| Literature DB >> 26639029 |
Shan-Shan Li1,2, Wen-Juan Li1,2, Tian-Jia Jiang1,2, Zhong-Gang Liu1,2, Xing Chen1, Huai-Ping Cong2, Jin-Huai Liu1, Yu-Ying Huang3, Li-Na Li3, Xing-Jiu Huang1,2.
Abstract
Iron oxide with different crystal phases (α- and γ-Fe2O3) has been applied to electrode coatings and been demonstrated to ultrasensitive and selective electrochemical sensing toward heavy metal ions (e.g., Pb(II)). A range of Pb(II) contents in micromoles (0.1 to 1.0 μM) at α-Fe2O3 nanoflowers with a sensitivity of 137.23 μA μM(-1) cm(-2) and nanomoles (from 0.1 to 1.0 nM) at γ-Fe2O3 nanoflowers with a sensitivity of 197.82 μA nM(-1) cm(-2) have been investigated. Furthermore, an extended X-ray absorption fine structure (EXAFS) technique was applied to characterize the difference of local structural environment of the adsorbed Pb(II) on the surface of α- and γ-Fe2O3. The results first showed that α- and γ-Fe2O3 had diverse interaction between Pb(II) and iron (hydro)oxides, which were consistent with the difference of electrochemical performance. Determining the responses of Cu(II) and Hg(II) as the most appropriate choice for comparison, the stripping voltammetric quantification of Pb(II) with high sensitivity and selectivity at γ-Fe2O3 nanoflower has been demonstrated. This work reveals that the stripping performances of a nanomodifier have to be directly connected with its intrinsic surface atom arrangement.Entities:
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Year: 2015 PMID: 26639029 DOI: 10.1021/acs.analchem.5b03570
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986