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胺封端的CdSe纳米晶体中的表面位点与连接

Surface Sites and Ligation in Amine-capped CdSe Nanocrystals.

作者信息

Cao Weicheng, Yakimov Alexander, Qian Xudong, Li Jiongzhao, Peng Xiaogang, Kong Xueqian, Copéret Christophe

机构信息

Department of Chemistry and Applied Biosciences, ETH Zürich, 8093, Zürich, Switzerland.

Department of Chemistry, Key Laboratory of Excited-State Materials of Zhejiang Province, Zhejiang University, Hangzhou, 310058, China.

出版信息

Angew Chem Int Ed Engl. 2023 Dec 11;62(50):e202312713. doi: 10.1002/anie.202312713. Epub 2023 Nov 9.

Abstract

Converting colloidal nanocrystals (NCs) into devices for various applications is facilitated by designing and controlling their surface properties. One key strategy for tailoring surface properties is thus to choose tailored surface ligands. In that context, amines have been universally used, with the goal to improve NCs synthesis, processing and performances. However, understanding the nature of surface sites in amine-capped NCs remains challenging, due to the complex surface compositions as well as surface ligands dynamic. Here, we investigate both surface sites and amine ligation in CdSe NCs by combining advanced NMR spectroscopy and computational modelling. Notably, dynamic nuclear polarization (DNP) enhanced Cd and Se 1D NMR helps to identify both bulk and surface sites of NCs, while Cd 2D NMR spectroscopy enables to resolve amines terminated sites on both Se-rich and nonpolar surfaces. In addition to directly bonding to surface sites, amines are shown to also interact through hydrogen-bonding with absorbed water as revealed by N NMR, augmented with computations. The characterization methodology developed for this work provides unique molecular-level insight into the surface sites of a range of amine-capped CdSe NCs, and paves the way to identify structure-function relationships and rational approaches towards colloidal NCs with tailored properties.

摘要

通过设计和控制胶体纳米晶体(NCs)的表面性质,有助于将其转化为适用于各种应用的器件。因此,定制表面性质的一个关键策略是选择定制的表面配体。在这种情况下,胺类被广泛使用,目的是改善纳米晶体的合成、加工和性能。然而,由于复杂的表面组成以及表面配体的动态变化,了解胺封端纳米晶体中表面位点的性质仍然具有挑战性。在这里,我们通过结合先进的核磁共振光谱和计算建模,研究了CdSe纳米晶体中的表面位点和胺连接。值得注意的是,动态核极化(DNP)增强的Cd和Se一维核磁共振有助于识别纳米晶体的体相和表面位点,而Cd二维核磁共振光谱能够解析富硒和非极性表面上的胺端基位点。除了直接与表面位点结合外,核磁共振显示胺类还通过氢键与吸附的水相互作用,计算结果进一步证实了这一点。这项工作开发的表征方法为一系列胺封端的CdSe纳米晶体的表面位点提供了独特的分子水平见解,并为识别结构-功能关系以及制备具有定制性质的胶体纳米晶体的合理方法铺平了道路。

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