Electrochemical Oxidation Performance Research Articles

Customization of Manganese Oxide Cathodes via Precise Electrochemical Lithium-Ion Intercalation for Diverse Zinc-Ion Batteries.

Manganese oxide-based aqueous zinc-ion batteries (ZIBs) are attractive energy storage devices, owing to their good safety, low cost, and ecofriendly features. However, various critical issues, including poor conductivity, sluggish reaction kinetics, and unstable structure still restrict their further development. Oxygen defect engineering is an effective strategy to improve the electrochemical performance of manganese oxides, but challenging in the accurate regulation of oxygen defects. In this work, an effective and controllable defect engineering strategy-controllable electrochemical lithium-ion intercalation - is proposed to tackle this issue. The incorporation of lithium ions and oxygen defects can promote the conductivity, lattice spacing, and structural stability of Mn2O3 (MO), thus improving its capacity (232.7mAhg-1), rate performance, and long-term cycling stability (99.0% capacity retention after 3000 cycles). Interestingly, the optimal ratio of intercalated lithium-ion varies at different temperature or mass-loading of MO, which provides the possibility to customize diverse ZIBs to meet different application conditions. In addition, the fabricated ZIBs present good flexibility, superior safety, and admirable adaptability under extreme temperatures (-20-100°C). This work provides an inspiration on the structural customization of metal oxide nanomaterials for diverse ZIBs, and sheds light on the construction of future portable electronics.

Synergy of Oxygen Vacancy and Surface Modulation Endows Hollow Hydrangea-like MnCo2O4.5 with Enhanced Capacitive Performance.

Surface chemistry and bulk structure jointly play crucial roles in achieving high-performance supercapacitors. Here, the synergistic effect of surface chemistry properties (vacancy and phosphorization) and structure-derived properties (hollow hydrangea-like structure) on energy storage is explored by the surface treatment and architecture design of the nanostructures. The theoretical calculations and experiments prove that surface chemistry modulation is capable of improving electronic conductivity and electrolyte wettability. The structural engineering of both hollow and nanosheets produces a high specific surface area and an abundant pore structure, which is favorable in exposing more active sites and shortens the ion diffusion distance. Benefiting from its admirable physicochemical properties, the surface phosphorylated MnCo2O4.5 hollow hydrangea-like structure (P-MnCoO) delivers a high capacitance of 425 F g-1 at 1 A g-1, a superior capability rate of 63.9%, capacitance retention at 10 A g-1, and extremely long cyclic stability (91.1% after 10,000 cycles). The fabricated P-MnCoO/AC asymmetric supercapacitor achieved superior energy and power density. This work opens a new avenue to further improve the electrochemical performance of metal oxides for supercapacitors.

Treatment of Organics in Wastewater Using Electrogenerated Gaseous Oxidants.

This work focuses on the comparison of the performance of direct electrochemical oxidation with indirect electrolysis mediated by gaseous oxidants in the treatment of diluted wastewater. To do this, energy consumptions of the electrolysis using mixed metal oxide (MMO) electrodes are compared with those required for the production and use of chlorine dioxide in the degradation of methomyl contained in aqueous solutions. Results demonstrate the feasibility of the mediated oxidation process and that this process is competitive with direct oxidation. The oxidants are produced under optimized conditions using the same anodic material applied for the direct degradation of organics, thus avoiding efficiency losses associated with mass transfer limitations in the degradation of dilute organic solutions. Thus, using the ClO2 gaseous oxidant, a concentration of 0.1 mM of methomyl from a solution containing 500 mL is completely removed with an energy consumption as low as 50 Wh. The application of the same energy to a direct electrolytic process for treating the same wastewater can only reach less than half of this removal. These findings may have a very important application in the use of electrochemical technology to achieve the remediation of persistent pollutants in wastewater, where their low concentrations typically make direct processes very inefficient.

