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首页> 外文期刊>Electrochimica Acta >Ultrasensitively photoelectronchemical determination of cysteine and coenzyme A with CdSe quantum dots-covered ZnO nanorods photoelectrode
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Ultrasensitively photoelectronchemical determination of cysteine and coenzyme A with CdSe quantum dots-covered ZnO nanorods photoelectrode

机译:用CDSE量子点覆盖ZnO纳米棒的半胱氨酸和辅酶A的超敏感光电子化学测定光电极

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A new photoelectrochemical system was fabricated by incorporating the cysteine or coenzyme A as electron donor into photoelectrochemical reaction of the nanostructured CdSe/ZnO photoelectrode to develop a photoelectrochemical method for the ultrasensitive determination of the cysteine and coenzyme A. The CdSe/ZnO photoelectrode was prepared by covering the CdSe quantum dots on the surface of ZnO nanorods arrays. The property of photoelectrode was investigated as photosensitive interface and electron acceptor, and its photoelectrochemical reaction was study with substrate. Under the 20 mW/cm(2) 410 nm visible light illuminations, the sensitive photocurrent response to the cysteine or coenzyme A was obtained at bias voltage 0 V. After the optimized experimental conditions, the photocurrent was proportional to the concentration of cysteine or the logarithm of coenzyme A concentration in the range of 1.00 x 10(-2)-20.0 mu mol/L and 2.00 x 10(-2)-50.0 mu mol/L, respectively. The detection sensitivity was 71.7 nA/mu mol/L for cysteine. The detection limit was estimated to be 6.00 x 10(-3) mu mol/L (S/N = 3) and 1.00 x 10(-2) mu mol/L (S/N = 3) for cysteine and coenzyme A, respectively. The other amino acids or common coenzymes were not interfering with the determination of cysteine and coenzyme A. Compared with other methods for the determination of cysteine and coenzyme A, the proposed method exhibits a wide measurement range, high sensitivity, and low cost. (c) 2018 Elsevier Ltd. All rights reserved.
机译:通过将半胱氨酸或辅酶A作为电子供体掺入纳米结构CDSE / ZnO光电极的光电化学反应来制造新的光电化学系统,以产生用于超细素和辅酶A的光电化学方法的光电化学方法。CDSE / ZnO光电极通过在ZnO纳米棒阵列表面上覆盖CDSE量子点。研究了光电极的性能作为光敏界面和电子受体,其光电化学反应与基材进行研究。在20mW / cm(2)410nm可见光灯下,在偏置电压0V下获得对半胱氨酸或辅酶A的敏感光电流响应。在优化的实验条件之后,光电流与半胱氨酸浓度成比例或辅酶的对数为1.00×10(-2)-20.0μmmol/ L和2.00×10(-2)-50.0μmmol/ l的浓度。用于半胱氨酸的检测灵敏度为71.7纳/ mu mol / l。检测限估计为半胱氨酸和辅酶A的6.00×10(-3)mm mol / l(s / n = 3)和1.00×10(-2)mm mol / l(s / n = 3),分别。其他氨基酸或常见辅酶不干扰半胱氨酸和辅酶A的测定。与测定半胱氨酸和辅酶A的其他方法相比,该方法表现出广泛的测量范围,高灵敏度和低成本。 (c)2018年elestvier有限公司保留所有权利。

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