Understanding the Origin of Higher Capacity for Ni-Based Disordered Rock-Salt Cathodes

• Published in: Chemistry of materials 2020-04, Vol.32 (8), p.3447-3461
• Main Authors: Cambaz, Musa Ali, Urban, Alexander, Pervez, Syed Atif, Geßwein, Holger, Schiele, Alexander, Guda, Alexander A, Bugaev, Aram L, Mazilkin, Andrey, Diemant, Thomas, Behm, R. Jürgen, Brezesinski, Torsten, Fichtner, Maximilian
• Format: Article
• Language: English
• ISSN: 0897-4756; 1520-5002
• DOI: 10.1021/acs.chemmater.9b05285

Lithium-excess disordered rock-salt oxides have opened up a new vista in search of high-capacity cathodes, resulting in a variety of new materials with versatile elemental compositions. This work introduces W6+ as a possible charge compensator and explores the solid-solution series Li1+x/100Ni1/2–x/120Ti1/2–x/120W x/150O2 (x = 0, 5, 10, 15, 20), which has been rationally developed based on concepts from percolation theory. Consistent with this understanding, the specific capacities increase from stoichiometric toward lithium-excessive compositions, while simultaneously capacity retention decreases considerably. Specifically, Li1.2Ni1/3Ti1/3W2/15O2 exhibits a first charge capacity of 246 mAh g–1, which exceeds the theoretical transition-metal redox capacity. To understand this peculiarity, we characterize the redox mechanism of nickel, titanium, tungsten, and oxygen using X-ray absorption spectroscopy, X-ray photoelectron spectroscopy, density functional theory calculations, and differential electrochemical mass spectrometry. We demonstrate that oxygen evolution takes place for Li1.2Ni1/3Ti1/3W2/15O2 predominantly above 4.4 V vs Li+/Li but was absent for the stoichiometric LiNi0.5Ti0.5O2. The oxygen oxidation causes instability of the anion framework, resulting in oxygen loss, which incurs severe capacity fading and leads to the observed voltage hysteresis. These findings provide important implications for the development and design of novel high-capacity lithium-excess nickel-based cathode materials.