Preparation of Ti/SnO2-Sb2O4-La Electrode with TiO2 Nanotubes Intermediate Layer and the Electrochemical Oxidation Performance of Rhodamine B.

A La-doped Ti/SnO2-Sb2O4 electrode with TiO2-NTs intermediate layer (Ti/TiO2-NTs/SnO2-Sb2O4-La) was created via the electrodeposition technique. The physicochemical and electrochemical properties of the electrode were analyzed through FESEM, XRD, XPS, CV, and LSV electrochemical tests. The results showed that TiO2-NTs were tightly packed on the surface of Ti substrate, thus improving the binding force of the SnO2-Sb2O4-La coating, offering greater specific surface area, more active spots, higher current response, and longer lifespan for the degradation of rhodamine B. The lifespan of the Ti/TiO2-NTs/SnO2-Sb2O4-La electrode reached 200 min (1000 mA cm-2, 1 M H2SO4), while the actual service life was up to 3699 h. Under the conditions of initial pH 3.0, Na2SO4 concentration of 0.1 M, current density of 30 mA cm-2, and initial rhodamine B concentration of 20 mg L-1, the color and TOC removal rate of rhodamine B reached 100% and 86.13% within 15 and 30 min, respectively. Rhodamine B was decomposed into acids, esters, and other molecular compounds under the action of •OH and SO4•- free radicals and electrocatalysis, and finally completely mineralized into CO2 and H2O. It is anticipated that this work will yield a novel research concept for producing DSA electrodes with superior catalytic efficacy and elevated stability.

Enhanced structural, electrical, and electrochemical performance of polyethylene oxides (PEO)‐based polymer electrolytes for solid state K+ ion batteries

AbstractFlexible polymer electrolytes with effective electrochemical characteristics must be developed to meet smart electronic technology demands. The current investigation explores the solid polymer electrolytes (SPEs) prepared by solution‐casting technique, using polyethylene oxides (PEO) doped with KCl salt in different weight percentages. The effect of the dopant on the chemical interactions and structural, optical, thermal, electrical, and electrochemical properties were studied using various strategies. It was found that the incorporation of KCl salt to PEO results in a three order of magnitude enhancement in ionic conductivity of polymer matrix from 10−9 to 10−6 S cm−1. The PEO doped with 20 wt.% KCl salt exhibited the highest ionic conductivity (4.32 × 10−6 S cm−1) and low activation energy (0.25 eV). According to the thermal analysis, the thermal stability of the films improved as the dopant concentration increased. Further, the electrochemical strength improved with increasing dopant concentration, according to cyclic voltammogram experiments. From the results of all the characterizations, PEO loaded with 20 wt.% KCl SPE system is a suitable candidate for use as an electrolyte in energy storage devices such as solid‐state batteries.

Preparation of La-doped Ti/SnO2-Sb2O4 anode and its electrochemical oxidation performance of rhodamine B.

In this paper, La-doped Ti/SnO2-Sb2O4 electrode was prepared by electrodeposition and used for electrochemical degradation of rhodamine B. The optimum preparation conditions of the electrode were optimized as deposition time of 15min and calcination at 500 ℃ for 2h. The water treatment conditions were selected as initial pH 3.0, electrolyte Na2SO4 concentration 0.1M, current density 30mAcm-2, and initial rhodamine B concentration 20mg L-1; the color and TOC removal of RhB reached 99.78% and 82.41% within 30min. The FESEM, XRD, XPS, CV, LSV, and EIS characterization studies demonstrated that Ti/SnO2-Sb2O4-1%La electrode had a dense structure and the highest oxygen evolution potential (2.14V) and lowest charge transfer resistance (0.198 Ω cm-2), indicating that doped La has lower energy consumption. Moreover, La doping can expand the specific surface area, active site, performance of pollutant degradation, and service life of the electrode. Especially, the service life of Ti/SnO2-Sb2O4-1%La is increased by three times, and the maximum life span reaches 90min (1000mAcm-2, 1M H2SO4). Free radical quenching experiments show that ·OH plays a major role in the degradation of RhB. The Ti/SnO2-Sb2O4-1%La electrode prepared in this paper and its results will provide data support and reference for the design of efficient electrocatalytic electrode.

