Difference between revisions of "Amorphous solid" - New World Encyclopedia

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[[Image:Candle with burnt wick.jpg|thumb|right|300px|Wax and paraffin are amorphous.]]
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[[File:Bulk Metallic Glass Sample.jpg|thumb|right|250px|Amorphous metals have low toughness, but high strength.]]
  
An '''amorphous solid''' is a [[solid]] in which there is no [[long-range order]]* in the positions of its [[atom]]s. On the other hand, if there is long-range atomic order, the solid is described as [[crystal|crystalline]] or [[Morphous solid|morphous]]. Most classes of solid materials can be found or prepared in an amorphous form. For instance, common window glass, many [[polymer]]s (such as [[polystyrene]]*), and even foods such as [[cotton candy]]* are amorphous solids.
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An '''amorphous solid''' is a [[solid]] in which there is no [[long-range order]] or repeating pattern in the positions of its [[atom]]s or [[molecule]]s. On the other hand, if there is long-range atomic order, the solid is described as [[crystal|crystalline]] or [[Morphous solid|morphous]].
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Most classes of solid materials can be found or prepared in an amorphous form. Examples of amorphous solids include window [[glass]], many [[polymer]]s (such as [[polystyrene]]), and the [[silicon]] in many [[Thin-film deposition|thin-film]] [[solar cell]]s. Even foods such as [[cotton candy]] are amorphous solids.
  
Amorphous materials are often prepared by rapidly cooling molten material. The cooling reduces the mobility of the material's molecules before they can pack into a more [[thermodynamics|thermodynamically]] favorable crystalline state.  Amorphous materials can also be produced by additives which interfere with the ability of the primary constituent to crystallize. For example addition of [[Sodium carbonate|soda]] to [[silicon dioxide]] results in window glass and the addition of [[diol|glycols]] to [[water]] results in a [[vitrification|vitrified]] solid.  
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== General approaches for preparing amorphous materials ==
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An amorphous material is often prepared by cooling its molten state rapidly. The cooling reduces the mobility of the material's atoms and molecules before they can pack into a [[thermodynamics|thermodynamically]] more favorable crystalline state.
  
Some materials, such as metals, are difficult to prepare in an amorphous state. Unless a material has a high melting temperature (as ceramics do) or a low crystallization energy (as polymers tend to), cooling must be done extremely rapidly.
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Amorphous materials can also be produced by additives that interfere with the ability of the primary constituent to crystallize. For example, the addition of [[sodium carbonate]] (soda) to [[silicon dioxide]] results in window glass, and the addition of [[diol|glycols]] to [[water]] results in a [[vitrification|vitrified]] solid.
  
Amorphous solids can exist in two distinct states, the 'rubbery' state and the 'glassy' state. The temperature at which the transition between the glassy and rubbery states is called their [[glass transition temperature]] or ''T''<sub>g</sub>.
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Some materials, such as metals, are difficult to prepare in an amorphous state. Unless a material has a high melting temperature (as ceramics do) or a low crystallization energy (as polymers tend to), cooling must be done extremely rapidly.
  
==Glasses==
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===Preparation of glasses===
In common parlance, the term [[glass]] refers to amorphous oxides, and especially silicates (compounds based on silicon and oxygen). Ordinary soda-lime [[glass]], used in windows and drinking containers, is created by the addition of [[Sodium carbonate|soda]] and lime ([[calcium oxide]]) to [[silicon dioxide]]. Without these additives silicon dioxide will (with slow cooling) form [[quartz]] crystals, not [[glass]].  
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:''Main article: [[Glass]]''
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A ''[[glass]]'' may be defined as an amorphous solid that is usually produced by mixing silica (silicon dioxide) with other chemicals at high heat, and allowing the mixture to cool without forming a crystalline structure. Ordinary, soda-lime glass, used for windows and drinking containers, is created by adding [[sodium carbonate|soda]] and lime ([[calcium oxide]]) to [[silicon dioxide]]. Without these additives, silicon dioxide will (with slow cooling) form [[quartz]] crystals, not glass.
  
