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  • 1
    Online Resource
    Online Resource
    The Electrochemical Society ; 2019
    In:  ECS Meeting Abstracts Vol. MA2019-01, No. 2 ( 2019-05-01), p. 147-147
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2019-01, No. 2 ( 2019-05-01), p. 147-147
    Abstract: Lithium phosphorus oxynitride (Lipon) is the most prominent example of glassy oxynitride electrolytes, which have demonstrated high ionic conductivities, stability over a wide voltage window, and resistance to Li dendrite formation. 1 Perhaps the greatest drawback of glassy oxynitride electrolytes is that expensive, high-vacuum deposition techniques have been necessary to produce electrolyte compositions with high ionic conductivity ( 〉 ~10 -6 S/cm). High-vacuum deposition techniques have low deposition rates (1 – 50 nm/min, which is less than 0.07 g/hr for Lipon at lab scale) and have only been successfully demonstrated for use in thin film batteries. Alternative processing routes for producing Lipon-like electrolytes could enable their wider usage as electrolytes and ionically conductive additives in commercially viable lithium metal and lithium-ion batteries. We have used scalable alternative processing to produce Lipon-like electrolyte nanopowders at a high throughput (5 g/hr at lab scale). This alternative processing method has successfully produced Lipon-like electrolytes that conventional ceramic and glass processing methods have been unable to produce. 2,3 The processed powders have a predominantly amorphous structure (x-ray diffraction), a particle size of ~100 nm (SEM), and a Lipon-like composition (energy dispersive x-ray spectroscopy and inductively coupled plasma optical emission spectroscopy). Neutron pair distribution function analysis has been coupled with ab initio molecular dynamics to verify that the Lipon-like nanopowders have local atomic structures (0 – 20 Å) that are nearly identical to conventionally sputtered Lipon. Impedance spectroscopy was used to measure the ionic conductivity and activation energy of unsintered Lipon-like nanopowder compacts. While interparticle contact resistance likely dominates these values, the unsintered Lipon-like nanopowder compact still demonstrated an ionic conductivity of 5.3 x 10 -7 S/cm at room temperature. Acknowledgements The information, data, and work presented herein was funded by the Advanced Research Projects Agency – Energy (ARPA-E), U.S. Department of Energy, under Award Number DE-AR0000775. This manuscript has been authored by UT-Battelle, LLC, under contract DE-AC05-00OR22725 with the U.S. Department of Energy. Electron microscopy experiments were conducted at ORNL’s Center for Nanophase Materials Sciences, which is a DOE Office of Science User Facility. Computing resources were provided by the Oak Ridge Leadership Computing Facility at the Oak Ridge National Laboratory. A portion of this research used resources at the Spallation Neutron Source, a DOE Office of Science User Facility operated by the Oak Ridge National Laboratory. Brendan Lewis, Rutuja Samant, Dora Cheung, and Bob Herbeck at Buffalo Manufacturing Works aided in the processing of later batches of Lipon-like material. Special thanks to: Brenda Smith, Chelsea Chen, Dale Hensley, and Robert Sacci at Oak Ridge National Laboratory. References 1 Bates, J. B.; Dudney, N. J.; Gruzalski, G. R.; Zuhr, R. A.; Choudhury, A.; Luck, C. F. Sputtering of lithium compounds for preparation of electrolyte films. Solid State Ionics , 1992 , 53-56 , 647-654. 2 Muñoz, F.; Durán, A.; Pascual, L.; Montagne, L.; Revel, B.; Rodrigues, A. C. M. Increased electrical conductivity of LiPON glasses produced by ammonolysis. Solid State Ionics , 2008 , 179 , 574-579. 3 Mascaraque, N.; Fierro, J. L. G.; Durán, A.; Muñoz, F. An interpretation for the increase of ionic conductivity by nitrogen incorporation in LiPON oxynitride glasses. Solid State Ionics , 2013 , 233 , 73-79.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2019
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  • 2
    Online Resource
    Online Resource
    The Electrochemical Society ; 2013
    In:  ECS Meeting Abstracts Vol. MA2013-02, No. 12 ( 2013-10-27), p. 838-838
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2013-02, No. 12 ( 2013-10-27), p. 838-838
    Abstract: Abstract not Available.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2013
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  • 3
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2016-02, No. 2 ( 2016-09-01), p. 162-162
