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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TL;DR: The current advances, existing limitations, along with the possible solutions in the pursuit of cathode materials with high voltage, fast kinetics, and long cycling stability are comprehensively covered and evaluated to guide the future design of aqueous ZIBs with a combination of high gravimetric energy density, good reversibility, and a long cycle life.
Abstract: Aqueous zinc ion batteries (ZIBs) are truly promising contenders for the future large-scale electrical energy storage applications due to their cost-effectiveness, environmental friendliness, intri...
726 citations
TL;DR: In this article, the authors considered the use of hydrogen as a way of using fuel cells and showed that hydrogen can play a significant role for intermediate time storage of a few hours to several days, and even for intermediate scale capacity energy storage.
Abstract: Pumped-Storage of Water: It is the most efficient; it is developed in very large scale capacity storage facilities which require specific sites; nevertheless, in the future due to its long lifetime it will play a significant role for intermediate time storage of a few hours to several days, and even for intermediate scale capacity energy storage. Electrochemical Energy Storage in Batteries: It is now used locally in some places that are not connected to the electricity network and on the smart grids for frequency regulation or small peak production shifts. Examples include sodium sulfur batteries (NaS) which are used in Japan; redox flow batteries under development, and some large scale lithium–ion batteries (LIBs) that are used in specific places. Storage via Hydrogen: The development of hydrogen as a way of using fuel cells is considered and seems very interesting from the pollution point of view at the local scale. From the technical point of view, most of the problems are almost solved. Nevertheless, hydrogen has to be produced and stored; and in this case, the yield is quite low, similar to that of the internal combustion engine. Electricity storage via hydrogen requires water electrolysis, H2 gas storage, and electricity production in fuel cells, all of which leads to a low efficiency and therefore, significant energy loss during electricity storage.
719 citations
TL;DR: This review comprehensively covering the studies on electrochemical materials for KIBs, including electrode and electrolyte materials and a discussion on recent achievements and remaining/emerging issues includes insights into electrode reactions and solid-state ionics and nonaqueous solution chemistry.
Abstract: Li-ion batteries (LIBs), commercialized in 1991, have the highest energy density among practical secondary batteries and are widely utilized in electronics, electric vehicles, and even stationary energy storage systems. Along with the expansion of their demand and application, concern about the resources of Li and Co is growing. Therefore, secondary batteries composed of earth-abundant elements are desired to complement LIBs. In recent years, K-ion batteries (KIBs) have attracted significant attention as potential alternatives to LIBs. Previous studies have developed positive and negative electrode materials for KIBs and demonstrated several unique advantages of KIBs over LIBs and Na-ion batteries (NIBs). Thus, besides being free from any scarce/toxic elements, the low standard electrode potentials of K/K+ electrodes lead to high operation voltages competitive to those observed in LIBs. Moreover, K+ ions exhibit faster ionic diffusion in electrolytes due to weaker interaction with solvents and anions than that of Li+ ions; this is essential to realize high-power KIBs. This review comprehensively covers the studies on electrochemical materials for KIBs, including electrode and electrolyte materials and a discussion on recent achievements and remaining/emerging issues. The review also includes insights into electrode reactions and solid-state ionics and nonaqueous solution chemistry as well as perspectives on the research-based development of KIBs compared to those of LIBs and NIBs.
651 citations
01 Mar 2019
619 citations
TL;DR: In this article, the challenges and recent developments related to rechargeable zinc-ion battery research are presented, as well as recent research trends and directions on electrode materials that can store Zn2+ and electrolytes that can improve the battery performance.
Abstract: The zinc-ion battery (ZIB) is a 2 century-old technology but has recently attracted renewed interest owing to the possibility of switching from primary to rechargeable ZIBs. Nowadays, ZIBs employing a mild aqueous electrolyte are considered one of the most promising candidates for emerging energy storage systems (ESS) and portable electronics applications due to their environmental friendliness, safety, low cost, and acceptable energy density. However, there are many drawbacks associated with these batteries that have not yet been resolved. In this Review, we present the challenges and recent developments related to rechargeable ZIB research. Recent research trends and directions on electrode materials that can store Zn2+ and electrolytes that can improve the battery performance are comprehensively discussed.
612 citations
References
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TL;DR: In this paper, the authors identify the redox potential paradox, E(Ni3+/Ni2+) > E (Ni4+ /Ni3+) in an identical structural framework, which is induced by transition of the oxides from Mott-Hubbard to negative charge-transfer regimes.
