Nano-on-micro approach for fabricating ternary metal oxy-hydroxide–based flexible supercapacitors

In the present work, we unveil a facile and effective method to directly grow Ni–Mo–Co oxy-hydroxide–based 3-dimensional hierarchical nanostructures on carbon microfibers (nano-on-micro) by using a facile hydrothermal synthesis route. Further, the electrochemical activity for directly grown fiber electrode as well as electrode formed by slurry coating of active material formed after hydrothermal reaction has been investigated. In this study, the metal ratios (nickel and cobalt) were selected to cover the wide spectrum of the concentration in order to obtain the optimum concentration for the best electrochemical performance. Electrochemical analysis of these ternary metal oxy-hydroxide–based active materials on the carbon microfiber shows significantly high electrochemical activity with a specific capacitance of 519 Fg−1 in hydrothermally activated sample and 890 Fg−1 in a slurry coated sample (at 1 Ag−1). This simple technique provides a novel method to fabricate high energy-storage devices with the advantage of being lighter and flexible and can be easily integrated for various flexible electronic applications potential applications including e-textiles, personal electronics, military apparel devices, and antimicrobial and biomedical textiles.

Effect of Calcination Temperature and Chemical Composition of PAN-Derived Carbon Microfibers on N2, CO2, and CH4 Adsorption

This work investigates the interplay of carbonization temperature and the chemical composition of carbon microfibers (CMFs), and their impact on the equilibration time and adsorption of three molecules (N2, CO2, and CH4). PAN derived CMFs were synthesized by electrospinning and calcined at three distinct temperatures (600, 700 and 800 °C), which led to samples with different textural and chemical properties assessed by FTIR, TGA/DTA, XRD, Raman, TEM, XPS, and N2 adsorption. We examine why samples calcined at low/moderate temperatures (600 and 700 °C) show an open hysteresis loop in nitrogen adsorption/desorption isotherms at −196.15 °C. The equilibrium time in adsorption measurements is nearly the same for these samples, despite their distinct chemical compositions. Increasing the equilibrium time did not allow for the closure of the hysteresis loop, but by rising the analysis temperature this was achieved. By means of the isosteric enthalpy of adsorption measurements and ab initio calculations, adsorbent/adsorbate interactions for CO2, CH4 and N2 were found to be inversely proportional to the temperature of carbonization of the samples (CMF-600 > CMF-700 > CMF-800). The enhancement of adsorbent/adsorbate interaction at lower carbonization temperatures is directly related to the presence of nitrogen and oxygen functional groups on the surface of CMFs. Nonetheless, a higher concentration of heteroatoms also causes: (i) a reduction in the adsorption capacity of CO2 and CH4 and (ii) open hysteresis loops in N2 adsorption at cryogenic temperatures. Therefore, the calcination of PAN derived microfibers at temperatures above 800 °C is recommended, which results in materials with suitable micropore volume and a low content of surface heteroatoms, leading to high CO2 uptake while keeping acceptable selectivity with regards to CH4 and moderate adsorption enthalpies.

Carbon Microstructures Synthesis in Low Temperature Plasma Generated by Microdischarges

The aim of this paper is to investigate the process of growth of different carbon deposits in low-current electrical microdischarges in argon with an admixture of cyclohexane as the carbon feedstock. The method of synthesis of carbon structures is based on the decomposition of hydrocarbons in low-temperature plasma generated by an electrical discharge in gas at atmospheric pressure. The following various types of microdischarges generated at this pressure were tested for both polarities of supply voltage with regard to their applications to different carbon deposit synthesis: Townsend discharge, pre-breakdown streamers, breakdown streamers and glow discharge. In these investigations the discharge was generated between a stainless-steel needle and a plate made of a nickel alloy, by electrode distances varying between 1 and 15 mm. The effect of distance between the electrodes, discharge current and hydrocarbon concentration on the obtained carbon structures was investigated. Carbon nanowalls and carbon microfibers were obtained in these discharges.

