There are still many problems that hinder the development of sodium-ion batteries (SIBs), including poor rate performance, short-term cycle lifespan, and inferior low-temperature property. Herein, excellent Na-storage performance in fluorophosphate (Na V (PO ) F ) cathode is achieved by lattice regulation based on charge balance theory. Lattice regulation of aliovalent Mn for V increases both electronic conductivity and Na -migration kinetics. Because of the maintaining of electrical neutrality in the material, aliovalent Mn -introduced leads to the coexistence of V and V from charge balance theory. It decreases the particle size and improves the structural stability, suppressing the large lattice distortion during cathode reaction processes. These multiple effects enhance the specific capacity (123.8 mAh g ), outstanding high-rate (68% capacity retention at 20 C), ultralong cycle (only 0.018% capacity attenuation per cycle over 1000 cycles at 1 C) and low-temperature (96.5% capacity retention after 400 cycles at -25 °C) performances of Mn -induced Na V Mn (PO ) F when used as cathode in SIBs. Importantly, a feasible sodium-ion full battery is assembled, achieving outstanding rate capability and cycle stability. The strategy of aliovalent ion-induced lattice regulation constructs cathode materials with superior performances, which is available to improve other electrode materials for energy storage systems.
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http://dx.doi.org/10.1002/smll.202102010 | DOI Listing |
Int J Mol Sci
January 2025
Winogradsky Institute of Microbiology, Research Center of Biotechnology, Russian Academy of Sciences, 119071 Moscow, Russia.
The Dps protein is the major DNA-binding protein of prokaryotes, which protects DNA during starvation by forming a crystalline complex. The structure of such an intracellular DNA-Dps complex is still unknown. However, the phenomenon of a decrease in the size of the Dps protein from 90 Å to 69-75 Å during the formation of a complex with DNA has been repeatedly observed, and no explanation has been given.
View Article and Find Full Text PDFAdv Mater
January 2025
State Key Laboratory of Organic-Inorganic Composites and College of Chemical Engineering, Beijing University of Chemical Technology, Beijing, 100029, People's Republic of China.
The confining effect is essential to regulate the activity and stability of single-atom catalysts (SACs), but the universal fabrication of confined SACs is still a great challenge. Here, various lattice-confined Pt SACs supported by different carriers are constructed by a universal co-reduction approach. Notably, Pt single atoms confined in the lattice of Ni(OH) (Pt/Ni(OH)) with a high electron-deficient state exhibit excellent activity for basic hydrogen evolution reaction (HER).
View Article and Find Full Text PDFPhys Chem Chem Phys
January 2025
School of Mechanical and Electrical Engineering, Lanzhou University of Technology, Lanzhou, 730050, China.
Previous researchers have conducted extensive investigations on the impact of various working conditions on fatigue damage. However, further research is still needed to understand the underlying mechanism of how the excitation frequency of cyclic loading affects the fatigue life. This article systematically discloses the phononic origin of atomic scale fatigue resonance, focusing on single-layer molybdenum disulfide (SL MoS) as a prototypical material.
View Article and Find Full Text PDFJ Hazard Mater
January 2025
Shandong Key Laboratory of Water Pollution Control and Resource Reuse, School of Environmental Science and Engineering, Shandong University, Qingdao 266237, China. Electronic address:
Clothianidin (CTD), a highly water soluble neonicotinoid insecticide, easily enters water through runoff. Developing eco-friendly materials to degrade CTD is essential. Nano zero valent iron (nZVI) is effective for contaminant removal, but it deactivates due to agglomeration.
View Article and Find Full Text PDFJ Hazard Mater
January 2025
School of Metallurgy and Environment, Central South University, Chinese National Engineering Research Center for Control and Treatment of Heavy Metal Pollution, Changsha 410083, China; School of Environment and Energy, South China University of Technology, the Key Laboratory of Pollution Control and Ecosystem Restoration in Industry Clusters (Ministry of Education), Guangdong Engineering and Technology Research Center for Environmental Nanomaterials, Guangzhou 510006, China.
The reactions at the mineral-solution interface govern whether heavy metals (HMs) ions are retained within minerals or migrate with the solution, thus influencing their cycling and fate. However, the mechanisms driving this differential behavior of HMs at the interface remain poorly understood. In this study, we present a novel paradigm for the selective retention of HMs ions at the mineral-solution interface.
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