4.8 Article

Elucidating the Limit of Li Insertion into the Spinel Li4Ti5O12

期刊

ACS MATERIALS LETTERS
卷 1, 期 1, 页码 96-102

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsmaterialslett.9b00099

关键词

-

资金

  1. Office of Vehicle Technologies of the U.S. Department of Energy, through the Advanced Battery Materials Research (BMR) Program (Battery500 Consortium) [DE-EE0007764]
  2. U.S. Department of Energy, Office of Science, Basic Energy Sciences [DE-SC0012118]
  3. National Science Foundation [ACI-1053575]
  4. Scientific User Facilities Division, Office of Basic Energy Sciences
  5. U.S. Department of Energy's Office of Energy Efficiency and Renewable Energy (EERE) [DE-EE0008444]
  6. Assistant Secretary for Energy Efficiency and Renewable Energy, Vehicle Technology Office of the U.S. Department of Energy through the Advanced Battery Materials Research (BMR) Program, including the Battery500 Consortium [DE-SC0012704]
  7. U.S. DOE Office of Science Facility, at Brookhaven National Laboratory [DE-SC0012704]

向作者/读者索取更多资源

In this work, we show that the well-known lithium-ion anode material, Li4Ti5O12, exhibits exceptionally high initial capacity of 310 mAh g(-1) when it is discharged to 0.01 V. It maintains a reversible capacity of 230 mAh g(-1), far exceeding the theoretical capacity of 175 mAh g(-1) when this anode is lithiated to the composition Li7Ti5O12. Neutron diffraction analyses identify that additional Li reversibly enters into the Li7Ti5O12 to form Li8Ti5O12. density functional theory (DFT) calculations reveal the average potentials of the Li4Ti5O12 to Li7Ti5O12 step and the Li7Ti5O12 to Li8Ti5O12 step are 1.57 and 0.19 V, respectively, which are in excellent agreement with experimental results. Transmission electron microscopy (TEM) studies confirm that the irreversible capacity of Li4Ti5O12 during its first cycle originates from the formation of a solid electrolyte interface (SEI) layer. This work clarifies the fundamental lithiation mechanism of the Li4Ti5O12, when lithiated to 0.01 V vs Li.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据