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Design of a Double-Photoelectrode Sensing System with a Metal–Organic Framework-Based Antenna-like Strategy for Highly Sensitive Detection of PD-L1

化学 天线(收音机) 纳米技术 金属有机骨架 材料科学 电信 有机化学 计算机科学 吸附
作者
Yamei Li,Shujun Wang,Yan Zhao,Yueyuan Li,Ping Wang,Hongqiang Xie,Peiqing Zhao,Yueyun Li,Qing Liu,Qin Wei
出处
期刊:Analytical Chemistry [American Chemical Society]
卷期号:95 (22): 8720-8727 被引量:11
标识
DOI:10.1021/acs.analchem.3c01516
摘要

Currently, the construction of heterojunctions as a method to enhance photoelectrochemical (PEC) activity has shown prospective applications in the analytical field. Restricted by carrier separation at the interface, developing a heterojunction sensing platform with high sensitivity remains challenging. Here, a double-photoelectrode PEC sensing platform was fabricated based on an antenna-like strategy by integrating MIL-68(In)–NH2, a p-type metal–organic framework (MOF) photocatalyst, as a photocathode with the type-II heterojunction of CdSe/MgIn2S4 as a photoanode synchronously. According to the ligand-to-metal charge transition (LMCT), the photo-generated carriers of MIL-68(In)–NH2 transferred from the organic ligand to the metal cluster, which provides an efficient antenna-like transfer path for the charge at the heterojunction interface. In addition, the sufficient Fermi energy difference between the double photoelectrode provides the continuous internal driving force required for rapid carrier separation at the anode detection interface, significantly improving the photoelectric conversion efficiency. Hence, compared with the traditional heterojunction single electrode, the photocurrent response of the double-photoelectrode PEC sensing platform developed using the antenna-like strategy is 2.5 times stronger. Based on this strategy, we constructed a PEC biosensor for the detection of programed death-ligand 1 (PD-L1). The elaborated PD-L1 biosensor exhibited sensitive and precise detection capability with a detection range of 1 × 10–5 to 1 × 103 ng/mL and a lower detection limit of 3.26 × 10–6 ng/mL and demonstrated the feasibility of serum sample detection, providing a novel and viable approach for the unmet clinical need of PD-L1 quantification. More importantly, the charge separation mechanism at the heterojunction interface proposed in this study provides new creative inspiration for designing sensors with high-sensitivity PEC performance.

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