Journal
CHEM
Volume 5, Issue 8, Pages 2195-2214Publisher
CELL PRESS
DOI: 10.1016/j.chempr.2019.06.010
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Funding
- State Key Research Development Program of China [2016YFA0204200]
- National Natural Science Foundation of China [21822603, 21773062, 21577036]
- Shanghai Pujiang Program [17PJD011]
- Fundamental Research Funds for the Central Universities [22A201514021]
- Korea Institute of Materials Science through the UC-KIMS Center for Innovation Materials for Energy and Environment [POC2930]
- UC Riverside through the UC-KIMS Center for Innovation Materials for Energy and Environment [POC2930]
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Great interest has recently emerged in the development of quantum dots (QDs) that are capable of direct white-light emission for solid-state lighting. The conventional synthesis routes often involve surface modification and ligand displacement, which usually lead to undesired QD aggregation and fluorescence quenching. Here, we report a new strategy to synthesize QDs (ZnS, CdS, CdTe, and CsPbBrxI3-x) directly in colloidal SiO2 to produce QD@SiO2 composites, displaying direct white-light emissions. By taking advantage of the NH4+ trapped inside the silica colloids, we introduce metal cations through ion-exchange reactions into the microporous network of silica and then produce QDs directly within the silica colloids. This trapped-NH4+ strategy represents a new platform for the synthesis of novel functional nanocomposites by allowing convenient incorporation of various nanoparticles into sol-gel-derived colloidal matrices.
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