Simplified Spray Pyrolysis Synthesis Enabling a Novel Dual‐Doping Strategy for Ultrahigh‐Rate Ni‐Rich Cathode Materials for Lithium‐Ion Batteries
Abstract
ABSTRACT Elemental doping has been extensively explored to address key challenges associated with Ni‐rich cathode material, such as Li/Ni cation mixing and anisotropic lattice strain, which hinder rapid Li + transport and accelerate mechanical degradation. However, single‐atom dopants typically improve only limited aspects of structural and electrochemical performance. In this study, we introduce a rational Zr─Ti co‐doping strategy via spray pyrolysis, in which Ti 4+ selectively modulates the local transition‐metal environment and the Ni oxidation state, while Zr 4+ strengthens the Ni‐rich lattice through robust Zr─O bonding. This synergistic doping suppresses detrimental phase transitions, stabilizes the oxygen sublattice, and mitigates microcrack formation, without aggravating Li/Ni disorder. To ensure homogeneous dopant incorporation, a spray pyrolysis approach utilizing Li‐containing precursor droplets was employed. This method offers uniform elemental distribution, simplified synthesis, and a reduced environmental footprint compared with conventional co‐precipitation techniques. As a result, Zr─Ti co‐doped Ni‐rich NCA microspheres (LiNi 0.85 Co 0.10 Al 0.04 Zr 0.007 Ti 0.003 O 2 ) synthesized via short‐time, low‐temperature calcination, exhibit excellent high‐rate capability (161 mA h g −1 at 10C). This work demonstrates that integrating dual‐dopant chemistry with a scalable spray pyrolysis process offers a promising pathway to concurrently enhance rate performance and structural integrity, providing a generalizable framework for the next generation of Ni‐rich cathode materials.
Fields of Study & Subjects
Advancements in Battery Materials
Advanced Battery Materials and Technologies
Extraction and Separation Processes
Publication details
- Journal / source
- Small
- Publisher
- Wiley
- Volume
- 22
- Issue
- 30
- Pages
- e14992–e14992
- Publication date
- 7 April 2026
- Language
- EN