Formation Of Oxygen Vacancies Research Articles

Mechanistic insights into the roles of copper in enhanced peroxymonosulfate activation for tetracycline degradation by copper ferrite composite catalyst

Tetracycline (TC) pollution has attracted great attention due to its wide use, non-biodegradability and potential carcinogenicity. Bimetallic catalysts/peroxymonosulfate (PMS) systems have been considered as powerful technologies for TC degradation. Although the excellent catalytic activity of copper ferrite (CuFe2O4) composite oxides for PMS has been already elucidated, the roles of increased Cu in the degradation especially from non-radical pathways are not clarified clearly. In this study, we prepared a series of CuO/CuFe2O4/Fe2O3 (CCF) catalysts to confirm the key role of molar ratios of Cu: Fe (ranging from 1:2 to 2:1) in the enhanced degradation. The optimized CCF-3 catalyst with the Cu: Fe molar ratio of 2:1 showed the best degradation efficiency up to 95.6 % and the fastest apparent degradation rate of 0.135 min−1 towards TC. In addition, the CCF-3/PMS system showed excellent adaptability and good stability in TC degradation. Importantly, a novel molecular-scale mechanism was proposed. Both radical (SO4∙-, ∙OH, O2∙ –) and non-radical (1O2, direct electron transfer) pathways were associated with the CCF-3/PMS catalytic system, where 1O2 played the dominant roles. The increased Cu significantly boosted the non-radical pathways via promoting the formation of oxygen vacancies (Ov) and its further conversion to 1O2, and facilitating electron transfer between bimetallic Cu/Fe interface. This work provides a deep insight into the formation and reaction mechanisms of non-radical species for CCF/PMS systems, and a novel foundation for the design of CuFe2O4 composite catalysts

Developing advanced oxygen electrodes for reversible protonic ceramic electrochemical cells via controlled bismuth doping on diverse perovskite lattice positions

The development of reversible protonic ceramic electrochemical cells (R-PCECs) is hampered by insufficient oxygen electrode activity. This study addresses this challenge by introducing bismuth (Bi) into different lattice sites (A-site, B-site, or both) of Ba(Co0.7Fe0.3)0.85Ta0.15O3-δ (BCFT) to develop novel oxygen electrode materials. Extensive characterizations and density functional theory calculations demonstrate that introducing Bi onto the B-site promotes oxygen vacancy formation and hydration, facilitates proton transportation and improves oxygen exchange ability, leading to the enhanced catalytic activity. In contrast, Bi on the A-site hinders performance. R-PCEC using Ba(Co0.7Fe0.3)0.75Bi0.10Ta0.15O3-δ (B-BCFT) oxygen electrode achieves exceptional performance in fuel cell (1.485 W cm−2 at 650 °C) and electrolysis modes (−1.839 A cm−2 at 1.4 V and 650 °C). Notably, B-BCFT demonstrates outstanding operational stability, lasting for 150 h in both modes and enduring 35 cycles of reversible operation. These results make B-BCFT a promising oxygen electrode material candidate for R-PCECs.

Experimental study on enrichment of heavy metals by modified mullite during co-combustion of lignite with eucalyptus wood

ABSTRACT Modifying the content of oxygen vacancies (OVs) has emerged as a crucial approach to tailoring silicate's adsorption properties, microstructure, conductivity, and catalytic performance. Some studies have reported the formation of OVs during ammonia treatment. However, there are limited studies on the production of OV-enriched mullite by treating it with N-containing compounds at low temperatures. In this work, formamide, urea, and ammonium acetate were used as ammonia-assisted reduction modifiers to induce oxygen vacancies in mullite at 30 ℃, 60 ℃, and 90 °C. The aim was to enhance the enrichment effect of heavy metals (Cr, Cu, Mn, Ni, Pb, Zn) during the co-combustion of coal and biomass. The modified mullite was analyzed by using X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET) surface area analysis, scanning electron microscopy (SEM), and Fourier transform infrared spectroscopy (FTIR). The results indicated that the particle size of mullite decreased, and the concentration of internal Al3+ ions and oxygen vacancies was enhanced. Coal-biomass-mullite combustion experiments were conducted in a tubular furnace at 900 °C, revealing a significant enhancement in the enrichment of heavy metals during the combustion process, particularly when the modification temperature was 60 °C using ammonium acetate as the modifier. This work holds significant importance for developing novel heavy metal adsorbents and the reduction of pollutant emissions from coal-biomass co-combustion in industrial applications.

