The biggest hurdle to the commercialization of perovskite solar cells is that organic–inorganic metal-halide perovskites tend to decompose into their consitutents in the presence of humidity and at high temperatures. Researchers have now made the devices more stable at high temperatures by adding an impermeable tin oxide and an aluminum-doped zinc oxide layer to a conventional perovskite cell architecture.
Typical perovskite solar cells employ an inverted cell architecture, in which positive charge carriers, or holes, are extracted from a PEDOT layer that is deposited on the transparent electrode. Electrons are extracted from the other electrode, which is a metal.
Thomas Riedl of the University of Wuppertal in Germany and his colleagues added a 20-nm-thick tin oxide (SnO x ) layer followed by a 100-nm-thick aluminum-doped zinc oxide (AZO) layer between the perovskite and the top metal electrode. The AZO is an excellent electron conductor, and the SnO x layer is crucial for blocking moisture. Cells with the protective bilayer lasted for more than 350 hours in ambient air with 50% humidity, whereas those without the SnO x layer degraded within tens of hours. The bilayer cells also lasted more than 1000 hours at 60°C, while those without the tin degraded within 100 hours. The work is reported in Nature Communications (doi:10.1038/ncomms13938).
Credit: Nature Communications.
Last summer, physicists at the University of Cambridge discovered that perov-skites can reuse photons multiple times.
By depositing thin perovskite films on textured surfaces, the Cambridge team, led by Felix Deschler and Richard Friend, has now been able to extract these recycled photons and boost the external photoluminescent quantum efficiency of devices. “We were surprised at the high gains in photoluminescence quantum efficiency we could achieve with our simple texturing approach, from 20% to almost 60%,” says Johannes Richter, lead author of the paper in Nature Communications (doi:10.1038/ncomms13941). This method could eventually improve power-conversion efficiencies in light-emitting diodes as well as solar cells.
Photon recycling involves light-generated electrons and holes recombining to produce a photon, and the process of charge separation and recombination continuing until the charges are extracted at the electrical contacts or the photons escape the film. The more photons that escape the film, the better the performance of the light-emitting devices or solar cells.
To increase every photon’s chance to leave the film at the film–air interface, the researchers trapped the photons in the perovskite layer. They achieved this by depositing the perovskite film on a randomly textured glass substrate with structures ranging from 100 nm to 1 µm, which caused the light to bounce around 30 times longer in the perovskite layer, hitting the film–air interface multiple times, explains Richter. On a planar film, the photon would leave the film at the interface between the film and the substrate.
Another approach to address perov-skites’ thermal stability is to use inorganic perovskites such as CsPbX3, where the cesium (Cs) cation is less volatile. There has been growing interest in perovskites for light-emitting field-effect transistors and phototransistors. By integrating organic and inorganic cations, a research team has made a triple cation perovskite Cs x (MA0.17FA0.83)1–x Pb(Br0.17I0.83)3 that has low amounts of electronic defects and better thermally stability.
Mohammad Khaja Nazeeruddin of the École Polytechnique Fédérale de Lausanne, Switzerland, Jin Jang of Kyung Hee University in South Korea, and their colleagues used the new material to make field-effect transistors that have mobilities over 2 cm2/V-s and inverters with voltage gains over 20. The researchers say that these are the best reported performances of such perovskite devices. The work is reported in Advanced Materials (doi:10.1002/adma.201602940).
Researchers at Florida State University have made a new organic–inorganic metal halide perovsite with a one-dimensional (1D) structure. The material has a 1D perovskite structure where the edge-sharing octahedral lead bromide chains [PbBr4 –2]n are surrounded by columnar cages formed by an organic cation (C4N2H14 2+) to form core–shell wires. Millions of these wires are stacked together to form a crystalline bundle.
The 1D structure is excellent at trapping electron–hole pairs called excitons. This leads to efficient bluish white-light emissions with photoluminescence quantum efficiencies of approximately 20% for the bulk single crystals and 12% for the microscale crystals, as reported in Nature Communications (doi:10.1038/ncomms14051). The material could open up a new way to make efficient light-emitting devices and phosphor materials for display applications.
