Chemistry:Bismuth ferrite

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Bismuth ferrite
Identifiers
3D model (JSmol)
Properties
BiFeO3
Molar mass 312.822 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Bismuth ferrite (BiFeO3, also commonly referred to as BFO in materials science) is an inorganic chemical compound with perovskite structure and one of the most promising multiferroic materials.[1] The room-temperature phase of BiFeO3 is classed as rhombohedral belonging to the space group R3c.[2][3][4] It is synthesized in bulk and thin film form and both its antiferromagnetic (G type ordering) Néel temperature (approximately 653 K) and ferroelectric Curie temperature are well above room temperature (approximately 1100K).[5][6] Ferroelectric polarization occurs along the pseudocubic direction ([math]\displaystyle{ \langle 111\rangle_c }[/math]) with a magnitude of 90–95 μC/cm2.[7][8]

Sample Preparation

Bismuth ferrite is not a naturally occurring mineral and several synthesis routes to obtain the compound have been developed.

Solid state synthesis

In the solid state reaction method[9] bismuth oxide (Bi2O3) and iron oxide (Fe2O3) in a 1:1 mole ratio are mixed with a mortar or by ball milling and then fired at elevated temperatures. Preparation of pure stoichiometric BiFeO3 is challenging due to the volatility of bismuth during firing which leads to the formation of stable secondary Bi25FeO39 (selenite) and Bi2Fe4O9 (mullite) phase. Typically a firing temperature of 800 to 880 Celsius is used for 5 to 60 minutes with rapid subsequent cooling. Excess Bi2O3 has also been used a measure to compensate for bismuth volatility and to avoid formation of the Bi2Fe4O9 phase.

Single crystal growth

Bismuth ferrite melts incongruently, but it can be grown from a bismuth oxide rich flux (e.g. a 4:1:1 mixture of Bi2O3, Fe2O3 and B2O3 at approximately 750-800 Celsius).[2] High quality single crystals have been important for studying the ferroelectric, antiferromagnetic and magnetoelectric properties of bismuth ferrite.

Chemical routes

Wet chemical synthesis routes based on sol-gel chemistry, modified Pechini routes,[10] hydrothermal[11] synthesis and precipitation have been used to prepare phase pure BiFeO3. The advantage of the chemical routes is the compositional homogeneity of the precursors and the reduced loss of bismuth due to the much lower temperatures needed. In sol-gel routes, an amorphous precursor is calcined at 300-600 Celsius to remove organic residuals and to promote crystallization of the bismuth ferrite perovskite phase, while the disadvantage is that the resulting powder must be sintered at high temperature to make a dense polycrystal.

Solution combustion reaction is a low-cost method used to synthesize porous BiFeO3. In this method, a reducing agent (such glycine, citric acid, urea, etc.) and an oxidizing agent (nitrate ions, nitric acid, etc.) are used to generate the reduction-oxidation (RedOx) reaction. The appearance of the flame, and consequently the temperature of the mixture, depends on the oxidizing/reducing agents ratio used.[12] Annealing up to 600 °C is sometimes needed to decompose the bismuth oxo-nitrates generated as intermediates. Since the content of Fe cations in this semiconductor material, Mӧssbauer spectroscopy is a proper technique to detect the presence of a paramagnetic component in the phase.

Thin films

The electric and magnetic properties of high quality epitaxial thin films of bismuth ferrite reported in 2003[1] revived the scientific interest for bismuth ferrite. Epitaxial thin films have the great advantage that their properties can be tuned by processing[13] or chemical doping,[14] and that they can be integrated in electronic circuitry. Epitaxial strain induced by single crystalline substrates with different lattice parameters than bismuth ferrite can be used to modify the crystal structure to monoclinic or tetragonal symmetry and change the ferroelectric, piezoelectric or magnetic properties.[15] Pulsed laser deposition (PLD) is a very common route to epitaxial BiFeO3 films, and SrTiO3 substrates with SrRuO3 electrodes are typically used. Sputtering, molecular-beam epitaxy (MBE),[16] metal organic chemical vapor deposition (MOCVD), atomic layer deposition (ALD), and chemical solution deposition are other methods to prepare epitaxial bismuth ferrite thin films. Apart from its magnetic and electric properties bismuth ferrite also possesses photovoltaic properties which is known as ferroelectric photovoltaic (FPV) effect.

