Concave gold nano-arrows (AuCNAs) for efficient catalytic reduction of 4-nitrophenol.

The catalytic oxidation of CO by single-atom transition metal catalysts has always been the focus of researchers. Herein, we report a strategy for the preparation of Cu single-atom anchored on MnO2 by oxalate chelation-assisted hydrothermal method, and the obtained Cu/MnO2–0.25 catalyst with the optimal molar ratio achieved about 90% CO conversion at 80 °C. The strong electronic interaction between Cu and MnO2 not only effectively inhibits the aggregation of Cu single atoms, but also the formed Cu-O-Mn hybrid structure activates the adjacent surface lattice oxygen, further improving the catalytic oxidation performance of CO at low and medium temperatures. The elevated activity is achieved at the single-atom active site by the Mars-van Krevelen (MvK) mechanism. This work provides a simple and reliable method for the rational design of stable transition metal single-atom catalysts and deepens the understanding of metal-support strong interactions (SMSI). 

Promotion effect of CO oxidation via activation of surface lattice oxygen by single atom Cu/MnO2 catalyst

The conversion of p-nitrophenol (4-NP) to p-aminophenol (4-AP) is of great significance for pharmaceutical and material manufacturing. In this work, Au-M@SiO2 (M = Rh, Pd, Ir, Pt) nanoparticles (NPs) with core-shell structures, which are expected to be excellent catalysts for the transformation of 4-NP to 4-AP, were synthesized by a facile one-pot one-step method. The structure and composition of the NPs were characterized through transmission electron microscopy, X-ray powder diffraction and X-ray photoelectron spectroscopy. Au-M@SiO2 (M = Rh, Pd, Ir, Pt) core-shell NPs showed excellent catalytic activity in the reduction of 4-NP, which is superior to most catalysts reported in the previous literature. The enhanced catalytic activity of Au-M@SiO2 core-shell NPs is presumably related to the bimetallic synergistic effect. This study provides a simple strategy to synthesize core-shell bimetallic NPs for catalytic applications. 

/pdf/one-pot-synthesis-of-au-m-sio2-m-rh-pd-ir-pt-core-shell-19du518c.pdf

One-pot synthesis of Au-M@SiO2 (M = Rh, Pd, Ir, Pt) core–shell nanoparticles as highly efficient catalysts for the reduction of 4-nitrophenol

Advances in CO catalytic oxidation on typical noble metal catalysts: Mechanism, performance and optimization

Boosting the efficiency of low-loaded Au on spongy Fe2O3 via interfacial ferric hydroxide for low-temperature CO oxidation

Highly efficient Au/Fe2O3 for CO oxidation: The vital role of spongy Fe2O3 toward high catalytic activity and stability.

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Highly efficient Au/Fe2O3 for CO oxidation: The vital role of spongy Fe2O3 toward high catalytic activity and stability.