On-site analysis of multiple analytes from different classes (such as heavy metals, proteins and small molecules), at the sensitivity required for a selected application, is a hard technological challenge. In this context, optical sensing in miniaturized systems has the largest potential. Baser on our previous findings,[1-3] we present here the design and optimization of a miniaturized optical sensor with multiple channels, capable of multimodal optical detection in each channel, and the proof-of-concept realization of sub-systems providing two complementary detection modes: plasmon enhanced fluorescence and localized surface plasmon resonance. The multichannel (enabling multiplexing) and multimodal optical sensor is designed to have a total size of one inch-square and optimized sensing performance, obtained by combining organic optoelectronic and nanoplasmonic components.
[12] M. Prosa et al., Adv. Funct. Mater. 31 (2021).
[13] M. Bolognesi et al., Adv. Mater. 2208719 (2023) 1–13.
[14] F. Floris et al., Mater. Proc. 14 (2023) 1–5.
Within light sensing optoelectronic devices, multijunction organic and hybrid photodetectors show a large potential. In particular, organic and hybrid phototransistors hold promises for high-sensitivity thanks to their inherent signal-amplification characteristics. However, often a trade-off between a large sensing area, a fast response, and a high specific detectivity is difficult to be achieved. Here we propose an alternative phototransistor concept, that relies on a geometrically engineered large area tri-channel architecture, applied to a multilayer hybrid phototransistor composed of an inorganic In2O3/ZnO n-type field-effect channel, and a top organic bulk-heterojunction or hybrid perovskite light-sensing layer. Up-scalable solution-processing of both the field-effect channel and the light-sensing layers are implemented. Different photoactive layers are used to corroborate and validate the proposed concept. The resulting phototransistor combines the characteristics of easy solution processing, a maximum responsivity of 10^5 A/W thanks to the large electron mobility of the In2O3/ZnO heterointerface, and a maximum specific detectivity of 10^15Jones (at a low gate voltage of 5V and under a low light illumination of 10 nW/cm2), thanks to the large sensing area which is fully exploited in the tri-channel architecture. The improved photoresponse characteristics are accompanied by a fast response (risetime <10ms down to the uW/cm2 of illumination), which is comparable to the time-response of analogous phototransistors in the conventional architecture. The experimental data are supported by device modelling, which helps highlighting the peculiar advantages of the proposed large area, tri-channel and multi-junction phototransistor architecture.
Despite fluorescent sensing is a reference method for the detection of a plethora of different compounds, the exploitation of this class of sensors is still limited to a few application scenarios as a result of the restricted availability of miniaturized, portable, and user-friendly devices.
Here, the smart combination of an organic photodiode (OPD), a Distributed Bragg Filter (DBR), and an organic light-emitting diode (OLED) is proven to provide a stacked device architecture capable of detecting fluorescent signals for a wide range of concentrations of “Rhodamine 700” ranging from 10-3 M to 10-6 M.
Despite fluorescent sensing is a reference method for the detection of a plethora of different compounds, the exploitation of this class of sensors is still limited to a few application scenarios as a result of the restricted availability of miniaturized, portable, and user-friendly devices.
Here, the smart combination of an organic photodiode (OPD), a Distributed Bragg Filter (DBR), and an organic light-emitting diode (OLED) is proven to provide a stacked device architecture capable of detecting fluorescent signals for a wide range of concentrations of “Rhodamine 700” ranging from 10-3 M to 10-5 M.
The integration of multiple devices in a single functional unit is boosting the advent of a series of compact optical sensors for rapid and on-site analysis. In this context, the huge potential of plasmonic-based sensors has been affected by the strict constraints of the detection scheme. The need for laboratory equipment, such as laser sources and expensive prism-based optics, results therefore in not-portable systems.
Here, an ultra-compact plasmonic sensor is demonstrated through the smart-integration of an organic light-emitting transistor (OLET), an organic photodiode (OPD), and a nanostructured plasmonic grating (NPG).[1] The direct integration of the OPD onto the planar structure of the OLET provided an unprecedented high degree of proximity of the light-source and light detecting areas, which enabled the exploitation of the angle-dependent sensing characteristics of the NPG.
