| 1. |
- Plakhova, Tatiana V., et al.
(författare)
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Towards the surface hydroxyl species in CeO2 nanoparticles
- 2019
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Ingår i: Nanoscale. - : ROYAL SOC CHEMISTRY. - 2040-3364 .- 2040-3372. ; 11:39, s. 18142-18149
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Tidskriftsartikel (refereegranskat)abstract
- Understanding the complex chemistry of functional nanomaterials is of fundamental importance. Controlled synthesis and characterization at the atomic level is essential to gain deeper insight into the unique chemical reactivity exhibited by many nanomaterials. Cerium oxide nanoparticles have many industrial and commercial applications, resulting from very strong catalytic, pro- and anti-oxidant activity. However, the identity of the active species and the chemical mechanisms imparted by nanoceria remain elusive, impeding the further development of new applications. Here, we explore the behavior of cerium oxide nanoparticles of different sizes at different temperatures and trace the electronic structure changes by state-of-the-art soft and hard X-ray experiments combined with computational methods. We confirm the absence of the Ce(III) oxidation state at the surface of CeO2 nanoparticles, even for particles as small as 2 nm. Synchrotron X-ray absorption experiments at Ce L-3 and M-5 edges, combined with X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM) and small angle X-ray scattering (SAXS) and theoretical calculations demonstrate that in addition to the nanoceria charge stability, the formation of hydroxyl groups at the surface profoundly affects the chemical performance of these nanomaterials.
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| 2. |
- Ambrozova, I., et al.
(författare)
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Microdosimetry for a carbon ion beam using track-etched detectors
- 2015
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Ingår i: Radiation Protection Dosimetry. - : Oxford University Press (OUP). - 0144-8420 .- 1742-3406. ; 166:1-4, s. 247-252
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Tidskriftsartikel (refereegranskat)abstract
- Track-etched detectors (TED) have been used as linear energy transfer (LET) spectrometers in heavy ion beams for many years. LET spectra and depth-dose distribution of a carbon ion beam were measured behind polymethylmethacrylate degraders at Heavy Ion Medical Accelerator in Chiba, Japan. The measurements were performed along monoenergetic beam with energy 290 MeV u-1 in different positions: (1) at beam extraction area, (2) at beginning, (3) maximum and (4) behind the Bragg peak region (0, 117, 147 and 151 mm of water-equivalent depth, respectively). The LET spectra inside and outside of the primary ion beam have been evaluated. TED record only heavy charged particles with LET above 8-10 keV μm-1, while electrons and ions with lower LET are not detected. The Geant4 simulation toolkit version 4.9.6.P01 has been used to estimate the contribution of non-detected particles to absorbed dose. Presented results demonstrate the applicability of TED for microdosimetry measurements in therapeutic carbon ion beams.
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| 3. |
- Boulanger, Nicolas, et al.
(författare)
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Enhanced Sorption of Radionuclides by Defect-Rich Graphene Oxide
- 2020
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Ingår i: ACS Applied Materials and Interfaces. - : American Chemical Society (ACS). - 1944-8244 .- 1944-8252. ; 12:40, s. 45122-45135
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Tidskriftsartikel (refereegranskat)abstract
- Extremely defect graphene oxide (dGO) is proposed as an advanced sorbent for treatment of radioactive waste and contaminated natural waters. dGO prepared using a modified Hummers oxidation procedure, starting from reduced graphene oxide (rGO) as a precursor, shows significantly higher sorption of U(VI), Am(III), and Eu(III) than standard graphene oxides (GOs). Earlier studies revealed the mechanism of radionuclide sorption related to defects in GO sheets. Therefore, explosive thermal exfoliation of graphite oxide was used to prepare rGO with a large number of defects and holes. Defects and holes are additionally introduced by Hummers oxidation of rGO, thus providing an extremely defect-rich material. Analysis of characterization by XPS, TGA, and FTIR shows that dGO oxygen functionalization is predominantly related to defects, such as flake edges and edge atoms of holes, whereas standard GO exhibits oxygen functional groups mostly on the planar surface. The high abundance of defects in dGO results in a 15-fold increase in sorption capacity of U(VI) compared to that in standard Hummers GO. The improved sorption capacity of dGO is related to abundant carboxylic group attached hole edge atoms of GO flakes as revealed by synchrotron-based extended X-ray absorption fine structure (EXAFS) and high-energy resolution fluorescence detected X-ray absorption near edge structure (HERFD-XANES) spectroscopy.
