Abstract
Er-doped 0.91(K0.5Na0.5)NbO3–0.09Sr(Mg0.5Ta0.5)O3 transparent fluorescent ceramics were prepared according to the traditional solid-phase method. The (K0.5Na0.5)NbO3 (KNN) ceramics were modified by introducing the second group elements Sr(Mg0.5Ta0.5)O3 and the rare-earth ions Er3+. Transparent ceramics' structural, optical, and electrical characteristics as a result of the effects of Er3+, investigations were done using 0.91KNN–0.09SMT: y wt% Er. Results show that the representative 0.91KNN–0.09SMT: 0.1 wt% Er ceramics sample has a light transmittance of 60% in the near infrared (1000 nm) band, and the optical band gap (Eg) is found to be 2.62 eV. Phase structure analysis has revealed that the doping of Er3+ does not alter the structure of the ceramic's pseudo-cube phase. Er-doped KNN-SMT ceramics exhibit better up-conversion luminescence properties and also retain electrical properties. The Er3+ makes the doped ceramics have luminescence properties upconverting. With the increase of doping amount, the luminescence intensity of ceramics increases gradually at first and then decreases. Moreover, the ceramic also has some features for energy storage.
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1 Introduction
Ceramics that are transparent exhibit outstanding chemical, mechanical and thermal stability [1,2,3]. As technology developed, some materials, such as sapphire for IR Windows, YAG (Yttrium aluminum garnet) for lasers, PZN-PT, and PbZn1/3Nb2/3O3–PbTiO3 for photoelectric purposes, have been developed as single crystals [4, 5]. Technically speaking, these single crystals pose a challenge to manufacture, which is the main factor preventing their use in mass production, it's critical to develop low-cost processes for producing transparent ceramics with suitable mechanical and optical qualities [6, 7]. Transparent pulse capacitors, sensors, storage, and transparent electronic components are all applications for transparent ferroelectric ceramics, a type of photoelectric ceramic that has exceptional optical and electrical properties [8,9,10,11].
Lead zirconate titanate (PZT) and La-doped lead zirconate titanate (PLZT) are transparent ferroelectric ceramic materials, which are commonly used in transparent ferroelectric ceramics, have large piezoelectric constants, electromechanical coupling coefficients, and outstanding photoelectric performance [2, 12, 13]. However, the use of lead-based ferroelectric materials has been restricted or outlawed in many nations due to the dangers they pose to the environment and public health, as a result, lead-free ferroelectric materials have been the focus of studies on rare-earth luminescence [14, 15]. Due to their large Piezoelectric constant and high Critical temperature, lead zirconate titanate (PZT) ferroelectric materials have been replaced by (K, Na)NbO3 (KNN)-based ceramics, which have received extensive study as lead-free piezoelectric systems [16,17,18,19,20,21,22].
Potassium niobate K0.5Na0.5NbO3 (KNN) is the prototypical ferroelectric transition metal base material without lead, is a solid solution with an A1+B5+O32+ perovskite structure of KNbO3 ferroelectric and NaNbO3 antiferroelectric in a ratio of 1:1. The ferroelectric and piezoelectric capabilities of the KNN's ABO3-type structure are good [23, 24]. Divalent ion Doping can affect how ceramic grains form and improve density, modify the phase structure, and enhance the electrical properties of ceramic samples by doping Sr2+(R = 0.144 nm, CN = 12) in the A and B positions of the second component of KNN ceramics [1, 25, 26]. Doped Mg2+ can obviously improve the optical electric conductivity [27, 28], doping Ta5+ makes dense ceramic, ferroelectric, piezoelectric, improved [29]. In order to attain high transparency, ferroelectric ceramics can have their grain polished, their porosity decreased, and their density raised with the addition of rare-earth ions (Re3+) [30]. In Sr3YLi(PO4)3F ceramics, co-doping of Ho3+ and Eu3+ can create deep traps that enhance the color contrast, Eu3+ doped KNN can create a deeper trap, enabling it to get a quicker response time and higher contrast in the color rendering [31, 32]. It is well-known that rare-earth elements are added to piezoelectric materials to enhance their electrical characteristics. These substances can also be utilized in luminous materials as active ions. Since rare-earth elements like Pr, Er, Eu, and Ho-doped in KNN ceramics, they exhibit luminous qualities. Fluorescent