Bibliometric analysis and systematic review of electrochemical methods for environmental remediation.

Electrochemical methods are increasingly favored for remediating polluted environments due to their environmental compatibility and reagent-saving features. However, a comprehensive understanding of recent progress, mechanisms, and trends in these methods is currently lacking. Web of Science (WoS) databases were utilized for searching the primary data to understand the knowledge structure and research trends of publications on electrochemical methods and to unveil certain hotspots and future trends of electrochemical methods research. The original data were sampled from 9080 publications in those databases with the search deadline of June 1st, 2022. CiteSpace and VOSviewer software facilitated data visualization and analysis of document quantities, source journals, institutions, authors, and keywords. We discussed principles, influencing factors, and progress related to seven major electrochemical methods. Notably, publications on this subject have experienced significant growth since 2007. The most frequently-investigated areas in electrochemical methods included novel materials development, heavy metal remediation, organic pollutant degradation, and removal mechanism identification. "Advanced oxidation process" and "Nanocomposite" are currently trending topics. The major remediation mechanisms are adsorption, oxidation, and reduction. The efficiency of electrochemical systems is influenced by material properties, system configuration, electron transfer efficiency, and power density. Electro-Fenton exhibits significant advantages in achieving synergistic effects of anodic oxidation and electro-adsorption among the seven techniques. Future research should prioritize the improvement of electron transfer efficiency, the optimization of electrode materials, the exploration of emerging technology coupling, and the reduction in system operation and maintenance costs.

A new method of alkalinity remediation for Cd-contaminated groundwater by PAAS-modified MgCO3/Mg(OH)2 colloid.

Mg(OH)2 dissolves slowly and can provide a long-term source of alkalinity, thus a promising alternative reagent for the in situ remediation of heavy metal polluted groundwater. Unfortunately, it exhibits a relatively poor stabilization effect on heavy metal Cd due to the higher solubility of the resulting stabilized product, Cd(OH)2. To overcome this limitation, we investigated the use of MgCO3/Mg(OH)2 colloid modified by sodium polyacrylate (PAAS) to remove Cd from groundwater. Through ultrasonic dispersion, the molecular chains of PAAS are broken, causing a transformation from flocculation to surface modification, resulting in the production of a stable colloid. The colloidal particles of MgCO3/Mg(OH)2 have a smaller size and a negatively charged surface, which significantly enhances their migration ability in aquifers. The combination of MgCO3 and Mg(OH)2 provides a complementary effect, where MgCO3 effectively precipitates Cd in the aquifer while Mg(OH)2 maintains the required pH level for stabilization. The optimal compounding ratio of MgCO3 to Mg(OH)2 for achieving the best stabilization effect on Cd is found to be 1:1. Column experiments demonstrate that the injection of MgCO3/Mg(OH)2 colloid substantially enhances Cd stability, reducing the exchangeable fraction of Cd in aquifer media from 88.61% to a range of 22.50-34.38%. Based on these results, the MgCO3/Mg(OH)2 colloid shows great potential as a reactive medium for remediating Cd-contaminated groundwater.

Light Addressable Potentiometric Sensors for Biochemical Imaging on Microscale: A Review on Optimization of Imaging Speed and Spatial Resolution.

Light addressable potentiometric sensors (LAPS) are a competitive tool for unmarked biochemical imaging, especially imaging on microscale. It is essential to optimize the imaging speed and spatial resolution of LAPS since the imaging targets of LAPS, such as cell, microfluidic channel, etc., require LAPS to image at the micrometer level, and a fast enough imaging speed is a prerequisite for the dynamic process involved in biochemical imaging. In this study, we discuss the improvement of LAPS in terms of imaging speed and spatial resolution. The development of LAPS in imaging speed and spatial resolution is demonstrated by the latest applications of biochemistry monitoring and imaging on the microscale.

"Wane and wax" strategy: Enhanced evolution kinetics of liquid phase Li2S4 to Li2S via mutually embedded CNT sponge/Ni-porous carbon electrocatalysts.