To avoid confusion, other types of glass often are referred to with a modifier, such as the term ''metallic glass'' to refer to [[amorphous metal]]lic alloys.
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===Preparation of "metallic glass"===
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Some amorphous [[metal]]lic [[alloy]]s can be prepared under special processing conditions, such as [[rapid solidification]], [[thin-film deposition]], or [[ion implantation]]. The term "metallic glass" refers only to amorphous metallic alloys that have been rapidly solidified. Materials produced by ion implantation or thin-film deposition are technically not called metallic glasses.
  
===Metallic glass===
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Even with special equipment, such rapid cooling is required that, for most metals, only a thin wire or ribbon can be made amorphous. This is adequate for many [[magnetism|magnetic]] applications, but thicker sections are required for most structural applications such as [[scalpel]] blades, [[golf club]]s, and cases for [[consumer electronics]].
Some amorphous metallic alloys can be prepared under special processing conditions (such as [[rapid solidification]], [[thin-film deposition]], or [[ion implantation]]), but the term "metallic glass" refers only to rapidly solidified materials.  
 
  
Even with special equipment, such rapid cooling is required that, for most metals, only a thin wire or ribbon can be made amorphous. This is enough for many [[magnetic]] applications, but thicker sections are required for most structural applications such as [[scalpel]] blades, [[golf club]]s, and cases for [[consumer electronics]].  Recent efforts have made it possible to increase the maximum thickness of glassy [[casting]]s, by finding alloys where [[kinetic]] barriers to crystallization are greater. Such alloy systems tend to have the following inter-related properties:
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Recent efforts have made it feasible to increase the maximum thickness of glassy [[casting]]s, by finding alloys that have greater [[kinetic]] barriers to crystallization. Such alloy systems tend to have the following interrelated properties:
*Many different solid [[phase (matter)|phase]]s are present in the equilibrium solid, so that any potential crystal will find that most of the nearby atoms are of the wrong type to join in crystallization
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*Many different solid [[phase (matter)|phase]]s are present in the equilibrium solid, so that any potential crystal will find that most of the nearby atoms are of the wrong type to join in crystallization.
*The composition is near a deep [[eutectic]], so that low melting temperatures can be achieved without sacrificing the slow diffusion and high liquid viscosity seen in alloys with high-melting pure components
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*The composition is near a deep [[eutectic]], so that low melting temperatures can be achieved without sacrificing the slow diffusion and high liquid viscosity found in alloys with high-melting pure components.
*Atoms with a wide variety of sizes are present, so that "wrong-sized" atoms interfere with the crystallization process by binding to atom clusters as they form.
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*[[Atom]]s with a wide variety of sizes are present, so that "wrong-sized" atoms interfere with the crystallization process by binding to atom clusters as they form.
One such alloy is the commercial "[[Liquidmetal]]", which can be cast in amorphous sections up to an inch thick.
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One such alloy is the commercial "[[Liquidmetal]]," which can be cast in amorphous sections up to an inch thick.
  
==Other synthesis routes==
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==Preparation by ion implantation==
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One way to produce a material without an ordered structure is to take a crystalline material and remove its internal order by damaging it. A practical, controllable way to do this is by firing [[ion (physics)|ions]] into the material at high speed, so that collisions inside the material knock all atoms from their original positions. This technique is known as ''[[ion implantation]]''. It produces amorphous solids only if the material is too cold for atoms to diffuse back to their original positions as the process continues.
  
