Aqueous Topological Synthesis of Au@semiconductor Core-Shell Nanocrystals with Morphology and Composition Engineering.

Inorg Chem

Key Laboratory of Medical Molecule Science and Pharmaceutical Engineering, Ministry of Industry and Information Technology, MOE Key Laboratory of Cluster Science, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing 100081, China.

Published: June 2024

AI Article Synopsis

  • - Core-shell nanocrystals (C-S NCs), especially noble metal@semiconductor types, have unique optical and electrical properties that make them highly desirable for various applications, including biological uses.
  • - A new aqueous strategy for synthesizing these C-S NCs using cation exchange reactions (CER) was developed, utilizing the safer and more environmentally friendly triphenylphosphine (TPP) instead of traditional solvents like tributyl phosphine (TBP).
  • - The produced Au@ZnS core-shell nanorods (C-S NRs) showed improved absorption properties, better biocompatibility, and high effectiveness in photodynamic therapy, demonstrating the potential of this new synthesis method.

Article Abstract

Core-shell nanocrystals (C-S NCs) are an essential class of materials whose structural engineering has attracted wide attention due to their tunable optical and electrical properties, especially noble metal@semiconductor (NMS) C-S NCs with flexible plasmon-exciton coupling. Due to their diverse critical applications, especially aqueous biological applications, herein we propose an aqueous topological strategy enabled by cation exchange reactions (CER) to synthesize various plasmonic Au@semiconductor C-S NCs, in which environmentally friendly triphenylphosphine (TPP) is used as an initiator instead of inflammable tributyl phosphine (TBP). The introduction of the milder, solid TPP facilitated a new aqueous CER strategy for synthesizing Au@semiconductor NCs with tailored chalcogenide compositions and morphologies. For example, the as-synthesized Au@ZnS C-S NRs had better absorption and biocompatibility and exhibited excellent photodynamic therapy efficacy.

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Source
http://dx.doi.org/10.1021/acs.inorgchem.4c01238DOI Listing

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