Applications

Being a room temperature multiferroic material and due to its ferroelectric photovoltaic (FPV) effect, bismuth ferrite has several applications in the field of magnetism, spintronics, photovoltaics, etc.

Photovoltaics

In the FPV effect, a photocurrent is generated in a ferroelectric material under illumination and its direction is dependent upon the ferroelectric polarization of that material. The FPV effect has a promising potential as an alternative to conventional photovoltaic devices. But the main hindrance is that a very small photocurrent is generated in ferroelectric materials like LiNbO3,[17] which is due to its large bandgap and low conductivity. In this direction bismuth ferrite has shown a great potential since a large photocurrent effect and above bandgap voltage[18] is observed in this material under illumination. Most of the works using bismuth ferrite as a photovoltaic material has been reported on its thin film form but in a few reports researchers have formed a bilayer structure with other materials like polymers, graphene and other semiconductors. In a report p-i-n heterojunction has been formed with bismuth ferrite nanoparticles along with two oxide based carrier transporting layers.[19] In spite of such efforts the power conversion efficiency obtained from bismuth ferrite is still very low.

References

  1. ↑ 1.0 1.1 Wang, J.; Neaton, B.; Zheng, H.; Nagarajan, V.; Ogale, S. B.; Liu, B.; Viehland, D.; Vaithyanathan, V. et al. (14 March 2003). "Epitaxial BiFeO3 Multiferroic Thin Film Heterostructures". Science 299 (5613): 1719–1722. doi:10.1126/science.1080615. PMID 12637741. Bibcode: 2003Sci...299.1719W. 
  2. ↑ 2.0 2.1 Kubel, Frank; Schmid, Hans (1990). "Structure of a Ferroelectric and Ferroelastic Monodomain Crystal of the Perovskite BiFeO3". Acta Crystallographica B46 (6): 698–702. doi:10.1107/S0108768190006887. http://archive-ouverte.unige.ch/unige:31426. 
  3. ↑ Catalan, Gustau; Scott, James F. (26 June 2009). "Physics and Applications of Bismuth Ferrite". Advanced Materials 21 (24): 2463–2485. doi:10.1002/adma.200802849. http://inside.mines.edu/~zhiwu/research/papers/E09_bfo.pdf. Retrieved 2 February 2012. 
  4. ↑ D. Varshney, A. Kumar, K. Verma, Effect of A site and B site doping on structural, thermal, and dielectric properties of BiFeO3 ceramics, https://doi.org/10.1016/j.jallcom.2011.05.106
  5. ↑ Kiselev, S. V.; Ozerov, R. P.; Zhdanov, G. S. (February 1963). "Detection of magnetic order in ferroelectric BiFeO3 by neutron diffraction". Soviet Physics Doklady 7 (8): 742–744. Bibcode: 1963SPhD....7..742K. 
  6. ↑ Spaldin, Nicola A.; Cheong, Sang-Wook; Ramesh, Ramamoorthy (1 January 2010). "Multiferroics: Past, present, and future". Physics Today 63 (10): 38. doi:10.1063/1.3502547. Bibcode: 2010PhT....63j..38S. http://www.mendeley.com/research/multiferroics-past-present-future-feature/. Retrieved 15 February 2012. 
  7. ↑ Chu, Ying-Hao; Martin, Lane W.; Holcomb, Mikel B.; Ramesh, Ramamoorthy (2007). "Controlling magnetism with multiferroics". Materials Today 10 (10): 16–23. doi:10.1016/s1369-7021(07)70241-9. 
  8. ↑ Seidel, J.; Martin, L. W.; He, Q.; Zhan, Q.; Chu, Y.-H.; Rother, A.; Hawkridge, M. E.; Maksymovych, P. et al. (2009). "Conduction at domain walls in oxide multiferroics". Nature Materials 8 (3): 229–234. doi:10.1038/NMAT2373. PMID 19169247. Bibcode: 2009NatMa...8..229S. 
