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Route to Stable Lead-Free Double Perovskites with the Electronic Structure of CH3NH3PbI3: A Case for Mixed-Cation Cs/CH3NH3/CH(NH2)22InBiBr6

机译:具有CH3NH3PBI3的电子结构的稳定无铅双钙钛矿:混合阳离子的情况Cs / Ch 3NH3 / Ch(NH2)2 2inbibr6

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摘要

During the past year, halide double perovskites attracted attention as potential lead-free alternatives to Pb-based halide perovskites. However, none of the compounds discovered so far can match the optoelectronic properties of MAPbI3 (MA = CH3NH3). Here we argue that, from the electronic structure viewpoint, the only option to make Pb-free double perovskites retaining the remarkable properties of MAPbI3 is to combine In and Bi as B(+) and B(3+) cations, respectively. While inorganic double perovskites such as Cs2InBiX6 were found to be unstable due to In(+) oxidizing into In(3+), we show that the +1 oxidation state of In becomes progressively more stable as the A-site cation changes from K to Cs. Hence, we propose the use of MA and FA [FA = CH(NH2)2] to stabilize A2InBiBr6 double perovskites. We show that the optoelectronic properties of A2InBiBr6 are remarkably similar to those of MAPbI3, and explore the mixed-cation (Cs/MA/FA)2InBiBr6 halide double perovskites.
机译:在过去的一年中,卤化物双重钙斯基氏植物引起了关注PB基卤化物钙矿的潜在无铅替代品。然而,到目前为止发现的化合物都不可以匹配MAPBI3(MA = CH3NH3)的光电性质。在这里,我们认为,从电子结构的观点来看,使PB的双重钙质的唯一选择是将MAPBI3的显着特性分别用于将其与B(+)和B(3+)阳离子组合。虽然发现如CS2INBIX6的无机双钙钛矿由于(+)氧化入(3+),但我们表明,随着A现场阳离子从K到的变化变化,+1氧化状态变得逐渐变得更稳定CS。因此,我们提出了使用MA和FA [FA = CH(NH2)2]以稳定A2INBIBR6双重钙锌矿。我们表明A2InbiBri6的光电性质与MAPBI3的光电性质非常相似,并探索混合阳离子(CS / MA / FA)2INBIBR6卤化物双钙锌矿。

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