Contact us: +91 9550333722 040 - 40102781
Structured search
India
Choose your country
Different countries will display different contents
Try our best to find the right business for you.
My chemicalbook

Welcome back!

HomeProduct name listLithium bis(trifluoromethanesulphonyl)imide

Lithium bis(trifluoromethanesulphonyl)imide

Synonym(s):Bis(trifluoromethylsulfonyl)amine lithium salt;LiTFSI;Lithium bistrifluoromethanesulfonimidate

  • CAS NO.:90076-65-6
  • Empirical Formula: C2F6LiNO4S2
  • Molecular Weight: 287.09
  • MDL number: MFCD00210017
  • EINECS: 415-300-0
  • SAFETY DATA SHEET (SDS)
  • Update Date: 2024-08-21 22:41:43
Lithium bis(trifluoromethanesulphonyl)imide Structural

What is Lithium bis(trifluoromethanesulphonyl)imide?

Description

Lithium bis(trifluoromethylsulphonyl)imide (LiTFSI) is normally used as a p-dopant?to enhance the conductivity and hole mobility of the?Spiro-OMeTAD for perovskite solar cells. It is believed that The function of LiTFSI in PSCs is?similar to that in solid-state dye-sensitised solar cells [2].

Description

Lithium bis(trifluoromethane)sulfonimide (LiTFSI) is a hydrophilic organic salt that has many uses in electric and electronic systems. Its bis(trifluoromethane)sulfonimide anion, often referred to as bistriflimide, has the useful property of coordinating weakly with cations.
LiTFSI ‘s other important property is its extremely high solubility in water: 21 molal or ≈6 kg/L of solution. Because of its solubility, it has been explored as an electrolyte for lithium-ion batteries, solar cells, and similar applications since at least the late 1980s. LiTFSI is a safer material than the formerly used salt, lithium hexafluorophosphate (LiPF6).
In a 2021 Nature article, André D. Taylor at New York University (New York City) and Yale University (New Haven, CT) and 18 colleagues there and at other institutions in the United States and the Republic of Korea reported a refinement in the use of LiTFSI in solar cells.
Photovoltaic cells made of inexpensive light-absorbing perovskites that have high power-conversion efficiencies have been developed over the past several years. To improve the cells’ ability to transport electrical charges, they are doped with a combination of LiTFSI and a semiconductor called Spiro-OMeTAD1; but this process is extremely slow.
Taylor and his fellow researchers solved the problem by bubbling carbon dioxide into a solution of spiro-OMeTAD and LiTFSI while irradiating the mixture with ultraviolet light. They then cast a film made from the solution onto the perovskite light absorber. The process can be completed in ≈1 min, compared with the older, hours-long doping procedure.
The authors state, “The CO2-treated interlayer exhibits approximately 100 times higher conductivity than a pristine [untreated] film while realizing stable, high-efficiency solar cells without any post-treatments.” They also report that their method is useful for doping π-conjugated polymers.
1. 2,2′,7,7′-Tetrakis[N,N-di(4-methoxyphenyl)amino]-9,9-spirobifluorene, CAS Reg. No. 207739-72-8.

Chemical properties

White hygroscopic powder

The Uses of Lithium bis(trifluoromethanesulphonyl)imide

It finds application in the preparation of rare-earth Lewis acid catalysts.

The Uses of Lithium bis(trifluoromethanesulphonyl)imide

Lithium bis(trifluoromethylsulfonyl)imide is used in the preparation of chiral imidazolium salt through an anion metathesis of the corresponding triflate organic electrolyte-based lithium batteries. It finds application in the preparation of rare-earth Lewis acid catalysts. It is also useful in primary and secondary lithium cells using organic liquid electrolytes and polymer batteries.

What are the applications of Application

Bis(trifluoromethane)sulfonimide lithium salt is an electrolyte

General Description

Bis(trifluoromethane)sulfonimide lithium salt is a synthetic reagent.

