ABSTRACT
Efficient photovoltaic devices must be efficient light emitters to reach the thermodynamic efficiency limit. Here, we present a promising prospect of perovskite photovoltaics as bright emitters by harnessing the significant benefits of photon recycling, which can be practically achieved by suppressing interfacial quenching. We have achieved radiative and stable perovskite photovoltaic devices by the design of a multiple quantum well structure with long (â¼3 nm) organic spacers with oleylammonium molecules at perovskite top interfaces. Our L-site exchange process (L: barrier molecule cation) enables the formation of stable interfacial structures with moderate conductivity despite the thick barriers. Compared to popular short (â¼1 nm) Ls, our approach results in enhanced radiation efficiency through the recursive process of photon recycling. This leads to the realization of radiative perovskite photovoltaics with both high photovoltaic efficiency (in-lab 26.0%, certified to 25.2%) and electroluminescence quantum efficiency (19.7 % at peak, 17.8% at 1-sun equivalent condition). Furthermore, the stable crystallinity of oleylammonium-based quantum wells enables our devices to maintain high efficiencies for over 1000 h of operation and >2 years of storage.
ABSTRACT
Metal halide perovskite (MHP)-based tandem solar cells are a promising candidate for use in cost-effective and high-performance solar cells that can compete with fossil fuels. To understand the research trends for MHP-based tandem solar cells, a general introduction to single-junction and multiple-junction MHP solar cells and the configuration of tandem devices is provided, along with an overview of the recent progress regarding various MHP-based tandem cells, including MHP/crystalline silicon, MHP/CuInGaS, MHP/organic photovoltaic, MHP/quantum dot, and all-perovskite tandem cell. Future research directions for MHP-based tandem solar cells are also discussed.
