Metal organic framework–derived core-shell CuO@NiO nanosphares as hole transport material in perovskite solar cell

Cu-Ni bimetallic organic frameworks were synthesized by a facile and stepwise solvothermal method, utilizing metal organic framework as precursor. Core-shell CuO@NiO nanospheres were obtained by calcining the bimetallic organic frameworks at 400° C in the air atmosphere. NiO nanospheres were also pr...

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Veröffentlicht in:Journal of solid state electrochemistry 2020-06, Vol.24 (6), p.1427-1438
Hauptverfasser: Hazeghi, Farzaneh, Mozaffari, Samaneh, Ghorashi, Seyed Mohammad Bagher
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description Cu-Ni bimetallic organic frameworks were synthesized by a facile and stepwise solvothermal method, utilizing metal organic framework as precursor. Core-shell CuO@NiO nanospheres were obtained by calcining the bimetallic organic frameworks at 400° C in the air atmosphere. NiO nanospheres were also prepared by calcining the Ni-BTC nanoparticles in the same conditions. Core-shell CuO@NiO and NiO nanoparticles synthesized by this procedure were employed in fabrication of perovskite solar cells (PSCs) as hole transport layer (HTL). In comparison with the performance of the NiO HTL–based PSC, device with core-shell CuO@NiO HTL exhibited a greater photon conversion efficiency 10.11% with a current density of 21.80 mA cm −2 , an open-circuit voltage of 0.91 V, and a fill factor of 0.51, which is about 15% higher than that of the PSC with NiO HTL (8.58%). The excellent performance of PSC based on core-shell CuO@NiO HTL is mainly attributed to the high extraction of charge carrier due to favorable energy level alignment between perovskite and hole transport layer, increase in HTL conductivity, and decrease of defect density in the surface and bulk of HTL. The stability test of devices showed outstanding long-term stability for the inorganic HTL-based PSCs. The devices with NiO and CuO@NiO HTLs maintained more than 52% and 60% of their original efficiency after 1920 h (80 days), respectively. In contrast, the cell with spiro-OMeTAD retained only 31.74% of its initial efficiency under the same storage conditions after 1248 h (52 days).
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Core-shell CuO@NiO nanospheres were obtained by calcining the bimetallic organic frameworks at 400° C in the air atmosphere. NiO nanospheres were also prepared by calcining the Ni-BTC nanoparticles in the same conditions. Core-shell CuO@NiO and NiO nanoparticles synthesized by this procedure were employed in fabrication of perovskite solar cells (PSCs) as hole transport layer (HTL). In comparison with the performance of the NiO HTL–based PSC, device with core-shell CuO@NiO HTL exhibited a greater photon conversion efficiency 10.11% with a current density of 21.80 mA cm −2 , an open-circuit voltage of 0.91 V, and a fill factor of 0.51, which is about 15% higher than that of the PSC with NiO HTL (8.58%). The excellent performance of PSC based on core-shell CuO@NiO HTL is mainly attributed to the high extraction of charge carrier due to favorable energy level alignment between perovskite and hole transport layer, increase in HTL conductivity, and decrease of defect density in the surface and bulk of HTL. The stability test of devices showed outstanding long-term stability for the inorganic HTL-based PSCs. The devices with NiO and CuO@NiO HTLs maintained more than 52% and 60% of their original efficiency after 1920 h (80 days), respectively. 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Core-shell CuO@NiO nanospheres were obtained by calcining the bimetallic organic frameworks at 400° C in the air atmosphere. NiO nanospheres were also prepared by calcining the Ni-BTC nanoparticles in the same conditions. Core-shell CuO@NiO and NiO nanoparticles synthesized by this procedure were employed in fabrication of perovskite solar cells (PSCs) as hole transport layer (HTL). In comparison with the performance of the NiO HTL–based PSC, device with core-shell CuO@NiO HTL exhibited a greater photon conversion efficiency 10.11% with a current density of 21.80 mA cm −2 , an open-circuit voltage of 0.91 V, and a fill factor of 0.51, which is about 15% higher than that of the PSC with NiO HTL (8.58%). The excellent performance of PSC based on core-shell CuO@NiO HTL is mainly attributed to the high extraction of charge carrier due to favorable energy level alignment between perovskite and hole transport layer, increase in HTL conductivity, and decrease of defect density in the surface and bulk of HTL. The stability test of devices showed outstanding long-term stability for the inorganic HTL-based PSCs. The devices with NiO and CuO@NiO HTLs maintained more than 52% and 60% of their original efficiency after 1920 h (80 days), respectively. 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Core-shell CuO@NiO nanospheres were obtained by calcining the bimetallic organic frameworks at 400° C in the air atmosphere. NiO nanospheres were also prepared by calcining the Ni-BTC nanoparticles in the same conditions. Core-shell CuO@NiO and NiO nanoparticles synthesized by this procedure were employed in fabrication of perovskite solar cells (PSCs) as hole transport layer (HTL). In comparison with the performance of the NiO HTL–based PSC, device with core-shell CuO@NiO HTL exhibited a greater photon conversion efficiency 10.11% with a current density of 21.80 mA cm −2 , an open-circuit voltage of 0.91 V, and a fill factor of 0.51, which is about 15% higher than that of the PSC with NiO HTL (8.58%). 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subjects Analytical Chemistry
Bimetals
Bulk density
Characterization and Evaluation of Materials
Chemistry
Chemistry and Materials Science
Circuits
Condensed Matter Physics
Copper
Copper oxides
Current carriers
Efficiency
Electrochemistry
Energy levels
Energy Storage
Metal-organic frameworks
Nanoparticles
Nanospheres
Nickel oxides
Open circuit voltage
Original Paper
Perovskites
Photovoltaic cells
Physical Chemistry
Roasting
Solar cells
Stability tests
Surface stability
Synthesis
title Metal organic framework–derived core-shell CuO@NiO nanosphares as hole transport material in perovskite solar cell
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