Rare Earth Ce Research Articles

Effect of Rare Earth Ce on Structure and Properties in 7CrSiMnMoV Die Steel Castings

In this study, rare earth (RE) Ce is used to modify the interaction between atoms in 7CrSiMnMoV die steel castings. The tensile properties are performed, and strengthening mechanism are analyzed by investigated fracture surface, and microstructure by optical microscopy (OM) and scanning electron microscope‐energy dispersive spectrometer (SEM‐EDS). And ab initio molecular dynamics (AIMD) is used to simulate the effect of the Ce element on the local atomic structure of the FeCeC system alloy steel. The results indicate the strength can increase from 722.55 to 1074.27 MPa, and the elongation can increase from 24.86% to 44.22% with a RE Ce concentration of 0.009%. It is attributed to that doping of Ce can inhibit the formation of network eutectic cementite, refine the lamellar spacing of pearlite, and even form granular cementite and martensite structures. AIMD simulation results show that C atoms tend to be surrounded by Fe, and the strong chemical bonds of FeC make the Fe‐centered C more stable with an increase in RE Ce concentration. And doping Ce can introduce new local topological and chemical orderings such that the FeCFe triplets predominantly form small and big angles shifting from near 75° and 136° to 47° and 81°, respectively.

Effect of rare earth Ce treatment on the microstructure and properties of 430 ferritic stainless steel bearing Sn and Cu

The effects of rare earth Ce on purifying molten steel, modifying inclusions and micro-alloying in 430 ferritic stainless-steel bearings with Sn and Cu has been studied in this paper. The results demonstrate that Ce can purify molten steel, modify inclusions, enhance the mechanical properties and improve the pitting and corrosion resistance of the experimental steel. Ce effectively purifies the molten steel, reducing the total oxygen (T. O) content to as low as 0.00086 wt.% and sulphur (S) content to 0.0020 wt.%. The transformation of inclusions in the steel follows the sequence of MnS·Al2O3 → CeAlO3 → Ce2O2S → Ce2O3 with increasing Ce content. The number of inclusions initially decreases and then increases, with the experimental steel containing 0.012 wt.% Ce showing the best cleaning effect. Additionally, Ce treatment only slightly improves the mechanical properties of the experimental steel, but significantly enhances its pitting corrosion resistance and intergranular corrosion resistance by changing the enrichment state of carbides and impurity elements at the grain boundaries. In detail, Ce can partially inhibit the precipitation of M23C6 type carbides at grain boundaries, thereby improving the intergranular corrosion resistance of the experimental steel.

Characterization of L12-Al3Ce phase and its purification mechanism in the Al-Ce-TiCN alloy

Rare earth element Ce has a positive purifying effect on Fe and Si impurities in pure aluminum. In this study, we unveiled the mechanism of Ce purification of Fe and Si impurities in commercial pure aluminum at the atomic scale via utilizing the properties of TiCN nanoparticles, which exhibit distribution along grain boundaries and impede solute atom diffusion at specific cooling rates. The transition phase L12-Al3Ce was characterized in aluminum, which is considered to be an important transition phase to purified products. Furthermore, High Angle Dark Field Scanning Transmission Electron Microscopy (HADDF-STEM) and 3D Atom Probe Tomography (3D-APT) results showed that Ce could respectively enrich the Fe and Si impurities, resulting in the formation of Al-Ce-Fe and Al-Ce-Si clusters. Density functional theory (DFT) results indicated that Fe and Si atoms can incorporate into L12-Al3Ce crystal, forming more stable structures and therefore giving rise to the formation of Al-Ce-Si and Al-Ce-Fe nanoclusters. This study provides atomic-scale insights into the mechanism of Ce purifying Fe and Si impurities in aluminum.

Long-term open-pit mining activities at the world's largest light rare earth mine significantly affect light rare earth elements in road dust over long distances

The long-term effects of decades of open-pit mining at the Bayan Obo deposit, the world's largest light rare earth mine, on the concentrations of several elements in road dust over long distances are unknown. Here, bulk road dust (BRD) and resuspended road dust (RRD) were collected from different distances from the mine for subsequent analysis of mining impacts. As a result of mining activities, light rare earth elements (LREEs), especially La, Ce, Pr and Nd, show different statistical and spatial variations compared to other elements. These LREEs decrease with increasing distance from the mine, and the values found in RRD are higher than those in other particle sizes. Mining emissions and soil have the most significant influence on these LREEs compared to other factors. Spatially, these four LREEs changed significantly over a large area (up to 60km from the mine) due to mining emissions. However, long-term mining activities affect these elements mainly through mining-contaminated soil as opposed to mining emissions. This study confirms the significant impact of mining activities on LREEs in road dust via a comprehensive data-driven framework, emphasizing the significant environmental effects of long-term open pit mining.

