| Literature DB >> 26674109 |
Jie Min1, Jun Liu1, Ming Lei2, Wenjun Wang3, Yakun Lu1, Linyu Yang1, Qian Yang1, Gang Liu4, Nan Su1.
Abstract
Parallelly aligned NiO hierarchical nanostructures were fabricated using a templated self-assembly method followed by calcinations, where rationally employed pluronic triblock copolymers (P123) are acting as molecular templates for geometrical manipulation of nanocrystals and short-chain alcohols are acting as cosolvents and cosurfactants. Such aligned nanostructure is constructed orderly with several ultrathin two-dimensional (2D) nanosheet subunits with an exceptionally small thickness of only 3 nm in a high degree of orientation and separation. Moreover, the number of assembled nanosheets in a unit can be tuned by changing the concentration of the involving P123. This is the first time to synthesize highly hierarchically ordered and bilaterally symmetrical nanostructures, distributed in diameter of around 200-300 nm, via self-assembly in the liquid phase without solid substrates. The as-synthesized NiO delivered high capacitances of 418 F/g at the current density of 2 A/g with well cycling stability (still maintained 85% after 2000 cycles) and 333 F/g at 10 A/g in rates performance after 60 cycles. These fine electrochemical performances are supposed to be attributed to the hierarchical structures with high specific surface area (SSA, ∼164.87 m(2)/g) and ordered multilevel mesopores, which facilitate the electrolyte accessibility and provide more active sites for redox reaction.Entities:
Keywords: P123-assisted self-assembly; high-rate performance; layers controllable; multilevel mesopores; parallelly aligned NiO hierarchical nanostructures; supercapacitor; ultrathin nanosheet subunits
Year: 2015 PMID: 26674109 DOI: 10.1021/acsami.5b09997
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229