4.7 Article

Enhanced rate performance of lithium-ion battery anodes using a cobalt-incorporated carbon conductive agent

期刊

INORGANIC CHEMISTRY FRONTIERS
卷 9, 期 14, 页码 3484-3493

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2qi00273f

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资金

  1. EPFL
  2. National Natural Science Foundation of China [52061135110, 21773279, 22075305]
  3. Chinese Academy of Sciences [ZDRW_CN_2020-1]
  4. Ningbo Science & Technology Innovation 2025 Major Project [2019B10050, 2019B10113, 2020Z101]
  5. Key Laboratory of Bio-Based Polymeric Materials of Zhejiang Province

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This paper introduces a new concept to enhance the rate capability of lithium-ion batteries by incorporating a small amount of metal species into the electron conductive agent. Experimental results show that the Si/C composite anode with oxidized Ketjen black (KJB) incorporated with cobalt (Co-ox-KJB) exhibits improved capabilities at high current densities. The improved electrochemical performance is attributed to enhanced electron conductivity, improved affinity towards the electrolyte, and an enhanced desolvation process.
Lithium-ion batteries with enhanced rate performance are of crucial importance for practical applications. Extensive studies on the structural design and surface modification of electrode materials with the aim of improving the rate performance have been reported. Here we describe a new concept to enhance the rate capability by incorporating a tiny amount of metal species into the electron conductive agent. We show that the Si/C composite anode exhibits increased capabilities at high current densities when oxidized Ketjen black (KJB) with incorporated cobalt (Co-ox-KJB) is used as the electron conductive agent. Compared with the pristine KJB, the reversible capacities of the Si/C electrode with the Co-ox-KJB are increased by 180% on average at 1.50 A g(-1) (279 mA h g(-1)vs. 73 mA h g(-1), respectively). A synergistic contribution from enhanced electron conductivity by Co incorporation, improved affinity towards the electrolyte and an enhanced desolvation process by surface functional groups is responsible for the improved electrochemical performance. This approach is applicable for super P-based electron conductive agents as well.

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