Study on the effect of rare earth Ce on the modification of sulfide inclusions in U71Mn heavy rail steel

In this paper, the directional modification behavior of rare earth Ce on sulfide inclusions in steel is studied by thermodynamic calculation and experiment methods, and the mechanism of directional modification of rare earth Ce on sulfide inclusions in U71Mn heavy rail steel is proved. The results show that U71Mn heavy rail steel contained more large-sized inclusions and their distribution is more concentrated without the addition of rare earth Ce element. After the addition of rare earth Ce element, the average size of sulfur-containing inclusions in the steel decrease from 5.22 μm to 1.85 μm, and the number density of sulfur-containing inclusions in the steel increase from 83.65 mm-2 to 217.68 mm-2, indicating that the number of sulfur-containing inclusions in the steel increases after the addition of Ce element, and more small-sized sulfur-containing inclusions will form in the steel. The addition of rare earth Ce element can effectively reduce the existence of large-sized inclusions in the steel and modify large-sized inclusions into small-sized inclusions.

Effect of Trace Rare Earth Element Cerium (Ce) on Microstructure and Mechanical Properties of High Strength Marine Engineering Steel

In this paper, FH460 special steel with rare earth element cerium (Ce) was selected, and the control group without Ce was set up. By changing the content of Ce, the microstructure, phase transition point, and mechanical properties of the test steel were observed to study the effect of trace rare earth element Ce on the microstructure and mechanical properties of high-strength marine engineering steel. The morphology and energy spectrum of inclusions in three kinds of test steels were observed by SEM, and the morphological changes in inclusions in FH460 high-strength marine engineering steel after adding Ce were investigated. The fracture morphology and energy spectrum analysis were carried out by combining the tensile test at room temperature and the gradient low temperature impact toughness test, and the effect of trace Ce on the mechanical properties of the test steel was comprehensively analyzed. The results show that the addition of Ce changes the phase transformation temperature of Ac1 and Ac3, and refines the original microstructure of the test steel. SEM observation showed that the addition of Ce changed the long strip MnS and polygonal irregular Al2O3 inclusions into ellipsoids, which reduced the size of inclusions. The gradient low temperature impact test shows that with the decrease in temperature, the fracture dimple depth of the three test sheets of steel decreases, and the Ce-containing test steel forms a deep dimple centered on rare earth inclusions, which hinders the crack propagation and significantly improves the low temperature impact toughness of the test steel.

Study on the effect of rare earth elements La, Ce, Y and Sc doping on the mechanical properties of aluminum–lithium alloys

In this paper, the effects of rare earth elements La, Ce, Sc, and Y on the bond strength of the aluminum–lithium alloy δ’ (Al3Li)/Al interface are investigated using first-principles calculations. The results show that the interfacial energy decreases after substitutional doping of Al atoms on both sides of the interface by rare earth elements, respectively, with values ranging from −2.0664 eV/Å2 to −1.9720 eV/Å2. The interfacial energy decreased by 2.0841 eV/Å2 and 2.0709 eV/Å2 when Ce and Sc elements replaced Al in the matrix, respectively. Uniaxial interfacial tensile simulations of Al/ Al3Li showed that the strain elongation of the material increased from 24 % to 42 % for the pure interface after doping with Sc elements at the interface. The same tensile tests yielded a maximum elongation at break of 3.25 % for Al-Li alloy after artificial aging at 0.6 % Sc content. Observation of the microstructure of the materials before and after rare earth doping using TEM reveals that the content of nanoscale Al3(Sc, Li) composite particles increases with the increase of Sc content after artificial aging at 185 °C for 10 h. Moreover, the presence of Al3Sc refines the precipitated phase of the alloy and improves the plastic toughness of the material.

