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• A sandwich-type signal off PEC sensor was constructed for PCT detection. • The photoactive matrix was Au NPs/BiOI NSs/B-TiO 2 NPs. • PbS/Co 3 O 4 was as a quenching signal label for signal amplification. • The PEC sensor exhibited a low detection limit of 0.02 pg/mL. A novel signal-off photoelectrochemical (PEC) immunosensor was proposed for procalcitonin (PCT) sensitive detection based on the Au nanoparticles/BiOI nanosheets/Black TiO 2 nanoparticles (Au NPs/BiOI NSs/B-TiO 2 NPs) as photoactive matrix and PbS quantum dots/Co 3 O 4 polyhedron (PbS/Co 3 O 4) as a quenching signal label for signal amplification. Concretely, BiOI NSs was fabricated by successive ionic layer absorption and reaction (SILAR) and formed the interlaced flake-like structure. Then Au NPs dropped on the BiOI NSs/B-TiO 2 NPs electrode forming Au NPs/BiOI NSs/B-TiO 2 NPs sensitization structure, which increased the utilization of visible light and accelerated electron transfer rate, resulting in a desirable PEC signal. PbS/Co 3 O 4 , an effective dual suppression signal quencher, was proposed for signal-off PEC immunosensor to weaken the photocurrent response because of the steric impedance, competitive absorption of light and competing consumption of electron donor. In this proposal, PCT was chosen to measure the performance of the suggested PEC immunosensor. Consequently, the fabricated PEC immunosensor showed a widely detection ranged from 0.1 pg/mL to 50 ng/mL and a low detection limit of 0.02 pg/mL (S/N = 3). What is more, the proposed PEC immunosensor possessed satisfactory selectivity, stability and reproducibility. [ABSTRACT FROM AUTHOR]

• It was the first application of GaON in PEC immunosensors. • An effectively cascade-like energy band edge level was obtained, which can effectively amplified PEC response. • The BiVO 4 /GaON/CdS label-free PEC immunosensor was successfully developed for determination of procalcitonin. In this paper, GaON with excellent photoelectrochemical (PEC) performance was adopted in PEC immunosensor for the first time. Based on CdS sensitized BiVO 4 /GaON composite material, a label-free PEC immunosensor was successfully developed for determination of procalcitonin (PCT). Firstly, BiVO 4 nanoarray was prepared by electrodeposition. Then GaON was added to form the BiVO 4 /GaON composite material, due to the greatly increasing charge transfer efficiency, the PEC signal increased by about 3 times. At last, CdS grew in situ on BiVO 4 /GaON composite that further expanded the light absorption range and improved the light utilization, and the PEC signal further increased again. This PEC immunosensor has a good linear relationship of 0.1 pg mL−1 - 50 ng mL−1 and the detection limitation of 0.03 pg mL−1 is calculated. Importantly, the BiVO 4 /GaON/CdS immunosensor platform showed good specificity and stability, and serum sample analysis have been performed with satisfactory results. [ABSTRACT FROM AUTHOR]

• Ferrocene carboxylic acid inhibited ECL behavior of Ru(bpy) 3 2+. • Ru(bpy) 3 2+ and n-butyl diethanolamine co-doped in silica nanoparticles. • The quenching mechanism was Fca+ decrease Ru(bpy) 3 2+ * through electron-transfer. • The sandwich quenching ECL immunosensor was used to detect procalcitonin. Herein, a quenching electrochemiluminescence (ECL) immunosensor was applied to detect procalcitonin (PCT) based on ferrocene carboxylic acid (Fca) quenching the ECL of Ru(bpy) 3 2+. Co-reactant n-butyl diethanolamine and Ru(bpy) 3 2+ co-doped in silica nanoparticles which grafted on g-C 3 N 4 surface (RuSiNPs-g-C 3 N 4) as luminophores. g-C 3 N 4 could immobilize large amounts of RuSiNPs due to large specific surface area, besides, its electrical conductivity also contributed to enhance the ECL intensity. N-butyl diethanolamine serving as alternative co-reactant promoted ECL efficiency. Zeolitic Zn2+-imidazolate cross-linked frame-work (ZIF-8) were served as the supporter to immobilize more amounts of Fca, which could remarkably decrease the ECL signal. The quenching mechanism mainly because that the oxidation species of Fca could further react with the excited states of Ru(bpy) 3 2+*. Under optimal experiment conditions, the proposed immunosensor presented a linear response range for detecting PCT from 5 pg mL−1 to 100 ng mL−1 with a detection limit of 0.85 pg mL−1 (S/N = 3). Furthermore, the proposed ECL immunosensor presented favorable specificity, good stability as well as excellent reproducibility, this strategy can offer a guiding significance in fundamental and clinical analysis of PCT. [ABSTRACT FROM AUTHOR]

