No abstract

Non-aqueous metal-oxygen batteries depend critically on the reversible formation/decomposition of metal oxides on cycling. Irreversible parasitic reactions cause poor rechargeability, efficiency, and cycle life and have predominantly been ascribed to the reactivity of reduced oxygen species with cell components. These species, however, cannot fully explain the side reactions. Here we show that singlet oxygen forms at the cathode of a lithium-oxygen cell during discharge and from the onset of charge, and accounts for the majority of parasitic reaction products. The amount increases during discharge, early stages of charge, and charging at higher voltages, and is enhanced by the presence of trace water. Superoxide and peroxide appear to be involved in singlet oxygen generation. Singlet oxygen traps and quenchers can reduce parasitic reactions effectively. Awareness of the highly reactive singlet oxygen in non-aqueous metal-oxygen batteries gives a rationale for future research towards achieving highly reversible cell operation.

Continuous monitoring of oxygen concentration is of great importance in many different areas of research which range from medical applications to food packaging. In the last three decades, significant progress has been made in the field of optical sensing technology and this review will highlight the one inherent to the development of oxygen indicators. The first section outlines the bioanalytical fields in which optical oxygen sensors have been applied. The second section gives the reader a comprehensive summary of the existing oxygen indicators with a critical highlight on their photophysical and sensing properties. Altogether, this review is meant to give the potential user a guide to select the most suitable oxygen indicator for the particular application of interest.

A simple, high resolution colormetric planar optode imaging approach is presented. The approach is simple and inexpensive yet versatile, and can be used to study the two-dimensional distribution and dynamics of a range of analytes. The imaging approach utilizes the inbuilt color filter of standard commercial digital single lens reflex cameras to simultaneously record different colors (red, green, and blue) of luminophore emission light using only one excitation light source. Using the ratio between the intensity of the different colors recorded in a single image analyte concentrations can be calculated. The robustness of the approach is documented by obtaining high resolution data of O 2 and pH distributions in marine sediments using easy synthesizable sensors. The sensors rely on the platinum(II)octaethylporphyrin (PtOEP) and lipophilic 8-Hydroxy-1,3,6-pyrenetrisulfonic acid trisodium (HPTS) salt derivate for O 2 and pH measurements, respectively. The brightness of both indicators is dramatically enhanced by making use of energy transfer from a donor molecule (Macrolex yellow coumarin). Furthermore, the emission from the donor serves as an internal reference for the O 2 sensor. The approach relies on semitransparent sensors, facilitating visual inspection of the sediment behind the sensors during measurements. Software for data acquisition and calibration will be available from the authors, whereas all hardware is available from a range of commercial sources. The total cost of the complete measuring system is approximately $3000 US.

Cyclometalated iridium(III) coumarin complexes represent new types of probes for optical oxygen sensing. In comparison to the most commonly used ruthenium(II) polypyridyl dyes and porphyrin complexes with platinum group metals, they possess much more efficient visible absorption and higher quantum yields, which results in much higher brightnesses. Spectral properties and oxygen sensitivity can be fine-tuned by varying the nature of the coumarin ligand and using respective monomeric or dimeric complexes. When incorporated in a model polystyrene film the probes show optimal dynamics of luminescence decay time for oxygen monitoring in the range from 0% to 100% air saturation. Cross-sensitivity to temperature is significantly lower than for the commonly used ruthenium(II)-tris-4,7-diphenyl-1,10-phenanthroline oxygen probe. The probes, however, exhibit significantly lower photostability, which restricts their application. If long-term measurements are not required, the probes can be successfully used for reliable monitoring of oxygen concentration. High brightness of the complexes makes them particularly attractive for application in thin films (for monitoring of fast processes) and various types of nano- and microparticles, including magnetic beads. If temperature compensation is not applied, the novel optodes result in the lower errors in determination of oxygen content.

A new intracellular O(2) (icO(2)) sensing probe is presented, which comprises a nanoparticle (NP) formulation of a cationic polymer Eudragit RL-100 and a hydrophobic phosphorescent dye Pt(II)-tetrakis(pentafluorophenyl)porphyrin (PtPFPP). Using the time-resolved fluorescence (TR-F) plate reader set-up, cell loading was investigated in detail, particularly the effects of probe concentration, loading time, serum content in the medium, cell type, density, etc. The use of a fluorescent analogue of the probe in conjunction with confocal microscopy and flow cytometry analysis, revealed that cellular uptake of the NPs is driven by nonspecific energy-dependent endocytosis and that the probe localizes inside the cell close to the nucleus. Probe calibration in biological environment was performed, which allowed conversion of measured phosphorescence lifetime signals into icO(2) concentration (μM). Its analytical performance in icO(2) sensing experiments was demonstrated by monitoring metabolic responses of mouse embryonic fibroblast cells under ambient and hypoxic macroenvironment. The NP probe was seen to generate stable and reproducible signals in different types of mammalian cells and robust responses to their metabolic stimulation, thus allowing accurate quantitative analysis. High brightness and photostability allow its use in screening experiments with cell populations on a commercial TR-F reader, and for single cell analysis on a fluorescent microscope.

The highly sensitive optical detection of oxygen including dissolved oxygen (DO) is of great interest in various applications. We devised a novel room-temperature-phosphorescence (RTP)-based oxygen detection platform by constructing core-shell nanoparticles with water-soluble polymethyloxazoline shells and oxygen-permeable polystyrene cores crosslinked with metal-free purely organic phosphors. The resulting nanoparticles show a very high sensitivity for DO with a limit of detection (LOD) of 60 nm and can be readily used for oxygen quantification in aqueous environments as well as the gaseous phase.

Highly photostable and strongly luminescent europium(III) beta-diketonate complexes are presented that can act as new probes for optical sensing of temperature. They can be excited with the light of a 405-nm LED and possess strong brightnesses. The decay times of the probes contained in a poly(vinyl methyl ketone) film and in poly(tert-butyl styrene) microparticles are highly temperature-dependent between 0 and 70 degrees C. The temperature-sensitive microparticles were dispersed, along with oxygen-sensitive microbeads consisting of a palladium porphyrin oxygen indicator in poly(styrene-co-acrylonitrile), in a thin layer of a hydrogel to give a dually sensing material which is excitable by a single light source. The two emissions can be separated by appropriate optical filters. The response to oxygen and temperature is described by 3D plots, and unbiased values can be obtained for temperature and oxygen, respectively, from the two luminescence signals if refined in an iteration step. The sensing scheme is intended for use in temperature-compensated sensing of oxygen, in contactless sensing of oxygen and temperature in (micro)biological and medical applications, in high-resolution oxygen profiling, and for simultaneous imaging of air pressure and temperature in wind tunnels.