Boosting energy storage: the role of lithium distribution in battery performance

An international research team from several institutions, including the ALBA Synchrotron, has come up with a new way to improve nickel-rich positive electrodes for lithium-ion batteries. Published in Nature Communications, the study sheds light on how lithium positioning impacts the electrochemical stability of the electrodes. The team also identified two optimized nickel-rich materials that open the door to more durable and effective lithium-ion battery systems.

As demand for rechargeable batteries grows, the need for sustainable and cost-effective materials to improve their lifespan and performance becomes increasingly critical. The next-generation lithium-ion batteries are being designed with new cathode active materials for high-performance energy storage that avoid hazardous materials like cobalt. Among the most promising positive electrode candidates are nickel-rich layered oxide materials. However, these materials face significant challenges in long-term stability due to structural degradation. A crucial yet frequently overlooked factor affecting their stability is the precise positioning of lithium atoms within the lattice—a characteristic extremely difficult to determine due to lithium’s weak interaction with standard X-ray methods.

A recent study published in Nature Communications addresses this challenge with advanced characterization techniques, including synchrotron X-ray and neutron diffraction, to analyse and optimize lithium distribution within nickel-rich electrodes. This work was a collaborative effort involving scientists from Shenzhen and Shanxi Universities (China), ICN2, and ICREA (Spain) alongside scientists from the ALBA Synchrotron, the Institute Laue-Langevin (France), the Karlsruhe Institute of Technology (Germany) and the UM6P (Morocco).

By adjusting lithium incorporation and adding multiple high-valence dopants (Nb⁵⁺, W⁶⁺, Mo⁶⁺), researchers identified two electrode materials with better durability and stability. The optimization of the material performance was also achieved by creating superlattice domains, that is ensuring that the distribution of the lithium ions is not random. Small changes in lithium occupancy in nickel-rich positive electrodes can significantly enhance electrochemical performance.  

Researchers examined the internal structure of these electrodes with a variety of techniques and synchrotron facilities. In particular, researchers monitored the real-time structural evolution of the nickel-rich positive electrodes during battery operation using in situ synchrotron X-ray diffraction (SXRD) at the MSPD beamline at ALBA. The high-resolution diffraction patterns provided by this beamline allowed the tracking of lithium positioning as well as of their phase transitions and lattice changes.

“The ability to study electrodes under operating conditions was critical to show how lithium occupancy influences stability and performance, which are both key parameters for the development of more durable Li-ion battery materials”, says Alexander Missyul, beamline scientist at MSPD.

This work identified two optimized electrode materials with important gains in battery cyclability. The first, with a lithium content of 1.08, stabilized the lithium/nickel exchange, and improved mechanical durability. The second, with a lithium content of 1.20, promoted oxygen redox activity, which helped electrode integrity at higher voltages. Both materials demonstrated a capacity retention of over 90% after extended cycling, significantly outperforming conventional nickel-rich electrodes.

Read more on ALBA website

Zn-air batteries: how working conditions impact cathode stability

Electrically rechargeable alkaline zinc-air batteries (RZAB) hold immense promise for future energy storage, offering a sustainable and cost-effective solution for both stationary and mobile applications. Zinc-air batteries operate on the coupled electrochemistry of zinc and oxygen. Reversible oxygen redox is enabled by a bifunctional gas-diffusion-electrode (GDE), that drives oxygen reduction during discharge and oxygen evolution during recharge. With present-day technologies, the alternation of these processes leads to the accumulation of damage, causing durability issues that still hamper implementation in real-life devices.

The aim of the present research is to fabricate a durable, efficient and sustainable bifunctional GDE. To achieve this objective, an insightful understanding of the electrode, jointly addressing molecular-level out-of-equilibrium electrochemistry and mesoscale architecture geometry evolution is required. The novel bifunctional GDE features a-MnO2 nanowires as oxygen reduction electrocatalyst and Ni@NiO core-shell nanoparticles as oxygen evolution electrocatalyst. The fabrication process consists in microwave-assisted hydrothermal synthesis of α-MnO2 nanowires, formulation of an ink with different contents of Ni/NiO nanoparticles, and spray-coating onto carbon paper, followed by thermal treatment.

Electrochemical performance is assessed using voltammetry, galvanostatic sequences representative of realistic operating conditions, and electrochemical impedance spectroscopy (EIS) in half-cell configuration. The novel GDEs exhibit remarkable oxygen reduction current densities, in excess of 200 mA cm-2, with improved stability during successive charge-discharge cycles. The addition of Ni@NiO nanoparticles lowers anodic overvoltages, mitigating carbon-support corrosion and enhancing overall GDE stability. However, the presence of Zn2+, released to the electrolyte by the anodic process, accelerates GDE failure due to the formation of inactive Zn-Mn-containing phases: this degradation mode is however mitigated by the Ni-based electrocatalyst, showing an anodic contribution also to poisoning.

Electrochemical measurements, combined with morphological SEM and TEM observations and STXM spectromicroscopy, performed at Elettra’s TwinMic beamline, allowed to pinpoint the degradation mechanisms, providing concrete guidance to overcome them. Specifically, electrochemical ageing, on the one hand, targets catalyst stability, triggering cathodic dissolution of Mn and anodic redeposition of MnO2 in less active forms, and, on the other hand, high anodic overvoltages, due to insufficient Ni-contaning electrocatalyst, favour oxygen bubble formation in the bulk of the active layer architecture, leading to cracking. Chemical degradation of the electrocatalysts causes nanorod agglomeration, growth of amorphous phases and Ostwald ripening of the Ni nanoparticles. Figures 1a and 2a display, respectively, ADHUC Mn L-edge spectra of a selection of samples tested in this study, accompanied by a typical chemical-state map, representative electrochemical results and TEM images. The alteration in the valence state of Mn and its space distribution can be readily inferred from stacks of absorption maps.

Read  more on Elettra website

Image: (a) Space-averaged spectra for indicated electrode conditions. (b) Corresponding (colour-coded) TEM micrographs and schematics of MnO2-evolution process. Elaborated with permission from the reference reported below.