4.8 Article

Transitional Metal Catalytic Pyrite Cathode Enables Ultrastable Four-Electron-Based All-Solid-State Lithium Batteries

Journal

ACS NANO
Volume 13, Issue 8, Pages 9551-9560

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.9b04538

Keywords

transitional metal catalytic pyrite; four electron storage; nanostructure engineering; pseudocapacitive behavior; density functional theory calculation

Funding

  1. National Key R&D Program of China [2018YFB0905400]
  2. National Natural Science Foundation of China [51872303]
  3. Zhejiang Provincial Natural Science Foundation of China [LD18E020004, LY18E020018]
  4. Natural Science Foundation of Ningbo [2018A610010]
  5. Youth Innovation Promotion Association CAS [2017342]
  6. Fujian Institute of Innovation, Chinese Academy of Sciences

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All-solid-state batteries can enable reversible four lithium ion storage for pyrite (FeS2) at a cutoff voltage of 1.0-3.0 V. However, strain/stress concentration generating electrode pulverization and sluggish electrochemical reaction of lithium sulfide and sulfur will affect the long cycling stability of the battery. Through experiments and density functional theory (DFT) calculations, it is proved that nanostructure engineering and electronic conduction improvement with introduction of catalytic cobalt can effectively improve the electrochemical activity of FeS2. The optimized loose structured Co0.1Fe0.9S2 based all -solid-state lithium batteries show reversible capacities of 860.5, 797.7, 685.8, and 561.8 mAh g(-1) after five cycles at 100, 200, 500, and 1000 mA g(-1), respectively, and a stable capacity of 543.5 mAh g(-1) can be maintained after cycling at a current density of 500 mA g(-1) for 100 cycles. Ex situ TEM and Raman results reveal that, after the first cycle, the reversible reaction 2Li(2)S + Fe <-> FeSy + (2 - y)S + 4Li(+) + 4e(-) proceeds from the following cycles onward, while nanocrystalline mackinawite FeS, Fe(III)-containing mackinawite FeS, and Fe3S4 are generated after the first discharge charge process. This work provides a facile method for improving the electrochemical performance for multi-electron reaction mechanism based all -solid-state lithium batteries.

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