Synthesis of N,S co-doped carbon dots for fluorescence turn-on detection of Fe2+ and Al3+ in a wide pH range

被引:16
作者
Song, Yanxi [1 ]
Xia, Xiaofeng [1 ]
Xiao, Zhongwen [2 ]
Zhao, Yong [3 ]
Yan, Mengjie [1 ]
Li, Jiayin [2 ]
Li, Hongqi [2 ]
Liu, Xiaotian [1 ]
机构
[1] Donghua Univ, Coll Environm Sci & Engn, 2999 North Renmin Rd, Shanghai 201620, Peoples R China
[2] Donghua Univ, Coll Chem Chem Engn & Biotechnol, 2999 North Renmin Rd, Shanghai 201620, Peoples R China
[3] Huainan Normal Univ, Sch Chem & Mat Engn, Huainan 232038, Anhui, Peoples R China
关键词
Carbon dots; N; S-doping; Fluorescence enhancement; Sensor; Fe2+; Al3+; SENSITIVE DETECTION; QUANTUM DOTS; SELECTIVE DETECTION; CITRIC-ACID; ALUMINUM; SENSOR; CELLS; PROBE; IONS; IRON;
D O I
10.1016/j.molliq.2022.120663
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
N,S co-doped carbon dots (N/S-CDs) was synthesized by using b-cyclodextrin as carbon source and Reactive Black 5 as nitrogen and sulfur source. The structure of the N/S-CDs was characterized and its performance for detection of Fe2+ and Al3+ was evaluated. Experimental results demonstrated that the N/S-CDs had good stability in 10 mmol/L brine and in a wide pH range of 3-12. The N/S-CDs exhibited high selectivity for detection of Fe2+ and Al3+ by dual-modal fluorescence enhancement and visualization with the naked eye over a wide pH range. The N/S-CDs displayed good anti-interference performance and low detection limits of 6.99 nmol/L for Fe2+ and 5.5 nmol/L for Al3+. The N/S-CDs responded to Al3+ rapidly within 3 min. Measurements on particle size, zeta potential, and UV-vis and FT-IR spectra suggested that Fe2+ enhanced fluorescence of the N/S-CDs by chelating while Al3+ promoted aggregation through com-bination with the N/S-CDs which responded to Al3+ by aggregation-induced enhancement of emission (AIEE) mechanism. (c) 2022 Elsevier B.V. All rights reserved.
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页数:13
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