Abstract

Phase-resolved luminescence chemical sensors provide the analyte determination based on the estimation of the luminescence lifetime. The lifetime is estimated from an analysis of the amplitudes and/or phases of the excitation and emission signals at one or several modulation frequencies. This requires recording both the excitation signal (used to modulate the light source) and the emission signal (obtained from an optical transducer illuminated by the luminescent sensing phase). The excitation signal is conventionally used as reference, in order to obtain the modulation factor (the ratio between the emission and the excitation amplitudes) and/or the phase shift (the difference between the emission and the excitation phases) at each modulation frequency, which are used to estimate the luminescence lifetime. In this manuscript, we propose a new method providing the luminescence lifetimes (based either on amplitudes or phases) using only the emission signal (i.e., omitting the excitation signal in the procedure). We demonstrate that the luminescence lifetime can be derived from the emission signal when it contains at least two harmonics, because in this case the amplitude and phase of one of the harmonics can be used as reference. We present the theoretical formulation as well as an example of application to an oxygen measuring system. The proposed self-referenced lifetime estimation provides two practical advantages for luminescence chemical sensors. On one hand, it simplifies the instrument architecture, since only one analog-to-digital converter (for the emission signal) is necessary. On the other hand, the self-referenced estimation of the lifetime improves the robustness against degradation of the sensing phase or variations in the optical coupling, which reduces the recalibration requirements when the lifetimes are based on amplitudes.

Highlights

  • Chemical sensing based on quenched luminescence has become increasingly popular in the last decades due to its versatility and accuracy at a reasonable cost [1,2,3,4,5,6]

  • We demonstrate that the luminescence lifetime can be derived from the emission signal when it contains at least two harmonics, because in this case the amplitude and phase of one of the harmonics can be used as reference

  • The phase-resolved luminescence spectroscopy is performed by applying a sinusoidal modulation to the light source, and the lifetime is estimated from the modulation factor and/or the phase shift [5,18,22,23,24,25]

Read more

Summary

Introduction

Chemical sensing based on quenched luminescence has become increasingly popular in the last decades due to its versatility and accuracy at a reasonable cost [1,2,3,4,5,6]. To the best of our knowledge, there is no previous proposal of self-referenced luminescence spectroscopy in the context of phase-resolved luminescence; the method described in this manuscript would provide the advantages of self-referencing to the accurate and inexpensive chemical sensors based on phase-resolved luminescence

Response of a Monoexponential Luminescent System
Conventional Estimation of the Lifetime
Lifetime Derived from the Amplitudes Referenced to the First Harmonic
Lifetime Derived from the Delay Referenced to the First Harmonic
Self-Referenced Lifetime Determination in a Simulation
Determination of the Analyte Concentration
Experimental Design
One-Site and Two-Sites Model Fitting the Experimental Data
Simulations of the Experiments Using the One-Site Model
Simulations of the Experiments Using the Two-Sites Model
Experimental Lifetimes Estimated with the Conventional Method
Experimental Lifetimes Estimated with the Self-Referenced Procedure
Accuracy in the Conventional and Self-Referenced pO2 Determination
Conclusions
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call