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BIOSENSORS & BIOELECTRONICS · 2017 · IF 7.78

Dual-responsive electrochemical immunosensor for prostate specific antigen detection based on Au-CoS/graphene and CeO2/ionic liquids doped with carboxymethyl chitosan complex

Yicheng Wei,Xiaojian Li,Xu Sun,Hongmin Ma,Yong Zhang,Qin Wei

Combining dual-signal channels of differential pulse voltammetry (DPV) and amperometric i–t curve, we developed an amplified sandwich-type electrochemical immunosensor for ultrasensitive detection of prostate specific antigen (PSA). Due to the large specific surface area and good adsorption property, 3-aminopropyltriethox functionalized CeO 2 mesoporous nanoparticles (NH 2 -M-CeO 2 ) was used for supporting toluidine blue (TB) as the electron transfer mediator and anti-PSA as the signal response. To prevent the leak of TB and facilitate the electron transfer property of NH 2 -M-CeO 2 , ionic liquids doped carboxymethyl chitosan (CMC/ILs) were incorporated and TB/M-CeO 2 /CMC/ILs complex was gotten to act as the label of anti-PSA (Ab 2 ). Meanwhile, Au-CoS/graphene was as the matrix materials modifying the electrode to immobilize anti-PSA (Ab 1 ). Specifically, Au-CoS/graphene cannot produce electrochemical signals through DPV method but can provide an obviously electrochemical signal towards catalysis hydrogen peroxide (H 2 O 2 ) through amperometric i–t curve method. At the time of detection, with the increase of concentrations of PSA, the DPV signals from TB/M-CeO 2 /CMC/ILs were increased and the amperometric i–t curve signals from the Au-CoS/graphene were decreased. Under the optimum conditions, the immunosensor demonstrated remarkable analytical performance of a linear range of 0.5   pg/mL to 50   ng/mL with a detection limit of 0.16   pg/mL for quantitative detection of PSA (S/N=3).

研究领域: 生物医学工程 · 分析化学
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Surfaces and Interfaces · 2024 · IF 5.7

Outside-to-inside: Efficacy comparation of Mn bulk and surface-doped TiO2{201} in E-fueled solar flow battery system

Ping Lu,Zixing Gu,Zihan Zhang,Huaneng Su,Qiang Ma,Chunsheng Li,Lei Wei,Qian Xu

The all-in-one E-fueled solar flow battery system that can be recharged with liquid fuel is a new type of power system. It can continuously convert solar energy into liquid fuel without relying on external power supply equipments. However, the interface between the photoanode and the electrolyte often exhibits unsteady behavior, resulting in poor performance of the system. In this work, the {201} facets are selected and the impact of two doping treatment strategies for TiO 2 {201} photoanode on the performance of the E-fueled solar flow battery system is systematically studied through the I-t curve, linear sweep voltammetry, Mott-Schottky plot. The results show that the un-biased photocharging current of bulk-doped TiO 2 can reach 2.7 mA·cm −2 in the battery system test, only relying on the self-built electric field at the interface, and the energy conversion efficiency approaches 2.67 %. In addition, the performance is analyzed by the combination of transmission electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy and other characterizations, with the aim of distinguishing the effects of bulk- and surface-doped Mn and accurately revealing the mechanism of their influences from the outside to the inside. Finally, the optimization rules of the un-biased light charging mode of the system are explored.

研究领域: 材料科学 · 电化学 · 太阳能转化 · 电池技术
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APPLIED SURFACE SCIENCE · 2022 · IF 7.392

Enhanced visible-light-driven photocatalytic activity of bi-phase titanium dioxide @ covalent organic framework Z-scheme system for photocatalytic removal of Cr (Ⅵ)

Yi Wen,Zheng Huang,Min Zhao,Longshan Zhao

The discharge of industrial heavy metal wastewater not only leads to environmental pollution, but also harms human health, so it is imperative to control heavy metal pollution. In the current work, a sequence of anatase/brookite TiO 2 @COF with different mass ratios, bi-phase TiO 2 and bare COF were successfully synthesized by simple hydrothermal synthesis. The photocatalytic activity of the prepared catalysts was assessed by reducing Cr(Ⅵ) in model pollutant (K 2 Cr 2 O 7 ). Under the condition of pH = 3, the Cr(Ⅵ) reduction rate of TiO 2 @COF-4 was as high as 99.19% in 30 min. The photocatalytic activity of TiO 2 @COF-4 remained stable in four consecutive cycles, suggesting that it has a potential application prospect for the removal of Cr(Ⅵ) in the actual environment. The morphology and structure of photocatalysts were observed by different techniques (SEM/EDS, HRTEM, BET analysis, XRD, FTIR and XPS). The specific reasons for the enhancement of photocatalytic performance of materials were explored by different methods (PL, UV–vis DRS, Mott-Schottky plots, I-T curves and EIS). Finally, we concluded that the photocatalytic system of TiO 2 @COF-4 may follow the typical direct Z- scheme mechanism. This work provides an effective solution for the water treatment of heavy metal pollution.

研究领域: 环境科学 · 材料科学 · 化学工程 · 纳米技术
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BIOSENSORS & BIOELECTRONICS · 2018 · IF 8.173

Dual mode competitive electrochemical immunoassay for B-type natriuretic peptide based on GS/SnO2/polyaniline-Au and ZnCo2O4/N-CNTs

Xuan Li,Li Liu,Xue Dong,Guanhui Zhao,Yueyuan Li,Juncong Miao,Jinglong Fang,Min Cui,Qin Wei,Wei Cao

A sensitive dual mode competitive electrochemical immunosensor for the detection of B-type natriuretic peptide (BNP) was successfully fabricated, which based on differential pulse voltammetry (DPV) and amperometric i-t curve response modes. Polyaniline (PAN) and tin dioxide (SnO 2 ) were loaded on graphene sheets (GS), which could effectively promote the electron transfer process, thereby amplifying the current signal and increasing the sensitivity of the immunosensor. To promote biocompatibility, gold nanoparticles (Au) were incorporated on GS/SnO 2 /PAN (GS/SnO 2 /PAN-Au). GS/SnO 2 /PAN-Au complex was gotten to act as the platform which could provide a clearly DPV signals. N-doped carbon nanotubes (N-CNTs) embellished by ZnCo 2 O 4 quantum dots (ZnCo 2 O 4 /N-CNTs) with excellent catalytic properties for the reduction of H 2 O 2 was gotten to act as the label of the antibody-BNP (Ab), providing an obviously current signal through amperometric i-t curve method. A large quantity of BNP could be stable loaded in the modified electrode via GS/SnO 2 /PAN-Au with excellent electrical conductivity and good biocompatibility , which could compete with target-BNP to combine Ab that labelled by ZnCo 2 O 4 /N-CNTs. Under the optimum conditions, the immunosensor exhibited remarkable analytical performance of a linear range from 0.01 pg/mL to 1 ng/mL with a detection limit of 3.4 fg/mL for quantitative detection of BNP (S/N = 3). This method was able to become a universal strategy for other biological detection.

研究领域: 电化学 · 生物化学 · 纳米技术 · 分析化学 · 生物医学工程
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