Graphene is a promising two-dimensional nanomaterial for many applications due to its exciting properties. In the past decade, a variety of techniques-each with its own set of advantages and disadvantages-have been developed to prepare graphene, and there are ongoing efforts to improve these techniques and to reveal new approaches. Here, we describe a simple and low-cost process for the bottom-up synthesis of graphene-like films. This new methodology involves a two-step procedure: (i) formation of polyaromatic ring structures by the repeated covalent coupling of aryl radicals generated from electrochemical reduction of polyhalogenated aromatic compounds in aprotic solvent, and (ii) production of carbon networks by heating of polyaromatic surface films. Accordingly, polymeric films were prepared on the electrodes by electrochemical reduction of polyhalogenated compounds such as hexafluorobenzene (HFB), hexachlorobenzene (HCB), and hexabromobenzene (HBB), and then polymer films were annealed at 400 °C for 30 min. The structure and surface characteristics of electrodeposited carbon films under self- and thermal-annealing conditions were studied by spectroscopic and morphological techniques. Also, the capacitance performance of the films was evaluated by means of cyclic voltammetry, galvanostatic charge-discharge, and electrochemical impedance spectroscopy. Results indicate that graphene-like carbon films can be achieved by use of the electrochemical approach under mild conditions without expensive equipment, and also that these carbon materials are very promising for low-cost energy-storage devices.

In this study, the influence of the film structure was investigated on the electrocatalytic oxygen reduction at GC electrodes covered with porphyrin and metalloporphyrin rings via the diazonium modification method. For that purpose, primarily, tetraphenylporphyrin (TPP) films on GC electrode surfaces were prepared by electroreduction of in situ generated diazonium salts of 5‐(4‐aminophenyl)‐10,15,20‐triphenylporphyrin (APP) and 5,10,15,20‐tetrakis(4‐aminophenyl)porphyrin (TAPP) molecules. Next, the formation of metalloporphyrin films on the modified surfaces was accomplished through the complexation reactions of surface porphyrin rings with metal ions in the salt solutions containing Mn(II), Fe(III) and Co(II) ions. The resulting porphyrin and metalloporphyrin layers were identified with XPS and ICP‐MS. The electrochemical barrier properties of the films on GC surfaces were examined by cyclic voltammetry in K3Fe(CN)6 aqueous solution. The electrocatalytic abilities of the resulting films were also investigated for the oxygen electrochemical reduction by employing cyclic voltammetry in PBS solutions saturated with oxygen. The results showed that the oxygen reduction potentials on modified GC electrodes were shifted to less negative potentials compared to that of bare GC electrode. Also, it was obtained that the oxygen reduction reaction was more effective on the GC electrodes modified with TPP rings by using TAPP molecules than those prepared by using APP molecules.

No abstract

Here, new carbon-based nanostructures were prepared by the one-step electrochemical method using hexagonal and pentagonal polychlorinated organic rings as carbon source. The electrochemical growth of carbon nanostructures on substrates was...