Published September 2014 | Version v1
Journal article

Mn-doped ZnFe2O4 nanoparticles with enhanced performances as anode materials for lithium ion batteries

  • 1. Laboratory of Quantum Engineering and Quantum Materials, School of Physics and Telecommunication Engineering, South China Normal University, Guangzhou 510006 (China)
  • 2. Engineering Research Center of Materials and Technology for Electrochemical Energy Storage, Guangzhou 510006 (China)
  • 3. Institute of Advanced Materials, Nanjing University of Technology, Nanjing 210009 (China)
  • 4. Department of Radiation Physics, Stanford University, Arastradero, PA 1070 (United States)

Description

Highlights: • Mn-doped ZnFe2O4 nanoparticles have been synthesized by hydrothermal method. • Zn0.96Mn0.04Fe2O4 electrode shows the highest reversible capacity of 1157 mA h g−1. • The Zn0.96Mn0.04Fe2O4 electrode shows promising cycling stability. - Abstract: Nanocrystalline Zn1−xMnxFe2O4 (x = 0, 0.02, 0.04, 0.06, 0.08, 0.1) have been successfully synthesized by one-step hydrothermal method. The morphologies and electrochemical performance of Mn-doped ZnFe2O4 in various proportions were investigated at room temperature, respectively. The Zn1−xMnxFe2O4 (x = 0.04) electrode in the as-synthesized samples showed the highest specific capacity of 1547 mA h g−1 and 1157 mA h g−1 in the initial discharge/charge process, with a coulombic efficiency of 74.8%. Additionally, excellent cycling stability was performed with a 1214 mA h g−1 capacity retention at a current density of 100 mA g−1 after 50 cycles. The corresponding mechanism was proposed which indicated that the Mn-doped ZnFe2O4 nanoparticles experienced an aggregation thermochemical reaction among ZnO, MnO and Fe2O3 subparticles

Availability note (English)

Available from http://dx.doi.org/10.1016/j.materresbull.2014.05.038

Additional details

Identifiers

DOI
10.1016/j.materresbull.2014.05.038;
PII
S0025-5408(14)00314-6;

Publishing Information

Journal Title
Materials Research Bulletin
Journal Volume
57
Journal Page Range
p. 127-134
ISSN
0025-5408
CODEN
MRBUAC

Optional Information

Copyright
Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.