Search Results (103)

The O3-type layered oxide materials have the advantage of high specific capacity, which makes them more competitive in the practical application of cathode materials for sodium-ion batteries (SIBs). However, the existing reported O3-type layered oxide materials still have a complex irreversible phase transition phenomenon, and the cycle life of batteries needs, with these materials, to be further improved to meet the requirements. Herein, we performed structural characterization and electrochemical performance tests on O3-NaNi_0.6−xFe_0.25Mn_0.15Mg_xO₂ (x = 0, 0.025, 0.05, and 0.075, denoted as NFM, NFM-2.5Mg, NFM-5.0Mg, and NFM-7.5Mg). The optimized NFM-2.5Mg has the largest sodium layer spacing, which can effectively enhance the transmission rate of sodium ions. Therefore, the reversible specific capacity can reach approximately 148.1 mAh g⁻¹ at 0.2C, and it can even achieve a capacity retention of 85.4% after 100 cycles at 1C, demonstrating excellent cycle stability. Moreover, at a low temperature of 0 °C, it also can keep capacity retention of 86.6% after 150 cycles at 1C. This study provides a view on the cycling performance improvement of sodium-ion layered oxide cathodes with a high theoretical specific capacity. Full article

Novel high-entropy perovskite oxide powders were synthesized using a sol-gel process. The B-site contained five cations: chromium, cobalt, iron, manganese, and nickel. The B-site cations were present on an equiatomic basis. The A-site cation was lanthanum, with calcium doping. The amount of A-site doping varied from 0 to 30 at%, yielding a composition of La_1−xCa_x(Co_0.2Cr_0.2Fe_0.2Mn_0.2Ni_0.2)O_3−δ. The resulting perovskite powders were pressurelessly sintered in air at 1400 °C for 2 h. Sintered densities were measured, and the grain structure was imaged via scanning electron microscopy to investigate the effect of doping. Samples were cut and polished, and their resistance was measured at varying temperatures in air to obtain the electrical conductivity and the mechanism that governs it. Plots of electrical conductivity as a function of composition and temperature indicate that the increased configurational entropy of the perovskite materials has a demonstrable effect. Full article

Lithium-rich layered oxide (LLO) has received extensive attention from researchers due to its high initial discharge capacity (≥250 mAh g⁻¹). However, defects such as its high initial irreversible capacity, voltage decay, and poor rate performance have severely limited its commercialization. These issues arise because the Li₂MnO₃ component in LLO is activated during the initial cycle, leading to the participation of lattice oxygen anions (O²⁻) in redox reactions. This results in irreversible oxygen loss (O₂) and subsequent structural phase transitions. To address these challenges, this study focuses on Li₁.₂Ni₀.₁₃Co₀.₁₃Mn₀.₅₄O₂ as the host material, utilizing abundant exposed (010) plane secondary particles and employing a vanadium (V) doping strategy to enhance electrochemical performance. The V forms strong V-O bonds with the lattice oxygen, effectively suppressing irreversible oxygen loss and improving structural stability. The results demonstrate that the LLO achieves the best electrochemical performance as the doping amount is 1 mol%, and the capacity retention improves from 74.5% (undoped) to 86% (V-doped) after 140 cycles at 0.5 C. Full article

La-doped Li_1.2Ni_0.13Mn_0.54Co_0.13O₂ cathode materials were successfully synthesized by the sol-gel method. The structure, morphology, element valence states, cyclic voltammetry, and cyclic properties were characterized to investigate the properties of the synthesized materials. The as-prepared La-doped Li_1.2Ni_0.13Mn_0.54Co_0.13O₂ materials exhibit well the crystalline hexagonal layered structures with lamellar-like particles featuring a rough surface. The optimal sample, designated as LLRMO-2 with 1/100 La³⁺ doping, delivers an impressive discharge capacity of 271.2 mAh g⁻¹ with a capacity retention of 87.8% after 100 cycles at the current density of 100 mA g⁻¹ compared with that of 203.5 mAh g⁻¹ with only 110.6 mAh g⁻¹ after 100 cycles for the pristine sample. Furthermore, the LLRMO-2 cathode exhibits a superior rate capability compared to the pristine sample and shows excellent cyclic performances with the capacity retention of 48.1% after 400 cycles. The voltage decay per cycle is only 1.60 mV, which is less than 3.70 mV of the pristine one. The enhanced capacity, rate capability, and cyclic performance observed in the La-doped Li-rich layered cathode can be attributed to the improved structural stability as well as the higher diffusion coefficient of lithium ions. These results suggest that the strategy of introducing La³⁺ into the transition metal slabs is an efficient approach for boosting electrochemical performances of Li-rich Mn-based cathode materials via enhancing structural stability. Full article

