Preparation of N-doped graphite oxide for supercapacitors by NH3 cold plasma

In this work, N-doped graphite oxide (GO-P) was prepared by cold plasma treatment of GO using a mixture of NH3 and Ar as the working gas. When the ratios of NH3:Ar were 1:2, 1:3, and 1:4, the specific capacitances of the GO-P(NH3:Ar1:2), GO-P(NH3:Ar1:3), and GO-P(NH3:Ar1:4) were 124.5, 187.7, and 134.6 Fg−1, respectively, which were 4.7, 7.1, and 5.1 times that of GO at the current density of 1 Ag−1. The capacitance retention of the GO-P(NH3:Ar1:3) was 80% when it was cycled 1000 times. The characterization results showed that the NH3 cold plasma could effectively produce N-doped GO and generate more active defects. The N/C ratio and the contents of pyridinic nitrogen and graphitic nitrogen of the GO-P(NH3:Ar1:3) were the highest. These were conducive to providing pseudocapacitance and reducing the internal resistance of the electrode. In addition, the ID/IG of the GO-P(NH3:Ar=1:3) (1.088) was also the highest, indicating the highest number of defects. The results of discharge parameters measurement and in situ optical emission spectroscopy diagnosis of NH3 plasma showed that the discharge is the strongest when the ratio of NH3:Ar was 1:3, thereby the generated nitrogen active species can effectively promote N-doping. The N-doping and abundant defects were the keys to the excellent electrochemical performance of the GO-P(NH3:Ar1:3). NH3 cold plasma is a simple and rapid method to prepare N-doped GO and regulate the N-doping to prepare high-performance supercapacitors.

Network-Like Platinum Nanosheets Enabled by a Calorific-Effect-Induced-Fusion Strategy for Enhanced Catalytic Hydrogenation Performance

In this paper, we report the construction of network-like platinum (Pt) nanosheets based on Pt/reduced graphite oxide (Pt/rGO) hybrids by delicately utilizing a calorific-effect-induced-fusion strategy. The tiny Pt species first catalyzed the H2-O2 combination reaction. The released heat triggered the combustion of the rGO substrate under the assistance of the Pt species catalysis, which induced the fusion of the tiny Pt species into a network-like nanosheet structure. The loading amount and dispersity of Pt on rGO are found to be crucial for the successful construction of network-like Pt nanosheets. The as-prepared products present excellent catalytic hydrogenation activity and superior stability towards unsaturated bonds such as olefins and nitrobenzene. The styrene can be completely converted into phenylethane within 60 min. The turnover frequency (TOF) value of network-like Pt nanosheets is as high as 158.14 h−1, which is three times higher than that of the home-made Pt nanoparticles and among the highest value of the support-free bimetallic catalysts ever reported under similar conditions. Furthermore, the well dispersibility and excellent aggregation resistance of the network-like structure endows the catalyst with excellent recyclability. The decline of conversion could be hardly identified after five times recycling experiments.

Effect of graphite oxide and exfoliated graphite oxide as a modifier for the voltametric determination of dopamine in presence of uric acid and folic acid

In the present work, exfoliated graphite oxide (E-GO) was prepared by sonicating graphite oxide (GO) (prepared by modified Hummer’s and Offemam methods). Prepared GO and E-GO were characterized using infrared absorption spectroscopy, X-ray diffraction, and scanning electron microscopy. The electrocatalytic properties of GO and E-GO towards detection of dopamine (DA), uric acid (UA), and folic acid (FA) were investigated using cyclic voltammetry and differential pulse voltammetry. Our results revealed that E-GO has a slighter advantage over the GO as an electrode modifier for detection DA, UA, and FA, which might be ascribed to the good conductivity of E-GO when compared to the GO.

Liquid “Syngas” Based on Supercritical Water and Graphite Oxide/TiO2 Composite as Catalyst for CO2 to Organic Conversion

The conversion of carbon monoxide into organic substances is one of the top topics of modern science due to the development of industry and the climate changes caused by it on the one hand, and the possibility of obtaining an economic effect on the other, as it could allow for partial recovery of fuels. A problem in this regard has always been the low solubility of CO2 in water, which eliminated the possibility of easy converting carbon dioxide into the liquid. The development of research on water critical states revealed the fact that water in a subcritical state has a much higher ability to dissolve gases. And this effect was used to obtain the "liquid synthesis gas" model presented in this paper. Equally important was the selection of an appropriate catalyst that would increase the efficiency of the conversion process by generating hydrogen in the system under the influence of cold plasma. In this work we present the studies of transformation of CO2 dissolved in supercritical water using partially reduced graphite oxide—nanometric titania composite (RGO-TiO2) as catalyst, due to the ability of RGO to generate hydrogen in the water environment (water splitting) under the influence of various physical factors, especially cold plasma. The RGO catalyst was stabilized with titanium oxide to obtain higher activity at lower RGO concentrations in the system. Therefore, research on conversions was preceded by a thorough analysis of CO2 solubility in supercritical water, as well as an analysis of the structural, morphological, and spectroscopic properties of the catalyst. Graphic Abstract General scheme of cold plasma reactor.