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| 4. |
- Boulanger, Nicolas, et al.
(författare)
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High Surface Area "3D Graphene Oxide" for Enhanced Sorption of Radionuclides
- 2022
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Ingår i: Advanced Materials Interfaces. - : John Wiley & Sons. - 2196-7350. ; 9:18
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Tidskriftsartikel (refereegranskat)abstract
- Here preparation of high surface area activated reduced graphene oxide (arGO) oxidized into a 3D analogue of defect-rich GO (dGO) is reported. Surface oxidation of arGO results in carbon to oxygen ratio C/O = 3.3, similar to the oxidation state of graphene oxide while preserving high BET surface area of about 880 m2 g−1. Analysis of surface oxidized arGO shows high abundance of oxygen functional groups which converts hydrophobic precursor into hydrophilic material. High surface area carbons provide the whole surface for oxidation without the need of intercalation and lattice expansion. Therefore, surface oxidation methods are sufficient to convert the materials into 3D architectures with chemical properties similar to graphene oxide. The "3D graphene oxide" shows high sorption capacity for U(VI) removal in an extraordinary broad interval of pH. Notably, the surface oxidized carbon material has a rigid 3D structure with micropores accessible for penetration of radionuclide ions. Therefore, the bulk "3D GO" can be used as a sorbent directly without dispersing, the step required for GO to make its surface area accessible for pollutants.
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| 5. |
- Kuzenkova, Anastasiia S., et al.
(författare)
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New insights into the mechanism of graphene oxide and radionuclideinteraction
- 2020
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Ingår i: Carbon. - : Elsevier. - 0008-6223 .- 1873-3891. ; 158, s. 291-302
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Tidskriftsartikel (refereegranskat)abstract
- The sorption of U(VI), Am(III)/Eu(III) and Cs(I) radionuclides by graphene oxides (GOs) synthesized byHummers’s, Brodie’s and Tour’s methods was studied through a combination of batch experiments withcharacterization by microscopic and spectroscopic techniques such as X-ray photoelectron spectroscopy(XPS), attenuated total reflection fourier-transform infrared spectroscopy (ATR-FTIR), high-energy resolutionfluorescence detected X-Ray absorption spectroscopy (HERFD-XANES), extended X-ray absorptionfine structure (EXAFS) and high resolution transmission electron microscopy (HRTEM). Remarkablydifferent sorption capacity and affinity of radionuclides was found towards GOs synthesized by Hummers’sand Brodie’s methods reflecting different structure and oxidation state of these materials.Mechanism underlying GO e radionuclide interaction is determined using variety of experimentaltechniques. For the first time it is shown here that GO - radionuclides interaction takes place on the smallholes or vacancy defects in the GO sheets. Mechanism of GO’s interaction with radionuclides wasanalyzed and specific functional groups responsible for this interaction were identified. Therefore, a newstrategy to produce improved materials with high capacity for radionuclides suggests the use perforatedand highly defected GO with a larger proportion of carboxylic functional groups.
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| 6. |
- Pchelkin, Stepan S., et al.
(författare)
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Algorithms for finding gaits of locomotive mechanisms : case studies for Gorilla robot brachiation
- 2016
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Ingår i: Autonomous Robots. - : Springer Science and Business Media LLC. - 0929-5593 .- 1573-7527. ; 40:5, s. 849-865
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Tidskriftsartikel (refereegranskat)abstract
- We consider a model of a 24-degree-of-freedom monkey robot that is supposed to perform a brachiation locomotion, i.e. to swing from one row of a horizontal ladder to the next one using the arms. The robot hand is constructed as a planar hook so that the contact point, about which the robot swings, is a passive hinge. We identify the 10 most relevant degrees of freedom for this underactuated mechanical system and formulate a tractable search procedure consisting on the following steps: (a) to introduce a parametrized family of coordination patterns to be enforced on the dynamics with respect to a path coordinate; (b) to formulate geometric equality constraints that are necessary to achieve a periodic locomotion; (c) to generate trajectories from integrable reduced dynamics associated with the passive hinge; (d) to evaluate the energetic cost of transport. Moreover, we observe that a linear approximation of the reduced dynamics can be used for trajectory generation, which allows us to incorporate computation of an approximate gradient of the cost function into the search algorithm significantly improving the computational efficiency.
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| 7. |
- Pchelkin, Stepan S., et al.
