No description available.

<p> Cathodic electrodeposition method has been developed for the fabrication of manganese oxide films for application in electrochemical supercapacitors (ES). The manganese oxide films prepared from KMn04 and NaMn04 aqueous solution showed an increasing deposition yield with the deposition time. The deposition rate decreases with increasing the concentration of deposition precursor. The obtained films were characterized using scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), X-ray diffraction analysis (XRD), thermogravimetric and differential thermal analysis (TGA/DTA). The SEM observations revealed uniform films of highly porous nanostructure on different substrates. The capacitive behavior of the deposits was investigated by cyclic voltammetry and chronopotentiometry method in 0.1M NaS04 aqueous solutions. As prepared deposits exhibited pseudocapacitive behavior in the potential window of 0-1.0 V versus SCE with excellent cyclability. A maximum specific capacitance (SC) of 353 Fig was obtained for the 45 μg/cm2 film deposited from KMn04 solution on stainless steel foil, at a scan rate of 2 m V /s in the 0.1 M Na2S04 solution. It was found that the SC decreased with increasing deposit thickness and scan rate. No significant effect was obtained on the films prepared from 20 mM KMn04 on stainless steel after heat treatment at various temperatures. The capacitance of as-prepared electrode did not change by changing the electrolyte from Na2S04 to K2S04 solutions. However, higher capacitance values were observed by using electrolyte with higher concentration. Different structures of manganese oxides were obtained when different deposition precursors were used. No significant difference in capacitive behavior was found between the films prepared from different deposition precursor. However it was concluded that conductivity of the film is key in determining the performance of the electrodes. The effect of substrates on the electrochemical behavior has also been investigated by using stainless steel and nickel foils. </p> / Thesis / Master of Applied Science (MASc)

Electrochemical supercapacitors (ESs) are currently under development for electronics and automotive applications due to their hybrid properties inherited from batteries and capacitors. ESs exhibit higher power densities than batteries and energy densities than capacitors, and offer long cyclic life and rapid charge-discharge suitable for many applications. A promising candidate of electrode materials is manganese dioxide (MnO2), which has the advantages of high theoretical capacitance, low cost and environmentally friendly. However, the low electronic and ionic conductivities of MnO2 have limited its performance for practical applications. It has been demonstrated in literature that composite materials, which consist of conductive additives such as multi-walled carbon nanotubes (MWCNTs) and MnO2 can address this problem, however further investigations are required to produce ESs with superior performance for real-world applications. In this dissertation, novel colloidal fabrication techniques have been developed and advanced dispersants were employed to fabricate advanced nanocomposite electrodes. MnO2-MWCNTs composite electrode was fabricated with use of multifunctional dispersant. The multifunctional dispersant cetylpyridinium chloride (CPC) showed good dispersion of MWCNTs and capability of forming complex with the precursor of MnO2, which improved the homogeneity of the composite and generated unique morphology. The MnO2-MWCNTs composite electrode fabricated exhibited remarkable areal capacitance at high active mass loadings. New scalable fabrication technique was developed for MnO2-MWCNTs by using high solubility sodium permanganate (NaMnO4) precursor. The fabricated composite electrode showed superior performance compared to electrodes fabricated by other colloidal techniques at similar mass loading. Liquid-liquid extraction was employed to address the problem of particles agglomeration upon drying. Bio-inspired advanced extractor lauryl gallate (LG) was used for liquid-liquid extraction of particles. LG has organic catechol group allowed for strong adsorption on inorganic particles. Using LG as an advanced extractor has facilitated the transfer of particles from aqueous to organic phase to prevent agglomeration associated with drying procedure and improved mixing with MWCNTs. Advanced dispersants from bile acid salts and charged aromatic dyes families such as sodium taurodeoxychloate (TDS) and tolonium chloride (TL) were used as MWCNTs dispersants, to fabricate composite electrode with alternative metal oxides such as Mn3O4 and V2O3. Furthermore, 3,4-dihydroxybenzaldhyde (DHB) was investigated as a dispersing agent for Mn3O4 and used to fabricate Mn3O4-MWCNTs composite electrode with TL by Schiff base formation. Mn3O4 offers the advantages of small particle size compared to MnO2, and can be converted to MnO2 by electrochemical cycling to enhance capacitive performance. V2O3 was considered as an alternative to MnO2 due to its metallic conductivity at room temperature. An activation procedure has been developed, which promoted the formation of capacitive V2O5 surface layer on conductive V2O3 to increase capacitance. The advanced dispersants have shown excellent dispersion of MWCNTs in aqueous solutions at low concentrations and facilitated the formation of homogeneous composite with Mn3O4 and V2O3. Activation procedures were developed for the Mn3O4 and V2O3 composite electrodes, and the electrodes with high active mass loadings showed exceptional performance after activation. / Thesis / Doctor of Philosophy (PhD) / In modern society, the demand for clean and renewable energy have grown drastically and there is a need in development of advanced energy storage devices. Currently, the most common energy storage devices are batteries or conventional capacitors. Batteries can store a large amount of energy, however they are limited by their low power performance. Capacitors can charge and discharge rapidly, but the amount of energy stored is relatively low. Other than batteries and capacitor, electrochemical supercapacitors are emerging energy storage devices that offer the advantages of high power and energy density, fast charge-discharge and long lifetime. The objective of this work was to develop advanced nanocomposite electrode materials for electrochemical supercapacitor applications. New colloidal processing strategies have been developed and advanced dispersants were employed for the fabrication of high performance nanocomposites for electrochemical supercapacitor applications. The results presented in this work showed exceptional performances compared to literature data and paved a new way for further developments.

