Self-assembly of nanoparticles

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Template:Primary sources Self-assembly is a phenomenon where the components of a system assemble themselves spontaneously via an interaction to form a larger functional unit. This spontaneous organization can be due to direct specific interaction and/or indirectly through their environment. Due to the increasing technological advancements, the study of materials in the nanometer scale is becoming more important. The ability to assemble nanoparticles into well-defined configuration in space is crucial to the development of electronic devices that are small but can contain plenty of information. The spatial arrangements of these self-assembled nanoparticles can be potentially be used to build increasingly complex structures leading to a wide variety of materials that can be used for different purposes.

At the molecular level, intermolecular force hold the spontaneous gathering of molecules into a well-defined and stable structure together. In chemical solutions, self-assembly is an outcome of random motion of molecules and the affinity of their binding sites for one another. In the area of nanotechnology, developing a simple, efficient method to organize molecules and molecular clusters into precise, pre-determined structure is crucial.

An example of self-assembly of nanoparticles in a solution. In this diagram, it can be seen that a disordered system formed an organized structure which can be due to specific interactions among the particles.


The study of self-assembly of nanoparticles is a new area in nanotechnology research. Scientists who are focusing their study on nanotechnology recognized that some properties of atoms and molecules enable them to arrange themselves into patterns. There are a variety of applications where the self-assembly of nanoparticles can be useful. For example, building sensors to detect chemical and biological molecules. In addition, it can also be used on creating computer chips with smaller component sizes, which can then allow more computing power to be stored on a chip. Recently, researchers were able to watch nanoparticles to self-assembly for the very first time in real-time. This research was done by scientists at the U.S. Department of Energy’s (DOE) Argonne National Laboratory. They had to use a transmission electron microscope (TEM) located at the Center for Nanoscale Materials to capture the quick movement of the nanoparticles into a self-assembled system.


Self-assembly is an equilibrium process where the assembled components are in equilibrium with the individual components. Self-assembly is driven by the minimization of Gibbs free energy. The minimization of Gibbs free energy is attained by the minimization of repulsive and the maximization of attractive molecular interactions.[1] In addition, the lower free energy is usually a result of a weaker intermolecular force between self-assembled moieties and is essentially enthalpic in nature.

The thermodynamics of the self-assembly process can be represented by a simple Gibbs free energy equation:

where if is negative, self-assembly is a spontaneous process. is the enthalpy change of the process and is largely determined by the potential energy/intermolecular forces between the assembling entities. is the change in entropy associated with the formation of the ordered arrangement. In general, the organization is accompanied by a decrease in entropy and in order for the assembly to be spontaneous the enthalpy term must be negative and in excess of the entropy term.[1] This equation shows that as the value of approaches the value of and above a critical temperature, the self-assembly process will become progressively less likely to occur and spontaneous self-assembly will not happen.

The self-assembly is governed by the normal processes of nucleation and growth. Small assemblies are formed because of their increased lifetime as the attractive interactions between the components lower the Gibbs free energy. As the assembly grows, the Gibbs free energy continues to decrease until the assembly becomes stable enough to last for a long period of time. The necessity of the self-assembly to be an equilibrium process is defined by the organization of the structure which requires non-ideal arrangements to be formed before the lowest energy configuration is found.


In a self-assembled structure a reasonable concentration of defects is present. Defects can be defined thermodynamically. In most cases, the thermodynamic driving force for self-assembly is provided by weak intermolecular interactions and is usually of the same order of magnitude as the entropy term.[1] In order for a self-assembling system to reach the minimum free energy configuration, there has to be enough thermal energy to allow the mass transport of the self-assembling molecules. For defect formation, the free energy of single defect formation is given by:

The enthalpy term, does not necessarily reflect the intermolecular forces between the molecules, it is the energy cost associated with disrupting the pattern and may be thought of as a region where optimum arrangement does not occur and the reduction of enthalpy associated with ideal self-assembly did not occur. An example of this can be seen in a system of hexagonally packed cylinders where defect regions of lamellar structure exist.

If is negative, there will be a finite number of defects in the system and the concentration will be given by:

N is the number of defects in a matrix of N0 self-assembled particles or features and is the activation energy of defect formation. The activation energy, , should not be confused with . The activation energy represents the energy difference between the initial ideally arranges state and a transition state towards the defective structure. At low defect concentrations, defect formation is entropy driven until a critical concentration of defects allows the activation energy term to compensate for entropy. There is usually an equilibrium defect density indicated at the minimum free energy. The activation energy for defect formation increases this equilibrium defect density.[1]

Particle Interaction

Intermolecular forces govern the particle interaction in self-assembled systems. The forces tend to be intermolecular in type rather than ionic or covalent because ionic or covalent bonds will “lock” the assembly into non-equilibrium structures. The types intermolecular forces seen in self-assembly processes are van der Waals, hydrogen bonds, and weak polar forces, just to name a few. In self-assembly, regular structural arrangements are frequently observed, therefore there must be a balance of attractive and repulsive between molecules otherwise an equilibrium distance will not exist between the particles. The repulsive forces can be electron cloud-electron cloud overlap or electrostatic repulsion.[1]


The processes by which nanoparticles self assemble are widespread and important. Understanding why and how self assembly occurs is key in reproducing and optimizing results. Typically, nanoparticles will self assemble for one or both of two reasons: molecular interactions and external direction.[2] Recently, researchers are more interested in the latter of these two reasons, and are able to apply external directing to a large variety of systems.

