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Structures of Ionic Solids

Structures of Ionic Solids

Edited By Shivani Poonia | Updated on Jul 02, 2025 06:28 PM IST

The ionic solids are a type of crystalline solid, formed by ions, which are held together by strong electrostatic forces known as ionic bonds. The general composition of these solids includes a repetitive pattern of cations (positively charged ions) and anions (negatively charged ions). The geometry for most ionic solids is connected with several factors, such as the dimensions and charges of the involved ions and how these ions can be packed into their most stable arrangement.

This Story also Contains
  1. NaCl (Rock Salt)
  2. CsCl
  3. ZnS (Zinc-Blende)
  4. CaF2 (Fluorite Structure)
  5. Na2O (Anti-Fluorite Structure)
  6. Some Solved Examples
  7. Summary
Structures of Ionic Solids
Structures of Ionic Solids

NaCl (Rock Salt)

  • In it CI- ions have CCP structure that is, FCC and Na+ ions occupy octahedral holes (voids) here.
  • Both Na+ and CI- have coordination number six. The number of formula units per unit cell is four. For example, halides of alkali metals (except CsX) like LiX, NaX, and KX, other halides like AgCl, AgBr, NH4Cl oxides like TiO, FeO, NiO.
  • rc + ra = a/2 and rNa+/rcl- must be 0.414 however, it is 0.525.

CsCl

  • Here Cl- ions are at the comers of a cube and Cs+ ions are in the cubic void (centered position) i.e. BCC like structure.
  • Here coordination number of both Cs+ and Cl- is 8 and here the number of formula units per unit cell is 1. rc + ra = √3a/2.
  • Here rCs+/rCl+ should be 0.732 but it is 0.93, e.g. CsX, TiBr, NH4Cl, NH4Br

ZnS (Zinc-Blende)

  • Here S2- occupies CCP or FCC arrangement while Zn2+ ions occupy alternate tetrahedral voids.
  • Only half of the total voids are occupied.
  • Here coordination number of both Zn2+ and S2- is four and here the number of formula units per unit cell is four. For example, ZnS, CuBr, Cul, Agl, etc.
    rc + ra = √3a/4

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CaF2 (Fluorite Structure)

  • Here Ca2+ occupies CCP and F- ions occupy all the tetrahedral voids.
  • Here coordination number of Ca2+ is 8 while for F- it is four and the effective number of Ca2+ and F- ions in a unit cell are 4 and 8 respectively, respectively the number of formula units per unit cell is four.
    rc + ra = √3a/4

Na2O (Anti-Fluorite Structure)

  • Here negative ions (O2-) occupy CCP while cations Na+ occupy all the tetrahedral voids.
  • Here coordination number of Na+ is four while for O2- it is eight, here the number of formula units per unit cell is four, and the effective number of Li+ and O2- ions in a unit cell are 8 and 4 respectively.
    rc + ra = √3a/4

Normal Spinel Structure (XY2O4)

  • Spinel is MgAl2O4, and spinel, in general, has the formula AB2O4. Here A is a divalent cation (Mg2+, Ca2+) and B is a trivalent cation Al3+.
  • Here Mg2+ occupy 1/8th of tetrahedral voids while oxide ions 1/ 8 of Al3+ occupy 1/2 of the octahedral voids.
  • As magnetic materials, these are used in telephones, and memory loops of computers.

Inverse Spinel Structure (Fe3O4, Magnetite)

  • In Fe3O4, Fe3+ and Fe2+ are present in 2:1 ratio.
  • Here oxides ions are in CCP while Fe2+ ions occupy 1 octahedral void while Fe3+ occupies 1 octahedral and 1 tetrahedral void.
  • Here O2- ions form the FCC unit cell.
  • Here the formula ratio of
    Fe2+ : Fe3+ : O2- = 1 : 2 : 4
  • MgFe2O4, Pb3O4, and Mn3O4 have also this type of structure.

