scholarly journals Rational Design of Alkali-Resistant NO Reduction Catalysts using a Stable Hexagonal V-Doped MoO3 Support for Alkali Trapping

ChemCatChem ◽  
2018 ◽  
Vol 10 (18) ◽  
pp. 3926-3926
Author(s):  
Xiaona Liu ◽  
Jiayi Gao ◽  
Yaxin Chen ◽  
Chao Li ◽  
Junxiao Chen ◽  
...  
ChemCatChem ◽  
2018 ◽  
Vol 10 (18) ◽  
pp. 3923-3923
Author(s):  
Xiaona Liu ◽  
Jiayi Gao ◽  
Yaxin Chen ◽  
Chao Li ◽  
Junxiao Chen ◽  
...  

ChemCatChem ◽  
2018 ◽  
Vol 10 (18) ◽  
pp. 3999-4003 ◽  
Author(s):  
Xiaona Liu ◽  
Jiayi Gao ◽  
Yaxin Chen ◽  
Chao Li ◽  
Junxiao Chen ◽  
...  

2019 ◽  
Vol 55 (66) ◽  
pp. 9853-9856 ◽  
Author(s):  
Chao Li ◽  
Zhiwei Huang ◽  
Xiaona Liu ◽  
Junxiao Chen ◽  
Weiye Qu ◽  
...  

A rationale was proposed for designing alkali-resistant SCR catalysts, which have common characteristics of separate active sites and alkali-trapping sites.


1999 ◽  
Vol 9 (8) ◽  
pp. 1801-1806 ◽  
Author(s):  
Parthasarathi Bera ◽  
K. C. Patil ◽  
V. Jayaram ◽  
M. S. Hegde ◽  
G. N. Subbanna

2017 ◽  
Vol 5 (22) ◽  
pp. 11340-11347 ◽  
Author(s):  
Lei Cao ◽  
Zhen-huan Li ◽  
Yu Gu ◽  
Dao-hao Li ◽  
Kun-mei Su ◽  
...  

Fe–N-CNBs-600 catalyst derived from fructose, NH3 and FeCl3 was prepared. The catalyst exhibits higher electrochemical properties in Zn–air batteries.


2021 ◽  
Vol 3 ◽  
Author(s):  
Yuan Wang ◽  
Xu Qian ◽  
Guokui Zheng ◽  
Ziqi Tian ◽  
Qiuju Zhang

Electrocatalytic nitrogen reduction reaction (NRR) is a promising and sustainable approach for ammonia production. Since boron as an active center possesses electronic structure similar to that of transition metals with d-orbitals (J. Am. Chem. Soc., 2019, 141 (7), 2884), it is supposed to be able to effectively activate the triple bond in N2. MXenes can be applied as substrates due to the large specific surface area, high conductivity, and tunable surface composition. In this work, the catalytic performance of a series of MXenes-supported single boron atom systems (labeled as B@MXenes) has been systematically studied by using density functional theory (DFT). B@Nb4C3O2, B@Ti4N3O2, and B@Ti3N2O2 were screened out owing to outstanding catalytic activity with limiting potentials of −0.26, −0.15, and −0.10 V, respectively. Further analysis shows that the unique property of boron that can intensely accept lone pair and back-donate the anti-bond of nitrogen contributes to the activation of inert triple bond. This work provides a new idea for the rational design of NRR catalyst and is of great significance for the future development of nitrogen reduction catalysts.


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