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Journal ArticleDOI

Sodium-ion batteries: present and future

19 Jun 2017-Chemical Society Reviews (The Royal Society of Chemistry)-Vol. 46, Iss: 12, pp 3529-3614
TL;DR: Current research on materials is summarized and discussed and future directions for SIBs are proposed to provide important insights into scientific and practical issues in the development of S IBs.
Abstract: Energy production and storage technologies have attracted a great deal of attention for day-to-day applications. In recent decades, advances in lithium-ion battery (LIB) technology have improved living conditions around the globe. LIBs are used in most mobile electronic devices as well as in zero-emission electronic vehicles. However, there are increasing concerns regarding load leveling of renewable energy sources and the smart grid as well as the sustainability of lithium sources due to their limited availability and consequent expected price increase. Therefore, whether LIBs alone can satisfy the rising demand for small- and/or mid-to-large-format energy storage applications remains unclear. To mitigate these issues, recent research has focused on alternative energy storage systems. Sodium-ion batteries (SIBs) are considered as the best candidate power sources because sodium is widely available and exhibits similar chemistry to that of LIBs; therefore, SIBs are promising next-generation alternatives. Recently, sodiated layer transition metal oxides, phosphates and organic compounds have been introduced as cathode materials for SIBs. Simultaneously, recent developments have been facilitated by the use of select carbonaceous materials, transition metal oxides (or sulfides), and intermetallic and organic compounds as anodes for SIBs. Apart from electrode materials, suitable electrolytes, additives, and binders are equally important for the development of practical SIBs. Despite developments in electrode materials and other components, there remain several challenges, including cell design and electrode balancing, in the application of sodium ion cells. In this article, we summarize and discuss current research on materials and propose future directions for SIBs. This will provide important insights into scientific and practical issues in the development of SIBs.

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Citations
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Journal ArticleDOI
TL;DR: In this article, a review of the recent developments of anode and cathode materials for PIBs, including several electrode materials in regards to synthesis, structure, electrochemical performance, and K-storage mechanisms is presented.

62 citations

Journal ArticleDOI
Li-Na Wang1, Xu Wu1, Fu-Ting Wang1, Xue Chen1, Jing Xu1, Ke-Jing Huang1 
TL;DR: V-doped 1T MoS2 nanosheets with a large layer spacing are grown on carbon cloth via a one-step hydrothermal method, providing an effective and eco-friendly route toward obtaining superior MoS 2 electrodes for high-performance Na+ storage.

62 citations

Journal ArticleDOI
Qing Xue1, Li Li1, Yongxin Huang1, Ruling Huang1, Feng Wu1, Renjie Chen1 
TL;DR: This simple surface modification method represents a promising means of mitigating issues currently associated with PB-based cathodes for PIBs and shows a lack of phase transition during the charge and discharge processes, possibly contributing to the excellent cycling stability.
Abstract: Potassium-ion batteries (PIBs) have received significant attention because of the abundant potassium reserves and similar electrochemistry of potassium to that of lithium. Because of the open framework and structural controllability, Prussian blue and its analogues (PB) are considered to be competitive cathodes of PIBs. However, the intrinsic lattice defects and poor electronic conductivity of PBs induce poor cycling performance and rate capability. Herein, we propose a polypyrrole-modified Prussian blue material (KHCF@PPy) via an in situ polymerization coating method for the first time. KHCF@PPy possesses a low defect concentration and improved electronic conductivity, and the electrode was found to exhibit 88.9 mA h g-1 discharge capacity at 50 mA g-1, with 86.8% capacity retention after 500 cycles. At a higher current density of 1000 mA g-1, the initial discharge capacity was 72.1 mA h g-1, which dropped slightly to 61.8 mA h g-1 after 500 cycles. The capacity decay rate was 0.03% per cycle. Detailed characterization showed a lack of phase transition during the charge and discharge processes and determined that K ions were not completely extracted from the monoclinic structure, possibly contributing to the excellent cycling stability. This simple surface modification method represents a promising means of mitigating issues currently associated with PB-based cathodes for PIBs.