Amorphous solids produced by other routes, such as [[ion implantation]] and [[thin-film deposition]] are, technically speaking, not glasses.
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==Preparation by thin-film deposition (cold deposition)==
 
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Techniques such as [[sputtering]] and [[chemical vapor deposition]] can be used to deposit a thin film of material onto a surface. If the surface is kept cold enough, the atoms being deposited will not, on average, have enough energy to diffuse along the surface and form ordered crystals. For every deposition technique, there is a substrate temperature below which the deposited film will be amorphous. Surface [[diffusion]] requires much less energy than diffusion through the bulk, so that these temperatures are often lower than those required to make amorphous films by ion implantation.
===Damage===
 
One way to produce a material without an ordered structure is to take a crystalline material and remove the order by damaging it.  A practical, controllable way to do this is by firing [[ions]] into the material at high speed, so that collisions inside the material knock all atoms from their original positions.  This technique is known as [[ion implantation]], and only forms amorphous solids if the material is too cold for atoms to diffuse back to their original positions as the process continues.
 
 
 
===Cold deposition===
 
Techniques such as [[sputtering]] and [[chemical vapour deposition]] can be used to deposit a thin film of material onto a surface. If the surface is kept cold, the atoms being deposited will not, on average, gain enough energy to diffuse along the surface until they find a place in an ordered crystal. For every deposition technique, there is a substrate temperature below which the deposited film will be amorphous. However, surface [[diffusion]] requires much less energy than diffusion through the bulk, so that these temperatures are often lower than those required to make amorphous films by ion implantation.
 
  
 
==Toward a strict definition==
 
==Toward a strict definition==
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It is difficult to make a distinction between truly amorphous solids and crystalline solids in which the crystal size is extremely small (less than two [[nanometer]]s). Even amorphous materials have some short-range order among the atomic positions (over distances of less than five nanometers). Furthermore, in very small [[crystal]]s, a large fraction of the [[atom]]s are located at or near the crystal's surface; relaxation of the surface and interfacial effects distort the atomic positions, decreasing the structural order. Even the most advanced structural characterization techniques, such as [[X-ray]] diffraction and transmission electron microscopy, have difficulty in distinguishing between amorphous and crystalline structures on these length scales.
  
It is difficult to make a distinction between truly amorphous solids and crystalline solids in which the size of the crystals is very small (less than two [[nanometre]]s). Even amorphous materials have some short-range order among the atomic positions (over length scales of less than five [[nanometre]]s). Furthermore, in very small [[crystal]]s a large fraction of the [[atom]]s are located at or near the surface of the crystal; relaxation of the surface and interfacial effects distort the atomic positions, decreasing the structural order. Even the most advanced structural characterization techniques, such as x-ray diffraction and transmission electron microscopy, have difficulty in distinguishing between amorphous and crystalline structures on these length scales.
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The transition from the liquid state to the glassy state, at a temperature below the equilibrium melting point of the material, is called the "[[glass transition]]." From a practical point of view, the glass transition temperature (T<sub>g</sub>) is defined empirically as the temperature at which the [[viscosity]] of the liquid exceeds a certain value (commonly 10<sup>13</sup> [[pascal second|pascal-seconds]]). The transition temperature depends on cooling rate, with the glass transition occurring at higher temperatures for faster cooling rates. The precise nature of the glass transition is the subject of ongoing research.
 
 
The transition from the liquid state to the glass, at a temperature below the equilibrium melting point of the material, is called the [[glass transition]]. From a practical point of view, the glass transition temperature is defined empirically as the temperature at which the [[viscosity]] of the liquid exceeds a certain value (commonly 10<sup>13</sup> [[pascal second|pascal-seconds]]). The transition temperature depends on cooling rate, with the glass transition occurring at higher temperatures for faster cooling rates. The precise nature of the glass transition is the subject of ongoing research. While it is clear that the glass transition is not a first-order thermodynamic transition (such as melting), there is debate as to whether it is a higher-order transition, or merely a kinetic effect.
 
