Stability Of Oxygen Vacancies Research Articles

Enhancing photocatalytic performance in Bi₂WO₆ nanolayers via ultrasound-assisted oxygen vacancy engineering

High-quality two-dimensional Bi₂WO₆ nanolayers were synthesized via hydrothermal processes, with oxygen vacancies introduced through an ultrasound-assisted alkali etching treatment. Comprehensive characterization using Raman spectroscopy, X-ray absorption spectroscopy (XAS), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and positron annihilation spectroscopy (PAS) confirmed the presence and effects of these vacancies on the structural and electronic properties of the nanolayers. Raman spectroscopy revealed shifts in vibrational modes, particularly a blue shift in the WO₆ octahedral vibration modes, indicative of oxygen vacancy formation. XPS analysis showed a reduction in the binding energies of the Bi 4f and W 4f orbitals, confirming an altered electronic environment. TEM images demonstrated significant lattice distortions in the oxygen-vacancy-rich regions, particularly disordered WO₆ octahedra and disrupted BiO bond lengths. These distortions are consistent with the structural disorder observed in XAS measurements, which highlighted a reduction in the coordination number of W atoms and a corresponding contraction of WO bond lengths. This charge redistribution between Bi and W atoms due to oxygen vacancies leads to localized structural perturbations, as further evidenced by PAS, which showed increased positron lifetimes associated with vacancy clusters, particularly around the Bi and W atoms. These vacancies create defective sites that trap photogenerated electrons, preventing their recombination with holes, thereby significantly enhancing photocatalytic performance. The enhanced photocatalytic activity was demonstrated by the nearly 98 % degradation of Rhodamine B dye under visible-light irradiation, a substantial improvement over the 70 % degradation achieved by the untreated sample. This work presents an innovative approach for generating stable oxygen vacancies in Bi₂WO₆ nanolayers and offers an in-depth understanding of the mechanisms that enhance photocatalytic performance, providing valuable insights for advancing photocatalysts designed for environmental remediation.

Tuning oxygen vacancies via photoinduced defect engineering in plasma pre-treated TiO2 for efficient solar-light-driven oxidation of trace methane

Photocatalysis employing cost-effective commercial titanium dioxide offers an ideal solution for eliminating trace methane emissions from livestock and poultry farming. However, significant challenges such as the rapid recombination of photogenerated carriers, a limited light absorption spectrum, and weak adsorption capabilities considerably hinder the effectiveness of titanium dioxide in the photocatalytic treatment of trace methane. This study proposes a novel approach to activate plasma pre-treated N-doped commercial anatase TiO2 into dual-defect TiO2 (N-doped TiO2-x) featuring stable and controllable oxygen vacancies (OV) through photoinduced defect engineering. Characterizations of the photocatalyst confirm the successful creation of surface defects, further evaluated through solar-light-driven CH4 (ppm level) removal investigations. The yield of this N-doped TiO2-x in converting CH4 is 4.84 μmol h−1, 44 times greater than that of unmodified TiO2, significantly outperforming previous studies. UV–Vis diffuse reflection spectra, and photoluminescence indicate that the modified commercial anatase TiO2 possesses a narrower band gap, efficient photogenerated carrier separation, and enhanced charge transfer. Furthermore, density functional theory (DFT) calculations demonstrate that the synergistic effects of oxygen vacancies and N doping enhance the adsorption and activation of both O2 and CH4 in the rate-determining step of the reaction. This innovative strategy holds considerable promise for modifying various materials for more efficient photocatalytic applications.

Sulfur filling activates vacancy-induced C–C bond cleavage in polyol electrooxidation

ABSTRACT Using the electrochemical polyol oxidation reaction (POR) to produce formic acid over nickel-based oxides/hydroxides (NiOxHy) is an attractive strategy for the electrochemical upgrading of biomass-derived polyols. The key step in the POR, i.e. the cleavage of the C–C bond, depends on an oxygen-vacancy-induced mechanism. However, a high-energy oxygen vacancy is usually ineffective for Schottky-type oxygen-vacancy-rich β-Ni(OH)2 (VSO-β-Ni(OH)2). As a result, both β-Ni(OH)2 and VSO-β-Ni(OH)2 cannot continuously catalyze oxygen-vacancy-induced C–C bond cleavage during PORs. Here, we report a strategy of oxygen-vacancy-filling with sulfur to synthesize a β-Ni(OH)2 (S-VO-β-Ni(OH)2) catalyst, whose oxygen vacancies are protected by filling with sulfur atoms. During PORs over S-VO-β-Ni(OH)2, the pre-electrooxidation-induced loss of sulfur and structural self-reconstruction cause the in-situ generation of stable Frenkel-type oxygen vacancies for activating vacancy-induced C–C bond cleavage, thus leading to excellent POR performances. This work provides an intelligent approach for guaranteeing the sustaining action of the oxygen-vacancy-induced catalytic mechanism in electrooxidation reactions.