Isosteric Enthalpy Behavior of CO2 Adsorption on Micro-Mesoporous Materials: Carbon Microfibers (CMFs), SBA-15, and Amine-Functionalized SBA-15

The isosteric enthalpy of adsorption (∆adsh ) of CO2 in three different micro and mesoporous materials was evaluated in this work. These materials were a microporous material with functional groups of nitrogen and oxygen (CMFs, carbon microfibers), a mesoporous material with silanol groups (SBA-15, Santa Barbara Amorphous), and a mesoporous material with amine groups (SBA-15_APTES, SBA-15 amine-functionalized with (3-Aminopropyl)-triethoxysilane). The temperature interval explored was between 263 K and 303 K, with a separation of 5 K between each one, so a total of nine CO2 isotherms were obtained. Using the nine isotherms and the Clausius–Clapeyron equation, the reference value for ∆adsh was found. The reference value was compared with those ∆adsh obtained, considering some arrangement of three or five CO2 isotherms. Finally, it was found that at 298 K and 1 bar, the total amount of CO2 adsorbed is 2.32, 0.53, and 1.37 mmol g−1 for CMF, SBA-15, and SBA-15_APTES, respectively. However, at a coverage of 0.38 mmol g−1, ∆adsh is worth 38, 30, and 29 KJ mol−1 for SBA-15_APTES, CMFs, and SBA-15, respectively. So, physisorption predominates in the case of CMF and SBA-15 materials, and the ∆adsh values significantly coincide regardless of whether the isotherms arrangement used was three or five. Meanwhile, in SBA-15_APTES, chemisorption predominates as a consequence of the arrangements used to obtain . This happens in such a way that the use of low temperatures (263–283 K) tends to produce higher ∆adsh values, while the use of high temperatures (283–303 K) decreases the ∆adsh values.

Enhanced catalytic ozonation of ibuprofen using a 3D structured catalyst with MnO2 nanosheets on carbon microfibers

Heterogeneous catalytic ozonation is an effective approach to degrade refractory organic pollutants in water. However, ozonation catalysts with combined merits of high activity, good reusability and low cost for practical industrial applications are still rare. This study aims to develop an efficient, stable and economic ozonation catalyst for the degradation of Ibuprofen, a pharmaceutical compound frequently detected as a refractory pollutant in treated wastewaters. The novel three-dimensional network-structured catalyst, comprising of δ-MnO2 nanosheets grown on woven carbon microfibers (MnO2 nanosheets/carbon microfiber), was synthesized via a facile hydrothermal approach. Catalytic ozonation performance of Ibuprofen removal in water using the new catalyst proves a significant enhancement, where Ibuprofen removal efficiency of close to 90% was achieved with a catalyst loading of 1% (w/v). In contrast, conventional ozonation was only able to achieve 65% removal efficiency under the same operating condition. The enhanced performance with the new catalyst could be attributed to its significantly increased available surface active sites and improved mass transfer of reaction media, as a result of the special surface and structure properties of this new three-dimensional network-structured catalyst. Moreover, the new catalyst displays excellent stability and reusability for ibuprofen degradation over successive reaction cycles. The facile synthesis method and low-cost materials render the new catalyst high potential for industrial scaling up. With the combined advantages of high efficiency, high stability, and low cost, this study sheds new light for industrial applications of ozonation catalysts.

Hybrid Carbon Microfibers-Graphite Fillers for Piezoresistive Cementitious Composites

Multifunctional structural materials are very promising in the field of engineering. Particularly, their strain sensing ability draws much attention for structural health monitoring applications. Generally, strain sensing materials are produced by adding a certain amount of conductive fillers, around the so-called “percolation threshold”, to the cement or composite matrix. Recently, graphite has been found to be a suitable filler for strain sensing. However, graphite requires high amounts of doping to reach percolation threshold. In order to decrease the amount of inclusions, this paper proposes cementitious materials doped with new hybrid carbon inclusions, i.e., graphite and carbon microfibers. Carbon microfibers having higher aspect ratio than graphite accelerate the percolation threshold of the graphite particles without incurring into dispersion issues. The resistivity and strain sensitivity of different fibers’ compositions are investigated. The electromechanical tests reveal that, when combined, carbon microfibers and graphite hybrid fillers reach to percolation faster and exhibit higher gauge factors and enhanced linearity.