Titanium Carbide Derived Nanoporous Carbon for Energy-Related Applications

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porous carbon
etching
adsorption
BET surface area
electron microscopy
small angle x-ray scattering
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Dash, Ranjan
Chmiola, John
Yushin, Gleb
Gogotsi, Yury
Laudisio, Giovanna
Singer, Jonathan
Kucheyev, Sergei
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High surface area nanoporous carbon has been prepared by thermo-chemical etching of titanium carbide TiC in chlorine in the temperature range 200–1200 °C. Structural analysis showed that this carbide-derived carbon (CDC) was highly disordered at all synthesis temperatures. Higher temperature resulted in increasing ordering and formation of bent graphene sheets or thin graphitic ribbons. Soft X-ray absorption near-edge structure spectroscopy demonstrated that CDC consisted mostly of sp2 bonded carbon. Small-angle X-ray scattering and argon sorption measurements showed that the uniform carbon-carbon distance in cubic TiC resulted in the formation of small pores with a narrow size distribution at low synthesis temperatures; synthesis temperatures above 800 °C resulted in larger pores. CDC produced at 600–800 °C show great potential for energy-related applications. Hydrogen sorption experiments at −195.8 °C and atmospheric pressure showed a maximum gravimetric capacity of ∼ 330 cm3/g (3.0 wt.%). Methane sorption at 25 °C demonstrated a maximum capacity above 46 cm3/g (45 vol/vol or 3.1 wt.%) at atmospheric pressure. When tested as electrodes for supercapacitors with an organic electrolyte, the hydrogen-treated CDC showed specific capacitance up to 130 F/g with no degradation after 10 000 cycles.

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2006-10-01
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Postprint version. Published in Carbon, Volume 44, Issue 12, 2006, pages 2489-2497. Publisher URL: http://dx.doi.org/10.1016/j.carbon.2006.04.035
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