Molten salt defect engineering regulation of Bi4TaO8Cl perovskite structure for boosting photo-Fenton degradation of antibiotics

Defect engineering offers a feasible avenue to ameliorate the photocatalytic activities of semiconductors, but the traditional preparation processes for introducing the defects would destroy the pristine morphology of the materials. Herein, a controllable defect engineering on CeO2 nanodots loaded Bi4TaO8Cl perovskite nanosheets was approached to synthesize well-defined CeO2/Bi4TaO8Cl (CE-BTC) heterojunction with stable oxygen vacancies (OVs) via a molten-salt-mediated strategy. Due to the coexistence of OVs and Ce4+/Ce3+ redox couple, the photo-Fenton degradation rate of ofloxacin by optimal CE-BTC heterojunction (0.09610 min−1) was 7.78 and 4.98 times higher than that by individual Bi4TaO8Cl and CeO2, respectively. Moreover, the CE-BTC also exhibited excellent degradation performance towards other antibiotics including norfloxacin, ciprofloxacin, tetracycline, and sulfamethoxazole, while maintaining good recyclability and stability. The high efficiency of CE-BTC was also attributed to its enhanced light-harvesting capability, low photogenerated carrier recombination, and minimal electron transfer resistance. Mechanism study indicated that ⋅OH and ⋅O2– were the dominant reactive species, whereas h+ also participated in the removal of ofloxacin with a lower contribution. This study demonstrated the enormous potential of CE-BTC heterojunction in the degradation and risk control of antibiotics, providing a promising strategy for designing highly dispersed heterojunction catalysts with surface defects.

Intrinsic doping and ageing of indium oxide thin films

Indium oxide (In2O3) is one of the most used materials for the synthesis of transparent electronics devices and currently tin-doped indium oxide (ITO) dominates the field of Transparent Conductive Oxides for most applications, from ICT to photovoltaics. In this work we present a study on the responses of indium oxide upon the formation, and stabilization, of point defects induced with different methods. After the deposition of In2O3 thin films via RF magnetron sputtering, treatments such as Ion Implantation (I.I.), Ultraviolet (UV) irradiation and Sun exposure were employed to generate oxygen vacancies as intrinsic dopants. Both I.I. and UV irradiations significantly improved the electrical conductivity of films, increasing the carrier density by up to 3 orders of magnitude. Moreover, after I.I. also the crystalline quality of the films was enhanced.To monitor the stability of oxygen vacancies upon exposure to ambient atmosphere, the ageing of samples was followed and recorded for a couple of weeks, reporting a fast and strong degradation of electrical properties. As a facile strategy to counteract the sheet resistance increase, samples were encapsulated in an ultra-thin (≈10 nm) SiO2 layer deposited via sputtering. Irradiated and encapsulated films retained a much lower sheet resistance throughout the observation time, preserving the samples conductivity.

High-Valence Cu Induced by Photoelectric Reconstruction for Dynamically Stable Oxygen Evolution Sites.

Oxygen vacancies are generally considered to play a crucial role in the oxygen evolution reaction (OER). However, the generation of active sites created by oxygen vacancies is inevitably restricted by their condensation and elimination reactions. To overcome this limitation, here, we demonstrate a novel photoelectric reconstruction strategy to incorporate atomically dispersed Cu into ultrathin (about 2-3 molecular) amorphous oxyhydroxide (a-CuM, M = Co, Ni, Fe, or Zn), facilitating deprotonation of the reconstructed oxyhydroxide to generate high-valence Cu. The in situ XAFS results and first-principles calculations reveal that Cu atoms are stabilized at high valence during the OER process due to Jahn-Teller distortion, resulting in para-type double oxygen vacancies as dynamically stable catalytic sites. The optimal a-CuCo catalyst exhibits a record-high mass activity of 3404.7 A g-1 at an overpotential of 300 mV, superior to the benchmarking hydroxide and oxide catalysts. The developed photoelectric reconstruction strategy opens up a new pathway to construct in situ stable oxygen vacancies by high-valence Cu single sites, which extends the design rules for creating dynamically stable active sites.

