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        <title>Nanoscale Research Letters - Latest Articles</title>
        <link>http://www.nanoscalereslett.com</link>
        <description>The latest research articles published by Nanoscale Research Letters</description>
        <dc:date>2013-05-25T00:00:00Z</dc:date>
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                                <rdf:li rdf:resource="http://www.nanoscalereslett.com/content/8/1/252" />
                                <rdf:li rdf:resource="http://www.nanoscalereslett.com/content/8/1/251" />
                                <rdf:li rdf:resource="http://www.nanoscalereslett.com/content/8/1/250" />
                                <rdf:li rdf:resource="http://www.nanoscalereslett.com/content/8/1/249" />
                                <rdf:li rdf:resource="http://www.nanoscalereslett.com/content/8/1/248" />
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                                <rdf:li rdf:resource="http://www.nanoscalereslett.com/content/8/1/246" />
                                <rdf:li rdf:resource="http://www.nanoscalereslett.com/content/8/1/245" />
                                <rdf:li rdf:resource="http://www.nanoscalereslett.com/content/8/1/244" />
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        <item rdf:about="http://www.nanoscalereslett.com/content/8/1/252">
        <title>Gold nanoparticles deposited on glass: physicochemical characterization and cytocompatibility</title>
        <description>Properties of gold films sputtered under different conditions onto borosilicate glass substrate were studied. Mean thickness of sputtered gold film was measured by gravimetry, and film contact angle was determined by goniometry. Surface morphology was examined by atomic force microscopy, and electrical sheet resistance was determined by two-point technique. The samples were seeded with rat vascular smooth muscle cells, and their adhesion and proliferation were studied. Gold depositions lead to dramatical changes in the surface morphology and roughness in comparison to pristine substrate. For sputtered gold structures, the rapid decline of the sheet resistance appears on structures deposited for the times above 100 s. The thickness of deposited gold nanoparticles/layer is an increasing function of sputtering time and current. AFM images prove the creation of separated gold islands in the initial deposition phase and a continuous gold coverage for longer deposition times. Gold deposition has a positive effect on the proliferation of vascular smooth muscle cells. Largest number of cells was observed on sample sputtered with gold for 20 s and at the discharge current of 40 mA. This sample exhibits lowest contact angle, low relative roughness, and only mild increase of electrical conductivity.</description>
        <link>http://www.nanoscalereslett.com/content/8/1/252</link>
                <dc:creator>Alena Reznickova</dc:creator>
                <dc:creator>Zdenka Novotna</dc:creator>
                <dc:creator>Nikola Kasalkova</dc:creator>
                <dc:creator>Vaclav Svorcik</dc:creator>
                <dc:source>Nanoscale Research Letters 2013, null:252</dc:source>
        <dc:date>2013-05-25T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1556-276X-8-252</dc:identifier>
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        <item rdf:about="http://www.nanoscalereslett.com/content/8/1/251">
        <title>Influence of nanoparticles of platinum on chicken embryo development and brain morphology</title>
        <description>Platinum nanoparticles (NP-Pt) are noble metal nanoparticles with unique physiochemical properties that have recently elicited much interest in medical research. However, we still know little about their toxicity and influence on general health. We investigated effects of NP-Pt on the growth and development of the chicken embryo model with emphasis on brain tissue micro- and ultrastructure. The embryos were administered solutions of NP-Pt injected in ovo at concentrations from 1 to 20 mug/ml. The results demonstrate that NP-Pt did not affect the growth and development of the embryos; however, they induced apoptosis and decreased the number of proliferating cells in the brain tissue. These preliminary results indicate that properties of NP-Pt might be utilized in brain cancer therapy, but potential toxic side effects must be elucidated in extensive follow-up research.</description>
        <link>http://www.nanoscalereslett.com/content/8/1/251</link>
                <dc:creator>Marta Prasek</dc:creator>
                <dc:creator>Ewa Sawosz</dc:creator>
                <dc:creator>Slawomir Jaworski</dc:creator>
                <dc:creator>Marta Grodzik</dc:creator>
                <dc:creator>Teresa Ostaszewska</dc:creator>
                <dc:creator>Maciej Kamaszewski</dc:creator>
                <dc:creator>Mateusz Wierzbicki</dc:creator>
