Abstract

From the history of commercial anode materials, Sn/C-based material is the focus to enhance the cycling performance. A chemical solution method is used to synthesize the Sn compounds / graphite composite anodes. At the first part of this study, the cycle life was enhanced by adjusting various pH values. The multi-phase Sn compound containing Sn6O4(OH)4, SnO2, Sn3(PO4)2were deposited on slices of graphite of sample pH6. They were expected to provide a higher spectator to Sn ratio for improved cycleability. These phases could be reduced to metallic Sn, resulting in buffer matrix during 1stcycle. Therefore, the sample pH6 exhibited the best of electrochemical performance. For the cell cycled between 0.001V and 1.5V, the 1stcharge capacity was 758 mAhg-1. Even after 50 cycles, the capacity remained higher than 460 mAhg-1. Synthesizing Sn compounds / graphite composite anodes at pH6 with different initial Sn concentrations improved the cycling performance in the second part of this study. When the Sn concentration reached 0.12M, multi-phases of Sn compounds were deposited on the slices of graphite and the amount of Sn was the maximum. The agglomeration of Sn clusters was suppressed by buffering agent generated by the multi-phase of Sn compounds containing Sn6O4(OH)4, SnO2, Sn3(PO4)2. Therefore, the sample Sn0.12 M exhibitedthe best cycling behavior among all. During cycling between 0.001 V and 1.5 V, the 1stcharge capacity was around 734 mAhg-1. The capacity remained as high as 440 mAhg-1 even after 50 cycles.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.