    Abstract: Capacity fade mechanisms can be difficult to pinpoint in conventional composite cathodes for Li-ion batteries. Capacity fade associated with the cathode can be caused by: (1) irreversible reactions involving the active material, possibly with the electrolyte, (2) degraded integrity of the composite structure, or (3) anode contamination by cathode dissolution products. Post-cycling characterization can be difficult, because these potential capacity fade mechanisms would occur in a complicated cathode structure with: porosity, possible microcracks, irregular surfaces, and multiple particulate phases (active material, binder, and conducting additive). Thin film cathodes were used to study how LiV 3 O 8 (LVO) microstructure affects cycling performance without the added complications associated with a conventional composite cathode structure. Thin film cathodes were produced by magnetron sputtering a Pt current collector layer and an LVO layer onto alumina disks. The thin film geometry with its uniform layered structure was well suited for analysis of pristine and cycled LVO cathodes by several characterization techniques, including transmission electron microscopy, energy dispersive x-ray spectroscopy, and x-ray photoelectron spectroscopy. The cycling performance of heat-treated thin film cathodes was directly compared to that of conventional composite cathodes with heat-treated sol-gel derived LVO powder. Thin film and sol-gel derived LVO cathodes showed excellent microstructural and electrochemical agreement as a function of heat-treatment temperature. Depending on heat-treatment temperature, the microstructure ranged from amorphous (as-deposited or low temperature heat-treatment) to coarse-grained crystalline material (higher temperature). The maximum specific capacity and the maximum capacity fade were both observed for LVO nanocrystalline material fired at intermediate temperature, where reduced capacity and reduced capacity fade were observed for higher and lower firing temperatures. Capacity fade was linked to vanadium dissolution, where amorphous LVO cathodes showed much lower vanadium dissolution than nanocrystalline LVO material. This work was supported as part of the Center for Mesoscale Transport Properties, an Energy Frontier Research Center funded by the U.S. Department of Energy, Office of Science, Basic Energy Sciences under Award # DE-SC0012673.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2016
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  • 4
    Online Resource
    Online Resource
    The Electrochemical Society ; 2014
    In:  ECS Meeting Abstracts Vol. MA2014-01, No. 15 ( 2014-04-01), p. 695-695
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2014-01, No. 15 ( 2014-04-01), p. 695-695
    Abstract: We have used computational thermodynamic approach to model Lithium-bearing mixed polyanion (LBMP) as an effort to predict electrochemical properties of glass cathode materials. Individual LBMP have been modeled within the framework of the compound energy formalism (CEF) as implemented in the CALPHAD (CALculation of PHAse Diagram) approach [1, 2]. To model the baseline material Li/FePO 4 thermodynamic descriptions for the crystalline solid and liquid phases of constituent Fe 2 O 3 and P 2 O 5 have been taken from the Scientific Group Thermodata Europe (SGTE) Substance Database and used as reference states. Thermodynamic model parameters for FePO 4 and Fe 4 (P 2 O 7 ) 3 have been self-consistently evaluated to reproduce Fe 2 O 3 -P 2 O 5 pseudo-binary phase diagram reported in the literatures. Afterward thermodynamic model parameters for the FePO 4 -LiFePO 4 pseudo-binary system has been evaluated to represent experimentally determined phase equilibrium data [3, 4]. The model successfully reproduces the miscibility gap at low temperatures by introducing positive interaction between FePO 4 and LiFePO 4 . FIG. 1. Calculated cell circuit voltage of Li x FePO 4 of crystalline and glass phases. Different ratios between the liquid and solid phases of LiFePO 4 and FePO 4 (L:S) have been used to model glass phase. From the developed thermodynamic database the open circuit voltage (OCV) of crystalline and glass Li/FePO 4 have been predicted by calculating chemical potential of Li (see FIG. 1). In order to model the Li x FePO 4 glass phase, different ratios between the liquid and solid phases of LiFePO 4 and FePO 4 (L:S) have been used and ideal mixing between two end-members have been assumed. The glassy form is more sloping, and has a significantly lower potential. Thermodynamic modeling of Li-Fe 2 O 3 -V 2 O 5 has been carried out to incorporate additional polyanion species in the model for the glass cathode materials. From the completed thermodynamic modeling of Li/FeVO 4 which combined with the baseline system, the cell voltage of Li/Fe 4 (0.5P 2 O 7 ×0.5V 2 O 7 ) 4 has been benchmarked against experimental measurements. The ratio between the solid and liquid thermodynamic descriptions to describe the electrochemical behavior of the LBMP glass materials has been established and will be used for other polyanion species to be added in the baseline system. Acknowledgement This work was supported by the Assistant Secretary for Energy Efficiency and Renewable Energy, Office of Vehicle Technologies of the U.S. Department of Energy References [1] L. Kaufman, H. Bernstein, Computer Calculation of Phase Diagram , New York, Academic Press Inc., 1970. [2] N. Saunders, A. P. Miodownik, CALPHAD (Calculation of Phase Diagrams): A Comprehensive Guide , Oxford, New York, Pergamon, 1998. [3] J. L. Dodd, R. Yazami, B. Fultz, Electrochem. Solid State Lett. , 9(3): A151-A5, 2006. [4] C. Delacourt, P. Poizot, J. M. Tarascon, C. Masquelier, Nature Mater. , 4(3): 254-60, 2005.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2014
