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      Screen printed carbon CsPbBr3 solar cells with high open-circuit photovoltage

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          Abstract

          Mesoporous carbon solar cells were prepared by infiltrating the porous substrate with inorganic CsPbBr 3 solution. The films were post-annealed at different temperatures; post-annealing at 400 °C strongly enhances the open circuit voltage (1.44 V) and cell efficiency (8.2%).

          Abstract

          Screen printed mesoporous carbon solar cells (mC-PSC) are a promising fully printable technology that does not require organic hole conductors, expensive metal contacts or vacuum processing. However, when infiltrated with the archetypal CH 3NH 3PbI 3 perovskite, mC-PSCs show low voltage which limits their use in innovative applications such as indoor light harvesting. Here we investigate both planar (C-PSC) and mesoporous (mC-PSC) carbon cells, based on all-inorganic CsPbBr 3. Pure CsPbBr 3 is a yellow material with an orthorhombic crystal structure at room temperature and a 2.3 eV band gap, which is not ideal for solar cell applications. However, CsPbBr 3 is thermally stable up to over 400 °C and high-voltage planar carbon solar cells, with open circuit voltages of up to 1.29 V and efficiencies up to 6.7% have been reported in the literature. We focus on the effect of the post-annealing temperature on the material properties and photovoltaic activity. XPS and XRD results show a non-linear trend with temperature, with significant improvements in composition between 200 and 300 °C. Both the mesoporous and planar champion devices were obtained after heat processing at 400 °C, reaching PCEs of 8.2% and 5.7% respectively. The average V oc for the planar and mesoporous devices were 1.33 V and 1.27 V respectively with a record 1.44 V for the best mC-PSC.

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          Anomalous Hysteresis in Perovskite Solar Cells.

          Perovskite solar cells have rapidly risen to the forefront of emerging photovoltaic technologies, exhibiting rapidly rising efficiencies. This is likely to continue to rise, but in the development of these solar cells there are unusual characteristics that have arisen, specifically an anomalous hysteresis in the current-voltage curves. We identify this phenomenon and show some examples of factors that make the hysteresis more or less extreme. We also demonstrate stabilized power output under working conditions and suggest that this is a useful parameter to present, alongside the current-voltage scan derived power conversion efficiency. We hypothesize three possible origins of the effect and discuss its implications on device efficiency and future research directions. Understanding and resolving the hysteresis is essential for further progress and is likely to lead to a further step improvement in performance.
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            One-Year stable perovskite solar cells by 2D/3D interface engineering

            Despite the impressive photovoltaic performances with power conversion efficiency beyond 22%, perovskite solar cells are poorly stable under operation, failing by far the market requirements. Various technological approaches have been proposed to overcome the instability problem, which, while delivering appreciable incremental improvements, are still far from a market-proof solution. Here we show one-year stable perovskite devices by engineering an ultra-stable 2D/3D (HOOC(CH2)4NH3)2PbI4/CH3NH3PbI3 perovskite junction. The 2D/3D forms an exceptional gradually-organized multi-dimensional interface that yields up to 12.9% efficiency in a carbon-based architecture, and 14.6% in standard mesoporous solar cells. To demonstrate the up-scale potential of our technology, we fabricate 10 × 10 cm2 solar modules by a fully printable industrial-scale process, delivering 11.2% efficiency stable for >10,000 h with zero loss in performances measured under controlled standard conditions. This innovative stable and low-cost architecture will enable the timely commercialization of perovskite solar cells.
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              Not All That Glitters Is Gold: Metal-Migration-Induced Degradation in Perovskite Solar Cells

              Perovskite solar cells (PSCs) have now achieved efficiencies in excess of 22%, but very little is known about their long-term stability under thermal stress. So far, stability reports have hinted at the importance of substituting the organic components, but little attention has been given to the metal contact. We investigated the stability of state-of-the-art PSCs with efficiencies exceeding 20%. Remarkably, we found that exposing PSCs to a temperature of 70 °C is enough to induce gold migration through the hole-transporting layer (HTL), spiro-MeOTAD, and into the perovskite material, which in turn severely affects the device performance metrics under working conditions. Importantly, we found that the main cause of irreversible degradation is not due to decomposition of the organic and hybrid perovskite layers. By introducing a Cr metal interlayer between the HTL and gold electrode, high-temperature-induced irreversible long-term losses are avoided. This key finding is essential in the quest for achieving high efficiency, long-term stable PSCs which, in order to be commercially viable, need to withstand hard thermal stress tests.
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                Author and article information

                Journal
                JMCAET
                Journal of Materials Chemistry A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                2018
                2018
                : 6
                : 38
                : 18677-18686
                Affiliations
                [1 ]Department of Chemistry
                [2 ]University of Bath
                [3 ]Bath BA2 7AY
                [4 ]UK
                [5 ]Centre for Sustainable Chemical Technologies
                [6 ]SPECIFIC
                [7 ]Swansea
                [8 ]Department of Chemical Engineering
                Article
                10.1039/C8TA07694D
                09aad817-b2cc-4a2a-9f51-54d6cc34f78f
                © 2018

                http://creativecommons.org/licenses/by/3.0/

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