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.
Citations
More filters
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
More filters
TL;DR: By critically analysing state-of-the-art technologies, this work aims to address the benefits and issues of graphene-based materials, as well as outline the most promising results and applications so far.
Abstract: Since its first isolation in 2004, graphene has become one of the hottest topics in the field of materials science, and its highly appealing properties have led to a plethora of scientific papers. Among the many affected areas of materials science, this 'graphene fever' has influenced particularly the world of electrochemical energy-storage devices. Despite widespread enthusiasm, it is not yet clear whether graphene could really lead to progress in the field. Here we discuss the most recent applications of graphene - both as an active material and as an inactive component - from lithium-ion batteries and electrochemical capacitors to emerging technologies such as metal-air and magnesium-ion batteries. By critically analysing state-of-the-art technologies, we aim to address the benefits and issues of graphene-based materials, as well as outline the most promising results and applications so far.
2,148 citations
TL;DR: A new electrode material, P2-Na(2/3)[Fe(1/2)Mn( 1/2)]O(2), that delivers 190 mAh g(-1) of reversible capacity in the sodium cells with the electrochemically active Fe(3+)/Fe(4+) redox will contribute to the development of rechargeable batteries from the earth-abundant elements operable at room temperature.
Abstract: Although sodium is an abundant element that can be electrochemically and reversibly extracted from and inserted into layered materials, the resulting reversible capacity for storing energy remains low. A manganese–iron–sodium-based electrode is now shown to exhibit a reversible capacity of 190 mAh g−1 due to electrochemically active Fe3+/Fe4+ redox reactions.
1,834 citations
TL;DR: In this article, the Im3 phase of high pressure KSbO3, the defect-pyrochlore structure illustrated by RbMgAlF6, and the carnegieite structure of high-temperature NaAlSiO4 were investigated.
1,733 citations
TL;DR: In this paper, a 3-volt secondary Na-ion battery possessing environmental and cost friendliness, Na+-shuttlecock hard-carbon/NaNi0.5Mn 0.5O2 cell, demonstrates steady cycling performance as next generation secondary batteries and an alternative to Li-ion batteries.
Abstract: Recently, lithium-ion batteries have been attracting more interest for use in automotive applications. Lithium resources are confirmed to be unevenly distributed in South America, and the cost of the lithium raw materials has roughly doubled from the first practical application in 1991 to the present and is increasing due to global demand for lithium-ion accumulators. Since the electrochemical equivalent and standard potential of sodium are the most advantageous after lithium, sodium based energy storage is of great interest to realize lithium-free high energy and high voltage batteries. However, to the best of our knowledge, there have been no successful reports on electrochemical sodium insertion materials for battery applications; the major challenge is the negative electrode and its passivation. In this study, we achieve high capacity and excellent reversibility sodium-insertion performance of hard-carbon and layered NaNi0.5Mn0.5O2 electrodes in propylene carbonate electrolyte solutions. The structural change and passivation for hard-carbon are investigated to study the reversible sodium insertion. The 3-volt secondary Na-ion battery possessing environmental and cost friendliness, Na+-shuttlecock hard-carbon/NaNi0.5Mn0.5O2 cell, demonstrates steady cycling performance as next generation secondary batteries and an alternative to Li-ion batteries.
1,679 citations
TL;DR: In this article, high precision voltage measurements and in situ x-ray diffraction indicate a sequence of three distinct phase transitions as varies from 1 to 0.4, two of which are situated slightly above and below and are caused by an order/disorder transition of the lithium ions.
Abstract: Electrochemical properties of are studied as Li is deintercalated from . High precision voltage measurements and in situ x‐ray diffraction indicate a sequence of three distinct phase transitions as varies from 1 to 0.4. Two of the transitions are situated slightly above and below and are caused by an order/disorder transition of the lithium ions. The order/disorder transition is studied as a function of temperature allowing the determination of an order/disorder phase diagram. In situ x‐ray diffraction measurements facilitate a direct observation of the effects of deintercalation on the host lattice crystal structure. The other phase transition is shown to be first order (coexisting phases are observed for ) involving a significant expansion of the parameter of the hexagonal unit cell. We report the variation of the lattice constants of with and show that the phase transition to the lithium ordered phase near is accompanied by a lattice distortion to a monoclinic unit cell with , , and . Finally we report an overall phase diagram for and .
1,529 citations