Diroll Benjamin T
Center for Nanoscale Materials , Argonne National Laboratory , Lemont , Illinois 60439 , United States.
J Phys Chem Lett. 2019 Sep 19;10(18):5623-5628. doi: 10.1021/acs.jpclett.9b02320. Epub 2019 Sep 10.
Intraband relaxation in polycrystalline films of hybrid perovskites methylammonium lead tribromide and methylammonium lead triiodide are studied by transient absorption spectroscopy from 80 K to >350 K. This temperature range spans the transitions of these materials from the high-temperature cubic phases, intermediate tetragonal phases, and low-temperature orthorhombic phases. The organic cation undergoes a distinct transition from an ordered lattice in the orthorhombic phase to a plastic crystal in cubic and tetragonal phases, which reportedly influences many optoelectronic properties. The much larger exciton binding energy of orthorhombic MAPbI (compared to cubic or tetragonal phases) or MAPbBr substantially changes the transient spectral responses of the materials by reducing the number of free carriers. However, for these measurements at low fluences, both MAPbBr and MAPbI exhibit subpicosecond intraband relaxation over the entire temperature range studied. Intraband relaxation becomes somewhat faster at higher temperatures, but freezing of organic cations are not accompanied by a discontinuity of the intraband relaxation time. These results suggest that configurational freedom of organic cations does not screen carriers from electron-phonon coupling.
通过瞬态吸收光谱法,在80 K至>350 K的温度范围内研究了混合钙钛矿甲基溴化铅和甲基碘化铅多晶薄膜中的带内弛豫。该温度范围涵盖了这些材料从高温立方相、中间四方相到低温正交相的转变。有机阳离子经历了从正交相中的有序晶格到立方相和四方相中的塑性晶体的明显转变,据报道这会影响许多光电性能。正交相MAPbI(与立方相或四方相相比)或MAPbBr的激子结合能大得多,通过减少自由载流子的数量,极大地改变了材料的瞬态光谱响应。然而,对于这些低通量测量,MAPbBr和MAPbI在整个研究温度范围内均表现出亚皮秒级的带内弛豫。在较高温度下,带内弛豫会变得稍快一些,但有机阳离子的冻结并未伴随着带内弛豫时间的不连续。这些结果表明,有机阳离子的构型自由度不会屏蔽载流子与电子-声子的耦合。