Abstract:This article presents an overview of the research highlights in graphene synthesis by Chemical Vapor Deposition (CVD). We discuss the growth mechanisms mainly over transition metals and alloys (with emphasis on Cu and Cu alloys), including new developments and experiments in transfer-free graphene growth on dielectric materials. We focus on the role of the different synthesis parameters, including thermodynamic aspects of the chemical process and physical, chemical and morphological properties of substrate catalyst. We discuss the relation among these parameters and the properties of the as-grown graphene. Some important relations are reviewed and addressed to the influence of the fundamental parameters and methods on the synthesis of high quality graphene.
In this study, we have employed infrared (IR) absorption spectroscopy, visible Raman spectroscopy, and x-ray absorption near edge structure (XANES) to quantify the hydrogen (H) content in hydrogenated amorphous carbon (a-C:H) films. a-C:H films with a hydrogen content varying from 29 to 47 at. % have been synthesized by electron cyclotron resonance chemical vapor deposition at low substrate temperatures (< 1 2 0 °C) applying a wide range of bias voltage, Vb, (-300 V < Vb < +100 V). With the application of high negative Vb, the a-C:H films undergo a dehydrogenation process accompanied by a sharp structural modification from polymer-to fullerenelike films. The trend in the H content derived from elastic recoil detection analysis (ERDA) is quantitatively reproduced from the intensity of the C -H bands and states in the IR and XANES spectra, respectively, as well as from the photoluminescence (PL) background drop in the Raman spectra. Using the H contents obtained by ERDA as reference data, semiquantitative expressions are inferred for the amount of bonded hydrogen as a function of the experimental spectroscopic parameters, i.e., the integrated area of the IR C -H stretching band at about 2900 cm-1, the PL background in visible Raman spectra, and the XANES intensity of the o-*-CH peak.
This paper deals with optical emission spectroscopy studies of low pressure (0.1-0.5 Torr) capacitively coupled radiofrequency hydrocarbon/argon-rich plasmas used for the synthesis of nanocarbon structures. The main goal of this paper is to obtain the electron temperature of such far-from-equilibrium plasmas as a function of the pressure, the excitation power and the argon content. In doing so, we have found that the argon upper energy levels used for electron temperature estimation remain close to corona balance. The latter has allowed us to use a modified Boltzmann plot technique to derive the electron temperature. It was found that, for the plasmas investigated, an increase of the argon population density (from 10% to 95%) leads to a pronounced decrease of the electron temperature while an increase of the processing pressure produces a moderate increase of the electron temperature. Additionally, the increase of the power from 50 to 300 W produces a very slight growth of the electron temperature.
Direct growth of graphene films on dielectric substrates (quartz and silica) is reported, by means of remote electron cyclotron resonance plasma assisted chemical vapor deposition r-(ECR-CVD) at low temperature (650°C). Using a two step deposition process- nucleation and growth- by changing the partial pressure of the gas precursors at constant temperature, mostly monolayer continuous films, with grain sizes up to 500 nm are grown, exhibiting transmittance larger than 92% and sheet resistance as low as 900 Ω·sq. The grain size and nucleation density of the resulting graphene sheets can be controlled varying the deposition time and pressure. In additon, first-principles DFT-based calculations have been carried out in order to rationalize the oxygen reduction in the quartz surface experimentally observed. This method is easily scalable and avoids damaging and expensive transfer steps of graphene films, improving compatibility with current fabrication technologies.
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