Ce Doping Research Articles

Effect of Ce and Sb doping on microstructure and thermal/mechanical properties of Sn-1.0Ag-0.5Cu lead-free solder

PurposeThe purpose of this study is to investigate the effects of Ce and Sb doping on the microstructure and thermal mechanical properties of Sn-1.0Ag-0.5Cu lead-free solder. The effects of 0.5%Sb and 0.07%Ce doping on microstructure, thermal properties and mechanical properties of Sn-1.0Ag-0.5Cu lead-free solder were investigated.Design/methodology/approachAccording to the mass ratio, the solder alloys were prepared from tin ingot, antimony ingot, silver ingot and copper ingot with purity of 99.99% at 400°C. X-ray diffractometer was adopted for phase analysis of the alloys. Optical microscopy, scanning electron microscopy and energy dispersive spectrometer were used to study the effect of the Sb and Ce doping on the microstructure of the solder. Then, the thermal characteristics of alloys were characterized by a differential scanning calorimeter (DSC). Finally, the ultimate tensile strength (UTS), elongation (EL.%) and yield strength (YS) of solder alloys were measured by tensile testing machine.FindingsWith the addition of Sb and Ce, the ß-Sn and intermetallic compounds of solders were refined and distributed more evenly. With the addition of Sb, the UTS, EL.% and YS of Sn-1.0Ag-0.5Cu increased by 15.3%, 46.8% and 16.5%, respectively. The EL.% of Sn-1.0Ag-0.5Cu increased by 56.5% due to Ce doping. When both Sb and Ce elements are added, the EL.% of Sn-1.0Ag-0.5Cu increased by 93.3%.Originality/valueThe addition of 0.5% Sb and 0.07% Ce can obtain better comprehensive performance, which provides a helpful reference for the development of Sn-Ag-Cu lead-free solder.

Magnetic properties and microstructure of Ce and Zr synergetic stabilizing Ti-lean SmFe12-based strip-casting flakes

Recently ThMn12-type samarium iron alloys have been promising materials for permanent magnets. Due to the high abundance and low cost, Ce as a possible stabilizer can be introduced into ThMn12-type alloys. The effect of Ce doping on the magnetic moment and phase stability in Ti-lean (Ce,Sm,Zr)(Fe,Co,Ti)12 compounds were predicted by the first-principles calculations. The CexSm0.8-xZr0.2(Fe0.8Co0.2)11.5Ti0.5 (x = 0–0.8) alloys with ThMn12 structure were produced by strip-casting into flakes by a wheel speed of 1.5 m/s and annealed at 1000 °C for 24 h. The Ce0.8Zr0.2(Fe0.8Co0.2)11.5Ti0.5 annealed flake shows a high saturation magnetization value of 13.6 kGs at room temperature. With the increase of Ce substitution in the annealed flakes, the content of α-(Fe,Co,Ti) phase decreases and the saturation magnetization increases. The 1:12 phase and the 1:9 phase have an orientation relationship that can be expressed as [0 0 –1]1:12//[100]1:9 and (020)1:12//(010)1:9. Besides, annealing process promotes the formation of 1:12 phase transformed from 1:9 phase. Coercivity is expected to be improved by obtaining uniform microstructure and suppressing the formation of soft α-(Fe,Co,Ti) phase in the ThMn12-based alloys.

Hydrothermal synthesis of Ce-doped SnS2 2D nanoplates with enhanced photocatalytic CO2 reduction performance

CO2 emissions caused by human activities seriously influence the climate of earth and hinder the sustainable development of humans and nature. Photocatalytic CO2 reduction is an effective method to convert CO2 into other chemicals and reduce CO2 emissions. Here, Ce doped SnS2 photocatalyst has been obtained by using a hydrothermal method. The phase and structure of obtained samples have been characterized and the photocatalytic CO2 reduction performance has been evaluated. The results show that Ce dopants can improve visible light absorption, increase the specific surface area, especially increase the adsorption of CO2. The influence of Ce doping concentration was investigated to optimize the photocatalytic performance. Compared to the pristine SnS2 photocatalyst, the Ce–SnS2 reached 46.9 μmol g−1 h−1 in the CO2 photo-reduced test, which is 3.21 times that of pristine SnS2 photocatalyst. The enhanced photocatalytic performance can be attributed to Ce dopant which increases the specific surface and CO2 absorption quantity, and reduces the recombination of photogenerated electrons and holes.

