纳米晶
卤化物
电致发光
钙钛矿(结构)
发光二极管
材料科学
光致发光
二极管
光电子学
量子效率
纳米技术
无机化学
化学
结晶学
图层(电子)
作者
Parth Vashishtha,Jonathan E. Halpert
标识
DOI:10.1021/acs.chemmater.7b01609
摘要
Perovskite nanocrystals have shown great promise as the basis of a new family of nanocrystal light-emitting diodes (LEDs). However, the external quantum efficiency and color stability of these materials still lag behind those of well-established technologies. Producing stable efficient red emitters with electroluminescence (EL) in the "pure" red range of 620–650 nm is a particular challenge. Here we present mixed halide CsPbBr3–xXx (X = I or Cl) peNC organic LEDs using peNC emitters with photoluminescence across the visible region to produce LEDs displaying EL across the visible spectrum. By focusing on the yellow-orange to deep red (560–680 nm) visible regime, we present evidence that field-driven halide separation in CsPbBr3–xIx peNCs is responsible for the observed red-shifting and splitting of the EL peaks. Greater compositional stability is demonstrated to be the key to higher efficiency, long-lived devices for deep red-emitting mixed halide peNCs with higher compositional concentrations of iodide.
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