h i g h l i g h t sZneMnO 2 battery was cycled at shallow DOD for more than 3000 cycles. Relatively low delivered cost of less than $150 per kWh. Mathematical model developed to understand the capacity fade mechanisms. Resistive film formation on the surface of MnO 2 particle during cycling. Change in SOC during cycling was used to measure capacity loss.
Keywords:Rechargeable zincemanganese dioxide battery Cycle life ZneMnO 2 battery model Capacity fade model Film resistance a b s t r a c t Batteries based on manganese dioxide (MnO 2 ) cathodes are good candidates for grid-scale electrical energy storage, as MnO 2 is low-cost, relatively energy dense, safe, water-compatible, and non-toxic. Alkaline ZneMnO 2 cells, if cycled at reduced depth of discharge (DOD), have been found to achieve substantial cycle life with battery costs projected to be in the range of $100 to 150 per kWh (delivered). Commercialization of rechargeable ZneMnO 2 batteries has in the past been hampered due to poor cycle life. In view of this, the work reported here focuses on the long-term rechargeability of prismatic MnO 2 cathodes at reduced DOD when exposed to the effects of Zn anodes and with no additives or specialty materials. Over 3000 cycles is shown to be obtainable at 10% DOD with energy efficiency >80%. The causes of capacity fade during long-term cycling are also investigated and appear to be mainly due to the formation of irreversible manganese oxides in the cathode. Analysis of the data indicates that capacity loss is rapid in the first 250 cycles, followed by a regime of stability that can last for thousands of cycles. A model has been developed that captures the behavior of the cells investigated using measured state of charge (SOC) data as input. An approximate economic analysis is also presented to evaluate the economic viability of ZneMnO 2 batteries based on the experiments reported here.
Gas sensing study of C2H4Li complex toward oxides viz. CO, CO2, NO, NO2, SO, and SO2 gas molecules has been carried out using ab initio method. Different possible configurations of gas molecule adsorption on C2H4Li complex are considered. The structural parameters of most stable configuration of gas molecule adsorbed complexes are thoroughly analysed. Electronic properties are studied using total density of states (DOS) plot. Charge transferred between the gas molecule and the substrate is studied using NBO charge analysis. Gas sensing of all the six gas molecules is possible at ambient conditions. Atom centred density matrix propagation (ADMP) molecular dynamics simulations confirmed that all the gas molecules remain adsorbed on C2H4Li complex at room temperature during the simulation. This study suggests that the C2H4Li complex acts as a novel gas sensing material for CO, CO2, NO, NO2, SO, and SO2 gas molecules at ambient conditions, below room temperature as well as at high pressure.
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