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Perovskite solar cell

About: Perovskite solar cell is a research topic. Over the lifetime, 4701 publications have been published within this topic receiving 216807 citations. The topic is also known as: PSC.


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Journal ArticleDOI
TL;DR: In this article, Magnesium iodide (MgI2) was first successfully used as a dopant into MAPbI3 perovskite prepared in humid air atmosphere.
Abstract: Despite the high efficiency of MAPbI3 perovskite solar cells, the long term stability and degradation in humid atmosphere are issues that still needed to be addressed. In this work, magnesium iodide (MgI2) was first successfully used as a dopant into MAPbI3 perovskite prepared in humid air atmosphere. Mg doping decreased the valence band level, which was determined from photoelectron yield spectroscopy. Compared to the pristine MAPbI3 perovskite film, the 1.0% Mg-doped perovskite film showed increased crystal grain size and formation of pinhole-free perovskite film. Performance of the solar cell was increased from 14.2% of the doping-free solar cell to 17.8% of 1.0% Mg-doped device. Moreover, 90% of the original power conversion efficiency was still retained after storage in 30–40% relative humidity for 600 h.

72 citations

Journal ArticleDOI
TL;DR: In this article, a colloidal PbS quantum dot was synthesized by a facile method and used as the inorganic hole-transporting material in a hybrid perovskite solar cell.
Abstract: Lead halide perovskite solar cells have attracted great interest due to their high efficiency and simple fabrication process. However, the high efficiency heavily relies on expensive organic hole-transporting materials (OHTMs) such as 2,2′,7,7′-tetrakis(N,N-di-p-methoxyphenylamine)-9,9′-spirobifluorene (spiro-MeOTAD), it is preferable to replace these expensive OHTMs by inorganic and low cost materials. Here, we report colloidal PbS quantum dots synthesized by a facile method and used as the inorganic hole-transporting material in a hybrid perovskite solar cell. By controlling the crystalline morphology of the perovskite capping layer, the recombination process is significantly retarded. Furthermore, a pure inorganic solar cell prepared by a two-step process demonstrated a nearly 8% power conversion efficiency due to efficient charge separation by a cascade of junctions and retarding charge recombination by a void-free capping layer. The stability of the inorganic solar cell was also tested with a little decay observed within ca. 100 h.

72 citations

Journal ArticleDOI
23 Jun 2022-Science
TL;DR: Liu et al. as mentioned in this paper showed that adding an ultrathin magnesium fluoride interlayer between the perovskite and C60 electron transport layer during growth facilitates mitigated nonradiative recombination.
Abstract: The performance of perovskite solar cells with inverted polarity (p-i-n) is still limited by recombination at their electron extraction interface, which also lowers the power conversion efficiency (PCE) of p-i-n perovskite-silicon tandem solar cells. A MgFx interlayer with thickness of ~1 nanometer at the perovskite/C60 interface favorably adjusts the surface energy of the perovskite layer through thermal evaporation, which facilitates efficient electron extraction and displaces C60 from the perovskite surface to mitigate nonradiative recombination. These effects enable a champion open-circuit voltage of 1.92 volts, an improved fill factor of 80.7%, and an independently certified stabilized PCE of 29.3% for a monolithic perovskite-silicon tandem solar cell ~1 square centimeter in area. The tandem retained ~95% of its initial performance after damp-heat testing (85°C at 85% relative humidity) for >1000 hours. Description A fluoride boost The wide-bandgap perovskite layer in perovskite-silicon tandem solar cells is still limited by high interface recombination at the electron extraction interface. Liu et al. show that adding an ultrathin magnesium fluoride interlayer between the perovskite and C60 electron transport layer during growth facilitates mitigated nonradiative recombination. An analysis of electronic structural data showed that conduction band bending of the perovskite and C60 facilitated electron extraction. A monolithic perovskite-silicon tandem solar cell with a certified power conversion efficiency of 29.3% retained about 95% of its initial performance for 1000 hours. —PDS The surface energy of the perovskite layer at the C60 interface is favorably adjusted with a magnesium fluoride interlayer.

72 citations

Journal ArticleDOI
TL;DR: In this paper, a perovskite solar cell with light illumination can increase the carrier concentration, thus enhancing charge recombination and causing the coexistence of high electric field and free carriers, and the cell shows a similar charge storage and junction mechanism to that of the multicrystalline silicon solar cell.
Abstract: Interplays between charge and electric field, which play a critical role in determining the charge transport, recombination, storage and hysteresis in the perovskite solar cell, have been systematically investigated by both electrical transient experiments and theoretical calculations. It is found that the light illumination can increase the carrier concentration in the perovskite absorber, thus enhancing charge recombination and causing the co-existence of high electric field and free carriers. Meanwhile, the cell shows a similar charge storage and junction mechanism to that of the multicrystalline silicon solar cell, where the junction electric field determines the charge collection and distribution. Furthermore, it is demonstrated that the static charge of both the doping and defect coming from ion (vacancy) migration can significantly influence the electric field inside the cell, thus affecting the charge collection and recombination, which could be the origins for the widely-concerned hysteresis behaviors.

71 citations

Journal ArticleDOI
TL;DR: In this paper, the authors outline the recent research progress on the metal cathode and HTM-free perovskite solar cells, which is a prospective solution to meet the growing energy demands.
Abstract: Recent developments in organic-inorganic halide perovskite solar cells created a sudden buzz in renewable energy community. Within a short span of time, the efficiency of perovskite solar cells (PSCs) soared from 2.1% (2006) to 22.1% (2017) by varying each component and device configuration. Recent works have been concentrated on the potential of PSCs to emerge as an economical technology. Elimination of hole transport material (HTM) and metal counter electrode in PSCs can overcome high cost and stability issues. In this review, we outline the recent research progress on the metal cathode and HTM-free PSCs, which is a prospective solution to meet the growing energy demands. Carbon materials are used as an alternative to the conventional metal cathode since, carbon materials possess unique qualities such as low cost, high stability, good conductivity and inherent water resistance. Introduction and discussions of this article include the evolution of PSCs, cost, device architectures, deposition techniques, the thickness of the spacer, morphology of counter electrode and stability.

71 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
2023225
2022409
2021631
2020770
2019835
2018780