Topic
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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TL;DR: It has been proved that this simple method is efficiently to improve the quality of ETL for high performance PSCs.
Abstract: Tin oxide (SnO2) is widely used in perovskite solar cells (PSCs) as an electron transport layer (ETL) material. However, its high surface trap density has already become a strong factor limiting PSC development. In this work, phosphoric acid is adopted to eliminate the SnO2 surface dangling bonds to increase electron collection efficiency. The phosphorus mainly exists at the boundaries in the form of chained phosphate groups, bonding with which more than 47.9% of Sn dangling bonds are eliminated. The reduction of surface trap states depresses the electron transport barriers, thus the electron mobility increases about 3 times when the concentration of phosphoric acid is optimized with 7.4 atom % in the SnO2 precursor. Furthermore, the stability of the perovskite layer deposited on the phosphate-passivated SnO2 (P-SnO2) ETL is gradually improved with an increase of the concentration. Due to the higher electron collection efficiency, the P-SnO2 ETLs can dramatically promote the power conversion efficiency (PCE) of the PSCs. As a result, the champion PSC has a PCE of 21.02%. Therefore, it has been proved that this simple method is efficient to improve the quality of ETL for high-performance PSCs.
66 citations
TL;DR: In this article, a self-consistent device model using solar cell Capacitance Simulator (SCAPS) was developed from experimental data of a 17.5% efficient perovskite solar cell.
66 citations
TL;DR: In this paper, a plasma-assisted atomic layer deposition (ALD) of nickel oxide (NiO) is carried out by adopting bis-methylcyclopentadienyl-nickel (Ni(MeCp)2) as precursor and O2 plasma as co-reactant, over a wide table temperature range of 50-300 °C.
Abstract: Low-temperature atomic layer deposition (ALD) offers significant merits in terms of processing uniform, conformal and pinhole-free thin films, with sub-nanometer thickness control. In this work, plasma-assisted atomic layer deposition (ALD) of nickel oxide (NiO) is carried out by adopting bis-methylcyclopentadienyl-nickel (Ni(MeCp)2) as precursor and O2 plasma as co-reactant, over a wide table temperature range of 50–300 °C. A growth rate of 0.32 A per cycle is obtained for films deposited at 150 °C with an excellent thickness uniformity on a 4 inch silicon wafer. Bulk characteristics of the NiO film together with its interfacial properties with a triple cation hybrid perovskite absorber layer are comprehensively investigated, with the aim of integrating NiO as hole transport layer (HTL) in a p–i–n perovskite solar cell (PSC) architecture. It is concluded that “key” to efficient solar cell performance is the post-annealing treatment of the ALD NiO films in air, prior to perovskite synthesis. Post-annealing leads to better wettability of the perovskite layer and increased conductivity and mobility of the NiO films, delivering an increase in short-circuit current density (Jsc) and fill factor (FF) in the fabricated devices. Overall, a superior 17.07% PCE is achieved in the post-annealed NiO-based PSC when compared to the 13.98% PCE derived from the one with pristine NiO.
66 citations
TL;DR: In this paper, the degradation of perovskite solar cells under operating situations through in situ X-ray diffraction and in situ x-ray absorption spectroscopies was investigated, which revealed that lead hydroxide iodide (PbIOH) was formed as an end decomposition product inside the cell.
Abstract: Photovoltaic performance of a perovskite solar cell is observed to decrease with increasing humidity, which might be attributed to the formation of hydrated intermediates leading to a decrease in extraction of photocarriers. However, direct evidence of the interplay between the perovskite layer and the photovoltaic performance under operating conditions (consecutive illumination) has not yet been reported. Herein, we investigated the degradation of perovskite solar cells under operating situations through in situ X-ray diffraction and in situ X-ray absorption spectroscopies, which revealed that lead hydroxide iodide (PbIOH), a new phase that has not previously been identified as the degradation product of perovskite solar cells, was formed as an end decomposition product inside the cell. The formation of PbIOH could break the interface inside and be the key reason behind the problem of reduced cell life. This work illustrates that in operando direct observation of the photo- and moisture-induced effects c...
66 citations
TL;DR: This work successfully fabricated highly efficient hole-blocking layer (HBL)-free PSCs through vigorously interrupting penetration of hole-transport material (HTM) into fluorine-doped tin oxide by a large grain based-CH3NH3PbI3 (MAPbI 3) film, thereby obtaining a PCE of 18.20%.
Abstract: There remains tremendous interest in perovskite solar cells (PSCs) in the solar energy field; the certified power conversion efficiency (PCE) now exceeds 20%. Along with research focused on enhancing PCE, studies are also underway concerning PSC commercialization. It is crucial to simplify the fabrication process and reduce the production cost to facilitate commercialization. Herein, we successfully fabricated highly efficient hole-blocking layer (HBL)-free PSCs through vigorously interrupting penetration of hole-transport material (HTM) into fluorine-doped tin oxide by a large grain based-CH3NH3PbI3 (MAPbI3) film, thereby obtaining a PCE of 18.20%. Our results advance the commercialization of PSCs via a simple fabrication system and a low-cost approach in respect of mass production and recyclability.
66 citations