Achieving High‐Voltage Stability in Li‐Rich Ni‐Rich Oxides with Local W/Ni(Li) Superstructure

Author:

Gao Xu12,Li Biao3,Rousse Gwenaëlle124,Morozov Anatolii V.5,Deschamps Michaël6,Elkaïm Erik7,Zhang Leiting8,Kummer Kurt9,Abakumov Artem M.5,Tarascon Jean‐Marie124ORCID

Affiliation:

1. Chimie du Solide‐Energie UMR 8260 Collège de France Paris Cedex 05 75231 France

2. Réseau sur le Stockage Electrochimique de l'Energie (RS2E) CNRS Amiens Cedex FR 3459 France

3. Beijing Key Laboratory of Theory and Technology for Advanced Battery Materials School of Materials Science and Engineering Peking University Beijing 100871 P. R. China

4. Sorbonne Université Paris 75005 France

5. Skolkovo Institute of Science and Technology Bolshoy Boulevard 30, bld. 1 Moscow 121205 Russia

6. CNRS UPR 3079 CEMHTI Univ. Orléans CS90055, 1D avenue de la Recherche Scientifique Orléans Cedex 2 45071 France

7. Synchrotron SOLEIL L'orme des Merisiers Saint Aubin BP 48 Gif sur Yvette 91192 France

8. Department of Chemistry – Ångström Laboratory Uppsala University Box 538 Uppsala SE‐751 21 Sweden

9. ESRF The European Synchrotron 71 Avenue des Martyrs, CS40220 Grenoble Cedex 9 38043 France

Abstract

AbstractCreating high‐energy‐density cathodes is crucial for building next‐generation lithium‐ion batteries. However, materials exploration along two main directions, namely Li‐rich or Ni‐rich oxides, has encountered bottlenecks. To get rid of the impasse, here a “Li‐rich Ni‐rich” route is consolidated by designing a new family of Li1+yNi(3‐5y)/3W2y/3O2 oxides with high‐voltage cycling stability up to 4.5 V and high capacities over 230 mAh g−1. It is discovered that W6+ is largely incorporated into the LiNiO2 lattice, forming W/Ni(Li) inverse honeycomb‐ordered nano‐domains. These Li‐rich domains enable reversible anionic redox, clearly demonstrated by X‐ray absorption spectroscopy, resonant inelastic X‐ray scattering, transmission electron microscopy, and nuclear magnetic resonance, which is linked to improved electrochemical performance. Furthermore, the incorporation of W6+ into the lattice proves to be the key to generating electrochemically active Li‐rich domains irrespective of Li stoichiometry given that a similar local structure is found in W‐substituted non‐Li‐rich oxides. This therefore implies the underestimated role of high‐valence cations in tuning the structure and electrochemistry of Ni‐rich oxides. These results underline the necessity of a Li‐rich composition in the request for reversible high capacity, reinforcing the promise of a “Li‐rich Ni‐rich” avenue for developing advanced cathodes.

Funder

Russian Science Foundation

Publisher

Wiley

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