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Green low-temperature-solution-processed in situ HI modified TiO2/SnO2 bilayer for efficient and stable planar perovskite solar cells build at ambient air conditions
摘要： Planar structures for halide perovskite solar cells with the high efficiencies typically use high-temperature processed TiO2 as the electron transporting layers (ETLs). Here, we demonstrate that an in-situ passivation strategy for TiO2 film through the introduction of HI during low-temperature preparation process. HI not only controls hydrolysis of TiO2 precursor but also eliminates defects and suppresses trap states in TiO2 film. Meanwhile, the double-layer architecture is constructed by coating TiO2 with SnO2 layer, the double ETLs can improve the photovoltaic performance of methylamine lead iodide (MAPbI3) perovskite solar cells. The TiO2(HI)/SnO2 ETL can effectively reduce the interfacial charge recombination and facilitate electron transfer. More importantly, the preparation of TiO2 and SnO2 are totally performed at low-temperature (150 °C) and the devices are fabricated in uncontrolled ambient conditions. Our best-performing planar perovskite cell using such a TiO2(HI)/SnO2 ETL has achieved a maximum power conversion efficiency (PCE) of 16.74%, and the devices exhibit good stability which maintaining 85% and 83% of their initial efficiency after heating at 100 °C for 22 h and under illuminating upon 1 sun irradiation for 6 h, respectively. Our results suggest a new approach for further improving the stability of PSCs fabricated in the air condition.
关键词： perovskite solar cell,electron transfer layer,ambient condition,TiO2/SnO2
更新于2025-09-12 10:27:22
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Controlled synthesis of nanocrystalline Nb:SrTiO <sub/>3</sub> electron transport layers for robust interfaces and stable high photovoltaic energy conversion efficiency in perovskite halide solar cells
摘要： Perovskite halides are of great attraction as efficient light absorption materials for solid-state solar cells, but the stability and photovoltaic energy conversion efficiency of perovskite solar cells (PSCs) are still limited by the interface structures and defects between their light-absorbing perovskite halides and electron transport layers (ETLs). Here, we report the ultraviolet (UV) light-induced degradation mechanism at the interfaces between perovskite halide and conventional TiO2 ETL materials, and provide a solution to overcome this drawback. UV-induced degradation is shown to be attributed to the formation of oxygen vacancies formed at the perovskite halide-ETL interface under UV light illumination, where the oxygen atoms released at the interface accelerate the decomposition of perovskite halide by inducing chemical reactions. Meanwhile, nanocrystalline SrTiO3 (STO) ETLs are revealed to be tunable in enabling high performance in PSCs under UV light illumination. Indeed, tuning the electronic structure of STO ETLs by Nb doping, in combination with the controllable removal of SrO phases segregated on the Nb-doped STO ETL surfaces, is exhibited to enable robust interface stability and stable high photovoltaic energy conversion efficiency for PSCs. Furthermore, we demonstrate that STO-based PSCs have no hysteresis due to low defect concentrations at the perovskite halide-STO ETL interfaces.
关键词： oxygen vacancy formation,electron transfer layer,perovskite oxides,photo stability,Perovskite solar cells
更新于2025-09-11 14:15:04