异质结
材料科学
氧气
纳米颗粒
纳米管
纳米结构
纳米技术
光催化
析氧
化学工程
光电子学
光化学
电化学
催化作用
碳纳米管
化学
电极
物理化学
有机化学
工程类
作者
Si Zhang,Hejie Zheng,Yuping Sun,Fen Li,Tongtong Li,Xiaoqiang Liu,Yanmei Zhou,Weiwei Chen,Huangxian Ju
标识
DOI:10.1016/j.bios.2020.112477
摘要
This work proposed an enhancing mechanism of both oxygen vacancies (OVs) and the heterostructure for amplifying the photoelectrochemical (PEC) aptasensing signal. The OVs were formed by in situ electrochemical reduction of TiO2 nanotube arrays (TNTAs), and well-separated Ag3VO4 nanoparticles (NPs) were then deposited on the TNTAs. The band gaps and positions of these nanomaterials were evaluated by Tauc equation and Mott-Schottky plots to verify the formation of the heterojunction. The OVs and heterojunction greatly enhanced the visible light absorption and improved the charge separation of TNTAs. The amplified PEC signal could be quenched by the resonance energy transfer between Ag3VO4 NPs and gold nanorods (Au NRs), which were labeled on the complementary DNA (cDNA) to the aptamer immobilized on the heterojunction. Upon the recognition of the aptamer to target analyte, the Au NR-cDNA was detached from the sensor, leading to a “signal-on” aptasensing strategy. Under optimal conditions, the PEC aptasensor displayed a detection limit of 0.015 pg mL−1 and a linear range from 0.02 to 300 ng mL−1 for 2,3',5,5'-tetrachlorobiphenyl.
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