Cathodic shift of onset potential for water oxidation on a Ti4+doped Fe2O3photoanode by suppressing the back reaction

2014 ◽  
Vol 7 (2) ◽  
pp. 752-759 ◽  
Author(s):  
Dapeng Cao ◽  
Wenjun Luo ◽  
Jianyong Feng ◽  
Xin Zhao ◽  
Zhaosheng Li ◽  
...  
2019 ◽  
Author(s):  
Pradip K. Das ◽  
Sarmistha Bhunia ◽  
Priyanka Chakraborty ◽  
Atanu Rana ◽  
Abhishek Dey ◽  
...  

Water oxidation is the primary step in both natural and artificial photosynthesis to convert solar energy in into chemical fuels. Herein, we report the first cobalt-based pincer catalyst for electrolytic water oxidation at neutral pH with high efficiency under electrochemical conditions. Most importantly, ligand (pseudo)aromaticity is identified to play an important role in the electrocatalysis. A significant potential jump (~300 mV) was achieved towards a lower positive value when the aromatized cobalt complex was transformed to a (pseudo)dearomatized cobalt species. This complex catalyzes the water oxidation in its high valent oxidation state at a much lower overpotential (~ 340 mV vs. NHE) based on the onset potential (0.5 mA/cm<sup>2</sup>) of catalysis at pH 10.5, outperforming all the other literature systems. These observations may provide a new strategy for the design of earth-abundant transition metal-based water oxidation catalysts.


2019 ◽  
Vol 258 ◽  
pp. 117962 ◽  
Author(s):  
Huiwen Lan ◽  
Yujian Xia ◽  
Kun Feng ◽  
Aimin Wei ◽  
Zhenhui Kang ◽  
...  

MRS Advances ◽  
2016 ◽  
Vol 1 (34) ◽  
pp. 2401-2407 ◽  
Author(s):  
Umanga De Silva ◽  
W. P. R. Liyanage ◽  
Manashi Nath

AbstractThe search for high-efficiency and environmentally benign water splitting catalysts has been on the rise since this process is a source of renewable, clean energy. However the process is inherently slow, especially for the production of O2 from H2O (water oxidation) due to the high electron count and energy intensive bond formation of the reaction. Hence the search for novel catalysts for oxygen evolution reactions (OER) has led researchers to focus on various families of compounds including oxides and recently selenides. Multifunctional nanostructures containing the semiconductor electrocatalyst grafted onto an optically active metallic component might boost the catalytic activity even further due to efficient charge injection. Magnetically active catalysts will also be lucrative since that might induce better adhesion of the oxygenated species at the catalytically active site. In this report we introduce multifunctional, magnetic Au3Pd–CoSe nanostructures as high-efficiency OER electrocatalysts. These multifunctional nanostructures were synthesized by a chemical vapor deposition (CVD) reaction with cobalt acetylacetonate and elemental selenium on Au-Pd sputter coated silica substrate at 800°C. The morphology of these multifunctional nanostructures were mostly bifunctional Janus-like nanoparticles as seen through scanning and transmission electron microscopy. They also showed soft ferromagnetic behavior. These bifunctional nanoparticles were coated on the anodes of a water oxidation cell and it was observed that these nanoparticles showed a higher OER activity with lower onset potential for O2 evolution as compared to the conventional oxide-based OER electrocatalysts.


2018 ◽  
Vol 1 (8) ◽  
pp. 4150-4157 ◽  
Author(s):  
Lang Pei ◽  
Bihu Lv ◽  
Shuangbao Wang ◽  
Zhentao Yu ◽  
Shicheng Yan ◽  
...  

2014 ◽  
Vol 176 ◽  
pp. 199-211 ◽  
Author(s):  
Yi-Hsuan Lai ◽  
Masaru Kato ◽  
Dirk Mersch ◽  
Erwin Reisner

