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Controlling the Intercalation Chemistry to Design High-Performance Dual-Salt Hybrid Rechargeable Batteries
We have conducted extensive theoretical and experimental investigations to unravel the origin of the electrochemical properties of hybrid Mg2+/Li+ rechargeable batteries at the atomistic and macroscopic levels. By revealing the thermodynamics of Mg2+ and Li+ co-insertion into the Mo6S8 cathode host...
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Published in: | Journal of the American Chemical Society 2014-11, Vol.136 (46), p.16116-16119 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | We have conducted extensive theoretical and experimental investigations to unravel the origin of the electrochemical properties of hybrid Mg2+/Li+ rechargeable batteries at the atomistic and macroscopic levels. By revealing the thermodynamics of Mg2+ and Li+ co-insertion into the Mo6S8 cathode host using density functional theory calculations, we show that there is a threshold Li+ activity for the pristine Mo6S8 cathode to prefer lithiation instead of magnesiation. By precisely controlling the insertion chemistry using a dual-salt electrolyte, we have enabled ultrafast discharge of our battery by achieving 93.6% capacity retention at 20 C and 87.5% at 30 C, respectively, at room temperature. |
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ISSN: | 0002-7863 1520-5126 |
DOI: | 10.1021/ja508463z |