Preparation and Characterization of Silica-Coated Magnetic–Fluorescent Bifunctional Microspheres

Bifunctional magnetic–fluorescent composite nanoparticles (MPQDs) with Fe3O4MPs and Mn:ZnS/ZnS core–shell quantum dots (QDs) encapsulated in silica spheres were synthesized through reverse microemulsion method and characterized by X-ray powder diffraction, scanning electron microscopy, transmission electron microscopy, vibration sample magnetometer, and photoluminescence (PL) spectra. Our strategy could offer the following features: (1) the formation of Mn:ZnS/ZnS core/shell QDs resulted in enhancement of the PL intensity with respect to that of bare Mn:ZnS nanocrystals due to the effective elimination of the surface defects; (2) the magnetic nanoparticles were coated with silica, in order to reduce any detrimental effects on the QD PL by the magnetic cores; and (3) both Fe3O4MPs and Mn:ZnS/ZnS core–shell QDs were encapsulated in silica spheres, and the obtained MPQDs became water soluble. The experimental conditions for the silica coating on the surface of Fe3O4nanoparticles, such as the ratio of water to surfactant (R), the amount of ammonia, and the amount of tetraethoxysilane, on the photoluminescence properties of MPQDs were studied. It was found that the silica coating on the surface of Fe3O4could effectively suppress the interaction between the Fe3O4and the QDs under the most optimal parameters, and the emission intensity of MPQDs showed a maximum. The bifunctional MPQDs prepared under the most optimal parameters have a typical diameter of 35 nm and a saturation magnetization of 4.35 emu/g at room temperature and exhibit strong photoluminescence intensity.


Introduction
Semiconductor quantum dots (QDs) have been widely explored as biomedical labeling agents [1][2][3][4]. However, the small-ensemble Stokes shift of intrinsic QDs can cause self-quenching. In addition, experimental results indicated that any leakage of cadmium from the QDs would be toxic and fatal to biological system [5], and cadmium-containing products can be environmentally problematic. Recently, Peng et al. [6][7][8] reported that doped QDs could not only replace cadmium in CdSe QDs with zinc, but also overcome a number of intrinsic disadvantages of undoped QDs emitters, i.e., strong self-quenching caused by their smallensemble Stokes shift (energy difference between absorption spectrum and emission band) [9] and sensitivity to thermal, chemical, and photochemical disturbances [10]. Mn 2? -doped ZnS QDs have been extensively investigated for use in various applications other than biomedical labeling, such as displays, sensors, and lasers [11][12][13]. In addition, the luminescence lifetime of Mn 2? -doped ZnS QDs is *1 ms. Such a long lifetime makes the luminescence from the nanocrystal readily distinguishable from any background luminescence. Therefore, Mn 2? -doped ZnS QDs could be potential candidates as fluorescent labeling agents, especially in biology [14]. Magnetic nanoparticles of iron oxides (MPs) also show many advantages in biological applications. One unique feature of magnetic nanoparticles is to respond well to magnetic control, which has led to several successful applications, including biological separation, protein purification, bacteria detection, and drug delivery [15,16]. Highly luminescent QDs could serve as luminescent markers, while magnetic nanoparticles could be easily manipulated under the external magnetic field. Therefore, combination of QDs and MPs to get fluorescent-magnetic bifunctional composite nanoparticles (MPQDs) has attracted intense attention in the past decade due to its appealing applications [17][18][19][20][21][22][23][24][25]. Surface modification of QDs and MPs with silica has led to improved stability, lower toxicity, and higher biocompatibility, and protection of the QDs against corrosion by the biological buffer. In addition, the rich and well-known surface chemistry of silica makes bioconjugation more convenient. However, it was still a challenge to obtain magnetic, multicolor barcoded nanospheres with controllable size and tunable readout.
In this work, we obtained water-soluble bifunctional MPQDs with Fe 3 O 4 MPs and Mn:ZnS/ZnS core-shell QDs encapsulated in silica spheres through reverse microemulsion method. The synthetic procedure was illustrated in Scheme 1. Our strategy could offer the following features: (1) the formation of Mn:ZnS/ZnS core/shell QDs resulted in enhancement in the photoluminescence (PL) intensity with respect to that of bare Mn:ZnS nanocrystals due to the effective elimination of the surface defects, and the QDs' chemical stability and photostability were also preserved [26]; (2) the magnetic MPs were coated with silica, so that no interference of the QD PL by the magnetic particles was expected [20,27]; and (3) both Fe 3 O 4 MPs and Mn:ZnS/ ZnS core-shell QDs were encapsulated in silica spheres, and the obtained MPQDs became water soluble. The obtained bifunctional MPQDs were characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), vibration sample magnetometer (VSM), and PL spectra. Besides the intensive PL, the MPQDs simultaneously exhibited magnetic properties and could be separated from solution using a permanent magnet. In a few words, the PL, magnetic, and water-soluble properties of the MPQDs would allow them to find a large range of applications for biolabeling, bioseparation, immunoassay, and diagnostics.

