The lithiumâÂÂsulfur battery (LiâÂÂS battery) is a type of rechargeable battery. It is notable for its high specific energy. The low atomic weight of lithium and moderate atomic weight of sulfur means that LiâÂÂS batteries are relatively light (about the density of water).
LithiumâÂÂsulfur batteries could displace lithium-ion cells because of their higher energy density and lower cost. The use of metallic lithium instead of intercalating lithium ions allows for much higher energy density, as less substances are needed to hold "lithium" and lithium is directly oxidized. LiâÂÂS batteries have a high theoretical specific energy (âÂÂ2600 Wh/kg for the Li/S redox chemistry), but practical cell-level specific energies in pouch-cell formats are typically ~300âÂÂ450 Wh/kg today; values above ~400 Wh/kg generally require high sulfur loading, lean-electrolyte operation, and limited excess lithium.
LiâÂÂS batteries with up to 1,500 charge and discharge cycles were demonstrated in 2017, but cycle life tests at commercial scale and with lean electrolyte have not been completed. As of early 2021, none were commercially available.
Several issues that have slowed acceptance. One is the polysulfide "shuttle" effect that is responsible for the progressive leakage of active material from the cathode, resulting in too few recharge cycles. Also, sulfur cathodes have low conductivity, requiring extra mass for a conducting agent in order to exploit the contribution of active mass to the capacity. Volume expansion of the sulfur cathode during S to LiS conversion and the large amount of electrolyte needed are also issues.
Progress has been made toward high-stability sulfurized-carbon cathodes. Sulfurized-carbon cathodes (e.g., sulfurized polyacrylonitrile, also known as SPAN) may offer some advantages. Their polysulfide shuttle free feature facilitates proper operation under lean electrolyte conditions (< 3 g÷(A÷h)<sup>âÂÂ1</sup>).
Although LiâÂÂS chemistry is attractive for its high theoretical energy density, practical pouch cells require minimizing inactive mass and operating under conditions that resemble commercial batteries. Some practical targets include: (i) high areal sulfur loading (typically âÂÂ¥5 mg<sub>s</sub> cm<sup>âÂÂ2</sup>) to avoid overestimating capacity in thin electrodes; (ii) lean electrolyte operation, often expressed as electrolyte-to-sulfur ratio E/S â¤5 üL mg/s (or electrolyte-to-capacity ratio E/C â²5 üL/mAh), because electrolyte can account for a large fraction of pouch-cell mass; and (iii) a controlled negative-to-positive capacity ratio (N/P), since excess lithium metal improves coin-cell cycling but strongly lowers cell-level energy density. These constraints are interdependent: increasing sulfur loading or lowering E/S improves projected energy density, but can also increase polarization and lower reversible capacity if ion/electron transport and interfacial stability are not maintained. Pouch-cell specific energies are often near 400âÂÂ450 Wh/kg are reached only when these metrics are satisfied simultaneously.
LiS batteries were invented in the 1960s, when Herbert and Ulam patented a primary battery employing lithium or lithium alloys as anodic material, sulfur as cathodic material and an electrolyte composed of aliphatic saturated amines. A few years later the technology was improved by the introduction of organic solvents as PC, DMSO and DMF yielding a 2.35âÂÂ2.5 V battery. By the end of the 1980s a rechargeable LiS battery was demonstrated employing ethers, in particular DOL, as the electrolyte solvent.
The critical parameters needed for achieving commercial acceptance have been described. Specifically, LiâÂÂS batteries need to achieve a sulfur loading of >5 mg÷cm<sup>âÂÂ2</sup>, a carbon content of <5%, electrolyte-to-sulfur ratio of <5 üL÷mg<sup>âÂÂ1</sup>, electrolyte-to-capacity ratio of <5 üL÷(mA÷h)<sup>âÂÂ1</sup>, and negative-to-positive capacity ratio of <5 in pouch-type cells.
They were used on the longest and highest-altitude unmanned solar-powered aeroplane flight (at the time) by Zephyr 6 in August 2008.
Chemical processes in the LiâÂÂS cell include lithium dissolution from the anode surface (and incorporation into alkali metal polysulfide salts) during discharge, and reverse lithium plating to the anode while charging.
At the anodic surface, dissolution of the metallic lithium occurs, with the production of electrons and lithium ions during the discharge and electrodeposition during the charge. The half-reaction is expressed as:
In analogy with lithium batteries, the dissolution / electrodeposition reaction causes over time problems of unstable growth of the solid-electrolyte interface (SEI), generating active sites for the nucleation and dendritic growth of lithium. Dendritic growth is responsible for the internal short circuit in lithium batteries and leads to the death of the battery itself.
