4.7 Article

Design and fabrication of high-entropy oxide anchored on graphene for boosting kinetic performance and energy storage

期刊

CERAMICS INTERNATIONAL
卷 48, 期 3, 页码 3344-3350

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.ceramint.2021.10.109

关键词

High entropy oxide; Pseudocapcitance; Electrochemical kinetics

资金

  1. National Natural Science Foundation of China [51901109]
  2. Shandong Provincial Universities Young Innovative Talent Incubation Program-Inorganic Nonmetallic Materials Research and Innovation Team
  3. Key Research and Development Plan of Shandong Province [2018YFJH0402]
  4. Colleges and Universities Twenty Terms Foundation of Jinan City [2019GXRC034]
  5. Guangdong Basic and Applied Basic Research Foundation [2019A1515110933, 2019A1515110554, 2020A1515111086, 2020A1515110219]
  6. Innovation Pilot Project of Integration of Science, Education and Industry of Shandong Province [2020KJC-CG04]

向作者/读者索取更多资源

The research successfully prepared HEO@G composite material, providing high capacity and cycling stability for lithium-ion batteries, and deeply analyzed the influence of graphene on the electrochemical properties of the composite electrode.
The rock salt structure of high entropy oxide (HEO) (Mg0.2Co0.2Ni0.2Cu0.2Zn0.2)O has promising prospects for energy materials. Here, we prepare HEO and calculate the entropy value S-mix >= 1.5R (R represents the gas constant), thus proving that HEO is obtained. In addition, we design and obtain HEO@G (HEO@Graphene) through the surface modification of HEO with graphene, which is analysed by X-ray diffraction, X-ray photoelectron spectroscopy, and high-resolution transmission electron microscopy to reveal the rock salt structure of HEO@G and the formation of a planar layer architecture on the surface of HEO by graphene. The electrode well design with HEO@G as the anode material for lithium-ion batteries provides a high capacity of 1225 mA h g(-1) in the first discharge at 100 mA g(-1) and maintains a discharge capacity of similar to 950 mA h g(-1) after 200 cycles. A reversible cycling capacity of 460 mA h g(-1) is obtained under the condition of multiple cycles at high speed. In terms of expansion, electrochemical impedance spectrometry and pseudocapacitance investigations deeply demonstrate that the addition of graphene enhances the diffusion dissemination coefficient of lithium ions in the composite electrode and changes the electrochemical kinetic properties of the composite anode. Such a modification approach for HEO will provide a reference in energy storage applications.

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