4.5 Article

CoP Nanoparticles Intertwined with Graphene Nanosheets as a Superior Anode for Half/Full Sodium-Ion Batteries

期刊

CHEMELECTROCHEM
卷 8, 期 11, 页码 2022-2027

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/celc.202100085

关键词

CoP; graphene; sodium-ion batteries; anode

资金

  1. National Natural Science Foundation of China [51772257]
  2. Major Basic Research Project of Shandong Natural Science Foundation [ZR2018ZC1459]
  3. Shandong Provincial Natural Science Foundation [ZR2020QB108, ZR2020QB123, ZR2018BB001]
  4. Yantai University Students Innovation and Entrepreneurship Training Program

向作者/读者索取更多资源

This study successfully prepared CoP/RGO aerogel material with high reversible capacity, superior rate capability, and outstanding durability. Electrochemical analysis results show fast reaction kinetics and high surface capacitive contribution in the CoP/RGO composite. The CoP/RGO//Na3V2(PO4)(3) sodium-ion full cells exhibit a high initial charge capacity, and this work provides new opportunities for synthesizing active anode materials for SIBs.
Conversion-type CoP is a promising anode candidate for sodium-ion batteries (SIBs) thanks to their abundant resources and high theoretical capacity. However, the low reversible capacity and inferior cycle life are two major obstacles that limit its practical application in SIBs. Herein, cobalt-based metal-organic framework derived CoP nanoparticles coupled with reduced graphene oxide (RGO) composite (CoP/RGO) has been successfully prepared. The optimized CoP/RGO presents a high reversible capacity (258.6 mAh g(-1) at 0.1 A g(-1)), superior rate capability (173 mAh g(-1) at 2 A g(-1)) and extraordinary durability (155 mAh g(-1) at 0.5 A g(-1) after 500 cycles with the per cycle capacity decay rate of only 0.065 %). In addition, electrochemical analyses reveal fast reaction kinetics and high surface capacitive contribution in CoP/RGO composite, which can be responsible for the excellent performance. Furthermore, the CoP/RGO//Na3V2(PO4)(3) sodium-ion full cells are assembled successfully and display an initial charge capacity of 231.1 mAh g(-1) at 0.1 A g(-1). Considering the low cost and great electrochemical performances, this work may provide some new opportunities for the synthesis of activity anode materials for SIBs.

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