Core/shell formation and surface segregation of multi shell icosahedral silver-palladium bimetallic nanostructures: A dynamic and thermodynamic study

2016 ◽  
Vol 174 ◽  
pp. 187-194 ◽  
Author(s):  
Jinasena W. Hewage
2016 ◽  
Vol 4 (23) ◽  
pp. 9038-9043 ◽  
Author(s):  
Shutang Chen ◽  
Sravan Thota ◽  
Xudong Wang ◽  
Jing Zhao

Hollow bimetallic nanostructures exhibit increased durability and utilization efficiency compared to their solid counterparts, and therefore have become promising new candidates for catalytic applications.


2020 ◽  
Vol 01 ◽  
Author(s):  
Bonamali Pal ◽  
Anila Monga ◽  
Aadil Bathla

Background:: Bimetallic nanocomposites have currently gained significant importance for enhanced catalytic applications relative to monometallic analogues. The synergistic interactions modified electronic and optical properties in the bimetallic (M1@M2) structural morphology e.g., core-shell /alloy nanostructures resulted in a better co-catalytic performance for TiO2 photocatalysis. Objective:: Hence, this article discusses the preparation, characterization, and co-catalytic activity of different bimetallic nanostructures namely, Cu@Zn, Pd@Au, Au@Ag, and Ag@Cu, etc. Method:: These bimetallic co-catalysts deposited on TiO2 possess the ability to absorb visible light due to surface plasmonic absorption and are also expected to display the new properties due to synergy between two distinct metals. As a result, they reveal the highest level of activity than the monometal deposited TiO2. Result:: Their optical absorption, emission, charge carrier dynamics, and surface structural morphology are explained for the improved photocatalytic activity of M1@M2 loaded TiO2 for the hydrogenation of certain organic compounds e.g., quinoline, crotonaldehyde, and 1,3-dinitrobenzene, etc. under UV/ visible light irradiation. Conclusion:: It revealed that the use of bimetallic core@shell co-catalyst for hydrogenation of important industrial organics by M1@M2-TiO2 nanocomposite demonstrates beneficial reactivity in many instances relative to conventional transition metal catalysts.


2007 ◽  
Vol 22 (9) ◽  
pp. 2531-2538 ◽  
Author(s):  
Mei Chee Tan ◽  
Jackie Y. Ying ◽  
Gan Moog Chow

Near infrared (NIR) absorbing nanoparticles synthesized by the reduction of HAuCl4 with Na2S exhibited absorption bands at ∼530 nm, and in the NIR region of 650–1100 nm. The NIR optical properties were not found to be related to the earlier proposed Au2S–Au core-shell microstructure in previous studies. From a detailed study of the structure and microstructure of as-synthesized particles in this work, S-containing, Au-rich, multiply-twinned nanoparticles were found to exhibit NIR absorption. They consisted of amorphous AuxS (where x = 2), mostly well mixed within crystalline Au, with a small degree of surface segregation of S. Therefore, NIR absorption was likely due to interfacial effects on particle polarization from the introduction of AuxS into Au particles, and not the dielectric confinement of plasmons associated with a core-shell microstructure.


Small ◽  
2021 ◽  
pp. 2104399
Author(s):  
Jingrun Zhu ◽  
Lihui Zhou ◽  
Yihua Zhu ◽  
Jianfei Huang ◽  
Lu Hou ◽  
...  

2020 ◽  
Vol 20 (8) ◽  
pp. 5223-5238
Author(s):  
Vanita Sharma ◽  
P. Jeevanandam

Considerable work is being carried out recently to develop nanomaterials which can act as photocatalyst under sunlight. In the present study, ZnO@CuS core–shell nanocomposites were synthesized and their photocatalytic activity has been investigated. The nanocomposites were prepared by thermal decomposition of a single molecular precursor, cyclo-tri-μ-thioacetamide-tris(chlorocopper(I)) complex ([Cu3TAA3Cl3]), in the presence of ZnO nanorods in diphenyl ether at 200 °C. The effect of reaction time and precursor concentration on copper sulfide shell formation have been investigated. The ZnO@CuS core–shell nanocomposites were characterized using different techniques such as XRD, FE-SEM, TEM, FT-IR, UV-Vis, DRS and XPS. As compared to bare ZnO nanorods, the ZnO@CuS nanocomposites show better photocatalytic activity towards degradation of congo red in an aqueous solution under sunlight.


Sign in / Sign up

Export Citation Format

Share Document