4.6 Article

A synergistic vertical graphene skeleton and S-C shell to construct high-performance TiNb2O7-based core/shell arrays

Journal

JOURNAL OF MATERIALS CHEMISTRY A
Volume 6, Issue 41, Pages 20195-20204

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c8ta06858e

Keywords

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Funding

  1. National Natural Science Foundation of China [51772272, 51502263, 51728204]
  2. Qianjiang Talents Plan D [QJD1602029]
  3. Startup Foundation for Hundred-Talent Program of Zhejiang University
  4. Fundamental Research Funds for the Central Universities [2018QNA4011]
  5. Program for Innovative Research Team in University of Ministry of Education of China [IRT13037]
  6. Key Science and Technology Innovation Team of Zhejiang Province [2010R50013]
  7. Supercomputing Center of University of Science and Technology of China

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Bespoke synthesis of wide-temperature high-power electrodes is of great importance for the development of advanced power-type lithium ion batteries (LIBs). Herein, we report a powerful combined solvothermal-electrodeposition (ST-ED) method to construct titanium niobium oxide (TiNb2O7) arrays sandwiched between a highly conductive vertical graphene (VG) skeleton and S-C shell forming a binder-free VG/TiNb2O7@S-C electrode. VG and S-C work cooperatively to establish an omnibearing conductive network on TiNb2O7 through internal and external integration. Positive advantages including large porosity, improved conductivity and enhanced structural stability are obtained in the VG/TiNb2O7@S-C core/shell arrays. Consequently, excellent electrochemical high-power performance at medium-high temperature (25 to 70 degrees C) is demonstrated for the designed VG/TiNb2O7@S-C electrodes, which show a high capacity from 284 to 354 mA h g(-1) at 1C, and 181 to 241 mA h g(-1) at 160C as the working temperature increases from 25 to 70 degrees C. Additionally, a remarkable high-temperature (70 degrees C) cycling span is proven for the VG/TiNb2O7@S-C electrode with a capacity of 203 mA h g(-1) at 40C after 5000 cycles. The synergistic positive effect from the VG and S-C shell is responsible for the enhancement of high-power capability. Our work paves the way for the fabrication of novel high-power electrodes for electrochemical energy storage.

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