硒化物
硒
量子点
光致发光
分散性
反应性(心理学)
硒化铅
纳米晶
吸收(声学)
材料科学
吸收光谱法
光电子学
硒化镉
红外线的
光化学
发射光谱
无机化学
量子产额
胶体
纳米技术
制作
航程(航空)
化学工程
红外光谱学
催化作用
作者
Jun‐Jie Zhang,Zhe Liu,Qingyu Wang,Yifan Chen,Xingyu Hu,Chenghua Sun,M. Lu,Zifeng Liu,Ning Dai,Yang Li
标识
DOI:10.1021/acs.jpclett.5c02547
摘要
Colloidal silver selenide (Ag2Se) quantum dots (QDs) are promising NIR-II emitters owing to their tunable emission and nontoxic compositions. However, current studies suffer from limited size tunability and poor photoluminescence quantum yields (PL QYs) due to conventional toxic organophosphine-based Se precursors with low reactivity. Here, we demonstrate a thermo-regulated synthetic strategy for size-tunable Ag2Se QDs employing safe and cost-effective SeO2 as the Se precursor. The mechanism of tuning the Se precursor reactivity derived from SeO2 by temperature control is thoroughly elucidated, enabling the controllable synthesis of monodisperse Ag2Se QDs with tunable absorption spectra and a broad size range from 3 to 15 nm. Furthermore, with a Au alloying strategy, we have successfully achieved tunable NIR-II emission (950-1250 nm) with a record-high PL QY of 53.59% at 1140 nm, along with superior photostability. The results will pave the way for eco-friendly Ag-chalcogenide QDs toward applications in biological and infrared optoelectronics.
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