Photoluminescent MoS2 quantum dots surrounded by nucleotides: an experimental and theoretical study

被引:0
作者
Karachevtsev, V. A. [1 ]
Kurnosov, N. V. [1 ]
Stepanian, S. G. [1 ]
Voloshin, I. M. [1 ]
Lytvyn, O. S. [2 ]
Plokhotnichenko, A. M. [1 ]
Adamowicz, L. [3 ]
机构
[1] NAS Ukraine, B Verkin Inst Low Temp Phys & Engn, 47 Nauky Ave, UA-61103 Kharkiv, Ukraine
[2] Borys Grinchenko Metropolitan Kyiv Univ, Bulvarno Kudriavska St 18-2, UA-04053 Kyiv, Ukraine
[3] Univ Arizona, Dept Chem & Biochem, Tucson, AZ 85721 USA
关键词
MoS2 quantum dots; Photoluminescence; Nucleotides; Liquid-phase exfoliation; DFT calculations; MoS2; defects; Two-dimensional nanostructures; ASSISTED EXFOLIATION; DICHALCOGENIDES; LUMINESCENT; NANOSHEETS;
D O I
10.1007/s11051-024-06144-7
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In recent years, the use of biomolecules as dispersants for the preparation of 2D nanomaterials by direct liquid-phase exfoliation (LPE) using ultrasonication has attracted increasing attention as a convenient and cost-effective approach to ensure simultaneously the biocompatibility of these nanostructures. In this work, we prepare MoS(2 )quantum dots (QDs) by the LPE method using deoxyadenosine monophosphate (dAMP) as an exfoliation agent that provides a good biocompatibility of the QDs too. As a result, a visible-range photoluminescence from MoS2 QDs surrounded by nucleotides is observed for the first time. Different structures of MoS2 QDs with dAMP are analyzed employing the DFT calculations. It is shown that dAMP can form coordination bonds with the Mo atoms located at the QD edges or at the defect sites where direct contacts with these atoms can occur. The covalent bonds facilitate strong adsorption of dAMP on a MoS2 QD. The structural flexibility of the nucleotide adsorbed on the MoS2 QD enables a combination of noncovalent stacking interaction of the nucleobase and a coordination bond of the phosphate group with the Mo atoms located at the edges to occur. This leads to the formation of a very energetically stable complex. [GRAPHICS] .
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