IOs) into a mixture of poly(lactic‐co‐glycolic‐acid)‐poly(ethylene glycol)‐folate (PLGA‐PEG‐FOL) and PLGA. The obtained NPs exhibit superparamagnetic properties and high fluorescence, which indicates that the lipid coated on IOs is effective at separating the conjugated polymer from IOs to minimize fluorescence quenching. These NPs are spherical in shape with an average diameter of ≈180 nm in water, as determined by laser light scattering. In vitro studies reveal that these dual‐modal NPs can serve as an effective fluorescent probe to achieve targeted imaging of MCF‐7 breast cancer cells without obvious cytotoxicity. In vivo fluorescence and magnetic resonance imaging results suggest that the NPs are able to preferentially accumulate in tumor tissues to allow dual‐modal detection of tumors in a living body. This demonstrates the potential of conjugated polymer based dual‐modal nanoprobes for versatile in vitro and in vivo applications in future. 相似文献
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走过了半个世纪的磁储存技术,小型化牵动着数据储存和计算机硬盘到达了从未有过的高度。正在研究发展的热辅助记录技术和图形媒介技术将会给磁记录硬盘带来更高的面密度,从而使小型化在磁储存的框架内还将有一段路可走。但由于其物理限制,磁硬盘无法永远继续小下去,人们正在寻找新的出路。因此除了对磁储存正在发展的两项新技术之外,特别是对完全另辟新路的非磁数据储存技术,如纳米机械AFM数据储存技术、全息光储存技术以及原子储存技术进行了论述,以显示当前该领域前沿科技的发展概貌。 相似文献
13.
Weida D. Chen A. Xavier Kohll Bichlien H. Nguyen Julian Koch Reinhard Heckel Wendelin J. Stark Luis Ceze Karin Strauss Robert N. Grass 《Advanced functional materials》2019,29(28)
In this paper the practical density of long‐term DNA storage is increased. Specifically, the DNA weight loading of silica sphere DNA storage is increased to 3.4 wt%, a ten‐fold increase compared to the previous state‐of‐the‐art. By applying a Layer‐by‐Layer (LbL) design with alternating layers of DNA and a polycationic molecule, namely polyethyleneimine (PEI), another dimension to DNA surface binding onto magnetic nanoparticles is added. A protective silica layer is grown on top of the multilayered nanoparticles to shield the DNA from external sources of damage. Accelerated aging experiments of the nanoparticles and the subsequent quantification of DNA stability via qPCR show a significantly lower degradation rate compared to unprotected DNA. The novel material is compared to previous DNA storage technologies, outperforming those in DNA storage density as well as stability. Finally, the storage of an 83 kB digital file in DNA through a successful readout of a 4991 oligonucleotide pool is demonstrated from particle encapsulation, through accelerated aging, to sequencing. 相似文献
14.
Microorganisms are widely used as the biotemplates for producing micro/nanomaterials owing to their unique features, such as exquisite morphology, renewable, and environmentally friendly. However, mass intracellular synthesis of uniformly dispersed nanoparticles (NPs) inside microorganisms is still challenging, especially in a predictable and controllable manner. Here, a facile and efficiency strategy is proposed to controllably produce highly dispersed and surfactant‐free Pd@Ag core–shell NPs within the Spirulina platensis (Sp.) cells. In this approach, the Sp. cells' permeability is enhanced by the hydrochloric acid treatment first, which enables the Pd NPs penetrate the cell envelope and distribute uniformly inside the cells, and then they can work as the catalytic seeds for the following electroless silver deposition, resulting in the intracellular fabrication of Pd@Ag core–shell NPs with no agglomeration. The Pd@Ag NPs show excellent catalytic activity (turnover frequency is up to 2893 h?1 for the 6.32 nm Pd@Ag NPs), good stability, and recyclability toward the 4‐nitrophenol reductions. The excellent properties are attributed to the asymmetrical core–shell structure, small size, and good dispersion of Pd@Ag NPs. Due to its facility, cost‐effectiveness, and versatility, this method can be expanded to other microorganisms, so it opens tremendous opportunities for various metallic nanoparticles intracellular synthesis as well as the practical application. 相似文献
15.
Yanjun Jiang Dong Yang Lei Zhang Qianyun Sun Xiaohui Sun Jian Li Zhongyi Jiang 《Advanced functional materials》2009,19(1):150-156
A novel approach combining layer‐by‐layer (LbL) assembly with biomimetic mineralization is proposed to prepare protamine–titiania hybrid microcapsules. More specifically, these microcapsules are fabricated by alternative deposition of positively charged protamine layers and negatively charged titania layers on the surface of CaCO3 microparticles, followed by dissolution of the CaCO3 microparticles using EDTA. During the deposition process, the protamine layer induces the hydrolysis and condensation of a titania precursor, to form the titania layer. Thereafter, the negatively charged titania layer allows a new cycle of deposition step of the protamine layer, which ensures a continuous LbL process. The morphology, structure, and chemical composition of the microcapsules are characterized by scanning electron microscopy, transmission electron microscopy, Fourier transform infrared, and X‐ray photoelectron spectroscopy. Moreover, these protamine–titania hybrid microcapsules are first employed as the carrier for the immobilization of yeast alcohol dehydrogenase (YADH), and the encapsulated YADH displays enhanced recycling stability. This approach may open a facile, general, and efficient way to prepare organic–inorganic hybrid materials with different compositions and shapes. 相似文献
16.
