Abstract:We report spectroelectrochemical studies to investigate the charge storage mechanism of composite polypyrrole/lignin electrodes. Renewable bioorganic electrode materials were produced by electropolymerization of pyrrole in the presence of a water-soluble lignin derivative acting as dopant. The resulting composite exhibited enhanced charge storage abilities due to a lignin-based faradaic processes, which was expressed after repeated electrochemical redox of the material. The in-situ FTIR spectroelectrochemistry… Show more
“…The peaks at 1040 cm −1 , 1331 cm −1 and 1420 cm −1 in both products correspond to O 2 2− species and 410 cm −1 corresponds to Zn-O bond38. The peaks at 3430, 2862, 1566, 1236, 965 cm −1 correspond to N-H, C-H, C=C, C-C-C and C-H sterching cofinfirming the presence of polypyrrole39. Figure 1c,d confirm single phasic cubic nanocrystalline ZnO 2 product (JCPDS card No.…”
Environmental hazard caused due to the release of dyes in effluents is a concern in many countries. Among the various methods to combat this problem, Advanced Oxidation Process, in which semiconductor photocatalysts are used, is considered the most effective one. These materials release Reactive Oxygen Species (ROS) such as hydroxyl radical and superoxide in suspension that degrade the dyes into non-toxic minerals. However, this process requires visible or UV light for activation. Hence, there is a need to develop materials that release ROS, both in the absence and in the presence of light, so that the efficiency of dye removal is enhanced. Towards this objective, we have designed and synthesized a new nanocomposite ZnO2/polypyrrole which releases ROS even in the dark. The ROS released in the dark and in light were estimated by standard methods. It is to be noted that ZnO2 degrades the dye only under UV light but not in dark or in the presence of visible light. We propose the mechanism of dye degradation in dark and light. The synergically coupled nanocomposite of ZnO2/ppy is the first example that degrades dyes in the dark, through advanced oxidation process without employing additional reagents.
“…The peaks at 1040 cm −1 , 1331 cm −1 and 1420 cm −1 in both products correspond to O 2 2− species and 410 cm −1 corresponds to Zn-O bond38. The peaks at 3430, 2862, 1566, 1236, 965 cm −1 correspond to N-H, C-H, C=C, C-C-C and C-H sterching cofinfirming the presence of polypyrrole39. Figure 1c,d confirm single phasic cubic nanocrystalline ZnO 2 product (JCPDS card No.…”
Environmental hazard caused due to the release of dyes in effluents is a concern in many countries. Among the various methods to combat this problem, Advanced Oxidation Process, in which semiconductor photocatalysts are used, is considered the most effective one. These materials release Reactive Oxygen Species (ROS) such as hydroxyl radical and superoxide in suspension that degrade the dyes into non-toxic minerals. However, this process requires visible or UV light for activation. Hence, there is a need to develop materials that release ROS, both in the absence and in the presence of light, so that the efficiency of dye removal is enhanced. Towards this objective, we have designed and synthesized a new nanocomposite ZnO2/polypyrrole which releases ROS even in the dark. The ROS released in the dark and in light were estimated by standard methods. It is to be noted that ZnO2 degrades the dye only under UV light but not in dark or in the presence of visible light. We propose the mechanism of dye degradation in dark and light. The synergically coupled nanocomposite of ZnO2/ppy is the first example that degrades dyes in the dark, through advanced oxidation process without employing additional reagents.