Superior performance of asymmetric supercapacitor based on Cu doped bismuth ferrite electrode

Electrochemical energy storage devices, like supercapacitors and batteries, are needed to meet the constantly increasing demands of portable energy devices. Many types of supercapacitor electrodes were synthesized and reported which include carbon-based materials, polymers, oxides and perovskites. In this work, we report on the fabrication of Cu doped bismuth ferrite (Cu-BiFeO3, Cu-BFO) nanoparticles via sol-gel procedure. In most of the doping cases the costly rare earth elements like La, Nd, Sm, Ce and Yb are used to replace Bi. Electrodes of Bi1-xCuxFeO3 where x have the values 0.0, 0.025, 0.05, 0.075, 0.1 and 0.15 were deposited on graphitic sheets. Optimum Cu doping value was found to be at x = 0.05. Cu2+ ions doping in place of Bi3+ ions will reveal the roles of oxygen vacancies, as determined from XPS. The estimated values of specific capacitance was found to be 732 F/g at 0.5 A/g for the electrode at x = 0.05 in three electrode system. 5%Cu-BFO//Carbon black asymmetric supercapacitor (ASC) device can be charged and discharged reversibly at cell voltage of 0.0 up to 1.5 V when using a 0.5 M Na2SO4 aqueous electrolyte. This configuration allows the ASC device to deliver a great energy density of 37.25 Wh/kg at a power density of 752 W/kg. The ASC device demonstrates excellent cycling stability, retaining 88.64 % of its initial specific capacitance after 5000 cycles. Increasing the Cu content up to 15 % causes instability in the crystal structure of BFO resulting on phase segregation into Bi2Fe4O9 along with BFO and deterioration in the electrode overall performance. XPS showed that replacement of Cu2+ in place of Bi3+ disturbs the neutrality and the chemical environment of the compound. Hence to achieve neutrality and ionic balance, oxygen vacancies increase and the Fe2+/Fe3+ ratio increases as well. Both oxygen vacancies and the change in the Fe ions ratio reduce electrochemical impedance and give rise to charge density. The homogenous distribution of the pores at x = 0.05 contributed greatly to its fast electrolyte ion diffusion that improved the observed capacitive properties. One has to mention here, that despite doping that contains ions with different ionic size and/or different oxidation state is unfavorable, to some extent, due to the changes they produce in the electronic structure and the chemical environment, nevertheless it is sometimes beneficial in creating new parameters in the structure that promote specific application like in the case of the current work, oxygen vacancies, increase in surface area and the mixed state valency.

(Ce, Nd) co-doped TiO2 NPs via hydrothermal route:Structural, optical, photocatalytic and thermal behavior

Rare earth (Ce, Nd) doped/co-doped titania (TiO2) nanoparticles were successfully produced by hydrothermal route. Titanium isopropoxide (IV), cerium nitrate hexahydrate and neodymium nitrate hexahydrate were utilized as raw/starting materials. The effect of Ce and Nd doping/co-doping in TiO2 were studied through different complementary tools such as XRD, FTIR, FE-SEM, EDX, XPS, UV–Visible, PL, photocatalytic and thermal analysis. XRD spectra revealed anatase tetragonal phase and cubic phase due to titania and ceria nanoparticles respectively. The crystallite size, lattice constants, volume and no. of unit cell were determined through XRD data. Optical studies revealed the band gap, urbach energy, extinction coefficient, refractive index, optical conductivity and photoluminescence emission wavelength. FTIR spectra investigated the chemical bondings and functional groups present in prepared samples. Optical absorption spectra confirmed that absorption edge is red shifted, indicating a decrease in band gap from 3.5 to 3.0 eV with the incorporation of rare earth ions (Ce, Nd) in TiO2 matrix. The rate of electron-hole pair recombination was reduced through co-doping of (Ce, Nd) in TiO2 lattice as exhibited by reduction in intensity of photo luminescence spectra. The photocatalytic efficiency was enhanced with the integration of rare earth metal ions in TiO2 matrix for different dyes such as rhodamine B (RhB) and malachite green (MG) with visible light irradiation. The degradation efficiency of (Ce, Nd) co-doped TiO2 NPs against RhB and MG dyes was found to be 89 and 95 % respectively. TGA analysis was carried out to find weight loss during different thermodynamic phases such as dehydration, decomposition and combustion, and crystallization. Various thermodynamic parameters such as activation energy, entropy and enthalpy were estimated by thermal analysis.

