Electrochemical Tests Research Articles

Electrochemical Activation of LiGaO2: Implications for Ga-Doped Garnet Solid Electrolytes in Li-Metal Batteries.

Ga-doped Li7La3Zr2O12 garnet solid electrolytes exhibit the highest Li-ion conductivities among the oxide-type garnet-structured solid electrolytes, but instabilities toward Li metal hamper their practical application. The instabilities have been assigned to direct chemical reactions between LiGaO2 coexisting phases and Li metal by several groups previously. Yet, the understanding of the role of LiGaO2 in the electrochemical cell and its electrochemical properties is still lacking. Here, we are investigating the electrochemical properties of LiGaO2 through electrochemical tests in galvanostatic cells versus Li metal and complementary ex situ studies via confocal Raman microscopy, quantitative phase analysis based on powder X-ray diffraction, energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, and electron energy loss spectroscopy. The results demonstrate considerable and surprising electrochemical activity, with high reversibility. A three-stage reaction mechanism is derived, including reversible electrochemical reactions that lead to the formation of highly electronically conducting products. The results have considerable implications for the use of Ga-doped Li7La3Zr2O12 electrolytes in all-solid-state Li-metal battery applications and raise the need for advanced materials engineering to realize Ga-doped Li7La3Zr2O12for practical use.

Regulating electronic structure of anionic oxygen by Ti4+ doping to stabilize layered Li-rich oxide cathodes for Li-ion batteries

Abstract Layered Li-rich oxide cathodes enable to activate lattice oxygen anions redox in the charge compensation process and provide superior high specific capacity over 250 mAh/g due to their unique configuration, and thus attracting great attentions as promising cathode candidates for Li-ion batteries. However, how to better stabilize the bulk lattice oxygen framework and surface structure, and slow down the release of oxygen, is still major bottleneck to develop high performance Li-rich materials. Transition metal ions with outer d0 electronic configuration have distortable configuration, which can accommodate the local structure and chemical environment of the material, and then improve structural stability. Herein this work, the d0 transition metal Ti4+ is used as doping element to improve the chemical and structural stability, capacity retention and lithium ion diffusion kinetics of Li-rich material. The role of Ti in the material modification is revealed through synchrotron-based soft X-ray absorption spectroscopy, XRD, XPS and electrochemical tests. The improvement in structural stability can be attributed to that Ti doping can adjust the hybridization of O2p and TM3d to regulate the local electronic structure of both bulk lattice oxygen and surface oxygen vacancies. It is hoped that this work should shed light on the development of high-performance cathode materials for Li-ion Batteries.

High‐Toughness Hydrated Polymer Electrolytes for Advanced Structural Supercapacitors

AbstractStructural supercapacitors that simultaneously bear mechanical loads and store electrical energy have exciting potential for enhancing the efficiency of various mobile systems. However, a significant hurdle in developing practical structural supercapacitors is the inherent trade‐off between their mechanical properties and electrochemical capabilities, particularly within their electrolytes. This study demonstrates a tough polymer electrolyte with enhanced multifunctionality made through the controlled hydration of a solid polymer electrolyte with poly(lactic acid) (PLA) and lithium salts. Characterization via differential scanning calorimetry, X‐ray diffraction, and Fourier transform infrared spectroscopy confirms the consistent amorphous solid solution phase in varying salt concentrations, whether dried or hydrated. Electrochemical tests and tensile tests are performed to evaluate the ionic conductivity and mechanical properties of these electrolytes. The results indicate that the strategic incorporation of water in the polymer electrolyte significantly enhances the ionic conductivity while preserving its mechanical properties. A specific composition demonstrated a remarkable increase in ionic conductivity (3.11 µS cm−1) coupled with superior toughness (15.4 MJ m−3), significantly surpassing the base polymer. These findings open new horizons for integrating electrochemical functionality into structural polymers without compromising their mechanical properties. Additionally, the paper reports the successful fabrication and testing of structural supercapacitor prototypes combining carbon fibers with fabricated electrolytes, showcasing their potential for diverse applications.

