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Solid-state chemistry

From Wikipedia, the free encyclopedia

Solid-state chemistry, also sometimes referred as materials chemistry, is the study of the synthesis, structure, and properties of solid phase materials, particularly, but not necessarily exclusively of, non-molecular solids. It therefore has a strong overlap with solid-state physics, mineralogy, crystallography, ceramics, metallurgy, thermodynamics, materials science and electronics with a focus on the synthesis of novel materials and their characterisation. Solids can be classified as crystalline or amorphous on basis of the nature of order present in the arrangement of their constituent particles.[1]


Silicon wafer for use in electronic devices
Silicon wafer for use in electronic devices

Because of its direct relevance to products of commerce, solid state inorganic chemistry has been strongly driven by technology. Progress in the field has often been fueled by the demands of industry, sometimes in collaboration with academia.[2] Applications discovered in the 20th century include zeolite and platinum-based catalysts for petroleum processing in the 1950s, high-purity silicon as a core component of microelectronic devices in the 1960s, and “high temperature” superconductivity in the 1980s. The invention of X-ray crystallography in the early 1900s by William Lawrence Bragg was an enabling innovation. Our understanding of how reactions proceed at the atomic level in the solid state was advanced considerably by Carl Wagner's work on oxidation rate theory, counter diffusion of ions, and defect chemistry. Because of his contributions, he has sometimes been referred to as the father of solid state chemistry.[3]

Synthetic methods

Given the diversity of solid state compounds, an equally diverse array of methods are used for their preparation.[1][4]

Oven techniques

For thermally robust materials, high temperature methods are often employed. For example, bulk solids are prepared using tube furnaces, which allow reactions to be conducted up to ca. 1100 °C.[5] Special equipment e.g. ovens consisting of a tantalum tube through which an electric current is passed can be used for even higher temperatures up to 2000 °C. Such high temperatures are at times required to induce diffusion of the reactants.

Tube furnace being used during the synthesis of aluminium chloride
Tube furnace being used during the synthesis of aluminium chloride

Melt methods

One method often employed is to melt the reactants together and then later anneal the solidified melt. If volatile reactants are involved, the reactants are often put in an ampoule that is evacuated of the mixture

By keeping the bottom of the ampoule in liquid nitrogen, and then sealed. The sealed ampoule is then put in an oven and given a certain heat treatment. In the presence of the molten flux, certain grain may grow rapidly within a matrix of finer crystallites. This produces abnormal grain growth (AGG), which may be desired or detrimental to the produced solid.

Solution methods

It is possible to use solvents to prepare solids by precipitation or by evaporation. At times the solvent is used as a hydrothermal that is under pressure at temperatures higher than the normal boiling point. A variation on this theme is the use of flux methods, where a salt of relatively low melting point is added to the mixture to act as a high temperature solvent in which the desired reaction can take place. this can be very useful

Gas reactions

Chemical vapour deposition reaction chamber
Chemical vapour deposition reaction chamber

Many solids react vigorously with reactive gas species like chlorine, iodine, oxygen etc. Others form adducts with other gases, e.g. CO or ethylene. Such reactions are often conducted in a tube that is open ended on both sides and through which the gas is passed. A variation of this is to let the reaction take place inside a measuring device such as a TGA. In that case stoichiometric information can be obtained during the reaction, which helps identify the products.

Chemical transport reactions are used to purify and to grow crystals of materials. The process is often carried out in a sealed ampoule. The transport process entails the addition small amount of a transport agent, e.g., iodine, which generates a volatile intermediate species that migrates (transports). The ampoule is then placed in an oven with two temperature zones.

Chemical vapour deposition is a method that is widely employed for the preparation of coatings and semiconductors from molecular precursors.[6]


New phases, phase diagrams, structures

Synthetic methodology and characterization often go hand in hand in the sense that not one but a series of reaction mixtures are prepared and subjected to heat treatment. The stoichiometry is typically varied in a systematic way to find which stoichiometries will lead to new solid compounds or to solid solutions between known ones. A prime method to characterize the reaction products is powder diffraction, because many solid state reactions will produce polycristalline ingots or powders. Powder diffraction will facilitate the identification of known phases in the mixture. If a pattern is found that is not known in the diffraction data libraries an attempt can be made to index the pattern, i.e. to identify the symmetry and the size of the unit cell. (If the product is not crystalline the characterization is typically much more difficult.)