Enhancement of piezoelectric properties of CaBi2Nb2O9 ceramics by Ce doping and direct reaction sintering

CaBi2Nb2O9 (CBN) with the Aurivillius phase has a high Curie temperature (TC) and remarkable fatigue resistance, which has great potential for application as high-temperature sensors. However, due to its low piezoelectric properties, its practical application remains a great challenge. In this paper, Ca1-xCexBi2Nb2O9 ceramics were prepared by the direct reaction sintering (DRS) and conventional preparation (CP) methods, respectively. The experimental results indicate that Ce doping can increase the piezoelectric coefficient d33 of CBN ceramics by about two times. Among them, the grain size of the samples prepared by the DRS method is finer and more uniform, and the d33 value of DRS samples is about 3.6–9.4 % higher than that of CP samples. The DRS sample Ca0·97Ce0·03Bi2Nb2O9 has a d33 value of 18.9 pC/N, a TC of 948 °C, and a resistivity of 1.1 × 105 Ω cm at 600 °C. This study shows that DRS method is an effective densification method, which can prepare CBN-based ceramics with excellent comprehensive properties, and provides an innovative preparation route to explore CBN-based ceramics with excellent piezoelectric properties.

Insights in the phase stability and performance enhancement mechanism of La2(Zr1-xCex)2O7 with reduced thermal conductivity

This study proposes a molten salt method-based process for the synthesis of Ce-doped pyrochlore-phase La2(Zr1-xCex)2O7, aiming to develop materials with excellent comprehensive properties, particularly for thermal barrier coatings. The results indicate that by employing the proposed method, the Ce doping level (x) can reach 0.4 for pyrochlore-phase La2(Zr1-xCex)2O7. However, high-temperature testing reveals a reduction in the phase stability of the samples. As the value of x increases, the temperature at which the samples exhibit the fluorite phase gradually decreases. DFT calculations on the crystal formation energy of La2(Zr1-xCex)2O7 confirm that an elevated level of Ce doping leads to an increase in crystal formation energy, indicating a decrease in phase stability. Subsequent thermal conductivity tests on La2(Zr1-xCex)2O7, along with theoretical thermal conductivity fitting, reveal a significantly greater fitting error for Ce doping at the Zr site compared to La site doping with other rare earth elements. Finally, XPS and EPR tests conducted on the samples doped at the Zr and La sites confirm that oxygen vacancies induced by high Ce doping levels play a crucial role in reducting the thermal conductivity of La2(Zr1-xCex)2O7.

Regulation of photoelectric properties of multi-element (Sn, Fe, Ce) co-doped anatase TiO2: The first principles study

The energy band structure, density of states and optical properties of multi-element (Sn, Fe, Ce) co-doped anatase titanium dioxide have been calculated using the first principles method. The results show that two-element (Sn, Fe, Ce) doping affects the energy band structure more than the single doping behaviour. Co-doping of two of the three elements (Sn, Fe, Ce) reduced the energy band gap values of TiO2 compared to pure anatase TiO2.The forbidden bandwidths of Sn and Ce were smaller than those of mono-doped Sn, but the co-doped system had higher bandwidth narrowing than that of the mono-doped system. The co-doping of Sn and Ce is 0.206 eV smaller than the single doping of Sn, and the co-doping of Sn and Fe is 0.56 eV smaller than the single doping of Sn. The utilization of the regional light absorption is increased, and the absorption spectra are red-shifted. It can be seen that the co-doping method is more favourable to the improvement of visible light response and visible photocatalytic activity of TiO2 than the single doping method.

Ce-doped LaMnO3-δ perovskite as an efficient ozonation catalyst for the degradation of high-concentration phenol wastewater

In this study, a series of La1−xCexMnO3-δ (x = 0, 0.1, 0.3, 0.5, 0.7, 0.9, 1.0) perovskites with different Ce doping ratios were synthesized by the citrate sol-gel method for catalytic ozonation degradation of phenol at high concentration. Among them, the La0.9Ce0.1MnO3-δ catalyst showed the best catalytic performance, increasing COD removal nearly three times compared with ozonation alone. The COD removal of the catalysts was 0.1 > 0.3 > 0 > 0.5 > 0.7 > 0.9 > 1.0, which corresponded to COD removal of 67.56 %, 58.12 %, 57.94 %, 53.68 %, 52.18 %, 49.19 %, and 39.24 %, respectively. SEM, BET, and XRD characterized the structural performance of the catalysts. The two critical parameters of catalyst dosage and pH were also optimized. Simultaneous reproducibility experiments demonstrated the good reusability of the catalyst. In addition, the catalytic degradation mechanism was investigated by the qualitative and quantitative detection of free radicals, EPR, fluorescence detection, XPS and TPD/TPR tests, which indicated that the surface hydroxyl groups, oxygen vacancies, and Mn(Ⅲ)/Mn(Ⅳ) and Ce(Ⅲ)/Ce(Ⅳ) redox pairs on the surface of the catalysts were the potential active sites for the decomposition of ozone to ROSs. The doping of Ce can effectively increase the number of active sites and promote the electron cycling process, thus generating large amounts of •OH and O2-•, effectively mineralizing phenol.

