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All-inorganic perovskite quantum dots as light-harvesting, interfacial, and light-converting layers toward solar cells

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TLDR
In this article, the authors focus on the latest development of all-inorganic perovskite quantum dots (AIPQDSCs) and analyze the current bottlenecks they are facing.
Abstract
Solution-processed colloidal lead halide perovskite quantum dots (QDs) are considered one of the promising candidates for next-generation photovoltaics (PVs) due to the excellent optoelectronic properties and low-cost synthetic process. In particular, all-inorganic perovskite (AIP) QDs exhibit better prospects due to their better stability. Although remarkable breakthroughs have been made in bulk perovskite solar cells (SCs), the AIP QD-based SCs (AIPQDSCs) are still on their way to catch up. A lot of reports have summarized the development of perovskite SCs, but few have focused on AIPQDSCs. In this review, we focus on the latest development of AIPQDSCs, and analyze the current bottlenecks they are facing. Also, various optimization means have been discussed to improve the performance of AIPQDSCs from two perspectives of QD materials and device structure, including compositional regulation, surface engineering, interface engineering, and optimization of the carrier transport layer. In addition, AIP QDs as converter for SCs are also presented. Since the stability of perovskite SCs is currently the most pressing issue, the device stability is also highlighted. In the end, a brief summary and perspectives are presented to look forward to the future development of AIPQDSCs.

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Citations
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ZnPc/CsPbBr3 QDs collaborative interface modification to improve the performance of CsPbBr3 perovskite solar cells

TL;DR: Zhang et al. as discussed by the authors introduced zinc phthalocyanine (ZnPc), CsPbBr3 quantum dots (QDs), and ZnPC mixed QDs in proper proportion as the interface modification layers of the PSCs, which can further enhance carrier extraction, suppress carrier recombination and improve performance of final devices.
References
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Journal ArticleDOI

Electron-hole diffusion lengths exceeding 1 micrometer in an organometal trihalide perovskite absorber.

TL;DR: In this article, transient absorption and photoluminescence-quenching measurements were performed to determine the electron-hole diffusion lengths, diffusion constants, and lifetimes in mixed halide and triiodide perovskite absorbers.
Journal Article

Electron-Hole Diffusion Lengths Exceeding 1 Micrometer in an Organometal Trihalide Perovskite Absorber

TL;DR: In this paper, transient absorption and photoluminescence-quenching measurements were performed to determine the electron-hole diffusion lengths, diffusion constants, and lifetimes in mixed halide and triiodide perovskite absorbers.
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Nanocrystals of Cesium Lead Halide Perovskites (CsPbX3, X = Cl, Br, and I): Novel Optoelectronic Materials Showing Bright Emission with Wide Color Gamut

TL;DR: The compelling combination of enhanced optical properties and chemical robustness makes CsPbX3 nanocrystals appealing for optoelectronic applications, particularly for blue and green spectral regions (410–530 nm), where typical metal chalcogenide-based quantum dots suffer from photodegradation.
Journal ArticleDOI

Formamidinium lead trihalide: a broadly tunable perovskite for efficient planar heterojunction solar cells

TL;DR: In this article, the effect of replacing the methylammonium cation in this perovskite was explored, and it was shown that with the slightly larger formamidinium lead trihalide cation, one can synthesise a peroviscite with a bandgap tunable between 1.48 and 2.23 eV.
Journal ArticleDOI

6.5% efficient perovskite quantum-dot-sensitized solar cell

TL;DR: Perovskite QD-sensitized 3.6 μm-thick TiO(2) film shows maximum external quantum efficiency (EQE) of 78.6% at 530 nm and solar-to-electrical conversion efficiency of 6.54% at AM 1.5G 1 sun intensity (100 mW cm(-2)), which is by far the highest efficiency among the reported inorganic quantum dot sensitizers.
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