scholarly journals Nitrogen Reduction to Ammonia on Atomic‐Scale Active Sites under Mild Conditions

Small Methods ◽  
2019 ◽  
Vol 3 (9) ◽  
pp. 1800501 ◽  
Author(s):  
Xiao Yan ◽  
Daolan Liu ◽  
Huanhuan Cao ◽  
Feng Hou ◽  
Ji Liang ◽  
...  
Author(s):  
Alexis T. Bell

Heterogeneous catalysts, used in industry for the production of fuels and chemicals, are microporous solids characterized by a high internal surface area. The catalyticly active sites may occur at the surface of the bulk solid or of small crystallites deposited on a porous support. An example of the former case would be a zeolite, and of the latter, a supported metal catalyst. Since the activity and selectivity of a catalyst are known to be a function of surface composition and structure, it is highly desirable to characterize catalyst surfaces with atomic scale resolution. Where the active phase is dispersed on a support, it is also important to know the dispersion of the deposited phase, as well as its structural and compositional uniformity, the latter characteristics being particularly important in the case of multicomponent catalysts. Knowledge of the pore size and shape is also important, since these can influence the transport of reactants and products through a catalyst and the dynamics of catalyst deactivation.


2021 ◽  
pp. 137695
Author(s):  
Chaoqun Ma ◽  
Naihua Zhai ◽  
Bingping Liu ◽  
Shihai Yan

Author(s):  
Jiangtian Li ◽  
Deryn Chu ◽  
David R Baker ◽  
Rongzhong Jiang

A seamless separation of intermediates (OHad and Had) to different active sites at atomic scale is realized on a Ni-O catalyst that is functionalized with low-coordinated oxygen and abundant vacancies....


Author(s):  
Liang Zhao ◽  
Rui Zhao ◽  
Yixiang Zhou ◽  
Xiaoxuan Wang ◽  
Xinyue Chi ◽  
...  

Electrochemical nitrogen reduction reaction (NRR) is an effective method for sustainable production of NH3. However, a robust NRR electrocatalyst is predominantly required in order to active the inert N2 molecule....


2020 ◽  
Vol 22 (17) ◽  
pp. 5730-5741
Author(s):  
Shuo Chen ◽  
Li-Li Ling ◽  
Shun-Feng Jiang ◽  
Hong Jiang

The defined catalyst (Co@NC) is prepared through the pyrolysis of the Co-centered metal–organic framework (MOF), in which Co active species (Co–Nx, surface Co NPs) and particle size play important roles in the catalytic hydrogenation of aromatic nitro compounds.


2021 ◽  
Vol 42 (4) ◽  
pp. 618-626 ◽  
Author(s):  
Zhifeng Dai ◽  
Yongquan Tang ◽  
Fei Zhang ◽  
Yubing Xiong ◽  
Sai Wang ◽  
...  

2018 ◽  
Vol 54 (34) ◽  
pp. 4250-4253 ◽  
Author(s):  
Benjamin L. Sheets ◽  
Gerardine G. Botte

A polymer gel electrolyte was implemented to enable the electrochemical reduction of nitrogen to ammonia at low temperature and pressure.


Nanoscale ◽  
2020 ◽  
Vol 12 (8) ◽  
pp. 4903-4908 ◽  
Author(s):  
Kang Liu ◽  
Junwei Fu ◽  
Li Zhu ◽  
Xiaodong Zhang ◽  
Hongmei Li ◽  
...  

Electrochemical nitrogen reduction reaction (NRR) is a promising route to produce ammonia under mild conditions. Single-atom W supported on BP was screened as a promising electrocatalyst with high catalytic activity, stability, and selectively for NRR.


2015 ◽  
Vol 1094 ◽  
pp. 168-173
Author(s):  
Xiu E Ren ◽  
Jian Hui Zhang ◽  
Xiao Dan Lv ◽  
Qi Dan Chen

Preferential adsorption takes place at the step ledge between adjacent crystal faces, which usually serve as active sites for breaking chemical bonds. In this paper, we present a structural model to interpret the habit modification of single crystals in terms of the step geometries relationship between crystal faces. A new series of high index faces parallel to the ledge between adjacent facets can be explicitly determined from the presence of the symmetry operators in the space group. The relative stability of these new faces undergoes a faceting transition, driven by the adsorbate-induced changes of the step configuration. Combined with the chemical bond-geometric approach, our predictions accurately reproduce the tapering evolutions of KDP crystals in the present of metallic ions. The current work provides a new insight on how changes affecting elementary steps on one face are translated into the emergence of a new crystallographic face.


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