Combined experimental and first principles look into (Ce, Mo) doped BiVO4

Here we investigated the effects of Ce and Mo doping on hydrothermally synthesized bismuth vanadate BiVO4 nanoparticles (NPs). The existence of monoclinic scheelite and tetragonal zircon phases of NPs was validated from Rietveld refinement of the powdered X-ray diffraction, room temperature Raman, and Fourier-transform infrared spectroscopy. The co-doping of Bi and V sites with respective Ce and Mo dopants in a mixed tetragonal zircon and monoclinic scheelite phases of BiVO4 lattice was corroborated from high-resolution transmission electron microscopy and X-ray photoelectron spectroscopy. The photoluminescence measurements revealed enhancement of photo-generated carrier recombination in (Ce, Mo) co-doped BiVO4 NPs which may have hampered its photocatalytic efficiency in degrading the methylene blue dye. The simulations based on Hubbard U corrected density functional theory (DFT+U) suggest that Mo and Ce co-doping introduced deep impurity states which may have facilitated the photo-generated carrier recombination detrimental to photocatalytic performance. The UV-vis diffuse reflectance measurements provided evidence for the presence of these defect states. In summary, this work may have presented a comprehensive experimental analysis of (Ce, Mo) doped BiVO4 supported by DFT simulations.

Bottom-Up Construction of Mesoporous Cerium-Doped Titania with Stably Dispersed Pt Nanocluster for Efficient Hydrogen Evolution.

Hydrogen generation is one of the crucial technologies to realize sustainable energy development, and the design of advanced catalysts with efficient interfacial sites and fast mass transfer is significant for hydrogen evolution. Herein, an in situ coassembly strategy was proposed to engineer a cerium-doped ordered mesoporous titanium oxide (mpCe/TiO2), of which the abundant oxygen vacancies (Ov) and highly exposed active pore walls contribute to good stability of ultrasmall Pt nanoclusters (NCs, ∼ 1.0 nm in diameter) anchored in the uniform mesopores (ca. 20 nm). Consequently, the tailored mpCe/TiO2 with 0.5 mol % Ce-doping-supported Pt NCs (Pt-mpCe/TiO2-0.5) exhibits superior H2 evolution performance toward the water-gas shift reaction with a 0.73 molH2·s-1·molPt-1 H2 evolution rate at 200 °C, which is almost 6-fold higher than the Pt-mpTiO2 (0.13 molH2·s-1·molPt-1 H2). Density functional theory calculations confirm that the structure of Ce-doped TiO2 with Ce coordinated to six O atoms by substituting Ti atoms is thermodynamically favorable without the deformation of Ti-O bonds. The Ov generated by the six O atom-coordinated Ce doping is highly active for H2O dissociation with an energy barrier of 2.18 eV, which is obviously lower than the 2.37 eV for the control TiO2. In comparison with TiO2, the resultant Ce/TiO2 support acts as a superior electron acceptor for Pt NCs and causes electron deficiency at the Pt/support interface with a 0.17 eV downshift of the Pt d-band center, showing extremely obvious electronic metal-support interaction (EMSI). As a result, abundant and hyperactive Ti3+-Ov(-Ce3+)-Ptδ+ interfacial sites are formed to significantly promote the generation of CO2 and H2 evolution. In addition, the stronger EMSI between Pt NCs and mpCe/TiO2-0.5 than that between Pt and mpTiO2 contributes to the superior self-enhanced catalytic performance during the cyclic test, where the CO conversion at 200 °C increases from 72% for the fresh catalyst to 99% for the used one. These findings reveal the subtle relationship between the mesoporous metal oxide-metal composite catalysts with unique chemical microenvironments and their catalytic performance, which is expected to inspire the design of efficient heterogeneous catalysts.

