Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/95723
Title: Graphene ultrathin film electrode for detection of lead ions in acetate buffer solution
Authors: Wang, Zhaomeng
Liu, Erjia
Issue Date: 2012
Source: Wang, Z., & Liu, E. (2013). Graphene ultrathin film electrode for detection of lead ions in acetate buffer solution. Talanta, 103, 47-55.
Series/Report no.: Talanta
Abstract: Few-layer graphene ultrathin films were synthesized via solid-state carbon diffusion from amorphous carbon (a-C) thin layers sputtering coated on Si substrates with or without a SiO2 layer, which an a-C layer was covered by a nickel (Ni) layer as a catalyst. When the Ni/a-C bilayer coated samples were heated at 1000 °C the carbon (C) atoms from the a-C layers diffused into the top Ni layers to form a C rich surface. Upon rapid cooling, the C atoms accumulated on the surface of the Ni layers and formed graphene ultrathin films through nucleation and growth processes. The formation of graphene ultrathin films was confirmed by Raman spectroscopy, high resolution transmission electron microscopy (HR-TEM), electron diffraction, field-emission scanning electron microscopy (FE-SEM) and 4-point probe. The synthesized graphene ultrathin films were used as working electrodes for detection of trace heavy metal ions (Pb2+, as low as 7 nM) in acetate buffer solutions (pH 5.3) using square wave anodic stripping voltammetry (SWASV). The effects of substrate surface condition and Ni layer thickness on the structure and electrochemical properties of graphene ultrathin film electrodes were investigated in detail. Compared to conventional diamond-like carbon (DLC) electrodes, the graphene electrodes developed in this study had better repeatability, higher sensitivity and higher resistance to passivation caused by surface active species.
URI: https://hdl.handle.net/10356/95723
http://hdl.handle.net/10220/11879
ISSN: 0039-9140
DOI: 10.1016/j.talanta.2012.10.005
Rights: © 2012 Elsevier B.V.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:MAE Journal Articles

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