Phosphine-Free Synthesis of Monodisperse and Size-Tunable Silver Selenide Quantum Dots via Thermo-Regulated Selenium Dioxide Reactivity for High-Efficiency NIR-II Emission
{"title":"Phosphine-Free Synthesis of Monodisperse and Size-Tunable Silver Selenide Quantum Dots via Thermo-Regulated Selenium Dioxide Reactivity for High-Efficiency NIR-II Emission","authors":"Junjie Zhang, , , Zhe Liu, , , Qingyu Wang, , , Yifan Chen, , , Xingyu Hu, , , Cong Sun, , , Mengya Lu, , , Zifeng Liu, , , Ning Dai, , and , Yang Li*, ","doi":"10.1021/acs.jpclett.5c02547","DOIUrl":null,"url":null,"abstract":"<p >Colloidal silver selenide (Ag<sub>2</sub>Se) 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 Ag<sub>2</sub>Se QDs employing safe and cost-effective SeO<sub>2</sub> as the Se precursor. The mechanism of tuning the Se precursor reactivity derived from SeO<sub>2</sub> by temperature control is thoroughly elucidated, enabling the controllable synthesis of monodisperse Ag<sub>2</sub>Se 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.</p>","PeriodicalId":62,"journal":{"name":"The Journal of Physical Chemistry Letters","volume":"16 38","pages":"10027–10034"},"PeriodicalIF":4.6000,"publicationDate":"2025-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Physical Chemistry Letters","FirstCategoryId":"1","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.jpclett.5c02547","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
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.
期刊介绍:
The Journal of Physical Chemistry (JPC) Letters is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, chemical physicists, physicists, material scientists, and engineers. An important criterion for acceptance is that the paper reports a significant scientific advance and/or physical insight such that rapid publication is essential. Two issues of JPC Letters are published each month.