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Title: Understanding the electrochemical lithiation/delithiation process in the anode material for lithium ion batteries NiFeOPO4/C using ex-situ X-ray absorption near edge spectroscopy and in-situ synchrotron X-ray

Journal Article · · Electrochimica Acta
 [1];  [2];  [3];  [4];  [4];  [4];  [5];  [3];  [6];  [7]
  1. Mohammed VI Polytechnic Univ., Ben Guerir (Morocco); Cadi Ayyad Univ., Marrakesh (Morocco); Argonne National Lab. (ANL), Argonne, IL (United States)
  2. Cadi Ayyad Univ., Marrakesh (Morocco)
  3. Mohammed VI Polytechnic Univ., Ben Guerir (Morocco)
  4. Argonne National Lab. (ANL), Argonne, IL (United States)
  5. Mohammed VI Polytechnic Univ., Ben Guerir (Morocco); Univ. Hassan 1er, Khouribga (Morocco)
  6. Argonne National Lab. (ANL), Argonne, IL (United States); Stanford Univ., Stanford, CA (United States); Imam Abdulrahman Bin Faisal Univ. (IAU), Dammam (Saudi Arabia)
  7. Mohammed VI Polytechnic Univ., Ben Guerir (Morocco); Cadi Ayyad Univ., Marrakesh (Morocco)

Here, nickel iron (III) oxyphosphate NiFeOPO4 (NFP) was successfully synthesized using solid-state route and modified with carbon layer using sucrose as carbon source. The electrochemical performances of the composite anode material NiFeOPO4/C (NFP/C) vs. Li+/Li0 were investigated at C/5 current rate and in a wide voltage window 0.01-3.0 V. During the first lithiation at C/5, NFP/C was able to uptake more than six lithium ions into the structure delivering a capacity of 736.63 mAh g-1. In this study, NFP phosphate was characterized using XRD, SEM, EDS mapping, and Raman spectroscopy. The first cycle was investigated using high energy spectroscopies including: in-situ synchrotron X-Ray Diffraction and ex-situ X-ray Absorption Near Edge Spectroscopy (XANES). In-situ synchrotron XRD revealed that the crystal structure of NFP/C undergoes structural transformations leading to lower degrees of crystallinity during the first lithiation. Ex-situ XANES measurements disclosed that the redox reaction of iron and nickel during the first lithiation and delithiation is reversible.

Research Organization:
Argonne National Lab. (ANL), Argonne, IL (United States)
Sponsoring Organization:
USDOE Office of Energy Efficiency and Renewable Energy (EERE), Vehicle Technologies Office (EE-3V). Battery Materials Research (BMR) Program; USDOE
Grant/Contract Number:
AC02-06CH11357
OSTI ID:
1477459
Alternate ID(s):
OSTI ID: 1495273
Journal Information:
Electrochimica Acta, Vol. 283, Issue C; ISSN 0013-4686
Publisher:
ElsevierCopyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 13 works
Citation information provided by
Web of Science

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