Zirconia: More and More Translucent

Abstract
Purpose of Review Yttria-stabilized zirconium dioxide, 3 mol% Y-TZP (zirconia, 3Y-TZP) was introduced as a prosthetic material to provide metal-free, tooth-colored, and durable material option for the patients. However, its optical properties are not ideal. This review describes the diferent strategies to increase translucency of zirconia material and summarizes the current knowledge of translucent zirconia for fxed prosthodontic applications.
Recent Findings One of the most common ways of increasing the translucency of zirconia is to add the cubic phase by increasing Y₂O₃ content. Y₂O₃ 4Y mol% and Y₂O₃ 5Y mol% partially stabilized zirconia materials seem to have better optical properties compared to 3Y-TZP materials but with less favorable mechanical properties.
Summary Despite the attempts to develop a translucent zirconia material, its optical properties are still far from those of natural tooth structures. Possible solution for achieving more translucent and durable zirconia material could be utilizing nanocrystalline zirconia. The production of nanocrystalline zirconia is yet very technique-sensitive, and the sintering process needs to be well controlled. Additional research in this feld is needed before recommendation for clinical use. In the future, the challenge will be in achieving balance between improved translucency without sacrifcing from mechanical properties. This would apply not only for subtractive but also additively manufactured zirconia ceramics.
Keywords Zirconia · Translucency · Monolithic · Prosthodontics · Dental materials

Introduction

Dental materials used for restoring teeth attempt to imitate translucency and light refectance of natural tooth structure. Glass ceramic materials suit best for this purpose, as their optical properties resemble the ones of enamel and dentine ^[1]. However, the lower mechanical properties of glass ceramic-based materials limit their use in load-bearing areas of the mouth ^{[2, 3]}. Yttria-stabilized zirconium dioxide, 3 mol% Y-TZP (zirconia, 3Y-TZP) was introduced as a prosthetic material to provide metal-free, tooth-colored, and durable material option for the patients ^[4]. However, due to polycrystal material structure, zirconia has some optical restrictions.

Color and translucency are essential components in esthetic appearance of a tooth or a dental restoration. Human perception of color is based on the light emission and its transmission, absorption, and refection on the surface of an object ^[5]. Individual interpretation of a color as well as the material properties and surrounding conditions (illumination and light) play a role in perception and producing a color in dentistry.

Diferent Phases of Zirconia

Un-stabilized zirconia exists in three different phases, depending on the surrounding temperature: monoclinic (m) <1170 °C, tetragonal (t) 1170–2370 °C, and cubic (c) >2370 °C ^[6]. Monoclinic zirconia grains are 3–5% larger compared to tetragonal ones. When un-stabilized zirconia material cools down from >1170 °C, tetragonal grains are transformed into monoclinic where 3–5% volume expansion occurs. The sudden volume expansion causes cracks and defects in the material, decreasing mechanical strength of monoclinic zirconia. Tetragonal zirconia instead has better mechanical properties, although it does not exist as such at room temperature. By partially stabilizing the zirconia with 3 mol% of Y₂O₃ tetragonal zirconia can be maintained also at room temperature ^{[6, 7]}.

As a meta-stable material, tetragonal zirconia has ability to resist crack propagation up to certain extend. The stress caused by a crack induces t-m transformation at the crack tip, which leads to local volume expansion of 3–5%, and the compressive stresses are preventing the crack propagation ^{[6, 7]}. This phenomenon, called transformation toughening, is the basis of high mechanical properties of tetragonal zirconia. On the other hand, t-m transformation can also lead to detrimental changes on material surface which occur due to environmental stresses such as presence of water, body fuids, or steamed water ^[8]. This phenomenon, low-temperature degradation or aging, can be caused for example by steam pressure in autoclave. Due the efect of water steam, tetragonal grains on material surface turn into monoclinic, which is leading to sudden volume expansion and water penetration into the material ^{[9, 10]}.

Mechanical Properties of 3Y‑TZP

Zirconia is by far the strongest ceramic material for dental applications. Flexural strength of 3% mol yttria-stabilized zirconia (3Y-TZP) is high, varying from 900 to 1400 MPa ^[11–13] and fracture toughness from 7.4 to 11.5 MPa m^{1/2 [14–16]}. On the other hand, fexural strength of lithium disilicate-based glass ceramic materials is varying between 330 and 550 MPa and fracture toughness from 1.39 to 2.04 ^{[17, 18]}. However, it has been shown that fexural strength of lithium disilicate-based glass ceramic materials is higher after adhesive bonding ^[19].