Tunnel-structured Na_0.44MnO₂ (NMO) has been extensively studied as a potential cathode for sodium-ion batteries (SIBs) due to its favorable cycling endurance, cost-effectiveness, environmental benignity, and notable air-moisture stability. However, limitations, such as sluggish ion diffusion kinetics, an insufficient Na⁺ storage capacity, and an unsatisfactory Jahn–Teller effect, impede its widespread application. To address these problems, this study proposes a co-doping strategy that involves the simultaneous introduction of a cation and an anion. The optimized cathode Na_0.44Mn_0.99Ni_0.01O_1.985F_0.015 demonstrates remarkable rate capabilities with average discharge capacities of 136.2, 133.0, 129.6, 124.0, 115.9, and 95.8 mAh g⁻¹ under current rates ranging from 0.1 to 5 C. Furthermore, it also exhibits exceptional long-term cyclability, retaining 86.5% and 89.4% capacity retention at 1 and 5 C after 200 and 400 cycles, respectively, accompanied by nearly 100% Coulombic efficiency. A comprehensive structural characterization and experimental analysis reveal that the synergistic incorporation of Ni and F can effectively adjust the lattice parameters and alleviate the Jahn–Teller distortion of the NMO cathode, thereby resulting in enhanced structural integrity, rapid ion transfer dynamics, and excellent sodium storage performance. Consequently, this investigation establishes a significant approach for optimizing tunnel-phase Mn-based cathodes through the synergistic effect of cation and anion co-doping, which promotes the practical implementation of advanced SIBs. Full article

The metal-based/ceramic interface structure is a key research focus in science, and addressing the stability of the interface has significant scientific importance as well as economic value. In this project, the work of adhesion, heat of segregation, electronic structure, charge density, and density of states for doped-M (M = Ti, Mg, Cu, Zn, Si, Mn, or Al) Ni (111)/Al₂O₃ (0001) interface structures are studied using first-principle calculation methods. The calculation results demonstrate that doping Ti and Mg can increase the bonding strength of the Ni–Al₂O₃ interface by factors of 3.4 and 1.5, respectively. However, other dopants, such as Si, Mn, and Al, have a negative effect on the bonding of the Ni–Al₂O₃ interface. As a result, the alloying elements may be beneficial to the bonding of the Ni–Al₂O₃ interface, but they may also play an opposite role. Moreover, the Ti and Mg dopants segregate from the matrix and move to the middle position of the Ni–Al₂O₃ interface during relaxation, while other dopants exhibit a slight segregation and solid solution in the matrix. Most remarkably, the segregation behavior of Ti and Mg induced electron transfer to the middle of the interface, thereby increasing the charge density of the Ni–Al₂O₃ interface. For the optimal doped-Ti Ni–Al₂O₃ interface, bonds of Ti–O and Ti–Ni are found, which indicates that the dopant Ti generates stable compounds in the interface region, acting as a stabilizer for the interface. Consequently, selecting Ti as an additive in the fabrication of metal-based ceramic Ni–Al₂O₃ composites will contribute to prolonging the service lifetime of the composite. Full article

