卤化物
量子点
发光二极管
二极管
制作
溶解度
溶解
材料科学
铯
光电子学
钙钛矿(结构)
配体(生物化学)
纳米技术
化学
无机化学
物理化学
结晶学
病理
受体
医学
生物化学
替代医学
作者
Sjoerd A. Veldhuis,Yan Fong Ng,Riyas Ahmad,Annalisa Bruno,Nur Fadilah Jamaludin,D. Bahulayan,Nripan Mathews,Subodh Mhaisalkar
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2018-02-01
卷期号:3 (3): 526-531
被引量:92
标识
DOI:10.1021/acsenergylett.7b01257
摘要
The synthesis of all-inorganic cesium lead halide perovskite quantum dots (QDs) typically requires high temperatures, stringent conditions, large quantities of surface ligands, and judicious purification steps to overcome ligand-induced charge injection barriers in optoelectronic devices. Low-temperature syntheses generally require lower ligand concentrations but are severely limited by the low solubility of the Cs precursor. We describe an innovative and general approach employing crown ethers under ambient conditions to overcome these solubility limitations. The crown ethers facilitate complete dissolution of the CsBr precursor, rendering CsPbBr3 QD inks practical for device fabrication. The resultant light-emitting diodes (LEDs) displayed bright green emission, with a current efficiency and external quantum efficiency of 9.22 cd A–1 and 2.64%, respectively. This represents the first LED based on CsPbBr3 QDs prepared at room temperature. Lastly, the crown ethers form core–shell structures, opening new avenues to exploit their strong coordination strength.
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