3Y‑TZP as a Prosthetic Material

Dental zirconia is a polycrystal material, which does not contain any glass phase ^[1]. Therefore, it is very opaque and can be used mainly as framework material for dental crowns and FDPs. For esthetic purposes, the framework has to be veneered with feldspathic ceramic.

In clinical studies about 3Y-TZP material, minor amounts of 1.9–5.9% framework fractures of multiple-unit FDPs have been seen in 5 to 10 years of follow-up time ^[20–22]. Typically, the multi-unit FDPs fracture on the connector area, and the frameworks are therefore often designed bulky in order to achieve enough stability for the connector areas. Veneering ceramic seems to be clinically the weakest link of 3Y-TZP restorations. Several factors can afect to the chipping rate of veneering ceramic including non-anatomical framework design, thickness of the veneering ceramic, fast cooling phase during porcelain fring process, uneven heat distribution in zirconia material, and glass transition temperature and thermal expansion of veneering ceramic as well as roughness of the veneering ceramic after occlusal adjustments ^[23–28]. Minor and major ceramic chippings, varying from 12 to 32 %, are reported in clinical studies on teeth over 8- to 10-year follow-up time ^{[21, 29]} and up to 50% in implant-supported restorations in 10-year follow-up time ^[30]. Size of the restoration afects the reported chipping rate as well. Single crowns have shown lower chipping rates ^[21] compared to long-span multiple-unit FDPs, as in a 10-year randomized controlled clinical trial, 4- to 5-unit FDPs have shown higher chipping rates compared to 3-unit FDPs ^[29]. Figure 1 illustrates a fractured 3Y-TZP multipleunit FDP after 3.7 years of use.

Fig. 1 Clinical failure of 7-unit 3Y-TZP FDP with framework fracture (black arrow) and veneer chipping (white arrow) after 3.7 years of clinical use

In order to avoid the chipping of the veneering ceramic, more translucent zirconia materials were introduced ^{[31, 32•, 33]}. These materials can be used monolithic, without veneering ceramic. Figure 2 illustrates a monolithic implant crown made of 5Y-TZP material.

Fig. 2 Monolithic, highly polished 5Y-TZP implant crown

Color and Translucency in Dentistry

The relationship between the colors is defned by Munsell color space ^[34]. The Munsell color space consists of three diferent parameters: hue, chroma, and value. Hue is defned as a color shade; value is describing lightness/brightness of a color shade; and chroma is the intensity of the color shade. When white light is passing through a prism, each hue of visible light range has diferent wave length, varying from 400 nm for violet to 700 nm for red color ^[35]. When white light is interacting with an object, some of the wavelengths are absorbed and some refected. The refected wavelengths produce the visual color. Hence, certain object can appear in diferent colors when diferent light sources are used. In human eye, more precise in the retina, cone and rod cells register the light and send to the brain signals, which will be interpreted as colors ^[36].

Numerical values of color can be calculated by using CIELAB color space. The International Commission on Illumination (CIE) has defined a system where values given by spectrophotometric device can be translated into color parameters of L*, a*, and b* ^[37]. L* applies to lightness of an object, a* to a hue scale of red to green, and b* to a hue scale of yellow to blue. Using the CIELAB color space enables comparison of different materials and objects in terms of color and appearance. However, the results of the CIELAB color space can be difficult to interpret in a clinical environment. CIEDE2000 color difference formula was therefore introduced for better correlation with visual inspection ^{[38, 39]}. In CIEDE2000 system, the total color difference (△E₀₀) is calculated from lightness (L), chroma (C), and hue (H). The system has also thresholds for visual perceptibility (△E₀₀=0.8) and acceptability (△E₀₀=1.8), which is functioning as a quality control tool for clinical assessments.

A recent in vitro study was comparing the color of anterior monolithic (ML) and veneered zirconia crowns ^[40]. The veneered crowns were fabricated with cutback technique and layered with either enamel layering material (bilayer, BL) or enamel and dentine layering materials (tri-layer, TL). The CIE L*a*b* values of the crowns (n=5) were measured with spectrophotometer, and the color diferences were calculated with CIEDE2000 formula. The lowest color diferences were seen on BL and TL crowns compared to ML in cervical and middle areas of the crowns. In all crown types, the cervical and middle areas were mostly under the visual perceptibility level (△E₀₀≤0.8).

