V. A. Karachevtsev, N. V. Kurnosov, S. G. Stepanian, I. M. Voloshin, O. S. Lytvyn, A. M. Plokhotnichenko, L. Adamowicz
{"title":"Photoluminescent MoS2 quantum dots surrounded by nucleotides: an experimental and theoretical study","authors":"V. A. Karachevtsev, N. V. Kurnosov, S. G. Stepanian, I. M. Voloshin, O. S. Lytvyn, A. M. Plokhotnichenko, L. Adamowicz","doi":"10.1007/s11051-024-06144-7","DOIUrl":null,"url":null,"abstract":"<div><p>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<sub>2</sub> 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 MoS<sub>2</sub> QDs surrounded by nucleotides is observed for the first time. Different structures of MoS<sub>2</sub> 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 MoS<sub>2</sub> QD. The structural flexibility of the nucleotide adsorbed on the MoS<sub>2</sub> 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.</p><h3>Graphical abstract</h3>\n<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":653,"journal":{"name":"Journal of Nanoparticle Research","volume":"26 10","pages":""},"PeriodicalIF":2.1000,"publicationDate":"2024-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Nanoparticle Research","FirstCategoryId":"88","ListUrlMain":"https://link.springer.com/article/10.1007/s11051-024-06144-7","RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
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 MoS2 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.
期刊介绍:
The objective of the Journal of Nanoparticle Research is to disseminate knowledge of the physical, chemical and biological phenomena and processes in structures that have at least one lengthscale ranging from molecular to approximately 100 nm (or submicron in some situations), and exhibit improved and novel properties that are a direct result of their small size.
Nanoparticle research is a key component of nanoscience, nanoengineering and nanotechnology.
The focus of the Journal is on the specific concepts, properties, phenomena, and processes related to particles, tubes, layers, macromolecules, clusters and other finite structures of the nanoscale size range. Synthesis, assembly, transport, reactivity, and stability of such structures are considered. Development of in-situ and ex-situ instrumentation for characterization of nanoparticles and their interfaces should be based on new principles for probing properties and phenomena not well understood at the nanometer scale. Modeling and simulation may include atom-based quantum mechanics; molecular dynamics; single-particle, multi-body and continuum based models; fractals; other methods suitable for modeling particle synthesis, assembling and interaction processes. Realization and application of systems, structures and devices with novel functions obtained via precursor nanoparticles is emphasized. Approaches may include gas-, liquid-, solid-, and vacuum-based processes, size reduction, chemical- and bio-self assembly. Contributions include utilization of nanoparticle systems for enhancing a phenomenon or process and particle assembling into hierarchical structures, as well as formulation and the administration of drugs. Synergistic approaches originating from different disciplines and technologies, and interaction between the research providers and users in this field, are encouraged.