Graphite Gr

C · CAS 7782-42-5

Graphite is the layered carbon that holds lithium between its sheets in most lithium-ion cells.

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

Evidence level

2 of 5

Lab-measured

Capacity

372 mAh/g

Swelling

About 10%

Heat

Film breaks down at 90 to 120 °C

Cold charging

106 mAh/g at -40 °C

A flight cell

155 Wh/kg

Recipe, share of the weight

  • C not statedCarbon

Best for

Mature, low-cost anode with high capacity per gram at a low lithiation voltage.

Weakest at

Fast or cold charging (lithium plating) and heating (its protective film starts to break down at about 90 to 120 C).

Risk at a glance

  • People Low. Mostly not hazardous; dust can explode
  • If it fails High. Lithium plating
  • Corrosion No data. No corrosion data recorded

Quick facts: Gr

Key properties of Gr
PropertyValueBasis
Density1.9 to 2.3 g/cm³1 sourced value

What is the density of Graphite?

Graphite has a density of 1.9 to 2.3 g/cm³. The source and test conditions are listed in the properties table on this page.

What is Graphite used for?

Uses recorded in the sources include ISS main lithium-ion battery cells; Lithium-ion anode in electric-vehicle batteries; Brake linings, lubricants and powdered metals.

Why it exists

Graphite is the layered carbon that holds lithium between its sheets in most lithium-ion cells. Lithium ions slot in between the carbon layers as the cell charges and leave as it discharges, so graphite serves as the anode, the negative electrode. NASA lists it as the anode material of the GS Yuasa lithium-ion cells chosen for the batteries of the International Space Station. It stores charge at a very low voltage, which is good for the energy of the cell, but that same low voltage means lithium metal can plate onto the surface when a cell is charged fast or cold.

Where it's used

International Space Station main power

The GS Yuasa 134 Ah cells are described by NASA as lithium cobalt oxide with a carbon-graphite anode. Twenty-four lithium-ion units, with 30 cells per battery, were planned to replace 48 nickel-hydrogen units on the station.

Recipe

C

Graphite is pure carbon. Its atoms form flat sheets of six-sided rings, like a honeycomb, and the sheets stack on each other with weak bonds between them, leaving room for lithium to sit between the layers. Natural graphite comes from geologic deposits: it is mined, concentrated, then ground and sorted by flake size. Synthetic graphite is made by heating hydrocarbon materials to a very high temperature until they turn into graphite, a process called thermal graphitization, most often done in an Acheson furnace.

What Gr is made of
IngredientShare of the weightWhat it does
Carbon C not stated Forms the layered sheets. Lithium ions enter between the sheets when the cell charges and leave when it discharges.

Weight shares are as printed in the sources.

What it can do

Capacity

372 mAh/g

The theoretical specific capacity of 372 mAh/g follows from the reaction to LiC₆, which holds one lithium atom for every six carbon atoms.

Swelling

About 10%

Graphite swells by around 10% on lithiation, and the spacing between its layers grows from about 0.335 nm when uncharged to about 0.370 nm when fully lithiated as LiC₆.

Heat

Film breaks down at 90 to 120 °C

The protective film on the anode, the solid electrolyte interphase, begins to decompose at about 90 to 120 °C and releases CO₂, H₂, CH₄ and sometimes HF. Reported onsets for thermal runaway of lithiated graphite range from 80 to 160 °C, depending on the lithiation state, electrolyte and aging. One comparison value gives 2,700 J/g of heat for fully lithiated graphite.

Cold charging

106 mAh/g at -40 °C

In a three-electrode Li/graphite cell, at -30 °C and -40 °C the graphite potential crossed 0 V versus Li/Li⁺ after only 160 and 106 mAh/g, against 412 mAh/g at -20 °C. Once the potential reaches 0 V, lithium plating begins.

A flight cell

155 Wh/kg

The GS Yuasa LSE134-101 cell with a 134 Ah nameplate is listed at 155 Wh/kg at beginning of life, and its charge temperature range is 10 to 35 °C. The slide's own nameplate energy and mass work out to about 140.5 Wh/kg.