Light refraction, dispersion, transmission, and absorption afect to the optical behavior and color appearance of each object. Translucency describes the extent to which light is transmitted through the object instead of being absorbed or refected ^[35]. Translucency can be evaluated by contrast ratio (CR), translucency parameter (TP), and refractory index (RI). CR is measured by evaluating the ratio of refectance of a specimen placed on a black background compared to a white background ^[41], whereas TP represents a color diference of a specimen placed on a black background compared to a white background ^[42]. Higher the TP value means higher translucency value. Materials with TP values ≤ 2 are considered opaque, while they are blocking black background ^[43].

Thickness of the material afects directly the translucency parameter (TP) of the zirconia materials. TP values of diferent generation zirconia materials in an in vitro study varied between 16.59–20.40 for 0.5-mm-thick specimens to 5.10–9.17 for 2.0-mm-thick specimens, showing that the thinner the material, the more translucent it is ^[44]. For 1-mm-thick specimens, TP values were varying between 11.16 and 15.82, whereas the previously reported TP value is 18.7 1-mm-thick enamel and 16.4 for 1 mm dentin ^[45].

The contrast ratio is known to decrease by increasing translucency ^[44]. The contrast ratio value 0 is considered translucent and a value of 1 as fully opaque ^[46]. The efect of sintering temperature to contrast ratio (CR) was investigated in an in vitro study ^[47]. CR values were measured on specimens sintered in 9 different temperatures from 1300 to 1700 °C. CR was varying from 0.85 for 1300 °C to 0.68 for 1700 °C diferences being statistically signifcant. In other words, CR was decreasing by increasing sintering temperature.

Refractive index (RI) defnes how much the path of light is refracted when entering a material. It depends on diferent wavelengths of light and interaction of light in diferent interfaces (grain/grain vs grain/pore) ^{[48, 49]}. 3Y-TZP material has higher RI than other ceramic materials, meaning that the material has high surface refection and low light transmission ^[49].

Strategies to Increase Translucency in Zirconia Material

There are several methods to increase the translucency of zirconia material. It is possible to modify the material structure by changing the sintering protocol and amount and type of dopants, leading to less light refraction and scattering from the material structure.

During the development of translucent zirconia, modifying 3Y-TZP microstructure was considered as one of the frst actions. Zirconia was made more translucent trying by increasing material density by eliminating the pores ^{[48, 50]}. The large diference in refractive index between the pores and zirconia material is causing the light scattering by the porosity and generating opaque optical appearance.

For the frst-generation zirconia materials, alumina was used as sintering aid (3mol% of Y₂O₃ and 0.25 wt% Al₂O₃), which additionally stabilized the material and made it more resistant to low-temperature degradation ^[48]. However, alumina dopant was making the material look opaquer. By decreasing the alumina content as well as adding other dopants like lanthanum oxide, the material translucency could be improved ^[51]. The optimal level of Al₂O₃ dopant used in more translucent generations of 3Y-TZP is <0.25 wt%, providing higher density and better translucency ^[51]. Other suggested dopants are lanthanum oxide La₂O₃, magnesium oxide MgO, and neodymium oxide Nd₂O₃ ^[52]. From diferent dopants, the Al³⁺, La³⁺, Mg²⁺, and Nd³⁺ cations are segregated to the grain boundaries providing hydrothermal stability. Dopants seem to have efect to grain size, since 3Y-TZP materials doped with diferent concentrations of Al₂O₃ only showed larger grain size than 3Y-TZP materials doped with Al₂O₃ and La₂O₃ ^[51]. When yttria content was increased to 5 mol% (5Y-TZP with 0.05 wt% Al₂O₃), the grain size was signifcantly larger. However, in the market, mainly Al₂O₃ doped zirconia materials have been available.

Other option for increasing translucency of zirconia is to increase the grain size. The larger the grains, the less light refection and scattering there will be from grain boundaries, leading to higher translucency ^{[48, 53, 54]}. Larger grain size can be achieved by increasing sintering time and temperature ^{[11, 47]}. Decreasing the grain size would also provide more translucent zirconia material. Also, in nanocrystalline structure, the translucency is dependent on grain size and thickness. Zhang was estimating in his study that for optimal translucency, 1.3 mm thick specimen would need a grain size of 82 nm, and 2 mm thick specimen would need a grain size of 70 nm ^[48]. Nanocrystalline structure could be a perfect solution for achieving a zirconia material with high translucency and high mechanical properties. However, the production process is still inaccurate resulting to defects and porosities.

