发光
材料科学
堆积
元动力学
静水压力
化学物理
卤化物
钙钛矿(结构)
分子物理学
格子(音乐)
结晶学
最大值和最小值
雅恩-泰勒效应
分子动力学
手性(物理)
凝聚态物理
发色团
激子
光电子学
密度泛函理论
纳米技术
飞秒
纳米电子学
流体静力平衡
化学
哈密顿量(控制论)
正交晶系
作者
Mariagrazia Fortino,Alessandro Mattoni,Sascha Feldmann,Adriana Pietropaolo
标识
DOI:10.1021/acs.jpclett.5c02393
摘要
High Resolution Image Download MS PowerPoint Slide The influence of hydrostatic pressure on the structure and circularly polarized luminescence (CPL) of the 2D chiral perovskite S -(MBA) 2 PbI 4 (MBA = methylbenzylammonium) is investigated and compared to that of a brominated derivative, employing parallel-bias metadynamics coupled with excited-state ab initio molecular dynamics and time-dependent DFT simulations. A stepwise increase in pressure is shown to promote noncovalent interactions above the Fermi level, which in turn amplifies CPL emission and even allows for switching its sign. A comparable effect can be obtained by brominating the aromatic ring of ( R )- or ( S )-methylbenzylammonium. Strain, arising from both intrinsic structural constraints and applied external pressure, can deform the lattice and distort the inorganic octahedra. These strain-induced distortions promote parallel stacking of the chiral ligands, resulting in a CPL response within stable free energy minima and enabling chiral memory. We conclude that interlayer interactions can act as a powerful tool for engineering chiroptical properties through external pressure or structure-induced strain (internal pressure), enabling the design of new stimulus-responsive materials or the tuning of existing ones via strain engineering.
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