Abstract

All-inorganic perovskite CsPbX<sub>3</sub> (X = Cl, Br and I) quantum dots (QDs) have been wildly utilized in optoelectronic devices due to their tunable photoluminescence, high photoluminescence quantum yield (PLQY), and narrow-line width photoluminescence. However, the blue luminescence PLQY of CsPbX<sub>3</sub> perovskite quantum dots is still lower than their red and green luminescence counterparts (PLQYs nearly 100%). Here in this work, we present a handy strategy to synthesise the ultra-small blue luminescence Tin-doped CsPbBr<sub>3</sub> perovskite QDs by supersaturated recrystallization synthetic approach at room temperature, and the particle size of as-prepared QDs is lower than 4 nm. The crystal structure and optical property of Tin doped CsPbBr<sub>3</sub> QDs are characterized by XRD, TEM, ultraviolet-visible spectrophotometer, and fluorescence spectrophotometer. The results show that the particle size of as-prepared QDs is slightly shrunk from 3.33 nm (SnBr<sub>2</sub> 0.03 mmol) to 2.23 nm (SnBr<sub>2</sub> 0.06 mmol) as the SnBr<sub>2</sub> adding quantity increases, but there is no obvious change in the lattice spacing of doped QDs. The partial substitution of Pb for Tin leads the optical spectra to blue-shift from 490 nm (SnBr<sub>2</sub> 0.03 mmol) to 472 nm (SnBr<sub>2</sub> 0.06 mmol). The highest PLQY and the strongest XRD diffraction of ultra-small Tin doped CsPbBr<sub>3</sub>blue luminescence QDs are obtained by adding SnBr<sub>2</sub> 0.05 mmol, and the blue luminescence peak is located at 472 nm with the PLQY of 53.4%. There is no any change in PL peak of Tin doped CsPbBr<sub>3</sub> QDs (SnBr<sub>2</sub> 0.05 mmol) by storing it under the ambient atmosphere for 15 days, and the PLQY of Sn<sup>2+</sup> doped QDs is still 80% of the initial after 15 days. It is concluded that the crystallization and optical property can be effectively improved in Tin doped CsPbBr<sub>3</sub> QDs by partially replacing appropriate quantity of Pb by Tin.

Highlights

  • Fitting results fitted by time-resolved PL decays curve of tin doped CsPbBr3 quantum dots

  • 当 SnBr2 添加量为 0.06 mmol 时, 合成的量子 点仍为蓝光发射, 但其 photoluminescence quantum yield (PLQY) 仅为 21.7%, 比添加 SnBr2 为 0.05 mmol 时降低了 31.7%, XRD 各晶 面衍射峰变弱

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Summary

Introduction

单个CsPbBr3钙钛矿量子点的荧光闪烁特性 Photoluminescence blinking properties of single CsPbBr3 perovskite quantum dots 物理学报. 当 SnBr2 添加量为 0.05 mmol 时合成的超小晶粒锡掺杂 CsPbBr3 量子点显示出最优的光学性能, 其粒径约为 2.91 nm, 对应的 XRD 各晶面 衍射峰强度最强, 荧光发射峰位于 472 nm 处, PLQY 最高, 达到了 53.4%, 在空气中存放 15 d 后, 其荧光发射 峰位置不发生明显改变, 荧光 PLQY 仍保留最初的 80%, 为 42.7%. 当 SnBr2 为 0.05 mmol 时, 合成的蓝光 (472 nm) 量子点 PLQY 最高, 为 53.4%, 荧光发射具有良好的稳定性, 在空气中存放 15 d 后, 其荧光发射峰不发生明显改变, 仍位于 472 nm 处, 属于蓝光发射, PLQY 仍保持最初的 80%, 为 42.7%. 图 1 锡掺杂 CsPbBr3 量子点的 XRD 谱 Fig. 1.

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