Electrochemical supercapacitors (ESs) are one of the most modern energy storage systems that offer a balance between power and energy densities in which the energy storage mechanisms could be an electrostatic double layer (EDLCs) and pseudocapacitive. In this thesis, hybrid asymmetric supercapacitors have been developed to optimize the advantages for different types of (ESs) such as high conductivity, stability, fast charge-discharge, and relatively high performance. These developments include high active mass loading electrodes based on multiwall carbon nanotubes (MWCNTs) and transition metal oxides with incubation of low binder percentage and a high mass loading of 40 mg cm-2 that guarantees high electrochemical performance at a wide potential range for different electrodes, especially the cathodic one. Novel synthesis techniques and different multi-dispersants have been demonstrated; a conception colloidal fabrication method has been developed to improve the morphology/dispersion for composites of Fe3O4/MWCNTs (M-CNTs) and NiFe2O4/MWCNTs. Firstly, an advanced synthesis method called particle extraction through a liquid-liquid interface (PELLI) has been developed to enhance the dispersion of the nanoparticles M-CNTs. Furthermore, palmitic acid (PA) has been used as a surfactant in the bottom-up (PELLI) to reduce the agglomeration of M-CNTs with high Gamma (𝛾𝛾) ratio (nanoparticles/MWCNTs). Moreover, different synthesis methods have been developed in the presence of celestine blue dye (CB) as a co-dispersant with advanced electrostatic interaction and coagulation mechanism that ensured well- dispersed of (Fe3O4, NiFe2O4) coated (MWCNTs) at high mass loading. Subsequently, more optimizations have been done to analyze the effect of different adsorption mechanisms by using other co-dispersant agents such as pyrocatechol violet (PV), azure A chloride (AA), and m-cresol purple (CP). Finally, cyclic voltammetry, galvanic charge-discharge (GCD), electrochemical impedance spectroscopy (EIS), and cyclic stability have been done for the fabricated electrodes and devices in neutral aqueous electrolytes that showed a relevant electrochemical performance in a large potential range. / Thesis / Doctor of Philosophy (PhD) / The rapid increase in human population has caused many economic problems, one of them the enormous energy consumption rate as compared to the limitations of sources available for clean and renewable energy sources. Energy storage systems can be classified into different types, e.g., chemical, electrochemical, thermal, and mechanical systems. Popular electrochemical energy storage systems, such as batteries and capacitors, are used for many important daily applications but have difficulties while optimizing power and energy densities. Here, electrochemical supercapacitors (ESs) are considered potential energy storage systems that could balance power and energy densities with fast charge-discharge and a long lifetime. The purpose of this research is to advance nanocomposite materials for electrochemical supercapacitor applications, where we use new colloidal approaches to fabricate high-performance electrochemical supercapacitor electrodes and devices. Our results reveal that these devices can have exceptional performance that facilitates new routes for their development.

