Open AccessSuper Mg2+ Conductivity around 10–3 S cm–1 Observed in a Porous Metal–Organic Framework
Author(s) -
Yoshiyuki Yoshida,
Teppei Yamada,
Yuan Jing,
Takashi Toyao,
Kenichi Shimizu,
Masaaki Sadakiyo
Publication year - 2022
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.2c01612
Subject(s) - chemistry , conductivity , analytical chemistry (journal) , ionic conductivity , inorganic chemistry , adsorption , metal , ion , molecule , electrical resistivity and conductivity , electrode , electrolyte , organic chemistry , electrical engineering , engineering
We first report a solid-state crystalline "Mg 2+ conductor" showing a superionic conductivity of around 10 -3 S cm -1 at ambient temperature, which was obtained using the pores of a metal-organic framework (MOF), MIL-101, as ion-conducting pathways. The MOF, MIL-101⊃{Mg(TFSI) 2 } 1.6 (TFSI - = bis(trifluoromethanesulfonyl)imide), containing Mg 2+ inside its pores, showed a superionic conductivity of 1.9 × 10 -3 S cm -1 at room temperature (RT) (25 °C) under the optimal guest vapor (MeCN), which is the highest value among all Mg 2+ -containing crystalline compounds. The Mg 2+ conductivity in the MOF was estimated to be 0.8 × 10 -3 S cm -1 at RT, by determining the transport number of Mg 2+ ( t Mg 2+ = 0.41), which is the level as high as practical use for secondary battery. Measurements of adsorption isotherms, pressure dependence of ionic conductivity, and in situ Fourier transform infrared measurements revealed that the "super Mg 2+ conductivity" is caused by the efficient migration of the Mg 2+ carrier with the help of adsorbed guest molecules.