Kinetic analysis of photoelectrochemical water oxidation by mesostructured Co-Pi/α-Fe2O3 photoanodes

2016 ◽  
Vol 4 (8) ◽  
pp. 2986-2994 ◽  
Author(s):  
Gerard M. Carroll ◽  
Daniel R. Gamelin

Kinetics measurements are used to clarify the effect of Co-Pi on solar water splitting by Co-Pi/α-Fe2O3 composite photoanodes.

2021 ◽  
Author(s):  
Qijun Meng ◽  
Biaobiao Zhang ◽  
Hao Yang ◽  
Chang Liu ◽  
Yingzheng Li ◽  
...  

Bismuth vanadate (BiVO4) is one of the most fascinating building blocks for the design and assembly of highly efficient artificial photosynthesis devices for solar water splitting. Our recent report has...


2018 ◽  
Vol 6 (32) ◽  
pp. 15593-15602 ◽  
Author(s):  
Zhongyuan Zhou ◽  
Shaolong Wu ◽  
Linling Qin ◽  
Liang Li ◽  
Liujing Li ◽  
...  

Dual-absorber photoelectrodes are attractive candidates for solar water splitting due to their broadened absorption spectrum and improved photovoltage compared to single-absorber systems.


Author(s):  
Bingjun Jin ◽  
Yoonjun Cho ◽  
Cheolwoo Park ◽  
Jeehun Jeong ◽  
Sungsoon Kim ◽  
...  

The photoelectrochemical (PEC) water splitting efficiency is profoundly restricted by the limited light harvesting, rapid charge recombination, and sluggish water oxidation kinetics, in which the construction of a photoelectrode requires...


2018 ◽  
Vol 8 (9) ◽  
pp. 1526 ◽  
Author(s):  
Sangmo Kim ◽  
Nguyen Nguyen ◽  
Chung Bark

Over the past few decades, solar water splitting has evolved into one of the most promising techniques for harvesting hydrogen using solar energy. Despite the high potential of this process for hydrogen production, many research groups have encountered significant challenges in the quest to achieve a high solar-to-hydrogen conversion efficiency. Recently, ferroelectric materials have attracted much attention as promising candidate materials for water splitting. These materials are among the best candidates for achieving water oxidation using solar energy. Moreover, their characteristics are changeable by atom substitute doping or the fabrication of a new complex structure. In this review, we describe solar water splitting technology via the solar-to-hydrogen conversion process. We will examine the challenges associated with this technology whereby ferroelectric materials are exploited to achieve a high solar-to-hydrogen conversion efficiency.


2019 ◽  
Author(s):  
Drialys Cardenas-Morcoso ◽  
Tsvetelina Merdzhanova ◽  
Vladimir Smirnov ◽  
Friedhelm Finger ◽  
Bernhard Kaiser ◽  
...  

2019 ◽  
Vol 9 (17) ◽  
pp. 4588-4597 ◽  
Author(s):  
Truong-Giang Vo ◽  
Hsin-Man Liu ◽  
Chia-Ying Chiang

In this work, the effect of photochemically modifying nanoporous bismuth vanadate in Co2+ solution in acetate buffer (abbreviated as Co–Ac) on water oxidation was thoroughly studied.


2019 ◽  
Vol 7 (39) ◽  
pp. 22274-22278 ◽  
Author(s):  
Chenchen Feng ◽  
Qi Zhou ◽  
Bin Zheng ◽  
Xiang Cheng ◽  
Yajun Zhang ◽  
...  

Spinel-structured NiCo2O4 nanosheets with dual-metal active sites, an ultrathin structure, and abundant oxygen vacancies were decorated for the first time on a BiVO4 photoanode for highly efficient PEC water oxidation.


2020 ◽  
Vol 8 (7) ◽  
pp. 3845-3850 ◽  
Author(s):  
Meirong Huang ◽  
Wenhai Lei ◽  
Min Wang ◽  
Shuji Zhao ◽  
Changli Li ◽  
...  

Large-scale BiVO4 photoanodes were prepared for solar water splitting. A photocurrent density of water oxidation of ∼2.23 mA cm−2 at 1.23 VRHE and ∼0.83% conversion efficiency at 0.65 VRHE were achieved, with <4% decay after 5 h of operation under harsh conditions.


2018 ◽  
Vol MA2018-01 (31) ◽  
pp. 1864-1864
Author(s):  
Chengxiang("CX") Xiang

Renewable hydrogen produced by solar water-splitting has the potential to balance the intermittent nature of the sunlight and support grid-scale energy storage. In a solar-driven water-splitting device, the cathode surface and the anode surface involve hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), which are tightly coupled with each other, that is, whenever one oxygen molecule was produced at the cathode surface, two hydrogen molecules were produced at the anode surface at the same time. In this talk, I will show some recent results on an alternative approach to solar water-splitting, where the electron and proton generated at OER was used to charge an aqueous vanadium solution in a 2.0 M sulfuric acid (pH = -0.16) electrolyte with near unity Faradaic efficiency, rather than being used directly to produce hydrogen at the cathode. The produced V2+ species in the cathode chamber was then passed through a MoCx based catalyst to produce hydrogen and to re-generate V3+ for the subsequent reduction, with an average hydrogen generation efficiency of 85% at different depths of charging. Coupled to a solar tracker, the solar-driven vanadium redox cell was charged outdoors under real-world illumination during the day and discharged at night to produce hydrogen with a daily average solar to hydrogen (STH) conversion efficiency of 5.8%.


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