Thermodynamic considerations of same-metal electrodes in an asymmetric cell

Abstract

Abstract An electrochemical cell contains three open thermodynamic systems that, in dynamic equilibrium, equalize their electrochemical potentials with that of their surrounding by forming an electric-double-layer-capacitor at the interface of the electrolyte with each of the two electrodes. Since the electrode/electrolyte interfaces are heterojunctions, the electrochemical potentials or Fermi levels of the two materials that contact the electrolyte at the two electrodes determine the voltage of a cell. The voltage is the sum of the voltages of the two interfacial electric-double-layer capacitors at the two electrode/electrolyte interfaces. A theoretical analysis of the thermodynamics that gives a quantitative prediction of the observed voltages in an asymmetric cell with an S8 relay at the positive electrode is provided. In addition, new discharge data and an X-ray photoelectron spectroscopy analysis of the lithium plated on the positive electrode of a discharged cell is presented. Ab initio, DFT methods were used to calculate the band structure and surface-state energies of the crystalline S8 solid sulfur relay. The theoretical exposition of the thermodynamics of the operative driving force of the chemical reactions in an electrochemical cell demonstrate that our initial experimental data and conclusions are valid. Other reported observations of lithium plating on the positive electrode, observations that were neither exploited nor their origins specified, are also cited.

Keywords

• Thermodynamics
• Electrochemical potentials
• Heterojunctions
• Batteries
• Solid state
• Double layer capacitors