Ferroelectric BiFeO3as an Oxide Dye in Highly Tunable Mesoporous All-Oxide Photovoltaic Heterojunctions
Type
ArticleKAUST Department
Materials Science and Engineering ProgramDate
2016-10-12Permanent link to this record
http://hdl.handle.net/10754/621629
Metadata
Show full item recordAbstract
As potential photovoltaic materials, transition-metal oxides such as BiFeO3 (BFO) are capable of absorbing a substantial portion of solar light and incorporating ferroic orders into solar cells with enhanced performance. But the photovoltaic application of BFO has been hindered by low energy-conversion efficiency due to poor carrier transport and collection. In this work, a new approach of utilizing BFO as a light-absorbing sensitizer is developed to interface with charge-transporting TiO2 nanoparticles. This mesoporous all-oxide architecture, similar to that of dye-sensitized solar cells, can effectively facilitate the extraction of photocarriers. Under the standard AM1.5 (100 mW cm−2) irradiation, the optimized cell shows an open-circuit voltage of 0.67 V, which can be enhanced to 1.0 V by tailoring the bias history. A fill factor of 55% is achieved, which is much higher than those in previous reports on BFO-based photovoltaic devices. The results provide here a new viable approach toward developing highly tunable and stable photovoltaic devices based on ferroelectric transition-metal oxides.Citation
Wang L, Ma H, Chang L, Ma C, Yuan G, et al. (2016) Ferroelectric BiFeO3as an Oxide Dye in Highly Tunable Mesoporous All-Oxide Photovoltaic Heterojunctions. Small. Available: http://dx.doi.org/10.1002/smll.201602355.Sponsors
This work was supported by King Abdullah University of Science and Technology (KAUST). L.C. and J.W. acknowledge support from the Ministry of Education, Singapore under Project Nos. MOE2013-T2-1-052 and AcRF Tier 1 RG126/14. H.M. and G.Y. also acknowledge for the support from the National Natural Science Foundation of China (11134004).Publisher
Wiley-BlackwellJournal
SmallISSN
1613-6810Additional Links
http://onlinelibrary.wiley.com/doi/10.1002/smll.201602355ae974a485f413a2113503eed53cd6c53
10.1002/smll.201602355