We report here an high specific surface area activated carbon loaded with hemin (H-PAC) synthesized by one-step in situ pyrolysis of paper. As the carrier of hemin, paper-derived activated carbon (PAC) showed high specific surface area (3157 m2 g-1) after optimization. The surface concentration of hemin in the material was effectively increased. In particular, PAC had a unique interconnected porous structure, which can be used as a continuous conductive framework and provide more active sites. Hemin maintained peroxidase-like activity and showed superior synergistic effect with PAC via pyrolysis, displaying rapid redox characteristics. Under optimized conditions, the composite exhibits high electro–catalytic activities for H2O2 reduction with a low detection limit of 0.087 μM, and high selectivity.
This paper describes a strategy for preparing free-standing reduced graphene oxide@Si nanoparticles (rGO@Si NPs) composite membranes. Graphene oxide (GO) was reduced and self-assembled synchronously with nanoparticles of silicon (Si NPs) on a metal surface and the composite film was subsequently used in a lithium-ion battery (LIB). This work describes several important novel aspects of the reported technology. Firstly, the composite membrane has a flexible self-supporting structure, allowing it to function as an anode material without requiring binders and current collectors. Secondly, the successful assembly of Si NPs and reduced Graphene oxide (rGO) sheets has enabled the production of the rGO@Si NPs composite film with high controllability and orderliness. Thirdly, the conductive nature of graphene has significantly decreased the resistivity while enhancing the electron transport capacity of the battery anode. Lastly, the robust and flexible structure of the graphene sheet has greatly mitigated the large volume variation in Si NPs during charging or discharging, resulting in the rGO@Si NPs composite film exhibiting excellent energy density and high-power density.
In this work, Fe–decorated nitrogen–doped carbon nanospheres are prepared for electrochemical monitoring of acetaminophen. Via a direct pyrolysis of the melamine–formaldehyde resin spheres, the well–distributed Fe–NC spheres were obtained. The as–prepared Fe–NC possesses enhanced catalysis towards the redox of acetaminophen for abundant active sites and high–speed charge transfer. The effect of loading Fe species on the electrochemical sensing of acetaminophen is investigated in detail. The synergistic effect of nitrogen doping along with the above–mentioned properties is taken advantage of in the fabrication of electrochemical sensors for the acetaminophen determination. Based on the calibration plot, the limits of detection (LOD) were calculated to be 0.026 μM with a linear range from 0–100 μM. Additionally satisfactory repeatability, stability, and selectivity are obtained.
We report here, a strategy to prepare Pt/Pd nanoparticles decorated with Co-N-C materials, where Co-N-C was obtained via pyrolysis of ZIF-67 directly. As-prepared Pt/Pd/Co-N-C catalysts showed excellent ORR performance, offered with a higher limit current density (6.6 mA cm−2) and similar half-wave potential positive (E1/2 = 0.84 V) compared with commercial Pt/C. In addition to an ORR activity, it also exhibits robust durability. The current density of Pt/Pd/Co-N-C decreased by only 9% after adding methanol, and a 10% current density loss was obtained after continuous testing at 36,000 s.
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