In this study, polypyrrole (PPy) prepared by chemical and electrochemical polymerization was investigated as the electrode of electrochemical supercapacitor (ES). New strategies were developed for the fabrication of nano-structured PPy and PPy based nano-composites, which included discovery of advanced anionic dopants and multi-functional nano-crystals, and development of co-dispersing agents. These methods improved the capacitive performance and cycle stability of PPy electrodes. The results indicated that high material loading and good capacitance retention of PPy was achieved using an electrochemical polymerization method and Ni plaque as the current collectors. Nano-crystalline (CTA)2S2O8 formed by a chemical precipitation method from solutions, containing anionic oxidant (S2O82-) and cationic surfactant (CTA+), could be used as the oxidant to synthesize PPy nano-fibers. We demonstrated that multi-wall carbon nanotubes (MWCNT) can be efficiently dispersed using such nano-crystals. Application of multi-functional nano-crystals is a conceptually new approach for the fabrication PPy coated MWCNT. Moreover, safranin and malachite green were found as universal dispersing and charging agents for cataphoretic deposition of graphene, MWCNT and PPy nano-fibers. It opens new strategies in colloidal and electrochemical processing of PPy nano-composites for ES electrodes. PPy coated MWCNT, prepared by the multi-functional nano-crystals (CTA)2S2O8, was employed for the fabrication of N-doped activated carbon-coated MWCNT (N-AC-MWCNT). The obtained N-AC-MWCNT was uniformly coated and possessed with high surface area. The use of N-AC-MWCNT enabled the fabrication of ES electrodes with high mass loading and high active material to current collector mass ratio. Symmetric and asymmetric ES cells, fabricated by N-AC-MWCNT and aqueous Na2SO4 electrolyte, showed high specific capacitance, good capacitance retention and large voltage window. The positive electrode of asymmetric ES, MnO2 coated MWCNT, was successfully prepared by the chemical reaction between KMnO4 and N-AC-MWCNT. The problem of degradation of MWCNT was avoided by the use of N-AC as the sacrificial carbon. Significant progress on ES technology has allowed for the development of capacitive dyes removal (CDR) methods using ES devices. In our study, porous carbon materials, N-doped activated carbon coated MWCNT (N-AC-MWCNT) and N-doped activated carbon nano-fibers (N-AC-NF), were developed as the electrodes for CDR applications. The experimental results indicated that capacitive performance of ES cells was influenced by the chemical structure, size, charge-to mass ratio, concentration and redox-active ligands of the dyes. CDR is a promising method for removal of various cationic and anionic dyes, which offers advantages of energy saving and simple electrode regeneration. / Thesis / Doctor of Philosophy (PhD)

Neste estudo foi investigado o processo de redução térmica do óxido de grafeno em médio vácuo como uma rota viável de baixo custo econômico para obtenção do óxido de grafeno reduzido para aplicação em supercapacitores. O objetivo principal foi estudar a influência da temperatura de processamento no grau de redução do óxido de grafeno utilizando um sistema de vácuo com bomba mecânica de duplo estágio. O processamento constituiu na exposição do óxido de grafeno em várias temperaturas (200, 400, 600, 800 e 1000 °C) com pressão reduzida (10-2mbar) condição de médio vácuo. Foram utilizadas técnicas convencionais para caracterização dos materiais precursores e processados, tais como: microscopia eletrônica de varredura (MEV), difração de raios-X (DRX) e espectroscopia no infravermelho com transformada de Fourier (FTIR). Com os resultados deste estudo foi demostrado que é possível obter o óxido de grafeno reduzido utilizando um sistema de vácuo com bomba mecânica de duplo estágio e temperaturas de processamento superiores a 200°C. / In this study the process of medium vacuum thermal reduction of the graphene oxide as a low cost route for obtaining reduced graphene oxide has been investigated. The main objective was to study the influence of the processing temperature on the degree of reduction of the graphene oxide using a vacuum system with two stage backing pump. The processing was carried out by exposing the graphene oxide at various temperatures (200, 400, 600, 800 e 1000 °C) with reduced pressure (10-2 mbar). Conventional techniques have been employed to the characterization of the starting and processed materials, such as: scanning electron microscopy (SEM), X-ray diffraction and Fourier transformed infrared spectroscopy (FTIR). With the results of this study it has been demonstrated that it is possible to obtain the reduced graphene oxide using a vacuum system with a two stage backing pump and processing temperatures superior to 200°C.

No description available.