A‐Site Defect Engineering Regulates Bimetallic Exsolution in Perovskite Oxide Boosting the Performance of Li–O2 Batteries

AbstractThe application life of Lithium–oxygen (Li–O2) batteries can be significantly affected by the formation and full decomposition of the discharge product Li2O2. After exsolution, the catalyst is designed to control the morphology and crystallinity of Li2O2 enhanced reversibility. In the perovskite exsolution system, the large amount of A‐site defects are introduced to induce the activation of lattice oxygen and the formation of oxygen vacancy, and promote the bimetallic exsolution from LaxFe0.8Cu0.1Co0.1O3. When x = 0.70, the distribution density of CuCo alloy and Cu metal increases and the size is smaller. Through exsolution process, the resulting oxygen vacancy and more doped ions exsolved expose a significant number of active sites that enhance the charge transfer and catalytic activity. Therefore, the charge resistance (Rct) smaller and can be better decomposed due to the generated small‐size Li2O2 with nano‐sheet morphology. Meanwhile, theoretical calculation shows that the exsolution of the catalyst enhances the adsorption of the intermediate LiO2 that makes the surface mechanism more advantageous. The reversibility of the battery is improved, and the cycle stability reaches 195 cycles. This work can serve as a guide for the development of exsolution that directs the design of high efficiency cathode catalyst.

Tuning of Oxygen Vacancies in Co3O4 Electrocatalyst for Effectiveness in Urea Oxidation and Water Splitting.

The development of an excellent multifunctional electrocatalyst that is based on non-precious metal is critical for improving the electrochemical processes of the hydrogen evolution reaction (HER), the oxygen evolution reaction (OER), and the urea oxidation reaction (UOR) in alkaline media. This study demonstrates that incorporating Mo into Co3O4 facilitated the formation of rich oxygen vacancies (Vo), which promotes effective nitrate adsorption and activation in urea electrolysis. Subsequently, in situ/operando X-ray absorption spectroscopy is used to explore the active sites in Mo-Co3O4-3 under OER, indicating the oxygen vacancies are first filled with OH• in Mo-Co3O4; facilitated the pre-oxidation of low-valence Co, and promoted the reconstruction/deprotonation of intermediate Co-OOH•. Mo-Co3O4-3 electrocatalysts show impressive HER, OER, and UOR with low overpotentials of 141 mV, 220 mV, and 1.32 V, respectively, at 10 mA cm-2 in an alkaline medium. Furthermore, in situ/Operando Raman spectroscopy results reveal the importance of CoOOH active sites for enhanced electrochemical performance in Mo-Co3O4-3 compared to the pure Co3O4. The urea electrolyzer with Mo-Co3O4 electrocatalysts acts as an anode and the cathode delivers 1.42 V at 10 mA cm-2. A viable approach to creating effective UOR electrocatalysts involves synergistic engineering exploiting doping and oxygen vacancies.

Overturned doping inert Ce into mesoporous CuO for enhanced peroxydisulfate activation and bisphenols degradation

Transition metal oxides have been recently investigated as excellent catalyst for peroxydisulfate (PDS) activation, but suffers from slow redox cycle of metal species. In this work, a novel avenue for facilitating valence cycles of Cu2+/Cu+ was proposed by overturned doping inert Ce into mesoporous CuO. Increased formation of active sites (Cu-Ce interface) and oxygen vacancy was achieved, resulting in accelerated interfacial electron transfer and facilitated valence cycles of Cu2+/Cu+. The Ce-doped mesoporous CuO (CeCuOx) exhibited greatly enhanced activity toward PDS activation and efficient removal of different bisphenols in a wide pH working range. The degradation of bisphenols followed a nonradical oxidation pathway based on electron transfer process (ETP), and CeCuOx@PDS complex was proved to be the primary reactive species. The CeCuOx/PDS system exhibited good stability and superior catalytic performance in complicated water matrix, and would be a promising catalyst for wastewater purification. This work provides a new prospect for boosting the redox behavior of metal active sites for environmental remediation.

Unraveling Oxygen Vacancies Effect on Chemical Composition, Electronic Structure and Optical Properties of Eu Doped SnO2.

