LiFe x Mn 1 -x PO 4 (LFMP) has emerged as a next-generation cathode material that bridges the cost-effectiveness, safety, and sustainability of LiFePO 4 (LFP) with the higher energy density of nickel-rich layered oxides without reliance on cobalt or nickel. However, the commercialization of LFMP is hindered by its intrinsically low electronic conductivity, one-dimensional tortuous Li + diffusion channels, and Mn-induced Jahn-Teller distortions. These factors, compounded by lattice strain during Fe 2+ /Fe 3+ and Mn 2+ /Mn 3+ redox transitions, lead to anisotropic stress, Li + transport barriers, increased internal resistance, and rapid capacity fade. This review systematically examines the structural and electrochemical behavior of LFMP across compositions, morphologies, and doping strategies. We analyze operando phase evolution, defect chemistry, and Li + migration pathways to elucidate the mechanistic origin of electrochemical fading. Particular emphasis is placed on solid solution stabilization, anti-site defect engineering, and elastic strain modulation via ion substitution and particle miniaturization. We synthesize insights across compositional design (multi-metal doping, Fe/Mn ordering), crystallographic defect control (e.g., anti-site Li + /M 2+ engineering), and morphological strategies (strain-accommodated nanoarchitectures), outlining approaches to extend solid-solution regimes and mitigate mechanical degradation. By bridging mechanistic understanding with scalable synthesis techniques, this review proposes a roadmap for the commercialization of LFMP as a strain-resilient, high-voltage cathode suitable for terawatt-scale energy storage.
Yang et al. (Sun,) studied this question.