transparent ceramics are fluorescent materials based on transparent ceramics that have been doped with various trace rare-earth elements to produce light that emits various colors when excited by light, primarily up-conversion (UC) and down-conversion (DC) luminescence [3, 33,34,35]. Under the excitation of lower energy long wave, the emission of higher energy short-wavelength light, with this property of materials are called up-conversion luminescent materials [36]. The up-conversion luminous materials provide high conversion efficiency, great absorption capacity, and stable physical and chemical properties [37, 38]. The choice of substrate material is very important, because the luminescence efficiency of up-conversion luminescent material is mainly affected by the crystal structure and anion of substrate material, and the coordination number, ion spacing and spatial structure position also affect the crystal structure [39]. The matrix of up-conversion luminescent materials is mainly sulfide, fluoride, halide, oxide and fluorine oxide materials. Among these, the oxide exhibits strong temperature resistance and, for the most part, relatively stable properties. When rare-earth oxides are properly doped, they can increase the luminous intensity of ceramics, and rare-earth ions' distinct energy level structures can provide optical characteristics [40]. The rare-earth doping type and lattice matching of the substrate material are also important. Appropriate radius of doped with rareearth ions also has the characteristics of the low phonon energy, lower phonon energy can improve the luminous efficiency. In conclusion, to improve luminescence characteristics to a greater extent, it is necessary to get closer to the rule of rare-earth doping [41]. Up-conversion luminescent materials have promising applications in optical disc technology, information processing, medical diagnosis, optical fiber amplifier and anti-counterfeiting.
Sr(Mg1/3Ta2/3)O3 (SMT), the second component's solid solution greatly slows down grain growth in this study's experiment, causing the ceramic sample's grains to expand to nanoscale size and significantly enhancing the ceramic sample's transmittance [42]. Appropriate addition of Er3+ can also improve the luminescence and electrical properties of transparent KNN-SMT ceramics, which can be efficiently applied to high performance multifunctional optoelectronic devices. The traditional solid-phase sintering procedure was used to prepare Er-doped 0.91KNN–0.09SMT transparent ceramics. Investigated were how Er3+ doping affected the ceramics' phase structure, transmittance, photoluminescence, and ferroelectric characteristics.
2 Experimental details
Using a traditional solid-phase approach, 0.91KNN–0.09SMT: y wt% Er (KNN–SMT: Er, y = 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8) was created. Anhydrous ethanol and ZrO2 beads were used as the ball-milling medium in tanks that were filled with the feedstock, including K2CO3 (99.5%), Na2CO3 (99.8%), Nb2O5 (99.99%), SrCO3 (99.9%), MgO (99.9%), Ta2O5 (99.9%), and Er2O3 (99.99%). To further mix the ingredients evenly, the powders were ball-milled for 12 h, calcined at 860 °C for 3 h, and then ball-milled again for 12 h to further mix the ingredients uniformly. Dried, thoroughly ground and sieved, to improve the fluidity of the powders, and then thoroughly agitated with polyvinyl alcohol with the mass fraction of 6 wt%. Once dried, completely ground and sieved, pressed into crude blanks of 12 mm diameter and 1 mm thickness under uniaxial pressure at 5 Mpa, and then maintained at 600 °C for 2 h to unload polyvinyl alcohol, and then sintered at 1170 °C for 3 h in order to fire the pellet body in the sintered ceramic sample, 0.3 mm of polishing was applied to the acquired samples.
X-ray diffractometer (XRD, D8 Advance, Bruker) determined the phases of the KNN-SMT: Er ceramics. The microstructure was viewed using a Field Emission scanning electron microscope (Quanta FEG-450, FEI Company, USA). UV–Vis spectrophotometer (UV-6100, Metash, China) measured the transmittance of light at 400–1000 nm from samples polished to a thickness of 0.3 mm. The ferroelectric system (TF Analyzer 2000HS, Germany) was used for testing of the hysteresis (P–E) buckles. Spectrophotometer (SENS-9000A, Zolix) conducted the measurement of fluorescence spectra under 980 nm excitation. The temperature-dependent dielectric properties were measured by a precision impedance analyzer (Agilent 4294A, USA).