• The signal indicator and matrix, Fe 3 S 4 -Pd, displayed excellent electrocatalytic activity for H 2 O 2 redox reaction. • Magnetic glassy carbon electrode was used to firmly immobilized the magnetic Fe 3 S 4 -Pd to achieve satisfied stability. • PBG nanomaterial played a role as the electron blocking label that realized a sensitive variation of current signal. • The signal-off sensing platform was successfully constructed, with a low detection limit of 130 fg/mL. Herein, a sandwich-type electrochemical (EC) immunosensor is proposed based on a special signal-off mode for the sensitive detection of procalcitonin (PCT) by utilizing Fe 3 S 4 loaded with Pd nanoparticles (Fe 3 S 4 -Pd) as a signal indicator and matrix and functionalized pineal mesoporous bioactive glass (PBG) as the label for signal amplification. Fe 3 S 4 -Pd not only shows excellent electrocatalytic activity for the H 2 O 2 redox reaction but is also firmly immobilized on a magnetic glassy carbon electrode due to its excellent magnetic properties; because of the above features, this immunosensor exhibits excellent sensitivity and stability, respectively. Glutaraldehyde is used as a cross-linking agent to bond the secondary antibodies (Ab 2) with PBG. It is worth mentioning that the electron transfer rate between the electrolyte and electrode is decreased significantly by PBG-Ab 2 ; thus, a sensitive variation in the current signal is observed, and a further improvement in the sensitivity of the immunosensor is realized. More importantly, the proposed signal-off sensing system has a wide linear detection range of 500 fg/mL to 50 ng/mL for PCT and a low detection limit of 130 fg/mL, which promotes it as a promising detection method for the sensitive detection of other biomarkers. [ABSTRACT FROM AUTHOR]

• A sandwich-type immunosensor for detection of PCT was designed. • CeO 2 -CuO-Au as platform can promote electron transfer. • Au@Ag-Th as signal labels can further effectually amplify the current signal. • The immunosensor presents prominent performance for PCT detection. Procalcitonin (PCT) is a kind of protein exists in the human blood. If the human bodies are infected with bacteria, fungi or parasites, the value of PCT in blood will be significantly raised. Thereby, we report an electrochemical immunosensor for measurement of PCT using gold nanoparticle (Au NP) decorated CeO 2 -CuO (CeO 2 -CuO-Au) as the platform and thionine modified Au@Ag heterojunction nanorods (Au@Ag-Th) as signal labels. Au NP decorated CeO 2 -CuO exhibits high surface area, high activity and good biocompatibility, which can immobilize more primary antibodies and promote electron transfer. The Au@Ag-Th provides good active sites to link secondary antibodies, further effectually amplify the current signal. This immunosensor exhibits a well-pleasing response with a limit detection of 0.17 pg mL−1 and linear detection between 0.5 pg mL−1 and 50 ng mL−1. Meanwhile, the high sensitivity, excellent specificity and acceptable human serum samples testing results of this method lead to potential applications in diagnosis of bacterial infections. [ABSTRACT FROM AUTHOR]