Lithium–sulfur battery

Lithium–sulfur battery
Specific energy 500 W·h/kg demonstrated
Energy density 350 W·h/L
Charge/discharge efficiency C/5 nominal
Cycle durability disputed
Nominal cell voltage cell voltage varies nonlinearly in the range 2.5–1.7 V during discharge; batteries often packaged for 3 V

The lithium–sulfur battery (Li–S battery) is a type of rechargeable battery, notable for its high specific energy.[1] The low atomic weight of lithium and moderate weight of sulfur means that Li–S batteries are relatively light (about the density of water). They were used on the longest and highest-altitude solar-powered aeroplane flight in August 2008.[2]

Lithium–sulfur batteries may succeed lithium-ion cells because of their higher energy density and reduced cost from the use of sulfur.[3] Currently the best Li–S batteries offer specific energies on the order of 500 W·h/kg, significantly better than most lithium-ion batteries, which are in the range of 150 to 200 W·h/kg. Li–S batteries with up to 1,500 charge and discharge cycles have been demonstrated.[4] As of early 2014, none were commercially available.[5] The key issue of Li–S battery is low electrical conductivity of sulfur cathode needing an extra mass for a conducting agent and the current research focus is to find highly conductive cathodes.[6]

Chemistry

Chemical processes in the Li–S 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.[7] 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 0.5–0.7 lithium ions per host atom.[8] Consequently, Li-S allows for a much higher lithium storage density. Polysulfides are reduced on the cathode surface in sequence while the cell is discharging:

S
8
Li
2
S
8
Li
2
S
6
Li
2
S
4
Li
2
S
3

Across a porous diffusion separator, sulfur polymers form at the cathode as the cell charges:

Li
2
S → Li
2
S
2
Li
2
S
3
Li
2
S
4
Li
2
S
6
Li
2
S
8
→ S
8

These reactions are analogous to those in the sodium–sulfur battery.

Most use a carbon/sulfur cathode and a lithium anode.[9] Sulfur is very cheap, but has practically no electroconductivity, 5×10−30 S⋅cm−1 at 25 °C.[10] A carbon coating provides the missing electroconductivity. Carbon nanofibers provide an effective electron conduction path and structural integrity, at the disadvantage of higher cost.[11]

One problem with the lithium–sulfur design is that when the sulfur in the cathode absorbs lithium, volume expansion of the LixS compositions happens, and predicted volume expansion of Li2S is nearly 80% of the volume of the original sulfur.[12] This causes large mechanical stresses on the cathode, which is a major cause of rapid degradation. This process reduces the contact between the carbon and the sulfur, and prevents the flow of lithium ions to the carbon surface.[13]

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.[14]

One of the primary shortfalls of most Li–S cells is unwanted reactions with the electrolytes. While S and Li
2
S
are relatively insoluble in most electrolytes, many intermediate polysulfides are not. Dissolving Li
2
S
n
into electrolytes causes irreversible loss of active sulfur.[15] 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,[16] LIPON, Li3N also exhibited promising performance.

Safety

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.[17]

Research

Research
Anode Cathode Date Source Specific Capacity after cycling Notes
Polyethylene glycol coated, pitted mesoporous carbon 17 May 2009 University of Waterloo[18] 1,110 mA⋅h/g after 20 cycles at a current of 168 mA⋅g−1[18] Minimal degradation during charge cycling. To retain polysulfides in the cathode, the surface was functionalized to repel (hydrophobic) polysulfides. In a test using a glyme solvent, a traditional sulfur cathode lost 96% of its sulfur over 30 cycles, while the experimental cathode lost only 25%.
Silicon nanowire Sulfur-coated, disordered carbon nanotubes 2011 Stanford University[19][20] 730 mA⋅h/g after 150 cycles (at 0.5C) An electrolyte additive boosted the faraday efficiency from 85% to over 99%.
Silicon nanowire/carbon Sulfur-coated, disordered carbon nanotubes made from carbohydrates 2013 CGS[21][22] 1,300 mA⋅h/g after 400 cycles (at 1C) Microwave processing of materials and laser-printing of electrodes.
Silicon carbon Sulfur 2013Fraunhofer Institute for Material and Beam Technology IWS[23] ? after 1,400 cycles
Copolymerized sulfur 2013University of Arizona[24][25] 823 mA⋅h/g at 100 cycles Uses "inverse vulcanization" on mostly sulfur with a small amount of 1,3-diisopropenylbenzene (DIB) additive
Porous TiO
2
-encapsulated sulfur nanoparticles
2013Stanford University[26][27] 721 mA⋅h/g at 1,000 cycles (0.5C) shell protects the sulfur-lithium intermediate from electrolyte solvent. Each cathode particle is 800 nanometers in diameter. Faraday efficiency of 98.4%.
Sulfur June 2013 Oak Ridge National Laboratory 1200 mA·h/g at 300 cycles at 60 °C (0.1C)

