Heteroatom doped carbon nanomaterials are often employed as advanced anode for Lithium ions battery (LIBs) in terms of their stable structure, high capacity and low cost. In this work, we… Click to show full abstract
Heteroatom doped carbon nanomaterials are often employed as advanced anode for Lithium ions battery (LIBs) in terms of their stable structure, high capacity and low cost. In this work, we proposed a novel strategy to synthesize high density (N, Ni, P) tri-doped echinus-like porous carbon spheres (PCS) by carbonizing a metal-organophosphine framework (MOPF) directly. The MOPF employs riboflavin sodium phosphate (C17H20N4NaO9P) as organic ligand as well as nitrogen and phosphorus source to conjugate with Ni(NO3)2·6H2O. As anode for LIBs, PCS was demonstrated that the discharge capacities were able to reach 386.5 mAh·g-1 after 100 cycles at current density of 0.05 A·g-1. Besides, the stable reversible capacities were obtained from ~459 mAh·g-1 to ~91.8 mAh·g-1 when current density varied from 0.05 to 1 A·g-1. The good anode performance is attributed to the unique structure of PCS and (N, Ni, P) tri-doping which introduces the additional capacities due to the presence of "reservoir effect". Moreover, the electrochemical analysis implied that the surface-limited capacitive behavior dominantly contributes to the lithium storage capacity of PCS anode.
               
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