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      Structural and Electrical Investigation of Cobalt-Doped NiO x /Perovskite Interface for Efficient Inverted Solar Cells

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          Abstract

          Inorganic hole-transporting materials (HTMs) for stable and cheap inverted perovskite-based solar cells are highly desired. In this context, NiO x , with low synthesis temperature, has been employed. However, the low conductivity and the large number of defects limit the boost of the efficiency. An approach to improve the conductivity is metal doping. In this work, we have synthesized cobalt-doped NiO x nanoparticles containing 0.75, 1, 1.25, 2.5, and 5 mol% cobalt (Co) ions to be used for the inverted planar perovskite solar cells. The best efficiency of the devices utilizing the low temperature-deposited Co-doped NiO x HTM obtained a champion photoconversion efficiency of 16.42%, with 0.75 mol% of doping. Interestingly, we demonstrated that the improvement is not from an increase of the conductivity of the NiO x film, but due to the improvement of the perovskite layer morphology. We observe that the Co-doping raises the interfacial recombination of the device but more importantly improves the perovskite morphology, enlarging grain size and reducing the density of bulk defects and the bulk recombination. In the case of 0.75 mol% of doping, the beneficial effects do not just compensate for the deleterious one but increase performance further. Therefore, 0.75 mol% Co doping results in a significant improvement in the performance of NiO x -based inverted planar perovskite solar cells, and represents a good compromise to synthesize, and deposit, the inorganic material at low temperature, without losing the performance, due to the strong impact on the structural properties of the perovskite. This work highlights the importance of the interface from two different points of view, electrical and structural, recognizing the role of a low doping Co concentration, as a key to improve the inverted perovskite-based solar cells’ performance.

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          High-performance and environmentally stable planar heterojunction perovskite solar cells based on a solution-processed copper-doped nickel oxide hole-transporting layer.

          An effective approach to significantly increase the electrical conductivity of a NiOx hole-transporting layer (HTL) to achieve high-efficiency planar heterojunction perovskite solar cells is demonstrated. Perovskite solar cells based on using Cu-doped NiOx HTL show a remarkably improved power conversion efficiency up to 15.40% due to the improved electrical conductivity and enhanced perovskite film quality. General applicability of Cu-doped NiOx to larger bandgap perovskites is also demonstrated in this study.
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            Interpretation and evolution of open-circuit voltage, recombination, ideality factor and subgap defect states during reversible light-soaking and irreversible degradation of perovskite solar cells

            Insights into the interplay of different recombination mechanisms and their origins (bulk, surface) are provided comparing fresh, light-soaked and aged devices. Metal halide perovskite absorber materials are about to emerge as a high-efficiency photovoltaic technology. At the same time, they are suitable for high-throughput manufacturing characterized by a low energy input and abundant low-cost materials. However, a further optimization of their efficiency, stability and reliability demands a more detailed optoelectronic characterization and understanding of losses including their evolution with time. In this work, we analyze perovskite solar cells with different architectures (planar, mesoporous, HTL-free), employing temperature dependent measurements (current–voltage, light intensity, electroluminescence) of the ideality factor to identify dominating recombination processes that limit the open-circuit voltage ( V oc ). We find that in thoroughly-optimized, high- V oc (≈1.2 V) devices recombination prevails through defects in the perovskite. On the other hand, irreversible degradation at elevated temperature is caused by the introduction of broad tail states originating from an external source ( e.g. metal electrode). Light-soaking is another effect decreasing performance, though reversibly. Based on FTPS measurements, this degradation is attributed to the generation of surface defects becoming a new source of non-radiative recombination. We conclude that improving long-term stability needs to focus on adjacent layers, whereas a further optimization of efficiency of top-performing devices requires understanding of the defect physics of the nanocrystalline perovskite absorber. Finally, our work provides guidelines for the design of further dedicated studies to correctly interpret the diode ideality factor and decrease recombination losses.
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              Tailoring solvent coordination for high-speed, room-temperature blading of perovskite photovoltaic films

              The efficiencies of small-pixel perovskite photovoltaics have increased to above 24%, while most reported fabrication methods cannot be transferred to scalable manufacturing process. Here, we report a method of fast blading large-area perovskite films at an unprecedented speed of 99 mm/s under ambient conditions by tailoring solvent coordination capability. Combing volatile noncoordinating solvents to Pb 2+ and low-volatile, coordinating solvents achieves both fast drying and large perovskite grains at room temperature. The reproducible fabrication yields a certified module efficiency of 16.4%, with an aperture area of 63.7 cm 2 . This method can be applied for various perovskite compositions. The perovskite modules also show a small temperature coefficient of −0.13%/°C and nearly fully recoverable efficiency after 58 cycles of shading, much better than commercial silicon and thin-film solar modules.
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                Author and article information

                Journal
                Nanomaterials (Basel)
                Nanomaterials (Basel)
                nanomaterials
                Nanomaterials
                MDPI
                2079-4991
                30 April 2020
                May 2020
                : 10
                : 5
                : 872
                Affiliations
                [1 ]Institute of Advanced Materials (INAM), Universitat Jaume I, Av. Sos Baynat, s/n, 12071 Castelló, Spain; z.rezay@ 123456ma.iut.ac.ir (Z.R.M.); barea@ 123456uji.es (E.M.B.); hassanab@ 123456uji.es (E.H.); julian@ 123456uji.es (B.J.-L.)
                [2 ]Department of Materials Engineering, Isfahan University of Technology, Isfahan 84156-83111, Iran; ahmad_k@ 123456cc.iut.ac.ir (A.K.); karimzadeh_f@ 123456cc.iut.ac.ir (F.K.); elhamhalvani@ 123456gmail.com (E.H.A.)
                [3 ]Textile Engineering Department, Textile Excellence & Research Centers, Amirkabir University of Technology, Tehran 15916-34311, Iran
                Author notes
                [* ]Correspondence: masi@ 123456uji.es (S.M.); sero@ 123456uji.es (I.M.-S.)
                Author information
                https://orcid.org/0000-0003-2601-7022
                https://orcid.org/0000-0001-9339-0180
                https://orcid.org/0000-0002-7561-5021
                https://orcid.org/0000-0003-1019-776X
                https://orcid.org/0000-0002-7373-1627
                Article
                nanomaterials-10-00872
                10.3390/nano10050872
                7279223
                32365967
                9cd0e26e-8500-4d0e-be1b-104896d4c037
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 24 March 2020
                : 15 April 2020
                Categories
                Article

                inverted planar perovskite solar cell,hole transport material,co-doped niox,perovskite morphology,electrical conductivity

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