Nanoporous Hollow Carbon Spheres Derived from Fullerene Assembly as Electrode Materials for High-Performance Supercapacitors

Author:

Shrestha Lok Kumar12ORCID,Wei Zexuan13,Subramaniam Gokulnath45ORCID,Shrestha Rekha Goswami1,Singh Ravi2,Sathish Marappan45,Ma Renzhi1,Hill Jonathan P.1ORCID,Nakamura Junji6,Ariga Katsuhiko13ORCID

Affiliation:

1. International Center for Materials Nanoarchitectonics (WPI-MANA), National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba 305-0044, Ibaraki, Japan

2. Department of Materials Science, Faculty of Pure and Applied Sciences, University of Tsukuba 1-1-1, Tennodai, Tsukuba 305-8573, Ibaraki, Japan

3. Department of Advanced Materials Science, Graduate School of Frontier Sciences, The University of Tokyo, 5-1-5 Kashiwanoha, Kashiwa 277-8561, Chiba, Japan

4. Electrochemical Power Sources Division, CSIR-Central Electrochemical Research Institute, Karaikudi 630003, Tamil Nadu, India

5. Academy of Scientific and Innovative Research (AcSIR), Ghaziabad 201002, Tamil Nadu, India

6. Mitsui Chemicals, Inc., Carbon Neutral Research Center (MCI–CNRC), International Institute for Carbon-Neutral Energy Research (I2CNER), Kyushu University, 744 Motooka, Nishi-ku, Fukuoka-shi 819-0395, Fukuoka, Japan

Abstract

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.

Funder

JSPS KAKENHI

Publisher

MDPI AG

Subject

General Materials Science,General Chemical Engineering

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