Carlos Martinez‐Boubeta Konstantinos Simeonidis David Serantes Iván Conde‐Leborán Ioannis Kazakis George Stefanou Luis Peña Regina Galceran Lluis Balcells Claude Monty Daniel Baldomir Manassis Mitrakas Makis Angelakeris 《Advanced functional materials》2012,22(17):3737-3744
The Fe‐MgO core‐shell morphology is proposed within the single‐domain nanoparticle regime as an enhanced magnetically driven hyperthermia carrier. The combinatory use of metallic iron as a core material together with the increased particle size (37–65 nm) triggers the tuning of dipolar interactions between particles and allows for further enhancement of their collective heating efficiency via concentration control. A theoretical universal estimation of hysteresis losses reveals the role of dipolar interactions on heating efficiency and outlines the strong influence of coupling effects on hyperthermia opening a novel roadmap towards multifunctional heat‐triggered theranostics particles. 相似文献
17.
Qingchen Dong Guijun Li Cheuk‐Lam Ho Chi‐Wah Leung Philip Wing‐Tat Pong Ian Manners Wai‐Yeung Wong 《Advanced functional materials》2014,24(6):857-862
Hard ferromagnetic (L10 phase) FePt alloy nanoparticles (NPs) with extremely high magnetocrystalline anisotropy are considered to be one of the most promising candidates for the next generation of ultrahigh‐density data storage system. The question of how to generate ordered patterns of L10‐FePt NPs and how to transform the technology for practical applications represents a key current challenge. Here the direct synthesis of L10 phase FePt NPs by pyrolysis of Fe‐containing and Pt‐containing metallopolymer blend without post‐annealing treatment is reported. Rapid single‐step fabrication of large‐area nanodot arrays (periodicity of 500 nm) of L10‐ordered FePt NPs can also be achieved by employing the metallopolymer blend, which possesses excellent solubility in most organic solvents and good solution processability, as the precursor through nanoimprint lithography (NIL). Magnetic force microscopy (MFM) imaging of the nanodot pattern indicates that the patterned L10 phase FePt NPs are capable of exhibiting decent magnetic response, which suggests a great potential to be utilized directly in the fabrication of bit patterned media (BPM) for the next generation of magnetic recording technology. 相似文献
18.
Brandon Mattix Timothy R. Olsen Thomas Moore Megan Casco Dan Simionescu Richard P. Visconti Frank Alexis 《Advanced functional materials》2014,24(6):800-807
Nanomaterials including gold nanoparticles, polymeric nanoparticles, and magnetic iron oxide nanoparticles are utilized in tissue engineering for imaging, drug delivery, and maturation. Prolonged presence of these nanomaterials within biological systems remains a concern due to potential adverse affects on cell viability and phenotype. Accelerating nanomaterial degradation within biological systems is expected to reduce the potential adverse effects in the tissue. Similar to biodegradable polymeric scaffolds, the ideal nanomaterial remains stable for sufficient time to accomplish its desired task, and then rapidly degrades once that task is completed. Here, surface modifications are reported to accelerate iron oxide MNP degradation mediated by polymer encapsulation, in which iodegradable coatings composed of FDA approved polymers with different degradation rates are used: poly(lactide) (PLA) or copolymer poly(lactide‐co‐glycolide) (PLGA). Results demonstrate that degradation of MNPs can be controlled by varying the content and composition of the polymeric nanoparticles used for MNP encapsulation (PolyMNPs). Incorporated into cellular spheroids, PolyMNPs maintain a high viability compared to non‐coated MNPs, and are also useful in magnetically patterning cellular spheroids into fused tissues for tissue engineering applications. Accelerated degradation compared to non‐coated MNPs makes PolyMNPs a viable alternative for removing nanomaterials from tissues after accomplishing their desired role. 相似文献
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《Advanced functional materials》2018,28(37)
Magnetic hyperthermia (MHT) and photothermal therapy (PTT) are emergent state‐of‐the‐art modalities for thermal treatment of cancer. While their mechanisms of action have distinct physical bases, both approaches rely on nanoparticle‐mediated remote onset of thermotherapy. Yet, are the two heating techniques interchangeable? Here, the heating obtained either with MHT or with PTT is compared. The heating is assessed in distinct environments and involves a set of nanomaterials differing in shape (spheres, cubes, stars, shells, and rods) as well as in composition (maghemite, magnetite, cobalt ferrite, and gold). The nanoparticle's heating efficacy in an aqueous medium is first evaluated. Subsequently, the heating efficiency within the cellular environment, where intracellular processing markedly decreases MHT, is compared. Conversely, endosomal sequestration could have a positive effect on PTT. Finally, iron oxide nanocubes and gold nanostars are compared in MHT and PTT in vivo within the heterogeneous intratumoral environment. Overall, two distinct therapeutic approaches, related to high dosage allowing MHT and low dosage associated with PTT, are identified. It is also demonstrated that PTT mediated by magnetic nanoparticles has an efficacy that is comparable to that of plasmonic nanoparticles, but only at significant nanoparticle dosages. At low concentrations, only plasmonic nanoparticles can deliver a therapeutic heating. 相似文献
20.
Yoann Prado Sandra Mazerat Eric Rivière Guillaume Rogez Alexandre Gloter Odile Stéphan Laure Catala Talal Mallah 《Advanced functional materials》2014,24(34):5402-5411
CsNiCr(CN)6 coordination nanoparticles with sizes ranging from 6 to 30 nm are highly diluted in an organic polymer matrix. Their static and dynamic magnetic behaviour allows unravelling of surface anisotropy and interparticle dipolar interaction effects. The single magnetic domain critical size is thus evaluated to be around 22 nm with a blocking temperature of 21 K (at ν = 1 Hz) and an effective energy barrier for the reversal of the magnetization of 426 K. 相似文献