4.7 Article

Ultrasensitive photoelectrochemical aptasensor for diclofenac sodium based on surface-modified TiO2-FeVO4 composite

Journal

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
Volume 413, Issue 1, Pages 193-203

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-020-02991-0

Keywords

Ti3+ self-doping; Oxygen vacancy; Ti3+-O-TiO2; FeVO4 heterojunction; Resonance energy transfer; Photoelectrochemical aptasensor

Funding

  1. National Natural Science Foundation of China [U1504215, 62071169, 21776061]
  2. program for Science & Technology Innovation Talents in Universities of Henan Province [19HASTIT037]
  3. program for Science & Technology Innovation Team in Universities of Henan Province [19IRTSTHN029]

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A photoelectrochemical aptasensing platform was developed by incorporating surface oxygen vacancy defects, Ti3+ self-doping, heterojunction, and resonance energy transfer, for the detection of diclofenac sodium. The platform demonstrated excellent signal amplification, a wide linear range, and a low detection limit.
Herein, a photoelectrochemical (PEC) aptasensing platform was designed by integrating surface oxygen vacancy (OV) defects, Ti3+ self-doping, the heterojunction, and resonance energy transfer (RET) effect into one platform for the detection of diclofenac sodium (DCF). Briefly, OV defects were introduced on TiO2 nanospheres with simultaneous Ti3+ self-doping, followed by a well-separated deposition of FeVO4 nanoparticles on TiO2 to obtain a Ti3+-O-TiO2/FeVO4 heterojunction. The surface modification of OVs, Ti3+ doping, and deposition of FeVO4 were confirmed by SEM, XPS, EPR, DRS, and PEC measurements. The surface OVs and doping of Ti3+ species created a new donor (defect) energy level under the conduction band of TiO2, which minimized the bandgap and thereby improved the visible light absorption of TiO2. Moreover, the capture of photo-excited electrons by surface OVs could hinder the electron-hole recombination. Due to the intimate surface contact and perfect energy matching between TiO2 and FeVO4, the formation of heterojunction decreased the bandgap and facilitated the electron-hole separation of TiO2. All these above events contributed to the enhancement of the PEC signals, which were then quenched by the RET effect between Ti3+-O-TiO2/FeVO4 and Au nanoparticle (AuNP)-labeled cDNA that had been attached to its complementary DCF aptamer on Ti3+-O-TiO2/FeVO4|ITO. The addition of target-DCF detached AuNP-labeled cDNA from the electrode to recover the photocurrent, resulting in a signal-on PEC aptasensor that exhibited a 0.1-500-nM linear range and a detection limit of 0.069 nM for DCF, attributed to the excellent amplification of the proposed aptasensing platform.

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