4.8 Article

Hollow Boron-Doped Si/SiOx Nanospheres Embedded in the Vanadium Nitride/Nanopore-Assisted Carbon Conductive Network for Superior Lithium Storage

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 11, 期 49, 页码 45612-45620

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.9b14912

关键词

lithium-ion batteries; silicon; silicon oxide; vanadium nitride; graphitization carbon

资金

  1. National Natural Science Foundation of China [51602210]
  2. Fundamental Research Funds for the Central Universities of China [2017SCU04A05, YJ201470]
  3. Fund Program for the Scientific Activities of Selected Returned Overseas Professionals in Sichuan Province, China [CRSBF2019764, CRSBF201814501]

向作者/读者索取更多资源

SiOx-based anode materials with high capacity and outstanding cycling performance have gained numerous attentions. Nevertheless, the poor electrical conductivity and non-negligible volume change hinder their further application in Li-ion batteries. Herein, we propose a new strategy to construct a hollow nanosphere with boron-doped Si/SiOx decorated with vanadium nitride (VN) nanoparticles and embedded in a nitrogen-doped, porous, and partial graphitization carbon layer (B-Si/SiOx@VN/PC). Benefiting from such structural and compositional features, the B-Si/SiOx@VN/PC electrode exhibits a stable cycling capacity of 1237.1 mA h g(-1) at a current density of 0.5 A g(-1) with an appealing capacity retention of 87.0% after 300 cycles. Additionally, it delivers high-rate capabilities of 1139.4, 940.7, and 653.4 mA h g(-1) at current densities of 2, 5, and 10 A g(-1), respectively, and ranks among the best SiOx-based anode materials. The outstanding electrochemical performance can be ascribed to the following reasons: (1) its hollow structure makes the Li+ transportation length decreased. (2) The existing nanopores facilitate the Li+ insertion/desertion and accommodate the volume variation. (3) The nitrogen-doped partial graphitization carbon enhances the electrical conductivity and promotes the formation of stable solid electrolyte interface layers during the repetitive Li+ intercalation/extraction process.

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