Co-reactant-on-Demand ECL: Electrogenerated Chemiluminescence by the in Situ Production of S2O82- at Boron-Doped Diamond Electrodes

被引:94
作者
Irkham [1 ]
Watanabe, Takeshi [1 ]
Fiorani, Andrea [2 ]
Valenti, Giovanni [2 ]
Paolucci, Francesco [2 ]
Einaga, Yasuaki [1 ,3 ]
机构
[1] Keio Univ, Dept Chem, 3-14-1 Hiyoshi, Yokohama, Kanagawa 2238522, Japan
[2] Univ Bologna, Dept Chem G Ciamician, Via Selmi 2, I-40126 Bologna, Italy
[3] JST ACCEL, 3-14-1 Hiyoshi, Yokohama, Kanagawa 2238522, Japan
关键词
ACETONITRILE-WATER SOLUTIONS; ELECTROCHEMILUMINESCENT DETECTION; ELECTROCHEMICAL REDUCTION; SELECTIVE DETECTION; AU NANOCLUSTERS; HYBRID MATERIAL; SYSTEM; COMPLEXES; EMISSION; GENERATION;
D O I
10.1021/jacs.6b09020
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A novel co-reactant-free electrogenerated chemiluminescence (ECL) system is developed where Ru(bpy)(3)(2+) emission is obtained on boron doped diamond (BDD) electrodes. The method exploits the unique ability of BDD to operate at very high oxidation potential in aqueous solutions and to promote the conversion of inert SO42- into the reactive co-reactant S2O82-. This novel procedure is rather straightforward, not requiring any particular electrode geometry, and since the co-reactant is only generated in situ, the interference with biological samples is minimized. The underlying mechanism is similar to that of the Ru(bpy)(3)(2+)/S2O82- system; however, the intensity of the emitted signal increases linearly with [SO42-] up to similar to 0.6 M, with possible implications for analytical uses of the proposed procedure.
引用
收藏
页码:15636 / 15641
页数:6
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