4.8 Article

N-Doped C@Zn3B2O6 as a Low Cost and Environmentally Friendly Anode Material for Na-Ion Batteries: High Performance and New Reaction Mechanism

Journal

ADVANCED MATERIALS
Volume 31, Issue 5, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.201805432

Keywords

anodes; Na-ion batteries; N-doped C; Zn3B2O6

Funding

  1. National Natural Science Foundation of China [21725103, 51472232]
  2. National Key R&D Program of China [2016YFB0100100, JCKY2016130B010]
  3. Jilin Province Science and Technology Development Plan Funding Project [20180101203JC, 20160101289JC]
  4. Changchun Science and Technology Development Plan Funding Project [18DY012]

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Na-ion batteries (NIBs) are ideal candidates for solving the problem of large-scale energy storage, due to the worldwide sodium resource, but the efforts in exploring and synthesizing low-cost and eco-friendly anode materials with convenient technologies and low-cost raw materials are still insufficient. Herein, with the assistance of a simple calcination method and common raw materials, the environmentally friendly and nontoxic N-doped C@Zn3B2O6 composite is directly synthesized and proved to be a potential anode material for NIBs. The composite demonstrates a high reversible charge capacity of 446.2 mAh g(-1) and a safe and suitable average voltage of 0.69 V, together with application potential in full cells (discharge capacity of 98.4 mAh g(-1) and long cycle performance of 300 cycles at 1000 mA g(-1)). In addition, the sodium-ion storage mechanism of N-doped C@Zn3B2O6 is subsequently studied through air-insulated ex situ characterizations of X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and Fourier-transform infrared (FT-IR) spectroscopy, and is found to be rather different from previous reports on borate anode materials for NIBs and lithium-ion batteries. The reaction mechanism is deduced and proposed as: Zn3B2O6 + 6Na(+) + 6e(-) reversible arrow 3Zn + B2O3 center dot 3Na(2)O, which indicates that the generated boracic phase is electrochemically active and participates in the later discharge/charge progress.

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