Single-Ion Li[superscript +], Na[superscript +], and Mg[superscript 2+] Solid Electrolytes Supported by a Mesoporous Anionic Cu–Azolate Metal–Organic Framework
A novel Cu(II)–azolate metal–organic framework (MOF) with tubular pores undergoes a reversible single crystal to single crystal transition between neutral and anionic phases upon reaction with stoichiometric amounts of halide or pseudohalide salts. The stoichiometric transformation between the two p...
| Main Authors: | , , |
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| Other Authors: | |
| Format: | Article |
| Language: | en_US |
| Published: |
American Chemical Society
2018
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| Online Access: | http://hdl.handle.net/1721.1/117532 https://orcid.org/0000-0002-7837-8412 https://orcid.org/0000-0003-3967-3395 https://orcid.org/0000-0002-1262-1264 |
| Summary: | A novel Cu(II)–azolate metal–organic framework (MOF) with tubular pores undergoes a reversible single crystal to single crystal transition between neutral and anionic phases upon reaction with stoichiometric amounts of halide or pseudohalide salts. The stoichiometric transformation between the two phases allows loading of record amounts of charge-balancing Li[superscript +], Na[superscript +], and Mg[superscript 2+] ions for MOFs. Whereas the halide/pseudohalide anions are bound to the metal centers and thus stationary, the cations move freely within the one-dimensional pores, giving rise to single-ion solid electrolytes. The respective Li[superscript +]-, Na[superscript +]-, and Mg[superscript 2+]-loaded materials exhibit high ionic conductivity values of 4.4 × 10[superscript –5], 1.8 × 10[superscript –5], and 8.8 × 10[superscript –7] S/cm. With addition of LiBF[subscript 4], the Li[superscript +] conductivity improves to 4.8 × 10[superscript –4] S/cm. These are the highest values yet observed for MOF solid electrolytes. |
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