
Journal of Energy Chemistry, Journal Year: 2024, Volume and Issue: unknown
Published: Nov. 1, 2024
Language: Английский
Journal of Energy Chemistry, Journal Year: 2024, Volume and Issue: unknown
Published: Nov. 1, 2024
Language: Английский
Advanced Energy Materials, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 19, 2025
Abstract Heterostructure engineering and active component reconstruction are effective strategies for efficient rapid charge storage in advanced sodium‐ion batteries (SIBs). Herein, sandwich‐type CoSe 2 @MXene composites used as a model to reconstruct new Cu Se@MXene heterostructures by situ electrochemical driving. The MXene core provides interconnected pathways electron ion conduction, while also buffering volumetric expansion stabilize the structure. This reconstructed heterointerface features abundant sodium sites, enhanced Na + adsorption, diffusion kinetics, thus increasing capacity. Moreover, elevated Co valence state during discharge process allows it act an reservoir provide additional supply Se conversion accelerate kinetics. When employed anode SIBs, electrode exhibits high capacity (694 mAh g −1 at 0.1 A ), excellent rate performance (425 20 exceptional durability (437 after 10 000 cycles 5 with 0.0014% decay per cycle). mechanism of is further revealed through ex characterization theoretical calculations. work approach designing conversion‐type anodes SIBs.
Language: Английский
Citations
3Advanced Functional Materials, Journal Year: 2025, Volume and Issue: unknown
Published: March 3, 2025
Abstract Molybdenum disulfide (MoS 2 ), characterized by its two‐dimensional structure and high theoretical specific capacity, is considered a prospective anode of Na‐ion battery. However, the cycling rate capabilities are hampered sluggish charge transfer kinetics poor structural stability. To overcome issues, most efforts have been focused on optimizing MoS . Nevertheless, rationally designing that can present rapid durable storage while ensuring large remains challenges. Herein, /MnS heterostructure featuring sphere‐like hollow morphology designed according to Ostwald ripening process Kirkendall effect. This construction effectively establish an interfacial built‐in electric field activated MnS , which exhibit P‐type N‐type semiconductor characteristics, respectively, thereby promoting electrochemical kinetics. Moreover, excellent stability after repeated (de)sodiation processes remarkably achieved thanks robust design, significantly achieving outstanding tolerance changes. Consequently, delivers capacity (594.8 mAh g −1 at 0.1 A superior performance (up 100 ultrastable capability (30 000 cycles with ≈81.4% retention). The work affords effective optimization tactic develop high‐performance conversion‐type electrodes for alkali‐ion batteries.
Language: Английский
Citations
1Journal of Alloys and Compounds, Journal Year: 2025, Volume and Issue: unknown, P. 178661 - 178661
Published: Jan. 1, 2025
Language: Английский
Citations
0Journal of Energy Chemistry, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 1, 2025
Language: Английский
Citations
0ACS Applied Materials & Interfaces, Journal Year: 2025, Volume and Issue: unknown
Published: Feb. 13, 2025
Owing to their layered structure and higher theoretical specific capacity, MoS2-based materials have evoked tremendous attention for sodium storage. However, sluggish ionic transport dynamics unavoidable volume variation always lead an unsatisfactory electrochemical performance, thereby hindering further development. Herein, the Se-doped MoS2 nanosheets confined in hollow mesoporous carbon nanospheres (MoSSe@C) were successfully prepared via a synergistic strategy combining defect design optimization. Thereinto, larger Se atom doping could regulate crystal provide abundant defects, leading increased conductivity, fast diffusion kinetics, active sites. Besides, it also effectively expand interlamellar spacing of internal nanosheets, releasing more intrafacial sites The external adapt fluctuation MoSSe@C electrode during repeated cycling. Furthermore, interior anion defects induced by exterior HMCs synergistically boost conductivity fasten redox kinetics electrode. As result, electronic is tailored both internally externally, contributing greatly rapid reaction dynamics. Thus, exhibits favorable performance (450/150 mAh g–1 at 0.1 A g–1) half/full cells, respectively.
Language: Английский
Citations
0ChemistrySelect, Journal Year: 2025, Volume and Issue: 10(12)
Published: March 1, 2025
Abstract A self‐supporting flexible electrode, composed of 1T phase MoS₂ nanosheets synthesized on carbon cloth, was fabricated using a one‐step hydrothermal method. This electrode material exhibits outstanding electrochemical performance when utilized as the anode for both lithium‐ion and sodium‐ion batteries. In batteries, capacity approximately 600 mAh g⁻¹ is retained after 150 cycles at current density 0.1 g⁻¹. high 500 sustained even 100 cycles. Compared to powder cloth with that has been grown treated through annealing, electrodes demonstrate enhanced performance. can be attributed substrate, which significantly enhances stability conductivity MoS₂. contrast, annealing induces transformation 1T‐phase into more stable yet less conductive 2H phase, thereby diminishing its efficiency. underscores benefits unannealed MoS₂‐carbon composite material.
Language: Английский
Citations
0Advanced Energy Materials, Journal Year: 2025, Volume and Issue: unknown
Published: April 21, 2025
Abstract Slow diffusion kinetics caused by the low conductivity and large volume changes of metal sulfides (MSs) during repeated sodiation/desodiation processes greatly limit implementation high‐rate sodium ion batteries (SIBs). To address this, inspired vacancy defect engineering, for first time, defective 3D In 2 S 3 /MXene nanostructure with high‐density vacancies strong interface bonding is developed as fast‐charging anode SIBs. This design enables material to have a Na + energy barrier (0.28 eV) absorption (−1.68 eV), resulting in high coefficient (5.01 × 10 −12 cm s −1 ) pseudocapacitive contribution 97.3%. Moreover, exhibits reversible multistep intercalation‐conversion reaction mechanism superior electrochemical kinetics. Consequently, assembled SIBs display performance (202.2 mAh g at 100 A long‐term cycling stability over 5000 cycles 0.0074% decay per cycle 20 . On this basis, Na‐ion full cell assembled, indicating practical application material. study sheds light on functional electrode materials long‐lifespan storage devices.
Language: Английский
Citations
0Advanced Science, Journal Year: 2024, Volume and Issue: unknown
Published: Nov. 4, 2024
Abstract Conversion‐type transition‐metal sulfides (CT‐TMSs) have been extensively studied as the anode of Li/Na/K‐ion batteries due to their high theoretical capacity. An issue with use material in battery is that a large capacity difference commonly observed. However, underlying mechanism leading problem still unknown. Here, mechanisms CT‐TMSs anodes storage are elucidated, which arises from conversion degree and size products. Specifically, increase ionic radius will cause insertion‐reaction ion diffuse energy barrier conversion‐reaction Gibbs free energies phase transformation decrease reaction kinetics, causes an products, thus reduction The amount products inevitably reduce spin‐polarized electrons injection into Fe corresponding ions during ion‐electron decoupling storage, reducing research clarifies Li/Na/K providing valuable insights for designing high‐capacity anodes.
Language: Английский
Citations
1Journal of Energy Chemistry, Journal Year: 2024, Volume and Issue: unknown
Published: Nov. 1, 2024
Language: Английский
Citations
0