Abstract

A novel method for preparation of BiFeO3 films via a simple solution-based CVD method is reported using for the first time a single-source heterobimetallic precursor [CpFe(CO)2BiCl2]. BiFeO3 films display ferroelectric and ferromagnetic ordering at room temperature and possess direct band-gaps between 2.0 and 2.2 eV. Photocatalytic testing for water oxidation revealed high activities under UVA (365 nm) and simulated solar irradiation, superior to that exhibited by a commercial standard (Pilkington Activ® TiO2 film) resulting in an apparent quantum yield of ∼24%.

Highlights

  • Water photolysis for H2 fuel generation has the potential to meet increasing energy demands whilst reducing the emission of harmful greenhouse gases into the atmosphere

  • Photocatalytic testing for water oxidation revealed high activities under UVA (365 nm) and simulated solar irradiation, superior to that exhibited by a commercial standard (Pilkington Activ® TiO2 film) resulting in an apparent quantum yield of $24%

  • AACVD of [CpFe(CO)2BiCl2] in THF solvent at a substrate temperature of 300 C resulted in the formation of adherent dark orange lms, passing the Scotch tape test, with complete substrate coverage

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Summary

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A simple, low-cost CVD route to thin films of BiFeO3 for efficient water photo-oxidation†. Blackman,*a Junwang Tang,b Paul Southern,c Paul M. A novel method for preparation of BiFeO3 films via a simple solutionbased CVD method is reported using for the first time a single-source heterobimetallic precursor [CpFe(CO)2BiCl2]. BiFeO3 films display ferroelectric and ferromagnetic ordering at room temperature and possess direct band-gaps between 2.0 and 2.2 eV. Photocatalytic testing for water oxidation revealed high activities under UVA (365 nm) and simulated solar irradiation, superior to that exhibited by a commercial standard (Pilkington Activ® TiO2 film) resulting in an apparent quantum yield of $24%

Introduction
Photocatalytic oxygen evolution
Results and discussion
Photoelectrochemical measurements
Solar lamp
Full Text
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