Flammability and Explosibility

Non flammable

Synthesis

5.91 g of anhydrous lithium fluoride and N-butyl-bistrifluoromethylsulfonimide 51.26 g. Add to 250 g of isopropyl acetate and reflux for 10 hours. It was filtered after being cooled to room temperature, and the filtrate was concentrated to dryness under reduced pressure.200 g of dichloromethane was added dropwise, and the mixture was stirred at 20 ° C for 2 hours and then filtered. Wash with dichloromethane. The filter cake was dried at 80 ° C to obtain 39.57 g of Lithium bis(trifluoromethanesulphonyl)imide. The yield is 90.7%.
Lithium bis(trifluoromethanesulphonyl)imide

Properties and Applications

Lithium bis(trifluoromethanesulphonyl)imide (LiTFSI) is a hydrophilic organic salt with many uses in electric and electronic systems. Its bis(trifluoromethane)sulfonimide anion, often called bistriflimide, is helpful in coordinating weakly with cations. LiTFSI's other important property is its extremely high solubility in water: 21 molal or ≈6 kg/L of solution. LiTFSI is safer than the formerly used salt, lithium hexafluorophosphate (LiPF6). To improve the cells' ability to transport electrical charges, researchers are doped with a combination of LiTFSI and a semiconductor called Spiro-OMeTAD1; however, this process is extremely slow. Taylor and his fellow researchers solved the problem by bubbling carbon dioxide into a solution of spiro-OMeTAD and LiTFSI while irradiating the mixture with ultraviolet light. They then cast a film from the solution onto the perovskite light absorber. The process can be completed in ≈1 minute, compared with the older, hours-long doping procedure.

Properties of Lithium bis(trifluoromethanesulphonyl)imide

Melting point: 234-238 °C(lit.)
Density  1,334 g/cm3
vapor pressure  0Pa at 25℃
Flash point: >100°C (>212°F)
storage temp.  Inert atmosphere,Room Temperature
solubility  H2O: 10 mg/mL, clear, colorless
form  Hygroscopic Powder
appearance hygroscopic white powder
color  White
Specific Gravity 1.334
Water Solubility  Soluble in water.
Sensitive  Moisture Sensitive
BRN  6625414
CAS DataBase Reference 90076-65-6(CAS DataBase Reference)
EPA Substance Registry System Methanesulfonamide, 1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]-, lithium salt (90076-65-6)
Boiling point: 234-238?°C (lit.)

Safety information for Lithium bis(trifluoromethanesulphonyl)imide

Signal word Danger
Pictogram(s)
ghs
Corrosion
Corrosives
GHS05
ghs
Skull and Crossbones
Acute Toxicity
GHS06
ghs
Health Hazard
GHS08
GHS Hazard Statements H314:Skin corrosion/irritation
H373:Specific target organ toxicity, repeated exposure
H412:Hazardous to the aquatic environment, long-term hazard
Precautionary Statement Codes P260:Do not breathe dust/fume/gas/mist/vapours/spray.
P273:Avoid release to the environment.
P280:Wear protective gloves/protective clothing/eye protection/face protection.
P303+P361+P353:IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.
P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

Computed Descriptors for Lithium bis(trifluoromethanesulphonyl)imide

InChIKey QSZMZKBZAYQGRS-UHFFFAOYSA-N

Related products of tetrahydrofuran

You may like

  • Lithium triflimide, 99%+ CAS 90076-65-6
    Lithium triflimide, 99%+ CAS 90076-65-6
    90076-65-6
    View Details
  • Bis(trifluoromethane)sulphonimide lithium salt, 99.95% CAS 90076-65-6
    Bis(trifluoromethane)sulphonimide lithium salt, 99.95% CAS 90076-65-6
    90076-65-6
    View Details
  • Lithium bis(trifluoromethanesulfonyl)imide 95% CAS 90076-65-6
    Lithium bis(trifluoromethanesulfonyl)imide 95% CAS 90076-65-6
    90076-65-6
    View Details
  • Lithium bis(trifluoromethanesulfonyl)imide, anhydrous, 99.99% CAS 90076-65-6
    Lithium bis(trifluoromethanesulfonyl)imide, anhydrous, 99.99% CAS 90076-65-6
    90076-65-6
    View Details
  • Lithium Bis(trifluoromethanesulfonyl)imide CAS 90076-65-6
    Lithium Bis(trifluoromethanesulfonyl)imide CAS 90076-65-6
    90076-65-6
    View Details
  • Bis(trifluoromethane)sulfonimide lithium salt CAS 90076-65-6
    Bis(trifluoromethane)sulfonimide lithium salt CAS 90076-65-6
    90076-65-6
    View Details
  • Bis(trifluoromethane)sulfonimide lithium salt CAS 90076-65-6
    Bis(trifluoromethane)sulfonimide lithium salt CAS 90076-65-6
    90076-65-6
    View Details
  • Lithium bis(trifluoromethanesulfonyl)imide CAS 90076-65-6
    Lithium bis(trifluoromethanesulfonyl)imide CAS 90076-65-6
    90076-65-6
    View Details
Statement: All products displayed on this website are only used for non medical purposes such as industrial applications or scientific research, and cannot be used for clinical diagnosis or treatment of humans or animals. They are not medicinal or edible.