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Sensing complex gaseous mixtures and identifying their composition and concentration have the potential to achieve unprecedented improvements in environmental monitoring, medical diagnostics, industrial safety, and the food/agriculture industry. Electronically transduced chemical sensors capable of recognizing and differentiating specific target gases and transducing these chemical stimuli in a portable electronic device offer an opportunity for impact by bridging the utility of chemical information with global wireless connectivity. Among electronically transduced chemical sensors, chemiresistors stand out as particularly promising due to combined features of low-power requirements, room temperature operation, non-line-of-sight detection, high portability, and exceptional modularity. Relying on changes in resistance of a functional material triggered by variations in the surrounding chemical environment, these devices have achieved part-per-billion sensitivities of analytes by employing conductive polymers, graphene, carbon nanotubes (CNTs), metal oxides, metal nanoparticles, metal dichalcogenides, or MXenes as sensing materials. Despite these tremendous developments, the need for stable, selective, and sensitive chemiresistors demands continued innovation in material design in order to operate in complex mixtures with interferents as well as variations in humidity and temperature. To fill existing gaps in sensing capabilities, conductive metal−organic frameworks (MOFs) and covalent organic frameworks (COFs) have recently emerged as a promising class of materials for chemiresistive sensing. In contrast to previously reported chemiresistors, these materials offer at least three unique features for gas sensing applications: (i) bottom-up synthesis from molecularly precise precursors that allows for strategic control of material−analyte interactions, (ii) intrinsic conductivity that simultaneously facilitates charge transport and signal transduction under low power requirements, and (iii) high surface area that enables the accessibility of abundant active sites and decontamination of gas streams by coordinating to and, sometimes, detoxifying harmful analytes. Through an emphasis on molecular engineering of structure−property relationships in conductive MOFs and COFs, combined with strategic innovations in device integration strategies and device form factor (i.e., the physical dimensions and design of device components), our group has paved the way to demonstrating the multifunctional utility of these materials in the chemiresistive detection of gases and vapors. Backed by spectroscopic assessment of material−analyte interactions, we illustrated how molecular-level features lead to device performance in detection, filtration, and detoxification of gaseous analytes. By merging the bottom-up synthesis of these materials with device integration, we show the versatility and scalability of using these materials in low-power electronic sensing devices. Taken together, our achievements, combined with the progress spearheaded on this class of materials by other researchers, establish conductive MOFs and COFs as promising multifunctional materials for applications in electronically transduced, portable, low-power sensing devices.
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Material and circuit design for organic electronic vapor sensors and biosensors
We summarize our recent results on material, device, and circuit structures for detection of volatile analytes in the atmosphere and proteins in aqueous solution. Common to both types of sensing goals is the design of materials that respond more strongly to analytes of interest than to likely interferents, and the use of chemical and electronic amplification methods to increase the ratio of the desired responses to the drift (signal/noise ratio). Printable materials, especially polymers, are emphasized. Furthermore, the use of multiple sensing elements, typically field-effect transistors, increases the selectivity of the information, either by narrowing the classes of compounds providing the responses, distinguishing time-dependent from dose-dependent responses, and increasing the ratio of analyte responses to environmental drifts. To increase the stability of systems used to detect analytes in solution, we sometimes separate the sensing surface from the output device in an arrangement known as a remote gate. We show that the output device may be an organic-based or a silicon-based transistor, and can respond to electrochemical potential changes at the sensing surface arising from a variety of chemical interactions.
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- PAR ID:
- 10159548
- Date Published:
- Journal Name:
- Proc. SPIE 11096, Organic and Hybrid Sensors and Bioelectronics XII, 110960A
- Volume:
- 11096
- Page Range / eLocation ID:
- 9
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Conference Paper:
- https://doi.org/10.1117/12.2530058