Electrochemical Oxidation Treatment of Organic Matter in Wastewater from Wet Fermentation of Yunnan Arabica Coffee

Electrochemical oxidation combined with reagents of O3, H2O2 and FeCl2 was conducted in this study to treat the wastewater from wet fermentation of Yunnan arabica coffee. In addition, the effect of oxidants on the efficiency of wastewater treatment, the binding capacities of the oxidants to proteins, the degradation of organic pollutants in the wastewater, and the formation of oxidized organic components were systematically investigated. The results reveal better performance of O3-combined electrochemical oxidation (63.60% COD removal efficiency) for treatment of organic species in coffee wastewater than that of the electrochemical processes with H2O2 (47.70% COD removal efficiency) and FeCl2 (34.48% COD removal efficiency). The synergy of the electrooxidation/O3 process (0.0133 A/cm2, 20 mg/L–2 L/min) could not only raise the pH value (3.70~4.20, 5.14~5.44) of the wastewater and reduce the NaOH dosage of 2.80~3.7 g/L, but also effectively degrade the proteins, lipids, unsaturated hydrocarbons, and carbohydrates, with a total chemical oxygen demand (COD) value above 20,000 mg/L. After the oxidation treatment, some organic components remained in the wastewater, including 31.94% of S-containing organics, lignin, condensed aromatic compounds, and aromatic structural compounds, which are difficult to be utilized by microorganisms. In addition, it was found that OH− could bind to proteins and affect the required amount of NaOH addition, whereas the protein binding energy of O3 is higher than that of H2O2, indicating a stronger ability of O3 to oxidize proteins. Therefore, the combination of O3 and electrochemical oxidation can be considered as an effective method to treat organic pollutants in the wastewater from wet fermentation of Yunnan arabica coffee.

Significant improvement in cycling and rate ability originating from regulation of bonding and transport channel via Ba2+ decoration in P2 layer oxide cathode

Nowadays, commercialization of layered transition metal oxides is hindered by irreversible phase transition during charging and discharging, low-capacity retention rate at high rate and slow Na+ diffusion kinetics. In this work, Ba2+ was introduced into the alkali metal layer to improve the electrochemical performance of layered transition metal oxides. XRD refinement and first principle calculations demonstrate that the introduced Ba2+ can effectively enlarge the distance between Na layers and reduce the potential barrier of sodium ion migration, thus leading to faster sodium ion diffusion kinetics. Simultaneously, charge distribution density calculation indicates that the introduced Ba2+ enhances overlap of electron clouds between transition metal (TM) and O, which result in more obvious covalence of TM-O bond, bigger electrostatic attraction between TM and O, and stronger bond energy of TM-O. These microstructures are beneficial to maintain structural stability and suppress the formation of OP4 phase during charging, which is demonstrated by XRD during charging and discharging process. The optimized Na0.6Ba0.012Mn0.62Ni0.22Fe0.16O2 provides reversible specific capacity of 133.8mAh g−1 at 0.5C (1C = 150mA g−1) and 122.1mAh g−1 at 2C. The strategy of regulating chemical bond environment by introducing Ba2+ achieves excellent the electrochemical performances and promotes the commercial development of sodium ion batteries.

Ameliorating electrochemical performance of Li-rich Mn-based cathodes for Li-ion batteries by Fe substitution

Ameliorating electrochemical performance of Li-rich Mn-based layered oxides (Li2MnO3, LMO) cathodes for lithium-ion batteries (LIBs) by Fe substitution.

