Development and challenges in perovskite scintillators for high-resolution imaging and timing applications

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Abstract

Inorganic scintillators play a major role in ionizing radiation detection due to their high versatility to detect multiple radiation sources such as X-rays, gamma-rays, alpha, beta, and neutron particles, and their fast and high light yield, making them especially convenient for imaging, spectroscopy, and timing applications. Scintillators-based detection systems are found, among various applications, in medical imaging, homeland security, high-energy physics, industrial control, oil drilling explorations, and energy management. This Review discusses advances and prospects of perovskite scintillators, particularly low-dimensional hybrid organic-inorganic perovskite crystals and all-inorganic perovskite nanocrystals. We highlight the promise of two-dimensional lithium-doped (PEA) ₂PbBr ₄ crystals and CsPbBr ₃ nanocrystals as scintillators with high light yields, exceeding 20 photons/keV, and fast decay times of less than 15 ns. Such a combination may result in fast-spectral X-ray imaging, an output count rate exceeding 30 Mcps/pixel in photon-counting computed tomography, and coincidence timing resolution of less than 100 ps in positron emission tomography. We review recent strategies to further improve light yield, decay time, and coincidence timing resolution through light-matter interactions such as extraction efficiency enhancement and Purcell-enhanced scintillators. These advancements in light yields and decay times of perovskite scintillators will be particularly useful in the medical and security applications.

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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

Loredana Protesescu, Sergii Yakunin, Maryna Bodnarchuk … (2015)

Metal halides perovskites, such as hybrid organic–inorganic CH3NH3PbI3, are newcomer optoelectronic materials that have attracted enormous attention as solution-deposited absorbing layers in solar cells with power conversion efficiencies reaching 20%. Herein we demonstrate a new avenue for halide perovskites by designing highly luminescent perovskite-based colloidal quantum dot materials. We have synthesized monodisperse colloidal nanocubes (4–15 nm edge lengths) of fully inorganic cesium lead halide perovskites (CsPbX3, X = Cl, Br, and I or mixed halide systems Cl/Br and Br/I) using inexpensive commercial precursors. Through compositional modulations and quantum size-effects, the bandgap energies and emission spectra are readily tunable over the entire visible spectral region of 410–700 nm. The photoluminescence of CsPbX3 nanocrystals is characterized by narrow emission line-widths of 12–42 nm, wide color gamut covering up to 140% of the NTSC color standard, high quantum yields of up to 90%, and radiative lifetimes in the range of 1–29 ns. 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.

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Organic-Inorganic Perovskites: Structural Versatility for Functional Materials Design.

Bayrammurad Saparov, David Mitzi (2016)

Although known since the late 19th century, organic-inorganic perovskites have recently received extraordinary research community attention because of their unique physical properties, which make them promising candidates for application in photovoltaic (PV) and related optoelectronic devices. This review will explore beyond the current focus on three-dimensional (3-D) lead(II) halide perovskites, to highlight the great chemical flexibility and outstanding potential of the broader class of 3-D and lower dimensional organic-based perovskite family for electronic, optical, and energy-based applications as well as fundamental research. The concept of a multifunctional organic-inorganic hybrid, in which the organic and inorganic structural components provide intentional, unique, and hopefully synergistic features to the compound, represents an important contemporary target.

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One-Year stable perovskite solar cells by 2D/3D interface engineering

G. Grancini, C. Roldán-Carmona, I. Zimmermann … (2017)

Despite the impressive photovoltaic performances with power conversion efficiency beyond 22%, perovskite solar cells are poorly stable under operation, failing by far the market requirements. Various technological approaches have been proposed to overcome the instability problem, which, while delivering appreciable incremental improvements, are still far from a market-proof solution. Here we show one-year stable perovskite devices by engineering an ultra-stable 2D/3D (HOOC(CH2)4NH3)2PbI4/CH3NH3PbI3 perovskite junction. The 2D/3D forms an exceptional gradually-organized multi-dimensional interface that yields up to 12.9% efficiency in a carbon-based architecture, and 14.6% in standard mesoporous solar cells. To demonstrate the up-scale potential of our technology, we fabricate 10 × 10 cm2 solar modules by a fully printable industrial-scale process, delivering 11.2% efficiency stable for >10,000 h with zero loss in performances measured under controlled standard conditions. This innovative stable and low-cost architecture will enable the timely commercialization of perovskite solar cells.