Elsevier

Ceramics International

Volume 42, Issue 6, 1 May 2016, Pages 7888-7894
Ceramics International

Short communication
Synthesis and electrochemical performances of MnxCoyNizCO3 as novel anode material

https://doi.org/10.1016/j.ceramint.2016.01.198Get rights and content

Abstract

Hydrothermal method was used to synthesize MnxCoyNizCO3 with morphology of microspheres. When the reactants MnSO4·H2O, CoSO4·7H2O and NiSO4·6H2O were in the molar ratio of 0.54:0.13:0.26, the product was Mn0.756Co0.133Ni0.111CO3, demonstrating the best electrochemical performances among all the prepared samples. The reversible discharge capacity of Mn0.756Co0.133Ni0.111CO3 maintained at 754 mA h g−1 after 200 cycles at the current density of 100 mA g−1 in the voltage range of 0.01–3 V. The ternary manganese–nickel–cobalt carbonates with suitable composition could be used as novel anode material for lithium-ion battery application.

Introduction

Possessing high energy density of lithium storage via a conversion reaction, transition metal carbonates have been proved as high-capacity anode materials for lithium-ion batteries [1]. It is well known that Mn owns perfect cycle life and safety, Ni offers high lithium storage capacity, Co possesses enhanced electronic conductivity [2]. Therefore, theoretically speaking, taking advantages of Mn, Co, and Ni elements, MnxCoyNizCO3 (x+y+z=1) should have ideal electrochemical performances. The specific electrochemical performances of MnxCoyNizCO3 strongly depend on the morphology, crystallinity and composition of metal elements (Mn, Co, Ni) of the sample [3].

In this work, the hydrothermal method was used to synthesize MnxCoyNizCO3 samples. The main purpose was to explore the optimal ratio of reactants for ideal electrochemical performances. The influence of crystallinity and morphology on electrochemical performances was also studied. The MnxCoyNizCO3 synthesized in our work behaved better electrochemical performances than those reported in other related works [4], [5], [6], [7].

Section snippets

Synthesis of the samples

All of the chemicals were of analytical grade, and they were used without further purification. MnSO4·H2O, CoSO4·7H2O, NiSO4·6H2O and suitable amount of urea were dissolved in distilled water. After magnetic stirring for 30 min, the solution was transferred into a 50 mL Teflon-lined stainless steel autoclave and maintained at 180 °C for 24 h. After air cooling to room temperature, the product was filtered and dried in vacuum at 100 °C for 24 h. We conducted four contrastive experiments here, the

Structure and morphology characterization

The XRD patterns of the samples are shown in Fig. 1. From the XRD patterns, we can see that all of the four samples take rhodochrosite MnCO3 as their main structure. The 2θ values of the diffraction peaks for the samples are in full accord with the standard rhodochrosite MnCO3 (JCPDS Card no. 83-1763). For the samples, the relative intensities of the main diffraction peaks appearing at about 24.5°, 31.7°, 37.8°, 41.8°, 45.5°, and 52.1° (2θ), corresponding to the lattice planes (0 1 2), (1 0 4),

Conclusion

Using the hydrothermal method, MnxCoyNizCO3 samples with different reactants ratios were synthesized successfully. All of the prepared samples took rhodochrosite MnCO3 as their main structure, possessing morphology of microspheres. When the mole ratio of reactants MnSO4·H2O, CoSO4·7H2O and NiSO4·6H2O was 0.54:0.13:0.26, the product was Mn0.756Co0.133Ni0.111CO3, owning the best morphology, crystallinity and electrochemical performances among all the prepared samples. The reversible discharge

Acknowledgments

Financial support provided by a National Natural Science Grant of China (No. 21476063) is gratefully acknowledged. The authors would also like to thank Dr. Tania Silver at the University of Wollongong for critical reading of the manuscript.

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