A mesocrystal is a material structure composed of numerous small crystals of similar size and shape, which are arranged in a regular periodic pattern. It is a form of oriented aggregation, where the small crystals have parallel crystallographic alignment but are spatially separated. [2]
When the sizes of individual components are at the nanoscale, mesocrystals represent a new class of nanostructured solids made from crystiallographically oriented nanoparticles. The sole criterion for determining whether a material is mesocrystal is the unique crystallographically hierarchical structure, not its formation mechanism. [3]
Helmut Cölfen discovered and named mesocrystals in 2005 during his studies on biominerals. [4] He suggested that their growth was due to a non-classical, self-assembly based process. [3]
Mesocrystal is an abbreviation for mesoscopically structured crystal, where individual subunits often form a perfect 3D order, as in a traditional crystal where the subunits are individual atoms. [3]
This is when a mesocrystal is formed by filling organic matrix compartments with crystalline matter. This crystalline matter would be oriented by the organic matrix. This is the process of biomineralization and this is how mesocrystals are produced in nature. [3]
In most cases mesocrystals form nanoparticles in solution. These nanoparticles aggregate and arrange in crystallographic formation, without any additives. [3] The main causes of this ordering are tensorial polarization forces and dipole fields. [5]
Formation with mineral bridges occur with the formation of nanocrystals. Growth is quenched at this stage by the absorption of a polymer into the nanoparticle surface. Now mineral bridges can nucleate at the defect site, within the growing inhibition layer on the nanocrystal. Through this, a new nanocrystal grows on the mineral bridge, and the growth is again stopped by the polymer. This process is repeated until the crystal builds up. [3]
This argument for formation of mesocrystals requires only a confined space that the reaction takes place in. As the nanoparticle grow into crystals, they have no choice but to align with each other in such a confined space. [3]
Mesocrystals have unique structural features and the physical and physiochemical properties that come from that structure have made them become a subject of interest. Mesocrystals are expected to have a role in many different applications. These include heterogeneous photocatalysts, electrodes, optoelectronics, biomedical materials, and lightweight structural materials. [5]
The properties that make mesocrystals viable for future applications are their shared properties with nanoparticulate, mesoporous, and single-crystal materials. Because mesocrystals are made up of nanoparticles, the properties of the nanoparticles themselves are, in some cases, passed to the whole mesocrystal structure. This allows for the practical application of mesocrystals because they are "potentially more stable analogues of nanoparticulate materials." High porosity is generally a quality of mesocrystals, this is the property shared with mesoporous materials. Closed, internal pores are good for thermal and dielectric insulation and the open pores then aid in absorption and could be utilized for medical delivery. Alternatively, a mesocrystal could have its pores filled and then it would be similar to a single-crystal material and have some unusual electronic and optical properties. The diversity of the properties of mesocrystals could allow them to be effectively utilized in many applications. [5]
The spines of sea urchins are composed of mesocrystals of calcite nano-crystals (92%) in a matrix of non-crystalline calcium carbonate (8%). This structure makes the spines hard but also shock-absorbing, which special property makes them effective defences against predators. [6] Mesocrystals also appear in the shells of some eggs, coral, chitin, and the shells of mussels. [3]
Nanomaterials describe, in principle, materials of which a single unit is sized between 1 and 100 nm.
A mesoporous material is a nanoporous material containing pores with diameters between 2 and 50 nm, according to IUPAC nomenclature. For comparison, IUPAC defines microporous material as a material having pores smaller than 2 nm in diameter and macroporous material as a material having pores larger than 50 nm in diameter.
Hydroxyapatite is a naturally occurring mineral form of calcium apatite with the formula Ca5(PO4)3(OH), often written Ca10(PO4)6(OH)2 to denote that the crystal unit cell comprises two entities. It is the hydroxyl endmember of the complex apatite group. The OH− ion can be replaced by fluoride or chloride, producing fluorapatite or chlorapatite. It crystallizes in the hexagonal crystal system. Pure hydroxyapatite powder is white. Naturally occurring apatites can, however, also have brown, yellow, or green colorations, comparable to the discolorations of dental fluorosis.
