Oxidative photo-deposition of chromia: tuning the activity for overall water splitting of the Rh/CrOx co-catalyst system

2017 ◽  
Vol 5 (33) ◽  
pp. 17248-17252 ◽  
Author(s):  
J. Menze ◽  
B. Mei ◽  
P. Weide ◽  
M. Muhler

By employing an oxidative photodeposition of CrOx the Rh/CrOx co-catalyst system was prepared on Ga2O3 and Ta2O5 resulting in up to 25% higher overall water splitting activities.

Author(s):  
Baojun Ma ◽  
Yuying Dang ◽  
Dekang Li ◽  
Xiaoyan Wang ◽  
Keying Lin ◽  
...  

2018 ◽  
Vol 6 (17) ◽  
pp. 7871-7876 ◽  
Author(s):  
Chong Wang ◽  
Bin Ma ◽  
Xingzhong Cao ◽  
Shan He ◽  
Jingbin Han ◽  
...  

A bridge-type interface was constructed in a Cu2O@ZnCr-LDH photocatalyst, and it imparts high efficiency for overall water splitting without any co-catalyst.


2019 ◽  
Vol 7 (12) ◽  
pp. 6708-6719 ◽  
Author(s):  
Kyoung-Won Park ◽  
Alexie M. Kolpak

Overall photocatalytic water splitting with a high efficiency has recently been observed for CoO nanoparticle suspensions in the absence of an applied bias or co-catalyst. This study clarifies the mechanism of spontaneous overall water splitting with the prominent efficiency observed on the CoO nanoparticle.


2015 ◽  
Vol 5 (6) ◽  
pp. 3416-3422 ◽  
Author(s):  
Guixia Zhao ◽  
Xiubing Huang ◽  
Federica Fina ◽  
Guan Zhang ◽  
John T. S. Irvine

A mediator-free Z-scheme overall water splitting photocatalyst system is achieved through the use of C3N4 (H2 generation catalyst) and WO3 (O2 generation catalyst) composite from a hydrothermal method, and Pt as co-catalyst under visible light (λ > 420 nm).


ChemistryOpen ◽  
2017 ◽  
Vol 6 (6) ◽  
pp. 701-705 ◽  
Author(s):  
Yang An ◽  
Benyan Xu ◽  
Yuanyuan Liu ◽  
Zeyan Wang ◽  
Peng Wang ◽  
...  

2016 ◽  
Vol 4 (48) ◽  
pp. 18730-18736 ◽  
Author(s):  
Ki-Yong Yoon ◽  
Hyo-Jin Ahn ◽  
Myung-Jun Kwak ◽  
Sun-I. Kim ◽  
Juhyung Park ◽  
...  

We report an efficient Ti-doped FeOOH (Ti-FeOOH) co-catalyst applied on SiOx thin layer coated Ti-doped porous Fe2O3 (Ti-PH) to realize an excellent water splitting photoelectrochemical cell.


Nanoscale ◽  
2018 ◽  
Vol 10 (22) ◽  
pp. 10420-10427 ◽  
Author(s):  
Taizo Yoshinaga ◽  
Masaki Saruyama ◽  
Anke Xiong ◽  
Yeilin Ham ◽  
Yongbo Kuang ◽  
...  

Cobalt doping into a Mn3O4 nanoparticle cocatalyst enhanced photocatalytic water splitting activity of a Mn3O4 cocatalyst/photocatalyst system.


2022 ◽  
Author(s):  
Yang Bai ◽  
Chao Li ◽  
Lunjie Liu ◽  
Yuichi Yamaguchi ◽  
Bahri Mounib ◽  
...  

The production of hydrogen from water via solar water splitting is a potential method to overcome the intermittency of the Sun’s energy by storing it as a chemical fuel. Inorganic semiconductors have been studied extensively as photocatalysts for overall water splitting, but polymer photocatalysts are also receiving growing attention. So far, most studies involving organic polymers report hydrogen production with sacrificial electron donors, which is unsuitable for large-scale hydrogen energy production. Here we show that a linear conjugated polymer photocatalyst can be used for overall water splitting to produce stoichiometric amounts of H2 and O2. We studied a range of different metal co-catalysts in conjunction with the linear polymer photocatalyst, the homopolymer of dibenzo[b,d]thiophene sulfone (P10). Photocatalytic activity was observed for palladium/iridium oxide-loaded P10, while other co-catalysts resulted in materials that showed no activity for overall water splitting. The reaction conditions were further optimized and the overall water splitting using the IrO2-loaded P10 was found to proceed steadily for an extended period (>60 hours) after the system stabilized. These results demonstrate that conjugated polymers can act as single component photocatalytic systems for overall water splitting when loaded with suitable co-catalysts, albeit currently with low activities. Significantly, though, organic polymers can be designed to absorb a large fraction of the visible spectrum, which can be challenging with inorganic catalysts. Transient spectroscopy shows that the IrO2 co-catalyst plays an important role in the generation of the charge separated state required for water splitting, with evidence for fast hole transfer to the co-catalyst. This solid-state approach should be transferable to other polymer photocatalysts, allowing this field to move away from sacrificial hydrogen production towards overall water splitting.


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