Lithium titanate LTO

Li4Ti5O12 · CAS 12031-95-7 · cubic, Fd-3m

Lithium titanate (Li4Ti5O12) is a spinel oxide used as a lithium-ion anode.

12 sources · Updated 2026-10-16 · CC BY 4.0

Evidence level

2 of 5

Lab-measured

Capacity

175 mAh/g in theory

Voltage

1.55 V

Size change

About 0.2%

Cycle life

20,000 to 30,000 cycles

Heat

383 J/g

Recipe, share of the weight

  • Li 6.0%Lithium
  • Ti 52.1%Titanium
  • O 41.8%Oxygen

Best for

Very long cycle life and fast charge, with no lithium plating and almost no size change.

Weakest at

Lower cell energy (high voltage, low capacity per gram) and gas generation with swelling in cells.

Risk at a glance

  • People None found. Not classified hazardous
  • If it fails High. Gassing and swelling
  • Corrosion Severe. LTO reacts with the carbonate solvents and makes gas that swells soft-pack cells.

Why it exists

Lithium titanate (LTO, Li₄Ti₅O₁₂) is a spinel oxide (cubic, space group Fd-3m) used as a lithium-ion anode. It works at a much higher voltage than graphite, near 1.55 V versus Li/Li⁺, and its structure barely changes size when lithium enters, a property called zero strain. Together these avoid lithium plating and allow very long cycle life, at the cost of lower cell energy. Its known weak point is that it reacts with carbonate electrolytes and generates gas, which swells soft-pack cells.

Where it's used

Toshiba SCiB cells

Toshiba says its SCiB cells use lithium titanium oxide in the anode. It names mild hybrid and hybrid cars, electric buses, trucks, factory vehicles, grid storage, trains, ships and substations as uses. It does not mention space.

A fast-charging car cell

A review reports that a Li₄Ti₅O₁₂ and LiFePO₄ 18650 cell type was used in a real car with the charge time cut to 5 minutes using a three-level charger. The car and maker are not named.

Recipe

Li4Ti5O12

Li₄Ti₅O₁₂ is a spinel oxide. Each formula unit combines four lithium atoms, five titanium atoms and twelve oxygen atoms.

What LTO is made of
IngredientAtoms per unitShare of the weightWhat it does
Lithium Li 4 6.0% The mobile species. Lithium ions enter and leave the spinel as the cell charges and discharges.
Titanium Ti 5 52.1% The redox center. Titanium changes oxidation state as lithium enters, near 1.55 V versus Li/Li⁺.
Oxygen O 12 41.8% Bonds with lithium and titanium to form the spinel framework, which barely changes size as lithium moves.

Weight shares are calculated from standard atomic weights.

What it can do

Capacity

175 mAh/g in theory

The theoretical specific capacity of the spinel is 175 mAh/g over a voltage window of 2.5 to 1.0 V versus Li/Li⁺. In a soft-pack full cell at a 0.5 C rate and 25 °C, the measured capacity of the LTO was 148.7 mAh/g, and 151.2 mAh/g for carbon-coated LTO. In a half-cell at 10 C discharge, porous crystallites delivered 140 mAh/g, and at 100 C about 70 mAh/g.

Voltage

1.55 V

The flat plateau of the two-phase Li₄Ti₅O₁₂ to Li₇Ti₅O₁₂ reaction sits at 1.55 V versus Li/Li⁺. That is about 1.2 V above a carbon anode, which lowers cell voltage and energy density.

Size change

About 0.2%

Inserting and removing lithium changes the volume by only around 0.2%, which is why the material is called zero strain. Graphite swells by around 10%.

Cycle life

20,000 to 30,000 cycles

An 800 mAh 18650 cell charged at 10C and discharged at 5C completed 20,000 cycles. A similar cell charged at 15C and discharged at 5C retained 95% after 30,000 cycles. These are test results reported in a review.

Heat

383 J/g

Electrochemically lithiated Li₄Ti₅O₁₂ released a total of 383 J/g in differential scanning calorimetry, with onset at 125 °C. The comparison value for fully lithiated graphite is 2,700 J/g, with onset at 100 °C.