The influence of Eu doping (0.5, 1 and 2 mol.%) and annealing in an oxygen-deficient atmosphere on the structure and optical properties of SnO2 nanoparticles were investigated in relation to electronic structure. The X-ray diffraction (XRD) patterns revealed single-phase tetragonal rutile structure for both synthesized and annealed Eu-doped SnO2 samples, except for the annealed sample with 2 mol.% Eu. The results of X-ray photoelectron spectroscopy (XPS) emphasized that europium incorporated into the SnO2 host lattice with an oxidation state of 3+, which was accompanied by the formation of oxygen vacancies under cation substitution of tetravalent Sn. Moreover, XPS spectra showed the O/Sn ratio, which has been reduced under annealing for creating additional oxygen vacancies. The pulse cathodoluminescence (PCL) demonstrated the concentration dependence of Eu site symmetry. Combination of XRD, XPS and PCL revealed that Eu doping and following annealing induce strongly disordering of the SnO2 crystal lattice. Our findings provide new insight into the interaction of rare-earth metals (Eu) with host SnO2 matrix and new evidence for the importance of oxygen vacancies for optical and electronic structure formation.

CoFe2O4 with the In-Situ Formed Oxygen Vacancies and Co Particles as an Efficient Bifunctional Catalyst for Rechargeable Zinc-Air Batteries.

Rechargeable zinc-air batteries (RZABs) are considered as one of the most promising clean energy device due to their abundant resources, low cost and environmental friendliness. However, their energy efficiency and cycle life are far from satisfactory due to the poor activity and stability of bi-functional electrocatalyst in air cathode. In this work, an efficient bi-functional catalyst (rGO-CoFe2O4/Co) was derived from its precursor (rGO-CoFe2O4) through a simple annealing process. Electrochemical measurements prove that rGO-CoFe2O4/Co with the in-situ formed Co nano particles and rich oxygen vacancies appears excellent oxygen reduction reaction and oxygen evolution reaction catalytic activity compared to its counterpart. Its half-wave potential is 0.81 V (vs RHE) and the OER overpotential is only 310 mV (vs RHE). In addition, rechargeable zinc-air batteries assembled with rGO-CoFe2O4/Co show the highest peak power density (128.9 mW cm-2) and cycling stability compared to rGO-CoFe2O4 and commercial Pt/C-RuO2 catalysts. This work provides a simple strategy for the design of advanced bifunctional catalysts.

A Study on Oxygen Vacancy Resistance Mechanism of V2O5

Introduction: Due to its magnetic and semiconductor properties, V2O5 has shown tremendous potential in resistive switching memory. Method: Therefore, this paper investigates the resistive mechanism of oxygen vacancies in V2O5. The formation energies of different oxygen vacancies are calculated. Results: The results indicate that oxygen vacancies tend to form single-component conductive filaments. In mixed oxygen vacancies clusters, the charge transfer characteristics and density of states of the V2O5-VO 13 vacancies are the most significant, which is consistent with the analysis of formation energy data. Conclusions: Additionally, the charge transfer of cluster oxygen vacancies was calculated, showing that V atoms directly connected to oxygen vacancies tend to lose electrons, while adjacent oxygen atoms are more likely to gain electrons. In V2O5-VO 12 and V2O5-VO 13, the number of electrons obtained by O2 and O16 exceeds the average by 36.4% and 33.2%. Thus, the formation of oxygen vacancies effectively improves the resistance characteristics of the V2O5.

Insights into Mechanisms of Reverse Water Gas Shift Activity Enhancement over Reverse Microemulsion‐Synthesized CuCeO2

AbstractCopper‐doped ceria (CuCeO2) catalysts with 0–26.5 Cu/(Cu+Ce) at% were synthesized via the reverse microemulsion method. X‐ray diffraction analysis of freshly synthesized and spent (post‐reaction) catalysts showed no separate phase of copper or copper oxide, indicating that Cu was incorporated into the CeO2 lattice, replacing Ce. Temperature programmed desorption experiments showed that the activation energy of CO2 desorption increased for higher Cu loadings, indicating stronger CO2 adsorption. This phenomenon was attributed to enhanced formation of oxygen vacancies due to Cu doping. X‐ray photoelectron spectroscopy further confirmed the enhanced generation of oxygen vacancies due to Cu incorporation. Catalytic performance evaluation with the H2/CO2 feed in the 300–600 °C range showed that all catalysts were 100 % selective to CO generation, with higher Cu loadings resulting in CO2 conversion close to equilibrium values at 500–600 °C. The activation energy of the reaction, determined through reaction tests, exhibited inverse relationship with the activation energy of CO2 desorption. The relationship between these two energy barriers is explored, providing valuable insights into the mechanism of RWGS activity enhancement.

