scholarly journals Reactivity and Mechanism of Photo- and Electrocatalytic Hydrogen Evolution by a Diimine Copper(I) Complex

Catalysts ◽  
2020 ◽  
Vol 10 (11) ◽  
pp. 1302
Author(s):  
Maria Drosou ◽  
Fotios Kamatsos ◽  
George Ioannidis ◽  
Athanasios Zarkadoulas ◽  
Christiana A. Mitsopoulou ◽  
...  

The tetrahedral copper(I) diimine complex [Cu(pq)2]BF4 displays high photocatalytic activity for the H2 evolution reaction with a turnover number of 3564, thus representing the first type of a Cu(I) quinoxaline complex capable of catalyzing proton reduction. Electrochemical experiments indicate that molecular mechanisms prevail and DFT calculations provide in-depth insight into the catalytic pathway, suggesting that the coordinating nitrogens play crucial roles in proton exchange and hydrogen formation.

2014 ◽  
Vol 5 ◽  
pp. 360-364 ◽  
Author(s):  
Jun Fang ◽  
Lisha Yin ◽  
Shaowen Cao ◽  
Yusen Liao ◽  
Can Xue

Pt@TiO2 core–shell nanostructures were prepared through a hydrothermal method. The dye-sensitization of these Pt@TiO2 core–shell structures allows for a high photocatalytic activity for the generation of hydrogen from proton reduction under visible-light irradiation. When the dyes and TiO2 were co-excited through the combination of two irradiation beams with different wavelengths, a synergic effect was observed, which led to a greatly enhanced H2 generation yield. This is attributed to the rational spatial distribution of the three components (dye, TiO2, Pt), and the vectored transport of photogenerated electrons from the dye to the Pt particles via the TiO2 particle bridge.


2009 ◽  
Vol 421-422 ◽  
pp. 554-557
Author(s):  
Soihiro Watanabe ◽  
Yousuke Narumi ◽  
Kenji Toda ◽  
Tadashi Ishigaki ◽  
Kazuyoshi Uematsu ◽  
...  

We synthesized Sr0.7La0.2[ ]0.1Bi2Ta2O9 (SBTL , [ ] vacancy), and measured their photocatalytic activity for water decomposition under UV light irradiation after acid treatment. They showed the high photocatalytic activity under UV light irradiation (H2 evolution (213μmol / h) , O2 evolution (82μmol / h)).


Author(s):  
Qiuchen Wang ◽  
Jun Ma ◽  
Gen Li ◽  
Tianxiang Zhao ◽  
Peng Chen ◽  
...  

Simultaneous photocatalytic reactions of H2 evolution and real wastewater degradation have drawn much attention to practical energy and environmental applications. While these applications of photocatalyst often suffer from the high...


2017 ◽  
Vol 46 (32) ◽  
pp. 10630-10634 ◽  
Author(s):  
Mei-Yan Gao ◽  
Shumei Chen ◽  
Lan-Xia Hu ◽  
Lei Zhang ◽  
Jian Zhang

This work reveals an interesting Ti–Cec system with various structures, where PTC-91 and PTC-94 have good photocatalytic activity and stability in water-splitting hydrogen evolution.


2011 ◽  
Vol 233-235 ◽  
pp. 1646-1649 ◽  
Author(s):  
Wen Quan Cui ◽  
Yue Li Qi ◽  
Jun Cheng ◽  
Jin Shan Hu ◽  
Ying Hua Liang

Pt/K2La2Ti3O10 was prepared by impregnating K2La2Ti3O10 into H2PtCl6 solution. The structure of the photocatalyst was studied by means of XRD, UV-Vis spectroscopy and XPS. And the photocatalytic activities of the samples were examined in a Pyrex reaction cell by splitting methanol solution. The result revealed that Pt/K2La2Ti3O10 photocatalyst showed much higher activity than pure K2La2Ti3O10 and kept a high photocatalytic activity even after 120 hours of illumination. XPS showed that the valence state of Pt was reduced from Ptto Pt0 during the illumination.


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