Electrocatalytic Degradation of Acyclovir by Three-Dimensional Porous Lead Dioxide Anodes: Condition Optimization, Kinetic Analysis and Degradation Mechanisms

A three-dimensional porous lead dioxide electrode (3D-PbO2) was developed by the template electrodeposition approach. Polystyrene microspheres were prepared by microemulsion polymerization, and then the polystyrene template was loaded on the PbO2 electrode by electrodeposition. Finally, a porous structure was formed by removing the template. Under these optimized conditions, the degradation of acyclovir could achieve complete removal, while the removal of COD was 29.59%. The electrochemical degradation process of acyclovir was consistent with the proposed primary reaction kinetics. The 3D-PbO2 electrode was comprehensively characterized using SEM, XRD, and XPS techniques. The SEM analysis revealed the presence of well-defined porous structures on the electrode surface, while the XRD results indicated a reduction in electrode crystal sizes. Additionally, the XPS analysis demonstrated a higher proportion of reactive oxygen species on the 3D-PbO2 electrode. The electrochemical properties of the electrode were investigated using CV and EIS. The experimental findings demonstrate that the 3D-PbO2 electrode exhibits a higher oxygen evolution potential and lower charge transfer resistance than the conventional PbO2 electrode. This study presents a viable approach to enhance the electrochemical oxidation performance of lead dioxide.

Pretreatment impact on electrochemically synthesized graphene oxide

The production of graphene oxide by the electrochemical method is more environmentally friendly, faster and suitable for mass production than the chemical method. Although this technique is very practical, the correct parameters must be selected to produce graphene oxide. Therefore, it is very important to investigate the factors affecting graphene oxide synthesis in the electrochemical process. In this study, the effect of pretreatment on graphene oxide produced by the electrochemical method was investigated. Structural characterization of the produced graphene oxide was carried out using X-ray diffraction, Raman spectroscopy and energy-dispersive X-ray spectroscopy, while morphological research was performed using scanning electron microscopy. Due to the increase in the electrochemical oxidation performance of dilute nitric acid with the effect of the pretreatment process, an effective increase in the oxygen content in the structure of graphene oxide was detected.

Dual Strategies with Anion/Cation Co-Doping and Lithium Carbonate Coating to Enhance the Electrochemical Performance of Lithium-Rich Layered Oxides.

Lithium-rich layered oxides (LLOs, Li1.2 Mn0.54 Ni0.13 Co0.13 O2 ) are widely used as cathode materials for lithium-ion batteries due to its high specific capacity, high operating voltage and low cost. However, the LLOs are faced with rapid decay of charge/discharge capacity and voltage, as well as interface side reactions, which limit its electrochemical performance. Herein, the dual strategies of sulfite/sodium ion co-doping and lithium carbonate coating were used to improve it. It founds that modified LLOs achieve 88.74 % initial coulomb efficiency, 295.3 mAh g-1 first turn discharge capacity, in addition to 216.9 mAh g-1 at 1 C, and 87.23 % capacity retention after 100 cycles. Mechanism research indicated that the excellent electrochemical performance benefits from the doping of both Na+ and SO3 2- , and it could significantly reduce the migration energy barrier of Li+ and promote Li+ migration. Meanwhile, anion and cation are co-doped greatly reduces the band gap of LLOs and increase its electrical conductivity, and its binding effect on Li+ is weakened, making it easier for Li+ to shuttle through the material. In addition, the lithium carbonate coating significantly inhibits the occurrence of interfacial side reactions of LLOs. This work provides a theoretical basis and practical guidance for the further development of LLOs with higher electrochemical performance.

