钝化
光致发光
钙钛矿(结构)
量子产额
材料科学
量子点
光电子学
发光二极管
卤化物
二极管
荧光粉
纳米技术
化学
无机化学
光学
荧光
结晶学
图层(电子)
物理
作者
Meiying Leng,Ying Yang,Zhengwu Chen,Wanru Gao,Jian Zhang,Liduo Wang,Deng‐Bing Li,Haisheng Song,Jianbing Zhang,Song Jin,Jiang Tang
出处
期刊:Nano Letters
[American Chemical Society]
日期:2018-08-14
卷期号:18 (9): 6076-6083
被引量:169
标识
DOI:10.1021/acs.nanolett.8b03090
摘要
Metal halide perovskite quantum dots (QDs) recently have attracted great research attentions. However, blue-emitting perovskite QDs generally suffer from low photoluminescence quantum yield (PLQY) because of easily formed defects and insufficient surface passivation. Replacement of lead with low toxicity elements is also preferred toward potential commercial applications. Here, we apply Cl-passivation to boost the PLQY of MA3Bi2Br9 QDs to 54.1% at the wavelength of 422 nm, a new PLQY record for blue emissive, lead-free perovskite QDs. Because of the incompatible crystal structures between MA3Bi2Br9 and MA3Bi2Cl9 and the careful kinetic control during the synthesis, Cl– anions are engineered to mainly locate on the surface of QDs acting as passivating ligands, which effectively suppress surface defects and enhance the PLQY. Our results highlight the potential of MA3Bi2Br9 QDs for applications of phosphors, scintillators, and light-emitting diodes.
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