How it compares

Graphite is one of two anodes in this collection, and the other is lithium titanate. Graphite stores much more charge per gram (372 mAh/g, against a lower figure for lithium titanate that is not entered here) and operates at a very low voltage. Its weaknesses are fast or cold charging, where lithium plates, and heating, where its protective film breaks down at about 90 to 120 °C. The table compares graphite 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
MeasurementGrLTO
Capacity and energy
Theoretical specific capacity372 mAh/g1175 mAh/g
Capacity reached before graphite potential falls to 0 V vs Li/Li+ (-20 C)412 mAh/g6no data
Capacity reached before graphite potential falls to 0 V vs Li/Li+ (-30 C)160 mAh/g7no data
Capacity reached before graphite potential falls to 0 V vs Li/Li+ (-40 C)106 mAh/g8no data
Thermal behavior and safety
Heat-release onset of carbon or graphite anodes80 to 160 °C3125 °C
DSC onset, fully lithiated graphite with electrolyteDSC100 °C5125 °C
SEI exothermic decomposition temperature rangeLiterature statement in a review90 to 120 °Cno data
Lifetime and stability
Volume change on cycling10 %20.2 %
Physical and electrical
Layer spacing, pristine graphiteStructural value quoted in a review0.335 nmno data
Layer spacing, fully lithiated LiC6Structural value quoted in a review0.37 nmno data
Specific gravity of graphite (carbon record)1.9 to 2.3 g/cm³4no data

Why choose it, and why not

Good for

  • A mature, low-cost anode with high capacity per gram at a low lithiation voltage.
  • Established in flight batteries, including the batteries of the International Space Station.

Watch out for

  • Fast or cold charging plates lithium metal on the surface, which loses active lithium and can be unsafe.
  • The protective film breaks down at about 90 to 120 °C, and the exposed lithiated graphite then reacts strongly with the electrolyte.
  • Graphite dust can explode in air and is electrically conductive, so it can short electronics.

Graphite is the proven workhorse anode. It stores a lot of charge cheaply, and it needs protection from fast charging, cold charging and heat.

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
MeasurementGrLTO
Capacity and energy
Specific energy of the ISS LSE134-101 cell (graphite anode, lithium cobalt oxide cathode)155 Wh/kg9no data
Temperature behavior
Allowed charge temperature of the ISS LSE134-101 cell10 to 35 °C10no data

Notes

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

Notes for the numbered rows
#MeasurementMethodConditionsCaveat
1Theoretical specific capacityFaraday calculation for one lithium per six carbon atoms (value as stated by the review)reaction graphite to LiC6, full lithiationstated as approximately 372 mAh/g—
2Volume change on cyclingStatement in a review of electrochemical dilatometry (operando electrode thickness measurement)event lithiation of graphitestated as around 10%—
3Heat-release onset of carbon or graphite anodesLiterature summary of calorimetry results in a reviewdepends on lithiation state, electrolyte composition, aging historynote reported range, not a single threshold—
4Specific gravity of graphite (carbon record)Reference value quoted in the PubChem carbon recordform graphite, general reference value for the element carbonnote not battery-grade electrode density—
5DSC onset, fully lithiated graphite with electrolyte—material fully lithiated graphitetest differential scanning calorimetry, comparison value given in an LTO papertest conditions for graphite not given in the abstractTotal heat for fully lithiated graphite was given as 2700 J/g (unit printed as "Jg" on the page, read as J/g).
6Capacity reached before graphite potential falls to 0 V vs Li/Li+ (-20 C)Constant-current charge with a lithium reference electrodetemperature C -20current 0.1 mA/cm2 (about C/24)cell three-electrode Li/graphite, 1 M LiPF6 in EC/DMC/DEC 1:1:1formation cycling noneAt 20 C and the same current, staging plateaus gave near-theoretical capacity (372 mAh/g). Reaching 0 V early means lithium plating starts before the graphite is full.
7Capacity reached before graphite potential falls to 0 V vs Li/Li+ (-30 C)Constant-current charge with a lithium reference electrodetemperature C -30current 0.1 mA/cm2 (about C/24)cell three-electrode Li/graphite, 1 M LiPF6 in EC/DMC/DEC 1:1:1formation cycling none—
8Capacity reached before graphite potential falls to 0 V vs Li/Li+ (-40 C)Constant-current charge with a lithium reference electrodetemperature C -40current 0.1 mA/cm2 (about C/24)cell three-electrode Li/graphite, 1 M LiPF6 in EC/DMC/DEC 1:1:1formation cycling none—
9Specific energy of the ISS LSE134-101 cell (graphite anode, lithium cobalt oxide cathode)Nameplate data in a NASA battery workshop presentationcell GS Yuasa LSE134-101, 134 A-hr nameplatestate beginning of lifeThe slide gives 155 Wh/kg, but its own nameplate energy of 496 Wh and cell mass of 3.53 kg work out to about 140.5 Wh/kg, so the slide is internally inconsistent.
10Allowed charge temperature of the ISS LSE134-101 cellTemperature range listed on the cell information slidecell GS Yuasa LSE134-101discharge range -10 to +35 CThe slide gives the range, not the reason for the lower charge limit.