(författare)
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On Orbital Stabilization for Industrial Manipulators : Case Study in Evaluating Performances of Modified PD plus and Inverse Dynamics Controllers
- 2017
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Ingår i: IEEE Transactions on Control Systems Technology. - 1063-6536 .- 1558-0865. ; 25:1, s. 101-117
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Tidskriftsartikel (refereegranskat)abstract
- Orbital stabilization is one of the available alternatives to the classical asymptotic stabilization, known as the reference tracking control, which is typically considered and implemented for controlling motions of industrial robot manipulators. Since asymptotic orbital stability means convergence of solutions of a closed-loop system to an orbit of a reference trajectory, instead of tracking it as a function of time, new feedback designs can potentially improve performance with respect to several key criteria for industrial manipulators such as absolute path accuracy for tool's motions and robustness to uncertainties in the model. The main outcomes of this paper are a new class of controllers that achieve asymptotic orbital stabilization of motions and a novel analytical method for analysis and redesign of system's dynamics using an excessive set of easy-to-compute transverse coordinates. The contributions have been validated in a series of experimental studies performed on a standard industrial robot ABB IRB 140 with the IRC5-system extended with an open control interface. The outcomes of the tests show that the proposed redesign allows achieving significantly reduced deviations of the actual trajectories from the desired ones at different ranges of speeds and for several different paths, often outperforming the state-of-the-art commercial implementations. A comprehensive discussion of one of such experiments is given.
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| 8. |
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| 9. |
- Amidani, Lucia, et al.
(författare)
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Understanding the size effects on the electronic structure of ThO2 nanoparticles
- 2019
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Ingår i: Physical Chemistry, Chemical Physics - PCCP. - : Royal Society of Chemistry (RSC). - 1463-9076 .- 1463-9084. ; 21:20, s. 10635-10643
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Tidskriftsartikel (refereegranskat)abstract
- Developing characterization techniques and analysis methods adapted to the investigation of nanoparticles (NPs) is of fundamental importance considering the role of these materials in many fields of research. The study of actinide based NPs, despite their environmental relevance, is still underdeveloped compared to that of NPs based on stable and lighter elements. We present here an investigation of ThO2 NPs performed with High-Energy Resolution Fluorescence Detected (HERFD) X-ray Absorption Near-Edge Structure (XANES) and with ab initio XANES simulations. The first post-edge feature of Th L-3 edge HERFD XANES disappears in small NPs and simulations considering non-relaxed structural models reproduce the trends observed in experimental data. Inspection of the simulations of Th atoms in the core and on the surface of the NP indeed demonstrates that the first post-edge feature is very sensitive to the lowering of the number of coordinating atoms and therefore to the more exposed Th atoms at the surface of the NP. The sensitivity of the L-3 edge HERFD XANES to low coordinated atoms at the surface stems from the hybridization of the d-Density of States (DOS) of Th with both O and Th neighboring atoms. This may be a common feature to other oxide systems that can be exploited to investigate surface interactions.
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| 10. |
- Boulanger, Nicolas, et al.
(författare)
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Super-oxidized “activated graphene” as 3D analogue of defect graphene oxide : oxidation degree vs U(VI) sorption
- 2023
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Ingår i: Journal of Hazardous Materials. - : Elsevier. - 0304-3894 .- 1873-3336. ; 457
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Tidskriftsartikel (refereegranskat)abstract
- Porous carbons are not favorable for sorption of heavy metals and radionuclides due to absence of suitable binding sites. In this study we explored the limits for surface oxidation of “activated graphene” (AG), porous carbon material with the specific surface area of ∼2700 m2/g produced by activation of reduced graphene oxide (GO). Set of “Super-Oxidized Activated Graphene” (SOAG) materials with high abundance of carboxylic groups on the surface were produced using “soft” oxidation. High degree of oxidation comparable to standard GO (C/O=2.3) was achieved while keeping 3D porous structure with specific surface area of ∼700–800 m2/. The decrease in surface area is related to the oxidation-driven collapse of mesopores while micropores showed higher stability. The increase in the oxidation degree of SOAG is found to result in progressively higher sorption of U(VI), mostly related to the increase in abundance of carboxylic groups. The SOAG demonstrated extraordinarily high sorption of U(VI) with the maximal capacity up to 5400 μmol/g, that is 8.4 – fold increase compared to non-oxidized precursor AG, ∼50 –fold increase compared to standard graphene oxide and twice higher than extremely defect-rich graphene oxide. The trends revealed here show a way to further increase sorption if similar oxidation degree is achieved with smaller sacrifice of surface area.
