Improved Electrochemical Performance of Self-Assembled Hierarchical Nanostructured Nickel Phosphide as a Negative Electrode for Lithium Ion Batteries

• Published in: Journal of physical chemistry. C Vol. 115; no. 48; pp. 23760 - 23767
• Main Authors: Lu, Y, Tu, J. P, Xiang, J. Y, Wang, X. L, Zhang, J, Mai, Y. J, Mao, S. X
• Format: Journal Article
• Language: English
• Published: American Chemical Society 08.12.2011
• Subjects: C: Nanops and Nanostructures
• ISSN: 1932-7447; 1932-7455
• DOI: 10.1021/jp208204u

Hierarchical, nanostructured nickel phosphide (h-Ni2P) spheres are synthesized by a one-pot reaction from an organic-phase mixture of nickel acetylacetonate, trioctylphosphine, tri-n-octylamine, and oleylamine (OAm). OAm is used as a surfactant to modify the surface morphology of Ni2P spheres. The h-Ni2P spheres are composed of ordered nanoparticles with 5–10 nm sizes and filled by amorphous carbon. The hierarchical structure can greatly increase the contact area between Ni2P and electrolyte, which provides more sites for Li+ accommodation, shortens the diffusion length of Li+, and enhances the reactivity of the electrode reaction. Also, the amorphous carbon and the hierarchical Ni2P nanostructures can buffer volume expansion and thus increase the electrode stability during cycling. In the context of storage behavior, the h-Ni2P electrode exhibits high capacity as well as Coulombic efficiency. After 50 cycles, the reversible capacity of h-Ni2P spheres is 365.3 mA h g–1 at 0.5 C and 257.8 mA h g–1 at 1 C, much higher than that of Ni2P spheres (97.2 mA h g–1 at 0.5 C). At a high rate of 3 C, the specific capacity of h-Ni2P is still as high as 167.1 mA h g–1.