Corrosion and compatibility

What happens when it meets other materials and environments.

Corrosion and compatibility
EnvironmentConcernWhat happens
Carbonate electrolyte during first charge (SEI formation) not rated On the first charge the electrolyte forms a protective film on the graphite, which can later crack and reform.1
Cracked SEI on lithiated graphite not rated A cracked film lets electrolyte reach lithiated graphite, which damages the surface and speeds heat generation.2
Propylene carbonate electrolyte not rated Propylene carbonate enters the graphite layers along with lithium, a damaging side reaction.3
Copper current collector (anode side) during over-discharge not rated Over-discharge dissolves the copper current collector, which can cause short circuits and capacity loss.4
Heated electrolyte-wet lithiated graphite not rated Once the film breaks down, heated lithiated graphite reacts strongly with the electrolyte.5
Corrosion details
#EnvironmentDetailsTest conditions
1 Carbonate electrolyte during first charge (SEI formation) Electrolyte is reduced on the graphite surface and forms a protective film (SEI) made of an inner inorganic layer (Li2CO3, LiF, Li2O) and an outer organic layer (ROCO2Li, ROLi). It protects the graphite, but it is not static: it can decompose, crack and reform during cycling or heating. voltage forms below about 1 V vs Li/Li+electrolyte carbonate solvents with LiPF6
2 Cracked SEI on lithiated graphite Cracks let electrolyte reach lithiated graphite, which can cause solvent co-intercalation, graphite exfoliation and further surface damage, and speeds up heat generation. trigger repeated cycling or thermal exposure
3 Propylene carbonate electrolyte Propylene carbonate co-intercalates into the graphite lattice along with lithium ions, a side reaction that dilatometry can detect. electrolyte propylene carbonate based
4 Copper current collector (anode side) during over-discharge Copper anode current collectors dissolve under over-discharge, which can cause contact loss, short circuits and capacity loss. trigger over-dischargegeneral statement for Li-ion batteries, not graphite specific
5 Heated electrolyte-wet lithiated graphite After the SEI breaks down, the exposed lithiated graphite reacts strongly and exothermically with carbonate solvents (EC, DMC, DEC), producing CO2, CH4 and other light hydrocarbons. This is the first major heat-release step in thermal runaway. temperature starts in the 50 to 160 C initiation window of thermal runaway

Risks and side effects

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

For people

Graphite is classified as not hazardous by some suppliers and as an irritant by others. The larger hazard is its dust.

Database entries
PubChem aggregates 2,727 reports from 27 notifications for the entry Carbon, which includes graphite. Of these, 55.1% report H319 (eye irritation) and 51.1% report H335 (respiratory irritation), while 40.2% say the substance does not meet GHS hazard criteria. Classification depends on the supplier and the grade.
A supplier sheet
A Sigma-Aldrich safety data sheet classifies graphite as not a hazardous substance or mixture, and notes that further processing of solids may form combustible dusts. Listed workplace limits include a NIOSH exposure limit of 2.5 mg/m³ and an ACGIH limit of 2 mg/m³, each averaged over a work shift.
Dust
An SGL Technic sheet states that graphite dust of 4 to 40 micrometre particle size can explode over a wide range of concentrations (class St1), that the dust can cause an electrical short, and that spilled powder is a slipping hazard.

If a cell overheats

These results come from laboratory studies and from reviews, not from incidents in the field.

