4.7 Article

Enhancing Li-S redox kinetics by fabrication of a three dimensional Co/CoP@nitrogen-doped carbon electrocatalyst

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 380, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2019.122595

Keywords

Co/CoP@NC; Synergistic effect; DFT calculations; Improved redox kinetics; Superior electrochemical performances

Funding

  1. Science and Technology Planning Project of Guangdong Province, China [2017B090916002]
  2. National Natural Science Foundation of China [51872098]
  3. Guangdong Natural Science Funds for Distinguished Young Scholar [2016A030306010]
  4. Guangdong Innovative and Entrepreneurial Research Team Program [2014ZT05N200]
  5. Natural Science Foundation of Guangdong Province [2018A030313944]
  6. China Postdoctoral Science Foundation [2019M652876]

Ask authors/readers for more resources

The design of sulfur hosts with high electrochemical activity and high sulfur loading plays a vital role in developing high-energy-density lithium-sulfur batteries. Herein, a novel type of sulfur cathode substrate is established via a facile two-step process, in which the Co and CoP nanoparticles are embedded in a three-dimensional (3D) porous nitrogen-doped carbon polyhedron (Co/CoP@NC). These Co and CoP nanograins not only act as polysulfides capturing centers but also the electrocatalysts effectively promoting the redox kinetics towards polysulfides conversion, as confirmed by the experimental results and DFT calculations. Meanwhile, the interconnected 3D porous N-doped carbon architecture contributed to Li+ transportation, electrolyte infiltration and relieves volume expansion of sulfur. Thus, Li-S batteries configured with the S@Co/CoP@NC cathode exhibit a remarkable enhancement in the rate capability and cycling performances. When sulfur content is controlled to be 75.8 wt%, the S@Co/CoP@NC cathode delivers an outstanding high-rate capability up to 30 C and low capacity decay rates of 0.033% and 0.03% per cycle over 1000 cycles at 1 C and 2 C, respectively.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available