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Synthesis of Sea Urchin-Like NiCo2O4 via Charge-Driven Self-Assembly Strategy for High-Performance Lithium-Ion Batteries.
Wang, Bin; Tsang, Chi-Wing; Li, Ka Ho; Tang, Yuanyuan; Mao, Yanping; Lu, Xiao-Ying.
Afiliação
  • Wang B; Hong Kong Applied Science and Technology Research Institute, Hong Kong, People's Republic of China.
  • Tsang CW; Faculty of Science and Technology, Technological and Higher Education Institute of Hong Kong, Hong Kong, People's Republic of China.
  • Li KH; Faculty of Science and Technology, Technological and Higher Education Institute of Hong Kong, Hong Kong, People's Republic of China.
  • Tang Y; School of Environmental Science and Engineering, Southern University of Science and Technology, Shenzhen, People's Republic of China.
  • Mao Y; Department of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen, People's Republic of China.
  • Lu XY; Faculty of Science and Technology, Technological and Higher Education Institute of Hong Kong, Hong Kong, People's Republic of China. xylu@vtc.edu.hk.
Nanoscale Res Lett ; 14(1): 6, 2019 Jan 07.
Article em En | MEDLINE | ID: mdl-30613904
ABSTRACT
In this study, hydrothermal synthesis of sea urchin-like NiCo2O4 was successfully demonstrated by a versatile charge-driven self-assembly strategy using positively charged poly(diallydimethylammonium chloride) (PDDA) molecules. Physical characterizations implied that sea urchin-like microspheres of ~ 2.5 µm in size were formed by self-assembly of numerous nanoneedles with a typical dimension of ~ 100 nm in diameter. Electrochemical performance study confirmed that sea urchin-like NiCo2O4 exhibited high reversible capacity of 663 mAh g-1 after 100 cycles at current density of 100 mA g-1. Rate capability indicated that average capacities of 1085, 1048, 926, 642, 261, and 86 mAh g-1 could be achieved at 100, 200, 500, 1000, 2000, and 3000 mA g-1, respectively. The excellent electrochemical performances were ascribed to the unique micro/nanostructure of sea urchin-like NiCo2O4, tailored by positively charged PDDA molecules. The proposed strategy has great potentials in the development of binary transition metal oxides with micro/nanostructures for electrochemical energy storage applications.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Nanoscale Res Lett Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Nanoscale Res Lett Ano de publicação: 2019 Tipo de documento: Article