A Two-Step Hydrothermal Synthesis Approach to Monodispersed Colloidal Carbon Spheres
© to the authors 2009
Received: 19 March 2009
Accepted: 6 May 2009
Published: 21 May 2009
This work reports a newly developed two-step hydrothermal method for the synthesis of monodispersed colloidal carbon spheres (CCS) under mild conditions. Using this approach, monodispersed CCS with diameters ranging from 160 to 400 nm were synthesized with a standard deviation around 8%. The monomer concentration ranging from 0.1 to 0.4 M is in favor of generation of narrower size distribution of CCS. The particle characteristics (e.g., shape, size, and distribution) and chemical stability were then characterized by using various techniques, including scanning electron microscopy (SEM), FT-IR spectrum analysis, and thermalgravity analysis (TGA). The possible nucleation and growth mechanism of colloidal carbon spheres were also discussed. The findings would be useful for the synthesis of more monodispersed nanoparticles and for the functional assembly.
Carbon-based material is one kind of the most important functional materials because of its unique electromagnetic, thermodynamical, and mechanical properties [1–3] that exhibit potential applications in many areas such as drug delivery, hydrogen storage, junction device, and sensors. Many attempts have been made in the synthesis of nanoparticles with shape control. Spherical nanoparticles are very commonly generated due to the minimum surface energy compared to other morphologies (e.g., films, tubes). Recently, carbon colloidal spheres (CCS) have become an interesting research object for many investigators owing to their potential applications, including high-density and high-strength carbon artifacts lithium storing materials [4–8], sacrificial template to fabricate hollow structures [9–16], catalyst support material in methanol electro-oxidation , and coating material in core/shell structure [7, 18, 19]. In addition, these carbon nanoparticles are also potential as building block materials for fabricating ordered close-packed arrays by self-assembly [10, 20], which is also an important research area in nanoscience.
The functional properties of nanoparticles are heavily dependent on their shapes, sizes, and size distribution. Various methods have been used to prepare carbon spheres, such as chemical vapor deposition , templating method , pyrolysis of carbon sources , and hydrothermal method. Among them, the hydrothermal method is widely used due to its advantages, such as high purity, controllable shape and size, and inexpensive operation . Moreover, the CCS produced by the hydrothermal approach have a hydrophilic surface covered with C–OH groups , which are available for further surface functional modification, as well as the CCS can be easily removed by oxidation at high temperature or by dissolving via enzyme in solution. Therefore, many studies focused on the synthesis of carbon colloids via the hydrothermal approach. For example, Wang et al.  were the first to report the hydrothermal synthesis of hard carbon spheres by using sugar as a precursor through heat treatment at 190 °C for 5 h. Li et al.  reported that the carbon spheres could be prepared with different sizes from 200 to 1,500 nm under different reaction times (2–10 h, at 160 °C). Later, Mi et al.  demonstrated a high-temperature method to produce carbon microspheres with size of 1–2 μm by heating at 500 °C for 12 h in a sealed autoclave. Despite some successes, limitations still exist in generating monodispersed CCS. This is because it is difficult to control or adjust the concentration of the precursor in a sealed system, which will affect the nucleation and growth, and hence the morphology and size of CCS. Therefore, to develop a simple and efficient method to prepare monodispersed CCS is still challenging.
In this work, we report for the first time the synthesis of monodispersed CCS by a two-step hydrothermal approach under mild conditions. A separated nucleation and growth process will be controlled in the proposed method. The particle characteristics (shape, size, distribution) are then characterized by using various techniques, including scanning electron microscopy (SEM), FT-IR spectrum analysis, and thermalgravity analysis (TGA). The possible growth mechanism of CCS prepared by the two-step synthesis approach is also discussed.
Synthesis of Carbon Colloids
This step aims to synthesize colloidal carbon particles that can serve as seeds in a two-step synthesis approach. In brief, 11.89 g glucose monohydrate (purchased from Tianjin Bodi Chemical Ind. Co. Ltd) was dissolved in 600 mL deionized water, followed by stirring and ultrasonication to insure the solution is homogeneous. The colorless solution was then transferred into a Teflon stainless steel autoclave with 1,000 mL capacity and then sealed closely. Subsequently, the sealed autoclave was heated to 180 °C for 4 h along with constant stirring at ~800 rpm, and then cooled to room temperature naturally. Finally, the suspension containing the as-prepared carbon colloids was transferred into a flask for further characterization and uses. It was found that the particle suspension shows different colors such as deep brown, puce, depending on the particle size.
Synthesis of Monodispersed CCS Particles
The morphology and size of the carbon colloidal particles were checked using scanning electron microscope (SHIMADZU, SSX-550, SUPERSCAN Scanning Electron Microscope). To prepare the SEM sample, a drop of the diluted suspension was placed on a glass slide and then it was coated with gold prior to examination. The average particle size was estimated based on the SEM image. FT-IR spectrum (Perkin Elmer, Spectrum one NTS) was used to identify the functional groups. Thermo-gravimetric analysis (HENVEN HCT-2 TG/DTA) was carried out in air for identification of particle stability.