Cadmium selenide is an inorganic compound with the formula CdSe. It is a black to red-black solid that is classified as a II-VI semiconductor of the n-type. It is a pigment, but applications are declining because of environmental concerns.
Cetrimonium bromide, also known with the abbreviation CTAB, is a quaternary ammonium surfactant with a condensed structural formula [(C16H33)N(CH3)3]Br.
Hybrid solar cells combine advantages of both organic and inorganic semiconductors. Hybrid photovoltaics have organic materials that consist of conjugated polymers that absorb light as the donor and transport holes. Inorganic materials in hybrid cells are used as the acceptor and electron transporter in the structure. The hybrid photovoltaic devices have a potential for not only low-cost by roll-to-roll processing but also for scalable solar power conversion.
Nanochemistry is an emerging sub-discipline of the chemical and material sciences that deals with the development of new methods for creating nanoscale materials. The term "nanochemistry" was first used by Ozin in 1992 as 'the uses of chemical synthesis to reproducibly afford nanomaterials from the atom "up", contrary to the nanoengineering and nanophysics approach that operates from the bulk "down"'. Nanochemistry focuses on solid-state chemistry that emphasizes synthesis of building blocks that are dependent on size, surface, shape, and defect properties, rather than the actual production of matter. Atomic and molecular properties mainly deal with the degrees of freedom of atoms in the periodic table. However, nanochemistry introduced other degrees of freedom that controls material's behaviors by transformation into solutions. Nanoscale objects exhibit novel material properties, largely as a consequence of their finite small size. Several chemical modifications on nanometer-scaled structures approve size dependent effects.
Nanocomposite is a multiphase solid material where one of the phases has one, two or three dimensions of less than 100 nanometers (nm) or structures having nano-scale repeat distances between the different phases that make up the material.
Nanoporous materials consist of a regular organic or inorganic bulk phase in which a porous structure is present. Nanoporous materials exhibit pore diameters that are most appropriately quantified using units of nanometers. The diameter of pores in nanoporous materials is thus typically 100 nanometers or smaller. Pores may be open or closed, and pore connectivity and void fraction vary considerably, as with other porous materials. Open pores are pores that connect to the surface of the material whereas closed pores are pockets of void space within a bulk material. Open pores are useful for molecular separation techniques, adsorption, and catalysis studies. Closed pores are mainly used in thermal insulators and for structural applications.
In biology, a test is the hard shell of some spherical marine animals and protists, notably sea urchins and microorganisms such as testate foraminiferans, radiolarians, and testate amoebae. The term is also applied to the covering of scale insects. The related Latin term testa is used for the hard seed coat of plant seeds.
Nanogeoscience is the study of nanoscale phenomena related to geological systems. Predominantly, this is investigated by studying environmental nanoparticles between 1–100 nanometers in size. Other applicable fields of study include studying materials with at least one dimension restricted to the nanoscale and the transfer of energy, electrons, protons, and matter across environmental interfaces.
Mesoporous silica is a form of silica that is characterised by its mesoporous structure, that is, having pores that range from 2 nm to 50 nm in diameter. According to IUPAC's terminology, mesoporosity sits between microporous (<2 nm) and macroporous (>50 nm). Mesoporous silica is a relatively recent development in nanotechnology. The most common types of mesoporous nanoparticles are MCM-41 and SBA-15. Research continues on the particles, which have applications in catalysis, drug delivery and imaging. Mesoporous ordered silica films have been also obtained with different pore topologies.
A crystallographic database is a database specifically designed to store information about the structure of molecules and crystals. Crystals are solids having, in all three dimensions of space, a regularly repeating arrangement of atoms, ions, or molecules. They are characterized by symmetry, morphology, and directionally dependent physical properties. A crystal structure describes the arrangement of atoms, ions, or molecules in a crystal.
