4.8 Article

Organic Light-Emitting Diode Sensing Platform: Challenges and Solutions

Journal

ADVANCED FUNCTIONAL MATERIALS
Volume 21, Issue 24, Pages 4744-4753

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.201101536

Keywords

OLED-based sensors; UV OLED-based sensors; microcavity OLED-based sensors; oxygen sensing; microlens arrays; outcoupling enhancement; bioanalyte sensing

Funding

  1. U.S. Department of Energy, Basic Energy Sciences, Materials Sciences and Engineering Division [DE-AC02-07CH11358]

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The organic light-emitting diode (OLED)-based sensing platform is gaining momentum due to unique attributes of the compact OLEDs that are used as excitation sources. This paper, however, points to issues related to this sensing platform that will affect many (bio)chemical sensing applications, in particular in photoluminescence (PL)-based sensors operated in the advantageous time domain, where pulsed OLEDs are utilized. The issues are related to the post-pulse electroluminescence (EL) profile, i.e., transient EL, which depends on the OLED materials and structure, and to the long-wavelength tail of the typically broad-band EL spectrum. Depending on materials and device structure, the transient EL may exhibit spikes peaking at similar to 100200 ns and mu s-long tails. As shown, these interfere with the determination of PL decay times (that are related to analyte concentrations) of sensing elements. The results also indicate that the long-wavelength tail of the EL spectrum contributes to the interfering post-pulse mu s-long EL tail. Hence, it is shown that the choice of OLED materials, the use of microcavity (mu C) OLEDs with tunable, narrower EL bands, and the use of UV OLEDs alleviate these issues, resulting in more reliable data analysis. Furthermore, a 2-D uniform 2 mu m-pitch microlens array that was previously used for improving light extraction from the OLEDs (J.-M. Park et al., Optics Express 2011, 19, A786) is used for directional PL scattering toward the photodetector, which leads to a similar to 2.13.8 fold enhancement of the PL signal. This behavior is shown for oxygen sensing, which is the basis for sensing of bioanalytes such as glucose, lactate, ethanol, cholesterol, and uric acid.

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