“…The polypyrrole/LS hybrid materials show a discharge capacity of 72 mA h g À1 and the capacity decreases dramatically aer 100 charge-discharge cycles. 7 The PEDOT/LS hybrid materials display a discharge capacity of 34 mA h g À1 and retain 83% of the capacity aer 1000 charge-discharge cycles. 6 The PEDOT/ LS/PAAQ hybrid materials present a discharge capacity of 80 mA h g À1 and a retention capacity of 80% aer 10 000 charge-discharge cycles.…”
Section: Electrochemical Characterization Of Electrodesmentioning
Lignin is a promising candidate for energy storage because of its abundance, wide geographic distribution, and low cost as it is mainly available as a low value product from processing of wood into paper pulp. Lignin contains large amounts of potential quinone groups, which can be oxidized and reduced in a two electron process. This redox reaction makes lignin suitable for charge storage. However, lignin is insulating and therefore conductive materials are necessary in lignin electrodes, for whom the cost of the conductive materials hinders the scalable application. Among the organic conductive materials, graphite is one of the cheapest and is easily acquired from nature. In this work, we combine graphite and lignosulfonate (LS) and fabricate LS/graphite organic electrodes under a solvent-free mechanical milling method, without additives. The graphite is sheared into small particles with a size range from 50 nm to 2000 nm. Few-layer graphene is formed during the ball milling process. The LS/graphite hybrid material electrodes with primary stoichiometry of 4/1 (w/w) gives a conductivity of 280 S m À1 and discharge capacity of 35 mA h g À1 . It is a promising material for the scalable production of LS organic electrodes.
“…The utility of the quinone/hydroquinone redox reaction to store charge has shown great potential in lignin/conjugated polymer polymeric complex system. [29][30][31][32] In these systems, lignin provides the quinone groups while the conducting polymer provides electrochemical accessibility to these functional groups. To further maximize the charge storage through quinone pseudocapacitance, we combined a conjugated polymer, PAAQ with integrated quinone, [33,34] with the PEDOT/lignin, resulting in a trihybrid electrode structure based on PEDOT/lignin complex and PAAQ (Figure 1a).…”
Section: Electrochemical Characterization Of Individual Electrode Matmentioning
lately. Supercapacitor devices allow a considerable amount of stored electric energy to be delivered rapidly, giving rise to high power capability in conjunction with long cycling life and high reversibility. [4][5][6][7] Nevertheless the demand for higher energy density supercapacitors is increasing, to be used as a storage device for renewable electricity.The development of new materials that improve the efficiency of energy conversion and storage is essential for a sustainable future. [8][9][10] These materials should be renewable, biodegradable, and have low cost. [11] Lignin is the second most abundant biopolymer on Earth, and complies with these characteristics. It is the largest natural source of quinone-aromatics chemical groups that can be employed to store and deliver charges by reversible Faradaic reactions. [12,13] However, the insulating nature of lignin limits the access to these functional redox groups. Therefore, it is necessary to form hybrids with other conductive materials such as conducting polymers [14] or carbon derivatives. [15][16][17] In order to harness the potential of conducting polymers as supercapacitor electrode materials, it is critical to improve their poor long-term stability and to increase their specific capacitance and energy density by fully utilizing the pseudo-capacitive redox processes. [18][19][20] In our previous work, we have constructed electrodes with hybrid materials based on electronic polymers and lignin derivatives. We found that the best combination was poly(3,4-ethylenedioxythiophene) PEDOT/lignin with a specific capacitance of 170 F g −1 . [21] We further investigated the interpenetrating network of poly(aminoanthraquinone) (PAAQ) and PEDOT with increased specific capacitance up to 383 F g −1 . [22] The development of hybrid electrode materials formed by electroactive and conducting components enable supercapacitor devices with intrinsic high specific power and improved energy density. These devices are described as symmetric SCs (SSCs) when both electrodes are identical, and asymmetric SCs (ASCs) when the material compositions of the positive and negative electrodes are different. The optimal performance is expected for asymmetric supercapacitors, because it may be possible to extend the operating voltage window of the cell, and its energy density thus becomes greater than that of the symmetric cells, as a consequence of electrodes operating reversibly in different potential ranges. [19,[23][24][25] A trihybrid bioelectrode composed of lignin, poly(3,4-ethylenedioxythiophene) (PEDOT), and poly(aminoanthraquinone) (PAAQ) is prepared by a two-step galvanostatic electropolymerization, and characterized for supercapacitor applications. Using PEDOT/Lignin as a base layer, followed by the consecutive deposition of PAAQ, the hybrid electrode PEDOT/Lignin/PAAQ shows a high specific capacitance of 418 F g −1 with small self-discharge. This trihybrid electrode material can be assembled into symmetric and asymmetric supercapacitors. The asymmetric supercapacitor uses PED...
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.