Synthesis of Mn:ZnS/ZnS Core/Shell Quantum Dots
Mn:ZnS/ZnS core/shell QDs were synthesized according to our recent reports [26]. Briefly, the stock solution was prepared by adding Zn(CH 3 COO) 2 Á2H 2 O and Mn(CH 3 COO) 2 Á2H 2 O into 100 mL 0.12 M TGA aqueous solution respectively. The Mn/Zn molar ratios in the four samples were fixed at 1%. Then the TGA-manganese solution reacted with Na 2 S aqueous solution at 80°C for 20 min to form small-size MnS core. In order to obtain Mn:ZnS/ZnS core/shell QDs, the TGA-zinc complex aqueous solution was injected into the MnS core solution at two-step. At the first step, 75% of TGA-zinc solution was injected into the MnS core solution under vigorously stirring and heated at 80°C for 10 h. The remaining TGAzinc solution was then injected into the mixture and heated at 80°C for another 2 h. The Mn:ZnS/ZnS core/shell QDs were obtained by adding excess ethanol to the solutions and then dried in vacuum.

Synthesis of Fe 3 O 4 Nanoparticles
Fe 3 O 4 nanoparticles were synthesized as reported by Massart et al. [28]. A mixture of 5.406 g of FeCl 3 Á6H 2 O and 2.780 g of FeCl 2 Á4H 2 O dissolved in 100 mL of highpurity water was placed in a 250-mL flask, following by the quick droplet-addition of 15 mL of 25% NH 4 OH. The mixture was irradiated with high-intensity ultrasound (600 W, 20 kHz) at room temperature in ambient air for Scheme 1 Synthesis of bifunctional magnetic fluorescent composite nanoparticles 1 h. After irradiation, the precipitate was centrifuged and washed using distilled water and ethanol for several times. It was then freeze-dried at 223 K for 4 h in vacuum.

Synthesis of Core-Shell Fe 3 O 4 @SiO 2 Nanoparticles
The core-shell Fe 3 O 4 @SiO 2 nanoparticles were synthesized as follows: 1 g of Fe 3 O 4 nanoparticles were added to 100 mL of 2.84 wt% sodium silicate solution and ultrasonically dispersed for 30 min. Then, 2 wt% H 2 SO 4 was used to adjust pH value of the solution to 9. The mixture was irradiated with high-intensity ultrasound (600 W, 20 kHz) at room temperature in ambient air for 1 h. Twenty-five milliliters cyclohexane, 3.2 mL n-hexanol, 8 mL TritonX-100, 1 mL of the as-prepared magnetic sol, and 1.5 mL of TEOS were added in a flask in turn under vigorous magnetic stirring. Thirty minutes after the microemulsion was formed, 1 mL NH 4 OH (25 wt%) was added to initiate the polymerization process. The silica growth was completed after 10 h of stirring. The final product was denoted as FS.

Synthesis of Silica-coated Magnetic-luminescent Bifunctional Nanocomposites
One milliliter of Mn:ZnS/ZnS aqueous solution (10 g/L), 1 mL TEOS, and 1 mL NH 4 OH (25 wt%) were in turn added into the above-mentioned FS and allowed to stir at room temperature for 5 h. Acetone was used to terminate the reaction, and the resultant precipitates of MPQDs were washed with water and ethanol for three times, and then dried in vacuum.

Characterization
The XRD patterns of the synthesized samples were obtained by a D/max-cA diffractometer using CuKa radiation (k = 0.15418 nm). The size and morphology of the as-synthesized products were determined by a XL30 S-FEG SEM and a JEM-3010 high-resolution TEM. The PL spectra of the samples were recorded with a Fluorescence Spectrophotometer F-4500. The room temperature magnetization in the applied magnetic field was performed by model JDM-13 vibrating sample magnetometer.

