This study demonstrates the influence of incorporating composites such as waste plastics derived graphene (WPDG) and manganese dioxide (MnO2) in the mesoporous carbon (CR) and their consequent characteristics. The CR having WPDG as composite is named as CRG and MnO2 containing CR composite is termed as CRM. CRG possess the surface area as high as 790 m²g-1 along with pore volume of 0.565 cc g-1 and radius of 3.82 nm. Cyclic voltammetry (CV) study suggested that CR and CRG showed non-Faradic capacitive behavior with almost rectangular shaped CV profiles at low scan rates and this shows the existence of electric double layer structure. On the other hand, pseudo-capacitance is observed for CRM. Galvanostatic charge/discharge investigation revealed that the specific capacitance can be enhanced by 6 times upon subsequent immobilization of WPDG in CR whereas 4-fold upgrading in the specific capacitance after treating CR with MnO2. Interestingly, CRM showed higher capacitance retention as compared to CRG and is attributed to its smaller value of equivalent series resistance as compared to CRG. Ragone plots shown that the higher energy and power densities are found for the case of CRG.
Abstract:We have synthesized a range of zwitterionic amphiphilic diblock copolymers with the same hydrophilic block (carboxybetaine) but with different hydrophobic blocks (n-butylmethacrylate (n-BMA) or 2-ethylhexylacrylate (EHA)) by the reversible addition-fragmentation chain transfer (RAFT) polymerization method. Herein, we systematically examined the role of hydrophobicity and salt concentration dependency of surface activity and micellization behaviour of block copolymer. Transition from surface active to non-surface active occurred with increasing hydrophobicity of the hydrophobic block of block copolymer (i.e., replacing P(n-BMA) by PEHA). Foam formation of block copolymer slightly decreased with the similar variation of the hydrophobic block of block copolymer. Block copolymer with higher hydrophobicity preferred micelle formation rather than adsorption at the air-water interface. Dynamic light scattering studies showed that block copolymer having P(n-BMA) produced near-monodisperse micelles, whereas block copolymer composed of PEHA produced polydisperse micelles. Zimm plot results revealed that the value of the second virial coefficient (A 2 ) changed from positive to negative when the hydrophobic block of block copolymer was changed from P(n-BMA) to PEHA. This indicates that the solubility of block copolymer having P(n-BMA) in water may be higher than that of block copolymer having PEHA in water. Unlike ionic amphiphilic block copolymer micelles, the micellar shape of zwitterionic amphiphilic block copolymer micelles is not affected by addition of salt, with a value of packing parameters of block copolymer micelles of less than 0.3.
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