The lithium-sulfur battery (Li-S) has been considered a promising energy storage system, however, in the practical application of Li-S batteries, considerable challenges remain. One challenge is the low kinetics involved in the conversion of Li2S4 to Li2S. Here, we reveal that highly dispersed Ni nanoparticles play a unique role in the reduction of Li2S4. Ni-porous carbon (Ni-PC) decorated in situ on a free-standing carbon nanotube sponge (CNTS/Ni-PC) enriches the current response of liquid phase Li2S4 and Li2S2 around the cathode more than 8.1 and 5.7 times higher than that of the CNTS blank sample, respectively, greatly boosting the kinetics and decreasing the reaction overpotential of Li2S4 reduction (lower Tafel slope and larger current response). Thus, with the same total overpotential, more space is provided for the concentration difference overpotential, allowing the more soluble polysulfide intermediates farther away from the surface of the conductive materials to be reduced based on the "wane and wax" strategy, and significantly improving the sulfur utilization. Consequently, S@CNTS/Ni-PC delivers excellent rate performance (812.4 mAh·g-1 at 2C) and a remarkable areal capacity of 10.1 mAh·cm-2. This work provides a viable strategy for designing a target catalyst to enhance the conversion kinetics in the Li2S4 reduction process.

A Simulation Optimization Factor of Si(111)-Based AlGaN/GaN Epitaxy for High Frequency and Low-Voltage-Control High Electron Mobility Transistor Application.

The effects of barrier layer thickness, Al component of barrier layer, and passivation layer thickness of high-resistance Si (111)-based AlGaN/GaN heterojunction epitaxy on the knee-point voltage (Vknee), saturation current density (Id-sat), and cut-off frequency (ft) of its high electron mobility transistor (HEMT) are simulated and analyzed. A novel optimization factor OPTIM is proposed by considering the various performance parameters of the device to reduce the Vknee and improve the Id-sat on the premise of ensuring the ft. Based on this factor, the optimized AlGaN/GaN epitaxial structure was designed with a barrier layer thickness of 20 nm, an Al component in the barrier layer of 25%, and a SiN passivation layer of 6 nm. By simulation, when the gate voltage Vg is 0 V, the designed device with a gate length of 0.15 µm, gate-source spacing of 0.5 µm, and gate-drain spacing of 1 µm presents a high Id-sat of 750 mA/mm and a low Vknee of 2.0 V and presents ft and maximum frequency (fmax) as high as 110 GHz and 220 GHz, respectively. The designed device was fabricated and tested to verify the simulation results. We demonstrated the optimization factor OPTIM can provide an effective design method for follow-up high-frequency and low-voltage applications of GaN devices.

Light addressable potentiometric sensor with well-ordered pyramidal pits-patterned silicon.

Light addressable potentiometric sensor (LAPS) with the structure of electrolyte-insulator-semiconductor is a kind of field effect sensor that detects local potential changes caused by protonation and deprotonation between electrolyte and insulator by light pulse. And scanned light pulse allows two-dimensional imaging of the distribution of chemical/biological species on the surface of sensor. An important challenge is to achieve low-cost, strong anti-interference and high-performance silicon-based LAPS. In this study, we propose to combine microsphere lithography with wet etching to fabricate well-ordered, tunable and low-cost pyramidal pits-patterned silicon as semiconductor of LAPS. The morphology and optical properties of pyramidal pits-patterned silicon are tested and analyzed. The sensing characteristics and the pH imaging performance of LAPS are tested and evaluated. The experiment results and theoretical analyses show that LAPS with pyramidal pits-patterned silicon has acceptable pH response, good long-term stability, and high performance in terms of photocurrent enhancement ratio, signal-to-noise ratio and pH imaging. This work can provide a simple, low-cost, strong anti-interference and high-performance device for pH-related chemical/biological analysis.

Molecular Simulation of Methane Adsorption Capacity of Matrix Components of Shale.

Shale gas occurs mainly as adsorption and free gas. Among them, whether the adsorbed gas can be gradually desorbed or not is a major cause of stable and high yield. The matrix component is the main factor affecting the adsorption capacity of shale. In this paper, by simulation software named Materials Studio (MS), using Molecular Dynamics Simulation and Monte Carlo Simulation, the adsorption capacity of different matrix components under specific conditions is studied and the four models: relative concentration model, diffusion coefficient model, saturated adsorption capacity model and isosteric heat of adsorption model, are built. The simulation models show that the mineral matrix has a significant impact on the adsorption of methane molecules in shale: kerogen I > smectite > chlorite > illite > quartz. Kerogen I has the strongest adsorption capacity with high-density thick layer adsorption. Under the temperature (369.97 K) and the formation pressure (28.07 MPa) and under the condition of 6.0 nm in the cylindrical hole, excess adsorption amount of kerogen I is 13.418%, the diffusion coefficient is only 0.046 Å2/ps, saturated adsorption amount is 3.060 cm3/g, and the amount of adsorption heat is 9.598 kJ/mol. As the adsorption force on the pore wall is not as strong as the interaction repulsion force between adsorbents within a short distance, the clay minerals all have 2~4 layers of narrow layer and low-density adsorption. The adsorption thickness of the single layer is inversely proportional to its adsorption capacity, and the adsorption capacity is positively correlated with the opportunity of exposing oxygen atoms to form hydrogen bonds. Quartz has no obvious adsorption potential for methane molecules. This study is conducive to the quantitative evaluation of shale gas adsorption capacity, selection of favorable blocks and advantageous zones of shale gas reservoirs, and the improvement of development efficiency.

