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  • 1
    In: Journal of Physics: Energy, IOP Publishing, Vol. 3, No. 3 ( 2021-07-01), p. 031501-
    Abstract: Batteries that extend performance beyond the intrinsic limits of Li-ion batteries are among the most important developments required to continue the revolution promised by electrochemical devices. Of these next-generation batteries, lithium sulfur (Li–S) chemistry is among the most commercially mature, with cells offering a substantial increase in gravimetric energy density, reduced costs and improved safety prospects. However, there remain outstanding issues to advance the commercial prospects of the technology and benefit from the economies of scale felt by Li-ion cells, including improving both the rate performance and longevity of cells. To address these challenges, the Faraday Institution, the UK’s independent institute for electrochemical energy storage science and technology, launched the Lithium Sulfur Technology Accelerator (LiSTAR) programme in October 2019. This Roadmap, authored by researchers and partners of the LiSTAR programme, is intended to highlight the outstanding issues that must be addressed and provide an insight into the pathways towards solving them adopted by the LiSTAR consortium. In compiling this Roadmap we hope to aid the development of the wider Li–S research community, providing a guide for academia, industry, government and funding agencies in this important and rapidly developing research space.
    Type of Medium: Online Resource
    ISSN: 2515-7655
    Language: Unknown
    Publisher: IOP Publishing
    Publication Date: 2021
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  • 2
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    The Electrochemical Society ; 2020
    In:  Journal of The Electrochemical Society Vol. 167, No. 10 ( 2020-06-26), p. 109003-
    In: Journal of The Electrochemical Society, The Electrochemical Society, Vol. 167, No. 10 ( 2020-06-26), p. 109003-
    Type of Medium: Online Resource
    ISSN: 1945-7111
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2020
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  • 3
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    The Electrochemical Society ; 2014
    In:  ECS Meeting Abstracts Vol. MA2014-02, No. 2 ( 2014-08-05), p. 58-58
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2014-02, No. 2 ( 2014-08-05), p. 58-58
    Abstract: Lithium-O 2 cells, with a theoretical specific energy of around 5 times higher than lithium-ion cells have the potential to become the technology powering tomorrow’s electric vehicles. However, since they were first reported by Abraham and Jiang[1] they have faced problems and setbacks. The principal problem was of instability of organic non-aqueous electrolytes to the superoxide ion formed as an intermediate discharge product [2] . Ionic liquids are a promising alternative to traditional carbonate based electrolytes, and indeed recent works have shown that Pyr 14 TFSI is relatively stable to superoxide [3–5]. Having identified a stable electrolyte we have then looked at the problem of electrode passivation by the insoluble and insulating discharge product lithium peroxide [6] , which produces a significant reduction on the practical capacity. This work continues our previous study on the use of ethylviologen triflate as a mediator/redox shuttle for the discharge reaction [7], with a study of mediator action by the shuttle molecule to achieve a 2-electron reduction of oxygen to form lithium peroxide away from the electrode surface. This eliminates electrode passivation as shown in Fig. 1. We will also present an in-depth study into the mechanism of oxygen reduction by ethylviologen triflate and other candidate mediators. The need for mediators for the charge reaction has also been stated by Bruce et al., [8] who found TTF to be a redox mediator in DMSO. Our own studies of TTF have found it to be unsuitable for use in in Pyr 14 TFSI due to its lower oxidation potential, so we have focused on the use of other compounds to carry electrons back to the electrode while the charge reaction converts the lithium peroxide back to oxygen. [1] K.M. Abraham, Z. Jiang, J. Electrochem. Soc. 143 (1996) 1–5. [2] F. Mizuno, S. Nakanishi, Y. Kotani, S. Yokoishi, H. Iba, Electrochemistry . 