3 Results and discussion
The optical transmittance spectra for Er-doped 0.91KNN–0.09SMT ceramics are displayed in Fig. 1a, ceramics Er-doped 0.91KNN–0.09SMT have a transparency of 44% to visible light (780 nm) and 60% to near infrared light (1000 nm) with an Er3+ doping concentration of 0.1 wt%, the ceramic has a extremely symmetric pseudo-cubic phase arrangement that renders it isotropic to light and lowers the quantity of light refraction at the grain frontiers. Er3+ doping changes the lattice of the ceramic, resulting in lattice expansion or contraction, affecting the symmetry of the ceramic structure. The interface reflection between the grains leads to serious loss of light intensity in the direction of light propagation. y = 0.6, the transmittance at 1000 nm is 40%; y > 0.8, the transmittance decreases to the minimum value, with the transmittance of 13% at 400 nm and 21% at 1000 nm. Therefore, the transmittance decreases with the increase of doping amount. In Fig. 1b shows the photographs of the ceramics (0.3 mm thickness), the lettering under the ceramics gradually blurs as the Er3+ content increases, which also indicates that the addition of rare-earth significantly reduces the transparency of the ceramics, especially when y > 0.6. The ceramic maintains its exceptional pellucidity despite the reduction in light transmission. Tauc equation can be used to determine the optical bandgap energy (Eg) from soaking up spectra, Eg is related to the absorption coefficient α as follows:
where h is Planck's constant and v is the frequency of the photon, the constant A. In addition, using the transmittance T, α can be determined as follows:
where t is the thickness of each tested sample [43].
Based on the ceramics' ability to transmit light illustrated in Fig. 1a, calculated and displayed in Fig. 2 is the Eg of Er-doped 0.91KNN–0.09SMT ceramics. The Eg of ceramics Er-doped 0.91KNN–0.09SMT is 2.62 eV, comparable to the pure KNN ceramic's Eg of 2.63 eV. However, when y = 0.8, the Eg is decreased to 2.29 eV. The ion substitution in 0.91KNN–0.09SMT ceramics doped with Er changes the electron occupancy state of the ceramics. Due to the increase of Er, the original equilibrium state is broken, and the energy band of ceramics also changes. The electron transition must take in sufficient energy. When the band gap is larger, some electrons will be blocked from the transition behavior, so more energy will be used for optical transmission, thus reducing optical loss. The lower Eg is more likely to transfer electrons from valence bands than the higher Eg, conversely, uses less energy for optical transportation, thus leading to the decline of the light transmission ability of ceramics. It can be seen that the Er3+ can change the ceramic band gap, and that the Eg lowers as the Er3+ doping level rises, deteriorating ceramics' ability to transmit light.
The XRD patterns of the Er-doped 0.91KNN–0.09SMT ceramics in the 2θ range of 20°–80°are displayed in Fig. 3a. Since the positions of all the peaks correspond to the standard map (PDF # 80-2497), and no impurity phases could be seen within the detection resolution of the XRD analyzer. As a result, it may be assumed that the dopant ions Er3+ have spread into the crystal lattices and created a solid solution that was stable with 0.91KNN-0.09SMT. The XRD patterns in the range of 45°–46.5° and Ta peaks above 60° were amplified to obtain greater peak details, as depicted in Fig. 3b and c, the fact that the diffraction peaks (200) and (220) do not split shows that the ceramics Er-doped 0.91KNN–0.09SMT preserves the pseudo-cubic phase's crystal structure.
In order to study the crystalline structure of the ceramics, the calculated lattice parameters of a, b, c, and the c/a ratio of the KNN–SMT: Er ceramics using the Jade 6.0 software package from the XRD data are provided in Table 1. When Er3+ (R = 0.089 nm, CN = 12) enters the lattice of 0.91KNN-0.09SMT ceramics, and the closest ion to it is Mg2+ (R = 0.072 nm, CN = 6), Ta5+ (R = 0.064 nm, CN = 6) and Nb5+ (R = 0.064 nm, CN = 6), the three ions undergo the swap and taking up the B-sites of the ceramic lattice, Er3+ has a slightly larger ionic radius, leading to the expansion of ceramic lattice, the diffraction peaks of XRD are shifted to a lower angle in the first instance. The amount of Mg2+ is minimal, and Ta5+ and Nb5+ will be substituted when the amount of Er3+ used for doping grows, the trivalent ions replace the pentavalent ions, increasing the anion gap, resulting in the shrinkage of the ceramic crystal lattice. Therefore, the Ta peak and (200) diffraction peak shift from low to high angle with the Er-doped.
