Ricardo Pinedo

One- or Two-Electron Transfer? The Ambiguous Nature of the Discharge Products in Sodium-Oxygen Batteries.

Rechargeable lithium-oxygen and sodium-oxygen cells have been considered as challenging concepts for next-generation batteries, both scientifically and technologically. Whereas in the case of non-aqueous Li/O2 batteries, the occurring cell reaction has been unequivocally determined (Li2O2 formation), the situation is much less clear in the case of non-aqueous Na/O2 cells. Two discharge products, with almost equal free enthalpies of formation but different numbers of transferred electrons and completely different kinetics, appear to compete, namely NaO2 and Na2O2. Cells forming either the superoxide or the peroxide have been reported, but it is unclear how the cell reaction can be influenced for selective one- or two-electron transfer to occur. In this Minireview, we summarize available data, discuss important control parameters, and offer perspectives for further research. Water and proton sources appear to play major roles.

How To Improve Capacity and Cycling Stability for Next Generation Li–O2 Batteries: Approach with a Solid Electrolyte and Elevated Redox Mediator Concentrations

Because of their exceptionally high specific energy, aprotic lithium oxygen (Li-O2) batteries are considered as potential future energy stores. Their practical application is, however, still hindered by the high charging overvoltages and detrimental side reactions. Recently, the use of redox mediators dissolved in the electrolyte emerged as a promising tool to enable charging at moderate voltages. The presented work advances this concept and distinctly improves capacity and cycling stability of Li-O2 batteries by combining high redox mediator concentrations with a solid electrolyte (SE). The use of high redox mediator concentrations significantly increases the discharge capacity by including the oxidation and reduction of the redox mediator into charge cycling. Highly efficient cycling is achieved by protecting the lithium anode with a solid electrolyte, which completely inhibits unfavored deactivation of oxidized species at the anode. Surprisingly, the SE also suppresses detrimental side reactions at the carbon electrode to a large extent and enables stable charging completely below 4.0 V over a prolonged period. It is demonstrated that anode and cathode communicate deleteriously via the liquid electrolyte, which induces degradation reactions at the carbon electrode. The separation of cathode and anode with a SE is therefore considered as a key step toward stable Li-O2 batteries, in conjunction with a concentrated redox mediator electrolyte.

New Insights into the Instability of Discharge Products in Na-O2 Batteries.

Sodium-oxygen batteries currently stimulate extensive research due to their high theoretical energy density and improved operational stability when compared to lithium-oxygen batteries. Cell stability, however, needs to be demonstrated also under resting conditions before future implementation of these batteries. In this work we analyze the effect of resting periods on the stability of the sodium superoxide (NaO2) discharge product. The instability of NaO2 in the cell environment is demonstrated leading to the evolution of oxygen during the resting period and the decrease of the cell efficiency. In addition, migration of the superoxide anion (O2(-)) in the electrolyte is observed and demonstrated to be an important factor affecting Coulombic efficiency.

Carbon-Free Cathodes: A Step Forward in the Development of Stable Lithium-Oxygen Batteries.

Lithium-oxygen (Li-O2 ) batteries are receiving considerable interest owing to their potential for higher energy densities than current Li-ion systems. However, the lack stability of carbon-based oxygen electrodes is believed to promote carbonate formation leading to capacity fade and limiting the cycling performance of the battery. To improve the stability and cyclability of these systems, alternative electrode materials are required. Metal oxides are mainly utilized at low current densities, whereas noble metals show outstanding performance at high current densities. Carbides appear to provide a good compromise between electrochemical performance and cost, which makes them interesting materials for further investigations. Here, a critical review of current carbon-free electrode research is provided with the goal of identifying routes to its successful optimization.

(Electro)chemical expansion during cycling: monitoring the pressure changes in operating solid-state lithium batteries

Solid-state lithium-ion batteries (SSBs) are a promising concept for future energy storage applications. Interestingly, the mechanical effects during operation of SSBs, and their correlation to the electrochemical performance, have rarely been investigated. In such systems, the rigid mechanical coupling between the active phases and the solid electrolyte will lead to more complex non-local strain effects than in the common liquid electrolyte-based lithium-ion batteries, where the chemical expansion or compression of the active phases is accommodated by the liquid electrolyte, and only local mechanical strain within the electrode particles exists. In this work we report on the pressure and height changes within typical solid-state batteries, which were measured in situ during galvanostatic cycling conditions. The continuous volume changes of both the anode and the cathode during lithiation/delithiation are responsible for a highly reproducible cycle of pressure changes during the operation of the solid-state battery cell. Bending and cracking of the solid-state battery cells are observed with X-ray tomography and provide evidence for the critical role of the macroscopic strain generated during cycling. Furthermore, these pressure and dilatometry measurements as well as X-ray tomography underline the importance of external confinement and pressure control for SSBs.