78 (2010) 403–405. [3] J.T. Frith, N. Garcia-araez, A.E. Russell, J.R. Owen, Prep. (n.d.). [4] I.M. AlNashef, M. a. Hashim, F.S. Mjalli, M.Q.A. Ali, M. Hayyan, Tetrahedron Lett. 51 (2010) 1976–1978. [5] S. Randström, G.B. Appetecchi, C. Lagergren, A. Moreno, S. Passerini, Electrochim. Acta . 53 (2007) 1837–1842. [6] V. Viswanathan, K.S. Thygesen, J.S. Hummelshøj, J.K. Nørskov, G. Girishkumar, B.D. McCloskey, et al., J. Chem. Phys. 135 (2011) 214704. [7] M.J. Lacey, J.T. Frith, J.R. Owen, Electrochem. Commun. 26 (2013) 74–76. [8] Y. Chen, S.A. Freunberger, Z. Peng, O. Fontaine, P.G. Bruce, Nat. Chem. 5 (2013) 489–94.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2014
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  • 4
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    The Electrochemical Society ; 2014
    In:  ECS Meeting Abstracts Vol. MA2014-02, No. 26 ( 2014-08-05), p. 1531-1531
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2014-02, No. 26 ( 2014-08-05), p. 1531-1531
    Abstract: In recent years, non-aqueous lithium-air batteries have been intensively investigated due to their high theoretical gravimetric energy, which is up to 10 times higher than lithium-ion batteries [1-4]. The discharge reaction involves the oxygen reduction reaction (ORR), forming either superoxide or peroxide. Superoxide formation is highly detrimental, because not only would the charge delivered by the battery be halved, but most importantly, superoxide induces the degradation of most known types of organic electrolytes [5-8] and carbon-containing electrodes [9-13]. Therefore, new catalysts enhancing the 2-electron reduction of oxygen in non-aqueous electrolytes are essential for the development of lithium-air batteries. Another issue in lithium-air batteries is that the reaction product, lithium peroxide, is insoluble and insulating. As a result, lithium peroxide deposits on the electrode surface and forms a passivation layer [14] , which leads to capacity fading. We have recently introduced the concept of redox shuttles as applied to solve the problem of electrode passivation in lithium-air batteries [15]. As illustrated in the figure on the example of ethyl viologen (EtV 2+ /EtV + ), a redox shuttle will displace the oxygen reduction reaction a short distance from the electrode surface, thus avoiding passivation. This work continues by investigating another advantage, which is the homogeneous catalysis of the oxygen reduction reaction. By combining electrochemical and UV-visible measurements, we have shown that ethyl viologen can act as a mediator for the 2-electron reduction of oxygen. This has the remarkable advantage of decreasing the lifetime of the highly reactive superoxide, which would be beneficial for the stability of electrolyte and electrode materials against irreversible degradation. Under appropriate reaction conditions, it was shown that the extent of degradation reactions undergone by ethyl viologen is 〈 2 %. In conclusion, ethyl viologen improves the selectivity of the oxygen reduction reaction towards the formation of lithium peroxide instead of the formation of degradation products or superoxide radical anions. References: [1] P.G. Bruce, S.A. Freunberger, L.J. Hardwick, J.M. Tarascon, Nat. Mater., 11 (2012) 19-29. [2] K. M. Abraham, Z. Jiang, J. Electrochem. Soc., 143 (1996) 1-5 [3] G. Girishkumar, B. McCloskey, A.C. Luntz, S. Swanson, W. Wilcke, J. Phys. Chem. Lett., 1 (2010) 2193-2203. [4] L.J. Hardwick, P.G. Bruce, Curr. Opin. Solid. St. M., 16 (2012) 178-185. [5] F. Mizuno, S. Nakanishi, Y. Kotani, S. Yokoishi, H. Iba, Electrochemistry, 78 (2010) 403-405. [6] S.A. Freunberger, Y. Chen, Z. Peng, J.M. Griffin, L.J. Hardwick, F. Barde, P. Novak, P.G. Bruce, J Am Chem Soc, 133 (2011) 8040-8047. [7] B.D. McCloskey, D.S. Bethune, R.M. Shelby, G. Girishkumar, A.C. Luntz, J. Phys. Chem. Lett., 2 (2011) 1161-1166. [8] G.M. Veith, N.J. Dudney, J. Howe, J. Nanda, J. Phys. Chem. C, 115 (2011) 14325-14333. [9] B.D. McCloskey, A. Speidel, R. Scheffler, D.C. Miller, V. Viswanathan, J.S. Hummelshøj, J.K. Nørskov, A.C. Luntz, J. Phys. Chem. Lett., 3 (2012) 997-1001. [10] D.M. Itkis, D.A. Semenenko, E.Y. Kataev, A.I. Belova, V.S. Neudachina, A.P. Sirotina, M. Havecker, D. Teschner, A. Knop-Gericke, P. Dudin, A. Barinov, E.A. Goodilin, Y. Shao-Horn, L.V. Yashina, Nano letters, 13 (2013) 4697-4701. [11] M. Leskes, A.J. Moore, G.R. Goward, C.P. Grey, J Phys Chem C Nanomater Interfaces, 117 (2013) 26929-26939. [12] G.A. Elia, J.