This study describes a new strategy to fabricate a special magnetic catalyst via facile coating Au-Pd nanoalloy catalysts onto a commercial magnetic stirring bar, without the incorporation of iron element. First, the abundant natural "waste" lignin was utilized as the reducing and stabilizing agent to prepare Au-Pd nanoalloys in a green manner. The Au-Pd nanoalloys were assumed to have a core-shell structure with an Au-rich core and a Pd-rich shell. The Au-Pd nanoalloys could be well dispersed in aqueous medium due to the stabilizing effect of lignin and be conveniently coated onto the surface of a commercial stirring bar. The AuPd nanoalloy catalyst exhibited excellent catalytic activities in the reduction of 4-nitrophenol to 4-amnophenol by NaBH, with a rate constant () of 0.239 min, which was higher than that of AuPd and AuPd nanoalloys and 4 times higher than that of a single-component Au or Pd nanoparticles. Besides, the catalytic ability of Au-Pd nanoalloy catalyst could be maintained even after seven cycles of catalysis. The catalytic rate constant was found to be positively correlated to the stirring speed of the bar. The scanning electron microscopy analysis revealed ravines and pores on the surface of lignin-nanoalloys composites, implying the possible mechanism of the catalytic activities. This study not only proved the feasibility of lignin for green synthesis of Au-Pd nanoalloys but also proposed a facile and innovated strategy for the future production of solid/liquid catalytic platforms where the developed method could be used to coat any surface interfacing the reagents.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641716 | PMC |
http://dx.doi.org/10.1021/acsomega.7b00830 | DOI Listing |
Noble metal nanoparticles and multi-materials thereof are processed on a substrate from aqueous solutions of the metallic ions, precluding any chemical additives/catalysts. The methods reported here take advantage of interactions between collapsing bubbles and the substrate that result in the generation of reducing radicals at the substrate surface and leading to the reduction of the metal ions on those sites, followed by nucleation and growth. Two selected substrates where these phenomena take place are nanocarbon and TiN.
View Article and Find Full Text PDFChem Commun (Camb)
September 2019
Jiangsu Key Laboratory of Pesticide Science and Department of Chemistry, College of Sciences, Nanjing Agricultural University, Nanjing 210095, P. R. China. and Beijing National Laboratory for Molecular Sciences and Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, P. R. China.
A series of gold/palladium nanoalloys stabilized by secondary phosphine oxides have been prepared for the first time. The nanocatalysts exhibit excellent regio- and chemo-selectivity in the hydrogenation of conjugated enynes, providing a mild and highly efficient way to access phosphinyl (Z) and (Z,Z)-[3]dendralenes.
View Article and Find Full Text PDFACS Appl Mater Interfaces
November 2018
Gold Catalysis Research Centre, State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences , Dalian 116023 , People's Republic of China.
Hybrid catalysts composed of gold-palladium nanoalloys that are sandwiched between layers of graphene oxide (GO) and lamellar TiO are synthesized via the deposition-reduction method. The resulting AuPd catalysts with different compositions of metal and support are fully characterized by a series of techniques, including X-ray diffraction, scanning transmission electron microscopy, X-ray photoelectron spectroscopy, and inductively coupled plasma mass spectrometry. The catalysts are also optimized against Au, Pd, GO, and TiO contents and employed in the direct synthesis of hydrogen peroxide (DSHP) from H and O.
View Article and Find Full Text PDFFaraday Discuss
September 2018
Cardiff Catalysis Institute, Cardiff University, School of Chemistry, Main Building, Park Place, Cardiff, CF10 3AT, UK.
A series of 1 wt% supported Au, Pd and AuPd nanoalloy catalysts were prepared via microwave assisted reduction of PdCl2 and HAuCl4 in a facile, one pot process. The resulting materials showed excellent activity for the direct synthesis of hydrogen peroxide from hydrogen and oxygen, with a synergistic effect observed on the addition of Au into a Pd catalyst. Detailed electron microscopy showed that the bimetallic particles exhibited a core-shell morphology, with an Au core surrounded by an Au-Pd shell, with a size between 10-20 nm.
View Article and Find Full Text PDFNanomaterials (Basel)
August 2017
The State Key Laboratory of Refractories and Metallurgy, School of Chemistry & Chemical Engineering, Wuhan University of Science and Technology, Wuhan 430081, China.
Due to the great potential to improve catalytic performance, gold (Au) and palladium (Pd) bimetallic catalysts have prompted structure-controlled synthesis of Au-Pd nanoalloys bounded by high-index facets. In this work, we prepared Au-Pd bimetallic nanoflowers (NFs) with a uniform size, well-defined dendritic morphology, and homogeneous alloy structure in an aqueous solution by seed-mediated synthesis. The prepared bimetallic NFs were fully characterized using a combination of transmission electron microscopy, Ultraviolet-Visible (UV-vis) spectroscopy, inductively coupled plasma optical emission spectroscopy, and cyclic voltammetry measurements.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!