Hydrogen Bonded Metal–Organic Supramolecule Functionalized BiVO4 Photoanode for Enhanced Water Oxidation Efficiency

2021 ◽  
pp. 130092
Author(s):  
Yun-Xiang Ma ◽  
Bin Gao ◽  
Jianping He ◽  
Jian-Fang Ma ◽  
Yanli Zhao
2021 ◽  
Vol 233 ◽  
pp. 01078
Author(s):  
Shuwei Zhang ◽  
Zhaoyu Wang ◽  
Xuejiao Yan ◽  
Jing Wang ◽  
Li Zhang ◽  
...  

Total organic carbon (TOC) can reflect the total amount of organic matter in water. This paper introduces the common methods of measuring organic carbon, including high temperature combustion method, potassium persulfate oxidation method, spectrometry, ozone oxidation chemiluminescence method, supercritical water oxidation method and so on. At present, high temperature combustion method is the most widely used method for TOC measurement in seawater, because of its high oxidation efficiency. TOC sensor needs to be developed to realize in-situ and long-term monitoring.


Author(s):  
Ferdinando Costantino ◽  
Alceo Macchioni ◽  
Giordano Gatto ◽  
Roberto Bondi ◽  
Fabio Marmottini

Clean production of renewable fuels is a great challenge of our scientific community. Iridium complexes have demonstrated a superior catalytic activity in the water oxidation (WO) reaction, which is a crucial step in water splitting process. Herein we have used a defective zirconium MOF with UiO-66 structure as support of a highly active Ir complex based on EDTA with formula [Ir(HEDTA)Cl]Na. The defects are induced by the partial substitution of tereftalic acid with smaller formiate groups. Anchoring of the complex occurs through a post-synthetic exchange of formiate anions, coordinated at the zirconium clusters of the MOF, with the free carboxylate group of the [Ir(HEDTA)Cl]-complex. The modified material was tested as heterogenous catalyst for the WO reaction by using Cerium Ammonium Nitrate as sacrificial agent. Although TOF and TON values are comparable to those of other iridium heterogenized catalysts, the MOF exhibits iridium leaching not limited at the first catalytic run, as usually observed, suggesting a lack of stability of the hybrid system under strong oxidative conditions.


2018 ◽  
Vol 140 (14) ◽  
pp. 4940-4944 ◽  
Author(s):  
Qianli Chu ◽  
Andrew J. E. Duncan ◽  
Giannis S. Papaefstathiou ◽  
Tamara D. Hamilton ◽  
Manza B. J. Atkinson ◽  
...  

Author(s):  
Hyein Park ◽  
Minjung Kang ◽  
Dong Won Kang ◽  
Chang Seop Hong

While preferential adsorption of ethane (C2H6) over ethylene (C2H4) is more advantageous in industrial separation technology, most porous materials such as metal-organic frameworks, covalent-organic frameworks, and hydrogen-bonded organic frameworks provide...


Inorganics ◽  
2019 ◽  
Vol 7 (10) ◽  
pp. 123 ◽  
Author(s):  
Giordano Gatto ◽  
Alceo Macchioni ◽  
Roberto Bondi ◽  
Fabio Marmottini ◽  
Ferdinando Costantino

Clean production of renewable fuels is a great challenge of our scientific community. Iridium complexes have demonstrated a superior catalytic activity in the water oxidation (WO) reaction, which is a crucial step in water splitting process. Herein, we have used a defective zirconium metal–organic framework (MOF) with UiO-66 structure as support of a highly active Ir complex based on EDTA with the formula [Ir(HEDTA)Cl]Na. The defects are induced by the partial substitution of terephthalic acid with smaller formate groups. Anchoring of the complex occurs through a post-synthetic exchange of formate anions, coordinated at the zirconium clusters of the MOF, with the free carboxylate group of the [Ir(HEDTA)Cl]− complex. The modified material was tested as a heterogeneous catalyst for the WO reaction by using cerium ammonium nitrate (CAN) as the sacrificial agent. Although turnover frequency (TOF) and turnover number (TON) values are comparable to those of other iridium heterogenized catalysts, the MOF exhibits iridium leaching not limited at the first catalytic run, as usually observed, suggesting a lack of stability of the hybrid system under strong oxidative conditions.


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