-B. Park, B. Scrosati, Y.-K. Sun, J. Hassoun, Electrochem. Commun., 34 (2013) 250-253. [13] M.M. Ottakam Thotiyl, S.A. Freunberger, Z. Peng, P.G. Bruce, J. Am. Chem. Soc., 135 (2012) 494-500. [14] V. Viswanathan, K.S. Thygesen, J.S. Hummelshoj, J.K. Norskov, G. Girishkumar, B.D. McCloskey, A.C. Luntz, J Chem Phys, 135 (2011) 214704. [15] M. J. Lacey, J. T. Frith, J. R. Owen, Electrochem. Comm., 26 (2013), 74-76.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2014
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  • 5
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    The Electrochemical Society ; 2020
    In:  Journal of The Electrochemical Society Vol. 167, No. 11 ( 2020-07-06), p. 110511-
    In: Journal of The Electrochemical Society, The Electrochemical Society, Vol. 167, No. 11 ( 2020-07-06), p. 110511-
    Type of Medium: Online Resource
    ISSN: 1945-7111
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    Publisher: The Electrochemical Society
    Publication Date: 2020
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  • 6
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    The Electrochemical Society ; 2022
    In:  ECS Meeting Abstracts Vol. MA2022-01, No. 2 ( 2022-07-07), p. 348-348
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2022-01, No. 2 ( 2022-07-07), p. 348-348
    Abstract: Preventing the decomposition reactions of electrolyte solutions is essential for extending the lifetime of lithium-ion batteries. However, the exact mechanism(s) for electrolyte decomposition at the positive electrode, and particularly the soluble decomposition products that form and initiate further reactions at the negative electrode, are still unknown. In this work, a combination of operando gas measurements and solution NMR was used to study decomposition reactions of the electrolyte solution at NMC (LiNi x Mn y Co 1-x-y O 2 ) and LCO (LiCoO 2 ) electrodes. A partially delithiated LFP (Li x FePO 4 ) counter electrode was used to selectively identify the products formed through processes at the positive electrode. Based on the detected soluble and gaseous products, two distinct routes with different onset potentials are proposed for the decomposition of the electrolyte solution at NMC electrodes. At low potentials ( 〈 80% state-of-charge, SOC), ethylene carbonate (EC) is dehydrogenated to form vinylene carbonate (VC) at the NMC surface, whereas at high potentials ( 〉 80% SOC), 1 O 2 released from the transition metal oxide chemically oxidises the electrolyte solvent (EC) to CO 2 , CO and H 2 O. The formation of water via this mechanism was confirmed by reacting 17 O-labelled 1 O 2 with EC and characterising the reaction products via 1 H and 17 O NMR spectroscopy. The water that is produced initiates secondary reactions, leading to the formation of the various products identified by NMR spectroscopy. Noticeably fewer decomposition products were detected in NMC/graphite cells compared to NMC/Li x FePO 4 cells, which is ascribed to the consumption of water (from the reaction of 1 O 2 and EC) at the graphite electrode, preventing secondary decomposition reactions. The insights on electrolyte decomposition mechanisms at the positive electrode, and the consumption of decomposition products at the negative electrode contribute to understanding the origin of capacity loss in NMC/graphite cells, and are hoped to support the development of strategies to mitigate the degradation of NMC-based cells.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2022
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  • 7
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    The Electrochemical Society ; 2016
    In:  ECS Meeting Abstracts Vol. MA2016-03, No. 2 ( 2016-06-10), p. 392-392
