Nanometer-Thick Carbon Coatings with Covalent Chemical Functionalization of Metal Oxide Nanoparticles for Environmental and Biological Applications

Metal oxide nanoparticles have many useful applications in environmental studies, as tracking agents in life sciences, and in nutrient delivery for nano-enhanced agriculture. A key challenge in controlling the behavior of metal oxide nanoparticles in aqueous media is that molecular ligands are unsta...

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Veröffentlicht in:ACS applied nano materials 2023-03, Vol.6 (5), p.3525-3536
Hauptverfasser: Kinsley, Paige C., Green, Curtis M., Borgatta, Jaya, Kruszynski Earl, Catherine E., Laudadio, Elizabeth D., Hamers, Robert J.
Format: Artikel
Sprache:eng
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Zusammenfassung:Metal oxide nanoparticles have many useful applications in environmental studies, as tracking agents in life sciences, and in nutrient delivery for nano-enhanced agriculture. A key challenge in controlling the behavior of metal oxide nanoparticles in aqueous media is that molecular ligands are unstable with respect to hydrolytic cleavage from the surfaces. This instability limits the practical application of metal oxide nanoparticles in aqueous media. We have developed a method for producing nanometer-thin carbon shells on the surface of Al2O3, Cr3+:Al2O3 (nanoruby), ZnO, and Fe3O4 (magnetite) metal oxides that provides a scaffold for subsequent covalent chemical functionalization. Fluorescence measurements using carbonized Cr3+:Al2O3 (nanoruby) confirm that these thin carbon coatings have relatively little impact on the optical properties, allowing bright emission with less than 50% decrease in fluorescence intensity compared to an identical nanoruby without carbon coating. We demonstrate the utility for functionalization by modifying C-coated Al2O3 with molecular ligands bearing positive and negative charges. This approach provides a pathway for functionalization of a broad range of metal oxide nanoparticles with molecular ligands that can confer specific molecular properties to the nanoparticle surfaces in aqueous media while taking advantage of the high strength and stability of C–C interfacial bonds between surface ligands and the carbon shell.
ISSN:2574-0970
2574-0970
DOI:10.1021/acsanm.2c05288