One key challenge facing room temperature Na-ion batteries lies in identifying earth-abundant, environmentally friendly and safe materials that can provide efficient Na storage sites in Na-ion batteries. Herein, we report such a material, polyoxometalate NaH[MnVO] (NMV), with entirely different composition and structure from those cathode compounds reported before. Ex-situ XPS and FTIR analyses reveal that NMV cathode behaves like an "electron/Na-ion sponge", with 11 electrons/Na acceptability per mole, which has a decisive contribution to the high capacity. The extraordinary structural features, evidenced by X-ray crystallographic analysis, of NaH[MnVO] with a flexible 2D lamellar network and 1D open channels provide diverse Na ion migration pathways, yielding good rate capability. First-principle calculations demonstrate that a super-reduced state, [MnVO], is formed with slightly expanded size (ca. 7.5%) upon Na insertion compared to the original [MnVO]. This "ion sponge" feature ensures the good cycling stability. Consequently, benefiting from the combinations of "electron/ion sponge" with diverse Na diffusion channels, when revealed as the cathode materials for Na-ion batteries, NaH[MnVO]/G exhibits a high specific capacity (ca. 190 mA h/g at 0.1 C), associates with a good rate capability (130 mA h/g at 1 C), and a good capacity retention (81% at 0.2 C). Our results promote better understanding of the storage mechanism in polyoxometalate host, enrich the existing rechargeable SIBs cathode chemistry, and enlighten an exciting direction for exploring promising cathode materials for Na-ion batteries.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acsnano.7b02062 | DOI Listing |
Small
January 2025
Fujian Provincial Key Laboratory of Quantum Manipulation and New Energy Materials, College of Physics and Energy, Fujian Normal University, Fuzhou, Fujian, 350117, China.
Single-atom materials provide a platform to precisely regulate the electrochemical redox behavior of electrode materials with atomic level. Here, a multifield-regulated sintering route is reported to rapidly prepare single-atom zinc with a very high loading mass of 24.7 wt.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Department of Chemistry, Colorado State University, Fort Collins, Colorado 80523, United States.
Conversion electrodes, such as antimony (Sb), are high energy density electrode materials for sodium-ion batteries (NIBs). These materials are limited in their performance due to the mechanical instability of these systems resulting from volume expansion of the material during cycling. Stabilizing conversion materials using a conductive polymer binder (CPB) protective layer is an effective way to enhance the performance of these materials.
View Article and Find Full Text PDFACS Nano
January 2025
Université Toulouse III Paul Sabatier, CIRIMAT, UMR-CNRS 5085, Toulouse Cedex 9 31062, France.
The rising demand for energy storage calls for technological advancements to address the growing needs. In this context, sodium-ion (Na-ion) batteries have emerged as a potential complementary technology to lithium-ion batteries (Li-ion). Among other materials, NaV(PO)F (NVPF) is a promising cathode for Na-ion batteries due to its high operating voltage and good energy density.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Department of Inorganic and Physical Chemistry, Indian Institute of Science, Bangalore 560012, India.
A stoichiometric cubic phase of zinc bismuth oxide ZnBiO (ZBO) is introduced as an anode for rechargeable Na-ion batteries. ZBO is synthesized using a coprecipitation method and characterized by various physicochemical techniques. Pristine ZBO shows a high cyclability in an ether-based electrolyte due to the formation of a robust interphase coupled with high Na conductivity.
View Article and Find Full Text PDFChem 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 PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!