Effects of rare earth on nitriding microstructure and properties of a La-Ce micro-alloyed Q235RE steel

Accelerating nitriding is an interesting topic in chemical heat treatment of ferrous parts. In order to have a deeper understanding of the catalysis principles of rare earth in nitriding, a Q235 carbon steel and a Q235RE steel micro-alloyed with rare earth elements La and Ce were nitrided respectively by plasma nitriding and gas nitriding. The microstructure, phase constitution, and composition of the nitrided specimens were analyzed. The hardness profile of nitriding layer and the brittleness of surface compound layer were measured. The results demonstrate that the Q235RE specimens obtained a higher hardness and deeper effective hardening layer than the Q235 specimens without rare earth microalloying. The rare earth catalysis effects were presented as the acceleration of nitrogen diffusion and the inhibition of nitride precipitation in the diffusion layer of the Q235RE specimens. In addition, the surface compound layer of the Q235RE specimens showed higher toughness and better adhesion to the matrix than that of the Q235 specimens, which is considered to be strongly related to the rare earth elements diffused into the compound and the enhanced residual compressive stress in the layer.

Gas‐Sensing Properties of NO on Ce‐Doped Zinc Oxide: A DFT Study

AbstractOne of the most prevalent pollutants that pollute the environment is nitrogen oxide (NOx). NO and NO2 gases, which are hazardous to both human health and the environment, are included in NOx. The rare earth element Ce doped metal oxide semiconductor (MOS) ZnO is employed to reveal their NO gas sensing properties. Based on density functional theory (DFT) calculations, the optimized surface of ZnO (0001), Ce‐doped ZnO (0001), adsorbate structure of NO, and adsorbate NO on the modified ZnO (0001) surface are obtained. The gas sensing properties are examined through adsorption energy, Bader charge analysis, charge density difference (CDD), charge transfer, band structure, total density of state (DOS), and partial density of states (PDOS). For the Ce‐doped ZnO (0001) surface the NO adsorption energy is more negative than the bare ZnO. From the observation of Bader charge analysis, the charge transfer value increases from the substrate to adsorbate after doping with Ce, which indicates that the Ce‐doped ZnO (0001) surface is more favorable for NO gas sensing. Favorable electronic properties and suitable adsorption energy of Ce‐doped ZnO can be a potential gas sensor for NO molecule. The obtained DFT results are also compared with the existing experimental results.

Effect of rare earth Ce and Y on microstructure and viscosity of ZL114A alloy

To investigate the impact of rare earth on the fluidity of casting aluminum alloy during the filling process, the study measured the effects of rare earth (Ce, Y) content and the mischmetal (Ce / Y) on the viscosity of ZL114A alloy melt using a viscosimeter. The results show that for a single rare earth element, when the addition amount of Ce and Y is 0.4 wt%, the grain size and viscosity reach a minimum, with average grain sizes of 45.42μm and 43.54μm respectively, and the solidification range decreases by 4.23°C and 4.61°C respectively, with Y having a better effect than Ce; compared with the alloy without rare earth elements, the grain growth mode changes from independent nucleation to outward extension form. For mixed rare earth elements, the refinement effect is better than that of a single rare earth element, but the viscosity is higher. When the Ce/Y mass ratio is 1/3, the grain size and viscosity reach a minimum, with an average grain size of 40.75μm and a solidification range shortened by 8.92°C; when the proportion of Y is higher, the alloy shows better refinement of the microstructure and viscosity improvement. Rare earth elements have the potential to enhance the fluidity and solidification structure of ZL114A alloy. This study offers valuable technical insights for optimizing the casting process and mold design.

Rare earth induced lattice distortion of Bi2WO6 to effectively improve photocatalytic performance: Experimental and DFT calculations

