Functional Mesoporous Carbon Research Articles

A green and high energy density asymmetric supercapacitor based on ultrathin MnO2nanostructures and functional mesoporous carbon nanotube electrodes

A green asymmetric supercapacitor with high energy density has been developed using birnessite-type ultrathin porous MnO(2) nanoflowers (UBMNFs) as positive electrode and functional mesoporous carbon nanotubes (FMCNTs) as negative electrode in 1 M Na(2)SO(4) electrolyte. Both of the electrode materials possess excellent electrochemical performances, with high surface areas and narrow pore size distributions. More significantly, the assembled asymmetric supercapacitor with optimal mass ratio can be cycled reversibly in the high-potential range of 0-2.0 V and exhibits an excellent energy density as high as 47.4 W h kg(-1), which is much higher than those of symmetric supercapacitors based on UBMNFs//UBMNFs and FMCNTs//FMCNTs supercapacitors. Furthermore, our asymmetric supercapacitor (ASC) device also exhibits a superior cycling stability with 90% retention of the initial specific capacitance after 1000 cycles and stable Coulombic efficiency of ~98%. These intriguing results exhibit great potential in developing high energy density "green supercapacitors" for practical applications.

Functional mesoporous carbon nanotubes and their integration in situ with metal nanocrystals for enhanced electrochemical performances

Functional mesoporous carbon nanotubes (MCNTs) and their integration in situ with Pt nanocrystals (Pt/MCNTs) have been designed and successfully developed via a facile route, which exhibited enhanced performances in energy storage and conversion applications.

Transition metal ion capture using functional mesoporous carbon made with 1,10-phenanthroline.

Functional mesoporous carbon has been built using 1,10-phenanthroline as the fundamental building block, resulting in a nanoporous, high surface area sorbent capable of selectively binding transition metal ions. This material had a specific surface area of 870 m2/g, an average pore size of about 30 Å, and contained as much as 8.2 wt% N. Under acidic conditions, where the 1,10-phenanthroline ligand is protonated, this material was found to be an effective anion exchange material for transition metal anions like [Formula: see text] and [Formula: see text]. 1,10-Phenanthroline functionalized mesoporous carbon ("Phen-FMC") was found to have a high affinity for Cu(II), even down to a pH of 1. At pHs above 5, Phen-FMC was found to bind a variety of transition metal cations (e.g. Co(II), Ni(II), Zn(II), etc.) from filtered ground water, river water and seawater. Phen-FMC displayed rapid sorption kinetics with Co(II) in filtered river water, reaching equilibrium in less than an hour, and easily lowering the [Co(II)] to sub-ppb levels. Phen-FMC was found to be more effective for transition metal ion capture than ion-exchange resin or activated carbon.

A novel low-temperature dendritic cyclotrimerization of 2,6-diacetyl pyridine leading to mesoporous carbon containing pyridine rings

A simple, direct synthesis of a mesoporous carbon containing pyridine rings is described. This synthesis utilizes the SiCl 4 induced cyclotrimerization of 2,6-diacetylpyridine to make a dendritic polymer, built of alternating benzene and pyridine rings. The cyclotrimerization allows for a high degree of crosslinking to take place at low temperatures stabilizing the mesostructure and allowing the carbonization to be carried out at only 600 °C, the lowest temperature reported to date for an N-doped mesoporous carbon. The functional mesoporous carbon so formed was found to have a surface area of 1275 m 2/g, 35 Å pores, and contain 6.8% N. XPS reveals two N-containing species, with the predominant species being pyridine N.

Functional mesoporous carbon built from the 1,10-phenanthroline building block: A new class of catalyst support

A simple synthesis of a high surface area catalyst support composed of a nanoporous carbon architecture built from a 1,10-phenanthroline precursor is described.