In the cold

55% at -40 °C

In a coin half-cell with a ternary carbonate electrolyte, LTO delivered 55.48% of its room-temperature capacity at -40 °C. The binary EC+DMC electrolyte almost failed to charge and discharge below -30 °C in the same study, so the electrolyte sets the limit.

How it compares

Lithium titanate is one of two anodes in this collection, and the other is graphite. It stores less charge per gram, 175 mAh/g in theory against 372 mAh/g for graphite, and it works at a higher voltage, which lowers cell energy. In exchange it avoids lithium plating, barely changes size, and lasts through tens of thousands of cycles in the tests collected here. The table compares lithium titanate with the other anodes in the collection.

The same measurements for each material, so you can compare them. Each row names the key condition under the value; the full conditions and methods are in the numbered notes under Technical details. Other materials are shown beside it; each was measured under its own conditions, so open its page before comparing closely. See the full ranking.

Benchmarks
MeasurementLTOGr
Capacity and energy
Theoretical specific capacity175 mAh/g1372 mAh/g
Porous nanocrystalline LTO at 10CHalf-cell result reported in a review140 mAh/g3no data
Porous nanocrystalline LTO at 100CHalf-cell result reported in a review70 mAh/gno data
Discharge capacity of LTO at -40 C relative to room temperature55.48 % of room-temperature capacity6no data
Voltage and potential
Working voltage plateau1.55 V vs Li/Li+2no data
Thermal behavior and safety
DSC onset, fully lithiated Li4Ti5O12 with electrolyteDSC125 °C780 to 160 °C
Lifetime and stability
Volume change on cyclingValue quoted in a review0.2 %410 %
Physical and electrical
Electronic conductivityValue quoted in the body text of a review1×10^-8 to 1×10^-7 S/cm5no data
Electronic conductivity as given in the abstractValue quoted in the abstract of a review1×10^-13 S/cmno data

Why choose it, and why not

Good for

  • Very long cycle life and fast charging, with no lithium plating and almost no change in size.
  • Established in commercial cells and named for vehicles, buses, trains, ships and grid storage by one manufacturer.

Watch out for

  • Lower cell energy, because of the high voltage and low capacity per gram.
  • Gas generation (hydrogen, carbon dioxide and carbon monoxide) swells soft-pack cells. The authors call gassing a grave safety concern and a main obstacle to wide use.
  • Poor performance in the cold with the wrong electrolyte.

LTO is the long-life, fast-charging anode. It gives up cell energy and has to be managed for gas, and in exchange it avoids lithium plating and barely changes size.

Technical details

For scientists and researchers. Everything above comes from the record below: every number with its method, its conditions and its source.

Cell-level benchmarks

Values for finished cells. These vary by manufacturer, so read the conditions in the notes. Other materials are shown beside it; each was measured under its own conditions, so open its page before comparing closely. See the full ranking.

Cell-level benchmarks
MeasurementLTOGr
Capacity and energy
Capacity of LTO in a NCM/LTO soft-pack cell, cycle 1148.7 mAh/g8no data
Capacity of LTO in a NCM/LTO soft-pack cell, cycle 400138.5 mAh/g9no data
Lifetime and stability
LTO//LiFePO4 18650 cell, stable capacityCycling test reported in a review20000 cycles10no data
LTO//LiFePO4 18650 cell, 95% capacity retentionCycling test reported in a review30000 cycles11no data
Hydrogen share of gas from charged NCM/LTO soft-pack cells stored 3 monthsGas chromatography of gas from the cells55.65 wt%12no data

Notes

The method, full conditions and any caveat for the numbered rows above.