To further investigate the effect of ion substitution in KNN-based crystals, Fig. 4a shows the Raman spectra of KNN–SMT: Er ceramics in the range of 100 to 900 cm−1 at room temperature. The Raman spectrum of KNN-based ceramics has 6 vibration modes: A1g, Eg, 2Flu, F2g and F2U [44]. Peaks below 200 cm−1 can be attributed to the translation mode of Na+/K+ cations and rotation of the NbO6 octahedron. The NbO6 octahedron F2u mode may also appear in this region, but its vibration is weak and almost flat with the baseline. The vibration mode F1u below 300 cm−1 can be identified as the vibration of A-site ions. When y = 0.1, Raman spectra within the range of 500–650 cm−1 can fit two peaks, namely A1g vibration mode near 612 cm−1 and Eg(v1) vibration mode near 555 cm−1, however, due to the increase of Er doping amount, the acromial 515 cm−1 on the left side of v1 began to protrude. In order to further study the changes in ceramic structure, the Gaussian fitting method was used to fit the peaks at 500–650 cm−1 in Fig. 4b. It can be seen that v1 shifted to the low wavenumber. With the increase of Er2+ doping, the ion spacing inside the NbO6 octahedron becomes longer and the interaction force decreases. When y = 0.6, the lattice cell volume reaches its maximum; when y > 0.6, v1 value increases, which is because Er2+ starts to replace cations, shortening ion spacing between NbO6 octahedrons, increasing bond energy, and strengthening ionic bond interaction. Figure 4c shows the Raman spectrum v1 peak shift and FWHM of KNN-SMT: Er ceramics with different Er doping amounts. FWHM is the half-peak width of v1. In KNN, the reduction of FWHM in v1 mode is due to the migration of NbO6 octahedron to low wavenumber, which weakens the interaction and effectively alleviates the lattice distortion. The characteristic peaks changed from flat at the beginning to sharp. Lattice defects caused by Er doping lead to the gradual sharpening of the two peaks on the left and right sides of v1. Also due to the increase of impurity caused by doping, the ceramics turned to asymmetric structure.
Figure 5 presents SEM images of the Er-doped 0.91KNN–0.09SMT ceramics. The grains of the Er-doped 0.91KNN–0.09SMT ceramics grew very firmly and with a good compactness, which is why they all have good transparency, according to the morphologies of the samples on the free surface. Doping before and after Er3+, the grain shape differentiation of ceramics is not obvious, ceramics' grain morphology is fuzzily defined, which is primarily cubic grain. If the ceramic is over-doped with Er3+, the growth of the grains is slowed, a few tiny erratic-shaped particles appear on the surface, the grain boundaries blur, and the density of the ceramic decreases due to the microstructure. Figure 6 shows the effect of Er3+ doping amount on ceramic density. The ceramic density measurement formula is shown according to Eq. (3):
m is the quality of the ceramic; \(h\) is the thickness and d is the diameter. When y = 0.1, the density is 4.03 g/cm3, and as the Er doping amount increases; the density is 3.73 g/cm3 when y = 0.8. It can be seen that when more and more Er is added, the density of ceramics becomes lower and lower, showing an obvious downward trend. The rationale is that adding heterogeneous Er prevents densification, which causes the density to drop and, as a result, the light transmittance to drop. Moreover, the presence of uneven particles and pores will lead to the intensification of the scattering characteristics of light through transparent ceramics, weakening the ability of the ceramic to transmit light. As the doping quantity of Er3+ increases, the grain size distribution of the ceramics becomes progressively more concentrated. Both over-sized and undersized grains have decreased. The overall trend can also be exhibited in the line in Fig. 7a–i. In Fig. 7i, it can be seen from the SEM photographs that the formation of ceramic grain was aided by the trace Er3+, where the average ceramic grain size increased from 0.174 to 0.193 μm from y = 0.2 to 0.3. In ceramics, sufficient Er3+ doping results in the emergence of widely spaced grain boundaries, which will impede grain growth. When y > 0.3, which decreases from 0.193 to 0.133 μm for KNN-SMT: Er. Due to the fact that the grain size is much lower than the visible light wavelength (400–900 nm), the optical transparency of the KNN–SMT: Er ceramic is greatly enhanced from y < 30% to y > 50%. In summary, the main factors contributing to the drop in the transmittance of ceramics are the establishment of more grain boundaries, the decline in density, and the continual reduction of grain size.
