State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences , Changchun 130022, Jilin, China.
Anal Chem. 2015 Feb 3;87(3):1903-10. doi: 10.1021/ac5041555. Epub 2015 Jan 9.
In this work, we report a green and simple strategy for the in situ growth of surfactant-free Au nanoparticles (Au NPs) on nitrogen-doped graphene quantum dots (Au NPs-N-GQDs). The formation of hybrid was achieved by just mixing the N-GQDs and HAuCl4·4H2O without addition of any other reductant and surfactant. High-resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS) characterizations clearly showed the formation of Au nanoparticles with predominantly exposed (111) facets which can provide more adsorption sites. Such nonsurfactant-capped Au NPs can provide naked catalytic surface with highly electrocatalytic activity. The Au NPs-N-GQDs exhibit high sensitivity and selectivity for electrochemical detection of hydrogen peroxide (H2O2) with a low detection limit of 0.12 μM and sensitivity of 186.22 μA/mM cm(2). Importantly, the Au NPs-N-GQDs-based electrochemical biosensor has shown great potential applications for detection of H2O2 levels in human serum samples and that released from human cervical cancer cells with satisfactory results. The present study demonstrates that such novel Au NPs-N-GQDs nanocomposite is promising for fabrication of nonenzymatic H2O2 biosensors.
在这项工作中,我们报告了一种绿色简单的策略,用于在氮掺杂石墨烯量子点(Au NPs-N-GQDs)上原位生长无表面活性剂的金纳米粒子(Au NPs)。通过混合 N-GQDs 和 HAuCl4·4H2O,无需添加任何其他还原剂和表面活性剂,即可实现杂化的形成。高分辨率透射电子显微镜(HRTEM)、X 射线衍射(XRD)和 X 射线光电子能谱(XPS)表征清楚地表明,形成了主要暴露(111)面的金纳米粒子,这可以提供更多的吸附位点。这种无表面活性剂覆盖的 Au NPs 可以提供具有高电催化活性的裸露催化表面。Au NPs-N-GQDs 对过氧化氢(H2O2)的电化学检测具有高灵敏度和选择性,检测限低至 0.12 μM,灵敏度为 186.22 μA/mM cm(2)。重要的是,基于 Au NPs-N-GQDs 的电化学生物传感器已显示出在检测人血清样品和人宫颈癌细胞释放的 H2O2 水平方面的巨大应用潜力,结果令人满意。本研究表明,这种新型的 Au NPs-N-GQDs 纳米复合材料有望用于制备非酶 H2O2 生物传感器。