Parametrisation and Use of a Predictive DFN Model for a High-Energy NCA/Gr-SiOx Battery

We demonstrate the predictive power of a parametrised Doyle-Fuller-Newman (DFN) model of a commercial cylindrical (21700) lithium-ion cell with NCA/Gr-SiOx chemistry. Model parameters result from the deconstruction of a fresh commercial cell to determine/confirm chemistry and microstructure, and also from electrochemical experiments with half-cells built from electrode samples. The simulations predict voltage proles for (i) galvanostatic discharge and (ii) drive-cycles. Predicted voltage responses deviate from measured ones by <1% throughout at least 95% of a full galvanostatic discharge, whilst the drive cycle discharge is matched to a 1-3% error throughout. All simulations are performed using the online computational tool DandeLiion, which rapidly solves the DFN model using only modest computational resource. The DFN results are used to quantify the irreversible energy losses occurring in the cell and deduce their location. In addition to demonstrating the predictive power of a properly validated DFN model, this work provides a novel simplifed parametrisation work that can be used to accurately calibrate an electrochemical model of a cell.

Microstructure and Discharge Performance of Aluminum Al 6061 Alloy as Anode for Electrolyte Activated Battery

Electrolyte activated battery finds its important use during natural disaster emergencies, such as floods and typhoons. Nevertheless, high corrosion rate will deteriorate the discharge performance of the battery and it is influenced by the type of electrolyte and discharge current. In this study, the corrosion and discharge performance of a commercial Al 6061 aluminum alloy as an anode are investigated at different discharge currents (0.001, 0.01, and 1 mA) and in different electrolytes, namely salt water, urea, and distilled water. Scanning electron microscopy results show that electrode in salt water has the most serious corrosion, followed by that of in urea and in distilled water. These electrode-electrolyte combinations are further investigated with potentiodynamic polarization, galvanostatic discharge, and electrochemical impedance spectroscopy (EIS) to understand their discharge potential, discharge behavior, and corrosion mechanism. Among all combinations, aluminum in water is found to have the highest discharge performance with discharge potentials ranging from 716 to 744 mV, regardless of discharge current.

Microstructure and Discharge Performance of Aluminum Al 6061 Alloy as Anode for Electrolyte Activated Battery

Electrolyte activated battery finds its important use during natural disaster emergencies, such as floods and typhoons. Nevertheless, high corrosion rate will deteriorate the discharge performance of the battery and it is influenced by the type of electrolyte and discharge current. In this study, the corrosion and discharge performance of a commercial Al 6061 aluminum alloy as an anode are investigated at different discharge currents (0.001, 0.01, and 1 mA) and in different electrolytes, namely salt water, urea, and distilled water. Scanning electron microscopy results show that electrode in salt water has the most serious corrosion, followed by that of in urea and in distilled water. These electrode-electrolyte combinations are further investigated with potentiodynamic polarization, galvanostatic discharge, and electrochemical impedance spectroscopy (EIS) to understand their discharge potential, discharge behavior, and corrosion mechanism. Among all combinations, aluminum in water is found to have the highest discharge performance with discharge potentials ranging from 716 to 744 mV, regardless of discharge current.

High-Performance Mg–Al–Bi Alloy Anode for Seawater Batteries and Related Mechanisms

Bi, a group 15 element, was added to magnesium alloys and applied to seawater batteries in marine operating machinery to improve the electrochemical performance and corrosion resistance of the battery. The electrochemical properties of as-cast pure Mg, Mg–8Al, and Mg–8Al–xBi alloy anodes in 3.5% NaCl solution were researched. Electrochemical impedance spectroscopy and an immersion test in 3.5% NaCl solution show that the Mg–8%Al–0.4%Bi alloy provides better corrosion resistance than Mg and the Mg–8Al alloy. The galvanostatic discharge results show that the Mg–8%Al–0.4%Bi alloy revealed better electrochemical properties and utilization efficiency in 3.5% NaCl solution. The Mg17Al12 and BiOCl phases formed during the discharge process of the Mg–8%Al–0.4%Bi alloy play an important role in improving the electrochemical performance and utilization efficiency of the alloy.

Influence of Fe and Ni Doped CuO Nanomaterials for High Performance Supercapacitors

This paper focuses on the synthesis of doped and undoped CuO nanoparticles using the sol-gel method, which has been prepared and described. Supercapacitor applications of as-synthesized nanomaterials were analyzed using cyclic voltammetry (CV), galvanostatic discharge (GCD) and electrochemical impedance spectroscopic (EIS) analysis. The cyclic voltammograms illustrated the quasi-rectangular shape which depicted the pseudocapacitance nature of the samples. The calculated specific capacitance of the prepared samples was 180, 253 and 303 (F/g) corresponding to CuO, Fe-CuO and Ni-CuO, respectively at the low current density and the EIS spectra show that the prepared Ni-CuO electrode exhibits low charge transfer resistance.

Modeling the Effect of the Loss of Cyclable Lithium on the Performance Degradation of a Lithium-Ion Battery

This paper reports a modeling methodology to predict the effect of the loss of cyclable lithium of a lithium-ion battery (LIB) cell comprised of a LiNi0.6Co0.2Mn0.2O2 cathode, natural graphite anode, and an organic electrolyte on the discharge behavior. A one-dimensional model based on a finite element method is presented to calculate the discharge behaviors of an LIB cell during galvanostatic discharge for various levels of the loss of cyclable lithium. Modeling results for the variation of the cell voltage of the LIB cell are compared with experimental measurements during galvanostatic discharge at various discharge rates for three different levels of the loss of cyclable lithium to validate the model. The calculation results obtained from the model are in good agreement with the experimental measurements. On the basis of the validated modeling approach, the effects of the loss of cyclable lithium on the discharge capacity and available discharge power of the LIB cell are estimated. The modeling results exhibit strong dependencies of the discharge behavior of an LIB cell on the discharge C-rate and the loss of cyclable lithium.

Highly Concentrated Aqueous Electrolyte With a Large Stable Potential Window for Electrochemical Double-Layer Capacitors

An active carbon (AC)/AC electrochemical capacitor, taking advantage of a high-concentrated lithium trifluoromethane sulfonate (LiTFS) or lithium bis(trifluoromethane sulfonyl) imide (LiTFSI) aqueous electrolyte, was demonstrated with an extended operating voltage of 2.5 V, which is the largest value till now for aqueous carbon-based capacitors. The AC electrode is entirely capacitive in these two electrolytes and the stable potential window of the single AC electrode can reach −1.2 to 1.2 V versus the saturated calomel electrode (SCE). The performance of the AC-based capacitor is evaluated in two- and three-electrode cells using a combination of electrochemical impedance (EIS), cyclic voltammetry (CV), galvanostatic discharge-charge, and self-discharge (SD, i.e., leakage current) measurements. At 0.5-mA cm−2 charge-discharge rate, the AC/AC capacitor presents 5.5 wh kg−1 and 4.5 wh kg−1 energy density for 20 m LiTFS and LiTFSI electrolyte, respectively. The results suggest that a thorough utilization of such lithium salt aqueous electrolytes with widening electrochemical stable potential window will no doubt lead to further development of electrochemical capacitors toward superior performance.