Zelang Jian,Clement Bommier,Langli Luo,Zhifei Li,Wentao Wang,Chongmin Wang,P. Alex Greaney,Xiulei Ji
出处
期刊:Chemistry of Materials [American Chemical Society] 日期:2017-02-27卷期号:29 (5): 2314-2320被引量:213
标识
DOI:10.1021/acs.chemmater.6b05474
摘要
Graphite is the commercial anode for lithium-ion batteries; however, it fails to extend its success to sodium-ion batteries. Recently, we demonstrated that a low-cost amorphous carbon—soft carbon exhibits remarkable rate performance and stable cycling life of Na-ion storage. However, its Na-ion storage mechanism has remained elusive, which has plagued further development of such carbon anodes. Here, we remedy this shortfall by presenting the results from an integrated set of experimental and computational studies that, for the first time, reveal the storage mechanism for soft carbon. We find that sodium ions intercalate into graphenic layers, leading to an irreversible quasi-plateau at ∼0.5 V versus Na+/Na as well as an irreversible expansion seen by in situ transmission electron microscopy (TEM) and X-ray diffraction (XRD). Such a high-potential plateau is correlated to the defective local structure inside the turbostratic stacking of soft carbon and the associated high-binding energies with Na ions, suggesting a trapping mechanism. On the other hand, soft carbon exhibits long sloping regions above and below the quasi-plateau during the first sodiation, where the sloping regions present highly reversible behavior. It is attributed to the more defects contained by soft carbon revealed by neutron total scattering and the associated pair distribution function studies.