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| 2. |
- Annamalai, Alagappan, et al.
(author)
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Influence of Sb5+ as a Double Donor on Hematite (Fe3+) Photoanodes for Surface-Enhanced Photoelectrochemical Water Oxidation
- 2018
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In: ACS Applied Materials and Interfaces. - : American Chemical Society (ACS). - 1944-8244 .- 1944-8252. ; 10:19, s. 16467-16473
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Journal article (peer-reviewed)abstract
- To exploit the full potential of hematite (α-Fe2O3) as an efficient photoanode for water oxidation, the redox processes occurring at the Fe2O3/electrolyte interface need to be studied in greater detail. Ex situ doping is an excellent technique to introduce dopants onto the photoanode surface and to modify the photoanode/electrolyte interface. In this context, we selected antimony (Sb5+) as the ex situ dopant because it is an effective electron donor and reduces recombination effects and concurrently utilize the possibility to tuning the surface charge and wettability. In the presence of Sb5+ states in Sb-doped Fe2O3 photoanodes, as confirmed by X-ray photoelectron spectroscopy, we observed a 10-fold increase in carrier concentration (1.1 × 1020 vs 1.3 × 1019 cm–3) and decreased photoanode/electrolyte charge transfer resistance (∼990 vs ∼3700 Ω). Furthermore, a broad range of surface characterization techniques such as Fourier-transform infrared spectroscopy, ζ-potential, and contact angle measurements reveal that changes in the surface hydroxyl groups following the ex situ doping also have an effect on the water splitting capability. Theoretical calculations suggest that Sb5+ can activate multiple Fe3+ ions simultaneously, in addition to increasing the surface charge and enhancing the electron/hole transport properties. To a greater extent, the Sb5+- surface-doped determines the interfacial properties of electrochemical charge transfer, leading to an efficient water oxidation mechanism.
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| 3. |
- Antlauf, Mathis, et al.
(author)
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Thermal Conductivity of Cellulose Fibers in Different Size Scales and Densities
- 2021
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In: Biomacromolecules. - : American Chemical Society (ACS). - 1525-7797 .- 1526-4602. ; 22:9, s. 3800-3809
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Journal article (peer-reviewed)abstract
- Considering the growing use of cellulose in various applications, knowledge and understanding of its physical properties become increasingly important. Thermal conductivity is a key property, but its variation with porosity and density is unknown, and it is not known if such a variation is affected by fiber size and temperature. Here, we determine the relationships by measurements of the thermal conductivity of cellulose fibers (CFs) and cellulose nanofibers (CNFs) derived from commercial birch pulp as a function of pressure and temperature. The results show that the thermal conductivity varies relatively weakly with density (ρsample = 1340–1560 kg m–3) and that its temperature dependence is independent of density, porosity, and fiber size for temperatures in the range 80–380 K. The universal temperature and density dependencies of the thermal conductivity of a random network of CNFs are described by a third-order polynomial function (SI-units): κCNF = (0.0787 + 2.73 × 10–3·T – 7.6749 × 10–6·T2 + 8.4637 × 10–9·T3)·(ρsample/ρ0)2, where ρ0 = 1340 kg m–3 and κCF = 1.065·κCNF. Despite a relatively high degree of crystallinity, both CF and CNF samples show amorphous-like thermal conductivity, that is, it increases with increasing temperature. This appears to be due to the nano-sized elementary fibrils of cellulose, which explains that the thermal conductivity of CNFs and CFs shows identical behavior and differs by only ca. 6%. The nano-sized fibrils effectively limit the phonon mean free path to a few nanometers for heat conduction across fibers, and it is only significantly longer for highly directed heat conduction along fibers. This feature of cellulose makes it easier to apply in applications that require low thermal conductivity combined with high strength; the weak density dependence of the thermal conductivity is a particularly useful property when the material is subjected to high loads. The results for thermal conductivity also suggest that the crystalline structures of cellulose remain stable up to at least 0.7 GPa.
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| 4. |
- Barbero, David, et al.
(author)
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Carbon nanotube networks : nano-engineering of SWNT networks for enhanced charge transport at ultralow nanotube loading
- 2014
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In: Advanced Materials. - : Wiley-VCH Verlagsgesellschaft. - 0935-9648 .- 1521-4095. ; 26:19, s. 3164-
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Journal article (peer-reviewed)abstract
- Arrays of nano-engineered carbon nanotube networks embedded in nanoscale polymer structures enable highly efficient charge transport as demonstrated by D. R. Barbero and co-workers on page 3111. An increase in charge transport by several orders of magnitude is recorded at low nanotube loading compared to traditional random networks in either insulating (polystyrene) or semiconducting (polythiophene) polymers. These novel networks are expected to enhance the performance of next generation hybrid and carbon based photovoltaic devices.