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2016-03, No. 2 ( 2016-06-10), p. 392-392
    Abstract: Increasing demand for lighter and more powerful batteries has driven research into alternative technologies. One system that has received significant attention is Lithium-Oxygen. This system exploits the reduction of oxygen to lithium peroxide, by lithium metal, to provide a theoretical specific energy of 3500 Wh kg -1 . One of the major problems facing the Lithium-Oxygen battery is the passivation of the air electrode caused by insoluble lithium oxides and lithium carbonate formed during cycling. These products are not completely oxidized during the charge  step and therefore accumulate within the electrode causing the capacity to fade with each cycle 1 . This work focuses on identifying solution based catalysts in non-aqueous electrolytes to facilitate the oxidation of these insoluble products 2 . The catalysts are oxidized at a higher potential than the lithium peroxide but undergo much faster electron transfer. Once oxidized the catalyst is able to oxidize any lithium peroxide or lithium carbonate remaining on the surface, unblocking the pores and therefore preserving the capacity over subsequent cycles. Analysis of the carbon electrode by x-ray diffraction is able to confirm Li 2 O 2  as the discharge product. While the evolution and consumption of oxygen during cycling has been studied using on-line mass spectrometry. The figure included displays cyclic voltammograms of oxygen reduction and evolution with (black) and without (red) a catalyst. This demonstrates that that incorporation of such a catalyst can significantly reduce electrode passivation and therefore dramatically improve the cycle life of the cell.  [1] Garcia-Araez, N.; Novák, P. Critical Aspects in the Development of Lithium–air Batteries. J. Solid State  Electrochem. 2013 , 17 , 1793–1807. [2] Lacey, M. J.; Frith, J. T.; Owen, J. R. A Redox Shuttle to Facilitate Oxygen Reduction in the Lithium Air Battery. Electrochem. commun. 2013 , 26 , 74–76. Fig. 1. Cyclic voltammogram of oxygen reduction and evolution at 50mV s -1 . Cell consisted of a two electrodes; a glassy carbon working electrode (3mm) and Lithium foil counter/ reference electrode. Figure 1
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2016
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  • 8
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    The Electrochemical Society ; 2014
    In:  ECS Meeting Abstracts Vol. MA2014-02, No. 1 ( 2014-08-05), p. 12-12
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2014-02, No. 1 ( 2014-08-05), p. 12-12
    Abstract: The global resources of lithium, essential for electric vehicle batteries, are a subject of some debate. Lithium resources are mainly from two types of deposit; brine (21.6 Mt of Li) and pegmatite (3.9 Mt of Li) 1 . The largest deposit of lithium reserves are the brine deposits in South America. Although existing lithium resources may be sufficient to support demand until the year 2100 (assuming that lithium batteries are recycled 1, 2) , lithium extraction is currently too complex, slow and inefficient to be economical 3, 4 . In current lithium industries, one of the most economical ways to extract lithium is by lime soda evaporation ; a solar evaporation and chemical plant process, which takes between 12 to 24 months. After the solar evaporation, the concentrated brine is pre-treated to a pH of 2 in order to remove Boron by a solvent extraction. Lime (CaO) is then added to remove magnesium, sulphate, and borate. Calcium left in the brine is removed by a small amount of soda ash or sodium carbonate (Na 2 CO 3 ). Then, the brine is heated to about 90°C and more soda ash is added to precipitate lithium carbonate 4, 5 . This lime soda evaporation is considered as a long-process of lithium extraction. Therefore, the objective of this work is to develop a new, fast and inexpensive approach to recover lithium chemically, from the lithium sources that contain other metal cations. Heterosite iron phosphate (FePO 4 ) is a discharged product of lithium iron phosphate (LiFePO 4 ). There are a few studies about the structure of heterosite