Volume 8, Issue 6 2000223
Full Paper

Enabling Dual-Ion Batteries via the Reversible Storage of Pyr14+ Cations into Coronene Crystal

Yaobing Fang

Yaobing Fang

Guangdong Engineering Technology Research Centre for Effective Storage and Utilization of Thermal Energy, School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou, 510640 China

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Wanying Bi

Wanying Bi

Guangdong Engineering Technology Research Centre for Effective Storage and Utilization of Thermal Energy, School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou, 510640 China

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Aiye Wang

Aiye Wang

Guangdong Engineering Technology Research Centre for Effective Storage and Utilization of Thermal Energy, School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou, 510640 China

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Wen Zheng

Wen Zheng

Guangdong Engineering Technology Research Centre for Effective Storage and Utilization of Thermal Energy, School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou, 510640 China

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Wenhui Yuan

Corresponding Author

Wenhui Yuan

Guangdong Engineering Technology Research Centre for Effective Storage and Utilization of Thermal Energy, School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou, 510640 China

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Li Li

Li Li

School of Environment and Energy, South China University of Technology, Guangzhou, 510006 China

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First published: 18 April 2020
Citations: 6

Abstract

Dual-ion batteries with pure ionic liquid electrolyte (IL-DIBs) have received increasing interest due to their sustainability, high operating voltage, and environmental friendliness. However, owing to the insertion/extraction of large-size ionic liquid cations, the conventional IL-DIBs with a graphite anode suffer from severe volume expansion and graphite exfoliation on the anode, causing a poor cycling performance. Herein, a novel IL-DIB is constructed by introducing a bulk organic material (coronene) as the anode, against a natural graphite cathode. The results show that, in a voltage window range from 1.0 to 4.4 V, the battery has a high discharge specific capacity of ≈73.3 mA h g−1 and exhibits a good cycling performance for 450 cycles with a lower capacity loss of 0.061 mA h g−1 per cycle at a current density of 300 mA g−1 (3 C). Notably, it still maintains a considerable capacity of ≈55.8 mA h g−1 at a high rate of 10 C. In addition, the reversible intercalation/de-intercalation of the Pyr14+ cations into/from the coronene anode is investigated by ex situ X-ray diffraction and Fourier transform infrared spectroscopy, showing an excellent structure stability of the coronene crystal during the charge–discharge process.

Conflict of Interest

The authors declare no conflict of interest.

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