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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: The underlying microscopic mechanism to be promoting the oriented growth of the perovskites crystals and reducing the defect concentration is unveiled, and the role of lead iodide is proposed.
Abstract: The presence of excess lead iodide in halide perovskites has been key for surpassing 20% photon-to-power conversion efficiency. To achieve even higher power conversion efficiencies, it is important to understand the role of remnant lead iodide in these perovskites. To that end, we explored the mechanism facilitating this effect by identifying the impact of excess lead iodide within the perovskite film on charge diffusion length, using electron-beam-induced current measurements, and on film formation properties, from grazing-incidence wide-angle X-ray scattering and high-resolution transmission electron microscopy. Based on our results, we propose that excess lead iodide in the perovskite precursors can reduce the halide vacancy concentration and lead to formation of azimuthal angle-oriented cubic α-perovskite crystals in-between 0° and 90°. We further identify a higher perovskite carrier concentration inside the nanostructured titanium dioxide layer than in the capping layer. These effects are consistent with enhanced lead iodide-rich perovskite solar cell performance and illustrate the role of lead iodide. Excess lead iodide in the mixed halide perovskites solar cells leads to high device performance but its origin remains elusive. Here Park et al. unveil the underlying microscopic mechanism to be promoting the oriented growth of the perovskites crystals and reducing the defect concentration.

247 citations

Journal ArticleDOI
TL;DR: This work demonstrates the use of perovskite solar cell packs with four single CH3NH3PbI3 based solar cells connected in series for directly photo-charging lithium-ion batteries assembled with a LiFePO4 cathode and a Li4Ti5O12 anode.
Abstract: Electric vehicles using lithium-ion battery pack(s) for propulsion have recently attracted a great deal of interest. The large-scale practical application of battery electric vehicles may not be realized unless lithium-ion batteries with self-charging suppliers will be developed. Solar cells offer an attractive option for directly photo-charging lithium-ion batteries. Here we demonstrate the use of perovskite solar cell packs with four single CH3NH3PbI3 based solar cells connected in series for directly photo-charging lithium-ion batteries assembled with a LiFePO4 cathode and a Li4Ti5O12 anode. Our device shows a high overall photo-electric conversion and storage efficiency of 7.80% and excellent cycling stability, which outperforms other reported lithium-ion batteries, lithium-air batteries, flow batteries and super-capacitors integrated with a photo-charging component. The newly developed self-chargeable units based on integrated perovskite solar cells and lithium-ion batteries hold promise for various potential applications.

247 citations

Journal ArticleDOI
TL;DR: In this paper, a functional hygroscopic polymer, poly(ethylene oxide), was applied to perovskite solar cells to make them more stable in a humid environment.
Abstract: Long-term device stability is one of the most critical issues that impede perovskite solar cell commercialization. Here we show that a thin layer of a functional hygroscopic polymer, poly(ethylene oxide), PEO, on top of the perovskite thin film, can make perovskite-based solar cells highly stable during operation and in a humid atmosphere. We prove that PEO chemically interacts with lead ions on the perovskite surface, and thus passivates undercoordinated defect sites. Importantly, defect healing by PEO not only results in an improvement of the photo-voltage but also makes the perovskite thin film stable. We demonstrate that the hygroscopic PEO thin film can prevent water inclusion into the perovskite film by screening water molecules, thus having a multi-functional role. Overall, such interface engineering leads to highly durable perovskite solar cells, which, in the presence of PEO passivation, retained more than 95% of their initial power conversion efficiency over 15 h illumination, under load, in ambient atmosphere without encapsulation. Our findings experimentally reveal the role of interface engineering in mastering the instability of perovskite materials and propose a general approach for improving the reliability of perovskite-based optoelectronic devices.

246 citations

Journal ArticleDOI
TL;DR: In this article, a spiro[fluorene-9,9′-xanthene] based molecular hole-transporting materials (X59) was developed via two-step synthesis from commercial precursors for perovskite solar cells.

244 citations

Journal ArticleDOI
TL;DR: Dopants for small molecule-based organic hole-transport layers impact both perovskite solar cells initial performance and long-term stability.
Abstract: Hybrid organic/inorganic perovskite solar cells (PSCs) have dramatically changed the landscape of the solar research community over the past decade, but >25 year stability is likely required if they are to make the same impact in commercial photovoltaics and power generation more broadly. While every layer of a PSC has been shown to impact its durability in power output, the hole-transport layer (HTL) is critical for several reasons: (1) it is in direct contact with the perovskite layer, (2) it often contains mobile ions, like Li+ – which in this case are hygroscopic, and (3) it usually has the lowest thermal stability of all layers in the stack. Therefore, HTL engineering is one method with a high return on investment for PSC stability and lifetime. Research has progressed in understanding design rules for small organic molecule hole-transport materials, yet, when implemented into devices, the same dopants, bis(trifluoromethane)sulfonimide lithium salt (LiTFSI) and tris(2-(1H-pyrazol-1-yl)-4-tert-butylpyridine)cobalt(III) tri[bis(trifluoromethane)sulfonimide] (FK209), are nearly always required for improved charge-transport properties (e.g., increased hole mobility and conductivity). The dopants are notable because they too have been shown to negatively impact PSC stability and lifetime. In response, new research has targeted alternative dopants to bypass these negative effects and provide greater functionality. In this review, we focus on dopant fundamentals, alternative doping strategies for organic small molecule HTL in PSC, and imminent research needs with regard to dopant development for the realization of reliable, long-lasting electricity generation via PSCs.

243 citations


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