Distinguishing Homogeneous from Heterogeneous Catalysis in Electrode-Driven Water Oxidation with Molecular Iridium Complexes

2011 ◽  
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James D. Blakemore ◽  
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Nicolas Marquet ◽  
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Matthias Bauer ◽  
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Small Science ◽  
2021 ◽  
Vol 1 (11) ◽  
pp. 2170027
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Chang Liu ◽  
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...  

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.


2017 ◽  
Vol 290 ◽  
pp. 10-18 ◽  
Author(s):  
Ilaria Corbucci ◽  
Kevin Ellingwood ◽  
Lucia Fagiolari ◽  
Cristiano Zuccaccia ◽  
Fausto Elisei ◽  
...  

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.


ChemInform ◽  
2014 ◽  
Vol 45 (13) ◽  
pp. no-no
Author(s):  
Aaron K. Vannucci ◽  
Leila Alibabaei ◽  
Mark D. Losego ◽  
Javier J. Concepcion ◽  
Berc Kalanyan ◽  
...  

2020 ◽  
Vol 2020 (10) ◽  
pp. 801-812 ◽  
Author(s):  
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Cornelis J. M. van der Ham ◽  
Velabo Mdluli ◽  
Markus Schmidtendorf ◽  
Helge Müller-Bunz ◽  
...  

2016 ◽  
Vol 128 (28) ◽  
pp. 8075-8079 ◽  
Author(s):  
Xiao Liu ◽  
Yoshifumi Maegawa ◽  
Yasutomo Goto ◽  
Kenji Hara ◽  
Shinji Inagaki

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