 
 
Glass is sometimes referred to as a [[Supercooling|supercooled]] liquid; this amounts to an assertion that the glass transition is purely a kinetic, rather than a thermodynamic effect. One argument against speaking this way is the fact that supercooled liquids flow whereas glass does not. In standard usage, the term [[Supercooling|supercooled]] means that the fluid is still a liquid but is at a temperature below its freezing point. For example, [[freezing rain]] falls in liquid form and freezes on contact because it is already below the freezing point. See [[pitch drop experiment]] and a related section in [[glass]].
 
 
 
Some examples of amorphous solids are [[glass]], [[polystyrene]], and the [[silicon]] in many [[Thin-film deposition|thin film]] [[solar cell]]s.
 
  
 
== Unsolved problems ==
 
== Unsolved problems ==
 
 
* What is the nature of the [[phase transition]] between a fluid or regular solid and a glassy [[phase (matter)|phase]]?
 
* What is the nature of the [[phase transition]] between a fluid or regular solid and a glassy [[phase (matter)|phase]]?
 
* What are the physical processes giving rise to the general properties of glasses?
 
* What are the physical processes giving rise to the general properties of glasses?
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* [[Polymer]]
 
* [[Polymer]]
  
== External links ==
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== References ==
*[http://www.ptbf.am.wroc.pl/v271/v271_17.pdf Vogel-Tammann-Fulcher Equation Parameters]
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* Chang, Raymond. ''Chemistry'', ninth ed. New York: McGraw-Hill Science/Engineering/Math, 2006. ISBN 0073221031
*[http://eprints.iisc.ernet.in/archive/00000257/01/kjrao.pdf Fragility thy name is glass]
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* Christie, John. [http://www.madsci.org/posts/archives/dec97/873687580.Ch.r.html What is the difference between an amorphous solid and a non-Newtonian fluid?"] School of Physical Chemistry, La Trobe University, Bundoora, Victoria, Australia, 1997. Retrieved November 21, 2007.
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* Neumann, Florin. 1996. [http://dwb.unl.edu/Teacher/NSF/C01/C01Links/www.ualberta.ca/~bderksen/florin.html "Glass: Liquid or Solid—Science vs. an Urban Legend"] Retrieved November 21, 2007.
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* Zallen, Richard. ''The Physics of Amorphous Solids''. New York: Wiley Classics Library, Wiley Interscience, New Ed edition, 1998. ISBN 0471299413
  
 
{{Phase_of_matter}}
 
{{Phase_of_matter}}
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[[Category:Physics]]
 
[[Category:Physics]]
 
[[Category:Chemistry]]
 
[[Category:Chemistry]]
[[Category:Phases of matter]]
 
  
 
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Latest revision as of 16:22, 17 November 2016

Amorphous metals have low toughness, but high strength.

An amorphous solid is a solid in which there is no long-range order or repeating pattern in the positions of its atoms or molecules. On the other hand, if there is long-range atomic order, the solid is described as crystalline or morphous.

Most classes of solid materials can be found or prepared in an amorphous form. Examples of amorphous solids include window glass, many polymers (such as polystyrene), and the silicon in many thin-film solar cells. Even foods such as cotton candy are amorphous solids.

General approaches for preparing amorphous materials

An amorphous material is often prepared by cooling its molten state rapidly. The cooling reduces the mobility of the material's atoms and molecules before they can pack into a thermodynamically more favorable crystalline state.

Amorphous materials can also be produced by additives that interfere with the ability of the primary constituent to crystallize. For example, the addition of sodium carbonate (soda) to silicon dioxide results in window glass, and the addition of glycols to water results in a vitrified solid.

Some materials, such as metals, are difficult to prepare in an amorphous state. Unless a material has a high melting temperature (as ceramics do) or a low crystallization energy (as polymers tend to), cooling must be done extremely rapidly.

Preparation of glasses

Main article: Glass

A glass may be defined as an amorphous solid that is usually produced by mixing silica (silicon dioxide) with other chemicals at high heat, and allowing the mixture to cool without forming a crystalline structure. Ordinary, soda-lime glass, used for windows and drinking containers, is created by adding soda and lime (calcium oxide) to silicon dioxide. Without these additives, silicon dioxide will (with slow cooling) form quartz crystals, not glass.

