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Significantly Enhancing the Lithium Ionic Conductivity of Metal–Organic Frameworks via a Postsynthetic Modification Strategy

Metal–organic frameworks (MOFs), due to their possessing a porous structure, are potential candidates for solid-state ionic conduction materials. Moreover, uncoordinated carboxylic acid groups (−COOH) of MOFs can be used as postsynthetic modification sites, which are favorable for lithium ion exchan...

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Bibliographic Details
Published in:Langmuir 2021-04, Vol.37 (13), p.3922-3928
Main Authors: Tian, Li, Xu, Xuebin, Liu, Meiying, Liu, Zixin, Liu, Zhiliang
Format: Article
Language:English
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Summary:Metal–organic frameworks (MOFs), due to their possessing a porous structure, are potential candidates for solid-state ionic conduction materials. Moreover, uncoordinated carboxylic acid groups (−COOH) of MOFs can be used as postsynthetic modification sites, which are favorable for lithium ion exchange. Herein, we synthesized a unique multiple carboxylic zinc metal–organic framework (Zn-MOF-COOH) containing uncoordinated carboxylic acid groups. Zn-MOF-COOLi was synthesized through deprotonation using LiOH via a straightforward acid–base reaction at room temperature (RT), thereby exhibiting better good electrochemical properties. The lithium ionic conductivity (σ) increased from 1.81 × 10–5 to 1.65 × 10–4 S·cm–1, lithium ion transference number (t Li+ ) rose from 0.67 to 0.77, and the electrochemical window improved from 2.0–5.5 to 1.5–6.5 V. This work offers a new strategy to improve the σ of MOFs and a new perspective toward manufacturing of high-performance solid-state ionic conduction materials.
ISSN:0743-7463
1520-5827
DOI:10.1021/acs.langmuir.1c00156