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| 11. |
- Cha, Gihoon, et al.
(författare)
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As a single atom Pd outperforms Pt as the most active co-catalyst for photocatalytic H-2 evolution
- 2021
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Ingår i: ISCIENCE. - : Elsevier BV. - 2589-0042. ; 24:8
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Tidskriftsartikel (refereegranskat)abstract
- Here, we evaluate three different noble metal co-catalysts (Pd, Pt, and Au) that are present as single atoms (SAs) on the classic benchmark photocatalyst, TiO2. To trap the single atoms on the surface, we introduced controlled surface vacancies (Ti3+-Ov) on anatase TiO2 nanosheets by a thermal reduction treatment. After anchoring identical loadings of single atoms of Pd, Pt, and Au, we measure the photocatalytic H-2 generation rate and compare it to the classic nanoparticle co-catalysts on the nanosheets. While nanoparticles yield the well-established the hydrogen evolution reaction activity sequence (Pt > Pd > Au), for the single atom form, Pd radically outperforms Pt and Au. Based on density functional theory (DFT), we ascribe this unusual photocatalytic co-catalyst sequence to the nature of the charge localization on the noble metal SAs embedded in the TiO2 surface.
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| 12. |
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| 13. |
- Francis, Z., et al.
(författare)
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Molecular scale track structure simulations in liquid water using the Geant4-DNA Monte-Carlo processes
- 2011
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Ingår i: Applied Radiation and Isotopes. - : Elsevier BV. - 0969-8043 .- 1872-9800. ; 69:1, s. 220-226
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Tidskriftsartikel (refereegranskat)abstract
- This paper presents a study of energy deposits induced by ionising particles in liquid water at the molecular scale Particles track structures were generated using the Geant4-DNA processes of the Geant4 Monte-Carlo toolkit These processes cover electrons (0 025 eV-1 MeV) protons (1 keV-100 MeV) hydrogen atoms (1 keV-100 MeV) and alpha particles (10 keV-40 MeV) including their different charge states Electron ranges and lineal energies for protons were calculated in nanometric and micrometric volumes
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| 14. |
- Goderis, Steven, et al.
(författare)
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Globally distributed iridium layer preserved within the Chicxulub impact structure
- 2021
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Ingår i: Science Advances. - : American Association for the Advancement of Science (AAAS). - 2375-2548. ; 7:9
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Tidskriftsartikel (refereegranskat)abstract
- The Cretaceous-Paleogene (K-Pg) mass extinction is marked globally by elevated concentrations of iridium, emplaced by a hypervelocity impact event 66 million years ago. Here, we report new data from four independent laboratories that reveal a positive iridium anomaly within the peak-ring sequence of the Chicxulub impact structure, in drill core recovered by IODP-ICDP Expedition 364. The highest concentration of ultrafine meteoritic matter occurs in the post-impact sediments that cover the crater peak ring, just below the lowermost Danian pelagic limestone. Within years to decades after the impact event, this part of the Chicxulub impact basin returned to a relatively low-energy depositional environment, recording in unprecedented detail the recovery of life during the succeeding millennia. The iridium layer provides a key temporal horizon precisely linking Chicxulub to K-Pg boundary sections worldwide.
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| 15. |
- Guo, J. H., et al.
(författare)
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The molecular structure of alcohol-water mixtures determined by soft-X-ray absorption and emission spectroscopy
- 2004
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Ingår i: Journal of Electron Spectroscopy and Related Phenomena. - : Elsevier BV. - 0368-2048 .- 1873-2526. ; 137-40:SI, s. 425-428
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Tidskriftsartikel (refereegranskat)abstract
- We have examined the influence of the intermolecular interaction on the local electronic structure by using X-ray absorption and emission spectra of liquid methanol, water, and their mixtures (in molar ratios of 9:1 and 7:3). We find a strong involvement of hydrogen bonding in the mixing of water and methanol molecules. The local electronic structure of water and methanol clusters, where water cluster is bridging within a 6-member open-ring structured methanol cluster, is separately determined. The experimental findings suggest an incomplete mixing of water-alcohol systems and a strong self- association between methanol chain and water cluster through hydrogen bonding. The enhancement of joint water-methanol open-ring structure owes the explanation to the loss of entropy of the aqueous solutions.
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| 16. |
- Ivaniuk, Khrystyna, et al.
