Size-controlled syntheses and hydrophilic surface modification of Fe3O4, Ag, and Fe3O4/Ag heterodimer nanocrystalsElectronic supplementary information (ESI) available: Fig. S1-S6. See DOI: 10.1039/c0dt00965b
High-quality, monodisperse, and size-controlled Fe 3 O 4 , Ag, and bifunctional Fe 3 O 4 /Ag heterodimer nanocrystals (NCs) have been synthesized successfully. In the synthesis of Fe 3 O 4 NCs, dodecanol was chosen as the substitute of 1,2-hexadecanediol and "size control" was achieved by...
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Zusammenfassung: | High-quality, monodisperse, and size-controlled Fe
3
O
4
, Ag, and bifunctional Fe
3
O
4
/Ag heterodimer nanocrystals (NCs) have been synthesized successfully. In the synthesis of Fe
3
O
4
NCs, dodecanol was chosen as the substitute of 1,2-hexadecanediol and "size control" was achieved by simply adjusting the proportion among the ligands instead of utilizing seed-mediated growth. In the synthesis of Ag NCs, organometallic silver acetylacetonate (Agacac) was used as precursors and tunable particle size could be easily obtained by adjusting the reaction temperatures. By using different sized Fe
3
O
4
NCs as seeds, Fe
3
O
4
/Ag heterodimer NCs with particle sizes tuned from 5 to 16 nm for Fe
3
O
4
and 4 to 8 nm for Ag were successfully synthesized and superparamagnetism were maintained. We found that the size of Ag attached on the Fe
3
O
4
NCs relied on the size of Fe
3
O
4
seed. UV-vis absorption spectra and TEM investigations revealed that the bigger the Fe
3
O
4
NCs seed used, the bigger the Ag NCs that were obtained from the heterodimer NCs. In addition, we demonstrated that all of these NCs were successfully transferred into water by surface modification with biocompatible carboxylic acid groups, which made them meet the basic requirement for biolabeling and biomedical applications.
High-quality, monodisperse Fe
3
O
4
(4-20 nm), Ag (4-9 nm), and bifunctional Fe
3
O
4
/Ag heterodimer nanocrystals have been synthesized and successfully transferred into water by surface modification. |
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ISSN: | 1477-9226 1477-9234 |
DOI: | 10.1039/c0dt00965b |