4.7 Article

Electrochemical reaction mechanism of amorphous iron selenite with ultrahigh rate and excellent cyclic stability performance as new anode material for lithium-ion batteries

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 389, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2020.124350

Keywords

Iron selenite; Heterointerfaces; Amorphous structures; Anode materials; Lithium-ion batteries

Funding

  1. National Research Foundation of Korea (NRF) - Korea government (MSIP) [NRF2019R1A2C2088047, NRF-2017R1A4A1014806]

Ask authors/readers for more resources

Metal selenite materials have unique advantages from forming metal oxide and selenide heterostructure nanocrystals, which assist in accelerating electron and lithium-ion transportation and providing more active sites via interfacial coupling, during the first cycle. In this study, synthesis of amorphous iron selenite materials derived via oxidation at a low temperature of 250 degrees C of crystalline iron selenide was firstly researched in detail, and their composite (FeSeO-C-CNT) with carbon materials was applied as an anode material for lithium-ion batteries. The reversible reaction mechanism of iron selenite with Li ions is described by the reaction: Fe2O3+ FeSe2 + xSeO(2) + (1 - x)Se + (4x + 12)Li+ (4x + 12)e(-) <-> 3Fe + (2x + 3)Li2O + 3Li(2)Se. FeSeO-C-CNT composite electrode showed high reversible capacities of 617 mA h g(-1) for the 1800th cycle even at an extremely high current density of 30 A g(-1), which surprisingly indicated that FeSeO-C-CNT is enabled to fully charge in a very short time of 72 s. This study demonstrated that amorphous iron selenite materials could be excellent candidates for new anode compositions with high capacities and fast electrochemical kinetics properties.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available