Large-scale Preparation of Black CeOx with Stable Oxygen Vacancies

Large-scale Preparation of Black CeOx with Stable Oxygen Vacancies

Dielectric probing of low-temperature degradation resistance of commercial zirconia bio-ceramics

ObjectivesTo investigate the effect of the stability of oxygen vacancies on the low-temperature degradation (LTD) resistance of two kinds of commercial zirconia-based materials (3Y-TZP ceramics and Ce-TZP/Al2O3 composites) via the dielectric probing methods. MethodsThe commercial 3Y-TZP ceramics and Ce-TZP/Al2O3 composites were prepared via conventional solid-state methods. Density, phase content, microstructure, strain, and biaxial flexural strength (BFS) of two materials were investigated using Archimedes method, XRD, SEM, strain-electric field (S-E) loops and ball-on-ring methods, respectively. The concentration of oxygen vacancies before and after LTD of two materials were evaluated using dielectric probing and XPS methods. ResultsThe XRD analysis revealed that compared to the 3Y-TZP ceramics, the Ce-TZP/Al2O3 composites showed better LTD resistance, without clear LTD. The greater LTD resistance for Ce-TZP/Al2O3 composites was associated with their stability of oxygen vacancies, by higher activation energy based on the dielectric measurements and XPS results. For the 3Y-TZP ceramics that underwent the tetragonal to the monoclinic phase transition during the LTD treatment, the concentration of their oxygen vacancies decreased after LTD. In addition, the Ce-TZP/Al2O3 composites exhibited higher flexural strength and potential fracture toughness based on the BFS testing and strain vs electric field measurement results, indicating a great potential for use in fixed restorative dental applications. SignificanceThis work suggested the stability of oxygen vacancies played a key role in the resistance to LTD. Optimizing the stability of the oxygen vacancies is key to the development of more reliable zirconia- based dental biomaterials with greater resistance to LTD.

Enhanced Light Absorption and Photo-Generated Charge Separation Efficiency for Boosting Photocatalytic H2 Evolution through TiO2 Quantum Dots with N-Doping and Concomitant Oxygen Vacancy.

Low-range light absorption and rapid recombination of photo-generated charge carriers have prevented the occurrence of effective and applicable photocatalysis for decades. Quantum dots (QDs) offer a solution due to their size-controlled photon properties and charge separation capabilities. Herein, well-dispersed interstitial nitrogen-doped TiO2 QDs with stable oxygen vacancies (N-TiO2-x-VO) are fabricated by using a low-temperature, annealing-assisted hydrothermal method. Remarkably, electrostatic repulsion prevented aggregation arising from negative charges accumulated in situ on the surface of N-TiO2-x-VO, enabling complete solar spectrum utilization (200-800 nm) with a 2.5 eV bandgap. Enhanced UV-vis photocatalytic H2 evolution rate (HER) reached2757µmol g-1 h-1, 41.6 times higher than commercial TiO2 (66µmol g-1 h-1). Strikingly, under visible light, HER rate was 189µmol g-1 h-1. Experimental and simulated studies of mechanisms reveal that VO can serve as an electron reservoir of photo-generated charge carriers on N-doped active sites, and consequently, enhance the separation rate of exciton pairs. Moreover, the negative free energy (-0.35 V) indicates more favorable thermodynamics for HER as compared with bulk TiO2 (0.66 V). This research work paves a new way of developing efficient photocatalytic strategies of HER that are applicable in the sustainable carbon-zero energy supply.

Decoupling electrolyte strategy for a high-voltage Na-ion hybrid capacitor based on NaFeO2 and activated carbon

