Ultra-fast microwave-assisted synthesis of photoluminescent carbon dots with an ultra-high quantum yield for H2O2 detection

被引:16
|
作者
Zhao, Xiaoyu [1 ,2 ,3 ]
Zhang, Mengyuan [4 ]
Zhang, Zhenghua [1 ,2 ,3 ]
机构
[1] Tsinghua Univ, Inst Environm Engn & Nanotechnol, Tsinghua Shenzhen Int Grad Sch, Shenzhen 518055, Guangdong, Peoples R China
[2] Tsinghua Univ, Guangdong Prov Engn Res Ctr Urban Water Recycling, Tsinghua Shenzhen Int Grad Sch, Shenzhen 518055, Guangdong, Peoples R China
[3] Tsinghua Univ, Sch Environm, Beijing 100084, Peoples R China
[4] South China Univ Technol, Sch Environm Sci & Engn, Guangzhou 510006, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Carbon dots; Photoluminescence; Nanomaterials; Microwave treatment; H; 2; O; detection; RATIOMETRIC FLUORESCENT NANOPROBE; ONE-STEP SYNTHESIS; HYDROGEN-PEROXIDE; COLOR EMISSION; CITRIC-ACID; NANODOTS; LIGHT; RED; CARBONIZATION; LUMINESCENCE;
D O I
10.1016/j.jece.2022.109008
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The conventional hydrothermal bottom-up synthesis for preparing carbon dots (CDs) usually requires stringent conditions and high energy consumption, whereas the quantum yield (QY) of CDs remains at a relatively low level. Herein, CDs exhibiting strong blue photoluminescence (PL) with an ultra-high QY (up to 94.4%) were prepared via a simple one-step microwave-assisted route using citric acid (CA) and o-phenylenediamine (o-PD) as precursors. The operating conditions, including reaction time, solvent species, amount of solvent, and precursor molar ratio, were optimized. The CDs synthesized within 3.5 min of microwave heating in ethylene glycol (EG) at a CA-to-PD molar ratio of 5:1 exhibited the highest QY (94.4%). A synergistic PL mechanism of the molecule state and carbon core state emissive centers was proposed according to the characterization results of CDs. Moreover, the proof-to-concept H2O2 fluorescent detection performances of the prepared CDs confirmed their great application potential as probe materials. Through directly mixing the CD products and H2O2, a strong PL response could be rapidly detected after merely 1 min, and the detection limit was calculated to be as low as 8.6 nM. Besides, the CDs exhibited high biocompatibility, making them suitable for in-vivo detection of H2O2. Therefore, this work provides a novel and efficient approach for synthesis of ultra-high QY CDs that can be directly applied in biological detection.
引用
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页数:10
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