Effect of T and P on Crystal Structure

  • On increasing the temperature of the CsCl structure coordination number decreases from 8:8 to 6:6.
    $\mathrm{CsCl} \xrightarrow{\Delta} \mathrm{NaCl}$ Structure
    8:8 6:6
  • On subjecting the NaCl structure to high pressure it will increase coordination number from 6:6 to 8:8.$\mathrm{NaCl} \xrightarrow{\text { highly pressurized }} \mathrm{CsCl}$ Structure
  • 6:6 8:8

Recommended topic video on(Structure of ionic solid)


Some Solved Examples

Example 1: The Ca2+ and F- are located in CaF2 crystal respectively at face-centred cubic lattice points and in

1) Tetrahedral voids

2)Half of tetrahedral voids

3)Octahedral voids

4)Half of the octahedral voids

Solution

As we have learned,

CaF2 (Fluorite Structure)

  • Here Ca2+ occupies CCP and F- ions occupy all the tetrahedral voids.
  • Here coordination number of Ca2+ is 8 while for F- it is four and the effective number of Ca2+ and F- ions in a unit cell are 4 and 8 respectively, here the number of formula units per unit cell is four.
    re + ra = √3a/4

-

In $\mathrm{CaF}_2$ crystal $\mathrm{Ca}^{2+}$ occupy all corners and face centre of the cube whereas $F^{-}$ occupy all tetrahedral
voids.

Therefore, Option(1) is correct

Example 2: n antifluorite structure, the negative ions:

1) Are arranged in ccp
2)Occupy tetrahedral voids

3)Are arranged in hcp

4)Occupy octahedral voids

Solution

As we have learned,

Na2O (Anti-Fluorite Structure)

  • Here negative ions (O2-) occupy CCP while cations Na+ occupy all the tetrahedral voids.
  • Here co-ordination number of Na' is four while for O2- it is eight, here number of formula units per unit cell is four and the effective number of Li+ and O2- ions in a unit cell are 8 and 4 respectively.
    re + ra = √3a/4

-

In antifluorite crystal i.e Na2O, the anions are arranged in cubic close packing while the cations occupy all the tetrahedral voids.
Therefore, Option(1) is correct

Example 3: The melting point of RbBr is $682^{\0} \mathrm{C}$, while that of NaF is $988^{\0} \mathrm{C}$. The principal reason that the melting point of NaF is much higher than that of RbBr is that:

1) The internuclear distance $r_c+r_a$ is greater for RbBr than that for NaF

2)These two crystals are not isomorphous

3)The bond in RbBr has more covalent character than the bond in NaF

4)The molar mass of NaF is smaller than that of RbBr

Solution

The internuclear distance is lesser for NaF than RbBr due to which there is a strong electrostatic force of attraction in NaF. Thus, the melting point of NaF is greater than RbBr.
Hence, the answer is the option (1).

Example 4: Ionic radii of cation $\mathrm{A}^{+}$ and anion $\mathrm{B}^{-}$ are 102 and 181ppm respectively. These ions are allowed to crystallize into an ionic solid. This crystal has cubic close packing for $\mathrm{B}^{-} \cdot \mathrm{A}^{+}$ is present in all octahedral voids. The edge length of the unit cell of the crystal AB is ____________ pm. (Nearest Integer)

1) 566

2)666

3)457

4)654

Solution

This crystal has cubic close paking for $\mathrm{B}^{-}$,
Means $\mathrm{B}^{\Theta}$ is present all corner and face centres , and $\mathrm{A}^{+}$ is present in all octahedral voids.


a = edge length of the unit cell of the crystal AB
$\begin{aligned} & \mathrm{a}=2 \mathrm{r}^{-}+2 \mathrm{r}^{+} \\ & \mathrm{a}=2 \times 181+2 \times 102 \\ & \mathrm{a}=362+204 \\ & \mathrm{a}=566 \mathrm{pm}\end{aligned}$
Ans = 566

Example 5: KF has a NaCl structure. What is the distance (in pm) between K+ and F- in KF. If density is 2.48 gm/cm3?

1) 268.8

2)537.5

3)155.3

4)5.375

Solution

Density formula :

$d=\frac{Z \times M}{a^3 \times N_A}$

For NaCl structure Z = 4

M for KF=58

$\begin{aligned} & 2.48=\frac{4 \times 58}{a^3 \times 6.02 \times 10^{23}} \\ & a^3=\frac{4 \times 58}{2.48 \times 6.02 \times 10^{23}}=150 \times 10^{-24} \\ & a=537.5 \mathrm{pm}\end{aligned}$


Rock salt structure or NaCl type structure -

$\mathrm{Cl}^{-}$ located at all corners and face center

$\mathrm{Na}^{+}$ located at all octahedral voids

Edge length $=2\left(r_{N a^{+}}+r_{C l^{-}}\right)$

Coordination number = 6:6
Thus, the distance between K+ and F- is $\frac{a}{2}=268.8 \mathrm{pm}$

Hence, the answer is (268.8 pm).