                <dc:creator>Andre Chwalibog</dc:creator>
                <dc:source>Nanoscale Research Letters 2013, null:251</dc:source>
        <dc:date>2013-05-24T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1556-276X-8-251</dc:identifier>
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        <prism:startingPage>251</prism:startingPage>
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        <title>SERS substrates formed by gold nanorods deposited on colloidal silica films</title>
        <description>We describe a new approach to the fabrication of surface-enhanced Raman scattering (SERS) substrates using gold nanorod (GNR) nanopowders to prepare concentrated GNR sols, followed by their deposition on an opal-like photonic crystal (OPC) film formed on a silicon wafer. For comparative experiments, we also prepared GNR assemblies on plain silicon wafers. GNR-OPC substrates combine the increased specific surface, owing to the multilayer silicon nanosphere structure, and various spatial GNR configurations, including those with possible plasmonic hot spots. We demonstrate here the existence of the optimal OPC thickness and GNR deposition density for the maximal SERS effect. All other things being equal, the analytical integral SERS enhancement of the GNR-OPC substrates is higher than that of the thick, randomly oriented GNR assemblies on plain silicon wafers. Several ways to further optimize the strategy suggested are discussed.</description>
        <link>http://www.nanoscalereslett.com/content/8/1/250</link>
                <dc:creator>Mikhail Tsvetkov</dc:creator>
                <dc:creator>Boris Khlebtsov</dc:creator>
                <dc:creator>Vitaly Khanadeev</dc:creator>
                <dc:creator>Victor Bagratashvili</dc:creator>
                <dc:creator>Peter Timashev</dc:creator>
                <dc:creator>Mikhail Samoylovich</dc:creator>
                <dc:creator>Nikolai Khlebtsov</dc:creator>
                <dc:source>Nanoscale Research Letters 2013, null:250</dc:source>
        <dc:date>2013-05-22T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1556-276X-8-250</dc:identifier>
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        <item rdf:about="http://www.nanoscalereslett.com/content/8/1/249">
        <title>Gold nanolayer and nanocluster coatings induced by heat treatment and evaporation technique</title>
        <description>The paper is focused on the preparation and surface characterization of gold coatings and nanostructures deposited on glass substrate. Different approaches for the layer preparation were applied. The gold was deposited on the glass with (i) room temperature, (ii) glass heated to 300&#176;C, and (iii) the room temperature-deposited glass which was consequently annealed to 300&#176;C. The sheet resistance and concentration of free carriers were determined by the van der Pauw method. Surface morphology was characterized using an atomic force microscopy. The optical properties of gold nanostructures were measured by UV&#8211;vis spectroscopy. The evaporation technique combined with simultaneous heating of the glass leads to change of the sheet resistance, surface roughness, and optical properties of gold nanostructures. The electrically continuous layers are formed for significantly higher thickness (18 nm), if the substrate is heated during evaporation process. The annealing process influences both the structure and optical properties of gold nanostructures. The elevated temperature of glass during evaporation amplifies the peak of plasmon resonance in the structures, the surface morphology being significantly altered.</description>
        <link>http://www.nanoscalereslett.com/content/8/1/249</link>
                <dc:creator>Anna Schaub</dc:creator>
                <dc:creator>Petr Slepi¿ka</dc:creator>
                <dc:creator>Irena Ka¿párková</dc:creator>
                <dc:creator>Petr Malinský</dc:creator>
                <dc:creator>Anna Macková</dc:creator>
                <dc:creator>Václav ¿vor¿ík</dc:creator>
                <dc:source>Nanoscale Research Letters 2013, null:249</dc:source>
        <dc:date>2013-05-22T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1556-276X-8-249</dc:identifier>
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        <prism:startingPage>249</prism:startingPage>
        <prism:publicationDate>2013-05-22T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.nanoscalereslett.com/content/8/1/248">
        <title>One-step large-scale synthesis of micrometer-sized silver nanosheets by a template-free electrochemical method</title>
