A crystal or crystalline solid is a solid material whose constituents (such as , , or ) are arranged in a highly ordered microscopic structure, forming a crystal lattice that extends in all directions. In addition, macroscopic are usually identifiable by their Geometry, consisting of flat faces with specific, characteristic orientations. The scientific study of crystals and crystal formation is known as crystallography. The process of crystal formation via mechanisms of crystal growth is called crystallization or solidification.
The word crystal derives from the Ancient Greek word κρύσταλλος (), meaning both "ice" and "rock crystal", κρύσταλλος, Henry George Liddell, Robert Scott, A Greek-English Lexicon, on Perseus Digital Library from κρύος (), "icy cold, frost". κρύος, Henry George Liddell, Robert Scott, A Greek-English Lexicon, on Perseus Digital Library
Examples of large crystals include , , and table salt. Most inorganic solids are not crystals but , i.e. many microscopic crystals fused together into a single solid. Polycrystals include most metals, rocks, ceramics, and ice. A third category of solids is , where the atoms have no periodic structure whatsoever. Examples of amorphous solids include glass, wax, and many .
Despite the name, lead glass, and related products are not crystals, but rather types of glass, i.e. amorphous solids.
Crystals, or crystalline solids, are often used in pseudoscientific practices such as Crystal healing, and, along with , are sometimes associated with spellwork in beliefs and related religious movements.Regal, Brian. (2009). Pseudoscience: A Critical Encyclopedia. Greenwood. p. 51.
Not all solids are crystals. For example, when liquid water starts freezing, the phase change begins with small ice crystals that grow until they fuse, forming a polycrystalline structure. In the final block of ice, each of the small crystals (called "" or "grains") is a true crystal with a periodic arrangement of atoms, but the whole polycrystal does not have a periodic arrangement of atoms, because the periodic pattern is broken at the grain boundary. Most macroscopic inorganic solids are polycrystalline, including almost all , , ice, rocks, etc. Solids that are neither crystalline nor polycrystalline, such as glass, are called , also called , vitreous, or noncrystalline. These have no periodic order, even microscopically. There are distinct differences between crystalline solids and amorphous solids: most notably, the process of forming a glass does not release the latent heat of fusion, but forming a crystal does.
A crystal structure (an arrangement of atoms in a crystal) is characterized by its unit cell, a small imaginary box containing one or more atoms in a specific spatial arrangement. The unit cells are stacked in three-dimensional space to form the crystal.
The symmetry of a crystal is constrained by the requirement that the unit cells stack perfectly with no gaps. There are 219 possible crystal symmetries (230 is commonly cited, but this treats chiral equivalents as separate entities), called Space group. These are grouped into 7 , such as cubic crystal system (where the crystals may form cubes or rectangular boxes, such as halite shown at right) or hexagonal crystal system (where the crystals may form hexagons, such as Ice Ih).
Euhedral crystals are those that have obvious, well-formed flat faces. Anhedral crystals do not, usually because the crystal is one grain in a polycrystalline solid.
The flat faces (also called ) of a euhedral crystal are oriented in a specific way relative to the underlying atomic arrangement of the crystal: they are planes of relatively low Miller index. The surface science of metal oxides, by Victor E. Henrich, P. A. Cox, page 28, google books link This occurs because some surface orientations are more stable than others (lower surface energy). As a crystal grows, new atoms attach easily to the rougher and less stable parts of the surface, but less easily to the flat, stable surfaces. Therefore, the flat surfaces tend to grow larger and smoother, until the whole crystal surface consists of these plane surfaces. (See diagram on right.)
One of the oldest techniques in the science of crystallography consists of measuring the three-dimensional orientations of the faces of a crystal, and using them to infer the underlying crystal system.