Results and Discussions
Structural and Morphological Characterization X-ray diffraction patterns of the samples are shown in  (Fig. 2a, b) shows that the Fe 3 O 4 /SiO 2 sample is composed of nanoparticles with a size in the range of about 20-40 nm. Figure 2c is the energy-dispersive X-ray (EDX) spectrum from Fig. 2b, further confirming that the Fe 3 O 4 / SiO 2 sample is composed of Fe, Si, and O, which is consistent with the XRD results (shown in Fig. 1b). A typical TEM image (Fig. 2d) shows that the size of Fe 3 O 4 /SiO 2 sample is about 15 nm. A typical SEM image (Fig. 3a, b) shows that the MPQDs sample is composed of nanoparticles with a size in the range of about 30-50 nm. Figure 3c is the EDX spectrum from Fig. 3b, further confirming that the MPQDs sample is composed of Fe, Si, O, Zn, and S, which is consistent with the XRD results (shown in Fig. 1c). A typical TEM image (Fig. 3d) shows that the size of the MPQDs sample is in the range of about 30 nm.

Optical Properties
Agekyan [30] reported that the interaction between the Fe 3 O 4 and the QDs would influence the PL properties of the nanocomposites. Hong et al. [31] reported that the PL properties of the magnetic-luminescent nanocomposites (Fe 3 O 4 /PE n /CdTe) were very sensitive to the distance between Fe 3 O 4 nanoparticles and CdTe QDs separated by the polyelectrolyte multilayers. The interaction between the two particle types was suppressed only after having deposited 21 layers of polyelectrolyte between the magnetic and the luminescent nanoparticles. In this paper, a dense silica shell was deposited on Fe 3 O 4 nanoparticles in order to prevent quenching of the QDs by the magnetic Fe 3 O 4 nanoparticles. Hence, control of silica coating on the surface of Fe 3 O 4 nanoparticles is an important consideration. With this in mind, we investigated several experimental parameters for silica formation with the aim of optimizing the resulting MPQDs fluorescence. Figure 4 showed the effect of the ratio of water to surfactant on the photoluminescence spectra of the MPQDs. It was found that the PL intensity increased with the decrease in the ratio of water to surfactant, and reached a maximum when R was 1:8. If the ratio of water to surfactant continued to decrease, namely \1:8, the PL intensity would decrease. Stjerndahl et al. [32] have reported that the SiO 2 shell thinned with the increasing water concentration. We have found that the optimal SiO 2 thickness was achieved when R was 1:8.

The Effects of the Ratio of Water to Surfactant
The Effect of the Amount of TEOS Figure 5 showed the effect of the amount of TEOS on the photoluminescence spectra of the MPQDs. It was found that the PL intensity increased with the decrease in the amount of TEOS, and reached a maximum when TEOS was 1.5 mL. If the amount of TEOS was too low, a silica shell did not form on the surface of the Fe 3 O 4 nanoparticles, while if the amount of TEOS was too high, loser and larger silica particles would form. The Effect of the Amount of NH 4 OH Figure 6 showed the effect of the amount of NH 4 OH on the photoluminescence spectra of the MPQDs. It was found that the PL intensity increased with the increase in the amount of NH 4 OH, and reached a maximum when NH 4 OH was 0.5 mL. If the amount of NH 4 OH continued to increase, namely more than 0.5 mL, the PL intensity would decrease. It was known that NH 4 OH catalyst accelerated the hydrolysis of TEOS proportionally. Rapid hydrolysis was preferred, to increase the monodispersity of the resulting particles and prevent competing reactions. Because the pH value of the solution increased with increasing NH 4 OH concentration, the electrostatic stabilization of the colloid should increase. Accordingly, the ionic strength of the solution increased, which destabilized the microemulsion system.    [37].
Overall, it must be concluded that the magnetic response of a system to an inert coating is rather complex and system specific, so that no firm correlations can be established at present. Therefore, the reasons for low magnetic of MPQDs should be further extensively studied in the future.

Conclusion
Water-soluble bifunctional MPQDs with Fe 3 O 4 MPs and Mn:ZnS/ZnS core-shell QDs encapsulated in silica spheres were synthesized through reverse microemulsion method. The effects of the parameters for the silica coating on the surface of Fe 3 O 4 , such as the ratio of water to surfactant (R), the amount of NH 4 OH, and the amount of TEOS, on the PL properties of MPQDs were studied. It was found that the silica coating on the surface of Fe 3 O 4 could effectively suppress the interaction between the Fe 3 O 4 and the QDs under the most optimal parameters, and the emission intensity of MPQDs showed a maximum. The bifunctional MPQDs prepared under the most optimal parameters have a typical diameter of 35 nm and a saturation magnetization of 4.35 emu/g at room temperature, and exhibit strong photoluminescence intensity. In a few words, the PL, magnetic, and water-soluble properties of the MPQDs would allow them to find a large range of applications for biolabeling, bioseparation, immunoassay, and diagnostics.