Microbial functional changes mark irreversible course of Tibetan grassland degradation.

The Tibetan Plateau's Kobresia pastures store 2.5% of the world's soil organic carbon (SOC). Climate change and overgrazing render their topsoils vulnerable to degradation, with SOC stocks declining by 42% and nitrogen (N) by 33% at severely degraded sites. We resolved these losses into erosion accounting for two-thirds, and decreased carbon (C) input and increased SOC mineralization accounting for the other third, and confirmed these results by comparison with a meta-analysis of 594 observations. The microbial community responded to the degradation through altered taxonomic composition and enzymatic activities. Hydrolytic enzyme activities were reduced, while degradation of the remaining recalcitrant soil organic matter by oxidative enzymes was accelerated, demonstrating a severe shift in microbial functioning. This may irreversibly alter the world´s largest alpine pastoral ecosystem by diminishing its C sink function and nutrient cycling dynamics, negatively impacting local food security, regional water quality and climate.

Electrodeposition of cobalt-iron bimetal phosphide on Ni foam as a bifunctional electrocatalyst for efficient overall water splitting.

To solve environmental pollution and energy crisis, it is essential to design an efficient, economical, and stable bifunctional electrocatalyst for water splitting to produce renewable energy sources H2 and O2. In this study, low-crystallinity and microspherical CoFe-P/NF catalyst synthesized by potentiostat electrodeposition on a foam nickel substrate had an excellent hydrogen evolution reaction (HER), oxygen evolution reaction (OER), and water splitting performance. In 1 M KOH solution, the CoFe-P/NF required the overpotentials of 45 mV for HER and 287 mV for OER in order to create a current density of 10 mA cm-2. Furthermore, the Tafel slope for HER and OER was measured as 35.4 and 43.2 mV dec-1, respectively. Serving as the bifunctional catalysts, the CoFe-P/NF electrode couple displays a low voltage of only 1.58 V at 10 mA cm-2 with an excellent long-term stability. Such remarkably properties of the CoFe-P/NF are attributed to the crystalline-amorphous phase structure, the synergistic effect of Co, Fe and P, and rapid separation of bubbles from the electrode surface. In summary, this study provides a new method for developing cost-effective catalyst towards green hydrogen production via water splitting.

Light-Addressable Potentiometric Sensors in Microfluidics.

The light-addressable potentiometric sensor (LAPS) is an electrochemical sensor based on the field-effect principle of semiconductors. It is able to sense the change of Nernst potential on the sensor surface, and the measuring area can be controlled by the illumination of a movable light. Due to the unique light-addressable ability of the LAPS, the chemical imaging system constructed with the LAPS can realize the two-dimensional image distribution detection of chemical/biomass. In this review, the advantages of the LAPS as a sensing unit of the microelectrochemical analysis system are summarized. Then, the most recent advances in the development of the LAPS analysis system are explained and discussed. In particular, this review focused on the research of ion diffusion, enzymatic reaction, microbial metabolism, and droplet microfluidics using the LAPS analysis system. Finally, the development trends and prospects of the LAPS analysis system are illustrated.

Platycodin D regulates high glucose-induced ferroptosis of HK-2 cells through glutathione peroxidase 4 (GPX4).