In Fig. 8a, the P-E hysteresis loops of KNN-SMT ceramics doped with different amounts of Er3+ obtained at the same electric field of 80 kV/cm. As can be seen, the electric hysteresis loop in the figure is characterized by "slender", which is consistent with the curve characteristics of relaxation ferroelectric materials and has high energy-storage efficiency. All Er-doped KNN-SMT ceramics exhibit P–E loops at saturation, it can be seen that after Er3+ doping, the ceramic P–E loops become narrower and it is seen that the rectangularity gradually decreases, indicating that Er3+ diminishes the ferroelectric property and enhances the relaxation property of the ceramics. Er3+ has the potential to fine-tune ceramic grains. Larger grain boundaries will restrict the mobility of domain walls, which also degrades the ceramics' ferroelectric properties. The maximum and residual polarization intensities Pm and Pr of ceramics continuously decrease as the amount of Er3+ doping increases. The fluctuation of ceramics' polarization intensity with increasing Er3+ doping levels is depicted in Fig. 8b. The graphic shows that the Pm and Pr both significantly dropped, the doping quantity rose from y = 0.1 to 0.2, causing the values of 16.4 C/cm2 and 2.89 C/cm2 to decrease to 12.6 C/cm2 and 1.54 C/cm2, respectively. Polarization gradually decreases and follows a similar changing trend after y ≥ 0.3. Figure 8a shows that the small coercive electric field Ec and the existence of polar nano regions makes the P–E loops became slimmer, because of the narrow P–E loops lead to less energy loss, which demonstrated the superior stability of energy-storage for KNN–SMT: Er ceramics. Using Eq. (4), it is possible to determine the ferroelectric ceramic's energy-storage density W based on the P–E hysteresis loops:
where P refers to the polarization and E to the electric field, following Eq. (5) can be used to calculate the recoverable energy-storage density Wrec:
Energy-storage efficiency η is another important measure for evaluating how well materials store energy, and it may be computed using Eq. (6):
The W and Wrec values of the KNN–SMT: Er ceramic samples are determined to be less than the critical failure strength using the P–E hysteresis loops of the KNN–SMT: Er ceramic samples as well as the equations stated above. Studying the energy-storage capabilities of ceramic samples with varying Er3+ doping contents [42]. Figure 8b was used to represent the energy-storage property of KNN–SMT: Er ceramic. As Er3+ is added, Wrec becomes more like the ceramic polarization change rule and has a general declining tendency, where Wrec and η are the energy-storage density and efficiency, while for y = 0.1 and 0.20, Wrec = 0.75 J/cm3, η = 68.9% and Wrec = 0.45 J/cm3, η = 71.4%, respectively. At y = 0.1, the KNN-SMT: Er ceramic's energy-storage density maximum value is attained, and when y = 0.2, the KNN-SMT: Er ceramic's efficiency maximum value is attained.
The KNN-SMT-Er curves measured at 1 kHz, 10 kHz, and 100 kHz, respectively, and the permittivity and dielectric loss as a function of temperature are shown in Fig. 9, with the test temperature ranging from ambient temperature to 500 °C, which shows the results of the experiment. The diagram shows that the ceramic dielectric peak Tm, which corresponds to the maximum dielectric constant εm, appears in the test temperature range. y = 0.1, Curie peak Tm = 36.9 °C, while the maximum εm to 1173, and the frequency dispersion, which is caused by the relaxation of ceramics. The position of Tm barely varies, which indicates that doping Er3+ has no discernible impact on the phase transition of ceramics and the phase transition temperature of various components is constant at roughly 46 °C, with more Er3+ doping, ceramics' maximum dielectric constant varies. Due to the modest quantity of doping, ceramics' dielectric constants tend to increase, with y = 0.2 and εm = 1539. When y > 0.3, the maximum dielectric constant continuously declines while the dielectric loss gradually rises. This phenomenon indicates that a large amount of Er3+ doping will weaken the dielectric characteristics of ceramics. Er3+ enters the lattice of KNN–SMT ceramics and replaces the ions at the B-site causing the ceramic lattice to expand. Subsequently, the stability of the octahedral structure of NbO6 is destroyed by the oxygen vacancy created during the substitution of Ta5+ and Nb5+, the ceramic's crystal lattice contracts, which eventually causes its maximum dielectric constant to drop as the quantity of Er3+ doping increases. The relationship between dielectric constant and temperature obeys the following formula:
where C is a constant; εm is the dielectric constant at Tm; ε is the dielectric constant at T > Tm; γ is the dispersion index, which describes the degree of dispersion of ferroelectrics at T > Tm. The γ value can be obtained by linear fitting [45].