Adding the amount of cubic phase by increasing yttria content is commonly used way of making zirconia more translucent ^{[55, 56]}. Cubic zirconia is optical isotropic, and therefore, light scattering at the grain boundaries is not seen ^{[51, 52]}. On the contrary, tetragonal zirconia is anisotropic in crystallographic directions (i.e., in optical properties tetragonal zirconia grains are birefringent) ^[55]. When the adjoining tetragonal grains do not have same crystallographic orientation, refractory index shows discontinuity at the grain boundaries leading to reductions in light transmittance and more opaque appearance.

There are several translucent zirconia materials with varying yttria content, most commonly 4 mol % and 5 mol% partially stabilized Y-TZP and 8 mol% fully yttria-stabilized 
zirconia (YSZ) ^{[48, 57, 58]}.

Graded zirconia was introduced more than a decade ago for making the optical and adhesive properties of 3Y-TZP better ^[31]. Glass powder composition was infltrated on 3Y-TZP surface, creating a structure where outer surface of an object had more esthetic layer, dense 3Y-TZP layer in the middle and inner glass layer for adhesive bonding. Specimens (thickness 1.4mm) with graded structure showed promising results in terms of critical load for radial cracking (1990 N) compared to monolithic specimens (1388 N). However, the method might be technique-sensitive and time-consuming, and the scientifc evidence is still scarce.

Finally, one of the more modern options for achieving better optical and esthetic outcomes is to combine layers of different Y₂O₃ mol% zirconia material (i.e., different translucency) as a multi-layered zirconia block/puck. The layers have different contents and pigment types, which leads to natural shade ^[59]. When fabricating a restoration with computer-aided design/computer-aided manufacturing (CAD/CAM) methods, the restoration is milled in such a way that the more translucent layer of zirconia is situated on the incisal edge of the restoration. A recent in vitro study was showing that there was no difference in translucency between the multi-layered 5 Y₂O₃ mol% and 4 Y₂O₃ mol% zirconia blocks ^[59]. However, another in vitro study was showing that fracture resistance of crown-shaped specimens was lower for multi-layered materials compared to conventional 3Y- and 4Y-TZP materials ^[60].

Efect of Dopants to 3Y‑TZP Material Properties

Zhang and co-workers were testing 3Y-TZP materials with diferent microstructure, and it could be seen that adding 0.25 wt% Al₂O₃ and 0.2 wt% La₂O₃ as a co-dopant resulted in higher amount of c-ZrO₂ compared to 3Y-TZP material doped with 0.25 wt% Al₂O₃ only ^[51]. Similar signifcant diference could also be seen in TP of these materials, 3Y-TZP 0.25 wt% Al₂O₃, and 0.2 wt% La₂O₃ being more translucent and having lower CR. By manipulating the grain boundaries with co-dopants, good long-term hydrothermal stability and higher mechanical properties could be achieved ^[52].

Mechanically, the bending strength was higher for 3Y-0.25Al specimens (997 MPa, SD 202) compared to 3Y-0.25Al-0.2La specimens (651 Mpa, SD 77). However, there were no diferences between 3Y-0.25Al-0.2La specimens and other specimens doped with diferent concentrations of La₂O₃ and Al₂O₃ ^[51].

Consequences of Making Zirconia Translucent

Changing the yttria content of zirconia material can have effect to several material properties. Additionally, when more c-phase is present, yttria is concentrated on tetragonal grains. Cubic zirconia is more brittle, and tetragonal zirconia has lower ability to transformation toughening, leading to lower mechanical properties ^[61].

Various in vitro studies show diferences in mechanical properties between diferent Y₂O₃ mol% zirconia materials with tendency to lower mechanical strength when increasing Y₂O₃ mol% and translucency ^{[32•, 57, 62–65]}. Flexural strength, fracture toughness, TP and CR values for diferent generations of zirconia are summarized in Table 1. The possible explanation for decrease in mechanical properties lies in the phase content of zirconia material, since c-phase does not seem to have as high mechanical properties as t-phase.

