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首页> 外文期刊>Chemistry of Materials: A Publication of the American Chemistry Society >Cesium Oleate Precursor Preparation for Lead Halide Perovskite Nanocrystal Synthesis: The Influence of Excess Oleic Acid on Achieving Solubility, Conversion, and Reproducibility
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Cesium Oleate Precursor Preparation for Lead Halide Perovskite Nanocrystal Synthesis: The Influence of Excess Oleic Acid on Achieving Solubility, Conversion, and Reproducibility

机译:铅卤化铯的前体制剂铅卤化物钙钛矿纳米晶体合成:过量油酸对溶解度,转化和再现性的影响

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摘要

In the colloidal synthesis of inorganic perovskite materials, cesium oleate (CsOL) is the most commonly used Cs precursor. Yet, despite its ubiquitous use in literature, CsOL has been observed to be insoluble at room temperature and leads to surprisingly inconsistent results in CsPbX3 nanocrystal synthesis, depending on the Cs salt from which the precursor is derived. We show that under the conditions used in most reports, the amount of oleic acid (OA) added, while stoichiometrically sufficient, still leads to incomplete conversion of the Cs salts to CsOL. This results in a mixture of Cs sources being present during the reaction, causing decreased homogeneity and reproducibility. When a 1:5 Cs:OA ratio is used, complete conversion is readily obtained, even under mild conditions, resulting in a precursor solution that is soluble at room temperature and yields identical synthetic results, regardless of the initial Cs source. Furthermore, H-1 nuclear magnetic resonance (NMR) of solutions prepared using varying Cs:OA ratios shows that the maximum ratio of Cs:OA obtainable in solution is 1:5, with any excess Cs present in the precipitate. We believe the use of a soluble, fully converted CsOL reagent will improve reproducibility for Cs-based perovskite synthesis and directly benefit synthetic methods based on microfluidics.
机译:在无机钙钛矿材料的胶体合成中,铯油(CSOL)是最常用的Cs前体。然而,尽管它在文献中无处不在,但已观察到CSOL在室温下不溶于令人惊讶的是,CSPBX3纳米晶合成的结果令人惊讶地不一致,这取决于前体的衍生物的CS盐。我们表明,在大多数报道中使用的条件下,添加的油酸(OA)的量,同时化学计量充分,仍然导致Cs盐对Csol的不完全转化。这导致CS源的混合物在反应过程中存在,导致均匀性降低和再现性。当使用1:5CS:OA比率时,即使在温和条件下,也可以容易地获得完全转化,从而导致在室温下可溶的前体溶液,并且不管初始CS源溶于相同的合成结果。此外,使用不同Cs制备的溶液的H-1核磁共振(NMR):OA比率表明,可在溶液中获得的Cs:OA的最大比为1:5,沉淀物中存在任何过量的Cs。我们认为使用一种可溶性的,完全转化的CSOL试剂将提高基于CS的钙钛矿合成的再现性,并直接受益于基于微流体的合成方法。

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