Phosphines in artificial photosynthesis: considering different aspects such as chromophores, water reduction catalysts (WRCs), water oxidation catalysts (WOCs), and dyads

2019 ◽  
Vol 3 (11) ◽  
pp. 2926-2953 ◽  
Author(s):  
J. Pann ◽  
H. Roithmeyer ◽  
W. Viertl ◽  
R. Pehn ◽  
M. Bendig ◽  
...  

Coordination complex systems containing phosphine ligands are used in artificial photosynthesis utilizing their unique stereoelectronic properties. Mono-, di- and tetraphosphines act as optimized ligand systems for complexation.

2019 ◽  
Vol 215 ◽  
pp. 141-161 ◽  
Author(s):  
Wolfgang Viertl ◽  
Johann Pann ◽  
Richard Pehn ◽  
Helena Roithmeyer ◽  
Marvin Bendig ◽  
...  

A pincer type ligand provides an additional coordination site or a proton relay depending on the metal oxidation state.


Inorganics ◽  
2019 ◽  
Vol 7 (3) ◽  
pp. 29 ◽  
Author(s):  
Christos Mavrokefalos ◽  
Greta Patzke

The expected shortage of fossil fuels as well as the accompanying climate change are among the major challenges of the 21st century. A global shift to a sustainable energy landscape is, therefore, of utmost importance. Over the past few years, solar technologies have entered the energy market and have paved the way to replace fossil-based energy sources, in the long term. In particular, electrochemical solar-to-hydrogen technologies have attracted a lot of interest—not only in academia, but also in industry. Solar water splitting (artificial photosynthesis) is one of the most active areas in contemporary materials and catalysis research. The development of low-cost, efficient, and stable water oxidation catalysts (WOCs) remains crucial for artificial photosynthesis applications, because WOCs still represent a major economical and efficient bottleneck. In the following, we summarize recent advances in water oxidation catalysts development, with selected examples from 2016 onwards. This condensed survey demonstrates that the ongoing quest for new materials and informed catalyst design is a dynamic and rapidly developing research area.


Author(s):  
Ravi Kumar Kunchala ◽  
Pushpendra . ◽  
Rimple Kalia ◽  
Sanyasinaidu Boddu

Artificial photosynthesis is a promising method that directly transforms solar energy into chemical energy. To achieve artificial photosynthesis, efficient water oxidation catalysts (WOCs) are essential. In nature, the manganese-oxo-calcium cluster...


2021 ◽  
Author(s):  
Yuta Tsubonouchi ◽  
Eman A. Mohamed ◽  
Zaki N. Zahran ◽  
Masayuki Yagi

Polypyridyl ruthenium(II) complexes have been widely researched as promising functional molecules. We have found unique photoisomerization reactions of polypyridyl ruthenium(II) aquo complexes. Recently we have attempted to provide insight into the mechanism of the photoisomerization of the complexes and distinguish between the distal−/proximal-isomers in their physicochemical properties and functions. Moreover, polypyridyl ruthenium(II) aquo complexes have been intensively studied as active water oxidation catalysts (WOCs) which are indispensable for artificial photosynthesis. The catalytic aspect and mechanism of water oxidation by the distal-/proximal-isomers of polypyridyl ruthenium(II) aquo complexes have been investigated to provide the guided thought to develop more efficient molecular catalysts for water oxidation. The recent progress on the photoisomerization and water oxidation of polypyridyl ruthenium(II) aquo complexes in our group are reviewed to understand the properties and functions of ruthenium complexes.


2019 ◽  
Vol 31 (50) ◽  
pp. 1902069 ◽  
Author(s):  
Sheng Ye ◽  
Chunmei Ding ◽  
Mingyao Liu ◽  
Aoqi Wang ◽  
Qinge Huang ◽  
...  

2021 ◽  
Vol 60 (3) ◽  
pp. 1806-1813
Author(s):  
Husain N. Kagalwala ◽  
Mahesh S. Deshmukh ◽  
Elamparuthi Ramasamy ◽  
Neelima Nair ◽  
Rongwei Zhou ◽  
...  

Solar RRL ◽  
2021 ◽  
Author(s):  
Matthew V. Sheridan ◽  
Benjamin D. Sherman ◽  
Yi Xie ◽  
Ying Wang

Inorganics ◽  
2018 ◽  
Vol 6 (4) ◽  
pp. 105 ◽  
Author(s):  
Laurent Sévery ◽  
Sebastian Siol ◽  
S. Tilley

Anchored molecular catalysts provide a good step towards bridging the gap between homogeneous and heterogeneous catalysis. However, applications in an aqueous environment pose a serious challenge to anchoring groups in terms of stability. Ultrathin overlayers embedding these catalysts on the surface using atomic layer deposition (ALD) are an elegant solution to tackle the anchoring group instability. The propensity of ALD precursors to react with water leads to the question whether molecules containing aqua ligands, such as most water oxidation complexes, can be protected without side reactions and deactivation during the deposition process. We synthesized two iridium and two ruthenium-based water oxidation catalysts, which contained an aqua ligand (Ir–OH2 and Ru–OH2) or a chloride (Ir–Cl and Ru–Cl) that served as a protecting group for the former. Using a ligand exchange reaction on the anchored and partially embedded Ru–Cl, the optimal overlayer thickness was determined to be 1.6 nm. An electrochemical test of the protected catalysts on meso-ITO showed different behaviors for the Ru and the Ir catalysts. The former showed no onset difference between protected and non-protected versions, but limited stability. Ir–Cl displayed excellent stability, whilst the unprotected catalyst Ir–OH2 showed a later initial onset. Self-regeneration of the catalytic activity of Ir–OH2 under operating conditions was observed. We propose chloride ligands as generally applicable protecting groups for catalysts that are to be stabilized on surfaces using ALD.


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