Effects of Surfactants on the Preparation of MnO2 and its Capacitive Performance

Amorphous hydrated manganese dioxide (MnO2) was prepared as an electrode material for supercapacitors by liquid co-precipitation in the presence of polyvinylpyrrolidone (PVP), polyethylene glycol (PEG) and sodium dodecylbenzenesulfonate (SDBS) respectively. The obtained samples were characterized by x-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), high-resolution transmission electron microscopy (HRTEM), and electrochemical methods. Physical characterizations confirmed that the addition of surfactants played an important role in the preparation of MnO2. The specific surface areas of MnO2 with the addition of PEG, SDBS and PVP were 169.92 m2/g, 137.40 m2/g and 196.64 m2/g, respectively, and the corresponding capacitances were 207.9 F/g, 187.5 F/g and 238.7 F/g. Compared with the sample without surfactants, the specific surface area and capacitance of the sample with the addition of PVP were improved by 92.2% and 53.1%, respectively. Moreover, the electrode showed good cycle stability at the current density of 120 mA/g, and 91.1% of its specific capacitance still remained after 500 cycles. It was concluded that this performance improvement was attributed to the electrostatic stabilization of the multivariate alkyl residue and cyano group (—NCO) as anchoring group, as well as the steric hindrance effect from lateral polarity groups of pentabasic ring in PVP structure.

Tea waste-supported hydrated manganese dioxide (HMO) for enhanced removal of typical toxic metal ions from water

A novel composite sorbent with hydrated manganese oxide (HMO) (<5 nm) highly dispersed on tea waste (TW), enjoying synergistic benefits from both materials, efficiently and selectively sorbed Pb(ii), Cd(ii), Cu(ii) and Zn(ii) from water.

Amorphous Manganese Dioxide as a Material for an Electrochemical Pseudocapacitor

The charge storage process of amorphous hydrated manganese dioxide (MnO2) as a pseudo-capacitor involves a fast redox reaction at the electrode surface. In order to understand the charge storage mechanism of MnO2 as a pseudo-capacitor in an aqueous KCl solution, we monitored the change of the capacitance by varying the pH of the solution, the cation of the electrolyte, the concentration of the KCl electrolyte, and the solvent. The charge storage mechanism of a metal oxide electrode such as MnO2 is concluded to involve a fast redox reaction through both the potassium ion exchange, MnO2 + δK+ + δe- ⇔ MnO2-δ(OK)δ and the proton exchange, MnO2 + δH+ + δe- ⇔ MnO2-δ(OH)δ dependent upon the availability of the cations in the electrolyte.