Promoting effect of CO2 on NiCr oxidation: Atomistic origins based on first principles.

The adsorption and dissociation of CO2 on both perfect and oxygen-deficient α-Cr2O3 (0001) surfaces, alongside the subsequent incorporation of the resulting C into the oxide lattice and its impact on oxide growth, are investigated using first-principles calculations. Our findings reveal that oxygen vacancies significantly enhance CO2 adsorption and promote its stepwise decomposition into C and O atoms. The resulting C can spontaneously dissolve into the oxide lattice through the oxygen vacancies. The presence of bulk dissolved C in the Cr2O3 lattice substantially enhances the formation, migration, and clustering of oxygen vacancies in the bulk. These results provide an atomic-level understanding of how CO2 accelerates the oxidation of chromia-forming alloys, offering microscopic insights for controlling oxide growth and mitigating oxidation-induced degradation of high-temperature alloys.

Promoting Surface Reconstruction in Spinel Oxides via Tetrahedral-Octahedral Phase Boundary Construction for Efficient Oxygen Evolution.

Understanding the origin of surface reconstruction is crucial for developing highly efficient lattice oxygen oxidation mechanism (LOM) based spinel oxides. Traditionally, the reconstruction has been achieved through electrochemical procedures, such as cyclic voltammetry (CV), linear sweep voltammetry (LSV). In this work, we found that the surface reconstruction in LOM-based CoFe0.25Al1.75O4 catalyst was an irreversible oxygen redox chemical reaction. And a lower oxygen vacancy formation energy (EO-V) could benefit the combination of the activated lattice oxygen atoms with adsorbed water molecular. Motivated by this finding, a strategy of phase boundary construction from Co tetrahedral to octahedral was employed to decrease EO-V in CoFe0.25Al1.75O4. The results showed that as the Co octahedral occupancy ratio rose to 64 %, a 3.5 nm-thick reconstructed layer formed on the catalyst surface with a 158 mV decrease in overpotential. Further experiments indicated that the coexistence of tetrahedral-octahedral (O-T) phase would result in lattice mismatch, promoting non-bonding oxygen states and lowering EO-V. Then more active lattice oxygen combined with H2O molecules to generate hydroxide ions (OH-), followed by soluble cation leaching, which enhanced the reconstruction process. This work provided new insights into the relationship between the intrinsic structure of pre-catalysts and surface reconstruction in LOM-based spinel electrocatalysts.

Enhancing Thermochemical Energy Storage Performance of Perovskite with Sodium Ion Incorporation

Perovskite materials are promising for thermochemical energy storage due to their ability to undergo redox cycling over a wide temperature range. Although BaCoO3 exhibits excellent air cycling properties, its heat storage capacity in air remains suboptimal. This study introduces Na into the lattice structure to enhance oxygen vacancy formation and mobility. DFT+U simulations of the surface structure of Na-doped BaCoO3−δ indicate that incorporating Na improves surface stability and facilitates the formation of surface oxygen vacancies. NaxBa1−xCoO3−δ compounds were synthesized using a modified sol–gel method, and their properties were investigated. The experimental results demonstrate that Na doping significantly enhances the redox activity of the material. The heat storage capacity increased by above 50%, with the Na0.0625Ba0.9375CoO3−δ solid solution achieving a heat storage density of up to 341.7 kJ/kg. XPS analysis reveals that Na doping increases the concentration of surface defect oxygen, leading to more active oxygen release sites at high temperatures. This enhancement in redox activity aligns with DFT predictions. During high-temperature cycling, the distribution of Na within the material becomes more uniform, and no performance degradation is observed after 300 cycles. Even after 450 cycles, Na0.0625Ba0.9375CoO3−δ retains over 96% of its initial redox activity, significantly outperforming fresh BaCoO3−δ. These findings elucidate the mechanism by which Na doping enhances the thermochemical heat storage performance of BaCoO3−δ and provide new insights for the design of perovskite-based materials.

Catalytic Fe2+ Cation Pair Site for Base-free N-Alkylation of Aromatic Amines with Alcohols.

