期刊
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 55, 期 22, 页码 6428-6432出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201601119
关键词
lithium-ion batteries; molecular design; multifunctional binders; noncovalent interactions; sulfur heterocyclic quinones
资金
- National NSFC [21231005]
- MOE [B12015, IRT13R30]
- Tianjin [13JCQNJC06400]
We report a rational design of a sulfur heterocyclic quinone (dibenzo[b,i] thianthrene-5,7,12,14-tetraone=DTT) used as a cathode (uptake of four lithium ions to form Li4DTT) and a conductive polymer [poly(3,4-ethylenedioxythiophene): poly(styrenesulfonate)=PEDOT:PSS) used as a binder for a high-performance rechargeable lithium-ion battery. Because of the reduced energy level of the lowest unoccupied molecular orbital (LUMO) caused by the introduced S atoms, the initial Li-ion intercalation potential of DTT is 2.89 V, which is 0.3 V higher than that of its carbon analog. Meanwhile, there is a noncovalent interaction between DTT and PEDOT:PSS, which remarkably suppressed the dissolution and enhanced the conductivity of DTT, thus leading to the great improvement of the electrochemical performance. The DTT cathode with the PEDOT:PSS binder displays a long-term cycling stability (292 mAhg(-1) for the first cycle, 266 mAhg(-1) after 200 cycles at 0.1 C) and a high rate capability (220 mAhg(-1) at 1 C). This design strategy based on a noncovalent interaction is very effective for the application of small organic molecules as the cathode of rechargeable lithium-ion batteries.
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