A crystal's crystallographic forms are sets of possible faces of the crystal that are related by one of the symmetries of the crystal. For example, crystals of galena often take the shape of cubes, and the six faces of the cube belong to a crystallographic form that displays one of the symmetries of the isometric crystal system. Galena also sometimes crystallizes as octahedrons, and the eight faces of the octahedron belong to another crystallographic form reflecting a different symmetry of the isometric system. A crystallographic form is described by placing the Miller indices of one of its faces within brackets. For example, the octahedral form is written as {111}, and the other faces in the form are implied by the symmetry of the crystal.
Forms may be closed, meaning that the form can completely enclose a volume of space, or open, meaning that it cannot. The cubic and octahedral forms are examples of closed forms. All the forms of the isometric system are closed, while all the forms of the monoclinic and triclinic crystal systems are open. A crystal's faces may all belong to the same closed form, or they may be a combination of multiple open or closed forms.
A Crystal habit is its visible external shape. This is determined by the crystal structure (which restricts the possible facet orientations), the specific crystal chemistry and bonding (which may favor some facet types over others), and the conditions under which the crystal formed.
Some crystals have formed by magmatic and metamorphic processes, giving origin to large masses of crystalline rock. The vast majority of igneous rocks are formed from molten magma and the degree of crystallization depends primarily on the conditions under which they solidified. Such rocks as granite, which have cooled very slowly and under great pressures, have completely crystallized; but many kinds of lava were poured out at the surface and cooled very rapidly, and in this latter group a small amount of amorphous or matter is common. Other crystalline rocks, the metamorphic rocks such as , and , are recrystallized. This means that they were at first fragmental rocks like limestone, shale and sandstone and have never been in a molten condition nor entirely in solution, but the high temperature and pressure conditions of metamorphism have acted on them by erasing their original structures and inducing recrystallization in the solid state.
Other rock crystals have formed out of precipitation from fluids, commonly water, to form druses or quartz veins. such as halite, gypsum and some limestones have been deposited from aqueous solution, mostly owing to evaporation in arid climates.
In addition, the same atoms may be able to form noncrystalline phases. For example, water can also form amorphous ice, while SiO2 can form both fused silica (an amorphous glass) and quartz (a crystal). Likewise, if a substance can form crystals, it can also form polycrystals.
For pure chemical elements, polymorphism is known as allotropy. For example, diamond and graphite are two crystalline forms of carbon, while amorphous carbon is a noncrystalline form. Polymorphs, despite having the same atoms, may have very different properties. For example, diamond is the hardest substance known, while graphite is so soft that it is used as a lubricant. Chocolate can form six different types of crystals, but only one has the suitable hardness and melting point for candy bars and confections. Polymorphism in steel is responsible for its ability to be heat treating, giving it a wide range of properties.
Polyamorphism is a similar phenomenon where the same atoms can exist in more than one amorphous solid form.
Crystallization is a complex and extensively-studied field, because depending on the conditions, a single fluid can solidify into many different possible forms. It can form a single crystal, perhaps with various possible phases, stoichiometry, impurities, defects, and crystal habit. Or, it can form a polycrystal, with various possibilities for the size, arrangement, orientation, and phase of its grains. The final form of the solid is determined by the conditions under which the fluid is being solidified, such as the chemistry of the fluid, the ambient pressure, the temperature, and the speed with which all these parameters are changing.
Specific industrial techniques to produce large single crystals (called boules) include the Czochralski process and the Bridgman technique. Other less exotic methods of crystallization may be used, depending on the physical properties of the substance, including hydrothermal synthesis, sublimation, or simply solvent-based crystallization.
Large single crystals can be created by geological processes. For example, selenite crystals in excess of 10 meter are found in the Cave of the Crystals in Naica, Mexico. For more details on geological crystal formation, see above.
Crystals can also be formed by biological processes, see above. Conversely, some organisms have special techniques to prevent crystallization from occurring, such as antifreeze proteins.
A few examples of crystallographic defects include (an empty space where an atom should fit), interstitial defects (an extra atom squeezed in where it does not fit), and (see figure at right). Dislocations are especially important in materials science, because they help determine the mechanical strength of materials.
