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Now showing 1 - 8 of 8
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    Dual-Zinc Electrode Electrochemical Desalination
    (Weinheim : Wiley-VCH Verlag, 2020) Dai, J.; Wang, J.; Hou, X.; Ru, Q.; He, Q.; Srimuk, P.; Presser, V.; Chen, F.
    Continuous and low-energy desalination technologies are in high demand to enable sustainable water remediation. Our work introduces a continuous desalination process based on the redox reaction of a dual-zinc electrode. The system consists of two zinc foils as redox electrodes with flowing ZnCl2 electrolyte, concentrated and diluted salt streams with three anion- and cation-exchange membranes (AEM and CEM) separated configuration (AEM|CEM|AEM). If a constant current is applied, the negative zinc electrode is oxidized, and electrons are released to the external circuit, whereas the positive zinc electrode is reduced, causing salt removal in the dilution stream. The results showed that brackish water can be directly desalted to 380.6 ppm during a continuous batch-mode process. The energy consumption can be as low as 35.30 kJ mol−1 at a current density of 0.25 mA cm−2, which is comparable to reverse osmosis. In addition, the dual-zinc electrode electrochemical desalination demonstrates excellent rate performance, reversibility, and batch cyclability through electrode exchange regeneration. Our research provides a route for continuous low-energy desalination based on metal redox mediators.
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    Carbide-Derived Niobium Pentoxide with Enhanced Charge Storage Capacity for Use as a Lithium-Ion Battery Electrode
    (Washington, DC : ACS Publications, 2020) Budak, Ö.; Geißler, M.; Becker, D.; Kruth, A.; Quade, A.; Haberkorn, R.; Kickelbick, G.; Etzold, B. J. M.; Presser, V.
    Nb2O5 has been explored as a promising anode material for use as lithium-ion batteries (LIBs), but depending on the crystal structure, the specific capacity was always reported to be usually around or below 200 mAh/g. For the first time, we present coarse-grained Nb2O5 materials that significantly overcome this capacity limitation with the promise of enabling high power applications. Our work introduces coarse-grained carbide-derived Nb2O5 phases obtained either by a one-step or a two-step bulk conversion process. By in situ production of chlorine gas from metal chloride salt at ambient pressure, we obtain in just one step directly orthorhombic Nb2O5 alongside carbide-derived carbon (o-Nb2O5/CDC). In situ formation of chlorine gas from metal chloride salt under vacuum conditions yields CDC covering the remaining carbide core, which can be transformed into metal oxides covered by a carbon shell upon thermal treatment in CO2 gas. The two-step process yielded a mixed-phase tetragonal and monoclinic Nb2O5 with CDC (m-Nb2O5/CDC). Our combined diffraction and spectroscopic data confirm that carbide-derived Nb2O5 materials show disordering of the crystallographic planes caused by oxygen deficiency in the structural units and, in the case of m-Nb2O5/CDC, severe stacking faults. This defect engineering allows access to a very high specific capacity exceeding the two-electron transfer process of conventional Nb2O5. The charge storage capacities of the resulting m-Nb2O5/CDC and o-Nb2O5/CDC are, in both cases, around 300 mAh/g at a specific current of 10 mA/g, thereby, the values are significantly higher than that of the state-of-the-art for Nb2O5 as a LIB anode. Carbide-derived Nb2O5 materials also show robust cycling stability over 500 cycles with capacity fading only 24% for the sample m-Nb2O5/CDC and 28% for o-Nb2O5/CDC, suggesting low degree of expansion/compaction during lithiation and delithiation.
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    High-performance ion removal via zinc–air desalination
    (Amsterdam : Elsevier, 2020) Srimuk, P.; Wang, L.; Budak, Ö.; Presser, V.
    Electrochemical processes enable a new generation of energy-efficient desalination technologies. While ion electrosorption via capacitive deionization is only suitable for brackish water with low molar strength, the use of Faradaic materials capable of reversible ion intercalation or conversion reactions allows energy-efficient removal of ions from seawater. However, the limited charge transfer/storage capacity of Faradaic materials indicates an upper limit for their desalination applications. Therefore, a new electrochemical concept must be explored to exceed the current state-of-the-art results and to push the desalination capacity beyond 100–200 mgNaCl/gelectrode. In this proof-of-concept work, we introduce the new concept of using metal–air battery technology for desalination. We do so by presenting performance data for zinc–air desalination (ZAD) in 600 mM NaCl. The ZAD cell provides a desalination capacity of 0.9–1.0 mgNaCl/cm2 (normalized to the membrane area; corresponding to 1300 mgNaCl/gZn) with a charge efficiency of 70% when charging/discharging the cell at 1 mA/cm2. The energy consumption of ZAD is 68–92 kJ/mol.
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    Emerging, hydrogen-driven electrochemical water purification
    (Amsterdam [u.a.] : Elsevier Science, 2022) Suss, M.E.; Zhang, Y.; Atlas, I.; Gendel, Y.; Ruck, E.B.; Presser, V.
