Photovoltaic effects in BiFeO3
14 Aug 2009-Applied Physics Letters (American Institute of Physics)-Vol. 95, Iss: 6, pp 062909-062909
TL;DR: In this article, the photovoltaic effect in ferroelectric BiFeO3 thin films was reported and the all-oxide heterostructures with SrRuO3 bottom and tin doped indium oxide top electrodes were characterized by open-circuit voltages ∼08-09V and external quantum efficiencies up to ∼10% when illuminated with the appropriate light.
Abstract: We report a photovoltaic effect in ferroelectric BiFeO3 thin films The all-oxide heterostructures with SrRuO3 bottom and tin doped indium oxide top electrodes are characterized by open-circuit voltages ∼08–09 V and external quantum efficiencies up to ∼10% when illuminated with the appropriate light Efficiencies are at least an order of magnitude larger than the maximum efficiency under sunlight (AM 15) thus far reported for ferroelectric-based devices The dependence of the measured open-circuit voltage on film thickness suggests contributions to the large open-circuit voltage from both the ferroelectric polarization and band offsets at the BiFeO3/tin doped indium oxide interface
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TL;DR: The ability of KBNNO to absorb three to six times more solar energy than the current ferroElectric materials suggests a route to viable ferroelectric semiconductor-based cells for solar energy conversion and other applications.
Abstract: Most known ferroelectric photovoltaic materials have very wide electronic bandgaps (that is, they absorb only high-energy photons) but here a family of perovskite oxides is described that have tunable bandgaps, allowing their use across the whole visible-light spectrum. The spontaneous electrical polarization that characterizes a ferroelectric material is attractive for solar-cell applications as the positive and negative charges generated by light absorption have a natural tendency to separate, making them easier to harvest efficiently. Unfortunately most known ferroelectrics have wide electronic bandgaps — that is they absorb only higher energy photons that make up a small fraction of the solar spectrum. Ilya Grinberg and colleagues now show that a classic ferroelectric can be chemically engineered to tune the bandgap over a broad range, achieving strong absorption and photocurrent generation across the solar spectrum. Ferroelectrics have recently attracted attention as a candidate class of materials for use in photovoltaic devices, and for the coupling of light absorption with other functional properties1,2,3,4,5,6,7. In these materials, the strong inversion symmetry breaking that is due to spontaneous electric polarization promotes the desirable separation of photo-excited carriers and allows voltages higher than the bandgap, which may enable efficiencies beyond the maximum possible in a conventional p–n junction solar cell2,6,8,9,10. Ferroelectric oxides are also stable in a wide range of mechanical, chemical and thermal conditions and can be fabricated using low-cost methods such as sol–gel thin-film deposition and sputtering3,5. Recent work3,5,11 has shown how a decrease in ferroelectric layer thickness and judicious engineering of domain structures and ferroelectric–electrode interfaces can greatly increase the current harvested from ferroelectric absorber materials, increasing the power conversion efficiency from about 10−4 to about 0.5 per cent. Further improvements in photovoltaic efficiency have been inhibited by the wide bandgaps (2.7–4 electronvolts) of ferroelectric oxides, which allow the use of only 8–20 per cent of the solar spectrum. Here we describe a family of single-phase solid oxide solutions made from low-cost and non-toxic elements using conventional solid-state methods: [KNbO3]1 − x[BaNi1/2Nb1/2O3 − δ]x (KBNNO). These oxides exhibit both ferroelectricity and a wide variation of direct bandgaps in the range 1.1–3.8 electronvolts. In particular, the x = 0.1 composition is polar at room temperature, has a direct bandgap of 1.39 electronvolts and has a photocurrent density approximately 50 times larger than that of the classic ferroelectric (Pb,La)(Zr,Ti)O3 material. The ability of KBNNO to absorb three to six times more solar energy than the current ferroelectric materials suggests a route to viable ferroelectric semiconductor-based cells for solar energy conversion and other applications.
1,041 citations
TL;DR: In this paper, a brief history of perovskite materials for photovoltaic applications is reported, the current state-of-the-art is distilled and the basic working mechanisms have been discussed.
