A review on radiation-induced nucleation and growth of colloidal metallic nanoparticles
© Abedini et al.; licensee Springer. 2013
Received: 9 September 2013
Accepted: 30 October 2013
Published: 13 November 2013
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© Abedini et al.; licensee Springer. 2013
Received: 9 September 2013
Accepted: 30 October 2013
Published: 13 November 2013
This review presents an introduction to the synthesis of metallic nanoparticles by radiation-induced method, especially gamma irradiation. This method offers some benefits over the conventional methods because it provides fully reduced and highly pure nanoparticles free from by-products or chemical reducing agents, and is capable of controlling the particle size and structure. The nucleation and growth mechanism of metallic nanoparticles are also discussed. The competition between nucleation and growth process in the formation of nanoparticles can determine the size of nanoparticles which is influenced by certain parameters such as the choice of solvents and stabilizer, the precursor to stabilizer ratio, pH during synthesis, and absorbed dose.
In the past few decades, revolutionary developments of science and engineering have moved at a very fast pace towards synthesis of materials in the nanosize region in order to achieve unique properties that are significantly different from those of the individual atoms and their bulk counterparts [1–3]. When the dimension of a particle decreases below 100 nm, it exhibits many intriguing properties that arise mainly from two physical effects. First, the quantization of electronic states becomes apparent leading to very sensitive size-dependent effects such as optical and magnetic properties [4, 5]. Second, the high surface-to-volume ratio alters the thermal, mechanical, and chemical properties of materials . Various nanoparticle synthesis approaches are available, which can be broadly classified into top-down and bottom-up approaches . In the former category, nanoparticles can be obtained by techniques such as milling or lithography which generates small particles from the corresponding bulk materials [8, 9]. However, in the latter approach, nanoparticles can be formed atom-by-atom in the gas phase, solid phase, or liquid phase . In the liquid phase, nanoparticles are chemically synthesized in a colloidal solution containing precursors, a reducing agent, a particle capping agent, and a solvent [11, 12]. Although colloidal synthesis has the potential to produce large quantity of nanoparticles with good control of size, shape, crystallinity, morphology, composition, and surface chemistry at reasonably low cost.
Colloids are composed of suspensions of one phase, either solid or liquid, in a second liquid phase . They are very attractive because of their huge surface-to-volume ratio and their high specific surface area. This insures contact of a large part of the particle atoms with the surrounding liquid, to form almost as soluble macromolecules, which leads to larger interactions or faster reactions . The colloids, which we are concerned with in this review, are particles of metallic elements with respect to their surrounding phase.
Most of the preparation techniques of the metal colloids are based on reduction of precursor metal ions in solution (aqueous or otherwise) in the presence of a stabilizing agent. The most widely used techniques are thermolysis , chemical reduction , sonochemical route [17, 18], and irradiation methods [19, 20]. One of the great advantages of the radiolytic synthesis in comparison with the other available methods lies in the fact that the experiment can be carried out at very mild conditions, such as ambient pressure and room temperature with high reproducibility . Another important advantage of this method is that the main reducing agent in the absence of oxygen is the hydrated electron which has a very negative redox potential. This enables any metal ions to be reduced to zero-valent metal atoms without using chemical reducing agents. Thus, the generation of primary atoms occurs as an independent event and at the origin; the atoms are separated and homogeneously distributed as were the ionic precursors [14, 22, 23]. In other words, two main factors which lead to formation of uniformly dispersed and highly stable nanoparticles without unwanted by-products of the reductants are homogeneous formation of nuclei and elimination of excessive chemical reducing agents. The choice of the absorbed dose is crucial in order to control the cluster size and crystal structure by precise tuning of nucleation and growth steps especially for multi-metallic clusters . Therefore, the radiation technique has proven to be an environmentally benign and low-cost method for preparation of a large quantity of size and structure controllable metal nanoparticles [24–26].
In this review, a few examples among recent works were selected in which colloidal metal particles were synthesized by radiolytic reduction method and used either as a part of elaborate structures.