The production of cellulose derived hybrid carbon nanofibre (CNF)/carbon nanotubes (CNTs) electrodes for the fabrication of supercapacitors and carbon fibre composites was investigated. The CNTs were grown via a floating catalyst chemical vapor deposition (CVD) method on the top surface of electrospun cellulose derived CNFs. These CNF and CNF/CNTs samples were then used as electrodes to produce liquid electrolyte-based supercapacitors. The growth of CNTs leads to an improvement of electrochemical performance compared to the plain CNFs. This improvement is due to the grown CNTs enlarging the reactive sites through enhanced surface area and porosity, and thereby increasing the conductivity of the system. CNTs have been also grown onto CNFs containing ferrocene and SiC particles. Composites were fabricated by combining the fibres and CNTs grown fibres with model polymers. The stress transfer properties of these materials have been estimated using an in situ Raman spectroscopic method by observing the shift of the Raman band during the tensile deformation of model polymer composites. Using this method, the elastic modulus of CNF/SiC/CNTs fibres has been estimated to be 208 ± 26 GPa. No shifts in the peak positions of bands relating to the carbon structure were obtained for in situ Raman spectroscopic studies of the CNF/CNTs fibres made from the ferrocene embedded fibres. This was thought to be due to the low yield of CNTs on the surface of the fibres. Furthermore, CNF/CNTs electrode-based structural supercapacitors, combining a solid electrolyte with the carbonized fibres, have been produced. These CNF/CNTs electrodes have a better capacitive performance than the plain CNF electrodes. There was a decrease in this performance with increased curing time of the resin, from 2 to 24 h, due to a lack of charge carrier mobility in the latter samples. A Raman spectroscopic study of the deformation of the carbon structures showed that the G-band shift towards a lower wavenumber position for the CNF and CNF/CNTs samples processed at a carbonization temperature of 2000 °C. Moduli of these fibres were estimated to be ~145 GPa and ~271 GPa, respectively, suggesting the growth of CNTs not only enhances the capacitive performance but also the mechanical properties of the structural supercapacitors. No Raman bend shift was found for the CNFs and CNF/CNTs samples processed below a carbonization temperature of 2000 °C, e.g. 900 °C and 1500 °C. This is because the graphitic structures are not well developed at carbonization temperatures below 1500 °C.

Neste trabalho foi proposto investigar as características de capacitores eletroquímicos de dupla camada elétrica (supercapacitores) utilizando como matéria prima um eletrólito biocompatível como rota viável de baixo custo econômico para obtenção de dispositivos eletrônicos para armazenamento de energia. O objetivo principal foi estudar a influência dos vários parâmetros de processamento nas características elétricas de supercapacitores à base de eletrólito neutro, utilizando, na preparação dos eletrodos oxido de grafeno reduzido via HDDR 400°C e o carbono ativado, também com baixa toxidade e impacto ambiental. O primeiro tópico consistiu na preparação de eletrólitos com diferentes concentrações para avaliar este parâmetro na curva de autodescarga dos supercapacitores. Alternativamente realizou-se a caracterização dos eletrodos preparados com oxido de grafeno reduzido via HDDR 400°C e carbono ativado por ensaios de voltametria cíclica em um analisador eletrônico computadorizado de supercapacitores, que resultou na determinação da capacitância específica do material precursor e das resistências internas. Foram utilizadas técnicas adicionais para caracterização dos materiais precursores e processados, tais como: microscopia eletrônica de varredura (MEV-EDS), difração de raios-X (DRX). / On this work was proposed research the electrochemical double layer capacitors characteristics (supercapacitors) using an environmentally compatible electrolyte as viable low economic cost path to obtain electronics devices for energy storage. The mains objective was to study the influence of the various processing parameters on electrical characteristics of supercapacitors based in neutral electrolyte, using in the preparation the activated carbon and reduced graphene oxide HDDR 400°C, also with low toxicity and environmentally impact. The first topic consisted in the preparation of electrolytes with different concentrations to evaluate this parameter in the self-discharge curve of supercapacitors. Alternatively was made characterization experiments of the activated carbon electrodes and rGO HDDR 400°C by cyclic voltammetry essays in an electronic computerized analyzer of supercapacitors that resulted in the determination of the precursor material specific capacitance and internal resistances Was utilized additional technics for characterization of precursor materials such as scanning electron microscopy (MEV-EDX) and X-ray diffraction (DRX).

