Superior performance enabled by supramolecular interactions in metal-organic cathode: the power of weak bonds

Journal Article · Fri Apr 15 00:00:00 EDT 2022 · Journal of Materials Chemistry. A

DOI:https://doi.org/10.1039/d2ta01463g· OSTI ID:1885217

Li, An-Che ^[1]; Chang, Cheng-Han ^[2]; Ivanov, Alexander S. ^[3]; Lo, Yi-An ^[1]; Popovs, Ilja ^[3]; Chen, Jeng-Lung ^[4]; Chuang, Yu-Chun ^[4]; Chang, Yu-Chung ^[4]; Chen, Bo-Hao ^[4]; Lee, Jui-Chin ^[1]; Chen, Teng-Hao ^[1]; Kaveevivitchai, Watchareeya ^[1]

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1. National Cheng Kung University, Tainan City (Taiwan)
2. Tamkang University, New Taipei City (Taiwan)
3. Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)
4. National Synchrotron Radiation Research Centre, Hsinchu (Taiwan)

Metal–organic-based electrode materials are increasingly appealing because both metal and organic linker are capable of undergoing redox processes, thus offering a high specific capacity. High porosity which can be achieved by the rational design of these materials is generally perceived as one of the major criteria for high rate performance. However, while Li-ion transport may be possible, oftentimes the counteranions (e.g., PF₆^-) and solvent molecules are co-inserted into the porous host lattice, potentially hindering Li-ion diffusion pathways. Here, in this study, we propose the concept of close-packed metal–organic cathode stabilized by multiple supramolecular interactions as a viable solution for exceptional electrochemical performance. This is illustrated in a modularly designed redox-active [CuL(Py)₂]_n (LH₄ = 1,4-dicyano-2,3,5,6-tetrahydroxybenzene, Py = pyridine). The mechanistic studies and DFT calculations confirm that the supramolecular interactions between its close-packed chains are the key to the flexible host lattice which only allows desolvated Li⁺ to intercalate, while these weak bonds also stabilize the inserted Li in the preferred hopping sites, creating optimal diffusion paths. The performance observed in this work is found to be among the best ever reported for metal–organic cathodes with a capacity as high as 255 mA h g^-1 at 65 mA g^-1 (0.25C) and a reversible capacity of 59 mA h g^-1 at ~26 A g^-1 (100C) corresponding to 81% retention after 1000 cycles. These findings reveal a potential new strategy towards metal–organic-based electrodes with high performance and enhanced cycling stability.

• Research Organization: Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States)
• Sponsoring Organization: Ministry of Science and Technology (MOST); National Cheng Kung University (NCKU); USDOE; USDOE Office of Science (SC), Basic Energy Sciences (BES). Materials Sciences & Engineering Division
• Grant/Contract Number: AC05-00OR22725
• OSTI ID: 1885217
• Alternate ID(s): OSTI ID: 1864383
• Journal Information: Journal of Materials Chemistry. A, Journal Name: Journal of Materials Chemistry. A Journal Issue: 37 Vol. 10; ISSN 2050-7488
• Publisher: Royal Society of Chemistry
• Country of Publication: United States
• Language: English

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36 MATERIALS SCIENCE