Effect of forming parameters on the corrosion performance of retrogression- and warm-formed AA7075 alloy sheets

ABSTRACT Retrogression forming (RF) and warm forming (WF) are used to remedy formability limitations of high-strength precipitation-hardened AA7075 alloy sheets. RF is a thermomechanical treatment combining retrogression heat treatment and the forming of initially peak-aged T6 temper. WF is a thermomechanical treatment of initially pre-aged temper. The present work examines the corrosion performance of retrogression- and warm-formed AA7075 alloy sheets by determining the optimal pre-aging temperature (80°C or 100°C), forming temperature (room temperature, 150–200°C), strain rate (1, 0.1, or 0.01 s−1), and heating rate (1.1 or 20°C·s−1) for conventional slow and novel fast-forming technologies. Several alternating- and direct-current electrochemical tests were administered, including electrochemical impedance spectroscopy, potentiodynamic polarization, and linear polarization resistance. Results showed that the corrosion performance (i.e., passive film and corrosion-resistant properties) of formed AA7075 sheets was directly proportional to pre-aging and WF temperatures, inversely proportional to the RF temperature, and mildly affected by strain/forming rate and heating rate during forming.

In situ Raman reveals the critical role of Pd in electrocatalytic CO2 reduction to CH4 on Cu-based catalysts.

Electrocatalytic CO2 reduction reaction (CO2RR) for CH4 production presents a promising strategy to address carbon neutrality, and the incorporation of a second metal has been proven effective in enhancing catalyst performance. Nevertheless, there remains limited comprehension regarding the fundamental factors responsible for the improved performance. Herein, the critical role of Pd in electrocatalytic CO2 reduction to CH4 on Cu-based catalysts has been revealed at a molecular level using in situ surface-enhanced Raman spectroscopy (SERS). A "borrowing" SERS strategy has been developed by depositing Cu-Pd overlayers on plasmonic Au nanoparticles to achieve the in situ monitoring of the dynamic change of the intermediate during CO2RR. Electrochemical tests demonstrate that Pd incorporation significantly enhances selectivity toward CH4 production, and the Faradaic efficiency (FE) of CH4 is more than two times higher than that for the catalysts without Pd. The key intermediates, including *CO2-, *CO, and *OH, have been directly identified under CO2RR conditions, and their evolution with the electrochemical environments has been determined. It is found that Pd incorporation promotes the activation of both CO2 and H2O molecules and accelerates the formation of abundant active *CO and hydrogen species, thus enhancing the CH4 selectivity. This work offers fundamental insights into the understanding of the molecular mechanism of CO2RR and opens up possibilities for designing more efficient electrocatalysts.

Conversion of cobalt from spent LIBs to Co3O4 electrode material for application in supercapacitors

ABSTRACT The cathode material of lithium-ion batteries (LIBs) is endowed with valuable metals, such as cobalt. The improper treatment of these batteries pollutes the environment and causes enormous resource waste. Therefore, the recovery of valuable metals from spent LIBs has attracted widespread attention. In this study, Co3O4 electrode materials were prepared by a simple homogeneous precipitation method and heat treatment using a leaching solution of spent LIBs-positive electrode material as the cobalt source. The crystal structure and morphology of the products were examined at different annealing temperatures, and their electrochemical performance was analyzed. The results show that low-temperature annealing contributes to grain refinement. The Co3O4 material prepared at 300°C annealing temperature has a rod-like structure with distinct pores and a specific surface area of 58.98 m2 g−1. Furthermore, electrochemical performance testing reveals that Co3O4 prepared at 300°C displays the best electrochemical performance as an electrode material, with a specific capacitance of 97.93 F g−1 and a cycle retention rate of 79.12% after 500 charge–discharge cycles. These findings demonstrate the feasibility of recycling valuable metal cobalt from spent LIBs cathode materials to produce Co3O4 materials for use as supercapacitor electrode materials, opening up new avenues for the recycling and utilisation of spent LIBs.