The mounting concern for renewable energies from ecologically conscious alternatives is growing in parallel with the demand for portable energy storage devices, fuelling research in the fields of electrochemical energy storage technologies. The supercapacitor, also known as electrochemical capacitor, is an energy storage device possessing a near infinite life-cycle and high power density recognized to store energy in an electrostatic double-layer, or through a pseudocapacitance mechanism as a result of an applied potential. The power density of supercapacitors far exceeds that of batteries with an ability to charge and discharge stored energy within seconds. Supercapacitors compliment this characteristic very well with a cycle life in excess of 106 cycles of deep discharge within a wide operational temperature range, and generally require no further maintenance upon integration. Conscientious of environmental standards, these devices are also recyclable. Electrochemical capacitors are currently a promising candidate to assist in addressing energy storage concerns, particularly in hybridized energy storage systems where batteries and supercapacitors compliment each other’s strengths; however specific challenges must be addressed to realize their potential. In order to further build upon the range of supercapacitors for future market applications, advancements made in nanomaterial research and design are expected to continue the materials development trend with a goal to improve the energy density through the development of a cost-efficient and correspondingly plentiful material. However, it is important to note that the characteristic power performance and exceptional life-cycle should be preserved alongside these efforts to maintain their niche as a power device, and not simply develop an alternative to the average battery. It is with this clear objective that this thesis presents research on an emerging carbon material derived from an abundant precursor, where the investigations focus on its potential to achieve high energy and power density, stability and integration with other electroactive materials. Activated carbons have been the dominant carbon material used in electric double-layer capacitors since their inception in the early 1970s. Despite a wide range of carbon precursors and activation methods available for the generation of high surface area carbons, difficulties remain in controlling the pore size distribution, pore shape and an interconnected pore structure to achieve a high energy density. These factors have restricted the market growth for supercapacitors in terms of the price per unit of energy storage. Activation procedures and subsequent processes for these materials can also be energy intensive (i.e. high temperatures) or environmentally unfriendly, thus the challenge remains in fabricating an inexpensive high surface-area electroactive material with favourable physical properties from a source available in abundance. Double-layer capacitive materials researched to replace active carbons generally require properties that include: high, accessible surface-area; good electrical conductivity; a pore size distribution that includes mesopore and micropore; structural stability; and possibly functional groups that lend to energy storage through pseudocapacitive mechanisms. Templated, fibrous and aerogel carbons offer an alternative to activated carbons; however the drawbacks to these materials can include difficult preparation procedures or deficient physical properties with respect to those listed above. In recent years nanostructured carbon materials possessing favourable properties have also contributed to the field. Graphene nanoplatelet (GNP) and carbon nanotube (CNT) are nanostructured materials that are being progressively explored for suitable development as supercapacitor electrodes. As carbon lattice structured materials either in the form of a 2-dimensional sheet or rolled into a cylinder both of these materials possess unique properties desirable in for electrode development. In the proceeding report, GNPs are investigated as a primary material for the synthesis of electrodes in both a pure and composite form. Three projects are presented herein that emphasize the suitability of GNP as a singular carbon electrode material as well as a structural substrate for additional electroactive materials. Investigation in these projects focuses on the electrochemical activity of the materials for supercapacitor devices, and elucidation of the physical factors which contribute towards the observed capacitance. An initial study of the GNPs investigates their distinct capacitive ability as an electric double-layer material for thin-film applications. The high electrically conductivity and sheet-like structure of GNPs supported the fabrication of flexible and transparent films with a thickness ranging from 25 to 100 nm. The thinnest film fabricated (25 nm) yielded a high specific capacitance from preliminary evaluation with a notable high energy and power density. Furthermore, fast charging capabilities were observed from the GNP thin film electrodes. The second study examines the use of CNT entanglements dispersed between GNP to increase the active surface area and reduce contact resistances with thin-film electrodes. Through the use MWNT/GNP and SWNT/GNP composites it was determined that tube aspect ratio influences the resulting capacitive performance, with the formation of micropores in SWNT/GNP yielding favourable results as a composite EDLC. The third study utilizes electrically conducting polypyrrole (PPy) deposited onto a GNP film through pulse electrodeposition for use as a supercapacitor electrode. Total pulse deposition times were evaluated in terms of their corresponding improvements to the specific capacitance, where an optimal deposition time was discovered. A significant increase to the total specific capacitance was observed through the integration PPy, with the majority charge storage being developed via psuedocapacitive redox mechanisms. A summary of the studies presented here centers on the development of GNP electrodes for application in high power supercapacitor devices. The potential use for GNP in both pure and composite electrode films is explored for electrochemical activity and capacitive capabilities, with corresponding physical characterization techniques performed to examine influential factors which contribute to the final results. The work emphasizes the suitability of GNP material for future investigations into their application as carbon or carbon composite electrodes in supercapacitor devices.