Microporous sulfur-doped carbon from thienyl-based polymer network precursors

Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG geförderten) Allianz- bzw. Nationallizenz frei zugänglich.This publication is with permission of the rights owner freely accessible due to an Alliance licence and a national licence (funded by the DFG, German Research Foundation) respectively.Porous sulfur-doped carbon was synthesised by using a thienyl-based polymer network as a precursor. The sulfur amount varies from 5–23 m% while the materials show microporosity with BET surface areas of up to 711 m2 g−1.DFG, EXC 314, Unifying Concepts in Catalysi

Synthesis of mesoporous composite materials of nitrogen-doped carbon and silica using a reactive surfactant approach

Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG geförderten) Allianz- bzw. Nationallizenz frei zugänglich.This publication is with permission of the rights owner freely accessible due to an Alliance licence and a national licence (funded by the DFG, German Research Foundation) respectively.Mesoporous composite materials of nitrogen-doped carbon and silica were synthesised in a one-step-process applying a soft templating procedure. The template used in the sol–gel synthesis of the silica is a cationic surfactant with distinct reactivity to form nitrogen-doped graphitic carbon upon heating. This reactivity is derived from the combination of the dicyanamide anion with a nitrogen-containing pyridinium cation, as it is known from ionic liquids used as nitrogen-doped carbon precursors. Thus applying this surfactant in a conventional sol–gel synthesis yields a silica gel doped with a precursor for N-doped carbon. By subsequent annealing mesoporous composite materials of silica and nitrogen-doped carbon are obtained

Nitrogen- and phosphorus-co-doped carbons with tunable enhanced surface areas promoted by the doping additives

Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG geförderten) Allianz- bzw. Nationallizenz frei zugänglich.This publication is with permission of the rights owner freely accessible due to an Alliance licence and a national licence (funded by the DFG, German Research Foundation) respectively.1-Butyl-3-methyl-pyridinium-dicyanamide (BMP-dca) is carbonised with tetra-alkyl-phosphonium-bromide additives yielding nitrogen- and phosphorus-co-doped carbons with enhanced BET surface areas promoted by the additives.DFG, EXC 314, Unifying Concepts in Catalysi

Nitrogen-doped coatings on carbon nanotubes and their stabilizing effect on Pt nanoparticles

Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG geförderten) Allianz- bzw. Nationallizenz frei zugänglich.This publication is with permission of the rights owner freely accessible due to an Alliance licence and a national licence (funded by the DFG, German Research Foundation) respectively.A homogeneous coating of nitrogen-doped carbon on carbon nanotubes is performed using ionic liquids. The N-doped material is employed as a support for nanoparticles. Electrochemical degradation behavior is monitored in situ and compared to an unmodified material. The strongly enhanced stability is explained on the basis of a Pt–nitrogen interaction.DFG, EXC 314, Unifying Concepts in Catalysi

Sulfur and nitrogen co-doped graphene for metal-free catalytic oxidation reactions

Sulfur and nitrogen co-doped reduced graphene oxide (rGO) is synthesized bya facile method and demonstrated remarkably enhanced activities in metal-free activation of peroxymonosulfate (PMS) for catalytic oxidation of phenol. Based on first-order kinetic model, S–N co-doped rGO (SNG) presents an apparent reaction rate constant of 0.043 ± 0.002 min -1 , which is 86.6, 22.8, 19.7, and 4.5-fold as high as that over graphene oxide (GO), rGO, S-doped rGO (S-rGO), and N-doped rGO(N-rGO), respectively. A variety of characterization techniques and density functional theory calculations are employed to investigate the synergistic effect of sulfur and nitrogen co-doping. Co-doping of rGO at an optimal sulfur loading can effectively break the inertness of carbon systems, activate the sp 2 -hybridized carbon lattice and facilitate the electron transfer from covalent graphene sheets for PMS activation. Moreover, both electron paramagnetic resonance (EPR) spectroscopy and classical quenching tests are employed to investigate the generation and evolution of reactive radicals on the SNG sample for phenol catalytic oxidation. This study presents anovel metal-free catalyst for green remediation of organic pollutants in water

Tuning the Catalytic Activity of Graphene Nanosheets for Oxygen Reduction Reaction via Size and Thickness Reduction

Currently, the fundamental factors that control the oxygen reduction reaction (ORR) activity of graphene itself, in particular the dependence of the ORR activity on the number of exposed edge sites remain elusive, mainly due to limited synthesis routes of achieving small size graphene. In this work, the synthesis of low oxygen content (< 2.5 +/-0.2 at %), few layer graphene nanosheets with lateral dimensions smaller than a few hundred nm was achieved using a combination of ionic liquid assisted grinding of high purity graphite coupled with sequential centrifugation. We show for the first time, that the graphene nanosheets possessing a plethora of edges exhibited considerably higher electron transfer numbers compared to the thicker graphene nanoplatelets. This enhanced ORR activity was accomplished by successfully exploiting the plethora of edges of the nanosized graphene as well as the efficient electron communication between the active edge sites and the electrode substrate. The graphene nanosheets were characterized by an onset potential of -0.13 V vs. Ag/AgCl and a current density of -3.85 mA/cm2 at -1 V, which represent the best ORR performance ever achieved from an undoped carbon based catalyst. This work demonstrates how low oxygen content nanosized graphene synthesized by a simple route can considerably impact the ORR catalytic activity and hence it is of significance in designing and optimizing advanced metal-free ORR electrocatalysts.Comment: corresponding author: [email protected], ACS Applied Materials and Interfaces 201

Biomass-derived three-dimensional porous N-doped carbonaceous aerogel for efficient supercapacitor electrodes

Functionalized carbonaceous materials with hierarchical structure and developed porosity are highly desired in energy storage and conversion fields. In this work, a facile and scalable hydrothermal methodology was established to synthesise three-dimensional (3D) N-doped carbonaceous aerogels using biomass-based starting materials and polypyrrole as N-source. The effect of different calcination temperatures on the structural properties, type and content of N-species and electrochemical performance of the 3D N-doped carbonaceous aerogels were uncovered. Thanks to the combinatorial effect of the appropriate N content and porous structure, the obtained samples exhibited excellent electrochemical performance, in particular, an outstanding specific capacitance of 281.0 F g-1 achieved on the sample calcined at 600 °C. This methodology offers a new fabrication strategy to prepare nanoscale carbonaceous materials with desirable morphology and hierarchical architecture of great potentials for the applications in energy fields