Surface Sites and Ligation in Amine‐capped CdSe Nanocrystals**

Author:

Cao Weicheng12,Yakimov Alexander1,Qian Xudong2,Li Jiongzhao2,Peng Xiaogang2,Kong Xueqian32,Copéret Christophe1ORCID

Affiliation:

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

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

3. Institute of Translational Medicine Shanghai Jiao Tong University Shanghai 200240 China

Abstract

AbstractConverting 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 113Cd and 77Se 1D NMR helps to identify both bulk and surface sites of NCs, while 113Cd 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 15N 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.

Funder

National Natural Science Foundation of China

China Scholarship Council

Publisher

Wiley

Subject

General Chemistry,Catalysis

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