Notes for the numbered rows
#MeasurementMethodConditionsCaveat
1Theoretical specific capacityValue quoted by the paper as the theoretical capacity of the spinelvoltage window 2.5 to 1.0 V vs Li/Li+reaction lithium insertion into the Li4Ti5O12 spinel (the source does not give the lithium count)—
2Working voltage plateauHalf-cell galvanostatic discharge, as summarized in a reviewreaction two-phase Li4Ti5O12 to Li7Ti5O12 plateaunote flat plateau, not an average over a sloping curve—
3Porous nanocrystalline LTO at 10C—rate 10C dischargeparticles porous crystallites 20 to 50 nm, 12 m2/gnote close to 175 mAh/g at C/2 per the same review—
4Volume change on cycling—event lithium insertion and extractionstated as around 0.2%attributed to Ohzuku et al. (zero-strain)—
5Electronic conductivity—material intrinsic Li4Ti5O12reason given empty Ti 3d stateThe abstract of the same paper states 1e-13 S/cm, so published figures disagree.
6Discharge capacity of LTO at -40 C relative to room temperatureGalvanostatic cycling after 4 h temperature equilibrationtemperature C -40rate 0.5Cvoltage window 1 to 2.5 V vs Li/Li+cell CR2025 coin half-cell vs lithium, 1 M LiPF6 in EC+EMC+DMC 1:1:1capacity at minus40 mAh g 86The binary EC+DMC electrolyte almost failed to charge and discharge below -30 C in the same study, so the electrolyte sets the limit.
7DSC onset, fully lithiated Li4Ti5O12 with electrolyte—material electrochemically lithiated Li4Ti5O12 from a Li-metal half-cell, with electrolytetest differential scanning calorimetrynote onset did not change noticeably with the amount of lithium insertedTotal heat of fully lithiated Li4Ti5O12 was 383 J/g, against 2700 J/g with onset 100 C for fully lithiated graphite (unit printed as "Jg" on the page, read as J/g). LTO's advantage here is mainly less heat, not a much later onset.
8Capacity of LTO in a NCM/LTO soft-pack cell, cycle 1Specific capacity of the LTO measured in the full cellrate 0.5C charge and dischargetemperature C 25cell soft-pack, Li(Ni1/3Co1/3Mn1/3)O2 cathode, 1 M LiPF6 in EC+DMC+EMC—
9Capacity of LTO in a NCM/LTO soft-pack cell, cycle 400Specific capacity of the LTO measured in the full cellrate 0.5C charge and dischargetemperature C 25cell soft-pack, Li(Ni1/3Co1/3Mn1/3)O2 cathode, 1 M LiPF6 in EC+DMC+EMCThe same cell type with carbon-coated LTO gave 151.2 mAh/g at cycle 1 and 151.3 mAh/g at cycle 400.
10LTO//LiFePO4 18650 cell, stable capacity—charge 10Cdischarge 5Ccell 18650, 800 mAh, nanostructured carbon-coated electrodes, flat 1.85 VSection 1 describes carbon-coated electrodes for this cell, while later text in the same paper calls the LTO anode carbon-free; the paper does not reconcile the two.
11LTO//LiFePO4 18650 cell, 95% capacity retention—charge 15Cdischarge 5Cretention 95%cell 18650, 800 mAh—
12Hydrogen share of gas from charged NCM/LTO soft-pack cells stored 3 months—storage fully charged, 25 C, 3 monthselectrolyte 1 M LiPF6 in EC+DMC+EMCother gases CO2 30.41 wt%, CO 10.00 wt%—

Corrosion and compatibility

What happens when it meets other materials and environments.