Effect of 0.3 at. % Ce on the corrosion resistance of Fe40Ni20Co20Cr20 high-entropy alloy in 3.5 wt% NaCl solution

The impact of trace Ce doping on the pitting behavior of Fe40Ni20Co20Cr20 high-entropy alloy in a 3.5 wt% NaCl solution was examined. The results indicate that the addition of trace Ce elements leads to a notable reduction in grain size and improved corrosion resistance of the alloy, the critical pitting potential of the alloy increased to 428 mv, and the corrosion resistance of the passivation film was significantly enhanced. This improvement can be mainly attributed to the strong surface activity of Ce, which promotes the formation of Cr2O3 in the passivation film, resulting in a more stable and protective film layer. The ΔE (difference between corrosion potential and zero charge potential) of the high-entropy alloys (HEAs) was negative, indicating a decrease in the adsorption capacity of the electrochemical interface for Cl−. This reduction helps to mitigate pitting corrosion on the surface of the passivation film caused by Cl− erosion.

The Cu/TiO2 adsorbent modified by Ce-doping removes trace phosphorus impurities from circular hydrogen of a polysilicon chemical vapor deposition furnace

There is an urgent need for efficient and cost-effective adsorbents for the removal of trace hydrogen phosphide (PH3) from the circular hydrogen systems in the polysilicon chemical vapor deposition furnaces. In this study, a straightforward and cost-effective method was used to synthesize a highly efficient adsorbent (Cex-Cuy/TiO2) for PH3 removal using TiO2 as the carrier and CuO as the active substance. Experimental findings demonstrated that optimal Ce doping amounts (nCu:nCe = 20:1) markedly enhanced the adsorbent's performance, with an adsorption capacity reaching as high as 149.14 mg g−1. Material characterization results indicated that Ce positively influenced the uniform dispersion of Cu on the TiO2 surface, and Ce doping increased the adsorbed oxygen content of the adsorbent, consequently enhancing its oxidation performance. The investigation of the reaction mechanism and causes of adsorbent deactivation revealed that the depletion of active substances (CuO) in the adsorbent and the accumulation of products such as Cu3P and phosphates are the primary factors contributing to its deactivation. Furthermore, high-temperature calcination could restore the activity of the adsorbent, indicating its great potential for engineering applications.

Balancing electron transfer and intermediate adsorption ability of metallic Ni-Fe-RE-P bifunctional catalysts via 4f-2p-3d electron interaction for enhanced water splitting

Balancing electron transfer and intermediate adsorption ability of bifunctional catalysts via tailoring electronic structures is crucial for green hydrogen production, while it still remains challenging due to lacking efficient strategies. Herein, one efficient and universal strategy is developed to greatly regulate electronic structures of the metallic Ni-Fe-P catalysts via in-situ introducing the rare earth (RE) atoms (Ni-Fe-RE-P, RE = La, Ce, Pr, and Nd). Accordingly, the as-prepared optimal Ni-Fe-Ce-P/CC self-supported bifunctional electrodes exhibited superior electrocatalytic activity and excellent stability with the low overpotentials of 247 and 331 mV at 100 mA cm−2 for HER and OER, respectively. In the assembled electrolyzer, the Ni-Fe-Ce-P/CC as bifunctional electrodes displayed low operation potential of 1.49 V to achieve a current density of 10 mA cm−2, and the catalytic performance can be maintained for 100 h. Experimental results combined with density functional theory (DFT) calculation reveal that Ce doping leads to electron decentralization and crystal structure distortion, which can tailor the band structures and d-band center of Ni-Fe-P, further increasing conductivity and optimizing intermediate adsorption energy. Our work not only proposes a valuable strategy to regulate the electron transfer and intermediate adsorption of electrocatalysts via RE atoms doping, but also provides a deep understanding of regulation mechanism of metallic electrocatalysts for enhanced water splitting.