The first step
Heating a charged cell breaks down the protective film at 90 to 120 °C. This releases CO₂, H₂, CH₄ and sometimes HF.
Then the graphite reacts
Once the film has broken down, the exposed lithiated graphite reacts strongly and exothermically with the carbonate solvents (EC, DMC and DEC), producing CO₂, CH₄ and other light hydrocarbons. This is the first major heat-release step in thermal runaway.
Pressure in the cell
The gases from the film breakdown raise the pressure inside the cell, which reaches the casing and neighbouring cells in a battery.
Lithium plating
Fast charging or low temperature polarizes the graphite so that its surface potential falls to or below 0 V versus Li/Li⁺. The result is loss of active lithium, capacity fade and potential safety risks.

Handling and storage

Storage
Keep the container tightly closed in a dry place. Avoid dust formation and provide exhaust ventilation where dust forms.
Protecting the film
Surface coating, an artificial interphase or surface-chemistry control can stabilise the film and delay the breakdown and heat release.
Reducing plating
Shortening the paths lithium must diffuse through the graphite (layer spacing, pores, particle size and morphology, edge sites) lowers polarization and plating tendency, at some cost in first-cycle efficiency and compaction density.
Spacecraft protection
The ISS batteries use two independent controls against thermal runaway, voltage and temperature monitoring of all 30 cells, cell-level fault isolation, radiant heat barriers between cell pairs, and vented gas directed away from neighbours.

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

Failure risks

Failure risks
FailureTrigger and consequence
Lithium platinghigh severityFast charging or low temperature polarizes the graphite so its surface potential falls to or below 0 V vs Li/Li+.Loss of active lithium, capacity fade and potential safety risks.
Cold charging cannot fill the graphitehigh severityCharging a Li/graphite cell below -20 CAt -30 C and -40 C the graphite potential crossed 0 V vs Li/Li+ after only 160 and 106 mAh/g, against 412 mAh/g at -20 C, so lithium intercalation drops sharply and competes with plating.
SEI decomposition starting thermal runawayhigh severityHeating of a charged cell, typically at high state of chargeExothermic SEI breakdown at 90 to 120 C releases CO2, H2, CH4 and sometimes HF, then lithiated graphite reacts with the electrolyte.

Side effects on surrounding parts

Side effects on surrounding parts
AffectsEffect
Cell casing and neighbouring cells in a batteryGases from SEI decomposition (CO2, H2, CH4, sometimes HF) raise pressure inside the cell.
Electronics near graphite powder handlingConductive graphite dust can cause an electrical short.

Handling and storage

  • Keep the container tightly closed in a dry place. Avoid dust formation and provide exhaust ventilation where dust forms.

Mitigations

  • Stabilize the SEI with surface coating, an artificial interphase or surface chemistry control, so that SEI breakdown and heat release are delayed.
  • Shorten lithium diffusion paths in the graphite (layer spacing, pores, particle size and morphology, edge sites) to lower polarization and plating tendency, at some cost in first-cycle efficiency and compaction density.
  • ISS lithium-ion battery safeguards: two independent controls against thermal runaway, voltage and temperature monitoring of all 30 cells, cell-level fault isolation, radiant heat barriers between cell pairs, and vented gas directed away from neighbours.

Supply and geography

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

Natural graphite

World mine production 1,800,000 t in 2025 (estimate, rounded), world reserves 310,000,000 t, resources above 800 million tons of recoverable graphite outside the US. Country figures for 2025e: China 1,400,000 t; Madagascar 80,000 t; Tanzania 75,000 t; Brazil 65,000 t; Mozambique 60,000 t; Russia 25,000 t; India 17,000 t. USGS states China produced an estimated 82% of world natural graphite in 2025, mostly crystalline flake.

Top producers (2025)
China 82%
Recycling
USGS: graphite is recycled mainly from refractory brick and linings, and the abundance of graphite in the world market inhibits more recycling; quantity of recycled graphite was not available.
Substitutes
Synthetic graphite powder and secondary synthetic graphite from machining graphite shapes compete for battery use

Graphite battery anode material (natural and synthetic), US trade

US imports of graphite battery anode material in the first 8 months of 2025 were 43,400 tons (28,100 tons in the same period of 2024); leading sources China 55%, Indonesia 31%, Republic of Korea 14%. Preliminary US antidumping duties on Chinese anode material were 93.50%, countervailing duties 11.58% to 721.03%. China exported 37,400 tons of spherical purified graphite in the first 9 months of 2025.

Recycling
Not stated for anode material in the source.