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| 5. |
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| 6. |
- Barbero, David, et al.
(author)
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Nano-engineering of SWNT networks for enhanced charge transport at ultralow nanotube loading
- 2014
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In: Advanced Materials. - : John Wiley & Sons. - 0935-9648 .- 1521-4095. ; 26:19, s. 3111-3117
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Journal article (peer-reviewed)abstract
- We demonstrate a simple and controllable method to form periodic arrays of highly conductive nano-engineered single wall carbon nanotube networks from solution. These networks increase the conductivity of a polymer composite by as much as eight orders of magnitude compared to a traditional random network. These nano-engineered networks are demonstrated in both polystyrene and polythiophene polymers.
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| 7. |
- Barbero, David R., et al.
(author)
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Ultralow Percolation Threshold in Nanoconfined Domains
- 2017
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In: ACS Nano. - : American Chemical Society (ACS). - 1936-0851 .- 1936-086X. ; 11:10, s. 9906-9913
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Journal article (peer-reviewed)abstract
- Self-assembled percolated networks play an important role in many advanced electronic materials and devices. In nanocarbon composites, decreasing the percolation threshold phi(c) is of paramount importance to reduce nanotube bundling, minimize material resources and costs, and enhance charge transport. Here we demonstrate that three-dimensional nanoconfinement in single-wall carbon nanotube/polymer nanocomposites produces a strong reduction in phi(c) reaching the lowest value ever reported in this system of phi(c) approximate to 1.8 X 10(-5) wt % and 4-5 orders of magnitude lower than the theoretical statistical percolation threshold oh phi(stat) Moreover, a change in network resistivity and electrical conduction was observed with increased confinement, and a simple resistive model is used to accurately estimate the difference in is in the confined networks. These results are explained in terms of networks' size, confinement, and tube orientation as determined by atomic force microscopy, electrical conductivity measurements, and polarized Raman spectroscopy. Our findings provide important insight into nanoscale percolated networks and should find application in electronic nanocomposites and devices.
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| 8. |
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| 9. |
- Barzegar, Hamid Reza, et al.
(author)
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Self-assembled PCBM nanosheets : a facile route to electronic layer-on-Layer heterostructures
- 2018
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In: Nano letters (Print). - : American Chemical Society (ACS). - 1530-6984 .- 1530-6992. ; 18:2, s. 1442-1447
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Journal article (peer-reviewed)abstract
- We report on the self-assembly of semicrystalline [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) nanosheets at the interface between a hydrophobic solvent and water, and utilize this opportunity for the realization of electronically active organic/organic molecular heterostructures. The self-assembled PCBM nanosheets can feature a lateral size of >1 cm2 and be transferred from the water surface to both hydrophobic and hydrophilic surfaces using facile transfer techniques. We employ a transferred single PCBM nanosheet as the active material in a field-effect transistor (FET) and verify semiconductor function by a measured electron mobility of 1.2 × 10–2 cm2 V–1 s–1 and an on–off ratio of ∼1 × 104. We further fabricate a planar organic/organic heterostructure with the p-type organic semiconductor poly(3-hexylthiophene-2,5-diyl) as the bottom layer and the n-type PCBM nanosheet as the top layer and demonstrate ambipolar FET operation with an electron mobility of 8.7 × 10–4 cm2 V–1 s–1 and a hole mobility of 3.1 × 10–4 cm2V–1 s–1.
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| 10. |
- Boulanger, Nicolas, et al.
(author)
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Aramid Based Slot Liners for Low Voltage Electric Motor Applications
- 2024
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In: 2024 IEEE Electrical Insulation Conference, EIC 2024. - : Institute of Electrical and Electronics Engineers (IEEE). - 9798350360431 - 9798350360448 ; , s. 17-21
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Conference paper (peer-reviewed)abstract
- The insulation in the stator of a low voltage electric motor has a double purpose: ensuring the electric insulation around the stator wiring as well as permitting a good evacuation of the generated heat. Improving the heat transfer properties of the slot liner within the stator while maintaining its electrical insulation properties allows for more efficient electric motors. This paper presents different types of composites based on an aramid matrix with boron nitride, zinc oxide and aluminum oxide fillers. The effect of the different filler materials on the thermal conductivity and the electric insulation properties of the slot liner are presented. Perspectives on the needs for a life cycle assessment of the slot liner constituents are evoked.
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