Yttria-stabilized zirconia

Yttria-stabilized zirconia (YSZ) is a ceramic in which the crystal structure of zirconium dioxide is made stable at room temperature by an addition of yttrium oxide. These oxides are commonly called "zirconia" (Zr O₂) and "yttria" (Y₂O₃), hence the name.

Stabilization

Pure zirconium dioxide undergoes a phase transformation from monoclinic (stable at room temperature) to tetragonal (at about 1173 °C) and then to cubic (at about 2370 °C), according to the scheme:

monoclinic (1173 °C) $\leftrightarrow$ tetragonal (2370 °C) $\leftrightarrow$ cubic (2690 °C) $\leftrightarrow$ melt

Obtaining stable sintered zirconia ceramic products is difficult because of the large volume change accompanying the transition from tetragonal to monoclinic (about 9%). Stabilization of the cubic polymorph of zirconia over wider range of temperatures is accomplished by substitution of some of the Zr⁴⁺ ions (ionic radius of 0.82 Å, too small for ideal lattice of fluorite characteristic for the tetragonal zirconia) in the crystal lattice with slightly larger ions, e.g., those of Y³⁺ (ionic radius of 0.96 Å). The resulting doped zirconia materials are termed stabilized zirconias.^[1]

Materials related to YSZ include calcia-, magnesia-, ceria- or alumina-stabilized zirconias, or partially stabilized zirconias (PSZ). Hafnia stabilized Zirconia is also known^{[citation needed]}.

Although 8-9 mol% YSZ is known to not be completely stabilized in the pure cubic YSZ phase up to temperatures above 1000 °C (Ref.^[2] and publications therein), commonly used abbreviations in conjunction with yttria-stabilized zirconia are:

Partly stabilized zirconia ZrO₂:
- PSZ - Partially Stabilized Zirconia
- TZP -Tetragonal Zirconia Polycrystal
- 4YSZ: with 4 mol-% Y₂O₃ partially Stabilized ZrO₂, Yttria Stabilized Zirconia
Fully stabilized zirconias ZrO₂:
- FSZ - Fully Stabilized Zirconia
- CSZ - Cubic Stabilized Zirconia
- 8YSZ - with 8 mol% Y₂O₃ Fully Stabilized ZrO₂
- 8YDZ - 8-9 mol% Y₂O₃-doped ZrO₂: owing the fact that the material is not completely stabilized and decomposes at high application temperatures, see paragraph next paragraphs^[2]^[3]^[4])

Thermal expansion coefficient

The thermal expansion coefficients depends on the modification of zirconia as follows:

Monoclinic: 7 · 10⁻⁶/K^[5]
Tetragonal: 12 · 10⁻⁶/K^[5]
Y₂O₃ stabilized: 10.5 · 10⁻⁶/K^[5]

Ionic conductivity of YSZ and its degradation

By the addition of yttria to pure zirconia (e.g., fully stabilized YSZ) Y³⁺ ions replace Zr⁴⁺ on the cationic sublattice. Thereby, oxygen vacancies are generated due to charge neutrality:^[6]

${\text{Y}}_{2}{\text{O}}_{3}\rightarrow 2{\text{Y}}_{\text{Zr}}^{'}+3{\text{O}}_{\text{O}}^{\text{x}}+{\text{V}}_{\text{O}}^{\bullet \bullet }$ with $[{\text{V}}_{\text{O}}^{\bullet \bullet }]={\frac {1}{2}}[{\text{Y}}_{\text{Zr}}^{'}]$ ,

meaning two Y³⁺ ions generate one vacancy on the anionic sublattice. This facilitates moderate conductivity of yttrium stabilized zirconia for O²⁻ ions (and thus electrical conductivity) at elevated and high temperature. This ability to conduct O²⁻ ions makes yttria-stabilized zirconia well suited for application as solid electrolye in solid oxide fuel cells.

For low dopant concentrations, the ionic conductivity of the stabilized zirconias increases with increasing Y₂O₃ content. It has a maximum around 8-9 mol% almost independent of the temperature (800-1200 °C).^[1]^[2] Unfortunately, 8-9 mol% YSZ (8YSZ, 8YDZ) also turned out to be situated in the 2-phase field (c+t) of the YSZ phase diagram at these temperatures, which causes the material's decomposition into Y-enriched and depleted regions on the nm-scale and, consequently, the electrical degradation during operation.^[3] The microstructural and chemical changes on the nm-scale are accompanied by the drastic decrease of the oxygen-ion conductivity of 8YSZ (degradation of 8YSZ) of about 40% at 950 °C within 2500 hrs.^[4] Traces of impurities like Ni, dissolved in the 8YSZ, e.g., due to fuel-cell fabrication, can have a severe impact on the decomposition rate (acceleration of inherent decomposition of the 8YSZ by orders of magnitude) such that the degradation of conductivity even becomes problematic at low operation temperatures in the range of 500-700 °C.^[7]

Nowadays, more complex ceramics like co-doped Zirconia (e.g., with Scandia, ...) are in use as solid electrolytes.