The radiolytic reduction has been proven to be a powerful tool to produce monosized and highly dispersed metallic clusters . The normal ionization radiations which are used for synthesis of nanoparticles are electron beam, X-ray, gamma-ray, and UV light. The metallic nanoparticles can be prepared in an aqueous solution in the presence of a stabilizer without using chemical reducing agents, namely by using of radiolytic method [26–29].
This mechanism avoids the use of additional reducing agents and the following side reactions. Moreover, by varying the dose of the irradiation, the amount of zero-valent nuclei can be controlled.
The charged dimer clusters M2+ may further be reduced to form a centre of cluster nucleation. The competition between the reduction of free metal ions and absorbed ones could be controlled by the rate of reducing agent formation .
where m, n and p represent the nuclearities, and x, y and z, symbolize the number of associated ions. The control of the final size depends on the limitation applied to the coalescence beyond certain nuclearity. For free clusters such as nanocolloids in solution, the coalescence may be limited by a polymeric molecule acting as a cluster stabilizer.
All nanostructured materials possess a huge surface energy due to the large surface area; thus, they are thermodynamically unstable or metastable. Overcoming the large surface energy to prevent the nanostructures from growing is one of the great challenges in the synthesis of nanomaterials . Nanoparticles, exclusively colloidal particles, in a short distance, are attracted to each other by the van der Waals force. If there is no counteracting force, the particles will aggregate and the colloidal system will be destabilized. The stability is achieved when the repulsion forces balance the attraction forces by electrostatic stabilization and/or steric stabilization.
There are several types of colloidal metal stabilizers which depend on the type of metal, method of preparation, and the application of the resultant metallic nanoparticles. For example, polymers having functional groups such as -NH2, -COOH, and -OH have high affinity for metal atoms; however, the use of stabilizers is not desirable for some applications such as catalysis. For example, activities of supported metal nanoparticle catalysts by coordination capture method are higher than those of polyvinyl-pyrrolidone (PVP)-stabilized metal colloidal catalysts [33, 34]. Due to functional groups namely C = O and N, and long polymer chains, PVP can associate with the metal nanoparticles [35, 36]. The functional groups containing lone pairs of electrons help in the stabilization of metal nanoparticles at their surfaces by covalent interaction, whereas the polymer chain restricts aggregation of metal nanoparticles by steric hindrance. For example, the long chains of PVP stretch out around nickel atom on the surface of the crystal, causing a steric hindrance effect and thus prevent particle growth effectively . Apart from this, PVP is a biocompatible polymer. Hence, nanoparticles synthesized in PVP can be used in biological applications.
where R-OH represents a PVA monomer.
The hydroxyl radicals almost exclusively react with PVA and the reduction of metal ions can take place both by hydrated electrons and the polymeric radicals PVA•.
The interactions between the surface of Ag colloids prepared by γ-irradiation and organic molecules containing ethanol and C12H25NaSO4 were discussed by Wang and his group . It was observed that these molecules can restrain the growth of Ag particles and produce a dendrite pattern. The interaction of metallic surfaces with the solvent makes the surfaces become homogeneous; thus, Ag particles lost the anisotropy which played an important role in the formation of dendritic patterns.
Another kind of stabilizer for metallic nanoparticles is inorganic compounds such as metal oxides. They were originally used as catalyst supports. The catalysts are generally transition noble metals (Pt, Re, Rh, etc.) supported on various oxides. For example, Al2O3 supported Ni nanocluster was synthesized via γ-irradiation by Keghouche and his co-workers . The solution of Ni(HCOO)2 · 7H2O, Al2O3, isopropanol, and ammonium hydroxide was γ-irradiated at a total dose of 100 kGy. Since alumina has an amphoteric character, it can play an important role in the fixation of metal ions.
When a mixed solution of two metal ionic precursors M+ and M'+ is irradiated, three main types of structures can be identified: intermetallic or alloyed structures, core/shell, and heterostructure [45, 46]. The reduction process of ionic solution is controlled by the respective redox potential of metallic ions which is the key factor to determine the structure of resultant particles.
Nanoparticles with alloy structure form when initial reduction reactions follow by mix coalescence and association of atoms and clusters with unreacted ions. These alternate associations and then reduction reactions progressively build bimetallic alloyed clusters .
