4.8 Article

Development of P3-K0.69CrO2 as an ultra-high-performance cathode material for K-ion batteries

Journal

ENERGY & ENVIRONMENTAL SCIENCE
Volume 11, Issue 10, Pages 2821-2827

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c8ee01365a

Keywords

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Funding

  1. Human Resources Development program of the Korea Institute of Energy Technology Evaluation and Planning (KETEP) - Ministry of Trade, Industry and Energy of the Korean government [20154010200840]
  2. Global Frontier R&D Programme at the Center for Hybrid Interface Materials (HIM), Ministry of Science, ICT & Future Planning [2013M3A6B1078875]
  3. Korea Evaluation Institute of Industrial Technology (KEIT) [20154010200840] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  4. National Research Foundation of Korea [2013M3A6B1078875] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Potassium-ion batteries (KIBs) are emerging as a promising energy storage technology because of their low cost and high energy density. However, the large size of K+ ions hinders the reversible electrochemical potassium (de)insertion in the host structure, limiting the selection of suitable electrode materials for KIBs. Herein, we designed and exploited a new layered oxide, P3-type K0.69CrO2 (hereafter denoted as P3-K0.69CrO2), as a high-performance cathode for KIBs for the first time. The proposed P3-K0.69CrO2 cathode was successfully synthesized via an electrochemical ion-exchange route and exhibited the best cycling performance for a KIB cathode material to date. A combination of electrochemical profiles, ex situ X-ray diffraction, and first-principles calculations was used to understand the overall potassium storage mechanism of P3-K0.69CrO2. Based on a reversible phase transition, P3-K0.69CrO2 delivers a high discharge capacity of 100 mA h g(-1) and exhibits extremely high cycling stability with approximate to 65% retention over 1000 cycles at a 1C rate. Moreover, the K-ion hopping into the P3-K0.69CrO2 structure was extremely rapid, resulting in great power capability of up to a 10C rate with a capacity retention of approximate to 65% (vs. the capacity at 0.1C).

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