在丝网印刷碳电极(SPCE)表面修饰石墨烯-壳聚糖(GPCS)复合膜和CeO2-Au纳米粒子,利用CeO2-Au纳米粒子对弓形虫特异性抗原(Tg-Ag)的固定,构建了用于弓形虫IgM抗体(Tg-IgM)检测的一次性电流型免疫传感器.采用扫描电镜(SEM)和透射电镜(TEM)...在丝网印刷碳电极(SPCE)表面修饰石墨烯-壳聚糖(GPCS)复合膜和CeO2-Au纳米粒子,利用CeO2-Au纳米粒子对弓形虫特异性抗原(Tg-Ag)的固定,构建了用于弓形虫IgM抗体(Tg-IgM)检测的一次性电流型免疫传感器.采用扫描电镜(SEM)和透射电镜(TEM)对该免疫传感器的修饰进行表征,利用循环伏安法(CV)、交流阻抗法(EIS)和差分脉冲伏安法(DPV)进行电化学性能检测.响应电流与Tg-IgM的浓度在7.5×10-4～24 AU mL-1的范围内呈线性相关,检测限为4.4×10-4AU mL-1.该免疫传感器具有良好的灵敏度、特异性、稳定性和重复性.与ELISA方法相比,该方法结果可靠,孵育时间短,可用于临床上Tg-IgM的检测.展开更多
CO2 selective reduction to CO with H2 over a CeO2-supported nano-Au catalyst at atmospheric pres- sure was investigated. A high CO2 conversion, approaching the thermodynamic equilibrium value, and nearly 100% CO selec...CO2 selective reduction to CO with H2 over a CeO2-supported nano-Au catalyst at atmospheric pres- sure was investigated. A high CO2 conversion, approaching the thermodynamic equilibrium value, and nearly 100% CO selectivity were obtained. The surface formate intermediates generated during the reverse water-gas shift reaction at 400 ℃ were identified using in situ diffuse-reflectance infra- red Fourier-transform spectroscopy. The formate consumption to give CO and H20, determined using mass spectrometry, indicated that the reaction proceeded via an associative formate mecha- nism; this contributes to the high Au/CeO2 catalytic activity at low temperatures.展开更多
文摘在丝网印刷碳电极(SPCE)表面修饰石墨烯-壳聚糖(GPCS)复合膜和CeO2-Au纳米粒子,利用CeO2-Au纳米粒子对弓形虫特异性抗原(Tg-Ag)的固定,构建了用于弓形虫IgM抗体(Tg-IgM)检测的一次性电流型免疫传感器.采用扫描电镜(SEM)和透射电镜(TEM)对该免疫传感器的修饰进行表征,利用循环伏安法(CV)、交流阻抗法(EIS)和差分脉冲伏安法(DPV)进行电化学性能检测.响应电流与Tg-IgM的浓度在7.5×10-4～24 AU mL-1的范围内呈线性相关,检测限为4.4×10-4AU mL-1.该免疫传感器具有良好的灵敏度、特异性、稳定性和重复性.与ELISA方法相比,该方法结果可靠,孵育时间短,可用于临床上Tg-IgM的检测.
基金supported by the National Natural Science Foundation of China (11475041, 11175036, 21373037)the Fundamental Research Funds for the Central Universities (DUT16QY49)~~
文摘CO2 selective reduction to CO with H2 over a CeO2-supported nano-Au catalyst at atmospheric pres- sure was investigated. A high CO2 conversion, approaching the thermodynamic equilibrium value, and nearly 100% CO selectivity were obtained. The surface formate intermediates generated during the reverse water-gas shift reaction at 400 ℃ were identified using in situ diffuse-reflectance infra- red Fourier-transform spectroscopy. The formate consumption to give CO and H20, determined using mass spectrometry, indicated that the reaction proceeded via an associative formate mecha- nism; this contributes to the high Au/CeO2 catalytic activity at low temperatures.
