Role of Synthesis in Evolution of Catalyst: Bulk, Dispersed to Single Atom

Author(s):  
Mrinal R. Pai ◽  
Sushma. A. Rawool ◽  
Rajendra V. Singh ◽  
Atindra Mohan Banerjee ◽  
A. K. Tripathi
Keyword(s):  
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Jingwen Pan ◽  
Baoyu Gao ◽  
Pijun Duan ◽  
Kangying Guo ◽  
Muhammad Akram ◽  
...  

Nonradical pathway-based persulfate oxidation technology is considered to be a promising method for high-salinity organic wastewater treatment.


2021 ◽  
Vol 286 ◽  
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Jing Li ◽  
Yanqing Zhang ◽  
Qi Cao ◽  
Yanmei Si ◽  
...  

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Sai Yao ◽  
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Menggai Jiao ◽  
...  

Electrochemical CO2 reduction reaction (CO2RR) is a very important approach to realize sustainable development. Single-atom catalysts show advantages in both homogeneous and heterogeneous catalysis, and considerable progress has been made...


Author(s):  
Anand S Burange ◽  
Awais Ahmad ◽  
Rafael Luque

Efforts to bridge the gap between homogeneous and heterogeneous catalysis include the use of surface organometallic chemistry, single atom catalysis and monodispersed metal nanoparticles, among others. In case of metal...


2022 ◽  
Vol 452 ◽  
pp. 214289
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Priyanka Aggarwal ◽  
Debasish Sarkar ◽  
Kamlendra Awasthi ◽  
Prashanth W. Menezes

Nano Energy ◽  
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Vol 125 (37) ◽  
pp. 20286-20300
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Robert H. Wells ◽  
Suming An ◽  
Prajay Patel ◽  
Cong Liu ◽  
Rex T. Skodje

2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Yujing Ren ◽  
Yan Tang ◽  
Leilei Zhang ◽  
Xiaoyan Liu ◽  
Lin Li ◽  
...  

Abstract Heterogeneous single-atom catalyst (SAC) opens a unique entry to establishing structure–performance relationship at the molecular level similar to that in homogeneous catalysis. The challenge lies in manipulating the coordination chemistry of single atoms without changing single-atom dispersion. Here, we develop an efficient synthetic method for SACs by using ethanediamine to chelate Pt cations and then removing the ethanediamine by a rapid thermal treatment (RTT) in inert atmosphere. The coordination chemistry of Pt single atoms on a Fe2O3 support is finely tuned by merely adjusting the RTT temperature. With the decrease in Pt-O coordination number, the oxidation state of Pt decreases, and consequently the hydrogenation activity increases to a record level without loss of chemoselectivity. The tunability of the local coordination chemistry, oxidation states of the metal, and the catalytic performance of single atoms reveals the unique role of SACs as a bridge between heterogeneous and homogeneous catalysis.


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