Efficient perovskite solar cells via improved carrier management
Jason J. Yoo,
Gabkyung Seo,
Matthew R. Chua,
Tae Gwan Park,
Yongli Lu,
Fabian Rotermund,
Young-Ki Kim,
Chan Su Moon,
Nam Joong Jeon,
Juan-Pablo Correa-Baena,
Vladimir Bulović,
Seong Sik Shin (),
Moungi G. Bawendi () and
Jangwon Seo ()
Additional contact information
Jason J. Yoo: Massachusetts Institute of Technology
Gabkyung Seo: Korea Research Institute of Chemical Technology
Matthew R. Chua: Massachusetts Institute of Technology
Tae Gwan Park: Korea Advanced Institute of Science and Technology
Yongli Lu: Massachusetts Institute of Technology
Fabian Rotermund: Korea Advanced Institute of Science and Technology
Young-Ki Kim: Ulsan National Institute of Science and Technology (UNIST)
Chan Su Moon: Korea Research Institute of Chemical Technology
Nam Joong Jeon: Korea Research Institute of Chemical Technology
Juan-Pablo Correa-Baena: Georgia Institute of Technology
Vladimir Bulović: Massachusetts Institute of Technology
Seong Sik Shin: Korea Research Institute of Chemical Technology
Moungi G. Bawendi: Massachusetts Institute of Technology
Jangwon Seo: Korea Research Institute of Chemical Technology
Nature, 2021, vol. 590, issue 7847, 587-593
Abstract:
Abstract Metal halide perovskite solar cells (PSCs) are an emerging photovoltaic technology with the potential to disrupt the mature silicon solar cell market. Great improvements in device performance over the past few years, thanks to the development of fabrication protocols1–3, chemical compositions4,5 and phase stabilization methods6–10, have made PSCs one of the most efficient and low-cost solution-processable photovoltaic technologies. However, the light-harvesting performance of these devices is still limited by excessive charge carrier recombination. Despite much effort, the performance of the best-performing PSCs is capped by relatively low fill factors and high open-circuit voltage deficits (the radiative open-circuit voltage limit minus the high open-circuit voltage)11. Improvements in charge carrier management, which is closely tied to the fill factor and the open-circuit voltage, thus provide a path towards increasing the device performance of PSCs, and reaching their theoretical efficiency limit12. Here we report a holistic approach to improving the performance of PSCs through enhanced charge carrier management. First, we develop an electron transport layer with an ideal film coverage, thickness and composition by tuning the chemical bath deposition of tin dioxide (SnO2). Second, we decouple the passivation strategy between the bulk and the interface, leading to improved properties, while minimizing the bandgap penalty. In forward bias, our devices exhibit an electroluminescence external quantum efficiency of up to 17.2 per cent and an electroluminescence energy conversion efficiency of up to 21.6 per cent. As solar cells, they achieve a certified power conversion efficiency of 25.2 per cent, corresponding to 80.5 per cent of the thermodynamic limit of its bandgap.
Date: 2021
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DOI: 10.1038/s41586-021-03285-w
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