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  • 5
    Online Resource
    Online Resource
    The Electrochemical Society ; 2013
    In:  ECS Meeting Abstracts Vol. MA2013-02, No. 8 ( 2013-10-27), p. 597-597
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2013-02, No. 8 ( 2013-10-27), p. 597-597
    Abstract: Abstract not Available.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2013
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  • 6
    Online Resource
    Online Resource
    The Electrochemical Society ; 2014
    In:  ECS Meeting Abstracts Vol. MA2014-01, No. 2 ( 2014-04-01), p. 282-282
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2014-01, No. 2 ( 2014-04-01), p. 282-282
    Abstract: Lithium iron phosphate is a commercially successful crystalline polyanionic material for use in lithium ion battery cathodes that has excellent specific capacity, cycleability, and safety performance. The success of lithium iron phosphate has lead researchers to explore other crystalline polyanionic materials [1-3], such as LiCoPO 4 , LiCoBO 3 , and Li 2 MnSiO 4 , which have higher theoretical capacities and/or higher redox potentials. Unfortunately, the experimentally measured capacities of these other crystalline polyanionic materials have not approached their excellent theoretical values typically due to low electrical conductivity and/or irreversible phase changes during cycling. In this paper, mixed polyanion glasses have been demonstrated as a new class of cathode materials that could actually achieve the excellent theoretical capacities of similar crystalline polyanionic materials by having higher electrical conductivity and no crystal structure changes. Electrical conductivity enhancement of glasses by orders of magnitude can be achieved by partial substitution of polyanions, such as vanadate or molybdate, for the network former in the glass (phosphate, borate, or silicate) [4]. Polyanion glasses do not undergo crystalline phase changes as lithium anions cycle in and out of their structure. Mixed polyanion glasses have been made by conventional melt-quench processing by graphite glass casting and splat quenching (FIG. 1). Iron pyrophosphate glasses have shown dramatic improvements in electrochemical performance with increased vanadate substitution. The specific capacity of iron pyrophosphate glass was negligible, but iron pyrophosphate glass with 50% vanadate substitution demonstrated 100% theoretical capacity in the intercalation reaction. In comparison, Padhi, et al. [5] have produced crystalline iron pyrophosphate cathodes that have only achieved 75% theoretical capacity. In addition, mixed polyanion glasses have demonstrated a high capacity second electrochemical reaction in addition to the intercalation reaction. X-ray absorption spectroscopy on glass cathodes has been performed at Brookhaven National Laboratory and has provided insights into electrochemical reaction mechanisms. Future research efforts have shifted to pursuing mixed polyanion glasses with high specific energies. FIG. 1. Splat quenching an iron phosphate glass melt (glass melt in glowing hot crucible about to be poured onto copper bottom copper chill plate) Acknowledgments: This work was supported by the Assistant Secretary for Energy Efficiency and Renewable Energy, Office of Vehicle Technologies of the U.S. Department of Energy under Contract No. DE-AC02-05CH11231, under the Batteries for Advanced Transportation Technologies (BATT) Program. Use of the National Synchrotron Light Source, Brookhaven National Laboratory, was supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, under Contract No. DE-AC02-98CH10886. The authors acknowledge the technical assistance of Paul Menchhofer, Jagjit Nanda, Surrendra Martha, Hui Zhou, and Loic Baggetto of Oak Ridge National Laboratory, Frank Delnick of Sandia National Laboratory, and Syed Khalid of Brookhaven National Laboratory. References: [1] A. Salah, et al., J. Power Sources , 140, 370-375 (2005). [2] V. Legagneur, et al., Solid State Ionics , 139, 37-46 (2001). [3] R. Dominko, et al., J. Power Sources , 174, 457-461 (2007). [4] M. Shapaan, et al., Physica B , 404, 2058-2064 (2009). [5] A. Padhi, et al., J. Electrochem. Soc. , 144, 1609-1613 (1997).