        <description>We have synthesized micrometer-sized Ag nanosheets via a facile, one-step, template-free electrochemical deposition in an ultra-dilute silver nitrate aqueous electrolyte. The nanosheet growth was revealed to occur in three stages: (1) formation of polygonal Ag nuclei on a substrate, (2) growth of {112}-faceted nanowire from the nuclei, and (3) anisotropic growth of (111)-planar nanosheets, approximately 20 to 50 nm in thickness and 10 &#956;m in width, in the &lt;112&gt;&#8722;direction. The vertical growth of the facet nanowire was induced by the strong interface anisotropy between the deposit and electrolyte due to the ultra-dilute concentration of electrolyte and high reduction potential. The thickness of Ag nanosheets was controllable by the adjustment of the reduction/oxidation potential and frequency of the reverse-pulse potentiodynamic mode.</description>
        <link>http://www.nanoscalereslett.com/content/8/1/248</link>
                <dc:creator>Sun Hwa Park</dc:creator>
                <dc:creator>Jin Gyeong Son</dc:creator>
                <dc:creator>Tae Geol Lee</dc:creator>
                <dc:creator>Hyun Min Park</dc:creator>
                <dc:creator>Jae Yong Song</dc:creator>
                <dc:source>Nanoscale Research Letters 2013, null:248</dc:source>
        <dc:date>2013-05-22T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1556-276X-8-248</dc:identifier>
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        <prism:startingPage>248</prism:startingPage>
        <prism:publicationDate>2013-05-22T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.nanoscalereslett.com/content/8/1/247">
        <title>Reduced graphene oxide aerogel with high-rate supercapacitive performance in aqueous electrolytes</title>
        <description>Reduced graphene oxide aerogel (RGOA) is synthesized successfully through a simultaneous self-assembly and reduction process using hypophosphorous acid and I2 as reductant. Nitrogen sorption analysis shows that the Brunauer-Emmett-Teller surface area of RGOA could reach as high as 830 m2 g-1, which is the largest value ever reported for graphene-based aerogels obtained through the simultaneous self-assembly and reduction strategy. The as-prepared RGOA is characterized by a variety of means such as scanning electron microscopy, transmission electron microscopy, X-ray diffraction, Raman spectroscopy, and X-ray photoelectron spectroscopy. Electrochemical tests show that RGOA exhibits a high-rate supercapacitive performance in aqueous electrolytes. The specific capacitance of RGOA is calculated to be 211.8 and 278.6 F g-1 in KOH and H2SO4 electrolytes, respectively. The perfect supercapacitive performance of RGOA is ascribed to its three-dimensional structure and the existence of oxygen-containing groups.</description>
        <link>http://www.nanoscalereslett.com/content/8/1/247</link>
                <dc:creator>Weijiang Si</dc:creator>
                <dc:creator>Xiaozhong Wu</dc:creator>
                <dc:creator>Jin Zhou</dc:creator>
                <dc:creator>Feifei Guo</dc:creator>
                <dc:creator>Shuping Zhuo</dc:creator>
                <dc:creator>Hongyou Cui</dc:creator>
                <dc:creator>Wei Xing</dc:creator>
                <dc:source>Nanoscale Research Letters 2013, null:247</dc:source>
        <dc:date>2013-05-21T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1556-276X-8-247</dc:identifier>
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        <prism:startingPage>247</prism:startingPage>
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        <item rdf:about="http://www.nanoscalereslett.com/content/8/1/246">
        <title>Noise and fluctuation relations of a spin diode</title>
        <description>We consider fluctuation relations between the transport coefficients of a spintronic system where mag-netic interactions play a crucial role. We investigate a prototypical spintronic device - a spin-diode -which consists of an interacting resonant level coupled to two ferromagnetic electrodes. We therebyobtain the cumulant generating function for the spin transport in the sequential tunnelling regime. Wedemonstrate the fulfilment of the nonlinear fluctuation relations when up and down spin currents arecorrelated in the presence of both spin-flip processes and external magnetic fields.</description>
        <link>http://www.nanoscalereslett.com/content/8/1/246</link>
                <dc:creator>Jong Soo Lim</dc:creator>
                <dc:creator>Rosa López</dc:creator>
                <dc:creator>David Sánchez</dc:creator>
                <dc:source>Nanoscale Research Letters 2013, null:246</dc:source>
        <dc:date>2013-05-20T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1556-276X-8-246</dc:identifier>
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                <prism:publicationName>Nanoscale Research Letters</prism:publicationName>
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        <prism:startingPage>246</prism:startingPage>
        <prism:publicationDate>2013-05-20T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.nanoscalereslett.com/content/8/1/245">
        <title>Nanopore detection of DNA molecules in magnesium chloride solutions</title>
