Skip to main content
Log in

Preparation and characterization of Li1.2Ni0.13Co0.13Mn0.54O2 cathode materials for lithium-ion battery

  • Original Paper
  • Published:
Ionics Aims and scope Submit manuscript

Abstract

Lithium-rich cathode materials Li1.2Ni0.13Co0.13Mn0.54O2 with (sample SF) and without (sample SP) formamide was synthesized by a spray-dry method. The crystalline structure and particle morphology of as-prepared materials were characterized by X-ray diffraction and scanning electron microscope. The specific surface area (SSA) of the Li1.2Ni0.13Co0.13Mn0.54O2 prepared from different routes was determined by a five-point Brunauer–Emmett–Teller (BET) method using N2 as absorbate gas. Being compared with the material synthesized without spray-drying process (sample CP), sample SP has much higher SSA. The additive formamide is helpful to form regular and solid precursor particles in spray-drying process, which results in a slightly aggregation of grains and reduction of SSA for sample SF. The electrochemical activities of the materials are closely related to their morphology and SSA. In the voltage range of 2–4.8 V at 25 °C, sample SP present a discharge capacity of 257 mAh g−1 at 0.1 C rate and 170 mAh g−1 at 1 C rate. The sample CP delivered only 136 mAh g−1 when discharged at 1 C rate. The elevated specific capacity and rate capability are attributed to smaller primary particle and higher SSA. Both cycle performance and rate capability of Li1.2Ni0.13Co0.13Mn0.54O2 were improved when formamide was used in spray-dry process. Discharge capacity of SF is 140.5 mAh g−1 at 2 C rate, and that of SP is 132.3 mAh g−1. Overlarge SSA of SP may provoke serious side reaction, so that its electrochemical performance was deteriorated.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

References

  1. Jarvis KA, Deng Z, Allard LF et al (2011) Chem Mater 23:3614

    Article  CAS  Google Scholar 

  2. Numata K, Sakaki C, Yamanaka S (1997) Chem Lett 8:725

    Article  Google Scholar 

  3. Lu Z, Dahn JR (2002) J Electrochem Soc 149:A815

    Article  CAS  Google Scholar 

  4. Wu X, Dong Z, Zheng J et al (2008) Natural Science 47:224

    Google Scholar 

  5. Kim MG, Jo M, Hong YS et al (2009) Chem Commun 2:218

    Article  Google Scholar 

  6. Li J, Klöpsch R, Stan MC et al (2011) J Power Sources 196:4821

    Article  CAS  Google Scholar 

  7. Kang SH, Johnson CS, Vaughey JT et al (2006) J Electrochem Soc 153:A1186

    Article  CAS  Google Scholar 

  8. Thackeray MM, Kang SH, Johnson CS et al (2006) Electrochem Commun 8:1531

    Article  CAS  Google Scholar 

  9. Rougier A, Gravereau P, Delmas C (1996) J Electrochem Soc 143:1168

    Article  CAS  Google Scholar 

  10. Kim J, Fulmer P, Manthiram A (1999) Mater Res Bull 34:571

    Article  CAS  Google Scholar 

  11. Ohzuku T, Ueda A, Nagayama M et al (1993) Electrochim Acta 38:1159

    Article  CAS  Google Scholar 

  12. Johnson CS, Li N, Lefief C et al (2008) Chem Mater 20:6095

    Article  CAS  Google Scholar 

  13. Ju SH, Kang YC (2010) J Alloys and Compd 506:913

    Article  CAS  Google Scholar 

  14. Yabuuchi N, Yoshii K, Myung ST et al (2011) J Am Chem Soc 133:4404

    Article  CAS  Google Scholar 

Download references

Acknowledgments

This work is supported by the National Science Foundation of China (project no. 20903061) and the National Basic Research Program of China (973 Program) (project no. 2011CB935902).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Jian Gao.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Gao, J., Huang, Z., Li, J. et al. Preparation and characterization of Li1.2Ni0.13Co0.13Mn0.54O2 cathode materials for lithium-ion battery. Ionics 20, 301–307 (2014). https://doi.org/10.1007/s11581-013-0991-1

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11581-013-0991-1

Keywords

Navigation