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Energy storage technologies with long storage duration are essential to stabilize electricity grids with a high share of intermittent renewable power. In a redox flow battery, the electrochemical conversion unit, where the charging and discharging reaction takes place, is spatially separated from the energy storage medium. In the all-vanadium redox flow battery (VRFB), a sulfuric acid aqueous electrolyte with dissolved vanadium ions is used as the storage medium. Vanadium is present in 4 different oxidation states, the redox couple vanadium(II) and (III) on the negative side of the cell, and vanadium(IV) and (V) on the positive side. This allows the battery to be repeatedly charged and discharged. A separator or membrane is used between the negative and positive electrode, which should selectively conduct the ions of the supporting electrolyte and minimize the passage of vanadium ions. Fluorinated membranes, such as Nafion™, are often used for this key component, but these ionomers were not originally developed for this application and therefore have functional shortcomings. Furthermore, the production and use of fluorinated materials is to be severely restricted or even banned in Europe. Therefore, the development of hydrocarbon-based membranes for the VRFB is of great importance. The study reported here focuses on polybenzimidazole polymers and membranes, which could be a promising materials class for next generation flow batteries. 

The mass loading of Si-graphite electrodes is often considered as a parameter of secondary importance when testing their performance. However, if a sacrificial additive is present in the electrolyte, the electrode loading becomes the battery cycle-life-determining factor. A lower loading was obtained by keeping slurry preparation steps unchanged from binder to binder and resulted in a longer lifetime for some of the binders. When the final loading was kept constant instead, the performance became independent of the binder used.

Evaluating potential electrolyte candidates is typically a lengthy procedure requiring long-term cycling experiments. To speed this process up, we have investigated potentiostatic lithium plating as a potential method for fast electrolyte suitability investigation. The applications of this methodology is not limited to liquid electrolytes, - effects of solid-state electrolytes, coatings, and other modifications can be readily assessed.

Lithium-rich layered oxides, containing cobalt, despite being promising high-capacity cathode materials, need alternatives to eliminate toxic and geopolitically restricted cobalt. An ongoing search for low-cost, Co-free Li-rich cathode materials with a better structural stability lead to investigation of Li_1.16Ni_0.19Fe_0.18Mn_0.46O₂ (LNFM), where cobalt is replaced by abundant iron. Our LNFM not only delivered a high capacity of 229 mAh/g but also has a stable average discharge voltage when cycled to upper cutoff potential of 4.8 V in additive-free electrolyte.

Fluoroethylene-carbonate is often referred to as a film-forming electrolyte additive for Li-ion batteries, resulting in high quality Solid–Electrolyte-Interphase on negative electrode, however, the underlying mechanism, even if thought to be known, has been only clarified due to our targeted experimental design, combining systematic electrochemical, chemical and microscopy characterization techniques. We have shown that first the formation of inorganic LiF-rich particles appear and only later the carbonate-rich film is actually formed.

The Lithium conducting electrolyte is a critical component of Li-ion batteries, as it has an important impact on performance and its durability, in particular in case of extreme environmental conditions. At low temperatures, a partial solidification can occur, while high temperatures can promote the degradation of the electrolyte. Using time-of-flight (ToF) neutron radiography, the possibility of imaging such changes in a fully non-invasive manner was demonstrated for the first time.

Control of interfacial reactivity at high-voltage is a key to high-energy-density Li-ion batteries. 2-aminoethyldiphenyl borate was investigated as an electrolyte additive to stabilize surface and bulk of both NCM851005 and graphite in the cell with upper cut-off voltage of 4.4 V vs Li+/Li. AEDB almost completely eliminated the “cross-talk” in the cell, by significantly reducing metal leaching from the cathode, preventing their deposition at the anode, and further electrolyte decomposition.

All-solid-state lithium ion batteries represent a promising battery technology for boosting the volumetric energy density and promising a superior safety. In this study excellent cycling stability of graphite anode material have been demonstrated in combination with sulfide-based solid electrolyte. Furthermore we evaluated the stability of the graphite-electrolyte interface by analyzing the normalized cumulative irreversible charge during cycling experiments.

X-ray photoemission electron microscopy (XPEEM) with its excellent spatial resolution is a well-suited technique to elucidate the complex electrode-electrolyte interface reactions in Li-ion batteries. It provides element-specific contrast images and enables the acquisition of local X-ray absorption spectra on single particles. Here we demonstrate the strength of post mortem measurements and we show the first electrochemical cell dedicated for operando experiments in all-solid-state batteries.

The vanadium redox flow battery (VRFB) is designed for grid-scale energy storage applications. Ion-exchange membranes are performance and cost relevant components of redox flow batteries. Currently used materials are largely ‘borrowed’ from other applications that have different functional requirements. For next generation VRFBs, it would be desirable to develop membrane materials based on low-cost porous separators with low resistance and high transport selectivity to minimize vanadium-ion and electrolyte crossover.

Degradation of the solid-electrolyte interface occurring during cycling is currently one of the most challenging issues for the development of all-solid-state batteries. Here we designed a unique electrochemical custom made cell for operando X-ray photoelectron spectroscopy (XPS) capable of maintaining high mechanical pressure with reliable electrochemistry and able to monitor in real-time the surface (electro-)chemical reactivity at the interfaces between the different composite.

A vanadium redox flow battery (VRFB) is a grid-scale energy storage device. Its energy conversion unit consists of a cell stack that comprises ion-exchange membranes to separate positive and negative electrode. The projected lifetime of a VRFB is 20 years and 7’000 charge-discharge cycles. Lifetime tests of membranes under application relevant conditions are therefore impractical, and the development of an accelerated stress test (AST) to assess the chemical stability of membranes is crucial.

Grid-scale storage of electricity is vital in energy scenarios with a high share of renewable electricity generation, such as wind and solar power. Redox flow batteries are particularly suited for intra-day time-shifting storage applications, yet investment costs need to be lowered for economic viability of the technology. We demonstrate a new ion conducting membrane that improves shortcomings of currently used materials and is potentially cheaper to produce.

The high-energy rechargeable Li-O₂ battery has been subject to intensive research worldwide during the past years. The Li-O₂ cell mainly comprises a negative (e.g. Li metal) and positive (e.g. porous carbon) electrode separated by an electronically insulating, but Li+ conducting electrolyte layer. In order to study the cell chemistry, a differential electrochemical mass spectrometry setup based on a set of valves, a pressure sensor and a quadrupole mass spectrometer has been developed.