Chemistry 754 - Solid State Chemistry Transition Metal Oxide Rock Salt and Rutile: Metal-Metal Bonding Chemistry 754 Solid State Chemistry Lecture 23 May.

Slides:



Advertisements
Similar presentations
Ch 10 Lecture 3 Angular Overlap
Advertisements

Ferromagnetism.
Coordination Chemistry II
Coordination Chemistry Bonding in transition-metal complexes.
Lectures Solid state materials
Placing electrons in d orbitals (strong vs weak field)
Coordination Chemistry Bonding in transition-metal complexes.
Transition metals, oxidations states and numbers
Spinel Structures. CFT aids in understanding the arrangements of metal ions in spinel structures (R.C. Chpt.12). READ R.C. WHERE SPINEL STRUCTURES ARE.
Lecture 26 MO’s of Coordination Compounds MLx (x = 4,6) 1) Octahedral complexes with M-L s-bonds only Consider an example of an octahedral complex.
Molecular Orbital Theory Edward A. Mottel Department of Chemistry Rose-Hulman Institute of Technology.
Lecture Notes by Ken Marr Chapter 11 (Silberberg 3ed)
Lecture 20 Dinuclear metal complexes with multiple M-M bonds 1) Transition metal-metal bonding: MO diagram Compared to main group elements, transition.
Metal-Metal Bonds Chapter 15. Metal-Metal Bonds Single, double, triple, and quadruple bonds are possible in transition metal complexes. –Figure 15-7;
Magnetism III: Magnetic Ordering
Ch 10 Lecture 2 Ligand Field Theory
Coordination Chemistry:
Coordination Chemistry II: Bonding
An Introduction to Band Theory, A Molecular Orbital Approach
Molecular orbital theory Overcoming the shortcomings of the valence bond.
Coordination Chemistry II
Magnetism and Magnetic Materials
CHE Materials Chemistry & Catalysis : Solid State Chemistry lecture 3 Rob Jackson LJ1.16,
IV. Electronic Structure and Chemical Bonding
Slide 2/26 Schedule Lecture 1: Electronic absorption spectroscopy Jahn-Teller effect and the spectra of d 1, d 4, d 6 and d 9 ions Lecture 2: Interpreting.
Colossal Magnetoresistance of Me x Mn 1-x S (Me = Fe, Cr) Sulfides G. A. Petrakovskii et al., JETP Lett. 72, 70 (2000) Y. Morimoto et al., Nature 380,
AP CHEMISTRY CHAPTER 9 BONDING 1. Hybridization 2.
Of bonds and bands How to understand MO theory for extended solids?
Unit 3 Summary. Crystal Field Theory x z y M n Which d-orbitals are effected the most?
Chemical Bonding II: Molecular Geometry and Hybridization of Atomic Orbitals Chapter 10.
Transition Metal Oxides Rock Salt and Rutile: Metal-Metal Bonding
How does benzene bond to a transition metal?
Lecture 7: M-M bonds d-bonds and bonding in metal clusters
Energy of 3 π bonding orbitals lower than energy of 2p (isolated) orbitals on C from which they come. π antibonding are higher than isolated 2p. Find experimentally.
Ch. 9 Molecular Geometry & Bonding Theories
CH. 23 TRANSITION ELEMENTS RECALL 1. characteristics of alkai & alkaline metals 2. Hund’s Rule 3. e - notation; elements / ions 4. why transition element?
Magnetism and Magnetic Materials DTU (10313) – 10 ECTS KU – 7.5 ECTS Sub-atomic – pm-nm With some surrounding environment and a first step towards the.
Applications of Spin-Polarized Photoemission P. D. Johnson, Annual Rev. Mater. Sci. 25 (1995) Combined spin –integrated/resolved detector: Giringhelli,
First Principle Design of Diluted Magnetic Semiconductor: Cu doped GaN
Sub-Topics Introduction to Transition Metals
Low-temperature properties of the t 2g 1 Mott insulators of the t 2g 1 Mott insulators Interatomic exchange-coupling constants by 2nd-order perturbation.
Transition Metal Oxide Perovskites: Band Structure, Electrical and Magnetic Properties Chemistry 754 Solid State Chemistry Lecture 22 May 20, 2002.
gg Delta bonds: (d xy ± d xy ) or (d x2-y2 ± d x2-y2 ) (d xy + d xy ) or (d x2-y2 + d x2-y2 )
Carbon’s valence electrons?. Hybrid Orbitals  Mixing of valence shell orbitals to form new similar orbitals for bonding electrons.
 The shape of a molecule plays an important role in its reactivity.  By noting the number of bonding and nonbonding electron pairs, we can easily predict.
Molecular Orbital Theory Bonding Models: Lewis Structures and VSEPR Valence Bond (VB) or Localized Electron (LE) Theory Molecular Orbital (MO) Theory Bonding.
Figure 23.2 Radii of transition metals as a function of group number.
Dr. S. M. Condren Chapter 9 Ionic and Covalent Bonding.
Introduction to Molecular Orbital Theory.
Magnetic Properties from Molecules to Solids
LII,III-Edges Absorption Coefficient
Covalent Bonding: Orbitals
Transition elements Introduction
Chapter 9 Bonding II: Molecular Geometry and Bonding Theories
Molecular Orbital Theory
Chemical Bonding II: Molecular Geometry and Hybridization of Atomic Orbitals Chapter 10.
Molecular Orbital Theory
Chemistry 141 Monday, November 27, 2017 Lecture 33 Pi bonding and MOs
Chemical Bonding II: Molecular Geometry and Hybridization of Atomic Orbitals Chapter 10 Copyright © The McGraw-Hill Companies, Inc.  Permission required.
Ionic vs Molecular
Chapter 10 Magnetic Properties Introduction 10
Chapter 3 Notes: First-row d-block Elements
Energy of 3 π bonding orbitals lower than energy of 2p (isolated)
Molecular Orbital Theory
Sigma (s) and Pi Bonds (p)
THE BIGGER PICTURE - TRENDS IN REAL SYSTEMS
Transition elements Introduction
Ch. 9 Molecular Geometry & Bonding Theories
KNOCKHARDY PUBLISHING
Presentation transcript:

