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Sökning: WFRF:(Barzegar Hamid Reza)

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1.
  • Barzegar, Hamid Reza, 1977-, et al. (författare)
  • C60/Collapsed Carbon Nanotube Hybrids : A Variant of Peapods
  • 2015
  • Ingår i: Nano letters (Print). - : American Chemical Society (ACS). - 1530-6984 .- 1530-6992. ; 15:2, s. 829-834
  • Tidskriftsartikel (refereegranskat)abstract
    • We examine a variant of so-called carbon nanotube peapods by packing C60 molecules inside the open edge ducts of collapsed carbon nanotubes. C60 insertion is accomplished through a facile single-step solution-based process. Theoretical modeling is used to evaluate favorable low-energy structural configurations. Overfilling of the collapsed tubes allows infiltration of C60 over the full cross-section of the tubes and consequent partial or complete reinflation, yielding few-wall, large diameter cylindrical nanotubes packed with crystalline C60 solid cores.
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2.
  • Barzegar, Hamid Reza, et al. (författare)
  • Electrostatically Driven Nanoballoon Actuator
  • 2016
  • Ingår i: Nano letters (Print). - : American Chemical Society (ACS). - 1530-6984 .- 1530-6992. ; 16:11, s. 6787-6791
  • Tidskriftsartikel (refereegranskat)abstract
    • We demonstrate an inflatable nanoballoon actuator based on geometrical transitions between the inflated (cylindrical) and collapsed (flattened) forms of a carbon nanotube. In situ transmission electron microscopy experiments employing a nanoelectromechanical manipulator show that a collapsed carbon nanotube can be reinflated by electrically charging the nanotube, thus realizing an electrostatically driven nanoballoon actuator. We find that the tube actuator can be reliably cycled with only modest control voltages (few volts) with no apparent wear or fatigue. A complementary theoretical analysis identifies critical parameters for nanotube nanoballoon actuation.
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3.
  • Barzegar, Hamid Reza, et al. (författare)
  • Nitrogen Doping Mechanism in Small Diameter Single-Walled Carbon Nanotubes : Impact on Electronic Properties and Growth Selectivity
  • 2013
  • Ingår i: The Journal of Physical Chemistry C. - : American Chemical Society (ACS). - 1932-7447 .- 1932-7455. ; 117:48, s. 25805-25816
  • Tidskriftsartikel (refereegranskat)abstract
    • Nitrogen doping in carbon nanostructures has attracted interest for more than a decade, and recent implementation of such structures in energy conversion systems has boosted the interest even more. Despite numerous studies, the structural conformation and stability of nitrogen functionalities in small diameter single-walled carbon nanotubes (SWNTs), and the impact of these functionalities on the electronic and mechanical properties of the SWNTs, are incomplete. Here we report a detailed study on nitrogen doping in SWNTs with diameters in the range of 0.8?1.0 nm, with well-defined chirality. We show that the introduction of nitrogen in the carbon framework significantly alters the stability of certain tubes, opening for the possibility to selectively grow nitrogen-doped SWNTs with certain chirality and diameter. At low nitrogen concentration, pyridinic functionalities are readily incorporated and the tubular structure is well pertained. At higher concentrations, pyrrolic functionalities are formed, which leads to significant structural deformation of the nanotubes and hence a stop in growth of crystalline SWNTs. Raman spectroscopy is an important tool to understand guest atom doping and electronic charge transfer in SWNTs. By correlating the influence of defined nitrogen functionalities on the electronic properties of SWNTs with different chirality, we make precise interpretation of experimental Raman data. We show that the previous interpretation of the double-resonance G?-peak in many aspects is wrong and instead can be well-correlated to the type of nitrogen doping of SWNTs originating from the p- or n-doping nature of the nitrogen incorporation. Our results are supported by experimental and theoretical data.
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4.
  • Barzegar, Hamid Reza, et al. (författare)
  • Palladium nanocrystals supported on photo-transformed C-60 nanorods : effect of crystal morphology and electron mobility on the electrocatalytic activity towards ethanol oxidation
  • 2014
  • Ingår i: Carbon. - : Elsevier BV. - 0008-6223 .- 1873-3891. ; 73, s. 34-40
  • Tidskriftsartikel (refereegranskat)abstract
    • We report on the synthesis and decoration of high-aspect-ratio crystalline C-60 nanorods (NRs) by functionalized palladium nanoparticles with an average size of 4.78 +/- 0.66 nm. In their pristine form, C-60 NRs suffer from partial damage in the solution-based decoration process resulting in poor crystallinity. However, by modifying the NR surface via in situ photochemical transformation in the liquid state, we are able to prepare highly stable NRs that retain their crystalline structure during the decoration process. Our method thus opens up for the synthesis of highly crystalline nanocomposite hybrids comprising Pd nanoparticles and C-60 NRs. Bys measuring the electron mobility of different C-60 NRs, we relate both the effect of electron mobility and crystallinity to the final electrocatalytic performance of the synthesized hybrid structures. We show that the photo-transformed C-60 NRs exhibit highly advantageous properties for ethanol oxidation based on both a better crystallinity and a higher bulk conductivity. These findings give important information in the search for efficient catalyst support.
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5.
