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  • 1
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2014-02, No. 2 ( 2014-08-05), p. 153-153
    Abstract: Storing the energy from renewable energy sources has become a critical issue in recent years. In order to develop a large-scale energy storage system (ESS) connected to green and sustainable energy beyond the conventional size of batteries, cost effectiveness must be the foremost requirement. For a large-scale ESS, battery electrode materials that are based on earth-abundant, readily available, and low-cost elements are highly desired. In this regard, using electrochemistry that utilizes an iron-based redox reaction combined with Na guest ions would be an optimal choice for such batteries because of the unlimited availability of Na from seawater and the ready availability of iron. However, only a limited number of such materials have been reported to date (NaFePO 4 , Na 2 FePO 4 F, NaFeSO 4 F, and Na 2 FeP 2 O 7 ). 1–6 Recently, we reported a new iron-based mixed-phosphate cathode, Na 4 Fe 3 (PO 4 ) 2 (P 2 O 7 ), which shows promising electrochemical properties in both Na- and Li-ion cells (H. Kim et al ., J. Am. Chem. Soc. 2012 , 134 , 10369−103722). 7 However, a fundamental understanding of the electrochemical reaction mechanism and structural stability under various conditions, which is essential for further development of this promising cathode, had not yet been achieved. In this report, we clarify the electrochemical reaction of Na 4 Fe 3 (PO 4 ) 2 (P 2 O 7 ) in Na-ion cells. We discovered that the electrode reaction is governed mainly by a one-phase reaction with a small volumetric change of less than 4%, despite significant distortion of pyrophosphate (P 2 O 7 ) occurring upon electrochemical cycling. Furthermore, the partially desodiated phases are thermally stable at temperatures up to 530 °C at all states of charge. With its open framework, high voltage (~3.2 V vs. Na), low volumetric change (~4%) and safety characteristics, Na 4 Fe 3 (PO 4 ) 2 (P 2 O 7 ) should be an outstanding candidate for a Na rechargeable battery electrode. References 1. Moreau, P.; Guyomard, D.; Gaubicher, J.; Boucher. F. Chem. Mater. 2010 , 22 , 4126–4128. 2. Lee, K. T; Ramesh, T. N.; Nan, F.; Botton, G.; Nazar, L. F. Chem. Mater. 2011 , 23 , 3593–3600. 3. Ellis, B. L.; Makahnouk, W. R. M.; Makimura, Y.; Toghill, K.; Nazar, L. F. Nat. Mater. 2007 , 6 , 749–753. 4. Barpanda, P.; Chotard, J.; Recham, N.; Delacourt, C.; Ati, M.; Dupont, L.; Armand, M.; Tarascon, J. –M. Inorg. Chem. 2010 , 49 , 7401–7413. 5. Barpanda, P.; Ye, T.; Nishimura, S.; Chung, S–C.; Yamada, Y.; Okubo, M.; Zhou, H.; Yamada, A. Electrochem. Commun. 2012 , 24 , 116–119. 6. Kim, H.; Shakoor, R. A.; Park, C.; Lim, S–Y.; Kim, J–S.; Jo, Y–N.; Cho, W.; Miyasaka, K.; Kahraman, R.; Jung, Y.; Choi, J. –W. Adv. Funct. Mater. 2012 , 23, 1147–1155. 7. Kim, H.; Park, I.; Seo, D. –H.; Lee, S.; Kim, S. –W.; Kwon, W. J.; Park, Y. –U.; Kim, C. S.; Jeon, S.; Kang, K. J. Am. Chem. Soc. 2012 , 134 , 10369−103722.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2014
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  • 2
    Online Resource
    Online Resource
    The Electrochemical Society ; 2013
    In:  ECS Meeting Abstracts Vol. MA2013-02, No. 14 ( 2013-10-27), p. 994-994
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2013-02, No. 14 ( 2013-10-27), p. 994-994
    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
    Online Resource
    Online Resource
    The Electrochemical Society ; 2014
    In:  ECS Meeting Abstracts Vol. MA2014-02, No. 5 ( 2014-08-05), p. 251-251
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2014-02, No. 5 ( 2014-08-05), p. 251-251
    Abstract: Only a small number of Li-containing cathode materials groups are considered for practical use in Li-ion battery systems. The possible candidates of cathode material were limited to the crystals that contain both redox-active element and lithium ion in the open framework. This concept has been conventionally considered as a standard for searching the cathode materials. But, it could be constraints to restrict the choices of materials for cathode in Li-ion battery systems. To expand the sight for seeking new positive electrode material, we suggested a novel strategy to use various kinds of Li-free transition metal ionic compounds (MX, M = transition metal, X = anion or polyanion group) as a positive electrode material by blending with a Li ionic compound (LiY, Y = anion or polyanion group) in nanoscale. [1] MX and LiY provided a redox couple and lithium ion supply for an electrochemical reaction. This concept is unconventional with general system of electrode material (Li ions and transition metal ions are in the same crystal system). In this case, transition metal