Organic−inorganic hybrid metal halides with structural flexibility and solution processability have been widely investigated for different application scenarios. However, the effective construction of phase-transition materials with a high phase-transition temperature (T tr ) for potential practical applications remains a great challenge, and reports on the regulation of T tr with significant enhancement have been rare. In this manuscript, we have realized a large T tr increase of 148 K in a layered hybrid lead iodide crystal (4-FTMBA) 4 Pb 3 I 10 (4-FTMBA = 4fluoro-N,N,N-trimethylbenzenaminium) by the H/F substitution strategy. Compared to the parent (TMBA) 4 Pb 3 I 10 (TMBA = N,N,Ntrimethylbenzenaminium), H/F substitution preserves the structural framework and crystal symmetry in (4-FTMBA) 4 Pb 3 I 10 . The introduction of heavier fluorine will significantly increase the motion barrier for the order−disorder transition, resulting in the remarkably improved T tr . Temperature-dependent crystal structures, Raman spectra, and dielectric analyses well support the phase-transition behavior. In addition, evident thermochromism with a tunable direct band gap in (4-FTMBA) 4 Pb 3 I 10 has been observed using UV−vis spectra. To the best of our knowledge, the achieved T tr enhancement of 148 K by H/F substitution is the highest among the organic−inorganic hybrid lead halide phase-transition materials. This finding would greatly inspire the rational design of functional materials with high performance.