scholarly journals Comparing the Catalytic Oxidation of Ethanol at the Solid–Gas and Solid–Liquid Interfaces over Size-Controlled Pt Nanoparticles: Striking Differences in Kinetics and Mechanism

Nano Letters ◽  
2014 ◽  
Vol 14 (11) ◽  
pp. 6727-6730 ◽  
Author(s):  
Andras Sapi ◽  
Fudong Liu ◽  
Xiaojun Cai ◽  
Christopher M. Thompson ◽  
Hailiang Wang ◽  
...  
Catalysts ◽  
2018 ◽  
Vol 8 (6) ◽  
pp. 226 ◽  
Author(s):  
Fudong Liu ◽  
Hailiang Wang ◽  
Andras Sapi ◽  
Hironori Tatsumi ◽  
Danylo Zherebetskyy ◽  
...  

2018 ◽  
Vol 123 (13) ◽  
pp. 7577-7583 ◽  
Author(s):  
Fudong Liu ◽  
Hui-Ling Han ◽  
Lindsay M. Carl ◽  
Danylo Zherebetskyy ◽  
Kwangjin An ◽  
...  

2014 ◽  
Vol 136 (29) ◽  
pp. 10515-10520 ◽  
Author(s):  
Hailiang Wang ◽  
Andras Sapi ◽  
Christopher M. Thompson ◽  
Fudong Liu ◽  
Danylo Zherebetskyy ◽  
...  

ChemCatChem ◽  
2021 ◽  
Author(s):  
Tobias Falk ◽  
Eko Budiyanto ◽  
Maik Dreyer ◽  
Christin Pflieger ◽  
Daniel Waffel ◽  
...  

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Tao Gan ◽  
Jingxiu Yang ◽  
David Morris ◽  
Xuefeng Chu ◽  
Peng Zhang ◽  
...  

AbstractActivation of O2 is a critical step in heterogeneous catalytic oxidation. Here, the concept of increased electron donors induced by nitrogen vacancy is adopted to propose an efficient strategy to develop highly active and stable catalysts for molecular O2 activation. Carbon nitride with nitrogen vacancies is prepared to serve as a support as well as electron sink to construct a synergistic catalyst with Pt nanoparticles. Extensive characterizations combined with the first-principles calculations reveal that nitrogen vacancies with excess electrons could effectively stabilize metallic Pt nanoparticles by strong p-d coupling. The Pt atoms and the dangling carbon atoms surround the vacancy can synergistically donate electrons to the antibonding orbital of the adsorbed O2. This synergistic catalyst shows great enhancement of catalytic performance and durability in toluene oxidation. The introduction of electron-rich non-oxide substrate is an innovative strategy to develop active Pt-based oxidation catalysts, which could be conceivably extended to a variety of metal-based catalysts for catalytic oxidation.


Molecules ◽  
2021 ◽  
Vol 26 (6) ◽  
pp. 1502
Author(s):  
Johannes M. Parikka ◽  
Karolina Sokołowska ◽  
Nemanja Markešević ◽  
J. Jussi Toppari

The predictable nature of deoxyribonucleic acid (DNA) interactions enables assembly of DNA into almost any arbitrary shape with programmable features of nanometer precision. The recent progress of DNA nanotechnology has allowed production of an even wider gamut of possible shapes with high-yield and error-free assembly processes. Most of these structures are, however, limited in size to a nanometer scale. To overcome this limitation, a plethora of studies has been carried out to form larger structures using DNA assemblies as building blocks or tiles. Therefore, DNA tiles have become one of the most widely used building blocks for engineering large, intricate structures with nanometer precision. To create even larger assemblies with highly organized patterns, scientists have developed a variety of structural design principles and assembly methods. This review first summarizes currently available DNA tile toolboxes and the basic principles of lattice formation and hierarchical self-assembly using DNA tiles. Special emphasis is given to the forces involved in the assembly process in liquid-liquid and at solid-liquid interfaces, and how to master them to reach the optimum balance between the involved interactions for successful self-assembly. In addition, we focus on the recent approaches that have shown great potential for the controlled immobilization and positioning of DNA nanostructures on different surfaces. The ability to position DNA objects in a controllable manner on technologically relevant surfaces is one step forward towards the integration of DNA-based materials into nanoelectronic and sensor devices.


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