4.7 Article

Regulating Na deposition by constructing a Au sodiophilic interphase on CNT modified carbon cloth for flexible sodium metal anode

Journal

JOURNAL OF COLLOID AND INTERFACE SCIENCE
Volume 611, Issue -, Pages 317-326

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2021.12.076

Keywords

Na metal anode; Au nanoparticles; Sodiophilic sites; Dendrite free; COMSOL simulation; In-situ optical microscopy investigation

Funding

  1. National Natural Science Foundation of China [U1804132]
  2. Zhongyuan Youth Talent support program of Henan province [ZYQR201912152]
  3. Academic Improvement Program of Physics of Zhengzhou University [2018WLTJ02]
  4. Zhengzhou University Youth Talent Start-up Grant

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A sodiophilic Na metal anode host is developed by sputtering gold nanoparticles into interconnected carbon nanotube modified carbon cloth. This structure effectively guides the uniform deposition of Na metal, resulting in stable cycle performance and long cycle life.
Na metal anode has attracted increasing attentions as the anode of sodium ion batteries (SIBs) due to its high theoretical capacity, low redox potential and high abundance. However, the formation of uncontrollable Na dendrite during repeated plating/stripping cycles hinders its further development and application. Herein, a sodiophilic Na metal anode host is developed by sputtering gold nanoparticles (Au NPs) into interconnected carbon nanotube modified carbon cloth (CNT/CC) to form a Au-CNT/CC architecture. Sodiophilic Au NPs effectively guide the Na metal uniform deposition and three-dimensional (3D) microporous structure offers a large surface area for nucleation and reducing the current densities. The regulated uniform Na metal deposition mechanism is investigated by the in-situ optical microscopy and simulation analysis. As a result, Au-CNT/CC electrode exhibits a low nucleation overpotential (2.2 mV) and stable cycle performance for 1600 h at 1 mA cm-2 with 2 mAh cm-2. Moreover, it even exhibits a long cycle stability for more than 800 h at 5 mA cm-2 with 2 mAh cm-2. To explore its application, a full cell coupled with a sodium vanadium phosphate coated with carbon layer (NVP@C) cathode is assembled and delivers an average discharge capacity of 80.6 mAh g-1 and coulombic efficiency of 99.6% for 400 cycles at 100 mAh g-1. Furthermore, a flexible pouch cell with Na@Au-CNT/CC as the anode is fabricated and demonstrated good flexibility and future application of wearable electronics. (c) 2021 Elsevier Inc. All rights reserved.

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