(författare)
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(Tetrafluorovinylphenyl)carbazole as a Multifunctional Material for OLED Applications
- 2023
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Ingår i: ACS APPLIED ELECTRONIC MATERIALS. - : AMER CHEMICAL SOC. - 2637-6113. ; 5:4, s. 2156-2168
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Tidskriftsartikel (refereegranskat)abstract
- The multifunctional materials for application in organic light-emitting devices (OLEDs) based on a single structural motif are very desired but quite rare species. Such structures allow simplifying the chemical variety within OLED heterostructures and thus reducing their cost, manufacturing time, and logistic efforts. In this paper, we report the 9-(2,3,5,6-tetrafluoro-4-vinylphenyl)carbazole molecule (Cz4FS) utilized as a fluorescent emitter, host material for quantum dot based OLEDs (QLEDs), acceptor part of the exciplex active layer, and monomer that can be used for the preparation of emissive polymers and copolymers. The external quantum efficiency (EQE) of the corresponding fluorescent OLED based on a Cz4FS single emitter doped into a 1,3-bis(carbazol-9-yl)benzene matrix is 4.2%, which is close to the theoretical limit and maximum brightness at the level of 3600 cd/m2. An OLED based on exciplex emission obtained utilizing Cz4FS as an acceptor demonstrates higher efficiency (5.3%) and much higher brightness near 25 000 cd/m2. A QLED based on Cz4FS as a host for CdSeS/ZnS core-shell quantum dots demonstrates excellent energy transfer from the Cz4FS matrix that results in a clear spectrum of quantum dots with an EQE of 2.3%, maximum of 19 000 cd/m2, and narrow spectral distribution. An OLED based on a Cz4FS-based polymer and copolymer demonstrates not extraordinary efficiency but low-efficiency roll-off in a wide range of current densities.
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| 17. |
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| 18. |
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| 19. |
- Kashtanov, Stepan, et al.
(författare)
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Structural conformation in a poly(ethylene oxide) film determined by X-ray emission spectroscopy
- 2007
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Ingår i: Journal of Physical Chemistry B. - : American Chemical Society (ACS). - 1520-6106 .- 1520-5207. ; 111:40, s. 11658-11661
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Tidskriftsartikel (refereegranskat)abstract
- The electronic structure of pol(ethylene oxide) (PEO) in a thin (< 1 mu) film sample was experimentally probed by X-ray emission spectroscopy. Both nonresonant and resonant X-ray emission spectra were simulated by using density functional theory (DFT) applied to four different models representing different conformations in the polymer. Calculated spectra were compared with experimental results for the PEO film. It was found that the best fit was obtained with the polymer conformation in PEO electrolytes from which the salt (LiMF6, M = P, As, or Sb) had been removed. This conformation is different from the crystalline bulk polymer and implies that film casting, commonly used to form electrolytes for Li polymer batteries, induces the same conformation in the polymer not depending upon the presence of salt.
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| 20. |
- Pachnerova Brabcová, Katerina, 1978, et al.
(författare)
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Clustered DNA damage on subcellular level: effect of scavengers
- 2014
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Ingår i: Radiation and Environmental Biophysics. - : Springer Science and Business Media LLC. - 1432-2099 .- 0301-634X. ; 53:4, s. 705-712
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Tidskriftsartikel (refereegranskat)abstract
- Clustered DNA damages are induced by ionizing radiation, particularly of high linear energy transfer (LET). Compared to isolated DNA damage sites, their biological effects can be more severe. We investigated a clustered DNA damage induced by high LET radiation (C 290 MeV u(-1) and Fe 500 MeV u(-1)) in pBR322 plasmid DNA. The plasmid is dissolved in pure water or in aqueous solution of one of the three scavengers (coumarin-3-carboxylic acid, dimethylsulfoxide, and glycylglycine). The yield of double strand breaks (DSB) induced in the DNA plasmid-scavenger system by heavy ion radiation was found to decrease with increasing scavenging capacity due to reaction with hydroxyl radical, linearly with high correlation coefficients. The yield of non-DSB clusters was found to occur twice as much as the DSB. Their decrease with increasing scavenging capacity had lower linear correlation coefficients. This indicates that the yield of non-DSB clusters depends on more factors, which are likely connected to the chemical properties of individual scavengers.
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| 21. |
- Pachnerova Brabcová, Katerina, 1978, et al.
