Defect engineering of NH2-MIL-88B(Fe) using different monodentate ligands for enhancement of photo-Fenton catalytic performance of acetamiprid degradation

2020 ◽  
Vol 398 ◽  
pp. 125684 ◽  
Author(s):  
Yuexin Wang ◽  
Zhen Zhong ◽  
Yaseen Muhammad ◽  
Hui He ◽  
Zhongxing Zhao ◽  
...  
2019 ◽  
Vol 32 (6) ◽  
pp. 1903915 ◽  
Author(s):  
Yuhang Qi ◽  
Lizhu Song ◽  
Shuxin Ouyang ◽  
Xichen Liang ◽  
Shangbo Ning ◽  
...  

Author(s):  
Zhiying Fan ◽  
Zheng Wang ◽  
Mirza Cokoja ◽  
Roland A. Fischer

A series of Cu(i)-enriched and Lewis basic site-containing defect-engineering MOFs was investigated for significantly enhanced catalytic performance in the click reaction and the A3 coupling.


2017 ◽  
Vol 900 ◽  
pp. 54-57
Author(s):  
Jia Jia Song ◽  
Zhen Feng Huang ◽  
Ji Jun Zou

The catalytic performance strongly relies on the composition, structure, and property of the material used. Earth-abundant tungsten oxides family (WOx≤3) has received considerable attention in photocatalysis, electrochemistry and catalytic hydrogenation due to its highly tunable structure and unique physicochemical properties. Substantial efforts have been made by us to improve the photocatalytic activity of WOx≤3 by enhancing light harvesting, charge transfer and separation, including defect engineering, morphology control, and hetero-junction construction. Additionally, the semiconductor-to-metal transition of WOx≤3 has been found with the increase of defect concentration, suggesting H2 can be activated on them in a similar way of a metal catalyst. As a result, WO2.72 also can function as a versatile and efficient catalyst for the saturation of olefins and selective transform of nitroarenes to anilines.


2020 ◽  
Vol 124 (36) ◽  
pp. 19563-19570
Author(s):  
Ye Yang ◽  
Junyao Li ◽  
Keqiu Chen ◽  
Qin-jun Chen ◽  
Yexin Feng

2019 ◽  
Vol 7 (38) ◽  
pp. 21704-21710 ◽  
Author(s):  
Chengying Guo ◽  
Xuejing Liu ◽  
Lingfeng Gao ◽  
Xiaojing Ma ◽  
Mingzhu Zhao ◽  
...  

Benefited from the optimized activity of active sites, adsorption energy and the proposed electron transfer property, the CoFe2O4 nanosheet with oxygen vacancies exhibited significantly enhanced water splitting catalytic performance.


2019 ◽  
Vol 9 (3) ◽  
pp. 811-821 ◽  
Author(s):  
Zhao-Meng Wang ◽  
Li-Juan Liu ◽  
Bo Xiang ◽  
Yue Wang ◽  
Ya-Jing Lyu ◽  
...  

The catalytic activity decreases as –(SiO)3Mo(OH)(O) > –(SiO)2Mo(O)2 > –(O)4–MoO.


2020 ◽  
Vol 8 (35) ◽  
pp. 18207-18214
Author(s):  
Dongbo Jia ◽  
Lili Han ◽  
Ying Li ◽  
Wenjun He ◽  
Caichi Liu ◽  
...  

A novel, rational design for porous S-vacancy nickel sulfide catalysts with remarkable catalytic performance for alkaline HER.


2016 ◽  
Vol 10 (3) ◽  
pp. 259-270
Author(s):  
Ludmila Matienko ◽  
◽  
Larisa Mosolova ◽  
Vladimir Binyukov ◽  
Gennady Zaikov ◽  
...  

Mechanism of catalysis with binary and triple catalytic systems based on redox inactive metal (lithium) compound {LiSt+L2} and {LiSt+L2+PhOH} (L2=DMF or HMPA), in the selective ethylbenzene oxidation by dioxygen into -phenylethyl hydroperoxide is researched. The results are compared with catalysis by nickel-lithium triple system {NiII(acac)2+LiSt+PhOH} in selective ethylbenzene oxidation to PEH. The role of H-bonding in mechanism of catalysis is discussed. The possibility of the stable supramolecular nanostructures formation on the basis of triple systems, {LiSt+L2+PhOH}, due to intermolecular H-bonds, is researched with the AFM method.


2019 ◽  
Author(s):  
M. Alexander Ardagh ◽  
Manish Shetty ◽  
Anatoliy Kuznetsov ◽  
Qi Zhang ◽  
Phillip Christopher ◽  
...  

Catalytic enhancement of chemical reactions via heterogeneous materials occurs through stabilization of transition states at designed active sites, but dramatically greater rate acceleration on that same active site is achieved when the surface intermediates oscillate in binding energy. The applied oscillation amplitude and frequency can accelerate reactions orders of magnitude above the catalytic rates of static systems, provided the active site dynamics are tuned to the natural frequencies of the surface chemistry. In this work, differences in the characteristics of parallel reactions are exploited via selective application of active site dynamics (0 < ΔU < 1.0 eV amplitude, 10<sup>-6</sup> < f < 10<sup>4</sup> Hz frequency) to control the extent of competing reactions occurring on the shared catalytic surface. Simulation of multiple parallel reaction systems with broad range of variation in chemical parameters revealed that parallel chemistries are highly tunable in selectivity between either pure product, even when specific products are not selectively produced under static conditions. Two mechanisms leading to dynamic selectivity control were identified: (i) surface thermodynamic control of one product species under strong binding conditions, or (ii) catalytic resonance of the kinetics of one reaction over the other. These dynamic parallel pathway control strategies applied to a host of chemical conditions indicate significant potential for improving the catalytic performance of many important industrial chemical reactions beyond their existing static performance.


2020 ◽  
Author(s):  
Adam Sapnik ◽  
Duncan Johnstone ◽  
Sean M. Collins ◽  
Giorgio Divitini ◽  
Alice Bumstead ◽  
...  

<p>Defect engineering is a powerful tool that can be used to tailor the properties of metal–organic frameworks (MOFs). Here, we incorporate defects through ball milling to systematically vary the porosity of the giant pore MOF, MIL-100 (Fe). We show that milling leads to the breaking of metal–linker bonds, generating more coordinatively unsaturated metal sites, and ultimately causes amorphisation. Pair distribution function analysis shows the hierarchical local structure is partially</p><p>retained, even in the amorphised material. We find that the solvent toluene stabilises the MIL-100 (Fe) framework against collapse and leads to a substantial rentention of porosity over the non-stabilised material.</p>


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