Abstract: There are only few semiconducting materials that have been shaping the progress of third generation photovoltaic cells as much as perovskites. Although they are deceivingly simple in structure, the archetypal AMX3-type perovskites have built-in potential for complex and surprising discoveries. Since 2009, a small and somewhat exotic class of perovskites, which are quite different from the common rock-solid oxide perovskite, have turned over a new leaf in solar cell research. Highlighted as one of the major scientific breakthroughs of the year 2013, the power conversion efficiency of the title compound hybrid organic–inorganic perovskite has now exceeded 18%, making it competitive with thin-film PV technology. In this minireview, a brief history of perovskite materials for photovoltaic applications is reported, the current state-of-the-art is distilled and the basic working mechanisms have been discussed. By analyzing the attainable photocurrent and photovoltage, realizing perovskite solar cells with 20% efficiency for a single junction, and 30% for a tandem configuration on a c-Si solar cell would be realistic.
1,033 citations
TL;DR: An insight into the analogies, state-of-the-art technologies, concepts, and prospects under the umbrella of perovskite materials (both inorganic-organic hybrid halideperovskites and ferroelectric perovkites) for future multifunctional energy conversion and storage devices is provided.
Abstract: An insight into the analogies, state-of-the-art technologies, concepts, and prospects under the umbrella of perovskite materials (both inorganic-organic hybrid halide perovskites and ferroelectric perovskites) for future multifunctional energy conversion and storage devices is provided. Often, these are considered entirely different branches of research; however, considering them simultaneously and holistically can provide several new opportunities. Recent advancements have highlighted the potential of hybrid perovskites for high-efficiency solar cells. The intrinsic polar properties of these materials, including the potential for ferroelectricity, provide additional possibilities for simultaneously exploiting several energy conversion mechanisms such as the piezoelectric, pyroelectric, and thermoelectric effect and electrical energy storage. The presence of these phenomena can support the performance of perovskite solar cells. The energy conversion using these effects (piezo-, pyro-, and thermoelectric effect) can also be enhanced by a change in the light intensity. Thus, there lies a range of possibilities for tuning the structural, electronic, optical, and magnetic properties of perovskites to simultaneously harvest energy using more than one mechanism to realize an improved efficiency. This requires a basic understanding of concepts, mechanisms, corresponding material properties, and the underlying physics involved with these effects.
1,015 citations
TL;DR: Bismuth perovskites have very promising properties for further development in solar cells and a power conversion efficiency of over 1% is obtained.
Abstract: Low-toxic bismuth-based perovskites are prepared for the possible replacement of lead perovskite in solar cells. The perovskites have a hexagonal crystalline phase and light absorption in the visible region. A power conversion efficiency of over 1% is obtained for a solar cell with Cs3 Bi2 I9 perovskite, and it is concluded that bismuth perovskites have very promising properties for further development in solar cells.
884 citations
TL;DR: A detailed overview of the energy harvesting technologies associated with piezoelectric materials along with the closely related sub-classes of pyroelectrics and ferro-electrics can be found in this article.
Abstract: This review provides a detailed overview of the energy harvesting technologies associated with piezoelectric materials along with the closely related sub-classes of pyroelectrics and ferroelectrics. These properties are, in many cases, present in the same material, providing the intriguing prospect of a material that can harvest energy from multiple sources including vibration, thermal fluctuations and light. Piezoelectric materials are initially discussed in the context of harvesting mechanical energy from vibrations using inertial energy harvesting, which relies on the resistance of a mass to acceleration, and kinematic energy harvesting which directly couples the energy harvester to the relative movement of different parts of a source. Issues related to mode of operation, loss mechanisms and using non-linearity to enhance the operating frequency range are described along with the potential materials that could be employed for harvesting vibrations at elevated temperatures. In addition to inorganic piezoelectric materials, compliant piezoelectric materials are also discussed. Piezoelectric energy harvesting devices are complex multi-physics systems requiring advanced methodologies to maximise their performance. The research effort to develop optimisation methods for complex piezoelectric energy harvesters is then reviewed. The use of ferroelectric or multi-ferroic materials to convert light into chemical or electrical energy is then described in applications where the internal electric field can prevent electron–hole recombination or enhance chemical reactions at the ferroelectric surface. Finally, pyroelectric harvesting generates power from temperature fluctuations and this review covers the modes of pyroelectric harvesting such as simple resistive loading and Olsen cycles. Nano-scale pyroelectric systems and novel micro-electro-mechanical-systems designed to increase the operating frequency are discussed.
