4.8 Article

Nanoscale tin-based intermetallic electrodes encapsulated in microporous copper substrate as the negative electrode with a high rate capacity and a long cycleability for lithium-ion batteries

期刊

NANO ENERGY
卷 2, 期 5, 页码 595-603

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.nanoen.2013.06.004

关键词

Lithium-ion batteries; Anode; Intermetallics; Capacity; Cycleability

资金

  1. NSFC [2093110426, 21003102, 21021002, 20833005]
  2. 973 program [209CB220102]
  3. 863 program [2011AA11A254]
  4. Solid State and Materials Chemistry Program of the Division of Materials Research at the U.S. National Science Foundation
  5. Division Of Materials Research
  6. Direct For Mathematical & Physical Scien [1006113] Funding Source: National Science Foundation

向作者/读者索取更多资源

The rate capacity and cycleability of a battery electrode are strongly determined by their chemistry and nano/microstructures. This is particularly true in developing next-generation lithium-ion batteries for electric vehicles. In this article, we report synthesis of nanometer tin based negative electrodes encapsulated in microporous copper substrates, which exhibit simultaneously high-rate and long-life performances. This intermetallic compound consists of an amorphous phase rich in Co, located at the boundaries of nanoscale crystalline Sn-Sb grains. The rate capacity retention is similar to 71.5% while increasing charge rate from 0.15 C (698.9 mAh g(-1)) to 25.0 C (500 mAh g(-1) at similar to 16 A g(-1)). Such a high rate performance is a result of novel chemistry (Sn50Sb44Co6) and high electrical conductivity of Cu framework. The cycling capacity is 549 mAh g(-1) at 0.2 C (1 C=650 mA g(-1)) after 300 cycles, and 493.6 mAh g(-1) at 0.4 C after 600 cycles. The Corich amorphous phase, along with the three dimensional porous structure, contributes to mitigating volume expansion/shrinkage during discharge/charge of the electrode. Our results suggest that the ternary Sn-Sb-Co intermetallic compound with the desirable chemistry and structure is a promising candidate as a high-rate and long-life negative electrode for lithium-ion batteries. (C) 2013 Elsevier Ltd. All rights reserved.

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