Fine Tuning the Composition and Nanostructure of Fe-Based Core-Shell Nanocatalyst for Efficient CO2 Hydrogenation

ChemNanoMat ◽  
2016 ◽  
Vol 2 (10) ◽  
pp. 989-996 ◽  
Author(s):  
Sharad Gupta ◽  
Vivek K. Jain ◽  
Dinesh Jagadeesan
Catalysts ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 452
Author(s):  
Michalis Konsolakis ◽  
Maria Lykaki

The rational design and fabrication of highly-active and cost-efficient catalytic materials constitutes the main research pillar in catalysis field. In this context, the fine-tuning of size and shape at the nanometer scale can exert an intense impact not only on the inherent reactivity of catalyst’s counterparts but also on their interfacial interactions; it can also opening up new horizons for the development of highly active and robust materials. The present critical review, focusing mainly on our recent advances on the topic, aims to highlight the pivotal role of shape engineering in catalysis, exemplified by noble metal-free, CeO2-based transition metal catalysts (TMs/CeO2). The underlying mechanism of facet-dependent reactivity is initially discussed. The main implications of ceria nanoparticles’ shape engineering (rods, cubes, and polyhedra) in catalysis are next discussed, on the ground of some of the most pertinent heterogeneous reactions, such as CO2 hydrogenation, CO oxidation, and N2O decomposition. It is clearly revealed that shape functionalization can remarkably affect the intrinsic features and in turn the reactivity of ceria nanoparticles. More importantly, by combining ceria nanoparticles (CeO2 NPs) of specific architecture with various transition metals (e.g., Cu, Fe, Co, and Ni) remarkably active multifunctional composites can be obtained due mainly to the synergistic metalceria interactions. From the practical point of view, novel catalyst formulations with similar or even superior reactivity to that of noble metals can be obtained by co-adjusting the shape and composition of mixed oxides, such as Cu/ceria nanorods for CO oxidation and Ni/ceria nanorods for CO2 hydrogenation. The conclusions derived could provide the design principles of earth-abundant metal oxide catalysts for various real-life environmental and energy applications.


2017 ◽  
Vol 19 (1) ◽  
pp. 270-280 ◽  
Author(s):  
Fenglin Liao ◽  
Xin-Ping Wu ◽  
Jianwei Zheng ◽  
Molly Meng-Jung Li ◽  
Anna Kroner ◽  
...  

We report a new Pd@Zn core–shell catalyst that offers a significantly higher kinetic barrier to CO/H2O formation in CO2 hydrogenation but facilitates CH3OH production at below 2 MPa with CH3OH selectivity at 70% as compared to 10% over Cu catalysts.


2020 ◽  
Vol 3 (4) ◽  
pp. 411-417 ◽  
Author(s):  
Xiaoben Zhang ◽  
Shaobo Han ◽  
Beien Zhu ◽  
Guanghui Zhang ◽  
Xiaoyan Li ◽  
...  

2015 ◽  
Vol 3 (26) ◽  
pp. 5189-5196 ◽  
Author(s):  
Hui Hou ◽  
Limei Chen ◽  
Haili He ◽  
Lizhen Chen ◽  
Zhenlu Zhao ◽  
...  

Fine-tuning the LSPR response of Au nanorod–polyaniline core–shell nanoparticles can achieve high photothermal efficiency and stability for cancer cell ablation.


2021 ◽  
Author(s):  
Ching-min Yeh ◽  
Thomas Jarrett ◽  
Yuan Gao ◽  
Chun-Xia Zhao ◽  
Andrew Whittaker ◽  
...  

<p>Designer biosurfactants can be used to stabilise and functionalise interfaces. One particularly promising use is the stabilisation of oil-in-water emulsions, enabling fine tuning physical, chemical and biological surface properties. The ability of emulsion systems to carry high payloads makes them attractive for applications in medicine, food and fragrances, and cosmetics. However, they have limited long-term stability. Here we sought to use the metal ion-chelating ability of the biosurfactant peptide, AM1, to precipitate the formation of a gold metal shell on AM1-stabilised emulsions by electroless plating. We found that replacing the commonly used zinc(II) with palladium(II) for coordination by histidine residues of adjacent AM1 peptides produced interfacial films that maintained elasticity at acidic pH. Proton NMR suggested a coordination mechanism independent of the imidazole ring of the histidines. Nevertheless. stabilisation of emulsions at low pH enabled the deposition of a gold shell, albeit by an unexpected mechanism. We propose that gold nanoparticles forming in bulk are adsorbed onto the peptide-stabilised interface, accumulating into a particulate coating. The resulting one-step method for nanoparticle precipitation and shell formation will be useful for the creation of biocompatible core-shell particles for applications where large payloads of hydrophobic active compounds require stability over long time periods.</p>


Nano Research ◽  
2021 ◽  
Author(s):  
Xiaoyun Guo ◽  
Zheng Hu ◽  
Jianxin Lv ◽  
Hui Li ◽  
Qinghua Zhang ◽  
...  

2021 ◽  
Author(s):  
Ching-min Yeh ◽  
Thomas Jarrett ◽  
Yuan Gao ◽  
Chun-Xia Zhao ◽  
Andrew Whittaker ◽  
...  

<p>Designer biosurfactants can be used to stabilise and functionalise interfaces. One particularly promising use is the stabilisation of oil-in-water emulsions, enabling fine tuning physical, chemical and biological surface properties. The ability of emulsion systems to carry high payloads makes them attractive for applications in medicine, food and fragrances, and cosmetics. However, they have limited long-term stability. Here we sought to use the metal ion-chelating ability of the biosurfactant peptide, AM1, to precipitate the formation of a gold metal shell on AM1-stabilised emulsions by electroless plating. We found that replacing the commonly used zinc(II) with palladium(II) for coordination by histidine residues of adjacent AM1 peptides produced interfacial films that maintained elasticity at acidic pH. Proton NMR suggested a coordination mechanism independent of the imidazole ring of the histidines. Nevertheless. stabilisation of emulsions at low pH enabled the deposition of a gold shell, albeit by an unexpected mechanism. We propose that gold nanoparticles forming in bulk are adsorbed onto the peptide-stabilised interface, accumulating into a particulate coating. The resulting one-step method for nanoparticle precipitation and shell formation will be useful for the creation of biocompatible core-shell particles for applications where large payloads of hydrophobic active compounds require stability over long time periods.</p>


2016 ◽  
Vol 109 (18) ◽  
pp. 183901 ◽  
Author(s):  
Mingyao Tang ◽  
Lin Zhou ◽  
Shuai Gu ◽  
Weidong Zhu ◽  
Yang Wang ◽  
...  

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