Scanning Electron Microscope (SEM)
Scanning Electron Microscope (SEM)

Once the unit cell of a new phase is known, the next step is to establish the stoichiometry of the phase. This can be done in a number of ways. Sometimes the composition of the original mixture will give a clue,

if one finds only one product -a single powder pattern- or if one was trying to make a phase of a certain composition by analogy to known materials but this is rare. Often considerable effort in refining the synthetic methodology is required to obtain a pure sample of the new material. If it is possible to separate the product from the rest of the reaction mixture elemental analysis can be used. Another way involves SEM and the generation of characteristic X-rays in the electron beam. X-ray diffraction is also used due to its imaging capabilities and speed of data generation.[7]

The latter often requires revisiting and refining the preparative procedures and that is linked to the question which phases are stable at what composition and what stoichiometry. In other words, what does the phase diagram looks like.[8] An important tool in establishing this is thermal analysis techniques like DSC or DTA and increasingly also, thanks to the advent of synchrotrons temperature-dependent powder diffraction. Increased knowledge of the phase relations often leads to further

X-ray diffractometer (XRD)
X-ray diffractometer (XRD)

refinement in synthetic procedures in an iterative way. New phases are thus characterized by their melting points and their stoichiometric domains. The latter is important for the many solids that are non-stoichiometric compounds. The cell parameters obtained from XRD are particularly helpful to characterize the homogeneity ranges of the latter.

Local structure

In contrast to the large structures of crystals, the local structure describes the interaction of the nearest neighbour atoms. Methods of nuclear spectroscopy use specific nuclei to probe the electric and magnetic fields around the nucleus. E.g. electric field gradients are very sensitive to small changes caused by lattice expansion/compression (thermal or pressure), phase changes, or local defects. Common methods are Mössbauer spectroscopy and perturbed angular correlation.

Further characterization

In many -but certainly not all- cases new solid compounds are further characterized[9] by a variety of techniques that straddle the fine line that (hardly) separates solid-state chemistry from solid-state physics. See Characterisation in material science.

Optical properties

For non-metallic materials, it is often possible to obtain UV/VIS spectra. In the case of semiconductors that will give an idea of the band gap.[10]


  1. ^ a b West, Anthony R. (2004). Solid State Chemistry and Its Applications. ISBN 981-253-003-7.
  2. ^ Kanatzidis, Mercouri G. (2018). "Report from the third workshop on future directions of solid-state chemistry: The status of solid-state chemistry and its impact in the physical sciences". Progress in Solid State Chemistry. 36 (1–2): 1–133. doi:10.1016/j.progsolidstchem.2007.02.002 – via Elsevier Science Direct.
  3. ^ Martin, Manfred (December 2002). "Life and achievements of Carl Wagner, 100th birthday". Solid State Ionics. 152–153: 15–17. doi:10.1016/S0167-2738(02)00318-1.
  4. ^ Cheetham, A. K.; Day, Peter (1988). Solid State Chemistry: Techniques. ISBN 0198552866.
  5. ^ "High Temperature Vacuum Tube Furnace GSL-1100 Operational Manual" (PDF).
  6. ^ Carlsson, Jan-Otto (2010). Handbook of Deposition Technologies for Films and Coatings (Third ed.). William Andrew. ISBN 978-0-8155-2031-3.
  7. ^ Schülli, Tobias U. (September 2018). "X-ray nanobeam diffraction imaging of materials". Current Opinion in Solid State and Materials Science. 22 (5): 188–201. Bibcode:2018COSSM..22..188S. doi:10.1016/j.cossms.2018.09.003.
  8. ^ cf. Chapter 12 of Elements of X-ray diffraction, B.D. Cullity, Addison-Wesley, 2nd ed. 1977 ISBN 0-201-01174-3
  9. ^ cf. Chapter 2 of New directions in Solid State Chemistry. C. N. R. Rao and J. Gopalakrishnan. Cambridge U. Press 1997 ISBN 0-521-49559-8
  10. ^ Cox, P. A. (1995). Transition Metal Oxides: An Introduction to Their Electronic Structure and Properties. Oxford Univ. Press. ISBN 978-0-19-958894-7.

External links

  • Media related to Solid state chemistry at Wikimedia Commons
  • [1], Sadoway, Donald. 3.091SC; Introduction to Solid State Chemistry, Fall 2010. (Massachusetts Institute of Technology: MIT OpenCourseWare)
This page was last edited on 9 February 2021, at 05:16
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