Single-Metal-Atom Dopants Increase the Lewis Acidity of Metal Oxides and Promote Nitrogen Fixation

2021 ◽  
pp. 4299-4308
Author(s):  
Jinsun Lee ◽  
Ashwani Kumar ◽  
Min Gyu Kim ◽  
Taehun Yang ◽  
Xiaodong Shao ◽  
...  
2021 ◽  
Vol 143 (35) ◽  
pp. 14169-14177
Author(s):  
Changchun Ye ◽  
Juzhe Liu ◽  
Qinghua Zhang ◽  
Xiaojing Jin ◽  
Yun Zhao ◽  
...  

Nanomaterials ◽  
2019 ◽  
Vol 9 (3) ◽  
pp. 401 ◽  
Author(s):  
Oscar E. Medina ◽  
Jaime Gallego ◽  
Daniela Arias-Madrid ◽  
Farid B. Cortés ◽  
Camilo A. Franco

The main objective of this work is the catalyst optimization of Fe2O3-, Co3O4-, NiO- and/or PdO- (transition element oxides—TEO) functionalized CeO2 nanoparticles to maximize the conversion of asphaltenes under isothermal conditions at low temperatures (<250 °C) during steam injection processes. Adsorption isotherms and the subsequent steam decomposition process of asphaltenes for evaluating the catalysis were performed through batch adsorption experiments and thermogravimetric analyses coupled to Fourier-transform infrared spectroscopy (FTIR), respectively. The adsorption isotherms and the catalytic behavior were described by the solid-liquid equilibrium (SLE) model and isothermal model, respectively. Initially, three pairs of metal oxide combinations at a mass fraction of 1% of loading of CeNi1Pd1, CeCo1Pd1, and CeFe1Pd1 nanoparticles were evaluated based on the adsorption and catalytic activity, showing better results for the CeNi1Pd1 due to the Lewis acidity changes. Posteriorly, a simplex-centroid mixture design of experiments (SCMD) of three components was employed to optimize the metal oxides concentration (Ni and Pd) onto the CeO2 surface by varying the oxides concentration for mass fractions from 0.0% to 2.0% to maximize the asphaltene conversion at low temperatures. Results showed that by incorporating mono-elemental and bi-elemental oxides onto CeO2 nanoparticles, both adsorption and isothermal conversion of asphaltenes decrease in the order CeNi1Pd1 > CePd2 > CeNi0.66Pd0.66 > CeNi2 > CePd1 > CeNi1 > CeO2. It is worth mentioning that bi-elemental nanoparticles reduced the gasification temperature of asphaltenes in a larger degree than mono-elemental nanoparticles at a fixed amount of adsorbed asphaltenes of 0.02 mg·m−2, confirming the synergistic effects between Pd and Fe, Co, and Ni. Further, optimized nanoparticles (CeNi0.89Pd1.1) have the best performance by obtaining 100% asphaltenes conversion in less than 90 min at 220 °C while reducing 80% the activation energy.


2019 ◽  
Author(s):  
Lewis Wilkins ◽  
Francois Gabbai

We describe our efforts towards the design of phosphine-based ligands featuring an electrophilic carbocationic moiety positioned to enter the secondary coordination sphere of the phosphine-bound metal atom. Using simple synthetic protocols, we have been able to obtain and fully characterize the complexes [(<i>o</i>-Ph<sub>2</sub>P(C<sub>6</sub>H<sub>4</sub>)Acr)AuCl]<sup>+</sup> ([<b>3</b>]<sup>+</sup>, Acr = 9-<i>N</i>-methylacridinium) and [(<i>o</i>-Ph<sub>2</sub>P(C<sub>6</sub>H<sub>4</sub>)Xan)AuCl]<sup>+</sup> ([<b>4</b>]<sup>+</sup>, Xan = 9-xanthylium). While only weak interactions occur between the gold atom and the methylium centers of these complexes, the more Lewis acidic [<b>4</b>]<sup>+</sup> readily reacts with chloride to afford a trivalent phosphine gold dichloride derivative (<b>7</b>) in which the metal atom is covalently bound to the former methylium center. This anion-induced Au(I)/Au(III) oxidation is accompanied by a conversion of the Lewis acidic methylium center in [<b>4</b>]<sup>+</sup> into an X-type ligand in <b>7</b>. This transformation leads us to conclude that the methylium center acts as a latent Z-type ligand poised to increase the Lewis acidity of the gold center, a notion supported by the carbophilic reactivity of these complexes.


