Cooperative effects of surface and interface treatments in a hematite (α-Fe2O3) photo-anode on its photo-electrochemical performance

Literature Information

Publication Date 2020-01-06
DOI 10.1039/C9SE01081E
Impact Factor 6.367
Authors

Mika Inaba, Woon Yong Sohn


View Original

Abstract

To enhance the efficiency of the oxygen evolution reaction of hematite (α-Fe2O3), we engineered both the surface of the hematite nanorods and the FTO/hematite interface simultaneously with an optimal annealing condition. We demonstrated that the enhancement of the photo-electrochemical performance of the hematite film treated by both methods was not just the summation of the improvements originating from each treatment but showed a significant cooperative effect. We clearly revealed that the strong electric field was effectively induced by the surface P doping with the concentration gradient profile, resulting in band bending even at 0 V vs. RHE. Furthermore, the dead layer was removed by the TiO2 underlayer, giving rise to Fermi level unpinning. We confirmed that the introduction of the TiO2 underlayer unpinning Fermi level enables building on the strength of the intrinsic long-lived holes generated by P doping, which is the origin of the cooperative effect.

Related Literature

The catalytic mechanism of glyceraldehyde 3-phosphate dehydrogenase from Trypanosoma cruzi elucidated via the QM/MM approach

Cláudio Nahum Alves, Jerônimo Lameira, Iñaki Tuñón, Sergio Martí, Vicent Moliner

2013-01-14 Paper

DOI: 10.1039/C3CP43968B

Formation of an electron hole doped film in the α-Fe2O3 photoanode upon electrochemical oxidation‡

Rita Toth, Michael Grätzel, Edwin C. Constable, Artur Braun

2012-10-09 Paper

DOI: 10.1039/C2CP42597A

Nanopatterning by ion implantation through nanoporous alumina masks

Wei Guan, Ian M. Ross, Umananda M. Bhatta, Jay Ghatak, Nianhua Peng, Beverley J. Inkson, Günter Möbus

2013-02-04 Communication

DOI: 10.1039/C3CP50196E

Mechanistic aspects of the linear stabilization of non-stationary electrochemical oscillations

Murilo F. Cabral, Raphael Nagao, Elton Sitta

2012-11-01 Paper

DOI: 10.1039/C2CP42890C

Polymer-regulated epitaxial crystallization of methanofullerene on mica

Lidong Zheng, Jiangang Liu, Yanchun Han

2012-11-05 Paper

DOI: 10.1039/C2CP42614E

Microlens array induced light absorption enhancement in polymer solar cells

Yuqing Chen, Max A. Noack

2013-01-24 Paper

DOI: 10.1039/C3CP50297J

Electron attachment to the dipeptide dialanine: influence of methylation on site selective dissociation reactions

Benjamin Puschnigg, Stefan E. Huber, Michael Probst, Katrin Tanzer, Violaine Vizcaino, Filipe Ferreira da Silva, Paul Scheier, Paulo Limão-Vieira, Stephan Denifl

2013-01-22 Paper

DOI: 10.1039/C3CP44230F

On the methods of calculation of the charge collection efficiency of dye sensitized solar cells

Luca Bertoluzzi, Shuai Ma

2013-02-04 Communication

DOI: 10.1039/C3CP44248A

Tunable photoluminescence from nc-Si/a-SiNx:H quantum dot thin films prepared by ICP-CVD

Basudeb Sain, Debajyoti Das

2013-01-17 Paper

DOI: 10.1039/C3CP43875A

You might also like

Compound Q&A

What industries use 4-(4-tert-Butylphenyl)-1H-pyrazol-3-amine (CAS: 1015845-73-4)?

4-(4-tert-Butylphenyl)-1H-pyrazol-3-amine finds applications in various industri...

1015845-73-44-(4-tert-Butylpheny...
Compound Q&A

What industries use H3TATAB (CAS: 63557-10-8)?

H3TATAB is used in the pharmaceutical industry for the synthesis of certain orga...

63557-10-8H3TATAB
Compound Q&A

What are the main uses of 1-Ethyl-3-fluorobenzene (CAS: 696-39-9)?

1-Ethyl-3-fluorobenzene (CAS: 696-39-9) is primarily used as a precursor in the ...

696-39-91-Ethyl-3-fluorobenz...
Compound Q&A

What are the main uses of 1-(tert-Butoxycarbonyl)-4-(4-methoxyphenyl)pyrrolidine-3-carboxylic acid (CAS: 851484-94-1)?

1-(tert-Butoxycarbonyl)-4-(4-methoxyphenyl)pyrrolidine-3-carboxylic acid is prim...

851484-94-11-(tert-Butoxycarbon...
Compound Q&A

What are the physical and chemical properties of 1-Cyclobutyl-4-piperidinone (CAS: 359880-05-0)?

1-Cyclobutyl-4-piperidinone (CAS: 359880-05-0) is a colorless or white crystalli...

359880-05-01-Cyclobutyl-4-piper...
Compound Q&A

What is Pyridine-2,6-dicarboxylic acid mono-tert-butyl ester (CAS: 575433-76-0)?

Pyridine-2,6-dicarboxylic acid mono-tert-butyl ester (CAS: 575433-76-0) is a che...

575433-76-0Pyridine-2,6-dicarbo...
Compound Q&A

What is the market or research trend for 2,3-Difluorophenylalanine (CAS: 236754-62-4)?

The market for 2,3-Difluorophenylalanine (CAS: 236754-62-4) is growing with incr...

236754-62-42,3-Difluorophenylal...
Compound Q&A

How is (2-Hydroxy-1-naphthyl)boronic acid (CAS: 898257-48-2) typically synthesized?

(2-Hydroxy-1-naphthyl)boronic acid can be synthesized through the reduction of 2...

898257-48-2(2-Hydroxy-1-naphthy...
1315351-28-0tert-Butyl (5-bromo-...
Compound Q&A

Are there alternatives to 5,7-Dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)-4H-chromen-3-yl beta-D-glucopyranoside (CAS: 19833-12-6) in synthesis?

While 5,7-Dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)-4H-chromen-3-yl beta-D-gluc...

19833-12-65,7-Dihydroxy-4-oxo-...
Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.