A randomized controlled trial to assess if changing sleep timing can improve glucose metabolism in people with prediabetes and type 2 diabetes

BackgroundSocial jetlag is a chronic disruption of sleep timing that is characterized by different sleep timing during workdays and free days. Social jetlag has been associated with disturbed glucose metabolism, insulin resistance, and increased risk of metabolic syndrome and type 2 diabetes. In this study, we aim to investigate whether a combination of bright light therapy in the morning, bright light reduction in the evening and sleep advance instructions for 3 weeks reduces social jetlag and if this results in improvement of glycemic and metabolic control, sleep, mood and quality of life after 3 and 12 weeks in people with prediabetes and type 2 diabetes and to assess possible mediators, compared to regular sleep habits.MethodsIn this randomized controlled trial, 60 people with prediabetes or type 2 diabetes with > 1 h social jetlag will be recruited. The intervention consists of bright light therapy (5000 lx) emitted by Vitamine-L (Lumie, UK) for 30 min each morning, combined with the advice to follow sleep advance instructions and to wear bright light-dimming goggles every evening for a period of 3 weeks. The control group adheres to their regular sleep habits and conditions. The primary outcome is glycated hemoglobin (HbA1c) after 12 weeks comparing the intervention and control in an intention-to-treat analysis. Secondary outcomes at 3 and 12 weeks are (1) social jetlag; (2) insulin sensitivity, fasting blood glucose, glucose-lowering medication use, and frequency of perceived hypoglycemia; (3) metabolic outcomes, including body mass index (BMI), waist circumference, body fat percentage, and blood pressure; (4) mood, including depression, fatigue and anxiety (measured with questionnaires); and (5) quality of life measured using EQ5D questionnaire. To assess other factors that might play a role as possible mediators, we will measure (para)sympathetic nervous system activity assessed with ECGs and electrochemical skin conductance tests, sleep quality and sleep phase distribution assessed with a sleep measuring headband (ZMax), the Dim Light Melatonin Onset in saliva samples (in a subgroup) at 3 and 12 weeks, the feeling of satiety and satiation with a 10-cm visual analog scale (VAS), diet using a food frequency questionnaire, and physical activity using an accelerometer (ActiGraph).DiscussionSocial jetlag can contribute to poorer glycemic control and metabolic control in those with type 2 diabetes. With this intervention, we aim to reduce social jetlag and thereby improve glycemic and metabolic control. This could offer a way to improve overall population health and to reduce the disease burden of type 2 diabetes.Trial registrationISRCTN registry ISRCTN11967109. Registered on 9 May 2024.

Platinum nanowires/MXene nanosheets/porous carbon ternary nanocomposites for in situ monitoring of dopamine released from neuronal cells

Dopamine is an important neurotransmitter in the body and closely related to many neurodegenerative diseases. Therefore, the detection of dopamine is of great significance for the diagnosis and treatment of diseases, screening of drugs and unraveling of relevant pathogenic mechanisms. However, the low concentration of dopamine in the body and the complexity of the matrix make the accurate detection of dopamine challenging. Herein, an electrochemical sensor is constructed based on ternary nanocomposites consisting of one-dimensional Pt nanowires, two-dimensional MXene nanosheets, and three-dimensional porous carbon. The Pt nanowires exhibit excellent catalytic activity due to the abundant grain boundaries and highly undercoordinated atoms; MXene nanosheets not only facilitate the growth of Pt nanowires, but also enhance the electrical conductivity and hydrophilicity; and the porous carbon helps induce significant adsorption of dopamine on the electrode surface. In electrochemical tests, the ternary nanocomposite-based sensor achieves an ultra-sensitive detection of dopamine (S/N = 3) with a low limit of detection (LOD) of 28 nM, satisfactory selectivity and excellent stability. Furthermore, the sensor can be used for the detection of dopamine in serum and in situ monitoring of dopamine release from PC12 cells. Such a highly sensitive nanocomposite sensor can be exploited for in situ monitoring of important neurotransmitters at the cellular level, which is of great significance for related drug screening and mechanistic studies.