62 citations

Journal ArticleDOI
14 Nov 2019-Chem
TL;DR: In this article, the authors employed chemical substitution in Na2/3TMO2 (TM = transition metal) layered compounds with different stacking modes: O3-Na 2/3Mg 1/3Ti 2/1/3O2 and P2-Na 1/6Mn 1/2O2 to improve the stability of high-voltage plateau and total reversible capacity.

62 citations

References
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Journal ArticleDOI
18 Nov 2011-Science
TL;DR: The battery systems reviewed here include sodium-sulfur batteries that are commercially available for grid applications, redox-flow batteries that offer low cost, and lithium-ion batteries whose development for commercial electronics and electric vehicles is being applied to grid storage.
Abstract: The increasing interest in energy storage for the grid can be attributed to multiple factors, including the capital costs of managing peak demands, the investments needed for grid reliability, and the integration of renewable energy sources. Although existing energy storage is dominated by pumped hydroelectric, there is the recognition that battery systems can offer a number of high-value opportunities, provided that lower costs can be obtained. The battery systems reviewed here include sodium-sulfur batteries that are commercially available for grid applications, redox-flow batteries that offer low cost, and lithium-ion batteries whose development for commercial electronics and electric vehicles is being applied to grid storage.

11,144 citations

Journal ArticleDOI
26 May 2006-Science
TL;DR: In this paper, a single epitaxial graphene layer at the silicon carbide interface is shown to reveal the Dirac nature of the charge carriers, and all-graphene electronically coherent devices and device architectures are envisaged.
Abstract: Ultrathin epitaxial graphite was grown on single-crystal silicon carbide by vacuum graphitization. The material can be patterned using standard nanolithography methods. The transport properties, which are closely related to those of carbon nanotubes, are dominated by the single epitaxial graphene layer at the silicon carbide interface and reveal the Dirac nature of the charge carriers. Patterned structures show quantum confinement of electrons and phase coherence lengths beyond 1 micrometer at 4 kelvin, with mobilities exceeding 2.5 square meters per volt-second. All-graphene electronically coherent devices and device architectures are envisaged.

4,848 citations

Journal Article
TL;DR: The transport properties, which are closely related to those of carbon nanotubes, are dominated by the single epitaxial graphene layer at the silicon carbide interface and reveal the Dirac nature of the charge carriers.
Abstract: Ultrathin epitaxial graphite was grown on single-crystal silicon carbide by vacuum graphitization. The material can be patterned using standard nanolithography methods. The transport properties, which are closely related to those of carbon nanotubes, are dominated by the single epitaxial graphene layer at the silicon carbide interface and reveal the Dirac nature of the charge carriers. Patterned structures show quantum confinement of electrons and phase coherence lengths beyond 1 micrometer at 4 kelvin, with mobilities exceeding 2.5 square meters per volt-second. All-graphene electronically coherent devices and device architectures are envisaged.

4,578 citations

Journal ArticleDOI
TL;DR: In this paper, the status of ambient temperature sodium ion batteries is reviewed in light of recent developments in anode, electrolyte and cathode materials, including high performance layered transition metal oxides and polyanionic compounds.
Abstract: The status of ambient temperature sodium ion batteries is reviewed in light of recent developments in anode, electrolyte and cathode materials. These devices, although early in their stage of development, are promising for large-scale grid storage applications due to the abundance and very low cost of sodium-containing precursors used to make the components. The engineering knowledge developed recently for highly successful Li ion batteries can be leveraged to ensure rapid progress in this area, although different electrode materials and electrolytes will be required for dual intercalation systems based on sodium. In particular, new anode materials need to be identified, since the graphite anode, commonly used in lithium systems, does not intercalate sodium to any appreciable extent. A wider array of choices is available for cathodes, including high performance layered transition metal oxides and polyanionic compounds. Recent developments in electrodes are encouraging, but a great deal of research is necessary, particularly in new electrolytes, and the understanding of the SEI films. The engineering modeling calculations of Na-ion battery energy density indicate that 210 Wh kg−1 in gravimetric energy is possible for Na-ion batteries compared to existing Li-ion technology if a cathode capacity of 200 mAh g−1 and a 500 mAh g−1 anode can be discovered with an average cell potential of 3.3 V.

3,776 citations