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2014
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  • 7
    Online Resource
    Online Resource
    The Electrochemical Society ; 2016
    In:  ECS Meeting Abstracts Vol. MA2016-02, No. 3 ( 2016-09-01), p. 500-500
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2016-02, No. 3 ( 2016-09-01), p. 500-500
    Abstract: Polyanion glasses are a relatively unexplored class of high capacity cathode materials (250-500 mAh/g) for applications in lithium ion batteries that can undergo intercalation and/or conversion electrochemical reactions. Unlike most crystalline polyanionic materials, polyanion glass materials can be varied widely in both the cation and polyanion composition. This huge compositional space presents an opportunity and a challenge: how do you tailor the glass composition to obtain optimal electrochemical performance? Glass composition is often discussed in terms of: glass formers, stabilizers, and fluxes. In our polyanion glass cathodes, glass formers (borate, phosphate, vanadate, and molybdate) provided the overall amorphous network of the glass and can be tailored to improve the conductivity and ionic transport. Our “stabilizers” typically contained the electrochemically active cation (iron, copper, cobalt, nickel, silver, antimony). Fluxes typically are associated with alkali ions and tend to reduce the chemical stability of the glass, and interestingly, flux cations include the lithium ions that diffuse into and out of the glass during cycling. Compositional substitution in the glass former, stabilizer, and flux of a polyanion glass cathode were shown to affect the 1 st cycle reversibility, long-term cycleability, and energy efficiency. Characterization was performed on as-produced glass, glass cathodes at different states of charge, and glass cathodes at different amounts of cycling to understand the fundamentals of the glass cathode structure and its associated electrochemical performance. X-ray absorption spectroscopy performed on glass cathodes at different states of charge showed valence changes in both the stabilizer cation and a glass former (vanadate) during electrochemical reactions. The valence change in the vanadate was identified as the primary source of 1 st cycle irreversible loss, whereas the valence changes in the stabilizer cation were typically reversible and were associated with gradual capacity fade during cycling. Transmission electron microscopy showed that metal nanoparticles formed uniformly throughout glass particles during the glass-state conversion reaction. IR & Raman spectroscopies of mixed polyanion glasses were used to identify key functional groups that were associated with reduced 1 st cycle irreversible loss and improved energy efficiency during cycling. This work was supported by the Assistant Secretary for Energy Efficiency and Renewable Energy, Office of Vehicle Technologies of the U.S. Department of Energy under Contract No. DE-AC02-05CH11231, under the Advanced Battery Materials Research (BMR) Program.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2016
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  • 8
    In: Surgical Endoscopy, Springer Science and Business Media LLC, Vol. 21, No. 7 ( 2007-07), p. 1170-1174
    Type of Medium: Online Resource
    ISSN: 0930-2794 , 1432-2218
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2007
    detail.hit.zdb_id: 1463171-4
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  • 9
    In: CARTILAGE, SAGE Publications, Vol. 3, No. 4 ( 2012-10), p. 342-350
    Abstract: The purpose of this study was to report the clinical outcomes of autologous chondrocyte implantation (ACI) procedures performed by a single orthopedic surgeon at a minimum of 7 years follow-up. Methods: A retrospective review of prospectively collected data was performed on 29 patients who underwent ACI of the knee between the years of 1998 and 2003. Prospective data were collected to assess changes in standardized outcome measures preoperatively and 2, 4, and 7 years postoperatively. All patients enrolled in the study were also recruited to undergo physical examination when possible. Results: The final cohort consisted of 29 patients with a mean final follow-up time of 8.40 years (range = 7.14-10.88 years). Comparing preoperative scores to 7-year postoperative values, the mean International Knee Documentation Committee (IKDC) score improved from 39.80 to 59.24 ( P 〈 0.001), mean Tegner-Lysholm score increased from 48.07 to 74.17 ( P 〈 0.001), SF-12 physical score improved from 40.38 to 48.66 ( P 〈 0.001), and SF-12 mental score improved from 44.14 to 48.98 ( P 〈 0.05). Significant improvement occurred in Knee Injury and Osteoarthritis Outcome Score (KOOS) pain (56.03 to 80.36), symptoms (54.19 to 74.75), activities of daily living (72.01 to 85.90), sports (23.34 to 55.34), and quality of life (24.56 to 56.03) ( P 〈 0.001). In addition, 7-year postoperative scores were at or near levels seen at 2 years (mean = 2.16; range = 0.94-4.03 years) and 4 years (mean = 4.43; range = 2.16-5.88 years) postoperatively, reflecting durable improvement. Subjectively, on a scale of 1 to 10 (10 being completely satisfied), the mean postoperative satisfaction rate was 8.14. Additionally, 88.9% of the patients would elect to have this surgery again if the same problem was to occur in the contralateral joint. Conclusions: The results of ACI in patients who present with symptomatic, full-thickness chondral defects remain durable at a minimum of 7-year follow-up with persistent, high levels of patient satisfaction. Level of Evidence: Case series; Level of evidence, IV.
    Type of Medium: Online Resource
    ISSN: 1947-6035 , 1947-6043
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2012
    detail.hit.zdb_id: 2515870-3
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  • 10
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2024
    In:  Educational Studies in Mathematics Vol. 115, No. 1 ( 2024-01), p. 93-110
    In: Educational Studies in Mathematics, Springer Science and Business Media LLC, Vol. 115, No. 1 ( 2024-01), p. 93-110
    Type of Medium: Online Resource
    ISSN: 0013-1954 , 1573-0816
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2024
    detail.hit.zdb_id: 2012239-1
    SSG: 17,1
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