期刊
ANALYTICAL CHEMISTRY
卷 91, 期 7, 页码 4889-4895出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.9b00787
关键词
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资金
- National Natural Science Foundation of China [21874063]
- Swiss National Science Foundation [200021_175622]
- Swiss National Science Foundation (SNF) [200021_175622] Funding Source: Swiss National Science Foundation (SNF)
We introduce here a general strategy to read out chronopotentiometric sensors by electrogenerated chemiluminescence (ECL). The potentials generated in chronopotentiometry in a sample compartment are used to control the ECL in a separate detection compartment. A three-electrode cell is used to monitor the concentration changes of the analyte, while the luminol-H2O2 system is responsible for ECL. The principle was shown to be feasible by theoretical simulations, indicating that the sampled times at a chosen potential, rather than traditional transition times, similarly give linear behavior between concentration and the square root of sampled time. With the help of a voltage adapter, the experimental combination between chronopotentiometry and ECL was successfully implemented. As an initial proof of concept, the ferro/ferricyanide redox couple was investigated. The square root of time giving maximum light output changed linearly with ferrocyanide concentration in the range from 0.70 to 4.81 mM. The method was successfully applied to the visual detection of carbonate alkalinity from 0.06 to 0.62 mM using chronopotentiometry at an ionophore-based hydrogen ion-selective membrane electrode. The measurements of carbonate in real samples including river water and commercial mineral water were successfully demonstrated.
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