Light-Induced Wavelength Dependent Self Assembly Process for Targeted Synthesis of Phase Stable 1D Nanobelts and 2D Nanoplatelets of CsPbI3 Perovskites

纳米晶 光致发光 材料科学 相(物质) 发光 钙钛矿(结构) 带隙 纳米技术 量子产额 光谱学 量子点 光电子学 荧光 结晶学 化学 光学 物理 量子力学 有机化学
作者
Avijit Pramanik,Sudarson Sekhar Sinha,Kaelin Gates,Jing Nie,Fengxiang X. Han,Paresh Chandra Ray
出处
期刊:ACS omega [American Chemical Society]
卷期号:8 (14): 13202-13212 被引量:5
标识
DOI:10.1021/acsomega.3c00477
摘要

Despite black cubic phase α-CsPbI3 nanocrystals having an ideal bandgap of 1.73 eV for optoelectronic applications, the phase transition from α-CsPbI3 to non-perovskite yellow δ-CsPbI3 phase at room temperature remains a major obstacle for commercial applications. Since γ-CsPbI3 is thermodynamically stable with a bandgap of 1.75 eV, which has great potential for photovoltaic applications, herein we report a conceptually new method for the targeted design of phase stable and near unity photoluminescence quantum yield (PLQY) two-dimensional (2D) γ-CsPbI3 nanoplatelets (NPLs) and one-dimensional (1D) γ-CsPbI3 nanobelts (NBs) by wavelength dependent light-induced assembly of CsPbI3 cubic nanocrystals. This article demonstrates for the first time that by varying the excitation wavelengths, one can design air stable desired 2D nanoplatelets or 1D nanobelts selectively. Our experimental finding indicates that 532 nm green light-driven self-assembly produces phase stable and highly luminescent γ-CsPbI3 NBs from CsPbI3 nanocrystals. Moreover, we show that a 670 nm red light-driven self-assembly process produces stable and near unity PLQY γ-CsPbI3 NPLs. Systematic time-dependent microscopy and spectroscopy studies on the morphological evolution indicates that the electromagnetic field of light triggered the desorption of surface ligands from the nanocrystal surface and transformation of crystallographic phase from α to γ. Detached ligands played an important role in determining the morphologies of final structures of NBs and NPLs from nanocrystals via oriented attachment along the [110] direction initially and then the [001] direction. In addition, XRD and fluorescence imaging data indicates that both NBs and NPLs exhibit phase stability for more than 60 days in ambient conditions, whereas the cubic phase α-CsPbI3 nanocrystals are not stable for even 3 days. The reported light driven synthesis provides a simple and versatile approach to obtain phase pure CsPbI3 for possible optoelectronic applications.

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