FePO 4 that report that it is more selective for lithium ions (Li + ) over sodium ions (Na + ). This structure displays excellent reversibility charge/discharge properties 6,7 . There small potential differences of the redox couple and the stability of LiFePO 4 over a wide range of pH in an aqueous solution are the main advantages of this structure to this application 6 . This work investigates a novel process that may prove to be more economical than the lime soda evaporation process for lithium extraction. Heterosite FePO 4 was used to selectively remove Li + from the brine with the aid of a reducing agent (sodium thiosulfate; Na 2 S 2 O 3 ). The resulting LiFePO 4 can be directly sent to lithium battery industries. In principle, the other cations could be retrieved back into the brine as shown in figure 1. We have examined and demonstrated the process of lithium insertion into a heterosite FePO 4 framework in aqueous salt solutions. In this process, the amount of Li + uptake can take up to 46 mg Li + /g solid and other cations (i.e. sodium, potassium, and magnesium) can take less than 3 mg/g solid . Furthermore, the re-lithiated FePO 4 performed satisfactorily as a positive electrode. This work could also be developed for future lithium recycling processes. References 1 S. E. Kesler, P. W. Gruber, P. a. Medina, G. a. Keoleian, M. P. Everson, and T. J. Wallington, Ore Geol. Rev. , 2012, 48 , 55–69 2 P. W. Gruber, P. a. Medina, G. a. Keoleian, S. E. Kesler, M. P. Everson, and T. J. Wallington, J. Ind. Ecol. , 2011, 15 , 760–775. 3 L. T. Peiro, G. V. Mendez and R. U. Ayres, Jom , 2013, 65 , 986-996. 4 D. E. Garrett, Handbook of lithium and natural calcium chloride: their deposits, processing, uses and properties , Elsevier Academic Press, Amsterdam, Boston, 2004 5 L. Moreno, Lithium Industry; A Strategic Energy Metal , Euro Pacific Canada Inc., 2013. 6 7. Z. Zhao, X. Si, X. Liu, L. He, and X. Liang, Hydrometallurgy , 2013, 133 , 75–83. 7 8. C. V. Ramana, a. Mauger, F. Gendron, C. M. Julien, and K. Zaghib, J. Power Sources , 2009, 187 , 555–564
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2014
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  • 9
    In: Enfermería Nefrológica, Sociedad Espanola de Enfermeria Nefrologica, Vol. 19, No. 1 ( 2016-02-24), p. 29-35
    Abstract: Los pacientes con enfermedad renal crónica estadio 5 tratados en diálisis presentan alteraciones cardiovasculares, musculoesqueléticas y psicosociales que afectan su capacidad física y funcional. La falta de actividad contribuye a un aumento de la mortalidad y al desarrollo de enfermedades crónicas. La calidad de vida relacionada con la salud es la evaluación que realiza el individuo respecto a su salud. El objetivo del estudio fue valorar y analizar la percepción de salud, la capacidad funcional, el estado nutricional y psicológico de los pacientes de hemodiálisis (HD) y diálisis peritoneal (DP). Realizamos un estudio descriptivo que incluyó todos los pacientes que realizaban diálisis en nuestro centro. Diseñamos una base de datos y analizamos las variables mediante el estadístico SPSS 21.El tamaño total de la muestra fue de 42 pacientes (21 HD- 21 DP). Los resultados mostraron un grupo homogéneo en la media de edad, con índice de Barthel y niveles de albúmina bajos similares, como describen otras series. Los resultados estadísticos muestran que los pacientes en HD son más sedentarios (p 〈 0,050), se sienten peor psicológica (p
    Type of Medium: Online Resource
    ISSN: 2255-3517 , 2254-2884
    Language: Unknown
    Publisher: Sociedad Espanola de Enfermeria Nefrologica
    Publication Date: 2016
    detail.hit.zdb_id: 2739231-4
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  • 10
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    The Electrochemical Society ; 2020
    In:  Journal of The Electrochemical Society Vol. 167, No. 8 ( 2020-05-05), p. 080520-
    In: Journal of The Electrochemical Society, The Electrochemical Society, Vol. 167, No. 8 ( 2020-05-05), p. 080520-
    Type of Medium: Online Resource
    ISSN: 1945-7111
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2020
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