Preparation of "metallic glass"

Some amorphous metallic alloys can be prepared under special processing conditions, such as rapid solidification, thin-film deposition, or ion implantation. The term "metallic glass" refers only to amorphous metallic alloys that have been rapidly solidified. Materials produced by ion implantation or thin-film deposition are technically not called metallic glasses.

Even with special equipment, such rapid cooling is required that, for most metals, only a thin wire or ribbon can be made amorphous. This is adequate for many magnetic applications, but thicker sections are required for most structural applications such as scalpel blades, golf clubs, and cases for consumer electronics.

Recent efforts have made it feasible to increase the maximum thickness of glassy castings, by finding alloys that have greater kinetic barriers to crystallization. Such alloy systems tend to have the following interrelated properties:

  • Many different solid phases are present in the equilibrium solid, so that any potential crystal will find that most of the nearby atoms are of the wrong type to join in crystallization.
  • The composition is near a deep eutectic, so that low melting temperatures can be achieved without sacrificing the slow diffusion and high liquid viscosity found in alloys with high-melting pure components.
  • Atoms with a wide variety of sizes are present, so that "wrong-sized" atoms interfere with the crystallization process by binding to atom clusters as they form.

One such alloy is the commercial "Liquidmetal," which can be cast in amorphous sections up to an inch thick.

Preparation by ion implantation

One way to produce a material without an ordered structure is to take a crystalline material and remove its internal order by damaging it. A practical, controllable way to do this is by firing ions into the material at high speed, so that collisions inside the material knock all atoms from their original positions. This technique is known as ion implantation. It produces amorphous solids only if the material is too cold for atoms to diffuse back to their original positions as the process continues.

Preparation by thin-film deposition (cold deposition)

Techniques such as sputtering and chemical vapor deposition can be used to deposit a thin film of material onto a surface. If the surface is kept cold enough, the atoms being deposited will not, on average, have enough energy to diffuse along the surface and form ordered crystals. For every deposition technique, there is a substrate temperature below which the deposited film will be amorphous. Surface diffusion requires much less energy than diffusion through the bulk, so that these temperatures are often lower than those required to make amorphous films by ion implantation.

Toward a strict definition

It is difficult to make a distinction between truly amorphous solids and crystalline solids in which the crystal size is extremely small (less than two nanometers). Even amorphous materials have some short-range order among the atomic positions (over distances of less than five nanometers). Furthermore, in very small crystals, a large fraction of the atoms are located at or near the crystal's surface; relaxation of the surface and interfacial effects distort the atomic positions, decreasing the structural order. Even the most advanced structural characterization techniques, such as X-ray diffraction and transmission electron microscopy, have difficulty in distinguishing between amorphous and crystalline structures on these length scales.

The transition from the liquid state to the glassy state, at a temperature below the equilibrium melting point of the material, is called the "glass transition." From a practical point of view, the glass transition temperature (Tg) is defined empirically as the temperature at which the viscosity of the liquid exceeds a certain value (commonly 1013 pascal-seconds). The transition temperature depends on cooling rate, with the glass transition occurring at higher temperatures for faster cooling rates. The precise nature of the glass transition is the subject of ongoing research.

Unsolved problems

  • What is the nature of the phase transition between a fluid or regular solid and a glassy phase?
  • What are the physical processes giving rise to the general properties of glasses?

See also

References
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 Phases of matter (list)
Solid | Liquid | Gas | Plasma
Colloid | Supercritical fluid | Superfluid | Supersolid | Degenerate matter | Quark-gluon plasma | Fermionic condensate | Bose-Einstein condensate | Strange matter
melting point | boiling point | triple point | critical point | equation of state | cooling curve

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