The development of heterogeneous Fe catalysts is very attractive due to the ubiquitous, abundant, and inexpensive nature of Fe as a resource. However, Fe oxides are commonly inert as catalysts and hence, the design and fabrication of active Fe sites are essential. Herein, the fabrication of an active Fe cation pair site by simple reduction treatment of SiO2-supported FeOx (FeOx/SiO2) is presented. The active Fe cation pair site was formed by the removal of the oxygen atom between Fe cations of the FeOx on SiO2, namely oxygen vacancy formation, which is induced by temperature-controlled reduction treatment. 773 K reduction maximized the Fe cation pair sites without the decomposition of FeOx species, which was an effective catalytic one for the N-alkylation of amines mainly proceeded through Meerwein-Ponndorf-Verley (MPV) type reduction, which is achieved by the stabilization of six-membered ring transition state derived from imines and alcohols over the open active site of the Fe cation pair site.

Glucose-assisted preparation of vacancy-rich ZnO sheets for photocatalytic activity enhancement

Vacancy-rich ZnO sheets with (1 0 0) facet were synthesized by the glucose-assisted calcination method. By introducing glucose to control the atmosphere, oriented growth of ZnO with oxygen vacancy was realized. Experimental results showed that the glucose-assisted calcination provided oxygen-poor environment for the formation of oxygen vacancy and promoted the transformation of ZnO from rods to sheets. ZnO sheets exhibited a high photocatalytic activity and regeneration ability. After 60 min of irradiation, methyl orange was completely decolorized and the degradation rate was still at 96 % after four-cycle experiments. The synergistic effect of oxygen vacancy and non-polar (1 0 0) facet improved the photocatalytic property of ZnO.

Modification of microstructure, optical, and electrical properties in 180 keV Co and Fe implanted Al1.5Ga0.5O3 thin-films

We report the microstructure, optical and electrical properties of Al1.5Ga0.5O3 thin films implanted by 180 keV Fe and Co ions. The X-ray diffraction pattern confirmed rhombohedral structure with R 3‾ c space group for pristine and Fe-implanted films. The Co-implanted films showed amorphous structure. SRIM simulations suggested oxygen vacancy in the films. The atomic force microscopy confirmed the formation of spherical-shaped particles (17–20 nm) in Co-implanted GaAlO_Si_550 films. The RMS roughness of the GaAlO_Si_550 films increased from 19 nm to 25 nm at higher Co-ion implantation fluences. X-ray photoelectron spectroscopy supported the formation of oxygen vacancy and non-stoichiometry at surface of the films. Electrical conductivity of the films enhanced up to 10−2- 10−3 S/m by metallic Fe- and Co ion implantation. Optical band gap was found at ∼3.85 eV for GaAlO_Al_550 and ∼4.04 eV for GaAlO_Si_550 pristine films. Optical band gap was stabilized in the range of 3.75–4.52 eV for Fe- and Co-implanted films, which can be useful for opto-electronic device applications in the UV and deep blue region.

Synthesis of low-temperature NH3-SCR catalysts for MnOx with high SO2 resistance using redox-precipitation method with mixed manganese sources

It remains a big challenge to enhance the SO2 resistance of catalyst in low-temperature NH3-SCR reduction. In this work, a series of MnOx-a%Mn (a = 0, 1, 3, 5, 10) catalysts were prepared by introducing manganese acetylacetonate during the reaction between lactic acid and KMnO4, based on the molar ratio of manganese acetylacetonate to KMnO4. Notably, MnOx-5 %Mn exhibited more than 95 % NO conversion and 100 % N2 selectivity at 80–240 °C. Moreover, the catalyst demonstrated excellent sulfur resistance by sustaining over 90 % NO conversion at 140 °C at the presence of 100 ppm SO2 for more than 6 h. Furthermore, XPS characterization indicated that adding manganese acetylacetonate enhanced electron transfer efficiency and improved the reduction capacity of the catalyst due to the interconversion between Mn3+ and Mn4+, which improved electron transfer efficiency. The enhanced reduction capacity of the catalyst promoted the formation of oxygen vacancies and surface-adsorbed oxygen species (Oα), avoiding over-oxidation of NH3. The results elucidated that manganese acetylacetonate could optimize the overall performance by modulating the synergistic effect between the oxidizing ability and surface acidity of the catalyst. Therefore, the MnOx-5 %Mn catalyst possessed a broad operational temperature window (40–240 °C) and SO2 resistance in the NH3-SCR reaction, indicating its potential for practical application.