Corrosion and compatibility
EnvironmentConcernWhat happens
Carbonate electrolyte with LiPF6, stored or cycled severe LTO reacts with the carbonate solvents and makes gas that swells soft-pack cells.1
Water and PF5 / HF from LiPF6 not rated The gas comes from LTO reacting with the solvent, not from water or HF.2
Deep discharge below about 1 V vs Li/Li+ moderate Discharging below about 1 V inserts extra lithium and builds a thick surface film.3
Normal working window (above 1 V vs Li/Li+) low In its normal window above 1 V, no surface film forms on LTO.4
Water during aqueous electrode processing, with an aluminium current collector moderate Water raises the slurry pH, which corrodes the aluminium current collector.5
Low-temperature carbonate electrolyte moderate In the cold the electrolyte thickens and the capacity falls.6
Corrosion details
#EnvironmentDetailsTest conditions
1 Carbonate electrolyte with LiPF6, stored or cycled LTO reacts with the carbonate solvents at its surface and makes H2, CO2 and CO, which swell soft-pack cells. The reaction happens in a thin outer layer of the (111) plane, which changes toward anatase TiO2. It occurs even in solvent with no LiPF6. storage 25 and 50 C, up to 3 monthscells soft-pack NCM/LTO, also 400 cycles at 0.5C and 25 Cworse at higher temperature (50 C reacts more than 25 C)
2 Water and PF5 / HF from LiPF6 The paper concludes the gas comes from the interaction of LTO with the solvent rather than from PF5 or water. In electrolyte, HF reacts with LTO to form Li2TiF6 and LiF on the surface. electrolyte 1 M LiPF6 in EC+DMC+EMC, 50 C soak
3 Deep discharge below about 1 V vs Li/Li+ Taking LTO down to 0.01 V inserts one extra lithium and also reduces electrolyte on the surface to form a thick SEI. voltage 0.01 V vs Li/Li+
4 Normal working window (above 1 V vs Li/Li+) The reaction at 1.55 V means no SEI is formed at the LTO surface, according to the review, which avoids SEI-related safety problems and allows other electrolytes than ethylene carbonate based ones. voltage 1.55 V plateau
5 Water during aqueous electrode processing, with an aluminium current collector LTO reacts with water, leaching lithium and raising the slurry pH (stabilizing above 11 when LTO is simply exposed to water, per the paper's citation). The high pH causes pitting corrosion of the aluminium current collector with hydrogen evolution, cracked coatings, poor adhesion and higher charge-transfer resistance. process water-based electrode slurry cast on battery-grade aluminium foilscope manufacturing step, not in-cell use
6 Low-temperature carbonate electrolyte At low temperature the electrolyte gets more viscous and less conductive, charge transfer and lithium diffusion in LTO slow down and capacity falls. temperature C -40electrolyte EC+EMC+DMC ternary vs EC+DMC binary

Risks and side effects

Hazards to people, what happens when a cell overheats, and how the material is handled and stored.

For people

Lithium titanate powder is not classified as hazardous by the supplier sheet we found, but toxicology data are mostly missing.

A supplier sheet
An MSE Supplies safety data sheet (revision 2020) for lithium titanate anode powder says it is not a hazardous substance or mixture under the OSHA hazard communication standard. Many toxicology and physical properties are listed as no data available.
Dust
Further processing of the solid may form combustible dusts, so this should be considered before processing.
In a fire
Fire products are titanium oxides and lithium oxides, and the powder is incompatible with strong oxidizing agents.

If a cell overheats

The evidence here is limited to one cell pairing and one test.

A cell with an LTO anode
In an accelerating-rate calorimetry test of 18650 cells with a Li₄Ti₅O₁₂ anode and a LiMn₂O₄ cathode, the authors report no thermal runaway, explosion or fire. This is one cathode pairing, and other cathodes and abuse modes were not covered.
Heat released
Fully lithiated Li₄Ti₅O₁₂ released 383 J/g in differential scanning calorimetry, against 2,700 J/g for fully lithiated graphite.
Gassing
LTO reacts with the carbonate solvents at its surface and makes hydrogen, carbon dioxide and carbon monoxide, which swell soft-pack cells. In one test the gas from fully charged cells stored for 3 months at 25 °C was 55.65 wt% hydrogen, 30.41 wt% carbon dioxide and 10.00 wt% carbon monoxide. The reaction is faster at high temperature.

