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首页> 外文期刊>Analytical chemistry >Electrogenerated Chemiluminescence. 66. The Role of Direct Coreactant Oxidation in the Ruthenium Tris(2,2′)bipyridyl/Tripropylamine System and the Effect of Halide Ions on the Emission Intensity
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Electrogenerated Chemiluminescence. 66. The Role of Direct Coreactant Oxidation in the Ruthenium Tris(2,2′)bipyridyl/Tripropylamine System and the Effect of Halide Ions on the Emission Intensity

机译:电产生的化学发光。 66.直接共反应物氧化在钌三(2,2')联吡啶/三丙胺体系中的作用以及卤离子对发射强度的影响

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We describe the electrogenerated chemiluminescence (ECL) processes of the (Ru(bpy)_(3))~(2+) (bpy=2,2′-bipyridyl)/tripropylamine (TPrA) system at glassy carbon, platinum, and gold electrodes. The electrochemical behavior of TPrA on different electrode materials and its influence on the ECL process are demonstrated. At glassy carbon electrodes, the direct oxidation of TPrA began at ~0.6 V vs SCE and exhibited a broad irreversible anodic peak. Two ECL waves were observed, one in the potential region more negative than 1.0 V vs SCE and one at more positive potentials. The first ECL process apparently occurs without the electrogeneration of (Ru(bpy)_(3))~(3+), in contrast to that of the second ECL wave. At Pt and Au electrodes, however, the formation of surface oxides significantly blocked the direct oxidation of TPrA. An ECL wave below 1.0 V did not appear at Pt and was very weak at gold. The ECL peaks at potentials of 1.1-1.2 V were also much weaker than those observed at the glassy carbon electrode. These results showed that the direct oxidation of TPrA played an important role in the ECL processes. Therefore, the enhancement of the TPrA oxidation current might lead to an increase in the ECL intensity. Small amounts of halide species were found to inhibit the growth of surface oxides on Pt and gold electrodes and led to an obvious increase of TPrA oxidation current. The anodic dissolution of gold in halide-containing solution was also important in activating the gold electrode surface. The electrochemical catalytic effect of bromide further promoted the oxidation of TPrA. A halide effect on ECL at Pt and Au electrodes was also evident. The most effective enhancement of ECL was observed at Au electrode in a bromide-containing solution. This effect was also found in an commercial flow-through instrument (IGEN) and provided a simple way to improve the detection sensitivity at low concentrations of (Ru(bpy)_(3))~(2+).
机译:我们描述了(Ru(bpy)_(3))〜(2+)(bpy = 2,2'-联吡啶基)/三丙胺(TPrA)系统在玻璃碳,铂和金上的电化学发光(ECL)过程电极。证明了TPrA在不同电极材料上的电化学行为及其对ECL工艺的影响。在玻璃碳电极上,TPrA的直接氧化在相对于SCE的约0.6 V处开始,并显示出宽的不可逆阳极峰。观察到两个ECL波,一个在电位区域中的电势比SCE负1.0 V,另一个在更大的正电位。与第二个ECL波相反,第一个ECL过程显然是在没有电生成(Ru(bpy)_(3))〜(3+)的情况下发生的。然而,在Pt和Au电极上,表面氧化物的形成显着阻止了TPrA的直接氧化。低于1.0 V的ECL波在Pt处没有出现,而在金时非常弱。电势为1.1-1.2 V的ECL峰也比在玻璃碳电极上观察到的ECL峰弱得多。这些结果表明,TPrA的直接氧化在ECL过程中起着重要作用。因此,TPrA氧化电流的增加可能导致ECL强度增加。发现少量卤化物会抑制Pt和金电极上表面氧化物的生长,并导致TPrA氧化电流明显增加。金在含卤化物溶液中的阳极溶解对于活化金电极表面也很重要。溴化物的电化学催化作用进一步促进了TPrA的氧化。铂和金电极上的ECL的卤化物效应也很明显。在含溴溶液中的金电极上观察到最有效的ECL增强。在商用流通式仪器(IGEN)中也发现了这种效应,并提供了一种简单的方法来提高低浓度(Ru(bpy)_(3))〜(2+)时的检测灵敏度。

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