Synthesis of Size-Controllable NiCo2S4 Hollow Nanospheres Toward Enhanced Electrochemical Performance

22Citations
Citations of this article
14Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Although the synthesis of novel nanostructured metal sulfides has been well established, further size-controllable optimization is still valuable to enhance their performance for various applications. Herein, a self-template method to size-controllably synthesize the hollow NiCo2S4 nanospheres is reported. Uniformly monodisperse NiCo precursors with diameter widely ranging from 97 to 550 nm are controllably synthesized and subsequently transformed into hollow NiCo2S4 nanospheres through in situ sulfidation. Smaller nanoparticles' diameter results in the hollow NiCo2S4 nanospheres larger surface area and thinner shell thickness and hence provides much more electrochemical active sites as well as facilitate the ion and electron transfer. Consequently, the hollow NiCo2S4 nanospheres—used as the electrode materials in supercapacitors—achieve 19% enhancement of specific capacity from 484.8 to 575.1 C g−1 through lowering the 42.5% diameter of hollow NiCo2S4 nanospheres from 407 to 234 nm. Moreover, the hollow NiCo2S4 nanospheres with 234 nm diameter exhibit superior rate capacity indicated by 49% capacity retention from 1 to 50 A g−1 and excellent cycling stability (77% after 2000 cycles). Furthermore, this method is a potentially general strategy in the size-controllable synthesis of the metal sulfides hollow nanostructures and results in the remarkable electrochemical applications.

Cite

CITATION STYLE

APA

Zhang, L., Zhang, H., Chu, X., Liu, F., Guo, C., & Yang, W. (2020). Synthesis of Size-Controllable NiCo2S4 Hollow Nanospheres Toward Enhanced Electrochemical Performance. Energy and Environmental Materials, 3(3), 421–428. https://doi.org/10.1002/eem2.12113

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free