Structural Study of Paraffin-Stabilized Methylammonium Lead Bromide Magic-Sized Clusters

拉曼光谱 光致发光 透射电子显微镜 溴化物 卤化物 材料科学 光谱学 正交晶系 吸收光谱法 化学 纳米技术 分析化学(期刊) 化学工程 结晶学 无机化学 有机化学 光电子学 晶体结构 光学 量子力学 物理 工程类
作者
Melissa Guarino‐Hotz,Jeremy L. Barnett,Kai-Chun Chou,Allison A. Win,Heng Zhang,Chengyu Song,Scott R. J. Oliver,Jin Z. Zhang
出处
期刊:Journal of Physical Chemistry C [American Chemical Society]
卷期号:127 (6): 3367-3376 被引量:12
标识
DOI:10.1021/acs.jpcc.2c08645
摘要

Metal halide perovskites, such as methylammonium lead bromide, have recently attracted considerable attention due to their interesting and useful photoelectric properties. Here, two types of methylammonium lead bromide magic-sized clusters (MSCs), passivated with oleylamine and oleic acid, were synthesized using ligand-assisted reprecipitation (LARP) and heated LARP (HLARP) methods. The optical properties of these MSCs were characterized using UV–vis electronic absorption and photoluminescence (PL) spectroscopies. The HLARP synthesis resulted in a two-fold increase in the PL quantum yield of the MSCs to 76%. The stability of the MSCs was tested using time-dependent PL spectroscopy. LARP MSCs in solution degraded completely after 14 days under ambient conditions, while HLARP MSCs lasted for 26 days. To stabilize them, the MSCs were added to a non-coordinating matrix, paraffin. Both MSCs showed significantly improved resistance to water with the addition of paraffin. Solid LARP MSCs lost all luminescence with and without the addition of paraffin by about 3 h. Solid HLARP MSCs without paraffin started to aggregate after 3 h, but paraffin stabilized HLARP MSC films were stable for 8 days. This improved stability in solid state form allowed for accurate, nonaggregated analysis using Raman spectroscopy, X-ray diffraction, and transmission electron microscopy. Raman spectroscopy revealed that the HLARP MSCs show an additional peak at 147 cm–1 compared to LARP MSCs, which is attributed to methylammonium. X-ray diffraction and transmission electron microscopy confirm that MSCs have a quasi-crystalline orthorhombic structure.
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