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      Flipping growth orientation of nanographitic structures by plasma enhanced chemical vapor deposition

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          Abstract

          Nanographitic structures (NGSs) with a multitude of morphological features are grown on SiO 2/Si substrates by electron cyclotron resonance-plasma enhanced chemical vapor deposition (ECR-PECVD).

          Abstract

          Nanographitic structures (NGSs) with a multitude of morphological features are grown on SiO 2/Si substrates by electron cyclotron resonance-plasma enhanced chemical vapor deposition (ECR-PECVD). CH 4 is used as a source gas with Ar and H 2 used as diluents. Field emission scanning electron microscopy, high resolution transmission electron microscopy (HRTEM) and Raman spectroscopy are used to study the structural and morphological features of the grown films. Herein we demonstrate how the morphology of these structures can be tuned from a planar to a vertical structure using a single control parameter, namely the level of dilution of CH 4 with Ar and/or H 2. Our results show that competitive growth and etching processes dictate the morphology of the NGSs. While an Ar-rich composition favors vertically oriented graphene nanosheets, an H 2-rich composition aids the growth of planar films. Raman analysis reveals the dilution of CH 4 with either Ar or H 2 or with the two in combination helps to improve the structural quality of the films. Line shape analysis of the Raman 2D bands shows a nearly symmetrical Lorentzian profile which confirms the turbostratic nature of the grown NGSs. This aspect is further elucidated by HRTEM studies where an elliptical diffraction pattern is observed. Based on these experiments, a comprehensive understanding is obtained of the growth and the structural properties of NGSs grown over a wide range of feedstock compositions.

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          Studying disorder in graphite-based systems by Raman spectroscopy.

          Raman spectroscopy has historically played an important role in the structural characterization of graphitic materials, in particular providing valuable information about defects, stacking of the graphene layers and the finite sizes of the crystallites parallel and perpendicular to the hexagonal axis. Here we review the defect-induced Raman spectra of graphitic materials from both experimental and theoretical standpoints and we present recent Raman results on nanographites and graphenes. The disorder-induced D and D' Raman features, as well as the G'-band (the overtone of the D-band which is always observed in defect-free samples), are discussed in terms of the double-resonance (DR) Raman process, involving phonons within the interior of the 1st Brillouin zone of graphite and defects. In this review, experimental results for the D, D' and G' bands obtained with different laser lines, and in samples with different crystallite sizes and different types of defects are presented and discussed. We also present recent advances that made possible the development of Raman scattering as a tool for very accurate structural analysis of nano-graphite, with the establishment of an empirical formula for the in- and out-of-plane crystalline size and even fancier Raman-based information, such as for the atomic structure at graphite edges, and the identification of single versus multi-graphene layers. Once established, this knowledge provides a powerful machinery to understand newer forms of sp(2) carbon materials, such as the recently developed pitch-based graphitic foams. Results for the calculated Raman intensity of the disorder-induced D-band in graphitic materials as a function of both the excitation laser energy (E(laser)) and the in-plane size (L(a)) of nano-graphites are presented and compared with experimental results. The status of this research area is assessed, and opportunities for future work are identified.
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            Uniaxial strain in graphene by Raman spectroscopy:\(G\)peak splitting, Grüneisen parameters, and sample orientation

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              Prepare dispersed CIS nano-scale particles and spray coating CIS absorber layers using nano-scale precursors

              In this study, the Mo-electrode thin films were deposited by a two-stepped process, and the high-purity copper indium selenide-based powder (CuInSe2, CIS) was fabricated by hydrothermal process by Nanowin Technology Co. Ltd. From the X-ray pattern of the CIS precursor, the mainly crystalline phase was CIS, and the almost undetectable CuSe phase was observed. Because the CIS powder was aggregated into micro-scale particles and the average particle sizes were approximately 3 to 8 μm, the CIS power was ground into nano-scale particles, then the 6 wt.% CIS particles were dispersed into isopropyl alcohol to get the solution for spray coating method. Then, 0.1 ml CIS solution was sprayed on the 20 mm × 10 mm Mo/glass substrates, and the heat treatment for the nano-scale CIS solution under various parameters was carried out in a selenization furnace. The annealing temperature was set at 550°C, and the annealing time was changed from 5 to 30 min, without extra Se content was added in the furnace. The influences of annealing time on the densification, crystallization, resistivity (ρ), hall mobility (μ), and carrier concentration of the CIS absorber layers were well investigated in this study.
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                Author and article information

                Journal
                RSCACL
                RSC Advances
                RSC Adv.
                Royal Society of Chemistry (RSC)
                2046-2069
                2015
                2015
                : 5
                : 111
                : 91922-91931
                Affiliations
                [1 ]Materials Science Group
                [2 ]Indira Gandhi Centre for Atomic Research
                [3 ]Kalpakkam-603102
                [4 ]India
                Article
                10.1039/C5RA20820C
                c4918cf1-5205-4f9c-b532-7c2d753c4aa0
                © 2015
                History

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