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固液界面的微波增强化学:全无机CsPbX纳米晶体的合成及阴离子诱导的结构和光学性质演变的揭示

Microwave-Enhanced Chemistry at Solid-Liquid Interfaces: Synthesis of All-Inorganic CsPbX Nanocrystals and Unveiling the Anion-Induced Evolution of Structural and Optical Properties.

作者信息

Thesika Kabalaraj, Vadivel Murugan Arumugam

机构信息

Advanced Functional Nanostructured Materials Research Laboratory (AFNM Lab), Centre for Nanoscience and Technology (CNST), Madanjeet School of Green Energy Technologies, Pondicherry University (A Central University), Dr. R. Venkataraman Nagar, Kalapet, Puducherry 605014, India.

出版信息

Inorg Chem. 2020 May 4;59(9):6161-6175. doi: 10.1021/acs.inorgchem.0c00294. Epub 2020 Apr 14.

Abstract

We demonstrate how microwaves could enhance the chemistry at interfaces of heterogeneous reactions involved in the microwave-solvothermal (MW-ST) synthesis of all-inorganic CsPbX (X = Cl, Br, I) perovskite nanocrystals (PNCs) within 6 min, unlike a conventional hot-injection method that requires 3 h. The enhanced MW-ST reaction rate was quantitatively analyzed by the Eyring equation, and it has been observed that the decreased activation free energy (Δ) and increased activation entropy (Δ) are caused by changes in the relative energies of reactants at their solid-liquid interfaces, leading to the formation of "hot spots", where microwave energy absorption is at its maximum. This rapid and homogeneous microwave heating could facilitate the self-assembly of uniformly distributed CsPbX nanocubes with precise control over the stoichiometric ratio, as confirmed by high-resolution transmission electron microscopy and energy-dispersive X-ray analyses. X-ray diffraction and Raman results indicate that lattice contraction and expansion in CsPbBrX have occurred because of an increase in the metal-halide bond length upon moving down the groups Cl → Br → I, as further ascertained by the Rietveld refinement studies. These anion-induced structural variations accordingly affected the electronic properties of MW-ST-synthesized CsPbX PNCs, which is apparent from the shifts in their conduction-band (CB) and valence-band (VB) positions. Consequently, the optical properties were also altered, resulting in a color-tuned emission from blue to red, with excellent photoluminescence quantum yields (up to 92%) and narrow emission line widths, as is evident from UV-vis and photoluminescence spectroscopy. The MW-ST-synthesized CsPbX PNCs were used as color-conversion layers for the fabrication of light-emitting diodes (LEDs) with commercial 456 nm UV-LED chips.

摘要

我们展示了微波如何在6分钟内增强全无机CsPbX(X = Cl、Br、I)钙钛矿纳米晶体(PNC)的微波溶剂热(MW-ST)合成中涉及的多相反应界面处的化学反应,这与需要3小时的传统热注入方法不同。通过艾林方程对增强的MW-ST反应速率进行了定量分析,并且观察到活化自由能(Δ)的降低和活化熵(Δ)的增加是由反应物在其固液界面处的相对能量变化引起的,导致形成“热点”,其中微波能量吸收达到最大值。这种快速且均匀的微波加热可以促进均匀分布的CsPbX纳米立方体的自组装,并精确控制化学计量比,高分辨率透射电子显微镜和能量色散X射线分析证实了这一点。X射线衍射和拉曼结果表明,由于沿Cl→Br→I族向下移动时金属卤化物键长增加,CsPbBrX中发生了晶格收缩和膨胀,里特韦尔德精修研究进一步证实了这一点。这些阴离子诱导的结构变化相应地影响了MW-ST合成的CsPbX PNCs的电子性质,这从它们的导带(CB)和价带(VB)位置的移动中可以明显看出。因此,光学性质也发生了改变,导致从蓝色到红色的颜色调谐发射,具有优异的光致发光量子产率(高达92%)和窄发射线宽,这从紫外可见光谱和光致发光光谱中可以明显看出。MW-ST合成的CsPbX PNCs被用作颜色转换层,用于制造具有商用456 nm紫外发光二极管(LED)芯片的发光二极管(LED)。

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