光电流
生物传感器
氧化还原
碘化物
材料科学
光电化学
催化作用
镍
化学
光化学
电极
纳米技术
光电子学
无机化学
电化学
冶金
物理化学
生物化学
作者
Rong Tan,Ying Qin,Mingsheng Lyu,Hengjia Wang,Jinli Li,Zhen Luo,Lili Hu,Wenling Gu,Chengzhou Zhu
出处
期刊:ACS Sensors
[American Chemical Society]
日期:2023-01-09
卷期号:8 (1): 263-269
被引量:11
标识
DOI:10.1021/acssensors.2c02125
摘要
Developing a self-checking photoelectrochemical biosensor with dual photocurrent signals could efficiently eliminate false-positive or false-negative signals. Herein, a novel biosensor with dual photocurrent responses was established for the detection of acetylcholinesterase activity. To achieve photocurrent polarity-switchable behavior, the iodide/tri-iodide redox couple was innovatively introduced to simultaneously consume the photoexcited electrons and holes, which circumvents the inconvenience caused by the addition of different hole- and electron-trapping agents in the electrolyte. Importantly, benefiting from the high catalytic activity, the enhanced photoelectric responsivity can be realized after decorating the counter electrode with nickel single-atom catalysts, which promotes a more efficient iodide/tri-iodide redox reaction under low applied voltages. It is envisioned that the proposed photocurrent polarity switching system offers new routes to sensitive and reliable biosensing.
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