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Building carbon structures inside hollow carbon spheres.

ABSTRACT: The synthesis and characterization of helical carbon nanofibers (CNFs) contained within a fully confined nanoreactor is described. In particular, hollow carbon spheres (od = ca. 310 nm; wall thickness ca. 20 nm) were infiltrated with Cu ions (1%) to produce CuO particles (<10 nm) and the CuO was converted to Cu particles at temperature of 300 °C. Acetylene was then used as a carbon source to grow helical CNFs within the hollow carbon spheres. The diameter and helicity of the CNFs was influenced by the Cu content within a hollow carbon sphere, the limited Cu sintering inside a sphere as well as the dimensions of the sphere. The procedures employed suggest that the philosophy of building other structures (and molecules) with any elements within confined nanoreactors is possible.

SUBMITTER: Gangatharan PM

PROVIDER: S-EPMC6650401 | biostudies-other | 2019 Jul

REPOSITORIES: biostudies-other

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Building carbon structures inside hollow carbon spheres.

Gangatharan Prakash M PM Maubane-Nkadimeng Manoko S MS Coville Neil J NJ

Scientific reports 20190723 1

The synthesis and characterization of helical carbon nanofibers (CNFs) contained within a fully confined nanoreactor is described. In particular, hollow carbon spheres (od = ca. 310 nm; wall thickness ca. 20 nm) were infiltrated with Cu ions (1%) to produce CuO particles (<10 nm) and the CuO was converted to Cu particles at temperature of 300 °C. Acetylene was then used as a carbon source to grow helical CNFs within the hollow carbon spheres. The diameter and helicity of the CNFs was influenced ...[more]

PMID: 31337805

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Project description:The energy storage performances of supercapacitors are expected to be enhanced by the use of nanostructured hierarchically micro/mesoporous hollow carbon materials based on their ultra-high specific surface areas and rapid diffusion of electrolyte ions through the interconnected channels of their mesoporous structures. In this work, we report the electrochemical supercapacitance properties of hollow carbon spheres prepared by high-temperature carbonization of self-assembled fullerene-ethylenediamine hollow spheres (FE-HS). FE-HS, having an average external diameter of 290 nm, an internal diameter of 65 nm, and a wall thickness of 225 nm, were prepared by using the dynamic liquid-liquid interfacial precipitation (DLLIP) method at ambient conditions of temperature and pressure. High temperature carbonization (at 700, 900, and 1100 °C) of the FE-HS yielded nanoporous (micro/mesoporous) hollow carbon spheres with large surface areas (612 to 1616 m2 g-1) and large pore volumes (0.925 to 1.346 cm3 g-1) dependent on the temperature applied. The sample obtained by carbonization of FE-HS at 900 °C (FE-HS_900) displayed optimum surface area and exhibited remarkable electrochemical electrical double-layer capacitance properties in aq. 1 M sulfuric acid due to its well-developed porosity, interconnected pore structure, and large surface area. For a three-electrode cell setup, a specific capacitance of 293 F g-1 at a 1 A g-1 current density, which is approximately 4 times greater than the specific capacitance of the starting material, FE-HS. The symmetric supercapacitor cell was assembled using FE-HS_900 and attained 164 F g-1 at 1 A g-1 with sustained 50% capacitance at 10 A g-1 accompanied by 96% cycle life and 98% coulombic efficiency after 10,000 consecutive charge/discharge cycles. The results demonstrate the excellent potential of these fullerene assemblies in the fabrication of nanoporous carbon materials with the extensive surface areas required for high-performance energy storage supercapacitor applications.

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Building carbon structures inside hollow carbon spheres.

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Building carbon structures inside hollow carbon spheres.

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