Handling and storage

Storage
Keep the container tightly closed in a dry, well-ventilated place, and avoid dust formation.
Controlling gas
A nanoscale carbon coating of about 5 nm, together with a stable surface film on the LTO, stopped visible swelling after 3 months of storage and 400 cycles in soft-pack cells. A 2 to 3 nm carbon layer applied by spray granulation of sucrose was reported to give a more stable film and suppress gas.
Water processing
LTO reacts with water and raises the slurry pH, which corrodes an aluminium current collector. Adding phosphoric acid to the aqueous slurry, tested up to 2.68 wt% of the LTO mass, buffers the pH and suppresses the corrosion.
In the cold
A ternary carbonate electrolyte (EC, EMC and DMC) gave better performance below 0 °C than a binary one.

Test details
The original wording and numbers from the sources, for readers who want them.

Failure risks

Failure risks
FailureTrigger and consequence
Gassing and swellinghigh severityInterfacial reaction of LTO with carbonate electrolyte, during storage and cycling, faster at high temperatureCell swelling; the authors call gassing a grave safety concern and a main obstacle to wide use of LTO batteries.
Thermal runaway of LTO/LiMn2O4 18650 cellslow severityAccelerated rate calorimetry test of 18650 cells with Li4Ti5O12 anode and LiMn2O4 cathodeThe authors report no thermal runaway, explosion or fire in that test. This is one cathode pairing; other cathodes and abuse modes were not covered.
Poor performance in the cold with the wrong electrolytemoderate severityCycling at or below -30 C with an EC+DMC binary electrolyteCells almost failed to charge and discharge below -30 C.

Side effects on surrounding parts

Side effects on surrounding parts
AffectsEffect
Pouch cells and packsGas from LTO surface reactions (H2, CO2, CO) is the main source of swelling in soft-pack batteries.
Cell energyLTO works about 1.2 V above a carbon anode, which lowers cell voltage and energy density.

Handling and storage

  • Keep the container tightly closed in a dry, well-ventilated place; avoid dust formation.

Mitigations

  • A nanoscale carbon coating (about 5 nm) plus a stable SEI film on LTO stopped visible swelling after 3 months of storage and 400 cycles in the soft-pack cells.
  • A 2 to 3 nm carbon layer applied by spray granulation of sucrose was reported to give a more stable SEI and suppress gas.
  • Adding phosphoric acid to the aqueous slurry (tested up to 2.68 wt% of the LTO mass) buffers the pH and suppresses the aluminium corrosion; the corrosion-free electrodes outperformed the acid-free ones.
  • Use of a ternary carbonate electrolyte (EC+EMC+DMC) gave better LTO performance below 0 C than a binary one.

Supply and geography

How common the raw materials are and where they come from.

Lithium

World mine production 290,000 t in 2025 (excluding the US, which is withheld), up from 222,000 t in 2024; reserves 37,000,000 t; identified resources about 150 million tons. Batteries were 88% of world lithium end use. Shares below are computed from the USGS table (country production / 290,000).

Top producers (2025)
Australia 31.7%, China 21.4%, Chile 19.3%, Zimbabwe 9.7%, Argentina 7.9%
Recycling
USGS: construction of lithium battery recycling plants continued throughout 2025; automotive firms and recyclers partnered.
Substitutes
Possible in batteries, ceramics, greases and glass; for primary battery anodes: calcium, magnesium, mercury, zinc

Titanium (sponge metal) and titanium dioxide pigment capacity

2025e world titanium sponge production 370,000 t (rounded), world pigment capacity 9,900,000 t. China 260,000 t of sponge and 6,000,000 t of pigment capacity. LTO is made from a titanium dioxide (anatase) precursor with a lithium compound, so pigment-grade TiO2 supply is the closer link than sponge metal. China's share of pigment capacity is 60.6% (6,000,000 of 9,900,000 t), computed here from the figures above; the producer shares listed below are for sponge metal. Shares computed from the USGS table.

Top producers (2025)
China 70.3%, Japan 14.3%, Russia 6.8%
Recycling
USGS: scrap data withheld; U.S. produced titanium powder from scrap metal from late 2024.
Substitutes
Aluminum, composites, steel and superalloys compete with titanium metal; calcium carbonate, kaolin and talc compete with TiO2 as pigment