4.8 Article

KCrS2 Cathode with Considerable Cyclability and High Rate Performance: The First K+ Stoichiometric Layered Compound for Potassium-Ion Batteries

期刊

SMALL
卷 14, 期 49, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.201803495

关键词

cathode; density functional theory; potassium-ion batteries; stability; sulfide

资金

  1. Creative Materials Discovery Program through the National Research Foundation of Korea (NRF) - Ministry of Science, ICT and Future [2015M3D1A1069710]
  2. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Education [NRF-2014R1A6A1030419]
  3. National Research Foundation of Korea [2015M3D1A1069710, 2014R1A6A1030419, 2015M3D1A1069707] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

KCrS2 is presented as a stable and high-rate layered material that can be used as a cathode in potassium-ion batteries. As far as it is known, KCrS2 is the only layered material with stoichiometric amounts of K+, which enables coupling with a graphite anode for full-cell construction. Cr(III)/Cr(IV) redox in KCrS2 is also unique, because LiCrS2 and NaCrS2 are known to experience S2-/S-2(2-) redox. O3-KCrS2 is first charged to P3-K0.39CrS2 and subsequently discharged to O3-K0.8CrS2, delivering an initial discharge capacity of 71 mAh g(-1). The following charge/discharge (C/D) shows excellent reversibility between O3-K0.8CrS2 and P3-K0.39CrS2, retaining approximate to 90% of the initial capacity during 1000 continuous cycles. The rate performance is also noteworthy. A C/D rate increase of 100-fold (0.05 to 5 C) reduces the reversible capacity only by 39% (71 to 43 mAh g(-1)). The excellent cyclic stability and high rate performance are ascribed to the soft sulfide framework, which can effectively buffer the stress caused by K+ deinsertion/insertion. During the transformation between P3-K0.39CrS2 and O3-K0.8CrS2, the material resides mostly in the P3 phase, which minimizes the abrupt dimension change and allows facile K+ diffusion through spacious prismatic sites. Structural analysis and density functional theory calculations firmly support this reasoning.

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