• 文献标题:   Understanding the Li-storage in few layers graphene with respect to bulk graphite: experimental, analytical and computational study
  • 文献类型:   Article
  • 作  者:   SONIA FJ, JANGID MK, ANANTHOJU B, ASLAM M, JOHARI P, MUKHOPADHYAY A
  • 作者关键词:  
  • 出版物名称:   JOURNAL OF MATERIALS CHEMISTRY A
  • ISSN:   2050-7488 EI 2050-7496
  • 通讯作者地址:   Indian Inst Technol
  • 被引频次:   16
  • DOI:   10.1039/c7ta01978e
  • 出版年:   2017

▎ 摘  要

In order to understand, clarify and provide confirmations in the contexts of the prevalent confusions concerning Li-storage in graphenic carbon (viz. the reduced dimensional scale of graphitic carbon), electrochemical lithiation/delithiation has been performed with CVD-grown fairly pristine well-ordered few-layer graphene films (FLG; similar to 7 layers; as a model material). Chronopotentiograms and cyclic voltammograms recorded with the FLG present distinct features corresponding to the transformation between different Li-GICs (i.e., 'staging') below 0.3 V against Li/Li+, thus confirming that 'classical' Li-intercalation does occur even at such reduced dimensional (nano) scale. Nevertheless, even in this lower potential window (our main focus here), Li-storage in FLG involves contributions from both diffusion-and surface-controlled mechanisms. The Li-capacities recorded with FLG just within this lower potential window, and also upon subtracting any possible contribution from the Cu current collector, were still similar to 3-4 times greater than those obtained with similarly grown thicker bulk graphite films (TBG: similar to 450 nm; Li-capacity recorded: similar to 380 mA h g(-1)). Contrary to the usual belief, the excess Li-capacity of FLG cannot be explained by the presence of extrinsic/intrinsic defects, which are nearly negligible in the FLG films under consideration. Simulation of Li-storage in graphene via DFT indicated that the excess capacity (after formation of the LiC6 configuration) is associated with additional stable Li-storage on the outer graphene surfaces in the forms of more than one Li-layer (but different from Li-plating) and segregation close to the 'stepped' (exposed) edges of the inner graphene layers (but not exactly at the edge sites). Overall, such predicted Li-storage mechanisms are in agreement with the experimentally observed contributions from both 'classical' Li-intercalation and surface-controlled processes (even at potentials below 0.3 V), which primarily account for the excess Li-capacities recorded with graphenic carbon.