期刊
JOURNAL OF PHYSICAL CHEMISTRY C
卷 112, 期 39, 页码 15570-15575出版社
AMER CHEMICAL SOC
DOI: 10.1021/jp805609y
关键词
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资金
- National Natural Science Foundation of China [20775014, 20735002, 20675016]
- Key Project of Chinese Ministry of Education [207052]
- Natural Science Foundation of Fujian Province of China [D0610009]
- SRF [XRC-0528]
The electrochemiluminescence (ECL) behaviors of tris(2,2-bipyridine)ruthenium(II)/triethylamine (Ru(bpy)3(2+)/TEA) in 1-butyl-3-methylimidazolium hexafluorophosphate (BMIPF6) ionic liquid were investigated and compared with those in aqueous solution (pH 7.0 PBS) at a gold electrode. It was found that the Ru(bpy)3(2+)/TEA system gave rise to one small and one large peak ECL peak at anodic process. The small anodic ECL peak observed around +0.90 V is due to the direct electrochemical oxidation of TEA at the gold electrode and further chemiluminescent reaction of its oxidative product with Ru(bpy)(3)(2+). The large anodic ECL peak found around +1.35 V results from the reversible electrochemical oxidation of Ru(bpy)(3)(2+) coupled with a slow following reaction of TEA with Ru(bpy)(3)(3+). The effects of viscosity and ionic strength of ionic liquid on diffusion coefficients, catalytic efficiency, and ECL intensity were investigated and discussed to reveal the ECL mechanism of Ru(bpy)(3)(2+)/TEA system in the ionic liquid of BMIPF6.
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