光致发光
卤化物
材料科学
钙钛矿(结构)
光电子学
纳米晶
量子点
硫系化合物
纳米技术
化学
无机化学
结晶学
作者
Loredana Proteşescu,Sergii Yakunin,Maryna I. Bodnarchuk,Franziska Krieg,Riccarda Caputo,Christopher H. Hendon,Ruoxi Yang,Aron Walsh,Maksym V. Kovalenko
出处
期刊:Nano Letters
[American Chemical Society]
日期:2015-01-29
卷期号:15 (6): 3692-3696
被引量:7315
摘要
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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