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A Controllable Synthesis of Rich Nitrogen‐Doped Ordered Mesoporous Carbon for CO<sub>2</sub> Capture and Supercapacitors

Advanced Functional Materials · 2012 · Vol. 23(18) · pp. 2322–2328
Jing WeiDandan ZhouZhenkun SunYonghui DengYongyao XiaDongyuan Zhao

Abstract

Abstract A controllable one‐pot method to synthesize N‐doped ordered mesoporous carbons (NMC) with a high N content by using dicyandiamide as a nitrogen source via an evaporation‐induced self‐assembly process is reported. In this synthesis, resol molecules can bridge the Pluronic F127 template and dicyandiamide via hydrogen bonding and electrostatic interactions. During thermosetting at 100 °C for formation of rigid phenolic resin and subsequent pyrolysis at 600 °C for carbonization, dicyandiamide provides closed N species while resol can form a stable framework, thus ensuring the successful synthesis of ordered N‐doped mesoporous carbon. The obtained N‐doped ordered mesoporous carbons possess tunable mesostructures ( p 6 m and Im $ \bar 3 $ m symmetry) and pore size (3.1–17.6 nm), high surface area (494–586 m 2 g −1 ), and high N content (up to 13.1 wt%). Ascribed to the unique feature of large surface area and high N contents, NMC materials show high CO 2 capture of 2.8–3.2 mmol g −1 at 298 K and 1.0 bar, and exhibit good performance as the supercapacitor electrode with specific capacitances of 262 F g −1 (in 1 M H 2 SO 4 ) and 227 F g −1 (in 6 M KOH) at a current density of 0.2 A g −1 .

Supercapacitor Materials and FabricationCovalent Organic Framework ApplicationsMetal-Organic Frameworks: Synthesis and ApplicationsMaterials scienceCarbonizationSupercapacitorMesoporous materialChemical engineeringCarbon fibersPyrolysisMoleculeSpecific surface areaNanotechnology
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