882 citations
References
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TL;DR: In this article, the authors describe a photovoltaic cell, created from low-to medium-purity materials through low-cost processes, which exhibits a commercially realistic energy-conversion efficiency.
Abstract: THE large-scale use of photovoltaic devices for electricity generation is prohibitively expensive at present: generation from existing commercial devices costs about ten times more than conventional methods1. Here we describe a photovoltaic cell, created from low-to medium-purity materials through low-cost processes, which exhibits a commercially realistic energy-conversion efficiency. The device is based on a 10-µm-thick, optically transparent film of titanium dioxide particles a few nanometres in size, coated with a monolayer of a charge-transfer dye to sensitize the film for light harvesting. Because of the high surface area of the semiconductor film and the ideal spectral characteristics of the dye, the device harvests a high proportion of the incident solar energy flux (46%) and shows exceptionally high efficiencies for the conversion of incident photons to electrical current (more than 80%). The overall light-to-electric energy conversion yield is 7.1-7.9% in simulated solar light and 12% in diffuse daylight. The large current densities (greater than 12 mA cm-2) and exceptional stability (sustaining at least five million turnovers without decomposition), as well as the low cost, make practical applications feasible.
26,457 citations
TL;DR: An ultrathin donor-acceptor solar cell composed entirely of inorganic nanocrystals spin-cast from solution is introduced, elucidates a class of photovoltaic devices with potential for stable, low-cost power generation.
Abstract: We introduce an ultrathin donor-acceptor solar cell composed entirely of inorganic nanocrystals spin-cast from solution. These devices are stable in air, and post-fabrication processing allows for power conversion efficiencies approaching 3% in initial tests. This demonstration elucidates a class of photovoltaic devices with potential for stable, low-cost power generation.
1,701 citations
TL;DR: It is found that bulk electric conduction in ferroelectric monodomain BiFeO3 crystals is highly nonlinear and unidirectional.
Abstract: Unidirectional electric current flow, such as that found in a diode, is essential for modern electronics. It usually occurs at asymmetric interfaces such as p-n junctions or metal/semiconductor interfaces with Schottky barriers. We report on a diode effect associated with the direction of bulk electric polarization in BiFeO3: a ferroelectric with a small optical gap edge of ∼2.2 electron volts. We found that bulk electric conduction in ferroelectric monodomain BiFeO3 crystals is highly nonlinear and unidirectional. This diode effect switches its direction when the electric polarization is flipped by an external voltage. A substantial visible-light photovoltaic effect is observed in BiFeO3 diode structures. These results should improve understanding of charge conduction mechanisms in leaky ferroelectrics and advance the design of switchable devices combining ferroelectric, electronic, and optical functionalities.
1,610 citations
TL;DR: An explanation of the photovoltaic effect, based on the asymmetry of the lattice, is proposed in this paper, which accounts for the light-induced index changes in LiNbO3.
Abstract: Photocurrents in doped LiNbO3 crystals are shown to be due to a bulk photovoltaic effect with saturation voltages in excess of 1000 V (∼105 V/cm). This effect accounts for the light‐induced index changes in LiNbO3. An explanation of the photovoltaic effect, based on the asymmetry of the lattice, is proposed.
1,053 citations
TL;DR: In this paper, the optical properties of epitaxial BiFeO3 thin films have been characterized in the visible range, showing an absorption onset near 2.17eV, a direct gap (2.667±0.005eV at 300K), and charge transfer excitations at higher energy.
Abstract: The optical properties of epitaxial BiFeO3 thin films have been characterized in the visible range. Variable temperature spectra show an absorption onset near 2.17eV, a direct gap (2.667±0.005eV at 300K), and charge transfer excitations at higher energy. Additionally, we report photoconductivity in BiFeO3 films under illumination from a 100mW∕cm2 white light source. A direct correlation is observed between the magnitude of the photoconductivity and postgrowth cooling pressure. Dark conductivities increased by an order of magnitude when comparing films cooled in 760 and 0.1Torr. Large increases in photoconductivity are observed in light.
440 citations