Ru(II) Bipyridyl Complex and TiO2 Nanocomposite Based Biomolecule-free Photoelectrochemical Sensor for Highly Selective Determination of Ultra-trace Hg2+ in Aqueous Systems
A biomolecule-free photoelectrochemical(PEC) probe(denoted as Ru-1) was designed, synthesized and coupled with TiO 2 nanoparticles(NPs) for the highly sensitive and selective PEC detection of Hg 2+ , a model analyte with hypertoxicity to both human health and ecosystem. The probe Ru-1 was designed w...
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Veröffentlicht in: | Chemical research in Chinese universities 2019-06, Vol.35 (3), p.370-376 |
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Sprache: | eng |
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Zusammenfassung: | A biomolecule-free photoelectrochemical(PEC) probe(denoted as Ru-1) was designed, synthesized and coupled with TiO
2
nanoparticles(NPs) for the highly sensitive and selective PEC detection of Hg
2+
, a model analyte with hypertoxicity to both human health and ecosystem. The probe Ru-1 was designed with Ru(II) bipyridyl complex as the chromophore, thiocyanate ligand as the recognition unit, and carboxylate group as the linkage site to connect Ru-1 to TiO
2
nanoparticles. Under irradiation, Ru-1 shows strong affinity to TiO
2
and good photophysical properties of strong visible light absorption, slow electron-hole(e-h
+
) recombination, and fast photoelectron injection to TiO
2
nanoparticles
via
the
π
-bridge of 4-(2,2′-bipyridin)-4-yl-thiophene moiety. However, the specific coordination of Hg
2+
with Ru-1
via
the thiol moiety in the thiocyanate enlarges the band gap of the complex and reduces the photocurrent significantly. The synergistic interaction between TiO
2
nanoparticles and the Ru-1 complex led to a selective PEC sensing strategy for Hg
2+
detection. Detectable linear ranges from 10
−12
g/mL to 10
−7
g/mL and from 10
−7
g/mL to 10
−3
g/mL were obtained without the interference from possibly co-existed metal ions. The good analytical performances indicate the chemical probe based biomolecule-free PEC platform may offer a new route for the detection of biologically and environmentally important small molecules. |
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ISSN: | 1005-9040 2210-3171 |
DOI: | 10.1007/s40242-019-8392-z |