  9. ↑ Sharma, Poorva; Varshney, Dinesh; Satapathy, S.; Gupta, P.K. (15 January 2014). "Effect of Pr substitution on structural and electrical properties of BiFeO3 ceramics". Materials Chemistry and Physics 143 (2): 629–636. doi:10.1016/j.matchemphys.2013.09.045. 
  10. ↑ Ghosh, Sushmita; Dasgupta, Subrata; Sen, Amarnath; Sekhar Maiti, Himadri (1 May 2005). "Low-Temperature Synthesis of Nanosized Bismuth Ferrite by Soft Chemical Route". Journal of the American Ceramic Society 88 (5): 1349–1352. doi:10.1111/j.1551-2916.2005.00306.x. 
  11. ↑ Han, J.-T.; Huang, Y.-H.; Wu, X.-J.; Wu, C.-L.; Wei, W.; Peng, B.; Huang, W.; Goodenough, J. B. (18 August 2006). "Tunable Synthesis of Bismuth Ferrites with Various Morphologies". Advanced Materials 18 (16): 2145–2148. doi:10.1002/adma.200600072. 
  12. ↑ Ortiz-Quiñonez, José-Luis; Pal, Umapada; Villanueva, Martin Salazar (10 May 2018). "Effects of Oxidizing/Reducing Agent Ratio on Phase Purity, Crystallinity, and Magnetic Behavior of Solution-Combustion-Grown BiFeO Submicroparticles". Inorganic Chemistry 57 (10): 6152–6160. doi:10.1021/acs.inorgchem.8b00755. PMID 29746118. 
  13. ↑ Mei, Antonio B.; Saremi, Sahar; Miao, Ludi; Barone, Matthew; Tang, Yongjian; Zeledon, Cyrus; Schubert, Jürgen; Ralph, Daniel C. et al. (2019-11-01). "Ferroelectric properties of ion-irradiated bismuth ferrite layers grown via molecular-beam epitaxy". APL Materials 7 (11): 111101. doi:10.1063/1.5125809. Bibcode: 2019APLM....7k1101M. 
  14. ↑ Müller, Marvin; Huang, Yen-Lin; Velez, Saul; Ramesh, Ramamoorthy; Fiebig, Manfred; Trassin, Morgan (2021-10-04). "Training the Polarization in Integrated La0.15Bi0.85FeO3-Based Devices". Advanced Materials 33 (52): 2104688. doi:10.1002/adma.202104688. PMID 34606122. 
  15. ↑ Zeches, R. J.; Rossell, M. D.; Zhang, J. X.; Hatt, A. J.; He, Q.; Yang, C.-H.; Kumar, A.; Wang, C. H. et al. (12 November 2009). "A Strain-Driven Morphotropic Phase Boundary in BiFeO3". Science 326 (5955): 977–980. doi:10.1126/science.1177046. PMID 19965507. Bibcode: 2009Sci...326..977Z. http://www.escholarship.org/uc/item/924223fh. 
  16. ↑ Mei, Antonio B.; Tang, Yongjian; Schubert, Jürgen; Jena, Debdeep; Xing, Huili (Grace); Ralph, Daniel C.; Schlom, Darrell G. (2019-07-01). "Self-assembly and properties of domain walls in BiFeO3 layers grown via molecular-beam epitaxy". APL Materials 7 (7): 071101. doi:10.1063/1.5103244. Bibcode: 2019APLM....7g1101M. 
  17. ↑ A. M. Glass, Von der Linde and T. J. Negran, High‐voltage bulk photovoltaic effect and the photorefractive process in LiNbO3,Appl. Phys. Lett.doi:10.1063/1.1655453
  18. ↑ Yang, S.Y.; Seidel, J.; Byrnes, S.J.; Shafer, P.; Yang, C.H.; Rossell, M.D.; Yu, P.; Chu, Y.H. et al. (2010). "Above-Bandgap Voltages from Ferroelectric Photovoltaic Devices.". Nature Nanotechnology 5 (2): 143–147. doi:10.1038/nnano.2009.451. PMID 20062051. Bibcode: 2010NatNa...5..143Y. http://www.escholarship.org/uc/item/6831m90k. 
  19. ↑ Chatterjee, S.; Bera, A.; Pal, A.J. (2014). "p–i–n Heterojunctions with BiFeO3 Perovskite Nanoparticles and p- and n-Type Oxides: Photovoltaic Properties". ACS Applied Materials & Interfaces 6 (22): 20479–20486. doi:10.1021/am506066m. PMID 25350523. https://ir.lib.uwo.ca/cgi/viewcontent.cgi?article=1058&context=biophysicspub. 

https://doi.org/10.1016/j.jallcom.2011.05.106



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