(författare)
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CONTRIBUTION OF INDIRECT EFFECTS TO CLUSTERED DAMAGE IN DNA IRRADIATED WITH PROTONS
- 2015
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Ingår i: Radiation Protection Dosimetry. - : Oxford University Press (OUP). - 0144-8420 .- 1742-3406. ; 166:1-4, s. 44-48
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Tidskriftsartikel (refereegranskat)abstract
- Protons are the dominant particles both in galactic cosmic rays and in solar particle events and, furthermore, proton irradiation becomes increasingly used in tumour treatment. It is believed that complex DNA damage is the determining factor for the consequent cellular response to radiation. DNA plasmid pBR322 was irradiated at U120-M cyclotron with 30 MeV protons and treated with two Escherichia coli base excision repair enzymes. The yields of SSBs and DSBs were analysed using agarose gel electrophoresis. DNA has been irradiated in the presence of hydroxyl radical scavenger (coumarin-3-carboxylic acid) in order to distinguish between direct and indirect damage of the biological target. Pure scavenger solution was used as a probe for measurement of induced OH center dot radical yields. Experimental OH center dot radical yield kinetics was compared with predictions computed by two theoretical models-RADAMOL and Geant4-DNA. Both approaches use Geant4-DNA for description of physical stages of radiation action, and then each of them applies a distinct model for description of the pre-chemical and chemical stage.
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| 22. |
- Pchelkin, Stepan, et al.
(författare)
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A dynamic human motion : coordination analysis
- 2015
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Ingår i: Biological Cybernetics. - : Springer Science and Business Media LLC. - 0340-1200 .- 1432-0770. ; 109:1, s. 47-62
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Tidskriftsartikel (refereegranskat)abstract
- This article is concerned with the generic structure of the motion coordination system resulting from the application of the method of virtual holonomic constraints (VHCs) to the problem of the generation and robust execution of a dynamic humanlike motion by a humanoid robot. The motion coordination developed using VHCs is based on a motion generator equation, which is a scalar nonlinear differential equation of second order. It can be considered equivalent in function to a central pattern generator in living organisms. The relative time evolution of the degrees of freedom of a humanoid robot during a typical motion are specified by a set of coordination functions that uniquely define the overall pattern of the motion. This is comparable to a hypothesis on the existence of motion patterns in biomechanics. A robust control is derived based on a transverse linearization along the configuration manifold defined by the coordination functions. It is shown that the derived coordination and control architecture possesses excellent robustness properties. The analysis is performed on an example of a real human motion recorded in test experiments.
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| 23. |
- Russell, Brandon K., et al.
(författare)
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Signatures of Non-linear Compton Scattering in Scattered Angular Spectra
- 2023
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Ingår i: Proceedings - Optica Nonlinear Optics Topical Meeting 2023, NLO 2023.
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Konferensbidrag (refereegranskat)abstract
- Simulated electron and photon angular spectra produced by non-linear Compton scattering using different models (LCFA, LMA, classical) are characterized. Signatures to differentiate between models are found and assessed for their ability to be measured experimentally.
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| 24. |
- Shipovskov, Stepan, et al.
(författare)
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Spraying enzymes in microemulsions of AOT in nonpolar organic solvents for fabrication of enzyme electrodes
- 2005
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Ingår i: Analytical Chemistry. - : American Chemical Society (ACS). - 1520-6882 .- 0003-2700. ; 77:21, s. 7074-7079
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Tidskriftsartikel (refereegranskat)abstract
- A new technique suitable for automated, large-scale fabrication of enzyme electrodes by air-spraying enzymes in organic inks is presented. Model oxidoreductases, tyrosinase (Tyr) and glucose oxidase (GOx), were adapted to octane-based ink by entrapment in a system of reverse micelles (RM) of surfactant AOT in octane to separate and stabilize the catalytically active forms of the enzymes in nonpolar organic media. Nonpolar caoutchouk polymer was also used to create a kind of "dry micelles" at the electrode/solution interface. Enzyme/RM/polymer-containing organic inks were air-brushed onto conductive supports and were subsequently covered by sprayed Nafion membranes. The air-brushed enzyme electrodes exhibited relevant bioelectrocatalytic activity toward catechol and glucose, with a linear detection range of 0.1-100 mu M catechol and 0.5-7 mM glucose; the sensitivities were 2.41 A M-1 cm(-2) and 2.98 mA M-1 cm(-2) for Tyr and GOx electrodes, respectively. The proposed technique of air-brushing enzymes in organic inks enables automated construction of disposable enzyme electrodes of various designs on a mass-production scale.
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