4.8 Article

Enhanced Electrochemical Performance of Sodium Manganese Ferrocyanide by Na3(VOPO4)2F Coating for Sodium-Ion Batteries

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 11, Issue 41, Pages 37685-37692

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.9b12041

Keywords

sodium-ion batteries; sodium manganese ferrocyanide; Na-3(VOPO4)(2)F; surface coating; cathode material

Funding

  1. National Natural Science Foundation of China [21573147, 21676165]
  2. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-AC02-06CH11357]
  3. Beijing Institute of Technology Teli Young Fellow Program [3090011181903]

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Sodium manganese ferrocyanide NaxMn[Fe(CN)(6)](y), is an attractive cathode material for sodium-ion batteries. However, NaxMn[Fe(CN)(6)](y) prepared by simple coprecipitation of Mn2+ and [Fe(CN)(6)](4-) usually shows poor cycling performance, which hinders its practical application. In this work, electrochemical performance of a Na1.6Mn[Fe(CN)(6)](0.9) (PBM) sample prepared by the simple precipitation method was greatly improved by coating with Na-3(VOPO4)(2)F (NVOPF) via a solution precipitation method. The as-prepared PBM@NVOPF with a coating quantity of 2.0% molar ratio showed enhanced rate capability and superior cyclic stability. The discharge capacities of PBM@NVOPF were 101.5 mA h g(-1) (1 C) and 91.4 mA h g(-1) (10 C), with a capacity retention of 84.3% after 500 cycles at 1 C, 20 degrees C. It also exhibited excellent cyclic stability at elevated temperature with an initial capacity of 109.5 mA h g(-1) and a capacity retention of 78.8% after 200 cycles at 1 C, 55 degrees C. In comparison, uncoated PBM showed a discharge capacity of 105.7 mA h g(-1) (1 C) and 76.7 mA h g(-1) (10 C), with a capacity retention of only 42.0% after 500 cycles at 1 C, 20 degrees C. The high-temperature performance of bare PBM was very poor, and the capacity retention was only 35.7% after 40 cycles because of serious Mn/Fe dissolution which caused structural deterioration of PBM. NVOPF coating protected the PBM from suffering corrosion in the electrolyte, thus ensured the framework stability of PBM during long-term cycling and contributed to the excellent electrochemical performance.

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