Sodium iron dioxide (NaFeO2) with high specific capacity, has been widely used as a kind of electrode materials for Na-ion batteries. When NaFeO2 is used as the battery-type electrode for aqueous Na-ion hybrid capacitors, there are a lot of technical challenges to meet, especially the narrow voltage window limited by the thermodynamic decomposition of water. We propose a novel decoupling electrolyte strategy to suppress the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER) on the NaFeO2 anode and the activated carbon (AC) cathode respectively, in order to expand the voltage window of the aqueous AC//NaFeO2 Na-ion hybrid capacitor. The alkaline anolyte (2 M NaOH) and the neutral catholyte (1 M Na2SO4) can be decoupled by the cation exchange membrane, which selectively allows the Na+ ions through the membrane to carry the electric currents in the charge/discharge process. The NaFeO2 sample with the stable crystal structure and oxygen vacancy defects, can provide a gravimetric specific capacitance of 101.1 F g−1 at 1 A g−1. Electrochemical kinetic analysis indicates that the capacitor-type behaviour is predominant in the electrochemical energy storage process of the AC//NaFeO2 Na-ion capacitor at the scan rates higher than 40 mV s−1. The AC//NaFeO2 Na-ion capacitor with the stable voltage window of 2 V, can provide an energy density of 12.6 Wh kg−1 at 1 kW kg−1. Due to its inhibiting effects on HER and OER, this decoupling electrolyte strategy holds great potential for constructing high-voltage aqueous energy storage devices.

Biomass-Derived Carbon Quantum Dots Chemical Bonding with Sn-Doped Bi2O2CO3 Endowed Fast Carriers' Dynamics and Stabilized Oxygen Vacancies for Efficient Decontamination of Combined Pollutants.

Surface defects on photocatalysts could promote carrier separation and generate unsaturated sites for chemisorption and reactant activation. Nevertheless, the inactivation of oxygen vacancies (OVs) would deteriorate catalytic activity and limit the durability of defective materials. Herein, bagasse-derived carbon quantum dots (CQDs) are loaded on the Sn-doped Bi2O2CO3 (BOC) via hydrothermal procedure to create Bi─O─C chemical bonding at the interface, which not only provides efficient atomic-level interfacial electron channels for accelerating carriers transfer, but also enhances durability. The optimized Sn-BOC/CQDs-2 achieves the highest photocatalytic removal efficiencies for levofloxacin (LEV) (88.7%) and Cr (VI) (99.3%). The elimination efficiency for LEV and Cr (VI) from the Sn-BOC/CQDs-2 is maintained at 55.1% and 77.0% while the Sn-BOC is completely deactivated after four cycle tests. Furthermore, the key role of CQDs in stabilization of OVs is to replace OVs as the active center of H2O and O2 adsorption and activation, thereby preventing reactant molecules from occupying OVs. Based on theoretical calculations of the Fukui index and intermediates identification, three possible degradation pathways of LEV are inferred. This work provides new insight into improving the stability of defective photocatalysts.

Bimetallic lattice doped fillers with durable oxygen vacancies for corrosion resistance of coated steel in hostile environments

A series of Ca-doped Co3O4 nano-sheets (Ca-Co3O4) rich in oxygen vacancies were prepared using the alkali precipitation method at different pH values and added to the coating. Scanning electron microscopy and X-ray diffraction were performed to confirm the successful synthesis of the nano-fillers. The electron paramagnetic resonance (EPR) and X-ray photoelectron spectroscopy (XPS) spectroscopy determined that the nano-filler has abundant oxygen vacancies. The corrosion resistance test results showed that the epoxy coating containing the Ca-Co3O4 (pH = 12.5) filler exhibited the best corrosion resistance. After 48 h of corrosion in a high-temperature and high-pressure oxygen-rich (HTHP-O2) environment, the |Z|0.01 Hz is 5 orders of magnitude higher than that of the pure Co3O4 coating. Furthermore, the scanning vibrating electrode technique and O2-adsorption-desorption test indicated that Ca-Co3O4 with durable and stable oxygen vacancies could provide a complete, stable and dense passive film for the substrate (Q235B steel). Because oxygen vacancies can selectively transport O2 to the coating-substrate interface ahead of other corrosive media.

The dynamic anti-corrosion of self-derived space charge layer enabling long-term stable seawater oxidation

Developing corrosion-resistant oxygen evolution electrocatalysts that can sustain seawater electrolysis is crucial but challenging for hydrogen production. Herein, we develop a bimetallic oxyhydroxide electrocatalyst with self-derived selenate space charge layer (SeO42− SCL) by in-situ electrochemically reconstructing cobalt-doped nickel diselenide (Co-NiSe2) pre-catalyst, enabling long-term stability for seawater electrolysis. In-situ experiments and theoretical results reveal the promoting effect of cobalt-doping on the reconstruction of NiSe2 and generation of dynamically stable oxygen vacancy sites. Importantly, the SeO42− SCL derived from the reconstruction process shows a dynamic anti-corrosion behavior, thus protecting metal species from dissolution and meanwhile without blocking the diffusion and adsorption of reactive species. Consequently, a two-electrode cell assembled by this Co-NiSe2 pre-catalyst as an anode, reaches an industrial current density (500 mA cm−2) at a cell voltage of 1.70 V, and that works stably for over 1500 h in alkaline seawater, which is of significance for promoting the practicality of low-cost catalysts.