The excellent visible light photocatalytic activity of bismuth-based photocatalysts has attracted the interest of many scholars at home and abroad. In this paper, rare earth (Sm, La, Ce, Eu) doped Bi2WO6 photocatalysts were prepared by a one-step hydrothermal method using bismuth nitrate and sodium tungstate as precursors. The microstructures and spectroscopic performances of prepared materials were investigated utilizing characterization methods, such as XRD, XPS, UV–vis, TEM, and N2 adsorption-desorption, etc., and the effluent removal performances were studied by using rhodamine B as a simulated degradation dye and the photodegradation mechanism was investigated in combination with DFT calculations. XRD indicates that the rare earth doping leads to the lattice distortion of the (131) crystal surface of Bi2WO6, and the relative amount of distortion is directly proportional to the photocatalytic activity; UV–vis spectra show that the absorption edge of Bi2WO6 is obviously red-shifted with the rare earth doping, and N2 adsorption-desorption curve show that the doped rare earths make the specific surface area of the sample effectively increased. Moreover, XPS spectrum suggests that the doped rare earth Ce and Eu often exist in the form of metastable oxidation states, and the transformation between Ce3+/Ce4+ and Eu2+/Eu3+ oxidation states is easy to form impurity energy levels between Bi2WO6, which make the energy level significantly enriched to broaden the absorption range and reduce band gap width of the material. DFT calculations further indicate that the rare earths successfully replace Bi sites. One of the main reasons for the improvement of photocatalytic activity is that rare earth doping is easier to replace Bi sites, leading to increased relative aberration; another one is that the arrangement of EVB and ECB in the photocatalytic mechanism is type-II, which contributes to red-shift of absorption edge and effective separation of electron-hole pairs in the photocatalytic process, thus improving the photocatalytic activity.

Investigation on the control of inclusions and tensile strength in Ce-treated P110-grade oil casing steel

This research added rare Earth elements Ce to the P110-grade oil casing steel to reveal their influence on the inclusions and tensile properties. The content of cerium in the steel varied from 0 to 452 ppm. Based on the classical thermodynamic calculation, the predominance diagram of Re-containing inclusions in P110-grade steel was obtained. The evolution route of the inclusions composition with the increasing cerium content in the steel was xCaO⋅yAl2O3 → Al2O3–CeAlO3 → Ce2O3–CeAlO3 → Ce2O3–Ce2O2S → Ce2O2S, which agreed well with the thermodynamic analysis. As the cerium content at 235 ppm, the size of Ce containing inclusions has a minimal size at 2.82 μm. Suitable Ce content can modify the big-size xCaO⋅yAl2O3 inclusions into small-size Re-containing inclusions. The results demonstrate that the tensile performance of this steel can be improved as the cerium content increases from 0 to 235 ppm. However, once the cerium content exceeds 235 ppm, further increases in cerium content led to a decline in performance. The experimental results shows that the presence of large-sized Ce2O2S inclusions and the change of microstructure, will lead to the decrease in tensile performance.

Determination of impurities in fertilizers purchased in Almaty (Kazakhstan)

Two solid (Double superphosphate and Phosphoric) and two liquid (Peat and Microfertilizer) fertilizers from Russia and Kazakhstan were evaluated with regard to macronutrients content (K, Ca), transition elements (Cr, Fe, Co, Zn, Hg), alkaline earth (Sr), semi-metals (As), rare earth elements (Ce, Eu, La, Nd, Sc, Sm, Tb, Yb) and Th and U. For analysis, the k0-INAA was used. For QA/QC purposes for k0-INAA the certified reference material BCR-320R channel sediment was used and irradiated together with the samples. The highest content of REEs was obtained in Double superphosphate, while in liquid fertilizers REEs were mostly below the limit of detection of the method used. Most elements in liquid organic fertilizers (Peat and Microfertilizer) were determined in insignificant level, except iron, which belongs to the essential micronutrients. The content of iron was at least 57 times higher in case of Peat fertilizer in comparison to Microfertilizer. Content of iron was higher in case of Phosphoric fertilizer than in Double superphosphate (about five times).

Construction of antimicrobial CeO2/Fe2O3 nanomaterials with enzyme-like activity and study of their mechanisms

This study employed rare earth element, Ce, and elemental Fe to prepare antimicrobial nanocomposites with enzyme-like activity. The materials were characterized by SEM, EDS, and XRD, as well as antimicrobial and drug resistance properties were tested. XPS analysis revealed a change in the valence state of Ce 3d in CeO2/Fe2O3 on addition of Fe. Furthermore, UV–vis spectral results showed that the band gap of the composite material decreased after composite formation. The creation of a heterogeneous structure was a significant factor responsible for enhancing the antimicrobial performance. The study analyzed the peroxidase (POD) activity of the materials using UV–vis spectroscopy. Results showed that the enzyme activity of the composites was significantly enhanced, compared to the individual materials. This enhancement combined with H2O2 to induce the production of ROS, resulted in a significant increase in the antimicrobial effect. The antimicrobial rate of the composite material exceeded 90 % at 250 µg/mL concentration. The antibacterial mechanism revealed that it primarily operated through synergistic effects of ROS, ionic dissolution, and damage by adsorption. It also had an apparent inhibitory effect on bacterial micro-organisms in water, which has wider application prospects.

