Self-assembly of nanoparticles

Transmission electron microscopy image of an iron oxide nanoparticle. Regularly arranged dots within the dashed border are columns of Fe atoms. Left inset is the corresponding electron diffraction pattern. Scale bar: 10 nm.[1]
Iron oxide nanoparticles can be dispersed in an organic solvent (toluene). Upon its evaporation, they may self-assemble (left and right panels) into micron-sized mesocrystals (center) or multilayers (right). Each dot in the left image is a traditional "atomic" crystal shown in the image above. Scale bars: 100 nm (left), 25 μm (center), 50 nm (right).[1]

Nanoparticles are classified as having at least one of its dimensions in the range of 1-100 nanometers (nm).[2] The small size of nanoparticles allows them to have unique characteristics which may not be possible on the macro-scale. Self-assembly is the spontaneous organization of smaller subunits to form larger, well-organized patterns.[3] For nanoparticles, this spontaneous assembly is a consequence of interactions between the particles aimed at achieving a thermodynamic equilibrium and reducing the system’s free energy. The thermodynamics definition of self-assembly was introduced by Professor Nicholas A. Kotov. He describes self-assembly as a process where components of the system acquire non-random spatial distribution with respect to each other and the boundaries of the system.[4] This definition allows one to account for mass and energy fluxes taking place in the self-assembly processes.

This process occurs at all size scales, in the form of either static or dynamic self-assembly. Static self-assembly utilizes interactions amongst the nano-particles to achieve a free-energy minimum. In solutions, it is an outcome of random motion of molecules and the affinity of their binding sites for one another. A dynamic system is forced to not reach equilibrium by supplying the system with a continuous, external source of energy to balance attractive and repulsive forces. Magnetic fields, electric fields, ultrasound fields, light fields, etc. have all been used as external energy sources to program robot swarms at small scales. Static self-assembly is significantly slower compared to dynamic self-assembly as it depends on the random chemical interactions between particles.[5]

Self assembly can be directed in two ways. The first is by manipulating the intrinsic properties which includes changing the directionality of interactions or changing particle shapes. The second is through external manipulation by applying and combining the effects of several kinds of fields to manipulate the building blocks into doing what is intended.[6] To do so correctly, an extremely high level of direction and control is required and developing a simple, efficient method to organize molecules and molecular clusters into precise, predetermined structures is crucial.[7]

  1. ^ a b Wetterskog, Erik; Agthe, Michael; Mayence, Arnaud; Grins, Jekabs; Wang, Dong; Rana, Subhasis; Ahniyaz, Anwar; Salazar-Alvarez, German; Bergström, Lennart (2014). "Precise control over shape and size of iron oxide nanocrystals suitable for assembly into ordered particle arrays". Science and Technology of Advanced Materials. 15 (5): 055010. Bibcode:2014STAdM..15e5010W. doi:10.1088/1468-6996/15/5/055010. PMC 5099683. PMID 27877722.
  2. ^ Dobson, Peter; King, Stephen; Jarvie, Helen (14 May 2019). "Nanoparticle". Britannica. Retrieved 6 May 2020.
  3. ^ Service, R. F. (2005). "How Far Can We Push Chemical Self-Assembly?". Science. 309 (5731): 95. doi:10.1126/science.309.5731.95. ISSN 0036-8075. PMID 15994541.
  4. ^ Kotov, Nicholas A. (14 December 2017). "Self-assembly of inorganic nanoparticles: Ab ovo". Europhysics Letters. 119 (6): 66008. Bibcode:2017EL....11966008K. doi:10.1209/0295-5075/119/66008. S2CID 126225656.
  5. ^ Wang, Ben; Zhang, Yabin; Guo, Zhiguang; Zhang, Li (24 October 2017). "Self-assembly of nanoparticles". materialstoday. Retrieved 6 May 2020.
  6. ^ Grzelczak, Marek; Vermant, Jan; Furst, Eric M.; Liz-Marzán, Luis M. (2010). "Directed Self-Assembly of Nanoparticles". ACS Nano. 4 (7): 3591–3605. doi:10.1021/nn100869j. ISSN 1936-0851. PMID 20568710.
  7. ^ Shinn, Eric; Hübler, Alfred; Lyon, Dave; Perdekamp, Matthias Grosse; Bezryadin, Alexey; Belkin, Andrey (2013). "Nuclear energy conversion with stacks of graphene nanocapacitors". Complexity. 18 (3): 24–27. Bibcode:2013Cmplx..18c..24S. doi:10.1002/cplx.21427. ISSN 1076-2787.

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