Rare earth Ce-doped W-type barium ferrites for tunable electromagnetic waves absorption performance

W-type ferrites possessing low cost and high chemical stability, show high potential in electromagnetic wave (EMW) absorption field. However, due to the low dielectric loss, developing high EMW absorption performance of W-type ferrites remains desired. Here, rare earth (RE) cerium (Ce)-doped W-type barium ferrites (Ba1-yCeyNi2Fe15.4O27, y = 0.1, 0.2, 0.3, 0.4, 0.5, 0.6) are prepared by a sol-gel approach. The influences of Ce doping are detailed analyzed. Ce ions with unpaired 4f electrons and strong spin-orbit coupling of angular momentum enhance the dielectric and magnetic properties of ferrites. Ba0.7Ce0.3Ni2Fe15.4O27 achieves the minimum reflection loss (RLmin) value of -52 dB while Ba0.6Ce0.4Ni2Fe15.4O27 showcases the widest effective absorption bandwidth (EAB) of 1.36 GHz associated with the RLmin reaching -38 dB, significantly outperforming the undoped ferrites. This work thus demonstrates a high-efficiency utilization of Ce for enhancing the EMW absorption performance of widely employed W-type barium ferrites, efficiently advancing the application field of RE elements.

Ce-doping at Mn site to enhance resistive switching performance of spinel MnCo2O4 resistive random access memory devices

The spinel Ce-doping MnCo2O4 (MCO) thin films were fabricated on Pt/Ti/SiO2/Si substrates for resistive switching (RS) layer using sol-gel spin-coating deposition method. The Pt/Mn0.925Ce0.075Co2O4/Pt (Pt/7.5MCC/Pt) device exhibits stabler and superior bipolar RS performance, the concentrated distribution of Reset/Set voltage as low as – 0.62/1.175 V, good cycle endurance and excellent time retention capability. The improvement in the RS performance of the Pt/7.5MCC/Pt devices can be attributable to the effective limitation of the random formation and rupture of conductive filaments by appropriate Ce doping. The carrier transport mechanism of the device at high resistance state can be dominated by the Schottky emission, whereas the carrier transport mechanism at low resistance state consistent with the Ohmic conduction. This work provides a potential performance improvement approach to design the resistive memory devices for data storage applications.

Photothermal effect and antimicrobial properties of cerium-doped bioactive glasses

Cerium (Ce) ions exhibit multifunctional biological properties, such as anti-inflammatory, antioxidant, antimicrobial, and anticancer properties. Consequently, the development of Ce-containing biomaterials with therapeutic characteristics has received considerable research attention. In this study, Ce-doped 13–93 bioactive glass (Ce-BG) was prepared using the conventional melt-quenching method. The physical phases, surface morphologies, elemental contents, and elemental valence states of the samples were analysed. The concentration of the ions released from the samples in deionised water was determined, and their ability to induce hydroxyapatite was evaluated. The photothermal properties were tested by irradiating the samples with an 808 nm laser. The results indicate that an increase in the Ce content within a certain range did not affect the amorphous structure and morphology of the bioactive glass. Ce content variation affected the photothermal effect of Ce-BG. The wet state powder sample could be rapidly heated up to 58.24 °C under 2 W/cm2 laser irradiation at 5 mol% Ce doping, showing the best photothermal performance. Further, bacterial experiments demonstrated the good antimicrobial effect of this sample. Simulated body fluid immersion experiments revealed the ability of the Ce-BG to induce hydroxyapatite production. Furthermore, in vitro cell culture studies showed that the Ce-BG was not toxic to MC3T3-E1 cells and induced cell proliferation after 3 days. Therefore, Ce-BG is a promising bioactive material because of its favourable photothermal effects, antimicrobial properties, and biocompatibility.

Effect of Ce doping on electromagnetic characteristics and absorbing properties of M-type barium ferrite

In this study, Ce3+-doped M-type barium ferrite BaCexFe12-xO19 (x = 0 ∼ 1.2) was prepared by sol-gel method. The effects of Ce3+ doping on the crystal structure, microstructure, electromagnetic properties and absorption properties of M-type barium ferrites were investigated. The results indicate that the crystal structure remains unchanged with the increase of Ce3+ doping. The crystal size of Ce3+ doped barium ferrite is in the micro-meter range, and the grain size remains almost constant with increasing doping. The addition of Ce3+ to the BaFe12O19 samples resulted in significant improvements in their electromagnetic and microwave absorption properties. These improvements were mainly due to the synergistic effect of magnetic and dielectric losses. Among the samples doped with different concentrations of Ce3+, BaCe0.2Fe11.8O19 exhibited the best absorption performance, which has a minimum reflection loss of −58 dB and an effective absorption bandwidth of 9.44 GHz at a matched thickness of 2.3 mm. This study proposes an efficient electromagnetic wave absorber with a wider effective absorption bandwidth.