Applications

YSZ has a number of applications:

For its hardness and chemical inertness (e.g., tooth crowns).
As a refractory (e.g., in jet engines).
As a thermal barrier coating in gas turbines
As an electroceramic due to its ion-conducting properties (e.g., to determine oxygen content in exhaust gases, to measure pH in high-temperature water, in fuel cells).
Used in the production of a solid oxide fuel cell (SOFC). YSZ is used as the solid electrolyte, which enables oxygen ion conduction while blocking electronic conduction. In order to achieve sufficient ion conduction, an SOFC with a YSZ electrolyte must be operated at high temperatures (800 °C-1000 °C). While it is advantageous that YSZ retains mechanical robustness at those temperatures, the high temperature necessary is often a disadvantage of SOFCs. The high density of YSZ is also necessary in order to physically separate the gaseous fuel from oxygen, or else the electrochemical system would produce no electrical power.^[8]^[9]
For its hardness and optical properties in monocrystal form (see "cubic zirconia"), it is used as jewelry.
As a material for non-metallic knife blades, produced by Boker and Kyocera companies.
In water-based pastes for do-it-yourself ceramics and cements. These contain microscopic YSZ milled fibers or sub-micrometer particles, often with potassium silicate and zirconium acetate binders (at mildly acidic pH). The cementation occurs on removal of water. The resulting ceramic material is suitable for very high temperature applications.
YSZ doped with rare-earth materials can act as a thermographic phosphor and a luminescent material.^[10]
Historically used for glowing rods in Nernst lamps.
As a high precision alignment sleeve for optical fiber connector ferrules.^[11]

References

^ ^a ^b H. Yanagida, K. Koumoto, M. Miyayama, "The Chemistry of Ceramics", John Wiley & Sons, 1996. ISBN 0 471 95627 9.
^ ^a ^b ^c Butz, Benjamin (2011). Yttria-doped zirconia as solid electrolyte for fuel-cell applications : Fundamental aspects. Südwestdt. Verl. für Hochschulschr. ISBN 978-3-8381-1775-1.
^ ^a ^b Butz, B.; Schneider, R.; Gerthsen, D.; Schowalter, M.; Rosenauer, A. (1 October 2009). "Decomposition of 8.5 mol.% Y2O3-doped zirconia and its contribution to the degradation of ionic conductivity". Acta Materialia. 57 (18): 5480–5490. doi:10.1016/j.actamat.2009.07.045.
^ ^a ^b Butz, B.; Kruse, P.; Störmer, H.; Gerthsen, D.; Müller, A.; Weber, A.; Ivers-Tiffée, E. (1 December 2006). "Correlation between microstructure and degradation in conductivity for cubic Y2O3-doped ZrO2". Solid State Ionics. 177 (37–38): 3275–3284. doi:10.1016/j.ssi.2006.09.003.
^ ^a ^b ^c Matweb: CeramTec 848 Zirconia (ZrO₂) & Zirconium Oxide, Zirconia, ZrO₂
^ Hund, F (1951). "Anomale Mischkristalle im System ZrO2–Y2O3. Kristallbau der Nernst-Stifte". Zeitschrift für Elektrochemie und Angewandte Physikalische Chemie. 55: 363–366.
^ Butz, B.; Lefarth, A.; Störmer, H.; Utz, A.; Ivers-Tiffée, E.; Gerthsen, D. (25 April 2012). "Accelerated degradation of 8.5 mol% Y2O3-doped zirconia by dissolved Ni". Solid State Ionics. 214: 37–44. doi:10.1016/j.ssi.2012.02.023.
^ Minh, N.Q. (1993). "Ceramic Fuel-Cells". Journal of the American Ceramic Society. 76 (3): 563–588. doi:10.1111/j.1151-2916.1993.tb03645.x.
^ De Guire, Eileen (2003). "Solid Oxide Fuel Cells". CSA. {{cite journal}}: Cite journal requires |journal= (help)
^ American Ceramic Society (29 May 2009). Progress in Thermal Barrier Coatings. John Wiley and Sons. pp. 139–. ISBN 978-0-470-40838-4. Retrieved 23 October 2011.
^ http://www.diamond-fo.com/en/products_catalogue_details.asp?section=2&group=e2000&source=Assemblies&family=10101