Chemistry Solid State Chemistry Transition Metal Oxide Rock Salt and Rutile: Metal-Metal Bonding Chemistry 754 Solid State Chemistry Lecture 23 May 22, 2002

Chemistry Solid State Chemistry Rock Salt and Rutile: Structure & Properties Octahedral Molecular Orbital DiagramOctahedral Molecular Orbital Diagram Rock Salt  *(t 2g ) and  *(e g ) BandsRock Salt  *(t 2g ) and  *(e g ) Bands M-M InteractionsM-M Interactions Properties 3d Transition Metal MonoxidesProperties 3d Transition Metal Monoxides Magnetic SuperexchangeMagnetic Superexchange Rutile  *(t 2g ) Bands, t  and t Rutile  *(t 2g ) Bands, t  and t  Properties MO 2 (M=Ti, V, Cr, Mo, W, Ru)Properties MO 2 (M=Ti, V, Cr, Mo, W, Ru) Double Exchange in CrO 2Double Exchange in CrO 2

Chemistry Solid State Chemistry Rock Salt Crystal Structure OM x y

Chemistry Solid State Chemistry Generic Octahedral MO Diagram a 1g (  ) t 1u (  ) e g (  ) t 2g (  ) t 1g & t 2u a 1g (  ) t 1u (  ) t 2g (  ) e g (  ) nd e g (d x2-y2, d z2 ) (n+1)d t 2g (d xy, d xz, d yz ) (n+1)s (n+1)p O 2p  (6) - t 2g, t 1u O 2p NB  (6)-t 1g, t 2u O 2p  (6) a 1g, t 1u, e g Transition Metal Oxygen

Chemistry Solid State Chemistry Simplified Band Structure nd e g (d x2-y2, d z2 ) (n+1)d t 2g (d xy, d xz, d yz ) (n+1)s (n+1)p O 2p  O 2p  (6) a 1g, t 1u, e g Transition Metal Oxygen M-O  M-O  O 2p NB M-O  [3] M-O  [2]  [4] Bands of interest

Chemistry Solid State Chemistry 3d Transition Metal Monoxides AFM = Antiferromagnetic

Chemistry Solid State Chemistry Orbital Overlap in the t 2g Band  point (k x =k y =k z =0) M M MM M M M MM M  point (k x =k y =  /a, k z =0) M-O  nonbonding M-M bonding M-O  antibonding M-M nonbonding Band Runs Uphill from  

Chemistry Solid State Chemistry Orbital Overlap in the e g Band  point (k x =k y =k z =0)  point (k x =k y =  /a, k z =0) M-O  nonbonding Band Runs Uphill from   M M M M M M M M M M M-O  antibonding

Chemistry Solid State Chemistry Band Structure Calculations SrTiO 3 TiO

Chemistry Solid State Chemistry Magnetic Structure What is the magnetic structure of MnO, FeO, CoO and NiO? Why do the electrons align themselves in an antiparallel fashion? Why does the Neel temperature (magnetic ordering temperature) increase from Mn  Fe  Co  Ni? AFMAFM egeg t 2g = egeg = Mn O

Chemistry Solid State Chemistry Magnetic Superexchange M-O-M Interaction is AFM (  ) when both TM have 1/2 filled configurations (d 5 -d 5 or d 3 -d 3 ) Mn O Mn Mn O V e g  t 2g  e g  t 2g  e g  t 2g  e g  t 2g  e g  t 2g  e g  t 2g  e g  t 2g  e g  t 2g  M-O-M Interaction is FM (  ) when 1/2 filled configuration overlaps with empty configuration (d 5 -d 3 ) e g superexchange is stronger than t 2g SE because of greater overlap.