This review analyzes TiO₂-based coatings formed by the plasma electrolytic oxidation (PEO) process of titanium for the photocatalytic degradation of methyl orange (MO) under simulated solar irradiation conditions. PEO is recognized as a useful technique for creating oxide coatings on various metals, particularly titanium, to assist in the degradation of organic pollutants. TiO₂-based photocatalysts in the form of coatings are more practical than TiO₂-based photocatalysts in the form of powder because the photocatalyst does not need to be recycled and reused after wastewater degradation treatment, which is an expensive and time-consuming process. In addition, the main advantage of PEO in the synthesis of TiO₂-based photocatalysts is its short processing time (a few minutes), as it excludes the annealing step needed to convert the amorphous TiO₂ into a crystalline phase, a prerequisite for a possible photocatalytic application. Pure TiO₂ coatings formed by PEO have a low photocatalytic efficiency in the degradation of MO, which is due to the rapid recombination of the photo-generated electron/hole pairs. In this review, recent advances in the sensitization of TiO₂ with narrow band gap semiconductors (WO₃, SnO₂, CdS, Sb₂O₃, Bi₂O₃, and Al₂TiO₅), doping with rare earth ions (example Eu³⁺) and transition metals (Mn, Ni, Co, Fe) are summarized as an effective strategy to reduce the recombination of photo-generated electron/hole pairs and to improve the photocatalytic efficiency of TiO₂ coatings. Full article

Nickel-rich cathode materials have emerged as ideal candidates for electric vehicles due to their high energy density; however, polycrystalline materials are prone to microcrack formation and unavoidable side reactions with electrolytes during cycling, leading to structural instability and capacity degradation. Herein, an Sr-doped single-crystalline nickel-rich LiNi_0.88Co_0.05Mn_0.07O₂/Sr cathode material is synthesized, with Sr doping levels controlled at x = 0.3%, 0.5%, 1 mol%. The nickel-rich LiNi_0.88Co_0.05Mn_0.07O₂/Sr cathode features particle sizes of approximately 2 μm, at a relatively low temperature. It inhibits the microcrack formation, prevents electrolyte penetration into the particle interior, and reduce side reactions, thereby enhancing structural stability. This enables the cathode to deliver a high initial discharge capacity of 205.3 mAh g⁻¹at 0.1 C and 170.8 mAh g⁻¹ at 10 C, within the voltage range of 2.7 V–4.3 V, and an outstanding capacity retention of 96.61% at 1 C after 100 cycles. These improvements can be attributed to the Sr-doping, which reduces the single-crystal growth temperature, effectively mitigating Li⁺/Ni²⁺ cation mixing. Moreover, the incorporation of Sr expands the interlayer spacing, thereby facilitating Li⁺ diffusion. The doping strategy employed in this work provides a new insight for low-temperature single-crystal materials synthesis, significantly improving the electrochemical performance of nickel-rich cathode materials. Full article

In this study, pure and Mg²⁺/Cr³⁺ co-doped Ni/Mn bimetallic oxides were used as precursors to synthesize pristine and doped LNMO samples. The LNMO samples exhibited the same crystal structure as the precursors. XRD analysis confirmed the successful synthesis of LNMO cathode materials using Ni/Mn bimetallic oxides as precursors. FTIR and Raman spectroscopy reveal that Mg²⁺/Cr³⁺ co-doping promotes the formation of the Fd3m disordered phase, effectively reducing electrochemical polarization and charge transfer resistance. Furthermore, co-doping significantly lowers the Mn³⁺ content on the LNMO surface, thereby mitigating Mn³⁺ dissolution. Significantly, Mg²⁺/Cr³⁺ co-doping induces the emergence of high-surface-energy {100} crystal facets in LNMO grains, which promote lithium-ion transport and, finally, enhance rate capability and cycling performance. Electrochemical analysis indicates that the initial discharge capacities of LNMO-0, LNMO-0.005, LNMO-0.010, and LNMO-0.015 were 126.4, 125.3, 145.3, and 138.2 mAh·g⁻¹, respectively, with capacity retention rates of 82.45%, 82.93%, 83.32%, and 82.08% after 100 cycles. Furthermore, the impedance of LNMO-0.010 prior to cycling was 97.38 Ω, representing a 14.35% reduction compared to the pristine sample. After 100 cycles, its impedance was only 58.61% of that of the pristine sample, highlighting its superior rate capability and cycling stability. As far as we know, studies on the synthesis of LNMO cathode materials via the design of Ni/Mn bimetallic oxides remain limited. Accordingly, this work provides an innovative approach for the preparation and modification of LNMO cathode materials. The investigation of Ni/Mn bimetallic oxides as precursors, combined with co-doping by Mg²⁺ and Cr³⁺, for the synthesis of high-performance LiNi_0.5Mn_1.5O₄ (LNMO) aims to provide insights into improving rate capability, cycling stability, reducing impedance, and enhancing capacity retention. Full article