One idealized concept for LiâÂÂS batteries, energy is stored in the sulfur cathode (S<sub>8</sub>). During discharge, the lithium ions in the electrolyte migrate to the cathode where the sulfur is reduced to lithium sulphide (Li<sub>2</sub>S). The sulfur is reoxidized to S<sub>8</sub> during the recharge phase. This idealized semi-reaction is therefore expressed as:
In reality the sulfur is reduced not to lithium sulphide but to lithium polysulphides (Li<sub>2</sub>S<sub>x</sub>, 2 ⤠x ⤠8) at decreasing chain length according to:
Depending on the battery, the final product is a mixture of Li<sub>2</sub>S<sub>2</sub> and Li<sub>2</sub>S. This contrasts with conventional lithium-ion cells, where the lithium ions are intercalated in the anode and cathodes. Each sulfur atom can host two lithium ions. Typically, lithium-ion batteries accommodate only 0.5âÂÂ0.7 lithium ions per host atom. Consequently, LiS allows for a much higher lithium storage density. Polysulfides are reduced on the cathode surface in sequence while the cell is discharging:
Across a porous diffusion separator, sulfur polymers form at the cathode as the cell charges:
These reactions are analogous to those in the sodiumâÂÂsulfur battery.
The main challenges of LiS batteries is the low conductivity of sulfur and its considerable volume change upon discharging and finding a suitable cathode is the first step for commercialization of LiS batteries. Therefore, carbon/sulfur cathode and a lithium anode are common. Sulfur is very cheap, but has practically no electroconductivity, 5Sâ cm<sup>âÂÂ1</sup> at 25ðC. A carbon coating provides the missing electroconductivity. Carbon nanofibers provide an effective electron conduction path and structural integrity, at the disadvantage of higher cost.
One problem with the lithiumâÂÂsulfur design is that when the sulfur in the cathode absorbs lithium, volume expansion of the Li<sub>x</sub>S compositions occurs, and predicted volume expansion of Li<sub>2</sub>S is nearly 80% of the volume of the original sulfur. This causes large mechanical stresses on the cathode, which is a major cause of rapid degradation. This process negatively affects the contact between the carbon and the sulfur, and prevents the flow of lithium ions to the carbon surface.
Mechanical properties of the lithiated sulfur compounds are strongly contingent on the lithium content, and with increasing lithium content, the strength of lithiated sulfur compounds improves, although this increment is not linear with lithiation.
One of the primary shortfalls of most LiâÂÂS cells is unwanted reactions with the electrolytes. While S and are relatively insoluble in most electrolytes, many intermediate polysulfides are not. Dissolving into electrolytes causes irreversible loss of active sulfur. Use of highly reactive lithium as a negative electrode causes dissociation of most of the commonly used other type electrolytes. Use of a protective layer in the anode surface has been studied to improve cell safety, i.e., using Teflon coating showed improvement in the electrolyte stability, LIPON, Li<sub>3</sub>N also exhibited promising performance.
Historically, the "shuttle" effect is the main cause of degradation in a LiS battery. The lithium polysulfide Li<sub>2</sub>S<sub>x</sub> (6 ⤠x ⤠8) is highly soluble in the common electrolytes used for LiS batteries. They are formed and leaked from the cathode and they diffuse to the anode, where they are reduced to short-chain polysulfides and diffuse back to the cathode where long-chain polysulfides are formed again. This process results in the continuous leakage of active material from the cathode, lithium corrosion, low coulombic efficiency and low battery life. Moreover, the "shuttle" effect is responsible for the characteristic self-discharge of LiS batteries, because of slow dissolution of polysulfide, which occurs also in rest state. The "shuttle" effect in a LiS battery can be quantified by a factor f<sub>c</sub> (0 < f<sub>c</sub> < 1), evaluated by the extension of the charge voltage plateau. The factor f<sub>c</sub> is given by the expression:
where k<sub>s</sub>, q<sub>up</sub>, [S<sub>tot</sub>] and I<sub>c</sub> are respectively the kinetic constant, specific capacity contributing to the anodic plateau, the total sulfur concentration and charge current.
Its initial capacity was 800 Ah/kg (classical LiCoO<sub>2</sub>/graphite batteries have a cell capacity of 100 Ah/kg). It decayed only very slowly, on average 0.04% each cycle, and retained 658 Ah/kg after 4000 cycles (82%).