Research Progress on the Application of Topological Phase Transition Materials in the Field of Memristor and Neuromorphic Computing.

Topological phase transition materials have strong coupling between their charge, spin orbitals, and lattice structure, which makes them have good electrical and magnetic properties, leading to promising applications in the fields of memristive devices. The smaller Gibbs free energy difference between the topological phases, the stable oxygen vacancy ordered structure, and the reversible topological phase transition promote the memristive effect, which is more conducive to its application in information storage, information processing, information calculation, and other related fields. In particular, extracting the current resistance or conductance of the two-terminal memristor to convert to the weight of the synapse in the neural network can simulate the behavior of biological synapses in their structure and function. In addition, in order to improve the performance of memristors and better apply them to neuromorphic computing, methods such as ion doping, electrode selection, interface modulation, and preparation process control have been demonstrated in memristors based on topological phase transition materials. At present, it is considered an effective method to obtain a unique resistive switching behavior by improving the process of preparing functional layers, regulating the crystal phase of topological phase transition materials, and constructing interface barrier-dependent devices. In this review, we systematically expound the resistance switching mechanism, resistance switching performance regulation, and neuromorphic computing of topological phase transition memristors, and provide some suggestions for the challenges faced by the development of the next generation of non-volatile memory and brain-like neuromorphic devices based on topological phase transition materials.

Creation of robust oxygen vacancies in 2D ultrathin BiOBr nanosheets by irradiation through photocatalytic memory effect for enhanced CO2 reduction

An interesting photocatalytic memory effect was found in 2D ultrathin BiOBr nanosheets, which endowed them the capability to trap photogenerated electrons on Bi3+ and Br- in this material system for an extended period of time and resulted in the creation of stable oxygen vacancies (Ov) by just visible light irradiation due to the charge balance requirement. Thus, a broader visible light absorption, more negative conduction band minimum, stronger piezoelectric response, better charge carrier separation and transfer, and enhanced CO2 adsorption and activation were occurred in these BiOBr nanosheets with prior visible light irradiation, all of which were beneficial for their enhanced CO2 reduction performances in photocatalysis, piezocatalysis, and photopiezocatalysis, respectively, than their counterparts without it. This work demonstrated a novel approach to create oxygen vacancies by light irradiation through the photocatalytic memory effect, which could be readily applied to similar photocatalyst systems to boost their performances and generate novel functionalities.

Catalyzing Generation and Stabilization of Oxygen Vacancies on CeO2-x Nanorods by Pt Nanoclusters as Nanozymes for Catalytic Therapy.

Although CeO2 nanomaterials have been widely explored as nanozymes for catalytic therapy, they still suffer from relatively low activities. Herein, the catalyzing generation and stabilization of oxygen vacancies on CeO2 nanorods by Pt nanoclusters via H2 gas reduction under mild temperature (350°C) to obtain Pt/CeO2- x , which can serve as a highly efficient nanozyme for catalytic cancer therapy, is reported. The deposited Pt on CeO2 by the atomic layer deposition technique not only can serve as the catalyst to generate oxygen vacancies under mild temperature reduction through the hydrogen spillover effect, but also can stabilize the generated oxygen vacancies. Meanwhile, the oxygen vacancies also provide anchoring sites for Pt forming strong metal-support interactions and thus preventing their agglomerations. Importantly, the Pt/CeO2- x reduced at 350°C (Pt/CeO2- x -350R) exhibits excellent enzyme-mimicking catalytic activity for generation of reactive oxygen species (e.g., ·OH) as compared to other control samples, including CeO2 , Pt/CeO2 , and Pt/CeO2- x reduced at other temperatures, thus achieving excellent performance for tumor-specific catalytic therapy to efficiently eliminate cancer cells in vitro and ablate tumors in vivo. The excellent enzyme-mimicking catalytic activity of Pt/CeO2- x -350R originates from the good catalytic activities of oxygen vacancy-rich CeO2- x and Pt nanoclusters.

