The present work describes the effects of dimethyl sulfoxide (DMSO) in KOH aqueous electrolyte on the performance of a zinc-air flow battery. Aqueous electrolytes containing 7 M KOH and (0 to 20)% v/v DMSO were studied revealing a critical role of DMSO on the dissolution and deposition of zinc. The anodic zinc dissolution process was studied via cyclic voltammetry, Tafel polarization and electrochemical impedance spectroscopy (EIS). The presence of DMSO showed improved zinc dissolution performance with the highest peak of zinc dissolution being the electrolyte containing 5% v/v DMSO. Tafel analysis demonstrated a significant decrease in polarization resistance and an increase in corrosion rate due to the introduction of DMSO to the electrolyte. This suggests that DMSO has the ability to suspend zinc oxide in the electrolyte, thus preventing passivation of the zinc surface. EIS results revealed that by adding DMSO to the electrolyte, charge transfer resistance increased. This is attributed to the formation of passive layers having arisen from DMSO adsorption, the formation of zincate ions in the vicinity of the zinc surface, and the deposition of discharged products. A difference in Nyquist plots was observed for 20% v/v DMSO/KOH and 0% v/v DMSO/KOH electrolytes implying non-Debye relaxation behavior taking place due to the surface effects. The electrolytes were implemented in a zinc-air flow battery. Maximum power densities of 130 mW/cm2 (5% v/v DMSO) and 125 mW/cm2 (20% v/v DMSO) were obtained and were observed to be about 43% and 28% higher than that of the DMSO-free electrolyte. Results indicated that when 20% v/v DMSO was added to KOH solution, there was 67% zinc utilization efficiency (550 mAh/g) which provided 20% improvement in discharge capacity. Further, the battery with 20% v/v DMSO demonstrated excellent cyclability. Overall, DMSO shows great promise for enhancement of zinc dissolution/deposition in zinc-air batteries.
Comparative study of Cu/ZnO/Al 2 O 3 (CZA) catalysts with different Cu loading in CO and CO 2 hydrogenation at 250 C under atmospheric pressure was investigated. Results showed that methanol was the major product for CO hydrogenation, while the main product for CO 2 hydrogenation was CO. High Cu loading catalyst exhibited high catalytic activity in both CO and CO 2 hydrogenation. Low Cu loading catalyst showed deactivation with time on stream after 1-2 h by coke formation containing both amorphous and graphitic cokes for both CO and CO 2 hydrogenation.
Herein, the formation and electrochemical performance of a novel binder-free turbostratic stacked/ well-ordered stacked δ-MnO2-carbon fiber composite cathodes in deep eutectic solvent (DES) based zinc-ion battery (ZIB) is reported. Results of morphological, elemental, and structural analyses revealed directly grown and interconnected δ-MnO2 crumpled nanosheets on a carbon fiber substrate. Moreover, an improvement via a simple annealing strategy in the stacking, surface area and conductivity of the δ-MnO2 sheets was observed. Annealing induces the rearrangement of δ-MnO2 sheets resulting in the transformation from turbostratic stacking to a well-ordered stacking of -MnO2 sheets, as indicated by the selected area electron diffraction (SAED) hexagonal single crystal pattern. Besides, the formation of the well-ordered stacking of -MnO2 sheets exhibited improved electrochemical performance and cyclability, as cathode material for ZIB. The novel strategy described in this study is an essential step for the development of binder-free δ-MnO2-C fiber composite with a well-ordered stacking of δ-MnO2 sheets. This study also demonstrated comparable electrochemical performance between the turbostratic -MnO2 sheets and the well-ordered stacked δ-MnO2 sheets.
Graphene and graphene-based hybrid materials have emerged as an outstanding supercapacitor electrode material primarily because of their excellent surface area, high electrical conductivity, and improved thermal, mechanical, electrochemical cycling stabilities. Graphene alone exhibits electric double layer capacitance (EDLC) with low energy density and high power density. The use of aerogels in a supercapacitor is a pragmatic approach due to its extraordinary properties like ultra-lightweight, high porosity and specific surface area. The aerogels encompass a high volume of pores which leads to easy soak by the electrolyte and fast charge-discharge process. Graphene aerogels assembled into three-dimensional (3D) architecture prevent there stacking of graphene sheets and maintain the high surface area and hence excellent cycling stability and rate capacitance. However, the energy density of graphene aerogels is limited due to EDLC type of charge storage mechanism. Consequently, 3D graphene aerogel coupled with pseudocapacitive materials such as transition metal oxides, metal hydroxides, conducting polymers, nitrides, chalcogenides show an efficient energy density and power density performance due to the presence of both types of charge storage mechanisms. This laconic review focuses on the design and development of graphene-based aerogel in the field of the supercapacitor. This review is an erudite article about methods, technology and electrochemical properties of graphene aerogel.
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