Summary

Ionic solids are composed of positive and negative ions held together by ionic bonds. The geometrical structure that the ions take in these solids is determined by the charge and size of the ions, thereby giving different stable structures such as simple cubic, body-centered cubic, and face-centered cubic forms, among others. Some important structures include patterns of rock salt, NaCl, and that of cesium chloride, CsCl,


Frequently Asked Questions (FAQs)

1. Why do some ionic solids conduct electricity when molten but not when solid?
In the solid state, ions are fixed in the crystal lattice and cannot move freely. When molten, the ions become mobile and can carry an electric current. This mobility of ions in the liquid state allows for electrical conductivity.
2. What is meant by a close-packed structure in ionic solids?
A close-packed structure refers to an arrangement of ions where they are packed as closely together as possible, maximizing the use of space. This efficient packing minimizes the overall energy of the system and is common in many ionic solids.
3. What is a unit cell in an ionic solid?
A unit cell is the smallest repeating unit of the crystal lattice that shows the full symmetry of the crystal structure. It is a conceptual tool used to describe and analyze the arrangement of ions in the entire crystal.
4. How does the size ratio of cations to anions affect the structure of ionic solids?
The size ratio of cations to anions influences the coordination number and the type of crystal structure formed. Larger size ratios typically result in higher coordination numbers and more complex structures, while smaller ratios lead to simpler structures with lower coordination numbers.
5. How does lattice energy relate to the stability of ionic solids?
Lattice energy is the energy released when gaseous ions combine to form a solid ionic compound. Higher lattice energy indicates stronger ionic bonds and greater stability of the ionic solid. It is influenced by factors such as ion charge and ion size.
6. What is meant by a body-centered cubic structure in ionic solids?
A body-centered cubic (BCC) structure is a crystal arrangement where ions occupy the corners of a cube and the center of the cube. This structure is found in some ionic solids and provides a balance between packing efficiency and ionic interactions.
7. How does pressure affect the structure of ionic solids?
Increased pressure can cause ionic solids to adopt more compact structures with higher coordination numbers. This can lead to phase transitions, where the crystal structure changes to accommodate the reduced volume, potentially altering the solid's properties.
8. What is the significance of the Born-Haber cycle in understanding ionic solid structures?
The Born-Haber cycle is a theoretical approach used to calculate lattice energy, which is crucial for understanding the stability and formation of ionic solids. It breaks down the formation of an ionic solid into several steps, providing insights into the energetics of the process.
9. How do ionic solids differ in their ability to dissolve in water?
The solubility of ionic solids in water depends on factors like lattice energy and hydration energy of the ions. Solids with lower lattice energies and higher hydration energies tend to be more soluble, as the energy required to break the crystal lattice is offset by the energy released during hydration.
10. What is the role of electronegativity in determining the structure of ionic solids?
Electronegativity differences between elements influence the degree of ionic character in the bonds. Larger differences typically result in more ionic character, affecting the strength of electrostatic interactions and, consequently, the crystal structure and properties of the solid.
11. How do ionic solids differ from covalent solids?
Ionic solids are composed of oppositely charged ions held together by electrostatic forces, while covalent solids consist of atoms or molecules bonded by shared electrons. Ionic solids typically have higher melting points, are brittle, and conduct electricity when dissolved or molten, unlike most covalent solids.
12. What is meant by the coordination number in ionic solids?
The coordination number in ionic solids refers to the number of oppositely charged ions directly surrounding a given ion in the crystal lattice. It depends on the relative sizes of the ions and affects the overall structure and properties of the solid.
13. What is an ionic solid?
An ionic solid is a crystalline structure composed of positively and negatively charged ions held together by strong electrostatic forces. These ions are arranged in a repeating three-dimensional pattern, forming a lattice structure.
14. Why are ionic solids typically hard and brittle?
Ionic solids are hard due to the strong electrostatic forces between ions. They are brittle because when stress is applied, layers of ions can shift, causing like charges to align and repel each other, leading to fractures along cleavage planes.
15. What determines the overall structure of an ionic solid?
The overall structure of an ionic solid is determined by the relative sizes of the ions, their charges, and the principle of maximum packing efficiency. These factors influence how the ions arrange themselves to minimize potential energy and maximize stability.
16. What is the rock salt (NaCl) structure, and why is it common?
The rock salt structure, named after sodium chloride, is a cubic arrangement where each ion is surrounded by six oppositely charged ions. It's common because it allows for efficient packing of ions with a 1:1 ratio and similar sizes, maximizing electrostatic interactions.
17. What is the significance of Madelung constant in ionic solids?
The Madelung constant is a numerical factor used in calculating the lattice energy of ionic crystals. It accounts for the sum of all electrostatic interactions in the crystal and varies depending on the specific crystal structure, providing insights into the stability of different ionic arrangements.
