scispace - formally typeset
Search or ask a question
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.

Content maybe subject to copyright    Report

Citations
More filters
Journal ArticleDOI
Yazhi Feng1, Qiu Zhang1, Shuang Liu1, Jian Liu1, Zhanliang Tao1, Jun Chen1 
TL;DR: In this paper, a cost-effective and eco-friendly aqueous sodium-manganese hybrid battery system using a graphite felt cathode, activated carbon anode, and hybrid electrolyte was proposed.
Abstract: Rechargeable aqueous sodium-ion batteries have become promising candidates for electrochemical grid-scale energy storage systems because of the rich natural abundance of sodium and the favourable safety of aqueous electrolytes. However, the electrochemical stability window of water limits the selection of electrode materials, and the poor performance of electrode materials hinders the comprehensive performance of the full batteries. In this work, a novel cost-effective and eco-friendly aqueous sodium–manganese hybrid battery system using a graphite felt cathode, activated carbon anode, and hybrid electrolyte (1 M Na2SO4 + 1 M MnSO4 + 0.1 M H2SO4) is proposed. The battery exhibits a discharge voltage of 1.2 V, a high coulombic efficiency (∼99.2%) and a lifetime of more than 7000 cycles. The hybrid system displays long cycling stability and high rate capability, demonstrating its feasibility for energy storage. It also provides a reference for the design of a new battery system that can be applied to develop high-performance aqueous sodium ion batteries for large-scale energy storage.

32 citations

Journal ArticleDOI
TL;DR: In this article, a comparative structural, Mossbauer, and electrochemical studies of the NaxMn2/3Fe1/3O2 and Naxmn1/2Fe 1/2O2 systems were conducted.
Abstract: The comparative structural, Mossbauer, and electrochemical studies of the NaxMn2/3Fe1/3O2 and NaxMn1/2Fe1/2O2 systems show that the change in the Mn/Fe ratio has a significant influence on the overlap between the Mn3+/4+ and Fe3+/4+ redox couples. The P2-type structure is maintained in the 0.3 < x < 0.8 domain. For the highest intercalation amount, structural distortions occur due to the Jahn–Teller effect of the Mn3+ ions. The macroscopic distortion results from a competition between the opposite effects of Mn3+ and Fe3+: the isotropic character of Fe3+ tends to prevent the macroscopic distortion. For the lower sodium amounts, the instability of the interstitial trigonal prismatic space leads to the formation, by slab gliding, of a very disordered structure. Even if this structural transition is reversible, a strong capacity fading is observed if the cell is charged above 4 V verus Na/Na+.

31 citations

Journal ArticleDOI
01 May 2020-Small
TL;DR: A universal strategy for synthesizing amorphous metals encapsulated into amorphously B, N co-doped carbon nanotubes by metal cation-assisted carbonization is explored and shows high capacity, excellent rate performance, and long cycle stability in SIBs anodes.
Abstract: Nearly inexhaustible sodium sources on earth make sodium ion batteries (SIBs) the best candidate for large-scale energy storage. However, the main obstacles faced by SIBs are the low rate performance and poor cycle stability caused by the large size of Na+ ions. Herein, a universal strategy for synthesizing amorphous metals encapsulated into amorphous B, N co-doped carbon (a-M@a-BCN; M = Co, Ni, Mn) nanotubes by metal cation-assisted carbonization is explored. The methodology allows tailoring the structures (e.g., length, wall thickness, and metals doping) of a-M@a-BCN nannotubes at the molecular level. Furthermore, the amorphous metal sulfide encapsulated into a-BCN (a-MSx @a-BCN; MSx : CoS, Ni3 S2 , MnS) nanotubes are obtained by one-step sulfidation process. The a-M@a-BCN and a-MSx @a-BCN possess the larger interlayer spacing (0.40 nm) amorphous carbon nanotube rich in heteroatoms active sites, making them exhibit excellent Na+ ions diffusion kinetics and capacitive storage behavior. As SIBs anodes, they show high capacity, excellent rate performance, and long cycle stability.

31 citations

Journal ArticleDOI
TL;DR: A three-dimensional hierarchical Ni3Se2 nanorod array grown in situ on foam Ni is the first to act as a carbon/binder-free electrode of SIBs via a one-step reversible conversion reaction.
Abstract: A three-dimensional hierarchical Ni3Se2 nanorod array (NA) grown in situ on foam Ni is the first to act as a carbon/binder-free electrode of SIBs via a one-step reversible conversion reaction. By a special decomposition–fusion process, the morphology and composition of the NA are regulated to obtain ultrahigh areal capacity, which is three times greater than that reported for other metal selenides.

31 citations

Journal ArticleDOI
01 Apr 2019

31 citations

References
More filters
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