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@ARTICLE{Nikolaev:861624,
author = {Nikolaev, Konstantin and Ermolenko, Yuri and Offenhäusser,
Andreas and Ermakov, S. and Mourzina, Youlia},
title = {{M}ultisensor {S}ystems by {E}lectrochemical {N}anowire
{A}ssembly for the {A}nalysis of {A}queous {S}olutions},
journal = {Frontiers in Chemistry},
volume = {6},
issn = {2296-2646},
address = {Lausanne},
publisher = {Frontiers Media},
reportid = {FZJ-2019-02070},
pages = {256},
year = {2018},
abstract = {The development of electrochemical multisensor systems is
driven by the need for fast, miniature, inexpensive,
analytical devices, and advanced interdisciplinary based on
both chemometric and (nano)material approaches. A
multicomponent analysis of complex mixtures in environmental
and technological monitoring, biological samples, and cell
culture requires chip-based multisensor systems with
high-stability sensors. In this paper, we describe the
development, characterization, and applications of
chip-based nanoelectrochemical sensor arrays prepared by the
directed electrochemical nanowire assembly (DENA) of noble
metals and metal alloys to analyze aqueous solutions. A
synergic action of the electrode transducer function and
electrocatalytic activity of the nanostructured surface
toward analytes is achieved in the assembled metal nanowire
(NW) sensors. Various sensor nanomaterials (Pd, Ni, Au, and
their multicomponent compositions) can be electrochemically
assembled on a single chip without employing multiple cycles
of photolithography process to realize multi-analyte sensing
applications as well as spatial resolution of sensor
analysis by this single-chip multisensor system. For
multi-analyte electrochemical sensing, individual
amperometric signals of two or more nanowires can be
acquired, making use of the specific electrocatalytic
surface properties of the individual nanowire sensors of the
array toward analytes. To demonstrate the application of a
new electrochemical multisensor platform, Pd-Au, Pd-Ni, Pd,
and Au NW electrode arrays on a single chip were employed
for the non-enzymatic analysis of hydrogen peroxide,
glucose, and ethanol. The analytes are determined at low
absolute values of the detection potentials with linear
concentration ranges of 1.0 × 10−6 − 1.0 × 10−3 M
(H2O2), 1.5 × 10−7 − 2.0 × 10−3 M (glucose), and 0.7
× 10−3 − 3.0 × 10−2 M (ethanol), detection limits of
2 × 10−7 M (H2O2), 4 × 10−8 M (glucose), and 5.2 ×
10−4 M (ethanol), and sensitivities of 18 μA M−1
(H2O2), 178 μA M−1 (glucose), and 28 μA M−1 (ethanol),
respectively. The sensors demonstrate a high level of
stability due to the non-enzymatic detection mode. Based on
the DENA-assembled nanowire electrodes of a compositional
diversity, we propose a novel single-chip electrochemical
multisensor platform, which is promising for acquiring
complex analytical signals for advanced data processing with
chemometric techniques aimed at the development of
electronic tongue-type multisensor systems for flexible
multi-analyte monitoring and healthcare applications.},
cin = {ICS-8},
ddc = {540},
cid = {I:(DE-Juel1)ICS-8-20110106},
pnm = {523 - Controlling Configuration-Based Phenomena (POF3-523)},
pid = {G:(DE-HGF)POF3-523},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:30009159},
UT = {WOS:000436840000001},
doi = {10.3389/fchem.2018.00256},
url = {https://juser.fz-juelich.de/record/861624},
}