フッ素化二次元ハイブリッドペロブスカイト（FPMA）₂PbI₄における圧力誘起構造、機械的、および光電子特性の調整可能性

We report a systematic high-pressure investigation of fluorinated two-dimensional hybrid perovskite (FPMA)₂PbI₄, combining in situ synchrotron powder X-ray diffraction (HP-PXRD), photoluminescence spectroscopy (HP-PL), and first-principles density functional theory (DFT) simulations. Under hydrostatic compression to 5.54 (±0.4) GPa, HP-PXRD exhibits anisotropic lattice contraction (a/a_o = 4.54%, b/b_o = 3.35%, c/c_o = 9.79%), leading to an isothermal bulk modulus of 15.6 (±1.3) GPa (K₀ = 29.9 TPa^-1) and incipient amorphization. DFT-optimized geometries confirm progressive PbI₆ octahedral flattening, concomitant to interlayer contraction, and intensification of F···I, F···H, and I···H interactions. Full elastic tensor analysis reveals moderate anisotropy (A_E = 2.09, A_G = 2.40), along with a broad Poisson's ratio of (-0.28 to 0.63), resulting from cooperating auxetic and conventional elastic deformations of the channels. HP-PL measurements show a continuous red shift to ∼616.9 from 535.4 nm, accompanied by progressive intensity quenching, which is ascribable to bond-contraction-driven bandgap reduction and pressure-amplified nonradiative recombination within a partially amorphized matrix. DFT band-structure computations reproduce pressure-dependent direct-gap narrowing, retaining the collinearity of the k-space valence-band maximum (VBM) and conduction-band minimum (CBM). Overall, this study demonstrates coupled structural, mechanical, and optoelectronic tunability in (FPMA)₂PbI₄, which underscores its potential for strain-engineered optoelectronic applications and flexible photonic systems with pressure-tunable emission across the visible range.