Author(s):  
A. Saravanan

Nitrogen fixation is a standout amongst the most significant concoction responses in the biological system of our planet. Under the regularly pressure of the petroleum product exhaustion emergency and anthropogenic worldwide environmental change with ceaseless CO2 emanation in the 21st century, examine focusing on the union of NH3 under gentle conditions in an economical and condition agreeable way is lively and flourishing. Thusly, the focal point of this survey is the cutting edge designing of effective photocatalysts for dinitrogen (N2) obsession toward NH3 amalgamation. Creating green and feasible techniques for NH3 combination under surrounding conditions, utilizing sustainable power source, is firmly wanted, by both modern and logical scientists. Photosynthesis for ammonia synthesis, which has as of late pulled in noteworthy consideration, straightforwardly creates NH3 from daylight, and N2 and H2O by means of photocatalysis. Photocatalysts containing copious surface oxygen-opportunities and coordinative unsaturated metal locales have been demonstrated to be equipped for actuating N2 reduction under fitting photoexcitation. A few impetus materials are examined which incorporate metal oxides, metals sulfides, carbon-based impetuses, and metal nitrides which are for the most part right now being sought after for their better use of their synergist property towards nitrogen fixation. This chapter portrays the photocatalytic reduction systems of nitrate towards unwanted items (nitrite, ammonium) and the more alluring item (dinitrogen).


2020 ◽  
Vol 22 (25) ◽  
pp. 13981-13988 ◽  
Author(s):  
Yao Tan ◽  
Ying Xu ◽  
Zhimin Ao

In this work, we explored the feasibility of transition metal atom embedded stanene as an effective catalyst for the nitrogen reduction reaction (NRR) based on first-principles calculations.


2006 ◽  
Vol 307 (1) ◽  
pp. 98-107 ◽  
Author(s):  
Arnaud Travert ◽  
Alexandre Vimont ◽  
Azziz Sahibed-Dine ◽  
Marco Daturi ◽  
Jean-Claude Lavalley
Keyword(s):  

2019 ◽  
Author(s):  
Lewis Wilkins ◽  
Francois Gabbai

We describe our efforts towards the design of phosphine-based ligands featuring an electrophilic carbocationic moiety positioned to enter the secondary coordination sphere of the phosphine-bound metal atom. Using simple synthetic protocols, we have been able to obtain and fully characterize the complexes [(<i>o</i>-Ph<sub>2</sub>P(C<sub>6</sub>H<sub>4</sub>)Acr)AuCl]<sup>+</sup> ([<b>3</b>]<sup>+</sup>, Acr = 9-<i>N</i>-methylacridinium) and [(<i>o</i>-Ph<sub>2</sub>P(C<sub>6</sub>H<sub>4</sub>)Xan)AuCl]<sup>+</sup> ([<b>4</b>]<sup>+</sup>, Xan = 9-xanthylium). While only weak interactions occur between the gold atom and the methylium centers of these complexes, the more Lewis acidic [<b>4</b>]<sup>+</sup> readily reacts with chloride to afford a trivalent phosphine gold dichloride derivative (<b>7</b>) in which the metal atom is covalently bound to the former methylium center. This anion-induced Au(I)/Au(III) oxidation is accompanied by a conversion of the Lewis acidic methylium center in [<b>4</b>]<sup>+</sup> into an X-type ligand in <b>7</b>. This transformation leads us to conclude that the methylium center acts as a latent Z-type ligand poised to increase the Lewis acidity of the gold center, a notion supported by the carbophilic reactivity of these complexes.


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