Integration of conductive electrodes with 3D tissue models can have great potential for applications in bioelectronics, drug screening, and implantable devices. As conventional electrodes cannot be easily integrated on 3D, polymeric, and biocompatible substrates, alternatives are highly desirable. Graphene offers significant advantages over conventional electrodes due to its mechanical flexibility and robustness, biocompatibility, and electrical properties. However, the transfer of chemical vapor deposition graphene onto millimeter scale 3D structures is challenging using conventional wet graphene transfer methods with a rigid poly (methyl methacrylate) (PMMA) supportive layer. Here, a biocompatible 3D graphene transfer method onto 3D printed structure using a soft poly ethylene glycol diacrylate (PEGDA) supportive layer to integrate the graphene layer with a 3D engineered ring of skeletal muscle tissue is reported. The use of softer PEGDA supportive layer, with a 105times lower Young's modulus compared to PMMA, results in conformal integration of the graphene with 3D printed pillars and allows electrical stimulation and actuation of the muscle ring with various applied voltages and frequencies. The graphene integration method can be applied to many 3D tissue models and be used as a platform for electrical interfaces to 3D biological tissue system.
A key challenge in bioelectronics is to establish and improve the interface between electronic devices and living tissues, enabling a direct assessment of biological systems. Sensors integrated with plant tissue can provide valuable information about the plant itself as well as the surrounding environment, including air and soil quality. An obstacle in developing interfaces to plant tissue is mitigating the formation of fibrotic tissues, which can hinder continuous and accurate sensor operation over extended timeframes. Electronic systems that utilize suitable biocompatible materials alongside appropriate fabrication techniques to establish plant-electronic interfaces could provide for enhanced environmental understanding and ecosystem management capabilities. To meet these demands, this study introduces an approach for integrating printed electronic materials with biocompatible cryogels, resulting in stable implantable hydrogel-based bioelectronic devices capable of long-term operation within plant tissue. These inkjet-printed cryogels can be customized to provide various electronic functionalities, including electrodes and organic electrochemical transistors (OECTs), that exhibit high electrical conductivity for embedded conducting polymer traces (up to 350 S/cm), transconductance for OECTs in the mS range, a capacitance of up to 4.2 mF g−1in suitable structures, high stretchability (up to 330% strain), and self-healing properties. The biocompatible functionalized cryogel-based electrodes and transistors were successfully implanted in plant tissue, and ionic activity in tomato plant stems was collected for over two months with minimal scar tissue formation, making these cryogel-based printed electronic devices excellent candidates for continuous, in-situ monitoring of plant and environmental status and health.
more » « less- Award ID(s):
- 1935594
- PAR ID:
- 10502811
- Publisher / Repository:
- Nature Partner Journals
- Date Published:
- Journal Name:
- npj Flexible Electronics
- Volume:
- 7
- Issue:
- 1
- ISSN:
- 2397-4621
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Abstract -
Abstract Organic electrochemical transistors (OECTs) have gained considerable attention due to their potential applications in emerging biosensor platforms. The use of conjugated polyelectrolytes (CPEs) as active materials in OECTs is particularly advantageous owing to their functional, water‐processable, and biocompatible nature, as well as their tunable electronic and ionic transport properties. However, there exists a lack of systematic studies of the structure‐property relationships of these materials with respect to OECT performance. This study shows how by tuning the molecular weight of self‐doped CPE (CPE‐K) it is possible to fabricate OECTs with a
µC *value of 14.7 F cm−1V−1s−1, one order of magnitude higher than previously reported CPE‐based devices. Furthermore, OECTs with a transconductance of 120 mS are demonstrated via device engineering. While CPE‐K batches with different molecular weights show good doping behavior and high volumetric capacitance, as confirmed by spectroelectrochemistry and electrochemical impedance spectroscopy, the medium molecular weight possesses the highest carrier mobility of ≈0.1 cm2V−1s−1leading to the highest transconductance. The enhanced charge transport is due to a favorable charge percolation pathway, as revealed by the combination of X‐ray analysis and conductive atomic force microscope. These insights provide guidelines for further improving the performance of CPE‐based OECTs. -
Abstract Organic electrochemical transistors (OECTs) have shown promise as transducers and amplifiers of minute electronic potentials due to their large transconductances. Tuning the OECT threshold voltage is important to achieve low‐powered devices with amplification properties within the desired operational voltage range. However, traditional design approaches have struggled to decouple channel and materials properties from threshold voltage, thereby compromising on several other OECT performance metrics, such as electrochemical stability, transconductance, and dynamic range. In this work, simple solution‐processing methods are utilized to chemically dope polymer gate electrodes, thereby controlling their work function, which in turn tunes the operation voltage range of the OECTs without perturbing their channel properties. Chemical doping of initially air‐sensitive polymer electrodes further improves their electrochemical stability in ambient conditions. Thus, OECTs that are simultaneously low‐powered and electrochemically resistant to oxidative side reactions under ambient conditions are demonstrated. This approach shows that threshold voltage, which is once interwoven with other OECT properties, can in fact be an independent design parameter, expanding the design space of OECTs.
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Abstract Low‐cost biosensors that can rapidly and widely monitor plant nutritional levels will be critical for better understanding plant health and improving precision agriculture decision making. In this work, fully printed ion‐selective organic electrochemical transistors (OECTs) that can detect macronutrient concentrations in whole plant sap are described. Potassium, the most concentrated cation in the majority of plants, is selected as the target analyte as it plays a critical role in plant growth and development. The ion sensors demonstrate high current (170 µA dec−1) and voltage (99 mV dec−1) sensitivity, and a low limit of detection (10 × 10−6
m ). These OECT biosensors can be used to determine potassium concentration in raw sap and sap‐like aqueous environments demonstrating a log‐linear response within the expected physiological range of cations in plants. The performance of these printed devices enables their use in high‐throughput plant health monitoring in agricultural and ecological applications. -
Cryogels, known for their biocompatibility and porous structure, lack mechanical strength, while 3D-printed scaffolds have excellent mechanical properties but limited porosity resolution. By combining a 3D-printed plastic gyroid lattice scaffold with a chitosan–gelatin cryogel scaffold, a scaffold can be created that balances the advantages of both fabrication methods. This study compared the pore diameter, swelling potential, mechanical characteristics, and cellular infiltration capability of combined scaffolds and control cryogels. The incorporation of the 3D-printed lattice demonstrated patient-specific geometry capabilities and significantly improved mechanical strength compared to the control cryogel. The combined scaffolds exhibited similar porosity and relative swelling ratio to the control cryogels. However, they had reduced elasticity, reduced absolute swelling capacity, and are potentially cytotoxic, which may affect their performance. This paper presents a novel approach to combine two scaffold types to retain the advantages of each scaffold type while mitigating their shortcomings.