| 1. |
- Petsagkourakis, Ioannis, et al.
(författare)
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Improved Performance of Organic Thermoelectric Generators Through Interfacial Energetics
- 2023
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Ingår i: Advanced Science. - : WILEY. - 2198-3844. ; 10:20
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Tidskriftsartikel (refereegranskat)abstract
- The interfacial energetics are known to play a crucial role in organic diodes, transistors, and sensors. Designing the metal-organic interface has been a tool to optimize the performance of organic (opto)electronic devices, but this is not reported for organic thermoelectrics. In this work, it is demonstrated that the electrical power of organic thermoelectric generators (OTEGs) is also strongly dependent on the metal-organic interfacial energetics. Without changing the thermoelectric figure of merit (ZT) of polythiophene-based conducting polymers, the generated power of an OTEG can vary by three orders of magnitude simply by tuning the work function of the metal contact to reach above 1000 mu W cm(-2). The effective Seebeck coefficient (S-eff) of a metal/polymer/metal single leg OTEG includes an interfacial contribution (V-inter/Delta T) in addition to the intrinsic bulk Seebeck coefficient of the polythiophenes, such that S-eff = S + V-inter/Delta T varies from 22.7 mu V K-1 [9.4 mu V K-1] with Al to 50.5 mu V K-1 [26.3 mu V K-1] with Pt for poly(3,4-ethylenedioxythiophene):p-toluenesulfonate [poly(3,4-ethylenedioxythiophene):poly(4-styrenesulfonate)]. Spectroscopic techniques are used to reveal a redox interfacial reaction affecting locally the doping level of the polymer at the vicinity of the metal-organic interface and conclude that the energetics at the metal-polymer interface provides a new strategy to enhance the performance of OTEGs.
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| 2. |
- Priyadarshini, Diana, et al.
(författare)
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Enzymatically Polymerized Organic Conductors on Model Lipid Membranes
- 2023
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Ingår i: Langmuir. - : AMER CHEMICAL SOC. - 0743-7463 .- 1520-5827. ; 39:23, s. 8196-8204
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Tidskriftsartikel (refereegranskat)abstract
- Seamless integration between biological systems and electricalcomponents is essential for enabling a twinned biochemical-electricalrecording and therapy approach to understand and combat neurologicaldisorders. Employing bioelectronic systems made up of conjugated polymers,which have an innate ability to transport both electronic and ioniccharges, provides the possibility of such integration. In particular,translating enzymatically polymerized conductive wires, recently demonstratedin plants and simple organism systems, into mammalian models, is ofparticular interest for the development of next-generation devicesthat can monitor and modulate neural signals. As a first step towardachieving this goal, enzyme-mediated polymerization of two thiophene-basedmonomers is demonstrated on a synthetic lipid bilayer supported ona Au surface. Microgravimetric studies of conducting films polymerizedin situ provide insights into their interactions with a lipid bilayermodel that mimics the cell membrane. Moreover, the resulting electricaland viscoelastic properties of these self-organizing conducting polymerssuggest their potential as materials to form the basis for novel approachesto in vivo neural therapeutics.
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| 3. |
- Strakosas, Xenofon, et al.
(författare)
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Metabolite-induced in vivo fabrication of substrate-free organic bioelectronics
- 2023
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Ingår i: Science. - : AMER ASSOC ADVANCEMENT SCIENCE. - 0036-8075 .- 1095-9203. ; 379:6634, s. 795-802
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Tidskriftsartikel (refereegranskat)abstract
- Interfacing electronics with neural tissue is crucial for understanding complex biological functions, but conventional bioelectronics consist of rigid electrodes fundamentally incompatible with living systems. The difference between static solid-state electronics and dynamic biological matter makes seamless integration of the two challenging. To address this incompatibility, we developed a method to dynamically create soft substrate-free conducting materials within the biological environment. We demonstrate in vivo electrode formation in zebrafish and leech models, using endogenous metabolites to trigger enzymatic polymerization of organic precursors within an injectable gel, thereby forming conducting polymer gels with long-range conductivity. This approach can be used to target specific biological substructures and is suitable for nerve stimulation, paving the way for fully integrated, in vivo-fabricated electronics within the nervous system.
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