Diabetic nephropathy (DN) is associated with inflammation. Platycodin D (PD) demonstrates anti-inflammatory activity. However, whether PD affects DN remains to be explored. Here, we aimed to discuss the role of PD in DN and its underlying mechanisms. High glucose (HG)-induced HK-2 cells were treated with PD, and cell viability was assessed using the Thiazolyl Blue Tetrazolium Bromide (MTT) assay. Ferroptosis-related factors such as lactate dehydrogenase (LDH) activity, lipid reactive oxygen species (ROS), iron (Fe2+) level, GSH level, and malondialdehyde (MDA) level were evaluated. Cell death was evaluated using the TUNEL assay. GPX4 expression was evaluated using Quantitative Real-time PCR (qRT-PCR) and Western blotting analysis. The results indicated that HG increased LDH activity, lipid ROS production, Fe2+ levels, and MDA levels and decreased GSH levels, suggesting that the HG condition induced ferroptosis. PD treatment inhibited ferroptosis in HG-induced cells, downregulated ACSL4 and TFR1 expression, and upregulated FTH-1 and SLC7A11 expression. PD reversed the effects of HG condition on cell death. Moreover, GPX4 expression was downregulated in HG-stimulated cells. Furthermore, we substantiated that PD suppressed ferroptosis by modulating GPX4 expression. In conclusion, PD inhibited ferroptosis in HG-induced HK-2 cells by upregulating GPX4 expression, suggesting that PD may be an effective drug for the clinical treatment of DN.

Nutrients in the rhizosphere: A meta-analysis of content, availability, and influencing factors.

Nutrient deficiency in most terrestrial ecosystems constrains global primary productivity. Rhizosphere nutrient availability directly regulates plant growth and is influenced by many factors, including soil properties, plant characteristics and climate. A quantitatively comprehensive understanding of the role of these factors in modulating rhizosphere nutrient availability remains largely unknown. We reviewed 123 studies to assess nutrient availability in the rhizosphere compared to bulk soil depending on various factors. The increase in microbial nitrogen (N) content and N-cycling related enzyme activities in the rhizosphere led to a 10% increase in available N relative to bulk soil. The available phosphorus (P) in the rhizosphere decreased by 12% with a corresponding increase in phosphatase activities, indicating extreme demand and competition between plants and microorganisms for P. Greater organic carbon (C) content around taproots (+17%) confirmed their stronger ability to store more organic compounds than the fibrous roots. This corresponds to higher bacterial and fungal contents and slightly higher available nutrients in the rhizosphere of taproots. The maximal rhizosphere nutrient accumulation was common for low-fertile soils, which is confirmed by the negative correlation between most soil chemical properties and the effect sizes of available nutrients. Increases in rhizosphere bacterial and fungal population densities (205-254%) were much higher than microbial biomass increases (indicated as microbial C: +19%). Consequently, despite the higher microbial population densities in the rhizosphere, the biomass of individual microbial cells decreased, pointing on their younger age and faster turnover. This meta-analysis shows that, contrary to the common view, most nutrients are more available in the rhizosphere than in bulk soil because of higher microbial activities around roots.

Impact of ZnO nanoparticles on soil lead bioavailability and microbial properties.

In the present study, we investigated the responses of microbial respiration and community structure, enzyme activity and DTPA-extractable Pb within 60 days of incubation in soils treated with Pb and nano-ZnO. The results showed that when the concentration of nano-ZnO exceeded 10 mg/kg, the concentration of DTPA-extractable Pb significantly decreased by 10.6%-21.3% on the 60th day of the experiment. The addition of nano-ZnO decreased the Pb-contaminated soil pH from 6.18 to 6.08 at 7 days, which is part of the reason for the ß-glucosidase activity change. Ten mg/kg nano-ZnO significantly reduced the qCO2 value, which represented the microbial energy demand for the conversion of carbon sources into biomass. Nano-ZnO improved the microbial diversity and richness of some metal-tolerant bacteria at 60 days. The findings provide deeper insight into the responses of soil microbes and Pb bioavailability in the presence of nano-ZnO particles.

Copper and Zirconium Codoped O3-Type Sodium Iron and Manganese Oxide as the Cobalt/Nickel-Free High-Capacity and Air-Stable Cathode for Sodium-Ion Batteries.

Considering the abundance of iron and manganese within the Earth's crust, the cathode O3-NaFe0.5Mn0.5O2 has shown great potential for large-scale energy storage. Following the strategy of introducing specific heteroelements to optimize the structural stability for energy storage, the work has obtained an O3-type NaFe0.4Mn0.49Cu0.1Zr0.01O2 that exhibits enhanced electrochemical performance and air stability. It displays an initial reversible capacity of 147.5 mAh g-1 at 0.1C between 2 and 4.1 V, a capacity retention ratio exceeding 69.6% after 100 cycles at 0.2C, and a discharge capacity of 70.8 mAh g-1 at a high rate of 5C, which is superior to that of O3-NaFe0.5Mn0.5O2. The codoping of Cu/Zr reserves the layered O3 structure and enlarges the interlayer spacing, promoting the diffusion of Na+. In addition, the structural stability and air stability observed by Cu-doping is well maintained via the incorporation of extra Zr favoring a highly reversible phase conversion process. Thus, this work has demonstrated an efficient strategy for developing cobalt/nickel-free high-capacity and air-stable cathodes for sodium-ion batteries.

