4.7 Article

(110)-Bridged nanoblocks self-assembled VS4 hollow microspheres as sodium-ion battery anode with superior rate capability and long cycling life

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 384, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2019.123385

Keywords

VS4; Hollow microspheres; Interaction of crystal lattices; Sodium-ion batteries; Anode

Funding

  1. National Natural Science Foundation of China [51672165, 21701107, 51702198]
  2. Doctoral Scientific Research Startup Foundation of Xi'an University of Technology [101-451119016]
  3. Postdoctoral Foundation of China [155660, 2016M592897XB]
  4. Natural Science Foundation of Shaanxi Province [2018JQ5107]
  5. National Key Research and Development Program of China [2017YFB0308303-03]
  6. Doctoral Scientific Research Startup Foundation of Shaanxi University of Science and Technology [2016QNBT-07]
  7. Platform construction for Imported talent of Shaanxi University of Science and Technology [134080038]
  8. Undergraduate Innovation and Entrepreneurship Training Program [201610708011]

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Development of three-dimensional self-assembled hollow nanoarchitectures combining functional shells and inner voids is an important approach for realizing high-rate and long-life battery electrodes. As a potential high-performance anode for sodium-ion batteries (SIBs), (1 1 0)-bridged nanoblocks self-assembled VS4 hollow microspheres (PNBH-VS 4 ) are controllably synthesized by a facile one-step hydrothermal method. The (1 1 0)bridged structure constructs the Na+ conducing channels and e(-) transfer paths among nano-grains and nanoblocks, and the self-assembled hollow structure presents the double space physical entrapment effect for the excessive volume change of nanoblocks, which synergistically improve the Na+ storage kinetics and structure stability. When employed as an anode for SIBs, PNBH-VS4 electrode exhibits the superior rate capability and long cycling life, outperforming those of the ever-reported VS4-based anode materials. At 0.2, 0.5, 1.0 and 2.0 A g the capacity can reach 629, 564, 428 and 400 mAh g(-1) after 250, 200, 350 and 700 cycles, respectively. Even at 5.0 A g(-1), the capacity can still stabilize at 309 mAh g(-1) after 1000 long cycles. In addition, it is revealed that PNBH-VS4 electrode undertakes the insertion and conversion reaction in the potential range of 0.50-3.00 and 0.05-0.50 V, respectively, where the main capacity contribution originates from the insertion reaction. Meanwhile, PNBH-VS4 electrode exhibits better insertion reversibility at lower current densities and conversion reversibility at higher current densities during cycling, respectively.

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