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LaFeO3 was synthesized via a low-energy solid-state route using commercial and tannic-acid-derived hematite as Fe precursors under identical processing (8 h milling + calcination at 800°C for 20 h, followed by 5 h post-milling), producing four samples. XRD confirms predominantly orthorhombic LaFeO3 (Pnma) in all cases, with residual hematite; the green-precursor samples show lower conversion and minor residual La2O3. Post-milling induces crystallite refinement and increased microstrain in all samples, with the green-precursor material exhibiting smaller crystallites (? 79 nm vs ? 91 nm) and more pronounced microstrain, reflecting its initially heterogeneous reaction pathway. Mössbauer spectroscopy shows a single LaFeO3 sextet, with reduced intensity in the green-precursor samples, consistent with residual non-reacted regions. FTIR and XPS reveal organic-derived species only in these samples, while SEM shows agglomerated micrometric structures of nanosized particles, slightly smaller on average. Room-temperature M–H curves confirm weak ferromagnetic behavior, and ZFC–FC measurements display features associated with minor hematite and strong thermal irreversibility, attributed to uncompensated spins enhanced by milling.