Honeycomb meshed working electrodes based on microsphere lithography for high-resolution chemical image sensor.

The chemical image sensor has attracted much attention because of its ability to visualize the spatial distribution of biochemical species in solution. However, the lateral diffusion of photo-generated carriers generated by illuminating backside of the substrate limits the spatial resolution of the sensor and the sharpness of the image. In this study, honeycomb meshed metal array based on microsphere lithography as working electrodes of the sensor is proposed. A focused light spot illuminates a plurality of periodic and ordered mesh holes and the metal electrodes adjacent to the mesh holes. For chemical imaging performance, sensors with honeycomb meshed working electrodes are developed for comparison with the sensor the flat working electrodes, and their spatial resolution is tested under the focused light spot with different sizes. Three interpretations of improved spatial resolution including enhanced recombination of the photo-generated holes by electrons during the initial stage of lateral diffusion and two boundary cases of modulated light illuminating meshed working electrodes on the substrate are elaborated. The experimental results show that the spatial resolution of sensor chips with honeycomb meshed working electrodes is better than that of the sensor with the flat working electrodes and is higher under the illumination condition of smaller light spots.

The critical role of titanium cation in the enhanced performance of P2-Na0.5Ni0.25Mn0.60Ti0.15O2 cathode material for sodium-ion batteries.

Tremendous effort has been devoted to develop durable electrode materials for sodium ion batteries. This work focuses on enhancing the reversibility of a cathode material Na0.5Ni0.25Mn0.75O2 by adopting the titanium cation doping strategy. The obtained P2-Na0.5Ni0.25Mn0.60Ti0.15O2 material shows smooth charge-discharge curves upon suppressing the Na+/vacancy ordering effect via the partial substitution of Mn4+ for Ti4+, and enhanced cycling performance. It exhibits a reversible capacity of 138 mA h g-1 at 0.5C, as well as a high rate capacity of 81 mA h g-1 at 5C between a cut-off voltage of 2 and 4 V, while long-term cycling stability is demonstrated with a capacity retention of 84% over 200 cycles. An enhanced cycling stability is also observed when the voltage is between 2 and 4.2 V. The feasibility of constructing a symmetrical Na-ion full cell with Na0.5Ni0.25Mn0.60Ti0.15O2 as cathode and anode electrodes is also demonstrated. The titanium cation doping results in reduced charge transfer impedance and an enhanced sodium cation diffusion coefficient, thus suggesting an efficient strategy to obtain a durable cathode material for sodium ion batteries.

Impact of manure on soil biochemical properties: A global synthesis.

Manure application mitigates land degradation and improves soil fertility. Despite many individual studies on manure effects, a comprehensive overview of its consequences for a broad range of soil properties is lacking. Through a meta-analysis of 521 observations spanning the experiments from days after pulse addition up to 113 years with continues manure input, we quantified and generalized the average responses of soil biochemical properties depending on climate factors, management, soil, and manure characteristics. Large increase of pools with fast turnover (microbial carbon (C) and nitrogen (N): +88% and +84%, respectively) compared to stable organic matter pools (+27% for organic C, and +33% for total N) reflects acceleration of C and N cycles and soil fertility improvement. Activities of enzymes acquiring C-, energy-, N-, phosphorus- and sulfur were 1.3-3.3 times larger than those in soil without manure for all study durations included. Soil C/N ratio remained unaffected, indicating the stability of coupled C and N cycles. Microbial C/N ratio decreased, indicating a shift towards bacterial domination, general increase of C and N availability and acceleration of element cycling. Composted manure or manure without mineral fertilizers induced the greatest increase compared to non-composted manure or manure with mineral fertilizers, respectively, in most biochemical properties. The optimal manure application rate for adjusting proper soil pH was 25 Mg ha-1 year-1. Among manure types, swine manure caused the greatest increase of N-cycle-related properties: microbial N (+230%), urease (+258%) and N-acetyl-ß-D-glucosaminidase (+138%) activities. Manure application strategies should avoid P and N losses and pollution via runoff, leaching or gaseous emissions due to fast mineralization and priming of soil organic matter. In conclusion, manure application favors C accumulation and accelerates nutrient cycling by providing available organic substances and nutrients and thus increasing enzyme activities.