Self Assembly by Molecular Interactions

Nanoparticles have the ability to assemble chemically through covalent or noncovalent interactions with their capping ligand.[3] The terminal functional group(s) on the particle are known as capping ligands. As these ligands tend to be complex and sophisticated, self-assembly can provide a simpler pathway for nanoparticle organization by synthesizing efficient functional groups.

Intermolecular Forces

Nanoparticles can self-assemble as a result of their intermolecular forces. As systems look to minimize their free energy, self assembly is one option for the system to achieve its lowest free energy thermodynamically.[2] Nanoparticles can be programmed to self assemble by changing the functionality of their side groups, taking advantage of weak and specific intermolecular forces to spontaneously order the particles. These direct interparticle interactions can be typical intermolecular forces such as hydrogen bonding or Van der Waals forces, but can also be internal charactaristics, such as hydrophobicity or hydrophilicity. For example, lipophilic nanoparticles have the tendency to self-assemble and form crystals as solvents are evaporated.[2] While these aggregations are based on intermolecular forces, external factors such as temperature and pH also play a role in spontaneous self-assembly.

Hamaker Interaction

As nanoparticle interactions take place on a nanoscale, the particle interactions must be scaled similarly. Hamaker interactions take into account the polarization characteristics of a large number of nearby particles and the effects they have on each other. Hamaker interactions sum all of the forces between all particles and the solvent(s) involved in the system. While Hamaker theory generally describes a macroscopic system, the vast number of nanoparticles in a self assembling system allows the term to be applicable. Hamaker constants for nanoparticles are calculated using Lifshitz theory, and can often be found in literature.

Hamaker Constants for Nanoparticles in Water
Material A131
Fe3O4[4] 22
-Fe2O3[4] 26
α-Fe2O3[4] 29
Ag[5] 33
Au[6] 45
All values reported in zJ [4] [5] [6]

Externally Directed Self Assembly

The natural ability of nanoparticles to self assemble can be replicated in systems that do not intrinsically self assemble. Directed self assembly (DSA) attempts to mimic the chemical properties of self-assembling systems, while simultaneously controlling the thermodynamic system to maximize self assembly.

Electric and Magnetic Fields

External fields are the most common directors of self-assembly. Electric and magnetic fields allow induced interactions to align the particles. The fields take advantage of the polarizability of the nanoparticle and its functional groups.[2] When these field-induced interactions overcome random Brownian motion, particles join to form chains and then assemble. At more modest field strengths, ordered crystal structures are established due to the induced dipole interactions. Electric and magnetic field direction requires a constant balance between thermal energy and interaction energies.

Flow Fields

Macroscopic Viscous Flow

Macroscopic viscous flow fields can direct self assembly of a random solution of particles into ordered crystals. However, the assembled particles tend to disassemble when the flow is stopped or removed.[2] Shear flows are useful for jammed suspensions or random close packing. As these systems begin in nonequilibrium, flow fields are useful in that they help the system relax towards ordered equilibrium. Flow fields are also useful when dealing with complex matrices that themselves have rheological behavior. Flow can induce anisotropic viseoelastic stresses, which helps to overcome the matrix and cause self assembly.

Large Amplitude Oscillatory Shear (LAOS)

Large amplitude oscillatory shear (LAOS) is most effective for particles that are 100 nm-1 µm in size.[2] Hard and soft shears can order in steady shear. However, this assembly strongly relies on particle volume fraction, particle interaction potentials, polydisterity, and shear rate and strain. The large amount of directing factors can cause complications in directing self assembly by LAOS. Diblock copolymer micells have recently been studied in regard to structuring nanoparticles in bulk.

Combination of Fields

The most effective self assembly director is a combination of fields.[2] If the fields and conditions are optimized, self assembly can be permanent and complete. When a field combination is used with nanoparticles that are tailored to be intrinsically responsive, the most complete assembly is observed. Combinations of fields allow the benefits of self assembly, such as scalability and simplicity, to be maintained while being able to control orientation and structure formation. Field combinations possess the greatest potential for future directed self assembly work.


