Wenchao Peng

Synthesis of porous reduced graphene oxide as metal-free carbon for adsorption and catalytic oxidation of organics in water

Activation of reduced graphene oxide (RGO) using CO2 to obtain highly porous and metal-free carbonaceous materials for adsorption and catalysis was investigated. A facile one-pot thermal process can simultaneously reduce graphene oxide and produce activated RGO without introducing any solid or aqueous activation agent. This process can significantly increase the specific surface area (SSA) of RGO from 200 to higher than 1200 m2 g−1, and the obtained materials were proven to be highly effective for adsorptive removal of both anionic (phenol) and cationic (methylene blue, MB) organics from water. Moreover, the activated RGO materials exhibited much better activity in effective activation of peroxymonosulfate (PMS) to produce sulfate radicals for oxidative degradation of MB.

2D Transition Metal Dichalcogenides and Graphene-Based Ternary Composites for Photocatalytic Hydrogen Evolution and Pollutants Degradation

Photocatalysis have attracted great attention due to their useful applications for sustainable hydrogen evolution and pollutants degradation. Transition metal dichalcogenides (TMDs) such as MoS2 and WS2 have exhibited great potential as cocatalysts to increase the photo-activity of some semiconductors. By combination with graphene (GR), enhanced cocatalysts of TMD/GR hybrids could be synthesized. GR here can act as a conductive electron channel for the transport of the photogenerated electrons, while the TMDs nanosheets in the hybrids can collect electrons and act as active sites for photocatalytic reactions. This mini review will focus on the application of TMD/GR hybrids as cocatalysts for semiconductors in photocatalytic reactions, by which we hope to provide enriched information of TMD/GR as a platform to develop more efficient photocatalysts for solar energy utilization.

Ti2C3Tx nanosheets as photothermal agents for near-infrared responsive hydrogels

Poly(N-isopropylacrylamide) (PNIPAM) is broadly applicable in many fields due to its temperature-induced phase transition property. Herein, a facile method to incorporate exfoliated Ti2C3Tx nanosheets in the PNIPAM network is reported. Due to compatibility, stability and photothermal properties of the incorporated Ti2C3Tx nanosheets, the obtained MXene/PNIPAM composite hydrogel shows excellent photothermal properties, expanding the pure thermal-responsive property of the PNIPAM hydrogel. Based on the smart composite hydrogel, remote light-control of the microfluidic pipeline is also demonstrated.

Preparation of Cuprous Oxide Mesoporous Spheres with Different Pore Sizes for Non-Enzymatic Glucose Detection

Mass transfer plays a significant role in a sensors performance, because the substrate can be detected only when it contacts with the active catalytic surface. In this work, cuprous oxide mesoporous nanospheres (Cu₂O MPNS) with different pore size distributions are fabricated and applied as electrocatalysts for glucose detection. The small pore Cu₂O (SP-Cu₂O, mean pore size of 5.3 nm) and large pore Cu₂O (LP-Cu₂O, mean pore size of 16.4 nm) spheres are prepared by the template method and an etching treatment. The obtained two kinds of Cu₂O MPNS exhibit high porosity with a similar specific surface area of 61.2 and 63.4 (m²·g-1), respectively. The prepared Cu₂O MPNS are used to construct an electrochemical non-enzymatic glucose sensor. The results show that the LP-Cu₂O exhibits better performance than SP-Cu₂O, which illustrates that the internal diffusion takes a great impact on the performance of the sensor. The LP-Cu₂O modified electrode possesses a high and reproducible sensitivity of 2116.9 μA mM-1·cm-2 at the applied potential of 0.6 V with a wide detection range of 0.003-7.8 mM and a low detection limit of 0.42 μM.

Magnetic Au-Ag-γ-Fe2O3/rGO Nanocomposites as an Efficient Catalyst for the Reduction of 4-Nitrophenol

In this paper, a facile route has been developed to prepare magnetic trimetallic Au-Ag-γ-Fe2O3/rGO nanocomposites. The impact of the preparation method (the intensity of reductant) on the catalytic performance was investigated. The nanocomposites were characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The prepared nanocomposites show fine catalytic activity towards the reduction reaction of 4-nitrophenol (4-NP). The nanocomposites also have superparamagnetism at room temperature, which can be easily separated from the reaction systems by applying an external magnetic field.