Hub Proteins Involved in RAW 264.7 Macrophages Exposed to Direct Current Electric Field.

At present, studies on macrophage proteins mainly focus on biological stimuli, with less attention paid to the responses of macrophage proteins to physical stimuli, such as electric fields. Here, we exploited the electric field-sensitive hub proteins of macrophages. RAW 264.7 macrophages were treated with a direct current electric field (dcEF) (200 mV/mm) for four hours, followed by RNA-Seq analysis. Differentially expressed genes (DEGs) were obtained, followed by Gene Ontology (GO), Kyoto Encyclopedia of Genes and Genomes pathway (KEGG) and protein-protein interaction (PPI) analysis. Eight qPCR-verified DEGs were selected. Subsequently, three-dimensional protein models of DEGs were modeled by Modeller and Rosetta, followed by molecular dynamics simulation for 200 ns with GROMACS. Finally, dcEFs (10, 50, and 500 mV/mm) were used to simulate the molecular dynamics of DEG proteins for 200 ns, followed by trajectory analysis. The dcEF has no obvious effect on RAW 264.7 morphology. A total of 689 DEGs were obtained, and enrichment analysis showed that the steroid biosynthesis pathway was most affected by the dcEF. Moreover, the three-dimensional protein structures of hub proteins were constructed, and trajectory analysis suggested that the dcEF caused an increase in the atomic motion of the protein in a dcEF-intensity-dependent manner. Overall, we provide new clues and a basis for investigating the hub proteins of macrophages in response to electric field stimulation.

Cellular processes involved in lung cancer cells exposed to direct current electric field.

With the rapid breakthrough of electrochemical treatment of tumors, electric field (EF)-sensitive genes, previously rarely exploited, have become an emerging field recently. Here, we reported our work for the identification of EF-sensitive genes in lung cancer cells. The gene expression profile (GSE33845), in which the human lung cancer CL1-0 cells were treated with a direct current electric field (dcEF) (300 mV/mm) for 2 h, was retrieved from GEO database. Differentially expressed genes (DEGs) were acquired, followed by Gene Ontology (GO), Kyoto Encyclopedia of Genes and Genomes pathway (KEGG) and protein-protein interaction (PPI) analysis. Hub genes were acquired and analyzed by various tools including the Human Protein Atlas, Kaplan-Meier analysis, Cytoscape, FunRich, Oncomine and cBioPortal. Subsequently, three-dimensional protein models of hub genes were modeled by Modeller 9.20 and Rosetta 3.9. Finally, a 100 ns molecular dynamics simulation for each hub protein was performed with GROMACS 2018.2. A total of 257 DEGs were acquired and analyzed by GO, KEGG and PPI. Then, 10 hub genes were obtained, and the signal pathway analysis showed that two inflammatory pathways were activated: the FoxO signaling pathway and the AGE-RAGE signaling pathway. The molecular dynamic analysis including RMSD and the radius of gyration hinted that the 3D structures of hub proteins were built. Overall, our work identified EF-sensitive genes in lung cancer cells and identified that the inflammatory state of tumor cells may be involved in the feedback mechanism of lung cancer cells in response to electric field stimulation. In addition, qualified three-dimensional protein models of hub genes were also constructed, which will be helpful in understanding the complex effects of dcEF on human lung cancer CL1-0 cells.

Low-Strain Reticular Sodium Manganese Oxide as an Ultrastable Cathode for Sodium-Ion Batteries.

Sodium-ion batteries (SIBs) are recognized as attractive alternatives for grid-scale electrochemical energy storage applications. Transition metal oxide cathodes represent one of the most dynamic materials for industrialization among the various cathodes for SIBs. Here, a cation-doped cathode Na0.44Mn0.89Ti0.11O2 with a tunnel structure is introduced, which undergoes a lowered volume change of only 5.26% during the Na+ insertion/extraction process. Moreover, the average Na+ diffusion coefficients are enhanced by more than 3-fold upon the doping of the Ti cation. The obtained cathode delivers a practically usable capacity of 119 mAh g-1 at 0.1 C as well as an enhanced discharge capacity of 96 mAh g-1 at 5 C. Durability is demonstrated by the retained 71 mAh g-1 after 1000 cycles, corresponding to a capacity retention of 74%. This work demonstrates that the reticular Na0.44Mn0.89Ti0.11O2 is a promising ultrastable cathode material for the development of long-life sodium-ion batteries.