The mechanism of alloyed structure formation by radiolysis has been studied in detail, for example for Al3+ and Ni2+ ionic solution under gamma irradiation by Abedini and her co-workers . Nickel ions can be reduced easier than aluminium ions, and as a result, when the precursor ion solution is irradiated, reduction occurs by successive steps. The unreacted ions are absorbed on the surface of the newly formed clusters to form a charged cluster. These ions then get reduced in situ by hydrated electrons to form alloyed structure.
The synthesis of metallic nanoparticles by irradiation is governed by a number of experimental parameters such as the choice of solvent and stabilizer, the precursor to stabilizer ratio, pH value during synthesis, and absorbed dose. All of these parameters determine the final ordering, particle size and distribution, and surface area of resultant nanoparticles. A preliminary study should be done in order to determine the best conditions for an efficient dispersion, and to prepare the further homogeneous fixation of the metal nanoparticles on the support.
It has been suggested that the reduction rate under irradiation can be modified by using the appropriate solvent. The reducing agents are the key parameters that can affect the speed of reduction and therefore the particle size and distribution. The hydrated electrons (E0 = -2.9 VNHE), produced by water radiolysis, are stronger reducing agents than 2-propyl radicals. The existence of different reducing agents in the media varies the speed of reduction that makes a broad size distribution.
The optimized pH corresponds to three issues namely, a compromise between the valence state and the charge of ionic precursor in relation with the electrostatic surface charge of the support, preventing reoxidation and minimizing the corrosion of the metallic nanoparticles, and preventing the preparation of unpleasant precipitation. For example, LIU et al.  have founded that Cu2+ ions in aqueous solution could be oxidized easily when the solution pH was lower than 9.
Nucleation and aggregation processes in the formation of bimetallic nanoparticles could be affected by varying the absorbed dose. The rates of growth could be determined by probabilities of the collisions between several atoms, between one atom and a nucleus, and between two or more nuclei . At low radiation doses, the concentration of unreduced metal ions is higher than the nucleus concentration because of low reduction rate. Thus, the unreduced ions can ionize bimetallic nanoparticles to form large bimetallic ions before they undergo reduction and aggregation processes to form even larger bimetallic nanoparticles. However, at higher doses, most of the metal ions are consumed during the nucleation process; therefore, the nucleus concentration is higher than the concentration of unreduced metal ions. As a result, the bimetallic nanoparticles are smaller in size at higher radiation doses .
A similar trend has been reported for PVP-capped Cu@CuAlO2-Al2O3 nanoparticles synthesized by gamma radiation in aqueous solution at various radiation doses . The average size of Cu@CuAlO2-Al2O3 nanoparticles decreased from 12 nm at 80 kGy to 4.5 nm at 120 kGy. Variation in the particle size could be referred to the difference in the rate of nucleation and growth processes.
By increasing the initial ion concentration, final size of metal nanoparticles increase . There are three main reasons for the results. Firstly, the rate of ion association that forms larger particles increases by increasing the concentration of metal ions. Secondly, particle aggregation occurs by collision of small particle in solution. The viscosity of the aqueous solution and subsequently the speed of particles movement can be changed by varying the ratio of polymer to ions. Increasing the concentration increases the number of ions and collision probability. Finally, the surface energy and further agglomeration of nanoparticles can be reduced by the adsorption of polymer molecules on the surface of metal nanoparticles [58, 59]. Therefore, increasing ion concentration reduces the polymer capping performance on the surface of nanoparticles which leads to the formation of larger particles.
In this review, we have surveyed the radiation-induced synthesis and the characterization studies of metallic nanoparticles especially prepared by gamma irradiation. It has been illustrated that the type of solvent, solution pH, precursors' concentration, and the absorbed dose do influence the composition, crystalline structure, particle size, size distribution, and optical properties of the final products. These effects are due to the variation in the nucleation, growth, and aggregation processes in the formation of colloidal metallic nanoparticles. This information could be useful in describing underlying principles in controlling the size of metal nanoparticles by analyzing different combinations of physical factors in monometallic and bimetallic nanoparticle formation.
The financial support from the Universiti Kebangsaan Malaysia (UKM) with project code DIP-2012-14 is acknowledged.
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