Study of process parameters and deposition mechanism of composite co-deposited Cu/Co-Mo-Ce on aluminum alloy surface

The 6061‑aluminum alloy is most used in marine engineering equipment. We used composite co-deposition to prepare a Cu/Co-Mo-Ce alloy coating on the aluminum alloy surface, which not only solved problems related to the ready corrosion of aluminum alloy in marine environments and the difficulty of directly preparing protective coatings but also solved problems associated with the fact that CoMo alloy form many holes by introducing the rare earth Ce. An exploration of the plating process revealed that when the concentration of the other main salts was unchanged and the concentration of Ce3+ was 0.012 mol·L−1, the Cu/Co-Mo-Ce had the flattest morphology, and the best corrosion resistance. The coatings were characterized and analyzed using SEM, EDS, XRD, and XPS. Finally, the ions deposition processes were tested via cyclic voltammetry and chronoamperometry and AC impedance.

The influence of rare earth elements (Ce, La, Y, Nd, Gd) on the microstructure, electrochemical and antibacterial properties of Al-Zn-In-Mg-Ti sacrificial anodes

The influence of incorporating rare earth elements (Ce, La, Y, Nd, Gd) on the performance of Al-Zn-In-Mg-Ti sacrificial anode was investigated. The results demonstrated that the addition of RE has lowered the open circuit potential of Al-Zn-In-Mg-Ti anode, and enhanced its self-corrosion resistance and activation properties. With 2 wt% RE content, the average grain sizes of the sacrificial anodes were reduced to below 100μm, exhibiting conspicuous grain refinement, which fostered an increase in the current efficiency. The current efficiencies of the anodes containing Ce, La, Y, and Nd respectively surpassed 90 %. Furthermore, the anodes with RE showed remarkable antibacterial property.

Co/Ce-MOF-Derived Oxygen Electrode Bifunctional Catalyst for Rechargeable Zinc-Air Batteries.

Improving the practicality of rechargeable zinc-air batteries relies heavily on the development of oxygen electrode catalysts that are low-cost, durable, and highly efficient in performing dual functions. In the present study, a catalyst with atomic Ce and Co distribution on a nitrogen-doped carbon substrate was prepared by doping the rare earth elements Ce and Co into a metal-organic framework precursor. Rare earth element Ce, known for its unique structure and excellent oxygen affinity, was utilized to regulate the catalytic activity. The catalyst prepared in this study demonstrated an exceptional electrocatalytic performance. At a current density of 10 mA cm-2, the catalyst exhibited an overpotential of 340 mV for the oxygen evolution reaction (OER), which was lower than that of commercial IrO2 (370 mV), while achieving a half-wave potential of 0.79 V for the process of oxygen reduction reaction (ORR), exhibiting a similar level of effectiveness as commercially accessible Pt/C catalysts (0.8 V). The catalyst's porous structure, interconnected three-dimensional carbon network, and large specific surface area are the factors contributing to the significant improvement in catalytic performance. Furthermore, in comparison to commercial Pt/C+IrO2, the catalyst exhibited good cycling stability and high efficiency in rechargeable zinc-air batteries.

Improved piezoelectric and photoluminescence properties in Ce-doped PSN-PMN-PT piezoelectric ceramics by multiscale coordination

The large piezoelectric coefficient (d33) and high mechanical quality factor (Qm) are essential for piezoelectric ceramics used in high-power devices. It is pity that the two parameters are usually opposite, with higher d33 corresponding to lower Qm. In order to well-balance the d33 and Qm, the rare-earth element Ce with multi-valence was introduced into the 0.06 Pb(Sc1/2Nb1/2)O3-0.61 Pb(Mg1/3Nb2/3)O3-0.33PbTiO3 (xCe-PSN-PMN-PT) ceramics in this work. The structure, electrical properties and optical properties of ceramics were systematically analyzed. Optimal electrical performances (d33 = 719 pC/N, Qm = 256, and dielectric loss tanδ = 0.007) were obtained in 0.02Ce-PSN-PMN-PT ceramics. These excellent performances originate from the multiscale coordination effects among defect dipoles, local structural heterogeneity, domain structure, phase structure, and grain size. The xCe-PSN-PMN-PT ceramics exhibit excellent photoluminescence properties in the blue wavelength range. Our research provides a new paradigm for deep-sea electro-optical communication.