Coupling Antisite Defect and Lattice Tensile Stimulates Facile Isotropic Li‐Ion Diffusion

Despite widely used as a commercial cathode, the anisotropic 1D channel hopping of lithium ions along the [010] direction in LiFePO4 prevents its application in fast charging conditions. Herein, an ultrafast nonequilibrium high‐temperature shock technology is employed to controllably introduce the Li–Fe antisite defects and tensile strain into the lattice of LiFePO4. This design makes the study of the effect of the strain field on the performance further extended from the theoretical calculation to the experimental perspective. The existence of Li–Fe antisite defects makes it feasible for Li+ to move from the 4a site of the edge‐sharing octahedra across the ab plane to 4c site of corner‐sharing octahedra, producing a new diffusion channel different from [010]. Meanwhile, the presence of a tensile strain field reduces the energy barrier of the new 2D diffusion path. In the combination of electrochemical experiments and first‐principles calculations, the unique multiscale coupling structure of Li–Fe antisite defects and lattice strain promotes isotropic 2D interchannel Li+ hopping, leading to excellent fast charging performance and cycling stability (high‐capacity retention of 84.4% after 2000 cycles at 10 C). The new mechanism of Li+ diffusion kinetics accelerated by multiscale coupling can guide the design of high‐rate electrodes. This work employs ultrafast nonequilibrium high‐temperature shock technology to controllably introduce Li–Fe antisite defects and lattice strain into the lattice of LiFePO4. The unique multiscale coupling structure promotes isotropic 2D interchannel Li+ hopping, leading to excellent fast charging performance and cycling stability. The new mechanism of Li+ diffusion kinetics accelerated by multiscale coupling can guide the design of high‐rate electrodes.