Preparation of Ti4O7 Reactive Electrochemical Membrane for Electrochemical Oxidation of Coking Wastewater

The effluent of coking wastewater comprises hundreds of refractory organics and is characterized by high toxicity and non-biodegradation. Electrochemical advanced oxidation processes (EAOPs) have been widely applied in the field of water purification. In this study, a Ti4O7 reactive electrochemical membrane (REM) was prepared using the plasma spraying method for the electro-oxidation of coking wastewater. The composition and surface morphology of the Ti4O7 REM were characterized via X-ray diffraction (XRD) and scanning electron microscopy (SEM), respectively. The computational fluid dynamics (CFD) simulation was used to compare the mass transfer performance of the Ti4O7 REM in traditional batch (TB) mode and flow-through (FT) mode. In the FT mode, the effects of current density and anode–cathode distance on the treatment efficiency were investigated, and the electrocatalytic performance of the anode on coking wastewater was analyzed. The results showed that the COD removal efficiency reached 76.2% with an energy consumption of 110.5 kWh kg−1 COD under the optimal condition. In addition, cathodic polarization provides an effective technique for maintaining the long-term activity of the Ti4O7 REM. The three-dimensional fluorescence results and UV-vis spectrum showed that the aromatic compounds could be effectively degraded using the Ti4O7 REM. The Ti4O7 REM demonstrated excellent performance of electrochemical oxidation and satisfactory stability, which had a strong potential for application in the field of practical wastewater and engineering practices that respond to the concept of sustainable development.

Effects of different vacancies in nickel hydroxides on the electrooxidation towards 5-hydroxymethylfurfural

The electrocatalytic oxidation of 5-hydroxymethylfurfural (HMFOR) emerges as an alternative pathway for the green production of valuable oxygenated chemicals owing to the catalyst innovation. The performance of nickel hydroxides, which are well-known for HMFOR, is still far from satisfactory as a result of the weak adsorption towards HMF, limited intrinsic activity and poor conductivity. Vacancy engineering provides an effective way to improve the catalytic ability of nickel hydroxides, nevertheless the role of different vacancies played in the HMFOR process is still unclear. Herein, a carbon-paper supported nickel hydroxide (Ni(OH)2/CP) with anionic vacancies (av-Ni(OH)2/CP) or cationic vacancies (cv-Ni(OH)2/CP) is employed for HMFOR study, with a special focus on the structure–function relationship between vacancy type and HMFOR performance. The successful introduction of different vacancies was manifested by electron paramagnetic resonance spectroscopy. X-ray photoelectron spectroscopy revealed the opposite roles of the anionic and cationic vacancies in modulating the electronic structure of Ni(OH)2. The time-dependent open-circuit potential measurements verified the different adsorption behavior of HMFOR on the surface of the catalysts. Benefiting from the well-tuned electronic structure and the enhanced adsorption ability, the av-Ni(OH)2/CP exhibits superior catalytic performance than the pristine Ni(OH)2/CP and the cv-Ni(OH)2/CP. More than 98.97% HMF can be converted using av-Ni(OH)2/CP as catalyst, with a remarkable yield of FDCA (98.51%) and a ultrahigh faradaic efficiency (98.46%) at 1.45 V. This work not only reports an excellent HMFOR electrocatalyst, but also elucidates the crucial effect of different vacancies on the electrochemical oxidation performance of Ni(OH)2 materials.

Degradation of the antibiotic ciprofloxacin in urine by electrochemical oxidation with a DSA anode

Ciprofloxacin (CIP) is a commonly prescribed fluoroquinolone antibiotic that, even after uptake, remains unmetabolized to a significant extent—over 70%. Unmetabolized CIP is excreted through both urine and feces. This persistent compound manages to evade removal in municipal wastewater facilities, leading to its substantial accumulation in aquatic environments. This accumulation raises concerns about potential risks to the health of various living organisms. Herein, we present a study on the remediation of CIP in synthetic urine by electrochemical oxidation in an undivided cell with a DSA (Ti/IrO2) anode and a stainless-steel cathode. Physisorbed hydroxyl radical formed at the anode surface from water discharge and free chlorine generated from Cl− oxidation were the main oxidizing agents. The effect of pH and current density (j) on CIP degradation was examined, and its total removal was easily achieved at pH ≥ 7.0 and j ≥ 60 mA cm−2 due to the action of free chlorine. The CIP decay always followed a pseudo-first-order kinetics. The components of the synthetic urine were also oxidized. The main nitrogenated species released was NH3. A very small concentration of free chlorine was quantified at the end of the treatment, thus demonstrating the good performance of electrochemical oxidation and its effectiveness to destroy all the organic pollutants. The present study demonstrates the simultaneous oxidation of the organic components of urine during CIP degradation, thus showing a unique perspective for its electrochemical oxidation that enhances the environmental remediation strategies.