Abstract: Raising the operating potential of the cathode materials in sodium-ion batteries is a crucial challenge if they are to outperform state-of-the-art lithium-ion batteries. Although the layered transition metal oxides, NaMO2 (M: transition metal), are the most promising cathode materials owing to their high theoretical capacity with much more stable nature than Li1–xMO2 system, factors influencing the redox potential have not yet been fully understood. Here, we identify redox potential paradox, E(Ni3+/Ni2+) > E(Ni4+/Ni3+), in an identical structural framework, namely, NaTi4+0.5Ni2+0.5O2 and NaFe3+0.5Ni3+0.5O2, which is induced by transition of the oxides from Mott–Hubbard to negative charge-transfer regimes. The origin of the unusually low E(Ni4+/Ni3+) is the surprisingly large contribution (over 80%) of oxygen orbital to the redox reaction, of which the primary effect on the electrochemical property is demonstrated for the first time, providing a firm platform to design better cathodes for advanced sodium-i...
82 citations
TL;DR: In this paper, the reactivity of hard carbon (called Na/HC below) in different solvents and electrolytes was studied by Accelerating Rate Calorimeter (ARC) and X-ray diffraction was used to analyse the products after all ARC experiments.
Abstract: Introduction Sodium-ion batteries are now receiving attention due to the low cost and abundance of sodium, compared to lithium [1]. Sodium cannot intercalate into graphitized carbon so nanoporous carbon is currently the most attractive negative electrode material for sodium-ion batteries [2]. In this work, the reactivity of sodium inserted hard carbon (called Na/HC below) in different solvents (EC, DEC, DMC, EC: DEC and EC: DMC) and electrolytes (NaPF6 EC: DEC and NaPF6 EC: DMC) was studied by Accelerating Rate Calorimeter (ARC) and X-ray diffraction was used to analyse the products of Na/HC after all ARC experiments.
82 citations
Dissertation•
01 Jan 2015
TL;DR: In this article, the authors proposed a graphene-wrapped anatase TiO2 nanofibers (rGO@TiO2 NFs) through an effective wrapping of reduced graphene oxide (RGO) sheets on electrospun TiO 2 NFs.
Abstract: Anatase TiO2 has been suggested as a potential sodium anode material, but the low electrical conductivity of TiO2 often limits the rate capability, resulting in poor electrochemical properties. To address this limitation, we propose graphene-wrapped anatase TiO2 nanofibers (rGO@TiO2 NFs) through an effective wrapping of reduced graphene oxide (rGO) sheets on electrospun TiO2 NFs. To provide strong electrostatic interaction between the graphene oxide (GO) sheets and the TiO2 NFs, poly(allylamine hydrochloride) (PAH) was used to induce a positively charged TiO2 surface by the immobilization of the -NH3+ group and to promote bonding with the negatively charged carboxylic acid (-COO−) and hydroxyl (-O−) groups on the GO. A sodium anode electrode using rGO@TiO2 NFs exhibited a significantly improved initial capacity of 217 mAh g−1, high capacity retention (85% after 200 cycles at 0.2C), and a high average Coulombic efficiency (99.7% from the second cycle to the 200th cycle), even at a 5C rate, compared to those of pristine TiO2 NFs. The improved electrochemical performances stem from highly conductive properties of the reduced GO which is effectively anchored to the TiO2 NFs.
82 citations
TL;DR: In this article, a new and facile synthesis of a tin-carbon nanocomposite and its electrochemical characterization is presented, which shows very stable cycling performance in a suitable potential range, and specific capacities of more than 180, 150, 130, and 90% for an applied specific current of 12.2.
81 citations
TL;DR: The ultrathin P123-assisted LTO (P-LTO) nanosheets show a rate capability much higher than that of the LTO sample without P123 in a Li battery with over 130 mAh g(-1) of capacity remaining at the 64C rate.
Abstract: Ultrathin Li4Ti5O12 (LTO) nanosheets with ordered microstructures were prepared via a polyether-assisted hydrothermal process. Pluronic P123, a polyether, can impede the growth of Li2TiO3 in the precursor and also act as a structure-directing agent to facilitate the (Li1.81H0.19)Ti2O5·2H2O precursor to form the LTO nanosheets with the ordered microstructure. Moreover, the addition of P123 can suppress the stacking of LTO nanosheets during calcining of the precursor, and the thickness of the nanosheets can be controlled to be about 4 nm. The microstructure of the as-prepared ultrathin and ordered nanosheets is helpful for Li+ or Na+ diffusion and charge transfer through the particles. Therefore, the ultrathin P123-assisted LTO (P-LTO) nanosheets show a rate capability much higher than that of the LTO sample without P123 in a Li battery with over 130 mAh g–1 of capacity remaining at the 64C rate. For intercalation of larger size Na+ ions, the P-LTO still exhibits a capacity of 115 mAh g–1 at a current rate ...
81 citations