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首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Infrared Spectroscopic Study of Vibrational Modes across the Orthorhombic-Tetragonal Phase Transition in Methylammonium Lead Halide Single Crystals
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Infrared Spectroscopic Study of Vibrational Modes across the Orthorhombic-Tetragonal Phase Transition in Methylammonium Lead Halide Single Crystals

机译:甲基铵卤化物单晶中正交 - 四方相转变振动模式的红外光谱研究

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Single crystals of the methylammonium (MA) lead halides MAPbI(3), MAPbBr(3), and MAPbCl(3) have been investigated using infrared spectroscopy with the aim of analyzing structural and dynamical aspects of processes that enable the ordering of the MA molecule in the orthorhombic crystal structure of these hybrid perovskites. Our temperature-dependent studies were focused on the analysis of the CH/NH rocking, C-N stretching, and CH/NH bending modes of the MA molecule in the 800-1750 cm(-1) frequency range. They deliver a direct comparison of the behaviors of the three halides on crossing the orthorhombic-tetragonal phase transition in MA lead halide single crystals. Drastic changes of all vibrational modes close to the phase transition were clearly observed. Additional spectral features that were not discussed previously are pointed out. The transformation of the two-dimensional orthorhombic hydrogen bond layers into a more three-dimensional arrangement in the tetragonal phase seems to be an important feature providing deeper insights into the mechanisms that lead to a free-rotating MA molecule in the inorganic host structure. The change of the molecule site symmetry in the tetragonal crystal structure seems to be an important feature of the orthorhombic-tetragonal phase transition. For low temperatures, it can be stated that the iodide is stronger influenced by hydrogen bonding than the bromide and the chloride.
机译:使用红外光谱研究已经研究了甲基铵(MA)铅卤化铅的单晶(3),MAPBBBR(3)和MAPBCL(3),目的是分析能够对MA分子排序的过程的结构和动态方面进行分析在这些杂交钙钛矿的正畸晶体结构中。我们的温度依赖性研究重点是在800-1750cm(-1)频率范围内的MA分子的CH / NH摇摆,C-N拉伸和CH / NH弯曲模式的分析。它们能够直接比较三卤化在马铅卤化物单晶中的正交 - 四方相转变中的三卤化物的行为。清楚地观察到靠近相变的所有振动模式的急剧变化。之前未讨论的附加光谱特征被指出。二维正畸氢粘合层的转化为四边形相中较多的三维布置似乎是一种重要的特征,提供更深的洞察力,进入导致无机宿主结构中的自由旋转MA分子的机构。四边形晶体结构中分子位点对称的变化似乎是正交 - 四方相转变的重要特征。对于低温,可以说碘化物的影响力比溴化物和氯化物更强。

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