18. What is the significance of Schottky defects in ionic solids?
Schottky defects are paired vacancies of cations and anions that maintain the overall charge neutrality of the crystal. These defects can significantly affect properties like ionic conductivity and diffusion rates within the solid, influencing its behavior in various applications.
19. How do ionic solids behave when exposed to electromagnetic radiation?
Ionic solids can interact with electromagnetic radiation in various ways. They may absorb certain wavelengths, leading to electronic transitions or lattice vibrations. This interaction can result in phenomena like color in some ionic compounds or their use in optical applications.
20. How do ionic solids behave under mechanical stress?
Under mechanical stress, ionic solids typically exhibit brittle behavior. The rigid nature of ionic bonds means that when sufficient force is applied, the crystal structure can suddenly break along cleavage planes rather than deforming plastically like metals.
21. What is Pauling's first rule, and how does it apply to ionic solid structures?
Pauling's first rule states that the coordination number of a cation is determined by the radius ratio of the cation to the anion. This rule helps predict the likely coordination number and structure of ionic compounds based on the relative sizes of the ions involved.
22. How do ionic radii affect the structure of ionic solids?
Ionic radii determine how closely ions can pack together and influence the coordination number. Larger ions typically lead to more open structures with lower coordination numbers, while smaller ions allow for denser packing and higher coordination numbers.
23. How does the charge of ions affect the structure of ionic solids?
The charge of ions influences the strength of electrostatic interactions and the coordination number. Higher charges typically lead to stronger interactions, higher coordination numbers, and more complex structures to balance the charges effectively.
24. How do defects in ionic solids affect their properties?
Defects in ionic solids, such as vacancies or interstitial ions, can significantly affect properties like electrical conductivity, color, and mechanical strength. They introduce irregularities in the crystal structure that can alter how the solid behaves under various conditions.
25. How does polymorphism occur in ionic solids?
Polymorphism in ionic solids occurs when a compound can exist in multiple crystal structures depending on conditions like temperature and pressure. Different polymorphs can have different properties despite having the same chemical composition.
26. What is the difference between stoichiometric and non-stoichiometric ionic compounds?
Stoichiometric ionic compounds have a fixed ratio of cations to anions that matches their chemical formula. Non-stoichiometric compounds deviate from this ideal ratio due to defects or substitutions, which can affect their properties and behavior.
27. How does temperature affect the structure of ionic solids?
Temperature can cause thermal expansion in ionic solids, increasing the average distance between ions. At very high temperatures, it can lead to phase transitions or melting, fundamentally altering the crystal structure.
28. How do ionic solids conduct heat compared to metals?
Ionic solids generally conduct heat poorly compared to metals. In metals, heat is conducted by free electrons, while in ionic solids, heat transfer occurs through vibrations of the crystal lattice (phonons), which is a less efficient process.
29. How do ionic solids contribute to the field of solid-state ionics?
Ionic solids are crucial in solid-state ionics, a field studying the movement of ions in solids. This area is important for developing technologies like solid-state batteries and fuel cells, where the controlled movement of ions through a solid material is essential for device function.
30. What is the relationship between crystal field theory and the color of ionic solids?
Crystal field theory explains how the electronic structure of transition metal ions is affected by surrounding ions in a crystal. This interaction can cause splitting of d-orbital energy levels, leading to the absorption of specific wavelengths of light and resulting in the characteristic colors of many ionic compounds.
31. How do ionic solids behave in non-aqueous solvents?
The behavior of ionic solids in non-aqueous solvents depends on the solvent's polarity and ability to solvate ions. Some ionic solids may dissolve in polar organic solvents, while others remain insoluble. This behavior is important in various chemical processes and applications.
32. What is the role of ionic solids in solid-state lighting technologies?
Ionic solids, particularly those containing rare earth elements, are crucial in solid-state lighting technologies like LEDs and phosphors. Their unique electronic structures allow for specific light emission properties, making them essential in creating efficient and color-tunable lighting solutions.
33. How do ionic solids contribute to the field of catalysis?
Ionic solids can act as catalysts or catalyst supports in various chemical reactions. Their surface structures, ability to exchange ions, and potential to create active sites make them valuable in heterogeneous catalysis, important in industrial processes and environmental applications.
34. What is the relationship between ionic solid structures and their magnetic properties?
The magnetic properties of ionic solids depend on the electronic configuration of the ions and their arrangement in the crystal structure. Some ionic compounds exhibit ferromagnetism, antiferromagnetism, or ferrimagnetism, which are influenced by the interactions between unpaired electrons in the crystal lattice.