Water electrolysis for hydrogen production has garnered significant attention due to its advantages of high efficiency, environmental friendliness, and abundant resources. Developing cost-effective, efficient, and stable materials for water electrolysis is therefore crucial. In this work, we synthesized a series of highly efficient multifunctional Mn-Co_1.29Ni_1.71O₄ electrocatalysts through an atomic doping strategy for alkaline electrocatalysts. The unique structure features and large specific surface area of these catalysts provide abundant active sites. The Mn-Co_1.29Ni_1.71O₄ catalysts exhibit an excellent oxygen evolution reaction (OER) performance in 1.0 M KOH electrolyte, with an overpotential of 334.3 mV at a current density of 10 mA cm⁻² and 373.3 mV at 30 mA cm⁻². Additionally, the catalysts also demonstrate a Tafel slope of 76.7 mV dec⁻¹ and outstanding durability. As hydrogen evolution reaction (HER) electrocatalysts, it shows an overpotential of 203.5 mV at −10 mA cm⁻² and a Tafel slope of 113.6 mV dec⁻¹. When the catalysts can be utilized for the overall water splitting, the catalyst requires a decomposition voltage of 1.96 V at 50 mA cm⁻². These results indicate that the high catalytic activity and stability of Mn-Co_1.29Ni_1.71O₄ samples make it a highly promising candidate for industrial-scale applications. Full article

High-performance electrode materials are fundamental to improving supercapacitor performance, serving as key factors in developing devices with high energy density, high power density, and excellent cyclic stability. Non-stoichiometric spinels with phase deficiencies can achieve electrochemical performance that surpasses that of stoichiometric materials, owing to their unique structural characteristics. In this study, we used a microwave-assisted method to synthesize a high-performance non-stoichiometric spinel material with phase deficiencies, Mn_0.5Co_2.5O₄, which displayed a wide potential window (1.13 V in a traditional aqueous three-electrode system) and high specific capacitance (716.9 F g⁻¹ at 1 A g⁻¹). More critically, through microwave-assisted doping engineering, nickel was successfully doped into the phase-deficient Mn_0.5Co_2.5O₄, resulting in a spinel material, Ni−Mn_0.5Co_2.5O₄, with significant lattice defects and a mixed 1D/2D morphology. The doping of nickel effectively promoted the high-state conversion of manganese valence states within the manganese cobaltite material, substantially increasing the quantity of highly active Co³⁺ ions. These changes led to an increase in the density of reactive sites, effectively promoting synergistic interactions, thereby significantly enhancing the material’s conductivity and energy storage performance. The specific capacitance of Ni−Mn_0.5Co_2.5O₄ reached 1180.6 F g⁻¹ at 1 A g⁻¹, a 64.7% improvement over the original Mn_0.5Co_2.5O₄; at a high current density of 10 A g⁻¹, the capacitance increased by 14.3%. Notably, the charge transfer resistance was reduced by a factor of 41.6. After 5000 cycles of testing, the capacity retention stood at 79.2%. This work reveals the effectiveness of microwave-assisted doping engineering in constructing high-performance non-stoichiometric spinel-type bimetallic oxide materials, offering advanced strategies for the development of high-performance electrode materials. Full article