Table 1 Flexural strength, fracture toughness, translucency parameter and contrast ratio of diferent zirconia generations

Same trend has also been seen in crown-shaped specimens. An in vitro study about implant crowns made of diferent generations of zirconia materials was showing that the fully stabilized (Y₂O₃ 8 mol%) zirconia crowns connected directly to the implant exhibited signifcantly lower fracture load values (140 N) compared to partially stabilized (Y₂O₃ 3 mol%) translucent zirconia crowns connected directly to implant (259 N) and partially stabilized (Y₂O₃ 3 mol%) translucent zirconia crowns connected with titanium base to implant (453 N) ^[75].

Previous in vitro studies show that the airborne particle abrasion increases the flexural strength of 3Y-TZP material ^{[76, 77]}. This is based on the t-m phase transformation-induced volume expansion on material surface, creating compressive stresses ^[77]. Another in vitro study comparing different generations of zirconia was showing that airborne particle abrasion was increasing the flexural strength of partially stabilized Y₂O₃ 3 mol% opaque and Y₂O₃ 3 mol% translucent zirconia but decreasing the flexural strength of fully stabilized Y₂O₃ 8 mol% zirconia ^[57]. The authors attributed the lower mechanical properties of Y₂O₃ 8 mol% zirconia are related to the high c-phase content and lower t-phase content of the material. When less t-grains are present, also less transformation toughening occurs. On the other hand, a study by Chevalier and co-workers demonstrated that the presence of cubic grains tend to reduce the material resistance to low-temperature degradation ^[78]. Yttrium stabilizer ions seem to enrich the cubic grains, while the adjacent tetragonal grains are less stable, and therefore, more t-m phase transformation takes place. This does not apply to longer sintering times or higher sintering temperatures but to aging conditions like moist environment.

The microstructure and phase content of zirconia material seem to have an impact on bond strength as well. Microtensile bond strength of airborne particleabraded conventional zirconia (3 mol% Y₂O₃) was shown to be significantly higher (20.86 Mpa, SD 5.12) than that of airborne particle-abraded translucent zirconia (5 mol% Y₂O₃) (16.39 Mpa, SD 4.36) ^[79]. This could be also related to the higher number of cubic grains in the material.

Micro‑layering, Staining, and Glazing

Despite attempts to develop a translucent zirconia material, its optical properties are still far from those of natural tooth structures. Possible solution for overcoming the translucency mismatch between zirconia material and natural dental structures and to avoid extensive veneering ceramic chippings could be micro-layering of the esthetic (buccal) surfaces of dental restorations ^[80]. In micro-layering workflow, zirconia framework is fabricated from translucent material block with no or very minimal cutback and veneered with <0.5-mm-thin ceramic layer which consist of fine-ground ceramic particles and a viscose liquid. Although in thin layer, the felspathic ceramic forms a three-dimensional network with natural looking depth effect as well as translucent, fluorescent, and opalescent optical properties. However, scientific evidence of micro-layering method is still lacking, and the potential risk of veneer chipping cannot be excluded at this point.

More natural looking appearance and depth effect can also be achieved by staining and glazing the zirconia framework. Staining of green-stage 3Y-TZP opaque zirconia might weaken the material’s mechanical properties ^[81]. In an in vitro study, staining was performed by dipping the specimens into the coloring liquid, and the increasing staining time was negatively afecting to fexural strength ^[81]. Similar efect was seen with 3Y-TZP translucent zirconia specimens stained by painting the surface with a brush ^[82], while increased fexural strength and decreased translucency parameter values were seen in specimens fabricated from 8 mol% fully yttria-stabilized zirconia. The diferences between diferent zirconia materials might be due to the material content and the amount of cubic zirconia present. Additionally, it has been shown that tension forces might cause delamination of the glazing layer on disc-shaped specimens ^[83]. However, clinically, this has not been reported so far, and it might not be a relevant problem.

Conclusions and Future Perspectives

When developing monolithic zirconia materials, more translucent nanocrystalline structures seem to be promising option ^[48]. They would provide substantial improvements in translucency while preserving strength properties. However, it seems to be difcult to produce well-dispersed homogenous starting powder containing controlled concentrations of stabilizing additives ^[84••]. Additional challenge is to avoid excessive grain growth and porosities during sintering process. The problems with producing methods remain to be solved by scientists in the future. Other possible options for developing more translucent and durable zirconia materials are further optimizing of the sintering process, grain size, and addition of diferent dopants.

The development of translucent zirconia materials continues, and new challenge will be in achieving the balance between improved translucency without sacrificing from mechanical properties. This would apply not only for subtractive but also additively manufactured zirconia ceramics ^[85–88].

References: Omitted