MIL-101(Fe) as a lithium-ion battery electrode material: a relaxation and intercalation mechanism during lithium insertion. Issue 8 (28th January 2015)

• Record Type: Journal Article
• Authors: Shin, JaeWook; Kim, Min; Cirera, Jordi; Chen, Shawn; Halder, Gregory J.; Yersak, Thomas A.; Paesani, Francesco; Cohen, Seth M.; Meng, Ying Shirley
• Is Part Of: Journal of materials chemistry. Volume 3:Issue 8(2015)
• Page Start: 4738
• Page End: 4744
• Publication Date: 2015-01-28
• Subjects: Materials -- Research -- Periodicals; Chemistry, Analytic -- Periodicals; Environmental sciences -- Research -- Periodicals; 543.0284
• DOI: 10.1039/c4ta06694d
• Languages: English
• ISSNs: 2050-7488

Abstract

Abstract : The electrochemical performance and mechanism of a MIL-101(Fe) metal–organic framework (MOF) as a lithium ion battery electrode is reported for the first time. Abstract : The electrochemical performance of a MIL-101(Fe) metal–organic framework (MOF) as a lithium ion battery electrode is reported for the first time. Iron metal centers can be electrochemically activated. The Fe 3+ /Fe 2+ redox couple is electrochemically active, but not reversible over many cycles. A comparison between ex situ and in operando X-ray absorption spectroscopy (XAS) on the Fe K-edge is presented. Our results indicate that the capacity fade is related to a time dependent, irreversible oxidation of Fe 2+ to Fe 3+ . These results are key in proving the importance of in operando XAS measurements. The MOF side reaction with an electrolyte has been computationally modeled. These results provide further insights on the mechanism responsible for the MOF lack of reversibility. Future guidelines for improving the reversibility of MOFs used as electrodes in Li-ion batteries based on the fine-tuning of the electronic structure of the material are proposed.