Electrodeposited Co-Doped Fe3O4 Thin Films as Efficient Catalysts for the Oxygen Evolution Reaction. (20th August 2016)
- Record Type:
- Journal Article
- Title:
- Electrodeposited Co-Doped Fe3O4 Thin Films as Efficient Catalysts for the Oxygen Evolution Reaction. (20th August 2016)
- Main Title:
- Electrodeposited Co-Doped Fe3O4 Thin Films as Efficient Catalysts for the Oxygen Evolution Reaction
- Authors:
- Han, Shan
Liu, Suqin
Yin, Shengjie
Chen, Lei
He, Zhen - Abstract:
- Abstract: The development of highly active electrocatalysts at a low cost is essential to the process of generating hydrogen fuel through electrochemical and photoelectrochemical water splitting. Here, we report a comprehensive investigation of the one-step electrodeposited cobalt-doped magnetite (Cox Fe3-x O4, 0 < x < 1) thin films as active and stable OER catalysts in alkaline solutions. The Cox Fe3-x O4 thin film electrode can be fabricated in minutes or even tens of seconds. The Co-doping concentration, thickness, and orientation of the Cox Fe3-x O4 films can be simply controlled by varying the deposition potential, deposition time, and the substrate, respectively. The dependences of the catalytic activity of the Cox Fe3-x O4 films on the composition, thickness, and orientation of growth are explored. The Cox Fe3-x O4 films exhibit greatly enhanced catalytic activities toward the OER compared to the Fe3 O4 thin film. The polycrystalline Cox Fe3-x O4 film deposited at −0.88 VAg/AgCl for 150 seconds exhibits the highest catalytic activity with an overpotential of ∼0.42 V at a current density of 10 mA cm −2, a Tafel slope of 53 mV dec −1, and an exchange current density of about 2.39 × 10 −10 A cm −2, which are comparable to those of Co3 O4 . Besides, the Cox Fe3-x O4 films possess good stability during the long-term electrolysis at a current density of 10 mA cm −2 in 1 M NaOH. The satisfactory catalytic activity and stability combined with the simplicity of fabricationAbstract: The development of highly active electrocatalysts at a low cost is essential to the process of generating hydrogen fuel through electrochemical and photoelectrochemical water splitting. Here, we report a comprehensive investigation of the one-step electrodeposited cobalt-doped magnetite (Cox Fe3-x O4, 0 < x < 1) thin films as active and stable OER catalysts in alkaline solutions. The Cox Fe3-x O4 thin film electrode can be fabricated in minutes or even tens of seconds. The Co-doping concentration, thickness, and orientation of the Cox Fe3-x O4 films can be simply controlled by varying the deposition potential, deposition time, and the substrate, respectively. The dependences of the catalytic activity of the Cox Fe3-x O4 films on the composition, thickness, and orientation of growth are explored. The Cox Fe3-x O4 films exhibit greatly enhanced catalytic activities toward the OER compared to the Fe3 O4 thin film. The polycrystalline Cox Fe3-x O4 film deposited at −0.88 VAg/AgCl for 150 seconds exhibits the highest catalytic activity with an overpotential of ∼0.42 V at a current density of 10 mA cm −2, a Tafel slope of 53 mV dec −1, and an exchange current density of about 2.39 × 10 −10 A cm −2, which are comparable to those of Co3 O4 . Besides, the Cox Fe3-x O4 films possess good stability during the long-term electrolysis at a current density of 10 mA cm −2 in 1 M NaOH. The satisfactory catalytic activity and stability combined with the simplicity of fabrication make the electrodeposited Cox Fe3-x O4 films economically and environmentally preferable compared to Co3 O4 as catalysts for the oxygen evolution reaction. … (more)
- Is Part Of:
- Electrochimica acta. Volume 210(2016)
- Journal:
- Electrochimica acta
- Issue:
- Volume 210(2016)
- Issue Display:
- Volume 210, Issue 2016 (2016)
- Year:
- 2016
- Volume:
- 210
- Issue:
- 2016
- Issue Sort Value:
- 2016-0210-2016-0000
- Page Start:
- 942
- Page End:
- 949
- Publication Date:
- 2016-08-20
- Subjects:
- electrodeposition -- CoxFe3-xO4 -- catalytic activity -- oxygen evolution reaction -- thin film
Electrochemistry -- Periodicals
Electrochemistry, Industrial -- Periodicals
541.37 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00134686 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.electacta.2016.05.194 ↗
- Languages:
- English
- ISSNs:
- 0013-4686
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3698.950000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 7553.xml