Stability of passive film and pitting susceptibility of 316 L stainless steel in the aggressive oilfield environment containing Cl−-CO2-O2

In this paper, the effects of chloride ions, oxygen, and carbon dioxide on the corrosion resistance of passive films formed on 316 L stainless steel were investigated in the aggressive oilfield environment using electrochemical testing and microscopic characterization techniques. The results showed that Cl− accelerated the anodic dissolution of the metal and compromised the structure and densification of the passive film, thus reducing its corrosion resistance. An increase in the partial pressure of carbon dioxide initially promotes pitting, but subsequently inhibited further corrosion development. The presence of oxygen enhanced the cathodic reaction and passive film formation, effectively preventing the invasion of aggressive chloride ions, thus inhibiting further corrosion. These findings provide a significant scientific basis for material selection and protection of oil extraction equipment in oilfield environments.

Effect of Cerium on Inclusion Evolution and Pitting Corrosion of Nb-Microalloyed Steel.

Nb-microalloyed steels are widely used in construction engineering fields due to their excellent mechanical properties, but they face serious corrosion problems in service environments. Pitting corrosion is the severest form of corrosion, and the types of inclusions are the leading cause to induce pitting corrosion. A new strategy is proposed to enhance the corrosion resistance of steels by achieving a beneficial transformation of inclusions with Ce treatment. In this paper, two types of Nb-microalloyed steels (0% Ce and 0.0058% Ce steel) were prepared to study the modification effect on inclusions in industrial production. The spherical CaS•C12A7 inclusions were modified to smaller ellipsoidal Ce2O2S inclusions, and the proportion of inclusions (0-2 μm) increased significantly from 27 to 66%, while large inclusions (>6 μm) disappeared. A kinetic model of inclusion evolution was established. The results of electrochemical tests indicated that the corrosion potential was positively shifted, and the corrosion current was reduced after Ce treatment. Additionally, the number of defects in the passivation film was decreased, and the corrosion resistance of the steel was significantly improved. The addition of Ce changed the types of inclusions and reduced the number of pitting nucleation points, which led to a remarkable reduction in the number and size of pitting pits. The mechanism of pitting corrosion induced by different types of inclusions was further investigated, and a pitting corrosion model was modeled based on the immersion experiments. Research results provide theoretical support for enhancing the corrosion resistance of steel.

A study on the evolution of microstructure of soil-rock mixtures based on the electrochemical conductive paths model under different rock and moisture content conditions

ABSTRACT To further improve the understanding of the evolution law of the microstructure of SRM in road engineering under moisture and rock content, the electrochemical impedance spectroscopy test under different moisture and rock conditions was carried out. This paper proposed an electrochemical model of different conductive paths based on different cementation states. The impact of rock and moisture content on the characteristic parameters of the conductive path model was analyzed. The results indicated the impedance spectrum curves became more pronounced with the continuous decrease in moisture content and increase in rock content. There was a well-defined exponential relationship between total impedance and both moisture and rock content. The total impedance decreased continuously with increasing moisture content and increased with increasing rock content. The characteristic parameters had practical significance in representing the microscopic structure. The moisture content primarily influenced the variation trends of the representation parameters by altering the channel width, length, and quantity of the continuous pore water solution pathways and the discontinuous rock-soil bonded bodies. The rock content affected the changes by compressing the external and internal pore water solution and soil particles, altering the compression and support between the continuous pore water solution pathways and the block rock framework.

