4.7 Article

Layered double hydroxides as high-performance anode material for potassium ion battery

Journal

JOURNAL OF ALLOYS AND COMPOUNDS
Volume 882, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2021.160711

Keywords

Potassium ion battery; Anode; Layered double hydroxides; Electrochemistry

Funding

  1. National Natural Science Foundation of China (NSFC) [61701434]
  2. Project Special Funding of Taishan Scholar [tsqn201909150]
  3. Natural Science Foundation of Shandong Province [ZR2020KF008]
  4. National Key Research and Development Program of China [2017YFB1401203, 2017YFA0700202]
  5. Shandong Province Higher Education Science and Technology Program [J17KA087]
  6. Qingchuang Science and Technology Plan of Shandong Universities [2019KJN001]

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Layered double hydroxides (LDHs) are investigated as anode materials for potassium ion batteries (PIBs), with MgFe-LDH showing higher K+ storage capacity but lower initial Coulombic efficiency compared to MgAl-LDH. The dominant mechanisms for K+ storage in these materials are electrical double layer effect and a faradaic process involving a conversion reaction between Fe3+ and Fe2+. The study suggests the potential of developing LDHs as efficient anode materials for PIBs.
In recent years, potassium ion batteries (PIBs) with capacitor-like rate performance and battery-like capacity are highly desirable. To this aim, layered double hydroxides (LDHs) are studied in this work to evaluate the feasibility of employing LDHs as anode materials for PIBs. Our results show MgFe-LDH that contains trivalent iron cations with variable valence states can deliver K+-storage capacity of 371.6 mAh g(-1) after running for 300 cycles at 0.1 A g(-1) with an initial Coulombic efficiency of 88.4%. In contrast, MgAl-LDH that represents LDHs excluding multivalent metal elements merely delivers a capacity of 195.3 mAh g(-1) under the same test condition but with a much higher initial Coulombic efficiency of 99.4%. Further study shows an electrical double layer effect is dominant to storing K+ for MgAl-LDH anode, while a faradaic process involving a conversion reaction between Fe3+ and Fe2+ is prevalent in MgFe-LDH anode. Rate performance of the MgFe-LDH/K cell shows its capacity retentions at 1, 2, 5, 10 A g(-1) are 60.9%, 51.3%, 42.9%, 39.5%, respectively, which exhibit cause-effect relationships with its intrinsic poor conductivity and a non-efficient grinding event at high current densities. Besides, by measuring EIS spectra at different temperatures, the apparent activation energy is calculated to be 79.5 kJ mol(-1). It is thus anticipated that this study will shed new light on developing LDHs as powerful anode materials for PIBs. (C) 2021 Elsevier B.V. All rights reserved.

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