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ACCEPTOR AND DONOR
DOPANTS IN KNN( POTASSIUM
SODIUM NIOBATE BASED
CERMICS
BY: HAMZA SUHARWARDI (MM-03)
INTRODUCTION
• It is peioelectric ceramic materials that is a promising alternative to lead-based
Piezo ceramics in the field of Electromechanical Conversion.
• American Elements manufactures potassium Sodium Niobate In both Research
and Bulk Quantity.
INTRODUCTION
• Nb2o5 was obtained from stanford materials corporation with 99.999% purity.
• whereas K2CO3 and Na2CO3 were obtained from fisher scientific with 99.9% anhydrous used.
• In addition to this, TiO2 was obtained from aldrich chemistry with 99.99%, and MnO2, SnO2, and SrCO3 were
obtained from aldrich with 99.9% purity each.
• Carbonates were dried at 300◦C, whereas all other oxides were heated at 900◦C for 24 h.
• 50 g of doped-KNN formulations
• Batches Of 50 g of Doped-KNN Formulations (K0.5Na0.5TixNb1−x O3−x/2 Where (0.0 ≤ X ≤ 0.05; K0.5Na0.5MnxNb1−x O3−x/2
Where (0.0 ≤ X ≤ 0.01) K0.5Na0.5NnxNb1−xO3−x/2 Where 0.0 ≤ X ≤ 0.03) And (K0.5Na0.5)1−xSrxNbo3 Where 0.0 ≤ X ≤ 0.07)
• It is prepared from dried raw powders in a hot condition (∼200◦C) to avoid the non-stoichiometric conditions caused by moisture,
especially in carbonates.
XRD (X-RAY DIFFRACTION)
• The XRD traces from KNN-50/50 doped with 1% Mn and 1% Ti both appear to be similar, but the
shape of 2θ ∼ 45◦ {220}, and {002} peaks shows a slight difference (figure 1). In both cases, the
intensity of the 2θ = 32◦ is lower than that of the undoped KNN. Increasing the concentration of Ti to
5% Ti emphasized the structural change observed at 1% Ti.
• There are a few studies on single Mn acceptor dopant in KNN. Peaks shifting toward higher 2θ is
evidence of shrinkage in the lattice volume, which took place for Mn2+ and Ti4+ acceptor dopants as
compared to the undoped KNN peak (shown in figure B : 2θ = 45–46◦ ).
• conversely, reported that XRD peaks shifted toward lower 2θ (i.e. Expansion in the lattice volume) in
the case of Mn4+ doped KNN. For KNN-50/50 doped with Sn4+, secondary peaks of SnO2 are visible
in figure 2. Moreover, within the resolution limits.
• There was no change in the trace of the major KNN peaks, confirming that Sn does not enter into
solid solution with KNN. investigated SnO2 and cuo co-doping in KNN and concluded that Sn4+
was not soluble after 1 mol%.
• It also reported insolubility issues for Sn4+ in KNN with secondary peaks visible in their XRD
data. The reasons behind the insolubility of Sn4+ issues in KNN is unclear, since Sn4+ has a
similar ionic radius to Nb5+ However, Sn4+ is more covalently bonded to O than Nb5+, which
may influence its solubility.
7
Thanks!
Any questions?
You can find me at
@hamzaahmed
hamzaahmed0696@gmail.com

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Acceptor AND DONOR DOPANTS IN KNN( Potassium Sodium Niobate BASED CERMICS.pptx

  • 1. ACCEPTOR AND DONOR DOPANTS IN KNN( POTASSIUM SODIUM NIOBATE BASED CERMICS BY: HAMZA SUHARWARDI (MM-03)
  • 2. INTRODUCTION • It is peioelectric ceramic materials that is a promising alternative to lead-based Piezo ceramics in the field of Electromechanical Conversion. • American Elements manufactures potassium Sodium Niobate In both Research and Bulk Quantity.
  • 3. INTRODUCTION • Nb2o5 was obtained from stanford materials corporation with 99.999% purity. • whereas K2CO3 and Na2CO3 were obtained from fisher scientific with 99.9% anhydrous used. • In addition to this, TiO2 was obtained from aldrich chemistry with 99.99%, and MnO2, SnO2, and SrCO3 were obtained from aldrich with 99.9% purity each. • Carbonates were dried at 300◦C, whereas all other oxides were heated at 900◦C for 24 h. • 50 g of doped-KNN formulations • Batches Of 50 g of Doped-KNN Formulations (K0.5Na0.5TixNb1−x O3−x/2 Where (0.0 ≤ X ≤ 0.05; K0.5Na0.5MnxNb1−x O3−x/2 Where (0.0 ≤ X ≤ 0.01) K0.5Na0.5NnxNb1−xO3−x/2 Where 0.0 ≤ X ≤ 0.03) And (K0.5Na0.5)1−xSrxNbo3 Where 0.0 ≤ X ≤ 0.07) • It is prepared from dried raw powders in a hot condition (∼200◦C) to avoid the non-stoichiometric conditions caused by moisture, especially in carbonates.
  • 4.
  • 5. XRD (X-RAY DIFFRACTION) • The XRD traces from KNN-50/50 doped with 1% Mn and 1% Ti both appear to be similar, but the shape of 2θ ∼ 45◦ {220}, and {002} peaks shows a slight difference (figure 1). In both cases, the intensity of the 2θ = 32◦ is lower than that of the undoped KNN. Increasing the concentration of Ti to 5% Ti emphasized the structural change observed at 1% Ti. • There are a few studies on single Mn acceptor dopant in KNN. Peaks shifting toward higher 2θ is evidence of shrinkage in the lattice volume, which took place for Mn2+ and Ti4+ acceptor dopants as compared to the undoped KNN peak (shown in figure B : 2θ = 45–46◦ ). • conversely, reported that XRD peaks shifted toward lower 2θ (i.e. Expansion in the lattice volume) in the case of Mn4+ doped KNN. For KNN-50/50 doped with Sn4+, secondary peaks of SnO2 are visible in figure 2. Moreover, within the resolution limits.
  • 6. • There was no change in the trace of the major KNN peaks, confirming that Sn does not enter into solid solution with KNN. investigated SnO2 and cuo co-doping in KNN and concluded that Sn4+ was not soluble after 1 mol%. • It also reported insolubility issues for Sn4+ in KNN with secondary peaks visible in their XRD data. The reasons behind the insolubility of Sn4+ issues in KNN is unclear, since Sn4+ has a similar ionic radius to Nb5+ However, Sn4+ is more covalently bonded to O than Nb5+, which may influence its solubility.
  • 7. 7 Thanks! Any questions? You can find me at @hamzaahmed hamzaahmed0696@gmail.com