Non-metallic Lewis acid sites enhance the activation of peracetic acid by cobalt-iron spinel for micropollutant decontamination: The critical role of Lewis acid sites as electron shuttles

Spinel is a common activator for peroxides, e.g., peracetic acid (PAA), in wastewater treatment, but suffers from insufficient electron transfer capacity at the active site and thus the limited activation capacity. Lewis acids are recognized for their capacity to interact with electrons and activate active sites, playing a crucial role in enhancing oxidant adsorption, shortening catalytic reaction distances, and increasing reaction kinetics. Herein, tellurium (Te), a typical Lewis acid, was introduced into cobalt-iron spinel (TCF) as an electron shuttler to improve the electron transfer capacity and thus boost the PAA activation. Results show that the degradation rate of sulfamethoxazole (SMX) with PAA activated via TCF is 4.0 times higher compared with cobalt-iron spinel (CF). Electron spin resonance (ESR) analysis and quenching experiments indicated acetylperoxyl radicals (CH3C(O)OO·) as the dominant reactive species in SMX degradation. Electrochemical tests revealed that the introduction of Lewis acid improved the charge transfer ability and charge utilization efficiency of the catalysts, exhibiting less electronic resistance and superior redox properties. Density functional theory (DFT) calculation suggests that the introduction of Lewis acid optimizes the electron distribution of the catalyst, and reduces the crucial reaction energy barriers for PAA activation. Additionally, the distinctive structural environment of Lewis acid renders TCF to exhibit excellent stability and resistance to complicated matrices in PAA activation. This work provides valuable insights into the Lewis acid regulating bimetallic catalyst performance and understanding the intrinsic interaction mechanisms, thereby establishing a critical groundwork for addressing prevailing wastewater treatment.

Graphitic Carbon Nitride as a Promising Visible-Light-Activated Support Boosting Platinum Nanoparticle Activity in Ethanol Electrooxidation.

In the present work, exfoliated graphitic carbon nitride (g-CN) is immobilized on carbon paper substrates by a simple electrophoretic route, and subsequently decorated with ultra-low amounts (≈μg/cm2) of Pt nanoparticles (NPs) by cold plasma sputtering. Optimization of preparative conditions allowed a fine tuning of Pt NPs size, loading and distribution and thus a controlled tailoring of g-CN/Pt interfacial interactions. Modulation of such features yielded g-CN-Pt-based anode materials with appealing activity and stability towards the ethanol oxidation reaction (EOR) in alkaline aqueous solutions, as revealed by electrochemical tests both in the dark and under irradiation. The present results provide new insights on the design of nano-engineered heterocomposites featuring improved performances thanks to Pt coupling with g-CN, a low-cost and environmentally friendly visible light-active semiconductor. Overall, this work might open attractive avenues for the generation of green hydrogen via aqueous ethanol electrolysis and the photo-promoted alcohol electrooxidation in fuel cells.

Performance repair of building materials using alumina and silica composite nanomaterials with electrodynamic properties

Abstract In recent years, the service life of building materials has become the focus of attention. Among them, the service life of concrete and steel bars is particularly affected by the corrosion of external ions (such as Cl−) in the environment. To solve this problem, a new type of composite nanocolloid was prepared through a controllable preparation method. The composite nanocolloid is prepared from aluminum chloride sol and silica sol as raw materials. The prepared colloidal particles have a particle size distribution between 10.5 and 17.5 nm, exhibiting excellent stability and dispersibility. In order to verify the improvement effect of the composite nanocolloid on the properties of building materials, the influence of it on the porosity of concrete and the anti-corrosion performance of steel bars was experimentally studied. The results indicate that the moisture absorption and dehumidification speed of concrete treated with composite nano colloids is slower, and the pore size distribution is mainly concentrated in 100–1,000 nm, indicating that the colloids can effectively optimize the pore structure of concrete. In addition, the processed steel plate samples showed high AC impedance values and low corrosion current logarithmic values in electrochemical testing, indicating that composite nanocolloids have a significant protective effect on the corrosion of steel bars, which can effectively improve the performance of building materials and extend their service life.

Corrosion suppression and strengthening of the Al-10Zn alloy by adding silica nanorods.

