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0-D, 1-D, 2-D Structures (not a chapter in our book!)

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Presentation on theme: "0-D, 1-D, 2-D Structures (not a chapter in our book!)"— Presentation transcript:

1 0-D, 1-D, 2-D Structures (not a chapter in our book!)
NANO 101 Introduction to Nanotechnology

2 Overview Bottom Up Top Down Chemistry! Milling Lithography
Large size distribution No control of shape Impurities Crystal Growth 0-D particles 1-D particles 2-D films Lithography

3 Top-Down Approaches Milling Lithography
Broad size distribution (tens to hundreds of nm) Varied shape and geometry Impurities and defects from milling Lithography Also includes bottom up method

4 Particle Requirements
Uniform size Uniform morphology Uniform chemical composition and crystal structure Monodispersed

5 Homogeneous Nucleation/
Supersaturated solution G = Gibbs free energy K = Boltzmann constant Co = equilibrium concentration T = temperature Ω = atomic volume Two competing forces Surface energy Volume energy N&N Fig. 3.2

6 Nucleation and Growth Rates
N&N Fig. 3.4

7 Hot Injection A way to separate nucleation and growth:
One ionic precursor is heated to ~ 300 C Other precursor is a room temp and injected Rapid nucleation occurs followed by temperature drop and growth phase

8 Hot Injection

9 Growth of Nanoparticles
Chem. Rev., 2014, 114 (15), pp 7610–7630

10 Making Nanoparticles Nucleation Diffusion from bulk to surface
Adsorption to surface Irreversible incorporation onto surface Growth If the slowest step is diffusion  uniform particles If the slowest step is layer by layer growth  non-uniform particles

11 Favoring Diffusion-limited Growth
Low concentrations Large diffusion distance High solution viscosity Introduce diffusion barrier Change rate of chemical reactions Reactants used Catalysts

12 Other Strategies: Heat up method – in situ formation of reactive precursors Slow addition of precursors – for RT growth

13 0-D Nanostructures: Surface Area and Energy
Surface energy increases with surface area Large surface energy = instability Driven to grow to reduce surface energy C. Nutzenadel et al., Eur. Phys. J. D. 8, 245 (2000).

14 Electrostatic Stabilization
Establish Surface Charge Density Adsorption of ions/charged species - +

15 Steric Stabilization “Capping” Anchored Adsorbed Irreversible binding
Random, weak

16 What is on the surface? Current area of research:
Probing the surface of platinum nanoparticles with 13CO by solid-state NMR and IR spectroscopies Nanoscale, 2014,6,

17 Example: Colloidal Gold
Comprehensive study on synthesis and properties of colloidal gold published by Faraday (1857) Classic method Precursor: dilute chlorauric acid (HAuCl4) Reducing agent: sodium citrate (NaC6H5O7) Reaction temperature: 100 °C Product: stable, uniform, ~20 nm particles

18 Colloidal Gold Particle Size
N&N Fig. 3.9

19 Colloidal Gold Particle Size
N&N Fig. 3.9

20 Synthesis of Metallic Nanoparticles
Reduction of metal complexes in dilute solutions Precursors Elemental metals, inorganic salts, metal complexes Reduction agents Stabilizers PVA Sodium polyacrylate

21 Other Methods Brust Synthesis Reverse Micelle

22 Influence of “Capping”
Addition of polymer stabilizer Used on surface to prevent agglomeration Affects growth by limiting growth site May interact with solute, catalyst, solvent Can affect morphology N&N Fig. 3.13

23 Growth of Pt Nanoparticles
Found that ligands can terminate growth instead of change growth rate.

24 Influence of Temperature
N&N Fig. 3.14

25 Influence of Concentration
J. Phys. Chem. B, Vol. 108, No. 40, 2004

26 Influence of Time Rhodium nanocrystals
J. Phys. Chem. C, Vol. 111, No. 16, 2007

27 Influence of pH Initial pH of reaction can affect size
SnO2 J. Phys. Chem. B, Vol. 108, No. 40, 2004

28 Formation of Nanoparticles in Solution
Advantages: Stabilization from agglomeration Extraction of nanoparticles from solvent Surface modification and application Mass production

29 MBE Quantum Dots Self-assemble due to lattice mismatch
Self-assemble due to lattice mismatch

30 How are these 0D? GaAs GaAs In As E

31 Formation of Nanoparticles on Substrates
Advantages: No ligands needed Very stable Ready for electronic application Access different materials easily


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