This discussion describes a direct comparison of photoelectrochemical (PEC) water oxidation activity between a photosystem II (PSII)-functionalised photoanode and a synthetic nanocomposite photoanode. The semi-biological photoanode is composed of PSII from the thermophilic cyanobacterium Thermosynechococcus elongatus on a mesoporous indium tin oxide electrode (mesoITO|PSII). PSII embeds all of the required functionalities for light absorption, charge separation and water oxidation and ITO serves solely as the electron collector. The synthetic photoanode consists of a TiO2 and NiOx coated nanosheet-structured WO3 electrode (nanoWO3|TiO2|NiOx). The composite structure of the synthetic electrode allows mimicry of the functional key features in PSII: visible light is absorbed by WO3, TiO2 serves as a protection and charge separation layer and NiOx serves as the water oxidation electrocatalyst. MesoITO|PSII uses low energy red light, whereas nanoWO3|TiO2|NiOx requires high energy photons of blue-end visible and UV regions to oxidise water. The electrodes have a comparable onset potential at approximately 0.6 V vs. reversible hydrogen electrode (RHE). MesoITO|PSII reaches its saturation photocurrent at 0.84 V vs. RHE, whereas nanoWO3|TiO2|NiOx requires more than 1.34 V vs. RHE. This suggests that mesoITO|PSII suffers from fewer limitations from charge recombination and slow water oxidation catalysis than the synthetic electrode. MesoITO|PSII displays a higher ‘per active’ site activity, but is less photostable and displays a much lower photocurrent per geometrical surface area and incident photon to current conversion efficiency (IPCE) than nanoWO3|TiO2|NiOx.


2014 ◽  
Vol 2 (19) ◽  
pp. 6727 ◽  
Author(s):  
Ming Li ◽  
Jiujun Deng ◽  
Aiwu Pu ◽  
Pingping Zhang ◽  
Hui Zhang ◽  
...  

2016 ◽  
Vol 18 (15) ◽  
pp. 10453-10458 ◽  
Author(s):  
Jiujun Deng ◽  
Xiaoxin Lv ◽  
Hui Zhang ◽  
Binhua Zhao ◽  
Xuhui Sun ◽  
...  

A significant cathodic shift of the onset potential and an enhancement of the photocurrent density can be found in the FeNiOOH-decorated hematite photoanode.


Nanoscale ◽  
2017 ◽  
Vol 9 (42) ◽  
pp. 16133-16137 ◽  
Author(s):  
Ke Dang ◽  
Xiaoxia Chang ◽  
Tuo Wang ◽  
Jinlong Gong

This paper describes an amorphous nickel boride (NiB) electrocatalyst loaded on porous BiVO4 for photoelectrochemical water oxidation. The NiB/BiVO4 photoanode exhibits an onset potential of 0.25 V versus the reversible hydrogen electrode (vs. RHE) and a photocurrent of 3.47 mA cm−2 at 1.23 V vs. RHE under simulated 100 mW cm−2 irradiation.


Catalysts ◽  
2018 ◽  
Vol 8 (11) ◽  
pp. 497 ◽  
Author(s):  
Lifei Xi ◽  
Kathrin Lange

Solar water splitting is a promising method for producing renewable fuels. Thermodynamically, the overall water splitting reaction is an uphill reaction involving a multiple electron transfer process. The oxygen evolution reaction (OER) has been identified as the bottleneck process. Hematite (α-Fe2O3) is one of the best photoanode material candidates due to its band gap properties and stability in aqueous solution. However, the reported efficiencies of hematite are notoriously lower than the theoretically predicted value mainly due to poor charge transfer and separation ability, short hole diffusion length as well as slow water oxidation kinetics. In this Review Article, several emerging surface modification strategies to reduce the oxygen evolution overpotential and thus to enhance the water oxidation reaction kinetics will be presented. These strategies include co-catalysts loading, photoabsorption enhancing (surface plasmonic metal and rare earth metal decoration), surface passivation layer deposition, surface chemical etching and surface doping. These methods are found to reduce charge recombination happening at surface trapping states, promote charge separation and diffusion, and accelerate water oxidation kinetics. The detailed surface modification methods, surface layer materials, the photoelectrochemical (PEC) performances including photocurrent and onset potential shift as well as the related proposed mechanisms will be reviewed.


2015 ◽  
Vol 3 (35) ◽  
pp. 17977-17982 ◽  
Author(s):  
Wanhong He ◽  
Ruirui Wang ◽  
Lu Zhang ◽  
Jie Zhu ◽  
Xu Xiang ◽  
...  

A multi-functional layered double hydroxide (LDH)-modified BiVO4 photoanode exhibits a tremendous cathodic shift of the onset potential and more than 2-fold enhancement in the oxidation efficiency and IPCE value.


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