800 mA·h/g at 300 cycles at 60 °C (1C)[28]

Solid lithium polysulfidophosphate electrolyte. Half the voltage of typical LIBs. Remaining issues include low electrolyte ionic conductivity and brittleness in the ceramic structure.[29][30]
Lithium Sulfur-graphene oxide nanocomposite with styrene-butadiene-carboxymethyl cellulose copolymer binder 2013 Lawrence Berkeley National Laboratory[31] 700 mA·h/g at 1,500 cycles (0.05C discharge)

400 mA·h/g at 1,500 cycles (0.5C charge/ 1C discharge)

Voltage between about 1.7 and 2.5 volts, depending on charge state. Lithium bis(trifluoromethanesulfonyl)imide) dissolved in a mixture of nmethyl-(n-butyl) pyrrolidinium bis(trifluoromethanesulfonyl)-imide (PYR14TFSI), 1,3-dioxolane (DOL), dimethoxyethane (DME) with 1 M lithium bis-(trifluoromethylsulfonyl)imide (LiTFSI), and lithium nitrate (LiNO
3
). High porosity polypropylene separator. Specific energy is 500 W⋅h/kg (initial) and 250 W⋅h/kg at 1,500 cycles (C=1.0)
Lithiated graphite Sulfur February 2014 Pacific Northwest National Laboratory 400 cycles Coating prevents polysulfides from destroying the anode.[32]
Lithiated graphene Sulfur/Lithium-sulfide passivation layer 2014 OXIS Energy[33][34] 240 mA·h/g (1000 cycles)

25 A·h/cell

Passivation layer prevents sulfur loss
Lithium sulfur batteries Carbon nanotube/Sulfur 2014 Tsinghua University [35] 15.1 mA·h⋅cm−2 at a sulfur loading of 17.3 mgS⋅cm−2 A free-standing CNT–S paper electrode with a high areal sulfur-loading was fabricated, in which short MWCNTs served as the short-range electrical conductive network and super-long CNTs acted as both the long-range conductive network and intercrossed binders.
Glass-coated sulfur with mildly reduced graphene oxide for structural support 2015 University of California, Riverside[36] 700 mA⋅h⋅g−1 (50 cycles)[37] Glass coating prevents lithium polysulfides from permanently migrating to an electrode
Lithium Sulfur 2016 LEITAT 500 W⋅h/kg ALISE H2020 project developing a Li-S battery for cars with new components and optimized regarding anode, cathode, electrolyte and separator

Commercialization

As of 2015 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 Li-S cells that provide 350 W⋅h/kg.[38] Sion claims to be in the process of volume manufacturing with availability by end of 2017.[39]

British firm OXIS Energy developed prototype lithium sulfur batteries that are currently operating in small scale, commercial, test applications. As of June 2015, OXIS Energy planned to sell its energy storage batteries from 2016.[40][41] Together with Imperial College London and Cranfield University, OXIS Energy published equivalent-circuit-network models for its cells.[42] With Lithium Balance of Denmark they built a prototype scooter battery system primarily for the Chinese market. The prototype battery has a capacity of 1.2kWh using 10Ah OXIS Long Life cells, weighs 60% less than lead acid batteries with a significant increase in range.[43] OXIS Energy has built a 3U, 3,000 W⋅h Rack-Mounted Battery that weighs only 25 kg and is fully scalable.[44] OXIS anticipates that its Lithium-Sulfur batteries will cost about $200/kWh in mass production.[45] OXIS has also been involved in the European Consortium for Lithium-Sulphur Power for Space Environments (ECLIPSE) H2020 project. This project is developing high-capacity Li-S batteries for satellites and launchers. [46]

Sony, which also commercialized the first lithium-ion battery, plans to introduce lithium–sulfur batteries to the market in 2020.[47]

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