Results and Discussion
One-step Approach for Carbon Colloids
One-step approach was used in this work to prepare carbon colloids that can serve as seeds for monodispersed CCS. Different experimental parameters were tested and optimized. Fig. 1shows the morphologies of the seeds produced under different concentrations of glucose monohydrate. At higher concentrations (e.g., 0.6, 1.0, and 1.5 M), the colloids are apt to aggregate and show a broad size distribution (diameters of 1–10 μm, Fig. 1a–c). When the concentration of glucose monomers decreases to 0.4 and 0.2 M, the size of particles reduces to ~300 nm (Fig. 1d) and ~220 nm (Fig. 1e), respectively. When the concentration was fixed at 0.1 M, the average diameter of the generated spheres is ~93 nm (see Fig. 1f), with a size distribution of standard deviation of ~11%. This suggested that one-step hydrothermal method could be used to prepare carbon colloids, but the size distribution is still wide, particularly for functional self-assembly.
The influence of reaction temperature on the formation of carbon colloids was also tested in this work. It was found that the suitable temperature range is 160–180 °C (Fig. 1), consistent with the literature [18, 31, 32]. When a low temperature (<140 °C) was used, it is hard to obtain carbon colloids even through a long reaction time (e.g., 24 h); while a high temperature (e.g., over 180 °C) was used, it led to the accelerated nucleation of glucose molecules and resulted in a burst nucleation with a steep decline of the monomer concentration, which would lead to the formation of multiple shapes and/or sizes in the product due to the durative polycondensation .
Two-Step Approach for Monodispersed CCS
In the optimization of experimental parameters, the concentration of the seeds added in second step can affect the morphologies/sizes of the final product. For example, when 600 mL seed suspension was fully used for the second-step nucleation and growth, the carbon particles obtained show diverse morphologies (elliptic and triquetrous) as shown in Fig. 2f; while one quarter of 600 mL (i.e., 150 mL) seed suspension or less was used, the monodispersed CCS could be preferentially generated (Fig. 2). In addition, various carbon sources were also investigated, including sucrose, starch, and glucose. Sucrose is a kind of disaccharide that decomposes to glucose and fructose easily, which could result in the formation of multi-size colloids. Starch was dissolved into hot water to produce gelatin, non-spherical particles formed in further hydrothermal treatment. Through careful comparison, the glucose is found to be preferential for the synthesis of monodispersed CCS under the reported conditions.
The mechanism governing nucleation and growth of the CCS in the two-step approach was discussed. Different growth mechanisms were proposed in the past. For example, Wang et al. [4–8] suggested that the formation of dewatering sugar spherules is similar to the emulsion polymerization procedure. At a certain temperature, the dehydration and polycondensation leads to the appearance of amphiphilic compound, and the formation of spherical micelles that can further nucleate by dewatering. Li et al. [18, 37] described the effect of critical supersaturation of glucose monomers and observed a nucleation burst when some macromolecules formed by intermolecular dehydration of linear or branchlike oligosaccharides. Recently, Yao et al. [31, 32] reported the transformation of fructose to 5-hydroxymethylfurfural through an intra-molecular dehydration process followed by subsequent formation of carbon spheres. Such a carbon sphere contains a dense hydrophobic core and a hydrophilic shell. Such differences in understanding particle nucleation and growth drive us to conduct such work.
In this case, the polymerization of glucose monomers is built up by intermolecular dehydration, which is critical to nucleation in the hydrothermal synthesis. It is supposed that in the homogeneous solution, the polymerization reaches supersaturation, and then nucleation occurs with the progress of dehydration and aromatization. In the proposed two-step synthesis approach, the active functional groups on the surface of the carbon colloids could react preferentially with the newly added monomers to form bigger particles instead of nucleation by the monomers themselves. This was also confirmed by the following theoretical explanation.
where the growth rate via diffusion-controlled mode is inversely proportional to the particle radius, consistent with the theory of Ostwald ripening . Our experimental observations (Fig. 2) are in good agreement with the Eq. 2.
where Δr is the standard deviation of the particle size distribution and is the mean particle radius. Equation 5 reveals that the change rate of standard deviation (d(Δr)/dt) depends strongly on the particle radius (r*) in equilibrium (supersaturation) in the diffusion-controlled mode. Higher supersaturation ( ) below the critical supersaturation makes better monodispersity (d(Δr)/dt < 0). Otherwise, lower supersaturation ( ) can broaden the size distribution (d(Δr)/dt > 0) even in the diffusion-controlled mode [38, 39]. In the proposed two-step approach, the standard deviation was reduced from 8.5% down to 6.9% with increasing the monomer concentration from 0.1 to 0.4 M (Fig. 3) indicating that a higher monomer concentration that determines the supersaturation is favorable for the narrow size distribution under the considerable conditions. On the basis of above-mentioned analysis, the diffusion-controlled mode may be dominant in the overall growth of particles in our proposed two-step synthesis method, which is apt to the formation of monodispersed particles.
We have demonstrated a facile two-step hydrothermal approach to the synthesis of monodispersed CCS under mild conditions. By this approach, the CCS size could be controlled in the range of 160–400 nm with a standard deviation 6–9%. Compared to the one-step approach, the proposed two-step approach could separately control the nucleation and growth of particles as far as possible, which is favorable for the narrow size distribution. It was noted that in the concentration range of 0.1–0.4 M, the higher the concentration of monomers the narrower the size distribution of carbon colloids. The nucleation and growth of the CCS might be attributed to the diffusion-controlled mode. This method could be extended into other systems for the fabrication of monodispersed particles with functional properties.
We gratefully acknowledge the financial support from the Program for Changjiang Scholars and Innovative Research Teams in University (PCSIRT, IRT0713), National Natural Science Fund for Distinguished Young Scholars (50425413), the Program for New Century Excellent Talents in University (NCET-25-0290), and the National Natural Science Foundation of China (50672014). We also thank our collaborators, Yuwei Sun and Wei Yi, for their essential contributions to this work.
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