CsPbBr3修饰ZIF-8纳米复合材料的合成及其光催化性能。

IF 4.6 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Alen Sam Thomas, Philip Nathaniel Immanuel, Neena Prasad, Achiad Goldreich, Jonathan Prilusky, Raanan Carmieli, Lena Yadgarov
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引用次数: 0

摘要

CsPbBr3 (CPB)钙钛矿纳米晶体(NCs)由于其出色的载流子迁移率、较长的扩散长度和高效的可见光吸收而引起了人们的极大兴趣,使其成为光催化、发光二极管(led)、太阳能电池和光电探测器的理想候选者。然而,它们的实际应用受到环境稳定性差的限制。为了解决这一挑战,我们采用了沸石咪唑盐框架(ZIF),特别是ZIF-8作为稳定基质,因为它具有优异的热稳定性和化学稳定性,高表面积和多种合成途径。采用优化的混合方法,将热注射制备的CPB NCs与ZIF-8相结合,合成了CPB/ZIF-8纳米复合材料,保证了NCs的均匀分布。电子显微镜(EM)分析证实了NCs在ZIF-8表面的均匀分布和控制良好。此外,傅里叶变换红外光谱(FTIR)显示了配体交换,其中ZIF-8结构的咪唑连接体取代了NCs配体。该工艺促进了后者的几乎外延附着,从而促进了集成过程中有效的电荷相互作用。事实上,我们观察到,在复合材料形成后,NCs的光致发光(PL)有92%的猝灭。这一发现进一步表明了有效的电荷分离和减少的电子-空穴复合。为了更深入地了解电荷转移机制,我们进行了电子顺磁共振(EPR)测量,以比较CPB和ZIF与CPB/ZIF复合材料的自由基生成能力。复合材料表现出优异的自由基生成能力,特别是羟基自由基(˙OH),表明电荷转移增强。这些发现表明该复合材料是一种非常有前途的光催化候选材料。在此基础上,我们以甲基橙(MO)和溴甲酚绿(BCG)为模型染料,通过染料降解实验探索了复合材料的光催化能力。与原始的ZIF和CPB纳米复合材料相比,CPB/ZIF纳米复合材料的光催化性能显著增强。其中,MO和BCG的降解率分别比CPB NCs高1.48倍和1.75倍。这一改进突出了CPB NCs与ZIF之间的有效相互作用,确立了CPB/ZIF纳米复合材料作为光催化和光电子应用的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis of CsPbBr3 decorated ZIF-8 nanocomposite for enhanced photocatalytic performance.

CsPbBr3 (CPB) perovskite nanocrystals (NCs) have attracted considerable interest due to their outstanding charge carrier mobility, long diffusion lengths, and efficient visible light absorption, making them ideal candidates for photocatalysis, light-emitting diodes (LEDs), solar cells, and photodetectors. However, their practical applications are limited by poor environmental stability. To address this challenge, we employ a zeolitic imidazolate framework (ZIF), specifically ZIF-8, as a stabilizing matrix for its exceptional thermal and chemical stability, high surface area, and versatile synthesis routes. The CPB/ZIF-8 nanocomposite was synthesized by integrating hot-injection-produced CPB NCs with ZIF-8 using an optimized mixing approach, ensuring a uniform NCs distribution. Electron microscopy (EM) analysis confirmed the well-controlled and uniform distribution of the NCs on the surface of the ZIF-8. Moreover, the Fourier-transform infrared spectroscopy (FTIR) revealed ligand exchange, where the imidazole linkers of the ZIF-8 structure replace the NCs ligands. The process advances almost epitaxial attachment of the latter, thus promoting effective charge interactions in the integration process. Indeed, we observe that upon formation of the composite, there is a 92% quenching in the photoluminescence (PL) of the NCs. This finding further indicates efficient charge separation and reduced electron-hole recombination. To gain deeper insight into the charge transfer mechanisms, we conducted electron paramagnetic resonance (EPR) measurements to compare the radical generation capabilities of CPB and ZIF with those of the CPB/ZIF composite. The composite exhibited superior radical generation capabilities, particularly hydroxyl radicals (˙OH), indicating enhanced charge transfer. These findings suggest that the composite is a highly promising candidate for photocatalysis. Building on these findings, we explored the photocatalytic abilities of the composite through dye degradation experiments, using methyl orange (MO) and bromocresol green (BCG) as model dyes. The CPB/ZIF nanocomposite demonstrated significantly enhanced photocatalytic performance compared to pristine ZIF and CPB NCs. Specifically, its degradation rates were 1.48× and 1.75× higher for MO and BCG, respectively, than those of CPB NCs. This improvement highlights the effective interaction between CPB NCs and ZIF, establishing the CPB/ZIF nanocomposite as a promising material for photocatalysis and optoelectronic applications.

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Nanoscale Advances
Nanoscale Advances Multiple-
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