  • Barzegar, Hamid Reza, et al. (författare)
  • Self-assembled PCBM nanosheets : a facile route to electronic layer-on-Layer heterostructures
  • 2018
  • Ingår i: Nano letters (Print). - : American Chemical Society (ACS). - 1530-6984 .- 1530-6992. ; 18:2, s. 1442-1447
  • Tidskriftsartikel (refereegranskat)abstract
    • We report on the self-assembly of semicrystalline [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) nanosheets at the interface between a hydrophobic solvent and water, and utilize this opportunity for the realization of electronically active organic/organic molecular heterostructures. The self-assembled PCBM nanosheets can feature a lateral size of >1 cm2 and be transferred from the water surface to both hydrophobic and hydrophilic surfaces using facile transfer techniques. We employ a transferred single PCBM nanosheet as the active material in a field-effect transistor (FET) and verify semiconductor function by a measured electron mobility of 1.2 × 10–2 cm2 V–1 s–1 and an on–off ratio of ∼1 × 104. We further fabricate a planar organic/organic heterostructure with the p-type organic semiconductor poly(3-hexylthiophene-2,5-diyl) as the bottom layer and the n-type PCBM nanosheet as the top layer and demonstrate ambipolar FET operation with an electron mobility of 8.7 × 10–4 cm2 V–1 s–1 and a hole mobility of 3.1 × 10–4 cm2V–1 s–1.
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6.
  • Barzegar, Hamid Reza, et al. (författare)
  • Solution-Based Phototransformation of C-60 Nanorods : Towards Improved Electronic Devices
  • 2013
  • Ingår i: Particle & particle systems characterization. - : Wiley-VCH Verlagsgesellschaft. - 0934-0866 .- 1521-4117. ; 30:8, s. 715-720
  • Tidskriftsartikel (refereegranskat)abstract
    • A modified liquid-liquid interface precipitation synthesis of C-60 nanorods, effects and opportunities following an in situ photochemical transformation in the liquid state, and an electronic characterization using a field-effect transistor (FET) geometry are reported. The nanorods feature a high aspect ratio of approximate to 10(3) and a notably small average diameter of 172 nm. Interestingly, it is found that a decreased nanorod diameter appears to correlate with distinctly improved electronic properties, and an average electron mobility of 0.30 cm(2) V-1 s(-1), as measured in a FET geometry, is reported for as-grown nanorods, with the peak value being an impressive 1.0 cm(2) V-1 s(-1). A photoexposure using green laser light ( = 532 nm) is demonstrated to result in the formation of a polymer-C-60 shell encapsulating a monomer-C-60 bulk; such photo-transformed nanorods exhibit an electron mobility of 4.7 x 10(-3) cm(2) V-1 s(-1). It is notable that the utilized FET geometry only probes the polymer-C-60 nanorod surface shell, and that the monomer-C-60 bulk is anticipated to exhibit a higher mobility. Importantly, photoexposed nanorods can be conveniently processed as a stabile dispersion in common hydrophobic solvents, and this finding is attributed to the insoluble character of the polymer-C-60 shell.
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7.
  • Barzegar, Hamid Reza, et al. (författare)
  • Spontaneous twisting of a collapsed carbon nanotube
  • 2017
  • Ingår i: Nano Reseach. - : Tsinghua University Press. - 1998-0124 .- 1998-0000. ; 10:6, s. 1942-1949
  • Tidskriftsartikel (refereegranskat)abstract
    • We study the collapsing and subsequent spontaneous twisting of a carbon nanotube by in situ transmission electron microscopy (TEM). A custom-sized nanotube is first created in the microscope by selectively extracting shells from a parent multi-walled tube. The few-walled, large-diameter daughter nanotube is driven to collapse via mechanical stimulation, after which the ribbon-like collapsed tube spontaneously twists along its long axis. In situ diffraction experiments fully characterize the uncollapsed and collapsed tubes. The experimental observations and associated theoretical analysis indicate that the origin of the twisting is compressive strain.
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8.
  • Barzegar, Hamid Reza, et al. (författare)
  • Synthesis of graphene nanoribbons inside boron nitride nanotubes
  • 2016
  • Ingår i: Physica status solidi. B, Basic research. - : Wiley. - 0370-1972 .- 1521-3951. ; 253:12, s. 2377-2379
  • Tidskriftsartikel (refereegranskat)abstract
    • We report on bottom-up synthesis of graphene nanoribbons inside boron nitride nanotubes, using coronene molecules as building blocks. The synthesized ribbons are one or two coronene molecules wide, depending on the diameter of the host nanotube. The encapsulated carbon nanostructures can be eliminated from the inner cavity of the filled boron nitride nanotube via oxidation without any damage to the nanotube structure.
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9.
  • Barzegar, Hamid Reza, et al. (författare)
  • Water assisted growth of C60 rods and tubes by liquid-liquid interfacial precipitation method
  • 2012
  • Ingår i: Molecules. - : MDPI. - 1431-5157 .- 1420-3049. ; 17:6, s. 6840-6853
  • Tidskriftsartikel (refereegranskat)abstract
    • C60 nanorods with hexagonal cross sections are grown using a static liquid-liquid interfacial precipitation method in a system of C60/m-dichlorobenzene solution and ethanol. Adding water to the ethanol phase leads instead to C60 tubes where both length and diameter of the C60 tubes can be controlled by the water content in the ethanol. Based on our observations we find that the diameter of the rods/tubes strongly depends on the nucleation step. We propose a liquid-liquid interface growth model of C60 rods and tubes based on the diffusion rate of the good C60 containing solvent into the poor solvent as well as on the size of the crystal seeds formed at the interface between the two solvents. The grown rods and tubes exhibit a hexagonal solvate crystal structure with m-dichlorobenzene solvent molecules incorporated into the crystal structure, independent of the water content. An annealing step at 200 °C at a pressure <1 kPa transforms the grown structures into a solvent-free face centered cubic structure. Both the hexagonal and the face centered cubic structures are very stable and neither morphology nor structure shows any signs of degradation after three months of storage.
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10.
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