期刊
INORGANIC CHEMISTRY
卷 53, 期 13, 页码 6494-6496出版社
AMER CHEMICAL SOC
DOI: 10.1021/ic500860t
关键词
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资金
- National Science Foundation CAREER award [DMR-1351538]
- Direct For Mathematical & Physical Scien
- Division Of Materials Research [1351538] Funding Source: National Science Foundation
Atomic-scale integration of polyether molecules and copper(II) chloride layers in a two-dimensional perovskite affords, to the best of our knowledge, the first example of extended Li+ cycling in a metal chloride electrode. The hybrid can cycle over 200 times as a cathode in a lithium battery with an open-circuit voltage of 3.2 V. In contrast, CuCl2 alone or the precursors to the hybrid cannot be cycled in a lithium battery, demonstrating the importance of the layered, organic inorganic architecture. This work shows that appropriate organic groups can enable Li+ cycling in inexpensive, nontoxic, metal halide electrodes, which is promising for large-scale applications.
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