Gradient Concentration Refilling of N Stabilizes Oxygen Vacancies for Enhanced Zn2+ Storage

AbstractThe introduction of oxygen vacancies into aqueous zinc ion battery (ZIB) cathodes can significantly improve the diffusion kinetics of Zn2+, endowing enhanced electrochemical performance. However, the stability of oxygen vacancies in batteries during aqueous electrolyte cycling has been overlooked. Here, the oxygen vacancy is stabilized by the refilling of different impurity atoms, and gradient concentration refilling of N achieves the most stable state of the oxygen vacancy with minimum formation energy (4.77 eV). The obtained Zn3V2O7(OH)2·2H2O with gradient N refilling of partial oxygen vacancies (N‐VO‐ZVO) achieves more stable oxygen vacancies and a low Zn2+ diffusion energy barrier (0.19 eV) with an ultra‐high rate performance of 186 mAh g−1 at 100 A g−1 and capacity retention rate of 84.9% after 10 000 cycles.

Semi‐Metallic Superionic Layers Suppressing Voltage Fading of Li‐Rich Layered Oxide Towards Superior‐Stable Li‐Ion Batteries

AbstractLi‐rich layered oxides (LRLOs) with greater specific capacity density are constrained by voltage attenuation and inferior rate performance because of irreversible oxygen release, metal dissolving and poor lithium‐ion transport capacity. Herein, a simple surface modification is designed to solve the performance degradation and structural collapse of LRLOs. Combining experiments with density functional theory (DFT) calculations, a semi‐metallic LiMn2O4‐like structure (LMO) with spin‐polarized conducting electrons, is introduced to the surface of the cathode restrains the activated surficial lattice oxygen ions by its stable oxygen vacancies. Additionally, Ni doping results in a fast‐ion conductor Li0.8Nb0.96Ni0.2O3structure (LNO) with lowered lithium ions diffusion barrier, which is tightly conjugating to substrate and synergistically reinforces the Li diffusion path through the cathode‐electrolyte interphase. Moreover, Mn dissolution is successfully relieved due to the decrease in Mn concentration in the coating layers. As a result, the modified material (LRLO@LMO@LNO) exhibits an ultra‐high discharge capacity of 120.4 mAh g−1even at 10 C with a very small discharge voltage attenuation of 313 mV after 600 cycles (0.52 mV per cycle) at 1 C. Undoubtedly, this method discloses a simple and effective approach to promote the practical utilization of high‐energy‐density.

Semi-Metallic Superionic Layers Suppressing Voltage Fading of Li-Rich Layered Oxide Towards Superior-Stable Li-Ion Batteries.

Li-rich layered oxides (LRLOs) with greater specific capacity density are constrained by voltage attenuation and inferior rate performance because of irreversible oxygen release, metal dissolving and poor lithium-ion transport capacity. Herein, a simple surface modification is designed to solve the performance degradation and structural collapse of LRLOs. Combining experiments with density functional theory (DFT) calculations, a semi-metallic LiMn2 O4 -like structure (LMO) with spin-polarized conducting electrons, is introduced to the surface of the cathode restrains the activated surficial lattice oxygen ions by its stable oxygen vacancies. Additionally, Ni doping results in a fast-ion conductor Li0.8 Nb0.96 Ni0.2 O3 structure (LNO) with lowered lithium ions diffusion barrier, which is tightly conjugating to substrate and synergistically reinforces the Li diffusion path through the cathode-electrolyte interphase. Moreover, Mn dissolution is successfully relieved due to the decrease in Mn concentration in the coating layers. As a result, the modified material (LRLO@LMO@LNO) exhibits an ultra-high discharge capacity of 120.4 mAh g-1 even at 10 C with a very small discharge voltage attenuation of 313 mV after 600 cycles (0.52 mV per cycle) at 1 C. Undoubtedly, this method discloses a simple and effective approach to promote the practical utilization of high-energy-density.

Enabling an Intrinsically Safe and High‐Energy‐Density 4.5 V‐Class Lithium‐Ion Battery with Synergistically Incorporated Fast Ion Conductors (Adv. Energy Mater. 18/2023)

Li-Ion Batteries In article number 2203999, Zhenpeng Yao, Chun Zhan, Jun Lu, and co-workers work toward the fabrication of intrinsically safe and high-energy-density 4.5 V-class Li-ion batteries. A sophisticated multifunctional surficial modification implemented by a neat one-step treatment is reported. An oxygen ion conductor introduced to the surface of the cathode restrains the activated surficial lattice oxygen ions by its stable oxygen vacancies, thereby dramatically enhancing battery safety.