Journal
ACS ENERGY LETTERS
Volume 2, Issue 8, Pages 1818-1824Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acsenergylett.7b00437
Keywords
-
Categories
Funding
- EPSRC [EP/M009521/0]
- MCC/Archer consortium [EP/L000202/1]
- EPSRC SUPERGEN
- Engineering and Physical Sciences Research Council [EP/L019469/1, EP/M009521/1, EP/L000202/1, EP/K016288/1] Funding Source: researchfish
- EPSRC [EP/M009521/1, EP/L019469/1, EP/L000202/1, EP/K016288/1] Funding Source: UKRI
Ask authors/readers for more resources
Organic-inorganic halide perovskites are attracting extraordinary attention in the field of energy materials. The reaction of hybrid lead halide perovskites with Li metal has recently been proposed for a number of potential applications. However, the mechanisms for Li uptake in such materials, such as intercalation and conversion, are still unknown. Using a combination of density functional theory and electrochemical and diffraction techniques, we consider Li intercalation and conversion reactions in CH3NH3PbI3, CH3NH3PbBr3, and CH3NH3PbCI3. Our simulations suggest that conversion reactions with Li are far more energetically preferable in these materials than Li intercalation. Calculations confirm the formation of Pb metal as a result of Li conversion in all three materials, and this is supported by X-ray diffraction analysis of CH3NH3PbBr3. The results of this study provide fresh insights into lithium and halide perovskite reactions that will hopefully drive further exploration of these materials for a wider variety of energy applications.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available