Published June 1, 2011 | Version v1
Journal article

Synthesis of boron/nitrogen substituted carbons for aqueous asymmetric capacitors

  • 1. Energy and Mineral Engineering, Pennsylvania State University, University Park, PA 16802 (United States)
  • 2. Materials Research Institute, Pennsylvania State University, 270 MRL Bldg., University Park, PA 16802 (United States)
  • 3. Energy Institute, Pennsylvania State University, University Park, PA 16802 (United States)
  • 4. Department of Chemical Engineering, The Pennsylvania State University, University Park, PA 16802 (United States)

Description

Highlights: → Synthesis of highly substituted boron and nitrogen containing carbons (BCN) for ultracapacitor applications. → Evidence for strong electroadsorption of protons on BCN. → Increased specific capacitance per unit area and improved cell voltage in aqueous asymmetric capacitors. - Abstract: Boron/nitrogen substituted carbons were synthesized by co-pyrolysis of polyborazylene/coal tar pitch blends to yield a carbon with a boron and nitrogen content of 14 at% and 10 at%, respectively. The presence of heteroatoms in these carbons shifted the hydrogen evolution overpotential to -1.4 V vs Ag/AgCl in aqueous electrolytes, providing a large electrochemical potential window (∼2.4 V) as well as a specific capacitance of 0.6 F/m2. An asymmetric capacitor was fabricated using the as-prepared low surface area carbon as the negative electrode along with a redox active manganese dioxide as the positive electrode. The energy density of the capacitor exceeded 10 Wh/kg at a power density of 1 kW/kg and had a cycle life greater than 1000 cycles.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.electacta.2011.03.112

Additional details

Identifiers

DOI
10.1016/j.electacta.2011.03.112;
PII
S0013-4686(11)00495-6;

Publishing Information

Journal Title
Electrochimica Acta
Journal Volume
56
Journal Issue
15
Journal Page Range
p. 5369-5375
ISSN
0013-4686
CODEN
ELCAAV

Optional Information

Copyright
Copyright (c) 2011 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.