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Solid state (Calculations & Doping)

Solid state (Calculations & Doping). Bonding in Solids. There are four types of solid: Molecular (formed from molecules) - usually soft with low melting points and poor conductivity.

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Solid state (Calculations & Doping)

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  1. Solid state(Calculations & Doping)

  2. Bonding in Solids • There are four types of solid: • Molecular (formed from molecules) - usually soft with low melting points and poor conductivity. • Covalent network (formed from atoms) - very hard with very high melting points and poor conductivity. • Ions (formed from ions) - hard, brittle, high melting points and poor conductivity. • Metallic (formed from metal atoms) - soft or hard, high melting points, good conductivity, malleable and ductile. Dr M S MEENA

  3. Crystalline Solids Determining Crystal Structure • crystalline solids have a very regular geometric arrangement of their particles • the arrangement of the particles and distances between them is determined by x-ray diffraction • in this technique, a crystal is struck by beams of x-rays, which then are reflected • the wavelength is adjusted to result in an interference pattern – at which point the wavelength is an integral multiple of the distances between the particles 3 Dr M S MEENA

  4. X-ray Crystallography 4 Dr M S MEENA

  5. Bragg’s Law • when the interference between x-rays is constructive, the distance between the two paths (a) is an integral multiple of the wavelength nl=2a • the angle of reflection is therefore related to the distance (d) between two layers of particles sinq= a/d • combining equations and rearranging we get an equation called Bragg’s Law 5 Dr M S MEENA

  6. Example –An x-ray beam at l=154 pm striking an iron crystal results in the angle of reflection q = 32.6°. Assuming n = 1, calculate the distance between layers. Dr M S MEENA

  7. n, q, l d HOW TO SOLVE….. Given: Find: • n = 1, q = 32.6°, l = 154 pm • d, pm Concept Plan: Relationships: Solution: Dr M S MEENA 7

  8. Unit Cells DR M S MEENA

  9. Unit Cells • Three common types of unit cell. • Primitive cubic, atoms at the corners of a simple cube, each atom shared by 8 unit cells; • Body-centered cubic (bcc), atoms at the corners of a cube plus one in the center of the body of the cube, corner atoms shared by 8 unit cells, center atom completely enclosed in one unit cell; • Face-centered cubic (fcc), atoms at the corners of a cube plus one atom in the center of each face of the cube, corner atoms shared by 8 unit cells, face atoms shared by 2 unit cells. Sudhir Kumar PGT (Chem.) KV Chamera -2

  10. Unit Cells • the number of other particles each particle is in contact with is called its coordination number • for ions, it is the number of oppositely charged ions an ion is in contact with • higher coordination number means more interaction, therefore stronger attractive forces holding the crystal together • the packing efficiency is the percentage of volume in the unit cell occupied by particles • the higher the coordination number, the more efficiently the particles are packing together 10 Dr M S MEENA

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  12. Simple Cubic 12

  13. Cubic Unit Cells - Simple Cubic • 8 particles, one at each corner of a cube • 1/8th of each particle lies in the unit cell • each particle part of 8 cells • 1 particle in each unit cell • 8 corners x 1/8 • edge of unit cell = twice the radius • coordination number of 6 2r 13

  14. Body-Centered Cubic 14

  15. Cubic Unit Cells - Body-Centered Cubic • 9 particles, one at each corner of a cube + one in center • 1/8th of each corner particle lies in the unit cell • 2 particles in each unit cell • 8 corners x 1/8 + 1 center • edge of unit cell = (4/Ö 3) times the radius of the particle • coordination number of 8 15

  16. Face-Centered Cubic 16

  17. Cubic Unit Cells - Face-Centered Cubic • 14 particles, one at each corner of a cube + one in center of each face • 1/8th of each corner particle + 1/2 of face particle lies in the unit cell • 4 particles in each unit cell • 8 corners x 1/8 + 6 faces x 1/2 • edge of unit cell = 2Ö 2 times the radius of the particle • coordination number of 12 17

  18. Ionic Crystals CsCl coordination number = 8 Cs+ = 167 pm Cl─ = 181 pm NaCl coordination number = 6 Na+ = 97 pm Cl─ = 181 pm 19

  19. Rock Salt Structures • coordination number = 6 • Cl─ ions (181 pm) in a face-centered cubic arrangement • ⅛ of each corner Cl─ inside the unit cell • ½ of each face Cl─ inside the unit cell • each Na+ (97 pm) in holes between Cl─ • octahedral holes • 1 in center of unit cell • ¼ of each edge Na+ inside the unit cell • Na:Cl = (¼ x 12) + 1: (⅛ x 8) + (½ x 6) = 4:4 = 1:1, • therefore the formula is NaCl 20

  20. Zinc Blende Structures • coordination number = 4 • S2─ ions (184 pm) in a face-centered cubic arrangement • ⅛ of each corner S2─ inside the unit cell • ½ of each face S2─ inside the unit cell • each Zn2+ (74 pm) in holes between S2─ • tetrahedral holes • 1 whole in ½ the holes • Zn:S = (4 x 1) : (⅛ x 8) + (½ x 6) = 4:4 = 1:1, • therefore the formula is ZnS 21

  21. Doping in Semiconductors • doping is adding impurities to the semiconductor’s crystal to increase its conductivity • goal is to increase the number of electrons in the conduction band • n-type semiconductors do not have enough electrons themselves to add to the conduction band, so they are doped by adding electron rich impurities • p-type semiconductors are doped with an electron deficient impurity, resulting in electron “holes” in the valence band. Electrons can jump between these holes in the valence band, allowing conduction of electricity 22

  22. Dr M S MEENA PGT CHEMISTRY KV-2 MRN MATHURAAGRA REGION Thank You Acknowledgements : Prentice Hall Publications Steven S. Zumdahl

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