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Selective Cation Exchange Enabled Growth of Lanthanide Core/Shell Nanoparticles with Dissimilar Structure
Hao Dong1, Ling-Dong Sun1, Lin-Dong Li1
1Beijing National Laboratory for Molecular Sciences, State Key Laboratory of Rare Earth Materials Chemistry and Applications, PKU-HKU Joint Laboratory in Rare Earth Materials and Bioinorganic Chemistry, College of Chemistry and Molecular Engineering, Peking University , Beijing 100871, China.
Researchers developed a novel method to create lanthanide core/shell nanoparticles with different structures. This technique enhances upconversion emission and prevents ion leakage, opening new possibilities for nanoparticle design.
Area of Science:
- Materials Science
- Nanotechnology
- Chemistry
Background:
- Core/shell nanostructures are crucial for advanced functionalities but are typically limited to isomorphic structures.
- Lanthanide-based nanomaterials are vital for photon conversion applications.
Purpose of the Study:
- To develop a method for creating lanthanide core/shell nanoparticles with dissimilar core and shell structures.
- To improve the performance of photon conversion materials through novel nanostructure engineering.
Main Methods:
- A selective cation exchange strategy was employed to construct heterostructured nanoparticles.
- Hexagonal NaLnF4 (lanthanide) cores were coated with cubic CaF2 shells.
- Surface structure evolution from hexagonal to cubic was induced via cation exchange.
Main Results:
- The heterostructured CaF2 shell significantly enhanced upconversion emission, increasing absolute quantum yield from 0.2% to 3.7%.
- The novel structure effectively suppressed interfacial diffusion and leakage of lanthanide ions (Ln3+).
Conclusions:
- This work presents a new approach for fabricating heterostructured core/shell nanoparticles with non-isomorphic components.
- The findings provide valuable insights for tuning nanoparticle properties and enhancing their performance in applications like photon conversion.
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