Crystalline (Ni1−xCox)5TiO7nanostructures grown in situ on a flexible metal substrate used towards efficient CO oxidation

Nanoscale ◽  
2017 ◽  
Vol 9 (32) ◽  
pp. 11713-11719 ◽  
Author(s):  
Yanan Jiang ◽  
Baodan Liu ◽  
Wenjin Yang ◽  
Lini Yang ◽  
Shujun Li ◽  
...  

Scalable (Ni1−xCox)5TiO7nanowire arrays were grownin situon a flexible titanium network substrate and exhibited superior catalytic performance for CO oxidation.

RSC Advances ◽  
2015 ◽  
Vol 5 (121) ◽  
pp. 100212-100222 ◽  
Author(s):  
Lin Li ◽  
Song-Hai Chai ◽  
Andrew Binder ◽  
Suree Brown ◽  
Shi-Ze Yang ◽  
...  

AuCo/MCF calcined at 500 °C for 1 h was found to produce the most active and stable catalyst for CO oxidation. In situ FTIR results of AuCo/MCF catalysts with different treatments.


Author(s):  
Qiuzhong Li ◽  
Caijie Wu ◽  
Ke Wang ◽  
Xiaoxiao Wang ◽  
Xun Chen ◽  
...  

A Au/TiO2-PD sample was prepared by the mild in situ photo-deposition method and follow by heat treatment. As compared to the Au/TiO2-DP prepared by deposition precipitation, this Au/TiO2-PD sample owned...


2017 ◽  
Vol 89 (4) ◽  
pp. 471-479
Author(s):  
Károly Lázár

Abstract Relocation of iron ions in microporous Fe-FER, (Al+Fe)-FER, Fe-MFI (FER: ferrierite, MFI: silicalite) and in mesoporous Fe-MCM-41 ferrisilicate (MCM: Mobile Crystalline Material) samples was followed during redox treatments primarily by tool of the in situ Mössbauer spectroscopy. Coexistence of various Fe3+ and Fe2+ species is demonstrated. In microporous Fe-FER and Fe-MFI existence of combined μ-oxo iron dimers, Fe3+FW-O-Fe2+EFW can be proposed. The presence of these dimers can easily be correlated with catalytic effect shown in certain oxidation processes. Structural rearrangement can also be revealed in mesoporous Fe-MCM-41 which result in improvement of catalytic performance in CO oxidation.


Nanomaterials ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 310
Author(s):  
Dohyeon Han ◽  
Doohwan Lee

Fine control of morphology and exposed crystal facets of porous γ-Al2O3 is of significant importance in many application areas such as functional nanomaterials and heterogeneous catalysts. Herein, a morphology controlled in situ synthesis of Al@Al2O3 core–shell architecture consisting of an Al metal core and a porous γ-Al2O3 shell is explored based on interfacial hydrothermal reactions of an Al metal substrate in aqueous solutions of inorganic anions. It was found that the morphology and structure of boehmite (γ-AlOOH) nano-crystallites grown at the Al-metal/solution interface exhibit significant dependence on temperature, type of inorganic anions (Cl−, NO3−, and SO42−), and acid–base environment of the synthesis solution. Different extents of the electrostatic interactions between the protonated hydroxyl groups on (010) and (001) facets of γ-AlOOH and the inorganic anions (Cl−, NO3−, SO42−) appear to result in the preferential growth of γ-AlOOH toward specific crystallographic directions due to the selective capping of the facets by adsorption of the anions. It is hypothesized that the unique Al@Al2O3 core–shell architecture with controlled morphology and exposed crystal-facets of the γ-Al2O3 shell can provide significant intrinsic catalytic properties with enhanced heat and mass transport to heterogeneous catalysts for applications in many thermochemical reaction processes. The direct fabrication of γ-Al2O3 nano-crystallites from Al metal substrate with in-situ modulation of their morphologies and structures into 1D, 2D, and 3D nano-architectures explored in this work is unique and can offer significant opportunities over the conventional methods.


Small Methods ◽  
2021 ◽  
pp. 2100202
Author(s):  
Tiantian Dai ◽  
Zanhong Deng ◽  
Xiaodong Fang ◽  
Huadong Lu ◽  
Yong He ◽  
...  

Micromachines ◽  
2021 ◽  
Vol 12 (7) ◽  
pp. 841
Author(s):  
Dong Tian ◽  
Yonghong Chen ◽  
Xiaoyong Lu ◽  
Yihan Ling ◽  
Bin Lin

An environmentally friendly method was proposed to prepare mesoporous Mobil Composition of Matter No.48 (MCM-48) using fly ash as the silica source. Silver nanoparticles were infiltrated on MCM-48 facilely by an in situ post-reduction method and evaluated as an effective catalyst for CO oxidation. The as-prepared MCM-48 and Ag/MCM-48 nanoparticles were characterized by XRD, N2 adsorption/desorption, and TEM. Investigations by means of XPS for Ag/MCM-48 were performed in order to illuminate the surface composition of the samples. Studies revealed the strong influence of the loading of Ag nanoparticles on catalysts in the oxidation of CO. CO conversion values for Ag/MCM-48 of 10% and 100% were achieved at temperatures of 220 °C and 270 °C, respectively, indicating that the Ag-decorated MCM-48 catalyst is extremely active for CO oxidation.


Catalysts ◽  
2019 ◽  
Vol 9 (4) ◽  
pp. 312 ◽  
Author(s):  
Antonella Glisenti ◽  
Andrea Vittadini

The effects of modifying the composition of LaCoO3 on the catalytic activity are predicted by density functional calculations. Partially replacing La by Sr ions has benefical effects, causing a lowering of the formation energy of O vacancies. In contrast to that, doping at the Co site is less effective, as only 3d impurities heavier than Co are able to stabilize vacancies at high concentrations. The comparison of the energy profiles for CO oxidation of undoped and of Ni-, Cu-m and Zn-doped (La,Sr)CoO3(100) surface shows that Cu is most effective. However, the effects are less spectacular than in the SrTiO3 case, due to the different energetics for the formation of oxygen vacancies in the two hosts.


CrystEngComm ◽  
2021 ◽  
Vol 23 (13) ◽  
pp. 2538-2546
Author(s):  
Min Yang ◽  
Guangshe Li ◽  
Huixia Li ◽  
Junfang Ding ◽  
Yan Wang ◽  
...  

For the first time, the growth behavior with size-dependent Fe occupancies at different sites of MgFe2O4 was examined. Hybrid catalysts of Pt/MgFe2O4 with a support size of 20.6 nm exhibited an optimal performance of CO oxidation.


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