Issue 37, 2015

Facile synthesis of core/shell ZnO/ZnS nanofibers by electrospinning and gas-phase sulfidation for biosensor applications

Abstract

This study describes a new method of passivating ZnO nanofiber-based devices with a ZnS layer. This one-step process was carried out in H2S gas at room temperature, and resulted in the formation of core/shell ZnO/ZnS nanofibers. This study presents the structural, optical and electrical properties of ZnO/ZnS nanofibers formed by a 2 nm ZnS sphalerite crystal shell covering a 5 nm ZnO wurtzite crystal core. The passivation process prevented free carriers from capture by oxygen molecules and significantly reduced the impact of O2 on nanostructure conductivity. The conductivity of the nanofibers was increased by three orders of magnitude after the sulfidation, the photoresponse time was reduced from 1500 s to 30 s, and the cathodoluminescence intensity increased with the sulfidation time thanks to the removal of ZnO surface defects by passivation. The ZnO/ZnS nanofibers were stable in water for over 30 days, and in phosphate buffers of acidic, neutral and alkaline pH for over 3 days. The by-products of the passivation process did not affect the conductivity of the devices. The potential of ZnO/ZnS nanofibers for protein biosensing is demonstrated using biotin and streptavidin as a model system. The presented ZnS shell preparation method can facilitate the construction of future sensors and protects the ZnO surface from dissolving in a biological environment.

Graphical abstract: Facile synthesis of core/shell ZnO/ZnS nanofibers by electrospinning and gas-phase sulfidation for biosensor applications

Supplementary files

Article information

Article type
Paper
Submitted
19 Apr 2015
Accepted
17 Aug 2015
First published
17 Aug 2015

Phys. Chem. Chem. Phys., 2015,17, 24029-24037

Author version available

Facile synthesis of core/shell ZnO/ZnS nanofibers by electrospinning and gas-phase sulfidation for biosensor applications

A. Baranowska-Korczyc, K. Sobczak, P. Dłużewski, A. Reszka, B. J. Kowalski, Ł. Kłopotowski, D. Elbaum and K. Fronc, Phys. Chem. Chem. Phys., 2015, 17, 24029 DOI: 10.1039/C5CP02278A

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