4.6 Article

Deciphering the lithium storage chemistry in flexible carbon fiber-based self-supportive electrodes

期刊

CARBON ENERGY
卷 4, 期 5, 页码 820-832

出版社

WILEY
DOI: 10.1002/cey2.173

关键词

density functional theory; flexible carbon fiber cloth; lithium-ion batteries; Ni5P4; self-supportive electrodes

资金

  1. National Natural Science Foundation of China [21875292, 21902188]
  2. National Key Research and Development Program of China [2019YFA0705702]
  3. Hunan Provincial Natural Science Foundation [2021JJ30087]
  4. Natural Science Foundation of Guangdong Province [2020A1515010798]
  5. Hunan Joint International Laboratory of Advanced Materials and Technology for Clean Energy [2020CB1007]

向作者/读者索取更多资源

This study reveals that Ni5P4 nanosheets prepared on CFC exhibit higher areal capacity and the high Li adsorption energy of CFC contributes to the superior Li-ion storage performance of CFC@Ni5P4.
Flexible carbon fiber cloth (CFC) is an important scaffold and/or current collector for active materials in the development of flexible self-supportive electrode materials (SSEMs), especially in lithium-ion batteries. However, during the intercalation of Li ions into the matrix of CFC (below 0.5 V vs. Li/Li+), the incompatibility in the capacity of the CFC, when used directly as an anode material or as a current collector for active materials, leads to difficulty in the estimation of its actual contribution. To address this issue, we prepared Ni5P4 nanosheets on CFC (denoted CFC@Ni5P4) and investigated the contribution of CFC in the CFC@Ni5P4 by comparing to the powder Ni5P4 nanosheets traditionally coated on a copper foil (CuF) (denoted P-Ni5P4). At a current density of 0.4 mA cm(-2), the as-prepared CFC@Ni5P4 showed an areal capacity of 7.38 mAh cm(-2), which is significantly higher than that of the P-Ni5P4 electrode. More importantly, theoretical studies revealed that the CFC has a high Li adsorption energy that contributes to the low Li-ion diffusion energy barrier of the Ni5P4 due to the strong interaction between the CFC and Ni5P4, leading to the superior Li-ion storage performance of the CFC@Ni5P4 over the pristine Ni5P4 sample. This present work unveils the underlying mechanism leading to the achievement of high performance in SSEMs.

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