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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, carbon nanotubes are incorporated into antimony carbon-nanotube composite electrodes (Sb/CNT) using a one-step electrodeposition procedure.

58 citations

Journal ArticleDOI
TL;DR: The first use of highly porous azo-linked polymers as a new redox-active electrode material for rechargeable sodium ion batteries is reported, eliminating the solubility issue of organic electrodes in common electrolytes and assisting in fast ionic transport and charge transfer rates.
Abstract: The use of redox-active organic materials in rechargeable batteries has the potential to transform the field by enabling lightweight, flexible, green batteries while replacing lithium with sodium would mitigate the limited supplies and high cost of lithium. Herein, we report the first use of highly porous azo-linked polymers (ALPs) as a new redox-active electrode material for rechargeable sodium-ion batteries. ALPs are highly cross-linked polymers and therefore eliminate the solubility issue of organic electrodes in common electrolytes, which is prominent in small organic molecules and leads to fast capacity fading. Moreover, the high surface area coupled with the π-conjugated microporous nature of ALPs facilitates electrolyte adsorption in the pores and assists in fast ionic transport and charge transfer rates. An average specific capacity of 170 mA h g-1 at 0.3 C rate was attained while maintaining 96% Coulombic efficiency over 150 charge/discharge cycles.

58 citations

Journal ArticleDOI
TL;DR: In this paper, the intrinsic relationship between the ion-embedding mechanisms and the electrochemical properties of the typical FeS2/Na (Li) cells was investigated by coupling operando magnetometry with electrochemical measurement.
Abstract: In spite of the excellent electrochemical performance in lithium-ion batteries (LIBs), transition-metal compounds usually show inferior capacity and cyclability in sodium-ion batteries (SIBs), implying different reaction schemes between these two types of systems. Herein, coupling operando magnetometry with electrochemical measurement, we peformed a comprehensive investigation on the intrinsic relationship between the ion-embedding mechanisms and the electrochemical properties of the typical FeS2/Na (Li) cells. Operando magnetometry together with ex-situ transmission electron microscopy (TEM) measurement reveal that only part of FeS2 is involved in the conversion reaction process, while the unreactive parts form "inactive cores" that lead to the low capacity. Through quantification with Langevin fitting, we further show that the size of the iron grains produced by the conversion reaction are much smaller in SIBs than that in LIBs, which may lead to more serious pulverization, thereby resulting in worse cycle performance. The underlying reason for the above two above phenomena in SIBs is the sluggish kinetics caused by the larger Na-ion radius. Our work paves a new way for the investigation of novel SIB materials with high capacity and long durability.

58 citations

Journal ArticleDOI
TL;DR: This work demonstrates the large π-conjugated porous frameworks (CPFs) as cathodes for OSIBs, motivated by the speculation that the CPFs are capable of enhancing charge transport, facilitating ionic diffusion, inhibiting dissolution, as well as improving stability.
Abstract: Organic sodium-ion batteries (OSIBs) are promising alternatives of inorganic lithium-ion batteries. The cathodes of OSIBs still suffer from low capacity, poor rate performance, and low cyclability. For the first time, we demonstrate the large π-conjugated porous frameworks (CPFs) as cathodes for OSIBs, motivated by the speculation that the CPFs are capable of enhancing charge transport, facilitating ionic diffusion, inhibiting dissolution, as well as improving stability. The batteries based on the obtained CPFs indeed delivered much better electrochemical performance than the small molecular construction units without any complex post-treatments. The moderate BET surface area of CPFs and the detailed analyses suggested that the micropores and the lamellar structure should be responsible for the fast ionic diffusion. We believe that this work will provoke growing interest of CPFs for OSIBs with functional molecular design toward high performance and pave a venue to achieve OSIBs in large-scale applications.

57 citations

Journal ArticleDOI
TL;DR: Oxygen-containing groups in carbon materials have been demonstrated to be effective in the anodic sodium-ion storage process; however, the effect of specific oxygencontaining groups on the sodium-...
Abstract: Oxygen-containing groups in carbon materials have been demonstrated to be effective in the anodic sodium-ion storage process; however, the effect of specific oxygen-containing groups on the sodium-...

57 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