Foreign In3+ treatment improving the photoelectrochemical performance of a hematite nanosheet array for water splitting

Nanoscale ◽  
2017 ◽  
Vol 9 (44) ◽  
pp. 17513-17523 ◽  
Author(s):  
Xianbao Bu ◽  
Guo Wang ◽  
Yang Tian

Foreign In3+ treatment enhances the PEC activity of water oxidation for the hematite nanosheet array.

2019 ◽  
Vol 14 (1) ◽  
Author(s):  
Zhou Cao ◽  
Yanling Yin ◽  
Peng Fu ◽  
Dong Li ◽  
Yulan Zhou ◽  
...  

Abstract Converting solar energy into sustainable hydrogen fuel by photoelectrochemical (PEC) water splitting is a promising technology to solve increasingly serious global energy supply and environmental issues. However, the PEC performance based on TiO2 nanomaterials is hindered by the limited sunlight-harvesting ability and its high recombination rate of photogenerated charge carriers. In this work, layered SnS2 absorbers and CoOx nanoparticles decorated two-dimensional (2D) TiO2 nanosheet array photoelectrode have been rationally designed and successfully synthesized, which remarkably enhanced the PEC performance for water splitting. As the result, photoconversion efficiency of TiO2/SnS2/CoOx and TiO2/SnS2 hybrid photoanodes increases by 3.6 and 2.0 times under simulated sunlight illumination, compared with the bare TiO2 nanosheet arrays photoanode. Furthermore, the TiO2/SnS2/CoOx photoanode also presented higher PEC stability owing to CoOx catalyst served as efficient water oxidation catalyst as well as an effective protectant for preventing absorber photocorrosion.


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.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Ki-Yong Yoon ◽  
Juhyung Park ◽  
Minsu Jung ◽  
Sang-Geun Ji ◽  
Hosik Lee ◽  
...  

AbstractTo boost the photoelectrochemical water oxidation performance of hematite photoanodes, high temperature annealing has been widely applied to enhance crystallinity, to improve the interface between the hematite-substrate interface, and to introduce tin-dopants from the substrate. However, when using additional dopants, the interaction between the unintentional tin and intentional dopant is poorly understood. Here, using germanium, we investigate how tin diffusion affects overall photoelectrochemical performance in germanium:tin co-doped systems. After revealing that germanium is a better dopant than tin, we develop a facile germanium-doping method which suppresses tin diffusion from the fluorine doped tin oxide substrate, significantly improving hematite performance. The NiFeOx@Ge-PH photoanode shows a photocurrent density of 4.6 mA cm−2 at 1.23 VRHE with a low turn-on voltage. After combining with a perovskite solar cell, our tandem system achieves 4.8% solar-to-hydrogen conversion efficiency (3.9 mA cm−2 in NiFeOx@Ge-PH/perovskite solar water splitting system). Our work provides important insights on a promising diagnostic tool for future co-doping system design.


Author(s):  
Wanqing Fang ◽  
Ai Qin ◽  
Yimin Lin ◽  
Rongzi Xv ◽  
Li Fu

BiVO4 is one of the most attractive photoanode materials for photoelectrochemical water splitting. Herein, cobalt phosphate (CoPi) modified BiVO4 (BiVO4/CoPi) photoanode is prepared by electrodeposition. The physical and chemical characterization...


Nanoscale ◽  
2018 ◽  
Vol 10 (3) ◽  
pp. 1153-1161 ◽  
Author(s):  
Ming Li ◽  
Xinglong Tu ◽  
Yanjie Su ◽  
Jing Lu ◽  
Jing Hu ◽  
...  

A facile solvothermal method is proposed for the controllable growth of vertically aligned In2S3 nanosheet arrays, which show remarkably enhanced photoelectrochemical performance for water oxidation after forming a heterojunction with ZnO.


2020 ◽  
Vol 49 (3) ◽  
pp. 588-592 ◽  
Author(s):  
Fusheng Li ◽  
Ziqi Zhao ◽  
Hao Yang ◽  
Dinghua Zhou ◽  
Yilong Zhao ◽  
...  

A cobalt oxide catalyst prepared by a flame-assisted deposition method on the surface of FTO and hematite for electrochemical and photoelectrochemical water oxidation, respectively.


2019 ◽  
Author(s):  
Jiajia Tao ◽  
Hong-Ping Ma ◽  
Kaiping Yuan ◽  
Yang Gu ◽  
Jianwei Lian ◽  
...  

<div>As a promising oxygen evolution reaction semiconductor, TiO2 has been extensively investigated for solar photoelectrochemical water splitting. Here, a highly efficient and stable strategy for rationally preparing GaON cocatalysts on TiO2 by atomic layer deposition is demonstrated, which we show significantly enhances the</div><div>photoelectrochemical performance compared to TiO2-based photoanodes. For TiO2@20 nm-GaON core-shell nanowires a photocurrent density up to 1.10 mA cm-2 (1.23 V vs RHE) under AM 1.5 G irradiation (100 mW cm-2) has been achieved, which is 14 times higher than that of TiO2 NWs. Furthermore, the oxygen vacancy formation on GaON as well as the band gap matching with TiO2 not only provides more active sites for water oxidation but also enhances light absorption to promote interfacial charge separation and migration. Density functional theory studies of model systems of GaON-modified TiO2 confirm the band gap reduction, high reducibility and ability to activate water. The highly efficient and stable systems of TiO2@GaON core-shell nanowires provide a deeper understanding and universal strategy for enhancing photoelectrochemical performance of photoanodes now available. </div>


RSC Advances ◽  
2021 ◽  
Vol 11 (15) ◽  
pp. 8751-8758
Author(s):  
Xiaonong Wang ◽  
Xiaoxia Li ◽  
Jingxiang Low

Photocatalytic water splitting provides an effective way to prepare hydrogen and oxygen.


Author(s):  
Di Li ◽  
Yingying Xing ◽  
Changjian Zhou ◽  
Yikai Lu ◽  
Shengjie Xu ◽  
...  

The high reaction energy barrier of the oxygen evolution reaction (OER) extremely reduces the efficiency of water splitting, which is not conducive to large-scale production of hydrogen. Due to the...


2019 ◽  
Vol 48 (31) ◽  
pp. 11934-11940 ◽  
Author(s):  
Jianmin Wang ◽  
Yunan Wang ◽  
Xinchao Xv ◽  
Yan Chen ◽  
Xi Yang ◽  
...  

Defective Fe3+ self-doped spinel ZnFe2O4 with abundant oxygen vacancies exhibits largely enhanced photoelectrochemical performance.


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