Another common type of crystallographic defect is an impurity, meaning that the "wrong" type of atom is present in a crystal. For example, a perfect crystal of diamond would only contain carbon atoms, but a real crystal might perhaps contain a few boron atoms as well. These boron impurities change the diamond color to slightly blue. Likewise, the only difference between ruby and sapphire is the type of impurities present in a corundum crystal.
In , a special type of impurity, called a dopant, drastically changes the crystal's electrical properties. Semiconductor devices, such as , are made possible largely by putting different semiconductor dopants into different places, in specific patterns.
Crystal twinning is a phenomenon somewhere between a crystallographic defect and a grain boundary. Like a grain boundary, a twin boundary has different crystal orientations on its two sides. But unlike a grain boundary, the orientations are not random, but related in a specific, mirror-image way.
Mosaicity is a spread of crystal plane orientations. A mosaicity consists of smaller crystalline units that are somewhat misaligned with respect to each other.
crystallize rapidly and are almost always polycrystalline, though there are exceptions like amorphous metal and single-crystal metals. The latter are grown synthetically, for example, fighter-jet turbines are typically made by first growing a single crystal of titanium alloy, increasing its strength and melting point over polycrystalline titanium. A small piece of metal may naturally form into a single crystal, such as Type 2 telluric iron, but larger pieces generally do not unless extremely slow cooling occurs. For example, iron are often composed of single crystal, or many large crystals that may be several meters in size, due to very slow cooling in the vacuum of space. The slow cooling may allow the precipitation of a separate phase within the crystal lattice, which form at specific angles determined by the lattice, called Widmanstatten patterns. Encyclopedia of the Solar System by Tilman Spohn, Doris Breuer, Torrence V. Johnson -- Elsevier 2014 Page 632
typically form when a metal reacts with a non-metal, such as sodium with chlorine. These often form substances called salts, such as sodium chloride (table salt) or potassium nitrate (saltpeter), with crystals that are often brittle and cleave relatively easily. Ionic materials are usually crystalline or polycrystalline. In practice, large salt crystals can be created by solidification of a molten fluid, or by crystallization out of a solution. Some ionic compounds can be very hard, such as oxides like aluminium oxide found in many gemstones such as ruby and synthetic sapphire.
Covalent bond solids (sometimes called covalent network solids) are typically formed from one or more non-metals, such as carbon or silicon and oxygen, and are often very hard, rigid, and brittle. These are also very common, notable examples being diamond and
Angelo State University: Formulas and Nomenclature of Ionic and Covalent Compounds
Weak van der Waals forces also help hold together certain crystals, such as crystalline , as well as the interlayer bonding in graphite. Substances such as , and wax form molecular bonds because the large molecules do not pack as tightly as atomic bonds. This leads to crystals that are much softer and more easily pulled apart or broken. Common examples include chocolates, candles, or viruses. Water ice and dry ice are examples of other materials with molecular bonding. Science for Conservators, Volume 3: Adhesives and Coatings by Museum and Galleries Commission -- Museum and Galleries Commission 2005 Page 57Polymer materials generally will form crystalline regions, but the lengths of the molecules usually prevent complete crystallization—and sometimes polymers are completely amorphous.
Quasicrystals are most famous for their ability to show five-fold symmetry, which is impossible for an ordinary periodic crystal (see crystallographic restriction theorem).
The International Union of Crystallography has redefined the term "crystal" to include both ordinary periodic crystals and quasicrystals ("any solid having an essentially discrete diffraction diagram").
Quasicrystals, first discovered in 1982, are quite rare in practice. Only about 100 solids are known to form quasicrystals, compared to about 400,000 periodic crystals known in 2004. The 2011 Nobel Prize in Chemistry was awarded to Dan Shechtman for the discovery of quasicrystals.
Not all crystals have all of these properties. Conversely, these properties are not quite exclusive to crystals. They can appear in or that have been made anisotropic by Work hardening or stress—for example, photoelasticity.
|
|