High performance optical oxygen sensors based on iridium complexes exhibiting interchromophore energy shuttling.

A doubly pyrene-grafted bis-cyclometallated iridium complex with engineered electronically excited states demonstrates reversible electronic energy transfer between adjacent chromophores giving rise to extremely long-lived red luminescence in solution (τ = 480 µs). Time-resolved spectroscopic studies afforded determination of pertinent photophysical parameters including rates of energy transfer and energy distribution between constituent chromophores in the equilibrated excited molecule (ca. 98% on the organic chromophores). Incorporation into a nanostructured metal-oxide matrix (AP200/19) gave highly sensitive O2 sensing films, as the detection sensitivity was 200-300% higher than with the commonly used PtTFPP and approaches the sensitivity of the best O2-sensing dyes reported to date.

Improved multifrequency phase-modulation method that uses rectangular-wave signals to increase accuracy in luminescence spectroscopy.

We propose a novel multifrequency phase-modulation method for luminescence spectroscopy that uses a rectangular-wave modulated excitation source with a short duty cycle. It is used for obtaining more detailed information about the luminescence system: the information provided by different harmonics allows estimating a model for describing the global frequency response of the luminescent system for a wide range of analyte concentration and frequencies. Additionally, the proposed method improves the accuracy in determination of the analyte concentration. This improvement is based on a simple algorithm that combines multifrequency information provided by the different harmonics of the rectangular-wave signal, which can be easily implemented in existing photoluminescence instruments by replacing the excitation light source (short duty cycle rectangular signal instead of sinusoidal signal) and performing appropriate digital signal processing after the transducer (implemented in software). These claims have been demonstrated by using a well-known oxygen-sensing film coated at the end of an optical fiber [a Pt(II) porphyrin immobilized in polystyrene]. These experimental results show that use of the proposed multifrequency phase-modulation method (1) provides adequate modeling of the global response of the luminescent system (R(2) > 0.9996) and (2) decreases the root-mean-square error in analytical determination (from 0.1627 to 0.0128 kPa at 0.5 kPa O2 and from 0.9393 to 0.1532 kPa at 20 kPa O2) in comparison with a conventional phase-modulation method based on a sinusoidally modulated excitation source (under equal luminous power conditions).

Direct observation of reversible electronic energy transfer involving an iridium center.

A cyclometalated iridium complex is reported where the core complex comprises naphthylpyridine as the main ligand and the ancillary 2,2'-bipyridine ligand is attached to a pyrene unit by a short alkyl bridge. To obtain the complex with satisfactory purity, it was necessary to modify the standard synthesis (direct reaction of the ancillary ligand with the chloro-bridged iridium dimer) to a method harnessing an intermediate tetramethylheptanolate-based complex, which was subjected to acid-promoted removal of the ancillary ligand and subsequent complexation. The photophysical behavior of the bichromophoric complex and a model complex without the pendant pyrene were studied using steady-state and time-resolved spectroscopies. Reversible electronic energy transfer (REET) is demonstrated, uniquely with an emissive cyclometalated iridium center and an adjacent organic chromophore. After excited-state equilibration is established (5 ns) as a result of REET, extremely long luminescence lifetimes of up to 225 µs result, compared to 8.3 µs for the model complex, without diminishing the emission quantum yield. As a result, remarkably high oxygen sensitivity is observed in both solution and polymeric matrices.

High performance optical sensing nanocomposites for low and ultra-low oxygen concentrations using phase-shift measurements.

The accurate and real-time measurement of low and ultra-low concentrations of oxygen using non-invasive methods is a necessity for a multitude of applications, from brewing beer to developing encapsulating barriers for optoelectronic devices. Current optical methods and sensing materials often lack the necessary sensitivity, signal intensity, or stability for practical applications. In this report we present a new optical sensing nanocomposite resulting in an outstanding overall performance when combined with the phase-shift measurement method (determination of luminescence lifetime in the frequency domain). For the first time we have incorporated the standard PtTFPP dye (PtTFPP = platinum(II) 5,10,15,20-meso-tetrakis-(2,3,4,5,6-pentafluorophenyl)-porphyrin) into AP200/19, a nanostructured aluminium oxide-hydroxide solid support. This sensing film shows an excellent sensitivity between 0 and 1% O2 (KSV = 3102 ± 132 bar⁻¹) and between 0 and 10% O2 (KSV = 2568 ± 614 bar⁻¹) as well as Δτ0.05% (62.53 ± 3.66%), which makes it 62 times more sensitive than PtTFPP immobilized in polystyrene and also 8 times more sensitive than PtTFPP immobilized on silica beads. Furthermore the phase-shift measurement method results in a significant improvement (about 23 times) in stability compared to the use of intensity recording methods. The film also displays full reversibility, long shelf stability (no change observed after 12 months), and it is not affected by humidity. To establish this sensing methodology and develop sensors over the full range of the visible light, we also studied three other dye-AP200/19 nanocomposites based on phosphorescent cyclometalated iridium(III) complexes.

Electrophoretic deposition as a new approach to produce optical sensing films adaptable to microdevices.

We report the fabrication of optical oxygen sensor films using electrophoretic deposition (EPD) of poly(styrene-co-maleic anhydride) nanoparticles containing the oxygen-sensitive dye platinum(ii) meso-tetra(pentafluorophenyl)porphine. Compared to other deposition methods, the EPD is simple and allows easy control over deposition, which is crucial for the implementation of optical sensing films in microdevices. By optimizing the synthesis of the functional nanoparticles, anodic EPD can be performed. The amount of deposited particles can be tuned by varying either the electrical potential or the deposition time. The sensing phases were characterized using a phase-modulation technique showing a Stern-Volmer constant (kSV1) between 45 and 52 bar(-1) for gas and of 20.72 bar(-1) in the aqueous phase without leaching of the particles from the surface. The small thickness of the layers lead to short response times (<0.4 s). This is the first time that polymeric optical sensing films have been obtained by EPD from dispersions of oxygen sensing nanoparticles.

In vitro oxygen sensing using intraocular microrobots.

We present a luminescence oxygen sensor integrated with a wireless intraocular microrobot for minimally-invasive diagnosis. This microrobot can be accurately controlled in the intraocular cavity by applying magnetic fields. The microrobot consists of a magnetic body susceptible to magnetic fields and a sensor coating. This coating embodies Pt(II) octaethylporphine (PtOEP) dyes as the luminescence material and polystyrene as a supporting matrix, and it can be wirelessly excited and read out by optical means. The sensor works based on quenching of luminescence in the presence of oxygen. The excitation and emission spectrum, response time, and oxygen sensitivity of the sensor were characterized using a spectrometer. A custom device was designed and built to use this sensor for intraocular measurements with the microrobot. Due to the intrinsic nature of luminescence lifetimes, a frequency-domain lifetime measurement approach was used. An alternative sensor design with increased performance was demonstrated by using poly(styrene-co-maleic anhydride) (PS-MA) and PtOEP nanospheres.