2014
DOI: 10.1038/ncomms5460
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Ultra-sensitive optical oxygen sensors for characterization of nearly anoxic systems

Abstract: Oxygen quantification in trace amounts is essential in many fields of science and technology. Optical oxygen sensors proved invaluable tools for oxygen measurements in a broad concentration range but until now neither optical nor electrochemical oxygen sensors were able to quantify oxygen in the sub-nanomolar concentration range. Herein we present new optical oxygen sensing materials with unmatched sensitivity. They rely on the combination of ultra-long decaying (several hundred milliseconds lifetime) phosphor… Show more

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Cited by 169 publications
(128 citation statements)
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“…Without resolving submicromolar concentrations, the linear extrapolation of the O 2 -gradient from above 1 to 2 lmol O 2 L -1 (the lower detection limit of many sensors) to zero O 2 severely underestimates the true extension of the submicromolar zone by up to several meters (online resource 2) and lowers the estimated depth of the oxic/anoxic interface. These observations are relevant for the interpretation of suboxic zones that are defined by the absence of both O 2 and H 2 S. If revisited with sensitive profiling equipment, such zones will probably turn out to be much thinner or even non-existing and processes like the oxidation of methane might actually occur at submicromolar O 2 concentrations rather than by anaerobic pathways (Canfield and Thamdrup 2009;Bethke et al 2011;Lehner et al 2014). …”
Section: Discussionmentioning
confidence: 99%
“…Without resolving submicromolar concentrations, the linear extrapolation of the O 2 -gradient from above 1 to 2 lmol O 2 L -1 (the lower detection limit of many sensors) to zero O 2 severely underestimates the true extension of the submicromolar zone by up to several meters (online resource 2) and lowers the estimated depth of the oxic/anoxic interface. These observations are relevant for the interpretation of suboxic zones that are defined by the absence of both O 2 and H 2 S. If revisited with sensitive profiling equipment, such zones will probably turn out to be much thinner or even non-existing and processes like the oxidation of methane might actually occur at submicromolar O 2 concentrations rather than by anaerobic pathways (Canfield and Thamdrup 2009;Bethke et al 2011;Lehner et al 2014). …”
Section: Discussionmentioning
confidence: 99%
“…to β-diketones) which dramatically reduces non-radiative deactivation of the excited triplet state. Indeed, the related work demonstrates that the BF 2 -chelated HPhN possesses extraordinary long phosphorescence decay time of about 300 ms. [73] Thus, back energy transfer is unlikely to significantly reduce the luminescence quantum yields and the main deactivation passway is the emission from 5 D 0 level of Eu(III). However, the back energy transfer may be responsible for extraordinary efficient quenching by molecular oxygen which will be discussed below.…”
Section: Absorption Spectramentioning
confidence: 99%
“…Moreover, they are not susceptible to drift caused by consumption of oxygen by the sensing dye. 32,49,50 In this study, an oxygen-sensitive fluorophore, [Ru(dpp) 3 ] 2þ Cl 2 -tris(4,7-diphenyl-1,10-phenanthroline)ruthenium(II) chloride (Sigma-Aldrich), was used as the oxygen indicator, due to its high photostability and moderate brightness. 33 It has a maximum excitation at a wavelength of 463 nm, while the maximum emission occurs at 618 nm.…”
Section: Fabrication Of Oxygen Sensormentioning
confidence: 99%