The behavior of Li/Na-ion capacitors (LICs/NICs) is largely limited by the low number of electroactive sites in conventional insertion-type anodes. In this work, we demonstrated a novel doping-vacancy double-defective and conversion-type Mn-O-F ultrafine nanowire (denoted as MnF-E) anode to boost the number of electroactive sites for enhanced LICs/NICs. Owing to the unique hetero oxygen-doping and intrinsic fluorine-vacancy double defects, the Mn-O-F nanowires exhibited superior electroactive sites and thus dramatically enhanced Li/Na-ion storage capability than pristine MnF micro/nano-crystals. Both the optimal MnF screened by orthogonal experiments and derived Mn-O-F anodes and commercial activated carbon (AC) cathode were used to construct MnF//AC and MnF-E//AC LICs/NICs, which were optimized by tuning the active mass ratios of the cathode/anode and the working voltage windows of the hybrid capacitors. The LICs/NICs based on the Mn-O-F anode demonstrated a considerably superior performance than the devices based on the MnF anode under the optimal voltages of 0-4 V and 0-4.3 V. The Mn-O-F anode exhibited dominant diffusion/surface-controlled kinetics for Li/Na-ion storage, respectively, showing a major conversion mechanism for the charge storage processes. This work provides a new concept of double-defective and conversion-type electrode materials to improve the Li/Na-ion storage capability and will have a significant impact on the relevant fields.
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http://dx.doi.org/10.1039/c9na00521h | DOI Listing |
Chem Sci
December 2024
Institute of Condensed Matter and Nanosciences, Molecular Chemistry, Materials and Catalysis, Université Catholique de Louvain Louvain-la-Neuve Belgium
Facilitating rapid charge transfer in electrode materials necessitates the optimization of their ionic transport properties. Currently, only a limited number of Li/Na-ion organic cathode materials have been identified, and those exhibiting intrinsic solid-phase ionic conductivity are even rarer. In this study, we present tetra-lithium and sodium salts with the generic formulae: A-Ph-CHP and A-Ph-PhP, wherein A = Li, Na; Ph-CHP = 2,5-dioxido-1,4-phenylene bis(methylphosphinate); Ph-PhP = 2,5-dioxido-1,4-phenylene bis(phenylphosphinate), as novel alkali-ion reservoir cathode materials.
View Article and Find Full Text PDFJ Mol Model
November 2024
Chemistry Department, Faculty of Science, King Abdulaziz University, P.O. Box 42805, 21589, Jeddah, Saudi Arabia.
Context: In recent years, rechargeable batteries have received considerable attention as a way to improve energy storage efficiency. Anodic (negative) electrodes based on Janus two-dimensional (2D) monolayers are among the most promising candidates. In this effort, the adsorption and diffusion of these Li, Na, and Mg ions on and through Janus 2D-TiSSe as anodic material was investigated by means of periodic DFT-D calculations.
View Article and Find Full Text PDFAdv Mater
November 2024
State Key Laboratory of Chemical Resource Engineering, College of Chemical Engineering, Beijing University of Chemical Technology, Beijing, 100029, P. R. China.
Carbonaceous materials hold great promise for K-ion batteries due to their low cost, adjustable interlayer spacing, and high electronic conductivity. Nevertheless, the narrow interlayer spacing significantly restricts their potassium storage ability. Herein, hierarchical N, S co-doped exfoliated holey graphene (NSEHG) with ultrahigh pyridinic/pyrrolic N (90.
View Article and Find Full Text PDFChemSusChem
August 2024
College of Engineering and Applied Sciences, Jiangsu Key Laboratory of Artificial Functional Materials, National Laboratory of Solid State Microstructures, Collaborative Innovation Centre of Advanced Microstructures, Frontiers Science Center for Critical Earth Material Cycling, Nanjing University, Nanjing, 210093, P. R. China.
Anionic redox chemistry has attracted increasing attention for the improvement in the reversible capacity and energy density of cathode materials in Li/Na-ion batteries. However, adverse electrochemical behaviors, such as voltage hysteresis and sluggish kinetics resulting from weak metal-ligand interactions, commonly occur with anionic redox reactions. Currently, the mechanistic investigation driving these issues still remains foggy.
View Article and Find Full Text PDFSci Rep
February 2024
Department of Physics, Indian Institute of Technology Patna, Bihta, 801103, India.
Transition metal oxides (TMO) are the preferred materials for metal ion battery cathodes because of their high redox potentials and good metal-ion intercalation capacity, which serve as an outstanding replacement for layered sulphide. In this work, using first-principles calculations based on Density functional theory approach, we explored the structural and electronic properties which comprise of adsorption and diffusion behaviour along with the analysis of voltage profile and storage capacity of Ru doped two-dimensional transition metal oxide [Formula: see text], [Formula: see text], and [Formula: see text] monolayers. The adsorption of alkali ions (Li, Na) to the surface of TMOs is strengthened by Ru-atom doping.
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