TY - JOUR
T1 - Electrogenerated Chemiluminescence for Chronopotentiometric Sensors
AU - Gao, Wenyue
AU - Jeanneret, Stéphane
AU - Yuan, Dajing
AU - Cherubini, Thomas
AU - Wang, Lu
AU - Xie, Xiaojiang
AU - Bakker, Eric
N1 - Publisher Copyright:
© 2019 American Chemical Society.
PY - 2019/4/2
Y1 - 2019/4/2
N2 - 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-H 2 O 2 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.
AB - 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-H 2 O 2 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.
UR - https://www.webofscience.com/wos/woscc/full-record/WOS:000463683300083
UR - https://openalex.org/W2083513236
UR - https://www.scopus.com/pages/publications/85063428372
M3 - Journal Article
SN - 0003-2700
VL - 91
SP - 4889
EP - 4895
JO - Analytical Chemistry
JF - Analytical Chemistry
IS - 7
ER -