Shen Juan, Luan Chaoran, Rowell Nelson, Li Yang, Zhang Meng, Chen Xiaoqin, Yu Kui
Institute of Atomic and Molecular Physics, Sichuan University, Chengdu, 610065 China.
Laboratory of Ethnopharmacology, Tissue-orientated Property of Chinese Medicine Key Laboratory of Sichuan Province, West China School of Medicine, West China Hospital, Sichuan University, Chengdu, 610065 China.
Nano Res. 2022;15(9):8564-8572. doi: 10.1007/s12274-022-4421-4. Epub 2022 May 31.
Little is known about how to precisely promote the selective production of either colloidal semiconductor metal chalcogenide (ME), magic-size clusters (MSCs), or quantum dots (QDs). Recently, a two-pathway model has been proposed to comprehend their evolution; here, we reveal for the first time that the size of precursors plays a decisive role in the selected evolution pathway of MSCs and QDs. With the reaction of cadmium myristate (Cd(MA)) and tri-n-octylphosphine selenide (SeTOP) in 1-octadecene (ODE) as a model system, the size of Cd precursors was manipulated by the steric hindrance of carboxylic acid (RCOOH) additive. Without RCOOH, the reaction produced both CdSe MSCs and QDs (from 100 to 240 °C). With RCOOH, the reaction produced MSCs or QDs when R was small (such as CH-) or large (such as CH-), respectively. According to the two-pathway model, the selective evolution is attributed to the promotion and suppression of the self-assembly of Cd and Se precursors, respectively. We propose that the addition of carboxylic acid may occur ligand exchange with Cd(MA), causing the different sizes of Cd precursor. The results suggest that the size of Cd precursors regulates the self-assemble behavior of the precursors, which dictates the directed evolution of either MSCs or QDs. The present findings bring insights into the two-pathway model, as the size of M and E precursors determine the evolution pathways of MSCs or QDs, the understanding of which is of great fundamental significance toward mechanism-enabled design and predictive synthesis of functional nanomaterials.
Supplementary material (additional optical absorption spectra, TEM, NMR, FT-IR, and XRD) is available in the online version of this article at 10.1007/s12274-022-4421-4.
关于如何精确促进胶体半导体金属硫族化物(ME)、魔法尺寸团簇(MSC)或量子点(QD)的选择性生成,人们了解甚少。最近,有人提出了一种双途径模型来理解它们的演化过程;在此,我们首次揭示前驱体的尺寸在MSC和QD的选定演化途径中起决定性作用。以肉豆蔻酸镉(Cd(MA))与三正辛基膦硒(SeTOP)在1-十八烯(ODE)中的反应作为模型体系,通过羧酸(RCOOH)添加剂的空间位阻来控制Cd前驱体的尺寸。在没有RCOOH的情况下,反应生成了CdSe MSC和QD(温度范围为100至240°C)。加入RCOOH后,当R较小时(如CH-)反应生成MSC,当R较大时(如CH-)反应生成QD。根据双途径模型,选择性演化分别归因于对Cd和Se前驱体自组装的促进和抑制。我们认为,羧酸的加入可能会与Cd(MA)发生配体交换,导致Cd前驱体尺寸不同。结果表明,Cd前驱体的尺寸调节了前驱体的自组装行为,从而决定了MSC或QD的定向演化。目前的研究结果为双途径模型带来了新的见解,因为M和E前驱体的尺寸决定了MSC或QD的演化途径,对其的理解对于功能纳米材料的机理驱动设计和预测合成具有重要的基础意义。
补充材料(额外的光吸收光谱、透射电子显微镜、核磁共振、傅里叶变换红外光谱和X射线衍射)可在本文的在线版本中获取,链接为10.1007/s12274-022-4421-4。