Solid Interfaces

Nano-particles can self assemble on solid surfaces after applying external forces (like magnetic, electric, and flow) as mentioned in the above section. Templates made of microstructures like carbon nanotubes or block polymers can also be used to assist in self assembly; they cause directed self assembly (DSA) in which active sites are embedded to selectively induce nanoparticle deposition. Such templates are considered as any object onto which different particles can be arranged into a structure with a morphology similar to that of the template.[7] Carbon nanotubes (microstructures), single molecules, or block copolymers are common templates.[7] Nanoparticles are often shown to self assemble within distances of nanometers and micrometers, but block copolymer templates can be used to form well-defined self-assemblies over macroscopic distances. By incorporating active sites to the surfaces of nanotubes and polymers, the functionalization of these templates can be transformed to favor self assembly of specified nanoparticles.

Liquid Interfaces

Pickering and Ramsden explained the idea of pickering emulsions when experimenting with paraffin-water emulsions with solid particles like iron oxide and silicon dioxide. They observed that the micron-sized colloids generated a resistant film at the interface between the two immiscible phases, inhibiting the coalescence of the emulsion drops.[8] These Pickering emulsions, as shown in the figure below, are formed from the self-assembly of colloidal particles in two-part liquid systems, such as oil-water systems. The desorption energy, which is directly related to the stability of emulsions depends on the particle size, particle-particle interaction and, of course, particle-water and particle-oil interactions.[8]

Self-assembly of solid nanoparticles at oil-water interface.

A decrease in total free energy was observed to be a result from the assembly of nanoparticles at an oil/water (O/W) interface. This is shown in the following equation in which a particle with radius r at an interface between oil (O) and water (W) results in a decrease of the initial interfacial energy E0 to E1; this difference in energy is ΔE1.

At a fixed γP/O, γP/W, and γO/W, the equation shows that the stability of a particle assembly is determined by the radius square. When moving to the interface, particles reduce the unfavorable contact between the immiscible fluids and decrease the interfacial energy. The decrease in total free energy for microscopic particles is much larger than that of thermal energy; this results in an effective confinement of large colloids to the interface. They are irreversibly bound to the interface. Nanoscopic particles are restricted to the interface by an energy reduction comparable to thermal energy. Thus, nanoparticles are easily displaced from the interface. A constant particle exchange then occurs at the interface; the rate of this exchange depends on particle size. The thermally activated escape of small particles occurs more often than larger particles.[8] For the equilibrium state of assembly, the total gain in free energy is smaller for smaller particles. Thus, large nanoparticles assemblies are more stable. This size dependence allows nanoparticles to self-assemble at the interface to attain its equilibrium structure. Micrometer- size colloids, on the other hand, may be confined in a non-equilibrium state. The interfacial tension and the wettability of a particle surface affect the desorption energy. The contact angle θ between the solid and the oil/water interface determines its wettability. As shown in the figure below, a contact angle θ greater than 90° favors a water-in-oil emersion while a contact angle θ less than 90° favors oil-in-water emulsion. These contact angles affect the stability of the emulsion.

Effects of contact angle on wettability.

A maximum desorption energy peak is observed at a contact angle of 90°. When the contact angle is greater than or less than this point, the desorption energy gradually decreases; thus, the stability of the emulsion decreases as well.


Material that consists with nano particles is called "nanostructured materials". The phase of "nanostructured material" implies two important ideas: i) that at lease some of the heterogeneity in materials is determined by the size range of nanostructures (~1-100 nm), and ii) these nanostructures might be synthesized and distributed (or organized), at least in part.[9] The study of self-assembly nanoparticles is important to understand the interaction between single particle in terms of applying them into different applications.


Model of multidimensional array of nano-particles. Particle could have two spins, spin up or down. Based on the spin directions, nano-particles will be able to store 0 and 1. Therefore, nanostructural material has a great potential to be new material that can be used widely electronic devices.

Self-assembly of nanoscale structures from functional nanoparticles has provided a powerful path to developing small and powerful electronic components. In the recent decade, it has been confirmed that organic compounds can be conductors or semiconductors. In addition to insulator, one of the opportunities in nanomaterials science is to use organic synthesis and molecular design to make electronically usefully structures starting with organic molecules. The difficulty of applied nanostructure material is nanoscale objects have always been difficult to work with because they cannot be characterized by molecular techniques and they are too small to see optically. 2D self assembly monodisperse particle colloids has a strong potential in dense magnetic storage media. Each colloid particle has the ability to store information as known as binary number 0 and 1 after applying it to a strong magnetic field. In the meantime, it requires a nanoscale sensor or detector in order to selectively choose the colloid particle.

Biological Applications

Drug Delivery

Block copolymers offer the ability to self-assemble into uniform, nanosized micelles[10][11] and accumulate in tumors via the enhanced permeability and retention effect.[12] Polymer composition can be chosen to control the micelle size and compatibility with the drug of choice. The challenges of this application are the difficulty of reproducing or controlling the size of self-assembly nano micelle, preparing predictable size-distribution, and the stability of the micelle with high drug load content.

See also


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