    Energy-efficient technologies for the remediation of water and generation of drinking water is a key towards sustainable technologies. Electrochemical desalination technologies are promising alternatives towards established methods, such as reverse osmosis or nanofiltration. In the last few years, hydrogen-driven electrochemical water purification has emerged. This review article explores the concept of desalination fuel cells and capacitive-Faradaic fuel cells for ion separation.
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    In situ tracking of defect healing and purification of single-wall carbon nanotubes with laser radiation by time-resolved Raman spectroscopy
    (Cambridge : Royal Society of Chemistry, 2015) Souza, N.; Zeiger, M.; Presser, V.; Mücklich, F.
    Defects and impurities in carbon nanotubes (CNTs), inherent to all synthesis routes, are generally addressed by thermal and/or chemical post treatments. These require atmosphere control, time-consuming temperature ramping, chemical handling, and often incur further defects. Furthermore, certain applications require nanotube treatments, such as dispersion, that cause further unwanted damage. Laser radiation was found to drastically increase purity, crystallinity and mean inter-defect distance while reducing defects, as indicated by Raman spectroscopy, effectively annealing our single-wall CNTs. Laser power density and radiation times, in other words, fluence, were optimised. When applied to CNTs with mechanically induced defects, these were almost fully eliminated. In addition to the tuned annealing of CNTs, unintentional sample modification can occur during Raman measurements if the influence of the power density and the exposure time are underestimated or disregarded. Fast laser radiation times and simple manipulation outdo common purification treatments. Additionally, selective shape and sitespecific parameters come into play such as interference patterns. Such arrangements of alternating tube quality, that is, in a CNT mat, could be interesting for preferred electronic conduction paths and find applications in, for example, interdigitated electrodes or sensors.
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    Capacitive deionization in organic solutions: Case study using propylene carbonate
    (Cambridge : Royal Society of Chemistry, 2016) Porada, S.; Feng, G.; Suss, M.E.; Presser, V.
    Capacitive deionization (CDI) is an emerging technology for the energy-efficient removal of dissolved ions from aqueous solutions. Expanding this technology to non-aqueous media, we present an experimental characterization of a pair of porous carbon electrodes towards electrosorption of dissolved ions in propylene carbonate. We demonstrate that application of CDI technology for treatment of an organic solution with an electrochemical stability window beyond 1.2 V allows for a higher salt removal capacity and higher charge efficiency as compared to CDI applied for treatment of aqueous electrolytes. Further, we show that using conductivity measurements of the stream emerging from the CDI cell combined with an equilibrium electric double-layer structure model, we can gain insights into charge compensation mechanisms and ion distribution in carbon nanopores.
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    Dispersion analysis of carbon nanotubes, carbon onions, and nanodiamonds for their application as reinforcement phase in nickel metal matrix composites
    (Cambridge : Royal Society of Chemistry, 2015) Reinert, L.; Zeiger, M.; Suárez, S.; Presser, V.; Mücklich, F.
    Dispersions of multi-wall carbon nanotubes, onion-like carbon, and nanodiamonds in ethylene glycol are produced using a homogenizer and an ultrasonic bath, altering the treatment time. The dispersed particles are then used as reinforcement phase for nickel matrix composites. These nanoparticles are chosen to represent different carbon hybridization states (sp2 vs. sp3) or a different particle geometry (0D vs. 1D). This allows for a systematic investigation of the effect of named differences on the dispersibility in the solvent and in the composite, as well as the mechanical reinforcement effect. A comprehensive suite of complementary analytical methods are employed, including transmission electron microscopy, Raman spectroscopy, dynamic light scattering, sedimentation analysis, zeta-potential measurements, scanning electron microscopy, electron back scatter diffraction, and Vickers microhardness measurements. It can be concluded that the maximum achievable dispersion grade in the solvent is similar, not altering the structural integrity of the particles. However, nanodiamonds show the best dispersion stability, followed by onion-like carbon, and finally multi-walled carbon nanotubes. The distribution and agglomerate sizes of the particles within the composites are in good agreement with the dispersion analysis, which is finally correlated with a maximum grain refinement by a factor of 3 and a maximum mechanical reinforcement effect for nanodiamonds.
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    Low voltage operation of a silver/silver chloride battery with high desalination capacity in seawater
    (London : Royal Society of Chemistry, 2019) Srimuk, P.; Husmann, S.; Presser, V.
    Technologies for the effective and energy efficient removal of salt from saline media for advanced water remediation are in high demand. Capacitive deionization using carbon electrodes is limited to highly diluted salt water. Our work demonstrates the high desalination performance of the silver/silver chloride conversion reaction by a chloride ion rocking-chair desalination mechanism. Silver nanoparticles are used as positive electrodes while their chlorination into AgCl particles produces the negative electrode in such a combination that enables a very low cell voltage of only Δ200 mV. We used a chloride-ion desalination cell with two flow channels separated by a polymeric cation exchange membrane. The optimized electrode paring between Ag and AgCl achieves a low energy consumption of 2.5 kT per ion when performing treatment with highly saline feed (600 mM NaCl). The cell affords a stable desalination capacity of 115 mg g-1 at a charge efficiency of 98%. This performance aligns with a charge capacity of 110 mA h g-1. © The Royal Society of Chemistry.