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首页> 外文期刊>Journal of nanoparticle research: An interdisciplinary forum for nanoscale science and technology >Room-temperature synthesis of pure perovskite-related Cs4PbBr6 nanocrystals and their ligand-mediated evolution into highly luminescent CsPbBr3 nanosheets
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Room-temperature synthesis of pure perovskite-related Cs4PbBr6 nanocrystals and their ligand-mediated evolution into highly luminescent CsPbBr3 nanosheets

机译:纯钙钛矿相关的CS4PBBR6纳米晶体的室温合成及其配体介导的进化到高度发光CSPBBR3纳米蛋白酶

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Currently, all-inorganic cesium lead-halide perovskite nanocrystals have attracted enormous attentions owing to their excellent optical performances. While great efforts have been devoted to CsPbBr3 nanocrystals, the perovskite-related Cs4PbBr6 nanocrystals, which were newly reported, still remained poorly understood. Here, we reported a novel room-temperature reaction strategy to synthesize pure perovskite-related Cs4PbBr6 nanocrystals. Size of the products could be adjusted through altering the amount of ligands, simply. A mixture of two good solvents with different polarity was innovatively used as precursor solvent, being one key to the high-yield Cs4PbBr6 nanocrystals synthesis. Other two keys were Cs+ precursor concentration and surface ligands. Ingenious experiments were designed to reveal the underlying reaction mechanism. No excitonic emission was observed from the prepared Cs4PbBr6 nanocrystals in our work. We considered the green emission which was observed in other reports originated from the avoidless transformation of Cs4PbBr6 into CsPbBr3 nanocrystals. Indeed, the new-prepared Cs(4)PbB(r)6 nanocrystals could transform into CsPbBr3 nanosheets with surface ligands mediated. The new-transformed two-dimensional CsPbBr3 nanosheets could evolve into large-size nanosheets. The influences of surface ligand density on the fluorescent intensity and stability of transformed CsPbBr3 nanosheets were also explained. Notably, the photoluminescence quantum yield of the as-transformed CsPbBr3 nanosheets could reach as high as 61.6% in the form of thin film. The fast large-scale synthesis of Cs4PbBr6 nanocrystals and their ligand-mediated transformation into high-fluorescent CsPbBr3 nanosheets will be beneficial to the future optoelectronic applications. Our work provides new approaches to understand the structural evolution and light-emitting principle of perovskite nanocrystals.
机译:目前,由于其优异的光学表演,全无机铯卤化物钙钛矿纳米晶体引起了巨大的注意。虽然巨大的努力已经致力于CSPBBR3纳米晶体,但新报道的钙钛矿相关的CS4PBBR6纳米晶体仍然仍然不知情。在这里,我们报道了一种新的室温反应策略,用于合成纯PeroVskite相关的CS4PBBR6纳米晶体。通过改变配体的量,可以通过改变配体的量来调整产品的大小。具有不同极性的两个良好溶剂的混合物创新用作前体溶剂,是高产CS4PBBR6纳米晶体合成的一个关键。其他两个键是Cs +前体浓度和表面配体。设计巧妙的实验旨在揭示潜在的反应机制。在我们的工作中,从制备的CS4PBBR6纳米晶体中观察到泻药排放。我们认为在其他报告中观察到的绿色排放来自CS4PBBR6的无需转化为CSPBBR3纳米晶体。实际上,新制备的Cs(4)PBB(R)6纳米晶体可以用介导的表面配体转化为CSPBBR3纳米片。新转换的二维CSPBBR3 NanosheS可以进化成大尺寸的纳米片。还解释了表面配体密度对转化的CSPBBR3纳米片荧光强度和稳定性的影响。值得注意的是,变化的CSPBBR3纳米片的光致发光量子产率可以以薄膜形式达到61.6%。 CS4PBBR6纳米晶体的快速大规模合成及其配体介导的转化为高荧光CSPBBR3纳米片将有利于未来的光电应用。我们的工作提供了了解佩洛夫斯基纳纳米晶体的结构演变和发光原理的新方法。

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