Literature DB >> 34984545

Theoretical investigation complexation characteristics and UV-Vis absorption spectral properties of CdTe QDs with four capping agents.

Qinghong Yang1, Xujiang Wan1, Yang Chen1, Hui Luo1, Yan Zheng2, Laicai Li3.   

Abstract

In this paper, density functional theory (DFT) and time-dependent density functional theory (TDDFT) are used to study the complexation characteristics CdTe QDs with four different capping agents, i.e. 3-mercaptopropionic acid (MPA), reduced glutathione (GSH), 1-thioglycerol (TG) and 2-mercaptoethanesulfonate (MES). The properties of these complexes are analyzed by the complexation free energies, bond lengths, LOL, ADCH charges, frontier molecular orbitals and the UV-Vis absorption spectra. The results indicate that the four capping agents could form stable complexes with CdTe QDs. Whether the four capping agents interact with (CdTe)6 or (CdTe)9, MES has the strongest complexation ability with CdTe QDs and the MES-complexes are the most stable. For (CdTe)6, A2-MES is the most stable configuration. The complexation free energy and bond length of A2-MES are - 74.50 kcal/mol and 2.461 Å, respectively. When (CdTe)9 as substrate, A4-MES is the most stable configuration and corresponding complexation free energy is - 100.97 kcal/mol, which is followed by A4-MPA (- 57.75 kcal/mol) and A3-TG (- 60.20 kcal/mol), while A4-GSH (- 44.47 kcal/mol) is the weakest. Moreover, the electron amount transferred from MES to CdTe QDs is the most, and the ADCH charge value is 1.47 e. The absorption intensity of UV-visible light after complexation is also the largest. This is consistent with the result of the complexation free energy. Thus, it can be seen that the complexation abilities of four capping agents are in order of MES > MPA≈TG > GSH.
© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  Capping agents; CdTe QDs; Complexation characteristics; Density functional theory; UV–vis Absorption spectroscopy

Year:  2022        PMID: 34984545     DOI: 10.1007/s00894-021-04940-9

Source DB:  PubMed          Journal:  J Mol Model        ISSN: 0948-5023            Impact factor:   1.810


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