Aluminum alloys have been widely studied because of their current engineering applications. Due to their high strength and lightweight, cracking can easily initiate on their surface, deteriorating their overall functional and structural properties and causing environmental attacks. The current study highlights the significant influence of incorporating 1 wt% silica nanostructure in aluminum-10 zinc alloys. The characteristics of the composites were examined using Vickers hardness, tensile, and electrochemical testing (OCP, Tafel, and EIS) at various artificial aging temperatures (423, 443, and 463 K). Silica nanorods may achieve ultrafine grains, increase hardness by up to 13.8%, increase σUTS values by up to 79% at 443 K, and improve corrosion rate by up to 89.4%, surpassing Al-10 Zn bulk metallics. We demonstrate that silica nanorods contribute to the creation of a superior nanocomposite that not only limits failure events under loading but also resists corrosion. Our findings suggest that silica nanocomposite can produce unique features for use in a variety of automotive, construction, and aerospace applications. This improvement can be attributed mainly to the large surface area of nano-silica particles, which alters the Al matrix. Microstructural, mechanical, and electrochemical studies revealed that the effects of structure refinement were dependent on nano-silica.

Performance repair of building materials using alumina and silica composite nanomaterials with electrodynamic properties

Abstract In recent years, the service life of building materials has become the focus of attention. Among them, the service life of concrete and steel bars is particularly affected by the corrosion of external ions (such as Cl−) in the environment. To solve this problem, a new type of composite nanocolloid was prepared through a controllable preparation method. The composite nanocolloid is prepared from aluminum chloride sol and silica sol as raw materials. The prepared colloidal particles have a particle size distribution between 10.5 and 17.5 nm, exhibiting excellent stability and dispersibility. In order to verify the improvement effect of the composite nanocolloid on the properties of building materials, the influence of it on the porosity of concrete and the anti-corrosion performance of steel bars was experimentally studied. The results indicate that the moisture absorption and dehumidification speed of concrete treated with composite nano colloids is slower, and the pore size distribution is mainly concentrated in 100–1,000 nm, indicating that the colloids can effectively optimize the pore structure of concrete. In addition, the processed steel plate samples showed high AC impedance values and low corrosion current logarithmic values in electrochemical testing, indicating that composite nanocolloids have a significant protective effect on the corrosion of steel bars, which can effectively improve the performance of building materials and extend their service life.

Two-Dimensional NiCo2S4 Nanosheets Deliver Efficient Oxygen Evolution Reaction

Introduction: The development of cost-effective and efficient catalysts plays a pivotal role in the realization of hydrogen production through electrochemical water splitting. Method: In this study, two-dimensional NiCo2S4 nanosheets weresynthesized usinga hydrothermal method followed by a sulfidation process. Results: The resulting materials were thoroughly characterized to understand their morphology and structure. The findings indicate that the NiCo2S4 nanosheets exhibit exceptional electrical conductivity and a high density of pores, which facilitate electrolyte infiltration and interfacial charge transfer during electrochemical reactions. Furthermore, the incorporation of S2− modulates the electronic structure of metal ions, reducing the oxidation potential of metal sites and promoting the surface reconstruction of the electrode to form active species. Electrochemical tests conducted in a 1 M KOH solution using the synthesized catalyst as the working electrode demonstrate an overpotential of merely 280 mV and 300 mV at a current density of 20 mA cm−2 and 40 mA cm−2 , respectively, which are much lower than those of NiCo-LDH electrodes (360 mV and 410 mV). Conclusion: Furthermore, the NiCo2S4 electrode delivers a remarkably low Tafel slope of 47.9 mV dec−1 . This investigation presents a novel approach to the development of efficient transition metal-based electrocatalysts.

The Preparation of N, P-Doped NiSe Nanorod Electrode Materials on Nickel Foam Using the Microwave Method for High-Performance Supercapacitors.