Chemistry Solid State Chemistry Rutile Crystal Structure z x y

Chemistry Solid State Chemistry MO 2 with the Rutile Structure

Chemistry Solid State Chemistry c/a Ratio in Rutile-Type Oxides VO 2 (T > 340K) Metallic V-V Even Spacing VO 2 (T < 340K) Metallic V-V Alternating MoO 2 Metallic Mo-Mo Alternating RuO 2 Metallic Ru-Ru Even Spacing CrO 2 Metallic Cr-Cr Even Spacing

Chemistry Solid State Chemistry M-M Overlap in the t 2g Band M-M  bonding M M M M M M M M M M-M  antibonding M-M  bonding  point k x =0 k y =0 k z =  /a M-M  antibonding M M M M M M M M M M-M  bonding M-M  antibonding  point k x =0 k y =0 k z = 

Chemistry Solid State Chemistry Combined M-O & M-M Effects The M-O  * and M-M bonding interactions both make a contribution to the t 2g band.The M-O  * and M-M bonding interactions both make a contribution to the t 2g band. The M-O  * interactions are dominant, but the M-M  interactions preturb the picture.The M-O  * interactions are dominant, but the M-M  interactions preturb the picture. As we fill up the t 2g band we can roughly think of the following picture in terms of M-M bonding strength.As we fill up the t 2g band we can roughly think of the following picture in terms of M-M bonding strength. M-M  d 1 TM Ion EFEF DOS M-M  d 2 TM Ion M-M   M-M  d 5 TM Ion M-M  d 6 TM Ion M-O   M-O  * ~ M-M  > M-M  > M-M 

Chemistry Solid State Chemistry + M-M  Tetragonal Structure (TiO 2,CrO 2, RuO 2 ) d e g d t 2g Oxygen 2p Transition Metal M-O  M-O  O 2p NB M-O  [2] M-O  [4] + M-M  Z = 2 (M 2 O 4 ) E F TiO 2 E F VO 2 E F CrO 2 E F RuO 2 Delocalized Electrons

Chemistry Solid State Chemistry Band Structure Calculations SrTiO 3 TiO 2

Chemistry Solid State Chemistry TiO 2 VO 2 CrO 2 Calculated Band Structure (Tetragonal, Z=2)

Chemistry Solid State Chemistry TiO 2 VO 2 CrO 2 Density of States (Tetragonal Structure)

Chemistry Solid State Chemistry M M M M a M M M M a M M M M a M M M M a M M M M a M M M M a TiO 2 Tetragonal Z=2 MoO 2 Monoclinic Z=4  point  point Bonding Antibonding M-M Short=Bonding M-M Long=Bonding M-M Short=AB M-M Long=AB M-M Short=Bonding M-M Long=AB M-M Short=AB M-M Long=Bonding

Chemistry Solid State Chemistry Pierls Distortion The dimerization which occurs in the rutile structure and it’s effects on the band structure are similar to the Pierls distortion we discussed for a 1D chain of Hydrogen atoms, except that it occurs on top of the M-O  * interactions. a a a a a a E k 0  /a EFEF E k 0 EFEF

Chemistry Solid State Chemistry M-O  M-O  O 2p NB M-M  [2] M-O  [8] M-O  [8] M-M  [2] d e g d t 2g Z = 4 (M 4 O 8 ) E F VO 2 E F MoO 2 Oxygen 2p Monoclinic Structure (VO 2,MoO 2 ) Delocalized Electrons M-O Antibonding Localized Electrons M-M Bonding

Chemistry Solid State Chemistry MoO 2 Monoclinic (Z=4) CrO 2 Tetragonal (Z=2) Mo-Mo  Mo-O  

Chemistry Solid State Chemistry CrO 2 and RuO 2 Why are alternating long-short M-M contacts, indicative of Metal-Metal bonding not observed in CrO 2 and RuO 2. The electron count suggests that the M-M  levels should be full and the M-M  * levels empty? There is a competition between localized M-M bonding and delocalized electronic transport in the M-O  * band. Favors M-M bonding and localized e Favors M-M bonding and localized e - Dominant in MoO 2 Favors delocalized transport in the M-O  * band Dominant in CrO 2 (poor overlap) RuO 2 (electron count) VO 2 Intermediate

Chemistry Solid State Chemistry Double Exchange CrO 2 is ferromagnetic. A property which leads to it’s use in magnetic cassette tapes. What stabilizes the ferromagnetic state? Localized t || electrons No M-M Bonding M M M M M M Delocalized t 2g  * electrons Ferromagnetic: Delocalized transport of t  * electrons allowed. t || t*t*t*t* t*t*t*t* Antiferromagnetic: Delocalized transport violates Hund’s Rule. Localized t || electrons polarize itinerant (delocalized) t 2g  * electrons. Magnetism and conductivity are correlated.