        <description>High translocation speed of a DNA strand through a nanopore is a major bottleneck for nanopore detection of DNA molecules. Here, we choose MgCl2 electrolyte as salt solution to control DNA mobility. Experimental results demonstrate that the duration time for straight state translocation events in 1&#160;M MgCl2 solution is about 1.3&#160;ms which is about three times longer than that for the same DNA in 1&#160;M KCl solution. This is because Mg2+ ions can effectively reduce the surface charge density of the negative DNA strands and then lead to the decrease of the DNA electrophoretic speed. It is also found that the Mg2+ ions can induce the DNA molecules binding together and reduce the probability of straight DNA translocation events. The nanopore with small diameter can break off the bound DNA strands and increase the occurrence probability of straight DNA translocation events.</description>
        <link>http://www.nanoscalereslett.com/content/8/1/245</link>
                <dc:creator>Yin Zhang</dc:creator>
                <dc:creator>Lei Liu</dc:creator>
                <dc:creator>Jingjie Sha</dc:creator>
                <dc:creator>Zhonghua Ni</dc:creator>
                <dc:creator>Hong Yi</dc:creator>
                <dc:creator>Yunfei Chen</dc:creator>
                <dc:source>Nanoscale Research Letters 2013, null:245</dc:source>
        <dc:date>2013-05-20T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1556-276X-8-245</dc:identifier>
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        <item rdf:about="http://www.nanoscalereslett.com/content/8/1/244">
        <title>Enhancement of light output power of GaN-based light-emitting diodes with photonic quasi-crystal patterned on p-GaN surface and n-side sidewall roughing</title>
        <description>In this paper, GaN-based light-emitting diodes (LEDs) with photonic quasi-crystal (PQC) structure on p-GaN surface and n-side roughing by nano-imprint lithography are fabricated and investigated. At an injection current of 20 mA, the LED with PQC structure on p-GaN surface and n-side roughing increased the light output power of the InGaN/GaN multiple quantum well LEDs by a factor of 1.42, and the wall-plug efficiency is 26% higher than the conventional GaN-based LED type. After 500-h life test (55[degree sign]C/50 mA), it was found that the normalized output power of GaN-based LED with PQC structure on p-GaN surface and n-side roughing only decreased by 6%. These results offer promising potential to enhance the light output powers of commercial light-emitting devices using the technique of nano-imprint lithography.</description>
        <link>http://www.nanoscalereslett.com/content/8/1/244</link>
                <dc:creator>Fang-I Lai</dc:creator>
                <dc:creator>Jui-Fu Yang</dc:creator>
                <dc:source>Nanoscale Research Letters 2013, null:244</dc:source>
        <dc:date>2013-05-17T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1556-276X-8-244</dc:identifier>
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        <prism:startingPage>244</prism:startingPage>
        <prism:publicationDate>2013-05-17T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.nanoscalereslett.com/content/8/1/243">
        <title>Facile approach to prepare multi-walled carbon nanotubes/graphene nanoplatelets hybrid materials</title>
        <description>A facile approach was developed to prepare multi-walled carbon nanotubes/graphene nanoplatelets hybrid materials through covalent bond formation. First, poly(acryloyl chloride) was grafted onto oxidized multi-walled carbon nanotubes through the reaction between the acyl chloride groups of poly and the hydroxyl groups of oxidized multi-walled carbon nanotubes. Second, the remaining acyl chloride groups of poly were allowed to react with the hydroxyl groups of hydroxylated graphene nanoplatelets. Scanning electron microscopy and transmission electron microscopy data showed that the multi-walled carbon nanotubes and graphene nanoplatelets were effectively connected with each other. And Fourier transform infrared spectroscopy data indicated the formation of covalent bonds between carbon nanotubes and graphene nanoplatelets. Conformational changes were monitored by Raman spectroscopy. This novel kind of carbon hybrid materials may have the potential application in a wide field, especially in increasing the toughness and strength of the matrix resin.</description>
        <link>http://www.nanoscalereslett.com/content/8/1/243</link>
                <dc:creator>Yuchen Jia</dc:creator>
                <dc:creator>Kejing Yu</dc:creator>
                <dc:creator>Kun Qian</dc:creator>
                <dc:source>Nanoscale Research Letters 2013, null:243</dc:source>
        <dc:date>2013-05-16T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1556-276X-8-243</dc:identifier>
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