Conventionally, LiS batteries employ a liquid organic electrolyte, contained in the pores of PP separator. The electrolyte plays a key role in LiS batteries, acting both on "shuttle" effect by the polysulfide dissolution and the SEI stabilization at anode surface. It has been demonstrated that the electrolytes based on organic carbonates commonly employed in Li-ion batteries (i.e. PC, EC, DEC and mixtures of them) are not compatible with the chemistry of LiS batteries. Long-chain polysulfides undergo nucleophilic attack on electrophilic sites of carbonates, resulting in the irreversible formation of by-products as ethanol, methanol, ethylene glycol and thiocarbonates. In LiS batteries are conventionally employed cyclic ethers (as DOL) or short-chain ethers (as DME) as well as the family of glycol ethers, including DEGDME and TEGDME. One common electrolyte is 1M LiTFSI in DOL:DME 1:1 vol. with 1%w/w di LiNO<sub>3</sub> as additive for lithium surface passivation.
Solid-state and gel electrolytes are being explored to improve safety and to suppress polysulfide shuttling by immobilizing sulfur species. Sulfide solid electrolytes provide high ionic conductivity and can enable shuttle-free operation, while polymer or composite electrolytes offer better mechanical compliance and wider processing windows. However, solid-state LiâÂÂS cells introduce new challenges, including large interfacial resistance at the sulfur/solid-electrolyte boundary and mechanical loss of contact due to the ~80% volume change during S â Li<sub>2</sub>S conversion. Recent all-solid-state LiâÂÂS prototypes therefore rely on engineered composite cathodes and interface designs to maintain continuous ionic and electronic pathways during cycling.
Because of the high potential energy density and the nonlinear discharge and charging response of the cell, a microcontroller and other safety circuitry is sometimes used along with voltage regulators to manage cell operation and prevent rapid discharge.
Lithium-sulfur (Li-S) batteries have a shorter lifespan compared to traditional Li-ion batteries. Its cycle life can be extended to over 1,000 cycles. One of the primary factors limiting the lifespan of Li-S batteries is the dissolution of polysulfides in the electrolyte, which leads to the shuttle effect and results in capacity loss over time. The operating temperature and cycling rate also play significant roles in determining the lifespan of Li-S batteries.
As of 2021 few companies had been able to commercialize the technology on an industrial scale. Companies such as Sion Power have partnered with Airbus Defence and Space to test their lithium sulfur battery technology. Airbus Defense and Space successfully launched their prototype High Altitude Pseudo-Satellite (HAPS) aircraft powered by solar energy during the day and by lithium sulfur batteries at night in real life conditions during an 11-day flight. The batteries used in the test flight utilized Sion Power's LiS cells that provide 350 Wâ h/kg. Lithium-metal batteries are an attractive alternative.
British firm OXIS Energy developed prototype lithium sulfur batteries. Together with Imperial College London and Cranfield University, they published equivalent-circuit-network models for its cells. With Lithium Balance of Denmark they built a prototype scooter battery system primarily for the Chinese market, which had a capacity of 1.2kWh using 10Ah Long Life cells, and weighed 60% less than lead acid batteries with a significant increase in range. They also built a 3U, 3,000Wâ h Rack-Mounted Battery that weighed only 25kg and was said to be fully scalable. They claimed their Lithium-Sulfur batteries would cost about $200/kWh in mass production. However, the firm entered bankruptcy (insolvency) status in May 2021.
Sony, which also commercialized the first lithium-ion battery, planned to introduce lithiumâÂÂsulfur batteries to the market in 2020, but has provided no updates since the initial announcement in 2015.
In 2022, the German company Theion claimed to introduce lithiumâÂÂsulfur batteries for mobile devices in 2023 and for vehicles by 2024.
In January 2023, Zeta Energy was awarded $4 million by the United States Department of Energy ARPA-E program to advance its lithium-sulfur batteries based on a sulfurized-carbon cathode and a vertically aligned carbon nanontube anode. Lyten started up a pilot production line making about 100 batteries a day.
In December 2024, automaker Stellantis and Zeta Energy announced a joint development agreement to advance lithiumâÂÂsulfur EV batteries, targeting commercial use around 2030 and highlighting cost savings from eliminating nickel and cobalt. In October 2024, Lyten announced plans to build a lithiumâÂÂsulfur gigafactory near Reno, Nevada, designed for up to ~10 GWh annual capacity, reflecting growing industrial interest in scaling LiâÂÂS technology. In August 2025, Lyten also agreed to acquire most of Northvolt's remaining assets and IP in Sweden and Germany, aiming to expand manufacturing and R&D capacity while continuing to mature LiâÂÂS cells for transportation and energy-storage markets. and in 2025 Lyten announced the acquisition of Swedish battery manufacturer Northvolt, including R&D, IP, labs and factories in Sweden, USA, Canada, Germany and Poland.