Developing more effective gold–support synergy is essential for enhancing the catalytic performance of supported gold nanoparticles (AuNPs) in the gas-phase oxidation of ethanol to acetaldehyde (AC) at lower temperatures. This study demonstrates a significantly improved Au–support synergy achieved by copper doping in LaMO₃ (M = Mn, Fe, Co, Ni) perovskites. Among the various Au/LaMCuO₃ catalysts, Au/LaMnCuO₃ exhibited exceptional catalytic activity, achieving an AC yield of up to 91% and the highest space-time yield of 764 g_AC g_Au⁻¹ h⁻¹ at 225 °C. Notably, this catalyst showed excellent hydrothermal stability, maintaining performance for at least 100 h without significant deactivation when fed with 50% aqueous ethanol. Comprehensive characterization reveals that Cu doping facilitates the formation of surface oxygen vacancies on the Au/LaMCuO₃ catalysts and enhances Au–support interactions. The LaMnCuO₃ perovskite stabilizes the crucial Cu⁺ species, resulting in a stable Au-Mn-Cu synergy within the Au/LaMnCuO₃ catalyst, which facilitates the activation of O₂ and ethanol at lower temperatures. The optimization of the reaction conditions further improves AC productivity. Kinetic studies indicate that the cleavages of both the O-H bond and the α-C-H bond of ethanol are the rate-controlling steps. Full article

Due to the advantages of high capacity, low working voltage, and low cost, lithium-rich manganese-based material (LMR) is the most promising cathode material for lithium-ion batteries; however, the poor cycling life, poor rate performance, and low initial Coulombic efficiency severely restrict its practical utility. In this work, the precursor Mn_2/3Ni_1/6Co_1/6CO₃ was obtained by the continuous co-precipitation method, and on this basis, different doping levels of aluminum–magnesium were applied to modify the electrode materials by high-temperature sintering. The first discharge capacity can reach 295.3 mAh·g⁻¹ for the LMR material of Li_1.40(Mn_0.666Ni_0.162Co_0.162Mg_0.005Al_0.005)O₂. The Coulombic efficiency is 83.8%, and the capacity retention rate remains at 84.4% after 300 cycles at a current density of 1 C for the Mg-Al co-doped LMR material, superior to the unmodified sample. The improved electrochemical performance is attributed to the increased oxygen vacancy and enlarged lithium layer spacing after trace magnesium–aluminum co-doping, enhancing the lithium-ion diffusion and effectively mitigating voltage degradation during cycling. Thus, magnesium–aluminum doping modification emerges as a promising method to improve the electrochemical performance of lithium-rich manganese-based cathode materials. Full article

The phase evolution of Li-rich Li-Mn-Ni-(Al)-O cathode materials upon heat treatments in the air at 900 °C was studied by X-ray and neutron powder diffraction. In addition, the structures of Li_1.26Mn_0.61−xAl_x Ni_0.15O₂, x = 0.0, 0.05, and 0.10, were refined from neutron powder diffraction data. For two-phase mixtures containing a monoclinic Li₂MnO₃ type phase M and a rhombohedral LiMn_0.5Ni_0.5O₂ type phase R, the structures, compositions, and phase fractions change with heat treatment time. This is realized by the substitution mechanism 3Ni²⁺ ↔ 2Li⁺ + 1Mn⁴⁺, which enables cation transport between the phases. A whole-powder pattern fitting analysis of size and strain broadening shows that strain broadening dominates. The X-ray domain size increases with heat treatment time and is larger than the sizes of the domains of M and R observed by electron microscopy. For heat-treated samples, the domain size is smaller for R than for M and decreases with increasing Al doping. Full article

With its distinctive multiple electrochemical reaction, iron vanadate (FeV₃O₉.2.6H₂O) is considered as a promising electrode material for energy storage. However, it has a relatively low practical specific capacitance. Therefore, using the low temperature sol–gel synthesis process, transition metal doping was used to enhance the electrochemical performance of layered structured FeV₃O₉.2.6H₂O (FVO). According to this study, FVO doped with transition metals with larger interlayer spacing exhibited superior electrochemical performance than undoped FVO. The Mn-doped FVO electrode showed the highest specific capacitance and retention of 143 Fg⁻¹ and 87%, respectively, while the undoped FVO showed 78 Fg⁻¹ and 54%. Full article