Experimental and DFT studies of mercury adsorption and oxidation on CuCo2O4(110) surface

Elemental mercury (Hg0) is a typical toxic pollutant in flue gas from coal-fired power plants. The specific role of oxygen transfer on Hg0 oxidation over CuCo2O4 oxygen carrier and the involved reaction mechanisms were systematically studied by experimental and theoretical methods. In this study, the CuCo2O4 oxygen carrier with spinel-structure was prepared with salt-assisted combustion method. To reduce the grain size and increase the specific surface area of the oxygen carrier, the optimal KCl: CuCo2O4 ratio of 1:1 was obtained. Oxygen uncoupling ability of CuCo2O4 oxygen carrier was very strong, and the oxygen-releasing performance was slightly decreased after ten cyclic processes. Simulation based on density functional theory (DFT) shows that CuCo2O4 has relative low oxygen vacancy formation energy and oxygen transport energy barrier, and the oxygen vacancy is the preferred O2 adsorption site. Hg0 removal experiments show that CuCo2O4 has a strong ability to remove Hg0. The proportion of Hg2+ increases with the temperature, and the proportion of HgP decreases accordingly. Simulation shows that the 3-Co site on the surface of the CuCo2O4 oxygen carrier is the optimum Hg0 adsorption site. CuCo2O4 is found as a strong oxygen-releasing oxygen carrier, which can effectively promote the oxidation of Hg0.

Valence state and redox property of Fe‐CNTs added CeO2/TiO2 catalyst

AbstractThe investigation focused on examining the impact of incorporating Fe‐carbon nanotubes (CNTs) on the valence state and oxygen vacancies, and the physicochemical parameters of the catalytic system. For the CeO2/TiO2 catalyst with Fe‐CNTs, no distinct X‐ray diffraction (XRD) peaks corresponding to Fe‐CNTs were observed. This indicated their uniform dispersion, supported by transmission electron microscopy (TEM) and scanning electron microscopy (SEM) imaging. X‐ray photoelectron spectroscopy (XPS) analysis was conducted to observe the changes in the valence state due to the addition of Fe‐CNTs. The concentration of Ce3+ on catalyst surface increased from 19.90% to 29.48% with an increased concentration of the chemisorbed oxygen species (Oα). This suggests that the addition of Fe‐CNTs into CeO2/TiO2 catalyst reduced Ce4+ on the catalyst surface, resulting in the formation of oxygen vacancies. Oxygen temperature‐programmed desorption (O2‐TPD) and hydrogen temperature‐programmed reduction (H2‐TPR) analyses showed both the adsorbed oxygen species and H2 consumption increased with adding Fe‐CNTs. Furthermore, the onset temperatures for O2 desorption and H2 consumption became lower, confirming the enhancement of catalytic redox properties.

Novel electrocatalyst with abundant oxygen vacancies enabling efficient two-electron water oxidation reaction for H2O2 synthesis

In the realm of electrocatalytic two-electron water oxidation reaction, the quest for efficient and selective catalysts poses a significant challenge in balancing productivity and activity, hindering the decentralized generation of hydrogen peroxide (H2O2) through electrochemical means. Addressing this hurdle, our study introduces a novel approach to crafting an effective and stable electrocatalyst for the two-electron water oxidation reaction (2e-WOR). Through the synthesis of magnesium stannite tungstate from a mixture of MgSnO3 and WO3, the engineer of a material with abundant oxygen vacancies is crucial for catalytic activity. This catalyst demonstrates exceptional performance, ascribed to its distinctive oxygen vacancies proximal to the active center Sn and electronic modulation by tungsten. Notably, Mg1-xSnWO6-x700 exhibits a remarkably low overpotential of 70 mV at 10 mA cm−2, coupled with a high faradic efficiency of 84 % for 2e- WOR at 2.6 V vs. RHE, maintaining consistent performance over 35 h. Furthermore, the formation of oxygen vacancies and the associated electronic transfer underscore the novelty and promise of our material in advancing the field of two-electron WOR. In sum, our electrocatalyst presents a cost-efficient and selective solution for water oxidation, offering potential avenues for enhancing H2O2 production.