A-Site Nonstoichiometric BaxCo0.4Fe0.4Zr0.1Y0.1O3-δ Cathode for Protonic Ceramics Fuel Cells.

Highly active triple (proton, oxygen-ion, and electron) conducting materials BaxCo0.4Fe0.4Zr0.1Y0.1O3-δ (BxCFZY, x = 0.9-1.1) were prepared and characterized as potential cathodes for protonic ceramic fuel cells (PCFCs) in this work. The crystal structure, oxygen vacancy concentration, electrical conductivity, oxygen ion transfer properties, and electrochemical performance of BxCFZY oxides were systematically evaluated. The electrical conductivity of BxCFZY decreases but oxygen vacancies increase with increasing Ba content, indicating that the charge compensation was mainly achieved by the production of oxygen vacancy rather than the increase in the valence of transition metal cations. The power density of 1170 mW cm-2 and the polarization resistance of 0.05 Ω cm2 were achieved at 700 °C for the anode-supported single cells with B1.1CFZY cathode, suggesting that the excess A site on the BxCFZY had a positive effect on the catalytic activity for the oxygen reduction reaction. Furthermore, the distribution of relaxation time (DRT) analysis method was adopted to determine the electrochemical processes of the cells with BxCFZY cathodes. The calculated results confirmed that the cell with B1.1CFZY cathode exhibited the optimum performance due to the best oxygen ion transfer properties in BxCFZY cathodes.

Improvements in the Electrochemical Performance of Sodium Manganese Oxides by Ti Doping for Aqueous Mg-Ion Batteries.

In recent times, the research on cathode materials for aqueous rechargeable magnesium ion battery has gained significant attention. The focus is on enhancing high-rate performance and cycle stability, which has become the primary research goal. Manganese oxide and its derived Na-Mn-O system have been considered as one of the most promising electrode materials due to its low cost, non-toxicity and stable spatial structure. This work uses hydrothermal method to prepare titanium gradient doped nano sodium manganese oxides, and uses freeze-drying technology to prepare magnesium ion battery cathode materials with high tap density. At the initial current density of 50 mA g-1 , the NMTO-5 material exhibits a high reversible capacity of 231.0 mAh g-1 , even at a current density of 1000 mA g-1 , there is still 122.1 mAh g-1 . It is worth noting that after 180 cycles of charging and discharging at a gradually increasing current density such as 50-1000 mA g-1 , it can still return to the original level after returning to 50 mA g-1 . Excellent electrochemical performance and capacity stability show that NMTO-5 material is a promising electrode material.

Single-atom Zr embedded Ti4O7 anode coupling with hierarchical CuFe2O4 particle electrodes toward efficient electrooxidation of actual pharmaceutical wastewater