Structural, magnetic and dielectric properties of cerium-doped manganese – cobalt ferrite nanoparticles

Co0.50Mn0.50Ce xFe2− xO4 (with x = 0.000, 0.025, 0.050 and 0.100) nanoparticles were synthesised through sol–gel method. The crystallite size and lattice constant are increased from 30 to 50 nm and 8.375 to 8.384 Å, respectively, with increasing Ce content. It was found that Fe3+ cations migrate towards octahedral sites with Ce doping. The optical band gap was decreased from 1.79 to 1.50 eV whereas saturation magnetisation was decreased from 57 to 49 emu/g with increase in Ce substitution. Maximum dielectric constant and minimum dielectric loss, maximum AC conductivity along with moderate magnetic properties were observed for x = 0.050. So, x = 0.050 may be a potential candidate for electromagnetic interference shielding applications.

Enhanced efficiency and thermal performance of multistage gradient doping Ce:YAG transparent ceramics for laser lighting

The key to realizing the applications of ceramic based laser lighting devices depends on the heat management capability of color converters. In order to sufficiently absorb the blue light and smoothen the temperature gradient of luminescent ceramics, multistage gradient doping Ce3+:Y3Al5O12 (Ce:YAG) transparent ceramics (TCs) with five different concentrations were designed, including 0.01 at%, 0.05 at%, 0.1 at%, 0.2 at% and 0.4 at% Ce. The composite green bodies were prepared by aqueous tape casting and multistage gradient doping Ce:YAG TCs, with concentrations from low to high, were fabricated by vacuum sintering. The in-line transmission values at 800 nm of composite structure Ce:YAG TCs could reach 80.3%. Under 21.13 W/mm2 blue laser excitation, the gradient doping Ce:YAG TC (1.32 mm) realized a high luminous efficacy of 280.3 lm/W, which was 15.8% higher than that of 0.15 at% Ce:YAG TC (240.27 lm/W). Finally, during lighting process, the input-output temperature differences (Tin-Tout) between excitation surface and light-exit surface of 0.15 at% Ce:YAG TC was 5 ℃, while that in gradient doping TC reduced by 50% (2.5 ℃). The results indicate that the multistage gradient doping Ce:YAG TCs will be an interesting color converter for high-power and energy-saving laser-driven lighting.

Cerium doped dibismuthoxysulfide flowers for boosting CO2 photoreduction

Photocatalytic CO2 conversion is one of the major ways to simultaneously decelerate the greenhouse effect and the energy crisis. In this work, cerium doped dibismuthoxysulfide (Ce–Bi2O2S) photocatalysts were fabricated via a hydrothermal method, and the influence of Ce doping on their photocatalytic CO2 reduction was evaluated under simulated solar irradiation. It was found that Ce4+/Ce3+ ions were successfully incorporated into the crystal lattice of Bi2O2S. The Ce–Bi2O2S with CO and CH4 generation rates of 5.11 μmol/g/h and 1.41 μmol/g/h, which was more than 1.9 and 2.0 times greater than those obtained for pure Bi2O2S, respectively. The enhanced CO2 reduction performance of Ce–Bi2O2S is ascribed to the acceleration of the charge separation in the presence of Ce4+/Ce3+. Therefore, this work provides a promising direction for design high-active Ce doped bismuth-containing photocatalysts for solar fuel generation.

Ce-doping enhanced ORR kinetics and CO2 tolerance of Nd1-xCexBaCoFeO5+δ (x = 0–0.2) cathodes for solid oxide fuel cells

Addressing challenges in oxygen reduction efficiency and CO2 endurance is essential for advancing the electrochemical energy conversion performance of solid oxide fuel cells (SOFCs). This investigation introduces an innovative strategy by employing Ce doping to enhance the oxygen reduction kinetics and CO2 resistance of NdBaCoFeO5+δ (NBCF) cathodes. Ce doping effectively regulates the oxygen vacancy content, the ratio of Co3+/Co4+ and Fe3+/Fe4+ in NBCF, leading to substantial improvements in oxygen exchange, lattice diffusion, and charge transfer processes. Consequently, a significant enhancement in the oxygen reduction reaction catalytic activity and CO2 endurance is achieved. At 800 °C, the introduction of 10 mol% Ce doping results in a 65.3% reduction in Rp, reaching 0.024 Ω cm2. Simultaneously, the power density experiences a 50.8% enhancement, reaching 1.0 W cm−2. The current investigation presents a novel avenue towards the advancement of next-generation high-efficiency and stable cathode materials for SOFCs.