| 1. |
- Forro, Csaba, et al.
(författare)
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Visualizing and Analyzing 3D Metal Nanowire Networks for Stretchable Electronics
- 2020
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Ingår i: Advanced Theory and Simulations. - : John Wiley & Sons. - 2513-0390. ; 3:8
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Tidskriftsartikel (refereegranskat)abstract
- Composites based on conductive nanowires embedded in elastomers are popular in a wide range of stretchable electronics applications where the requirements are either a stable or a highly increasing electrical resistance upon strain. Despite the widespread use of such composites, their production is not based in solid theoretical grounds but rather in empirical observations. The lack of such a framework is due to limitations in the methods for studying nanowire meshes, in particular the lack of knowledge on the spatial distribution of the nanowires and the change of their position under strain. This hurdle is overcome by collecting 3D reconstructed X-ray tomographies of silver nanowires embedded in polydimethylsiloxane (PDMS) under variable deformations and the missing structural information of the nanomaterial is obtained by unsupervised artificial intelligence image analysis. This allowed to reveal the precise assembly mechanisms of nanowire systems and derive a precise analytical formula for the piezoresistive response of the composite and finally to simulate the behavior of arbitrary samples in-silico.
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| 2. |
- Marie, Rodolphe, et al.
(författare)
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Use of PLL-g-PEG in micro-fluidic devices for localizing selective and specific protein binding
- 2006
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Ingår i: Langmuir. - : American Chemical Society (ACS). - 0743-7463 .- 1520-5827. ; 22:24, s. 10103-10108
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Tidskriftsartikel (refereegranskat)abstract
- By utilizing flow-controlled PLL-g-PEG and PLL-g-PEGbiotin modification of predefined regions of a poly-(dimethylsiloxane) (PDMS) micro-fluidic device, with an intentionally chosen large (similar to 1 cm(2)) internal surface area, we report rapid (10 min), highly localized (6 x 10(-6) cm(2)), and specific surface-based protein capture from a sample volume (100 mu L) containing a low amount of protein (160 attomol in pure buffer and 400 attomol in serum). The design criteria for this surface modification were achieved using QCM-D (quartz crystal microbalance with energy dissipation monitoring) of serum protein adsorption onto PLL-g-PEG-modified oxidized PDMS. Equally good, or almost as good, results were obtained for oxidized SU-8, Topas, and poly(methyl metacrylate) (PMMA), demonstrating the generic potential of PLL-g-PEG for surface modification in various micro-fluidic applications.
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| 3. |
- Sotiriou, Georgios A., et al.
(författare)
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Non-Toxic Dry-Coated Nanosilver for Plasmonic Biosensors
- 2010
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Ingår i: Advanced Functional Materials. - : Wiley. - 1616-301X .- 1616-3028. ; 20:24, s. 4250-4257
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Tidskriftsartikel (refereegranskat)abstract
- The plasmonic properties of noble metals facilitate their use for in vivo bio-applications such as targeted drug delivery and cancer cell therapy. Nanosilver is best suited for such applications as it has the lowest plasmonic losses among all such materials in the UV-visible spectrum. Its toxicity, however, can destroy surrounding healthy tissues and thus, hinders its safe use. Here, that toxicity against a model biological system (Escherichia coli) is "cured" or blocked by coating nanosilver hermetically with a about 2 nm thin SiO(2) layer in one-step by a scalable flame aerosol method followed by swirl injection of a silica precursor vapor (hexamethyldisiloxane) without reducing the plasmonic performance of the enclosed or encapsulated silver nanoparticles (20-40 nm in diameter as determined by X-ray diffraction and microscopy). This creates the opportunity to safely use powerful nanosilver for intracellular bio-applications. The label-free biosensing and surface biofunctionalization of these ready-to-use, non-toxic (benign) Ag nanoparticles is presented by measuring the adsorption of bovine serum albumin (BSA) in a model sensing experiment. Furthermore, the silica coating around nanosilver prevents its agglomeration or flocculation (as determined by thermal annealing, optical absorption spectroscopy and microscopy) and thus, enhances its biosensitivity, including bioimaging as determined by dark field illumination.
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| 4. |
- Stauffer, Flurin, et al.
(författare)
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Soft Electronic Strain Sensor with Chipless Wireless Readout: Toward Real-Time Monitoring of Bladder Volume
- 2018
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Ingår i: Advanced Materials Technologies. - : WILEY. - 2365-709X. ; 3:6
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Tidskriftsartikel (refereegranskat)abstract
- Sensing mechanical tissue deformation in vivo can provide detailed information on organ functionality and tissue states. To bridge the huge mechanical mismatch between conventional electronics and biological tissues, stretchable electronic systems have recently been developed for interfacing tissues in healthcare applications. A major challenge for wireless electronic implants is that they typically require microchips, which adds complexity and may compromise long-term stability. Here, a chipless wireless strain sensor technology based on a novel soft conductor with high cyclic stability is reported. The composite material consists of gold-coated titanium dioxide nanowires embedded in a soft silicone elastomer. The implantable strain sensor is based on an resonant circuit which consists of a stretchable plate capacitor and a coil for inductive readout of its resonance frequency. Successful continuous wireless readout during 50% strain cycles is demonstrated. The sensor element has a Youngs modulus of 260 kPa, similar to that of the bladder in order to not impair physiological bladder expansion. A proof-of-principle measurement on an ex vivo porcine bladder is presented, which shows the feasibility of the presented materials and devices for continuous, wireless strain monitoring of various tissues and organs in vivo.
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