35. What is the role of ionic solids in energy storage technologies?
Ionic solids are crucial in various energy storage technologies. They serve as electrolytes in batteries, as ion conductors in fuel cells, and as materials for capacitors. Understanding and manipulating their structures is key to developing more efficient and higher-capacity energy storage devices.
36. How do ionic solids contribute to the field of photocatalysis?
Certain ionic solids, particularly metal oxides, are important in photocatalysis. Their electronic structure allows them to absorb light and generate electron-hole pairs, which can drive chemical reactions. This property is utilized in applications like water purification and solar fuel production.
37. What is the relationship between ionic solid structures and their piezoelectric properties?
Piezoelectric properties in ionic solids arise from non-centrosymmetric crystal structures that allow for the generation of an electric charge in response to applied mechanical stress. Understanding these structures is crucial for developing materials used in sensors, actuators, and energy harvesting devices.
38. What is Frenkel defect, and how does it affect ionic solids?
A Frenkel defect occurs when an ion moves from its normal lattice position to an interstitial site, creating a vacancy and an interstitial ion. This defect can affect properties like ionic conductivity and is more common in solids with large differences in cation and anion sizes.
39. What is an antistructure, and how does it relate to ionic solids?
An antistructure is a crystal structure where the positions of cations and anions are reversed compared to a known structure. Understanding antistructures helps in predicting and analyzing the possible arrangements of ions in different compounds, expanding our knowledge of ionic solid structures.
40. How do ionic solids contribute to the field of materials science?
Ionic solids are important in materials science for their unique properties, including high melting points, specific electrical behaviors, and optical characteristics. They are used in various applications, from ceramics and electronic components to catalysts and energy storage materials.
41. What is the role of ionic solids in geochemistry?
In geochemistry, ionic solids play a crucial role in understanding mineral formation, rock composition, and geological processes. The structures and properties of ionic minerals provide insights into Earth's history, current composition, and ongoing geological activities.
42. How do impurities affect the properties of ionic solids?
Impurities can significantly alter the properties of ionic solids. They can introduce color, change electrical conductivity, affect mechanical strength, and modify chemical reactivity. Understanding and controlling impurities is crucial in many applications of ionic materials.
43. What is the relationship between ionic solid structures and their melting points?
The melting point of an ionic solid is generally related to its lattice energy. Structures with higher lattice energies, typically those with higher charges or smaller ions, tend to have higher melting points due to the stronger electrostatic forces holding the crystal together.
44. What is the significance of the radius ratio rule in predicting ionic solid structures?
The radius ratio rule, based on the ratio of cation to anion radii, helps predict the likely coordination number and, consequently, the crystal structure of ionic compounds. It's a useful tool for understanding how ion sizes influence the overall arrangement in ionic solids.
45. How do ionic solids contribute to the development of advanced ceramics?
Ionic solids are fundamental to many advanced ceramics, providing properties like high hardness, thermal stability, and specific electrical characteristics. Understanding ionic structures allows for the design of ceramics with tailored properties for applications in electronics, energy, and aerospace industries.
46. How do ionic solid structures influence their thermal expansion properties?
The thermal expansion of ionic solids is related to their crystal structure and the strength of ionic bonds. More tightly packed structures with stronger bonds generally exhibit lower thermal expansion, which is important in applications where dimensional stability under temperature changes is crucial.
47. What is the significance of superionic conductors in the context of ionic solids?
Superionic conductors are a special class of ionic solids where one ion species is highly mobile within a rigid framework of other ions. These materials show exceptionally high ionic conductivity, making them important for applications in solid-state batteries and fuel cells.
48. How do ionic solids behave under extreme conditions, such as very high pressures?
Under extreme pressures, ionic solids can undergo significant structural changes. These may include phase transitions to denser structures, changes in coordination numbers, or even metallization in some cases. Studying these behaviors provides insights into material properties under extreme conditions, relevant to geophysics and materials science.
49. How do ionic solid structures influence their optical properties?
The optical properties of ionic solids, such as transparency, refraction, and birefringence, are directly related to their crystal structures. The arrangement of ions affects how light interacts with the material, leading to properties useful in optical devices, gemstones, and other applications.
50. What is the significance of point defects in ionic solids?
Point defects, such as vacancies and interstitials, play a crucial role in the properties of ionic solids. They can affect ionic conductivity, color, and reactivity. Understanding and controlling these defects is important in tailoring materials for specific applications, from semiconductors to catalysts.

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