Electrocatalytic oxidation is commonly restricted by low degradation efficiency, slow mass transfer, and high energy consumption. Herein, a synergetic electrocatalysis system was developed for removal of various drugs, i.e., atenolol, florfenicol, and diclofenac sodium, as well as actual pharmaceutical wastewater, where the newly-designed single-atom Zr embedded Ti4O7 (Zr/Ti4O7) and hierarchical CuFe2O4 (CFO) microspheres were used as anode and microelectrodes, respectively. In the optimal reaction system, the degradation efficiencies of 40 mg L–1 atenolol, florfenicol, and diclofenac sodium could achieve up to 98.8%, 93.4%, and 85.5% in 120 min with 0.1 g L–1 CFO at current density of 25 mA cm–2. More importantly, in the flow-through reactor, the electrooxidation lasting for 150 min could reduce the COD of actual pharmaceutical wastewater from 432 to 88.6 mg L−1, with a lower energy consumption (25.67 kWh/m3). Meanwhile, the electrooxidation system maintained superior stability and environmental adaptability. DFT theory calculations revealed that the excellent performance of this electrooxidation system could be ascribed to the striking features of the reduced reaction energy barrier by single-atom Zr loading and abundant oxygen vacancies on the Zr/Ti4O7 surface. Moreover, the characterization and experimental results demonstrated that the CFO unique hierarchical structure and synergistic effect between electrodes were also the important factors that could improve the system performance. The findings shed light on the single-atom material design for boosting electrochemical oxidation performance.

How Do Impurities in Electrolytes Affect the Electrochemical Performance of Oxides in Lithium-Ion Batteries?

The recovery and treatment of spent LIBs has already been studied extensively. On one hand, the hydrometallurgical recovery of cathode materials has aroused widespread attention because of its low energy consumption and benefit to the environment. On another hand, the purification of the materials reclaimed from spent batteries is a challenging process with high probability that, later, some remaining impurities such as transition metal carbonates and sulfates could be released into the electrolyte. In this way the impurity content will have a serious impact on the final performance of the battery. To this point different electrochemical and analytical measurements were conducted to elucidate the effects of impurities in the electrolyte formulation, specifically Li, Mn, Co, Ni, and Al carbonates, sulfates, and acetates. The base LP30 electrolyte was intentionally contaminated with a maximum concentration of selected impurity to study the effects of the contaminated electrolyte on the electrode. Different combinations and varieties were explored correspondingly. Test setups were based on both, NMC811 in half cells (vs. Li) and symmetrical Li||Li cells, and the influence of contaminations was thus exploited on the Li counter electrode and on the NMC811 in Li||NMC811 configuration. A number of standard and advanced electrochemical test techniques such as CC-CV, electrochemical impedance, rate capability tests, GITT, and CV was applied for a fully understanding of the electrochemical characteristics of standard cathode active materials such as NMC811 when electrolytes with (artificially downgraded) low purity levels are present. The presentation will focus on discussion of results regarding the presence of transition metals Ni, Co, and Mn as impurities in the electrolyte which showed a significant impact on the electrochemical performance of the tested cells. When the concentration of the impurities increases, both the overpotentials at the cathode and the rate of capacity decay during cycling increase as well. The data shown will be very helpful for the researchers to understand the impact of impurities on the performance of oxide-based LIB cathode materials.

Advanced Vanadium Oxides for Sodium‐Ion Batteries

AbstractSodium‐ion batteries (SIBs) represent one of the current research frontiers owing to their low cost, intrinsic safety, environmental friendliness, and other unique features. In the current era, a myriad of investigations are conducted towards the exploration of advanced electrode materials with exceptional energy/power density, superior rate capability, and ultralong cycling life. Notably, vanadium oxides electrode materials have received great attention due to their diversity in chemical compositions and attractive electrochemical properties. In this review, comprehensive and detailed compendium regarding the latest developments and breakthroughs of highly promising vanadium oxides‐based electrode materials for advanced‐performance SIBs are elucidated. The crystal structures, electrochemical performance, structure‐property relationships and sodium storage mechanization of various vanadium oxides are discussed. In addition, further improvement strategies, including lattice engineering, nanostructuring design, surface modification and 3D porous architecting, are summarized. Finally, potential directions of resolving emergent challenges and forward prospects on augmenting the performance of vanadium oxides‐based electrode materials to facilitate their commercial application in SIBs are proposed. This review provides pioneering understanding of vanadium oxides‐based materials and guiding directions for the development viability of future cutting‐edge SIBs.