钝化
光致发光
钙钛矿(结构)
碘化物
蒽
卤化物
半导体
材料科学
载流子
有机半导体
带隙
发色团
化学物理
化学
光化学
纳米技术
无机化学
光电子学
结晶学
图层(电子)
作者
Jake Hardy,Sai Shruthi Murali,Calum K. Gordon,Paul Hume,Nathaniel J. L. K. Davis
标识
DOI:10.1021/acs.jpcc.3c05843
摘要
Researchers are actively exploring ways to effectively link organic chromophores with bulk semiconductors to facilitate efficient energy transfer between the two materials. However, this goal is usually hindered by poor interface formation between organic-molecular materials and inorganic semiconductors. Mixed-dimensional metal halide perovskites represent a potential solution to this problem, as they intimately connect the organic and inorganic constituents in the crystal lattice. In this study, we present our research into the integration of an anthracene derivative into narrow-bandgap mixed-dimensional lead iodide perovskites. While looking for evidence of energy transfer, we instead found that bulk thin films of methylammonium lead iodide can suffer from defect states that affect charge carriers of a particular energy, resulting in excitation energy-dependent photoluminescent lifetimes and photoluminescence quantum yields. The incorporation of anthracene and conversion into a mixed-dimensional perovskite reduced the detrimental effects of this defect, highlighting another beneficial aspect of reduced dimensionality, which has meaningful implications for potential photovoltaic devices based on these types of materials.
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