Carbide-derived carbon (CDC), also known as tunable nanoporous carbon, is the common term for carbon materials derived from carbide precursors, such as binary (e.g. SiC, TiC), or ternary carbides, also known as MAX phases (e.g., Ti2AlC, Ti3SiC2). CDCs have also been derived from polymer-derived ceramics such as Si-O-C or Ti-C, and carbonitrides, such as Si-N-C. CDCs can occur in various structures, ranging from amorphous to crystalline carbon, from sp2- to sp3-bonded, and from highly porous to fully dense. Among others, the following carbon structures have been derived from carbide precursors: micro- and mesoporous carbon, amorphous carbon, carbon nanotubes, onion-like carbon, nanocrystalline diamond, graphene, and graphite. Among carbon materials, microporous CDCs exhibit some of the highest reported specific surface areas (up to more than 3000 m2/g). By varying the type of the precursor and the CDC synthesis conditions, microporous and mesoporous structures with controllable average pore size and pore size distributions can be produced. Depending on the precursor and the synthesis conditions, the average pore size control can be applied at sub-Angstrom accuracy. This ability to precisely tune the size and shapes of pores makes CDCs attractive for selective sorption and storage of liquids and gases (e.g., hydrogen, methane, CO2) and the high electric conductivity and electrochemical stability allows these structures to be effectively implemented in electrical energy storage and capacitive water desalinization.
Nanocellulose is a term referring to nano-structured cellulose. This may be either cellulose nanocrystal, cellulose nanofibers (CNF) also called nanofibrillated cellulose (NFC), or bacterial nanocellulose, which refers to nano-structured cellulose produced by bacteria.
The Stöber process is a chemical process used to prepare silica particles of controllable and uniform size for applications in materials science. It was pioneering when it was reported by Werner Stöber and his team in 1968, and remains today the most widely used wet chemistry synthetic approach to silica nanoparticles. It is an example of a sol-gel process wherein a molecular precursor is first reacted with water in an alcoholic solution, the resulting molecules then joining together to build larger structures. The reaction produces silica particles with diameters ranging from 50 to 2000 nm, depending on conditions. The process has been actively researched since its discovery, including efforts to understand its kinetics and mechanism – a particle aggregation model was found to be a better fit for the experimental data than the initially hypothesized LaMer model. The newly acquired understanding has enabled researchers to exert a high degree of control over particle size and distribution and to fine-tune the physical properties of the resulting material in order to suit intended applications.
Mesoporous organosilica are a type of silica containing organic groups that give rise to mesoporosity. They exhibit pore size ranging from 2 nm - 50 nm, depending on the organic substituents. In contrast, zeolites exhibit pore sizes less than a nanometer. PMOs have potential applications as catalysts, adsorbents, trapping agents, drug delivery agents, stationary phases in chromatography and chemical sensors.
Amorphous calcium carbonate (ACC) is the amorphous and least stable polymorph of calcium carbonate. ACC is extremely unstable under normal conditions and is found naturally in taxa as wide-ranging as sea urchins, corals, mollusks, and foraminifera. It is usually found as a monohydrate, holding the chemical formula CaCO3·H2O; however, it can also exist in a dehydrated state, CaCO3. ACC has been known to science for over 100 years when a non-diffraction pattern of calcium carbonate was discovered by Sturcke Herman, exhibiting its poorly-ordered nature.
MCM-41 is a mesoporous material with a hierarchical structure from a family of silicate and alumosilicate solids that were first developed by researchers at Mobil Oil Corporation and that can be used as catalysts or catalyst supports.
Nanoparticle drug delivery systems are engineered technologies that use nanoparticles for the targeted delivery and controlled release of therapeutic agents. The modern form of a drug delivery system should minimize side-effects and reduce both dosage and dosage frequency. Recently, nanoparticles have aroused attention due to their potential application for effective drug delivery.