The most effective 3D layout of integration, including the optimal size and relative positioning of the three elements (i.e. OLET, OPD, and NPG), was unravelled by an advanced simulation tool, which also predicted the signal variation of the sensor under different conditions. Accordingly, the effectiveness of the new plasmonic-based detection scheme was demonstrated by the dependence of the OPD photocurrent on the surrounding environment of the NPG. In particular, a variation of the OPD photocurrent of about 10-9 A was recorded when exposing the NPG from water to alcoholic solutions at different concentrations.
A miniaturized plasmonic sensor with a total size of 0.1 cm3 was therefore obtained through the smart integration of nanometer-thick optoelectronic and plasmonic components.
[1] M. Prosa, et. al. Adv. Funct. Mater. 2021, 2104927. https://doi.org/10.1002/adfm.202104927
Optical sensors are demonstrating the largest potential for Lab-on-a-chip (LOC) systems to perform sensitive, quantitative, and fast sensing for healthcare and environmental monitoring. Among all options, biosensors based on refractometric sensing schemes combine high sensitivity with label-free detection, however, most of them still have not yet been miniaturized in LOC devices for the analysis of biological targets. Here, we demonstrate for the first time a fully miniaturized optical biosensor based on plasmonic-sensing that enables quantitative detection of biological analytes that are potentially found in milk (lactoferrin, streptomycin). The sensor relies on the unprecedented combination of i) miniaturized, monolithically integrated, and cost-effective optical transduction elements such as organic light-emitting diodes and organic photodiodes, and ii) immunoassay-based bio-recognition elements, for highly sensitive and specific localized surface plasmon resonance (LSPR) based detection via a nanostructured plasmonic grating. The sensor is also equipped with portable read-out electronics and microfluidic circuitry, allowing fast, reproducible and reliable functioning. The quantitative response is calibrated through reference samples and it allows reaching a limit of detection of 10-4 refractive index units (RIU) as LSPR sensor. The quantitative and analyte-specific detection is demonstrated for lactoferrin in the laboratory, giving a sensitivity as low as 9 ug/mL. The presented work opens the way for the universal application of optical biosensors in LOC devices, for on-site food analysis, and health monitoring, among others.
This work received funding from the European Union's Horizon 2020 research and
innovation programme under grant agreement no. 780839 (MOLOKO) and no. 101016706 (h-ALO).
KEYWORDS: Solar cells, Organic photovoltaics, Polymers, Capacitance, Temperature metrology, Heterojunctions, Interfaces, Video, Current controlled current source
Bulk Heterojunction (BHJ) solar cells have reached Power Conversion Efficiencies (PCE) over 10% but to be a competitive product long lifetimes are mandatory. In this view, guidelines for the prediction and optimization of the device stability are crucial to generate improved materials for efficient and stable BHJ devices. For encapsulated cells, degradation mechanisms can be mainly ascribed to external agents such as light and temperature. In particular, thermal degradation appears to be related not only to the BHJ morphology but also to the adjacent interfaces. Therefore, in order to have a complete description of the thermal stability of a BHJ cell, it is necessary to consider the entire stack degradation processes by using techniques enabling a direct investigation on working devices.
Here, five different donor polymers were selected and the OPV performance of the corresponding BHJ devices were monitored during the thermal degradation at 85°C, showing an exponential decay of the corresponding PCEs. In parallel, we measured the geometrical capacitance of analogous OPV devices as a function of temperature and we observed that at a defined temperature (TMAX), typical for each polymer-based device, the capacitance starts to decrease. Combining all these results we found an evident and direct correlation between TMAX and the PCE decay parameters (obtained from capacitance-temperature an thermal measurements, respectively). This implies that the capacitance-method here presented is a fast, reliable and relatively simple method to predict the thermal stability of BHJ solar cells without the need to perform time-consuming thermal degradation tests.
Access to the requested content is limited to institutions that have purchased or subscribe to SPIE eBooks.
You are receiving this notice because your organization may not have SPIE eBooks access.*
*Shibboleth/Open Athens users─please
sign in
to access your institution's subscriptions.
To obtain this item, you may purchase the complete book in print or electronic format on
SPIE.org.
INSTITUTIONAL Select your institution to access the SPIE Digital Library.
PERSONAL Sign in with your SPIE account to access your personal subscriptions or to use specific features such as save to my library, sign up for alerts, save searches, etc.