Herein, graphite is proposed as a reliable Ca-intercalation anode in tetraglyme (G). When charged (reduced), graphite accommodates solvated Ca-ions (Ca-G) and delivers a reversible capacity of 62 mAh g that signifies the formation of a ternary intercalation compound, Ca-G·C. Mass/volume changes during Ca-G intercalation and the evolution of in operando X-ray diffraction studies both suggest that Ca-G intercalation results in the formation of an intermediate phase between stage-III and stage-II with a gallery height of 11.41 Å. Density functional theory calculations also reveal that the most stable conformation of Ca-G has a planar structure with Ca surrounded by G, which eventually forms a double stack that aligns with graphene layers after intercalation. Despite large dimensional changes during charge/discharge (C/D), both rate performance and cyclic stability are excellent. Graphite retains a substantial capacity at high C/D rates (e.g., 47 mAh g at 1.0 A g s vs 62 mAh g at 0.05 A g) and shows no capacity decay during as many as 2000 C/D cycles. As the first Ca-shuttling calcium-ion batteries with a graphite anode, a full-cell is constructed by coupling with an organic cathode and its electrochemical performance is presented.
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http://dx.doi.org/10.1002/advs.201902129 | DOI Listing |
Chem Mater
January 2025
Department of Materials Science and Engineering, University of California, Berkeley, California 94704, United States.
Multivalent-ion batteries offer an alternative to Li-based technologies, with the potential for greater sustainability, improved safety, and higher energy density, primarily due to their rechargeable system featuring a passivating metal anode. Although a system based on the Ca/Ca couple is particularly attractive given the low electrochemical plating potential of Ca, the remaining challenge for a viable rechargeable Ca battery is to identify Ca cathodes with fast ion transport. In this work, a high-throughput computational pipeline is adapted to (1) discover novel Ca cathodes in a largely unexplored space of "empty intercalation hosts" and (2) develop material design rules for Ca-ion mobility.
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