The ceramics' dispersion index was determined, and the findings are depicted in Fig. 10 to help further examine the cause of the frequency spread of the ceramic dielectric constant. This figure draws the test frequency of 1 kHz scatter plot and fitting a straight line, the slope of the straight line is γ. With γ value to determine the relaxation ferroelectrics [46]. The ion doping level increases, which causes the ceramic sample's crystal structure to expand and contract, distorting the local lattice and causing the polar nanoregion to form. This results in the ceramic sample's evident relaxation behavior. According to the results of the fitting, Er-doped 0.91KNN–0.09SMT ceramics can be considered to be a relaxation ferroelectric because the dispersion index values fall within the range of typical relaxor ferroelectrics.
The up-conversion emission spectra of the ceramics at 980 nm excitation are shown in Fig. 11a, observe that the green and red emission bands are present in the spectrum, and that the brightness of the brilliant red peak is low, as can be seen in Fig. 11a after applying magnification. It is clear from Fig. 11b and the energy transition theory of ceramics up-conversion luminescence that the energy transitions of 4S3/2 → 4I15/2 and 4F9/2 → 4I15/2 are responsible for the emission peaks of ceramics at 550 nm and 655 nm, respectively. The emission peak shape of the ceramics remains unchanged, that is Stark splitting does not occur, indicating that the crystal field near Er3+ does not change during the phase transition of the ceramics. As the amount of Er3+ doping grows, the photoluminescence intensity of ceramics rises, then falls. As the degree of Er3+ doping is varied from y = 0.1 to 0.4, the light intensity of the ceramic samples between the two component dots increases. When y = 0.4, the emission intensity of green light of ceramic sample reaches the strongest, which is about 2 × 104, but the emission intensity of red light is still quite feeble at this point. Because the symmetry of the position of Er3+ in Er-doped 0.91KNN–0.09SMT ceramics has a significant impact on the luminescence intensity of ceramics [47]. When Er3+ replaces Mg2+, Ta5+ and Nb5+, progressively lost the symmetry of the crystal structure, so the luminous intensity of ceramics starting to wane at y > 0.4, even y = 0.7 or 0.8, the samples already have difficulty exhibiting a typical conversion emission peak. Furthermore, the up-conversion luminescence intensity of the ceramics is also affected by the crystal defects; the presence of a vacancy in the crystal can trap a photon, weakening the up-conversion emission intensity of the ceramic.
4 Conclusions
Using the traditional solid-phase approach to dope rare-earth Er3+ in KNN–SMT, up-conversion luminous transparent ferroelectric ceramics were created. The structure, transparency, up-conversion luminescence, and electrical characteristics of the ceramics are significantly impacted by Er3+ doping. With an increase in Er3+ doping, the transmittance considerably drops from y = 0.1 to y = 0.8, and at 1000 nm, it drops from 60 to 20%. The doping of Er3+ did not alter the ceramics' pseudo-cubic phase structure, which persisted when the maximum luminescence intensity of 2.0 × 104 was obtained at y = 0.4, but it did give the ceramics up-conversion luminescence features. When y = 0.1, Wrec = 0.75 J/cm3; when y = 0.2, η = 71.4%. Ceramics are relaxor ferroelectrics, it is a versatile optoelectronic material.
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This work is supported by the National Nature Science Foundation of China (61965007) and Guangxi Key Laboratory of Information Materials, (Guilin University of Electronic Technology), P. R. China (201007-Z).
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All authors jointly participated in the data collection and experimental program exploration. Data collection, analysis and initial manuscript were completed by first author: LW. Revision and refinement of the manuscript was performed by the corresponding author: HW and the manuscript was published with the consent of all authors.
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Wang, L., Wang, J., Liu, K. et al. Impact of Er addition on the electrical, optical, and transmittance characteristics of 0.91KNN–0.09SMT ferroelectric ceramics. J Mater Sci: Mater Electron 34, 1038 (2023). https://doi.org/10.1007/s10854-023-10455-1
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DOI: https://doi.org/10.1007/s10854-023-10455-1