Transition metal selenides have the leading position in the field of energy storage and conversion due to their high theoretical capacity, good electrical conductivity, and cycling stability. Nickel is widely used for the construction of positive electrodes in devices due to its good conductivity, variable valence state, and ideal redox activity. NiSe materials have high internal resistance and are prone to volume change during charging and discharging, thus affecting the practical application of this electrode material, and the reported NiSe materials have not achieved a more desirable capacity value. Therefore, in this study, N, P-NiSe nanoelectrode materials were prepared using nickel foam as the nickel source and hexachlorocyclotriphonitrile as the nitrogen and phosphorus dopant using an efficient, energy-saving, and simple microwave method. It was also characterised by XRD and XPS to confirm the successful preparation of N, P-NiSe materials. In addition, the material yielded a high capacitance value (3184 F g-1) and good cycling stability (72% of the initial capacitance value was retained after 4000 cycles) in electrochemical tests. To demonstrate its excellent suitability for practical applications, an asymmetric supercapacitor was assembled using N, P-NiSe as the anode and activated carbon as the cathode. At an operating voltage of 1.6 V, the device achieved an energy density of 289.06 Wh kg-1 and a power density of 799.26 W kg-1 and retained 80% of its initial capacity after 20,000 cycles.

Selenium-induced anion vacancy and active site migration stimulating remarkable sulfide Na-Ion storage

Heterojunctions and controllable anionic vacancies are perceived to be powerful means of ameliorating the performance of sodium-ion batteries assignable to their unique physical and chemical properties. However, the mechanism by which heterojunction and vacancy structures affect sodium-ion battery storage remains to be systemically explored. In this study, the Se doped CoS2@CoS1.035@Carbon (Se-CoS2@CoS1.035@C) heterostructure with anion vacancy was synthesized by a one-step calcination. These heterostructures with lower metal oxidation states and anionic vacancies exhibit exceptional Na+ storage performance (554.3 mA h g−1 after 1500 cycles at 5.0 A g−1). Both electrochemical tests and theoretical calculations demonstrate excellent pseudocapacitive behavior and enhanced Na+ adsorption during discharge because of anionic vacancies and Se doping. Additionally, introducing weaker Co-Se bonds and extending Co-S and Co-Se bonds reduce binding energies, which effectively accelerates the conversion reaction. Our findings provide a feasible way to rationally design and facilely prepare heterostructured anode materials with rich anionic vacancies for sodium-ion batteries.

Phase structure and electrochemical properties of A5B19 La0.8-xPrxMg0.2Ni3.8 (x = 0–0.3) hydrogen storage alloy anode material

The La0.8-xPrxMg0.2Ni3.8 (x = 0, 0.05, 0.1, 0.2, 0.3) alloy were synthesized useing the induction melting method. X-ray diffraction, scanning electron microscope, electron probe micro analyzer, and electrochemical tests were used to analyze the structure and electrochemical performance of the La0.8-xPrxMg0.2Ni3.8 (x = 0–0.3) alloy. It was studied how the Pr element affected the electrochemical characteristics and microstructure of the A5B19 La-Mg-Ni based hydrogen storage alloy. The results show that the alloy consists of the CaCu5-LaNi5 phase, 2 H-Pr5Co19 phase, and 3R-Ce5Co19 phase. The abundance of the A5B19 phase increase with the increase of Pr content, while the abundance of the LaNi5 phase decrease, and the addition of Pr promotes the formation of the 2 H-Pr5Co19 phase. According to the results of the electrochemical test, every sample has good activation qualities, and the activation can be completed in 3–4 times. The activation properties are not significantly altered by the addition of Pr. The maximum discharge capacity increases at first, then decreases, reaching the highest 371.15 mAh g−1 at x = 0.2. The cyclic stability gradually improves with increasing content of Pr, and the maximum capacity retention rate reaches 85.80 % after 100 cycles. The primary factor influencing the alloy's high rate discharge ability is the exchange current density. With the increase of the exchange current density, the high rate discharge performance is gradually enhanced.