ion and Li ion in the nanocomposite do not exist in the same crystal system and spatially separated as a mixture of MX and LiY. In this paper, we will introduce and discuss about the transition metal oxide system as a redox couple among the infinite possible combinations of lithium ionic compounds and metal ionic compounds. Transition metal oxides such as FeO, MnO were considered as promising anode materials due to the earth abundance and large capacity from conversion reaction. [2] Although they have redox potential below 1 V as anode material, [3][4] we will show that this transition metal oxides can be applied to the cathode materials (3 V-class) by making nanocomposite with lithium ionic compound. To better understand the mechanisms during electrochemical cycling we have performed XPS, XANES/EXAFS analysis, allowing us to study the local environment change of Fe or Mn during the charge and discharge reaction. FeO and MnO showed different aspects during the electrochemical reaction in terms of electrochemical activity and local environment change. We will discuss about the reaction mechanism in detail. [1] S.-W. Kim, K-Y. Nam, D.-H. Seo, J. Hong, H. Kim, H. Gwon, and K. Kang, Nano Today , 7 , 168 (2012) [2] P. Poizot, S. Laruelle, S. Grugeon, L. Dupont, and J.-M. Tarascon, Nature , 407 , 496 (2000) [3] M. Gao, P. Zhou, P. Wang, J. Wang, C. Liang, J. Zhang, and Y. Liu, J. Alloy. Compd. , 565 , 97 (2013) [4] X. Li, D. Li, L. Qiao, X. Wang, X. Sun, P. Wang, and D. He, J. Mater. Chem. , 22 , 9189 (2012)
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2014
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  • 4
    Online Resource
    Online Resource
    The Electrochemical Society ; 2014
    In:  ECS Meeting Abstracts Vol. MA2014-04, No. 2 ( 2014-06-10), p. 204-204
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2014-04, No. 2 ( 2014-06-10), p. 204-204
    Abstract: Developing low-cost and high-performance energy storage devices is important for sustainable energy utilization. Recently, sodium (Na) ion batteries have been highlighted as a possible competitor to lithium (Li) ion batteries because of their potential merit in the cost effectiveness. Na resources are earth-abundant, and Na electrochemistry shares many similarities with Li. However, their relatively low energy/power densities and unreliable cycle stability need to be addressed. In this work, we propose a novel high-performance cathode for Na rechargeable batteries based on functionalized graphene nanoplatelets. Starting from natural graphite, functionalized graphene nanoplatelets were fabricated via simple scalable routes, which could control the chemical composition and porous nanostructure of the sample in one-step. By using surface reactions between Na and functionals on graphene nanoplatelets, (i) no significant lattice change occurred during battery cycling, and (ii) much faster Na kinetics could be achieved through porous network without solid-state diffusion.[1] Furthermore, the high electrical conductivity of the material could aid in improving the rate capability.[2] While previous studies of graphite-based electrodes are mostly found in anode applications for NIB and only very recently its cathode application was discovered, [3, 4] this work manipulated the carbon into a cathode with a tunability of composition and nanostructure by simple one-step chemical modification. The functionalized graphene cathode could deliver the energy of ~500 Wh kg -1 without capacity decay during 300 battery cycles and could also exhibit an unprecedentedly high power of ~55 kW kg -1 with a less-than-10 s charge/discharge rate for NIB. References [1] H. Kim, H.-D. Lim, S.-W. Kim, J. Hong, D.-H. Seo, D.-c. Kim, S. Jeon, S. Park, K. Kang, Sci. Rep., Scalable Functionalized Graphene Nano-platelets as Tunable Cathodes for High-performance Lithium Rechargeable Batteries 3 (2013) 1506. [2] S.-M. Oh, S.-T. Myung, J. Hassoun, B. Scrosati, Y.-K. Sun, Electrochem. Commun., Reversible NaFePO 4 electrode for sodium secondary batteries 22 (2012) 149-152. [3] Y.-X. Wang, S.-L. Chou, H.-K. Liu, S.-X. Dou, Carbon, Reduced graphene oxide with superior cycling stability and rate capability for sodium storage 57 (2013) 202-208. [4] Z. Wang, L. Qie, L. Yuan, W. Zhang, X. Hu, Y. Huang, Carbon, Functionalized N-doped interconnected carbon nanofibers as an anode material for sodium-ion storage with excellent performance 55 (2013) 328-334.
    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
    Korean Academy of Addiction Psychiatry ; 2017
    In:  Korean Academy of Addiction Psychiatry Vol. 21, No. 1 ( 2017-04-30), p. 30-37
    In: Korean Academy of Addiction Psychiatry, Korean Academy of Addiction Psychiatry, Vol. 21, No. 1 ( 2017-04-30), p. 30-37
    Type of Medium: Online Resource
    ISSN: 1226-6035
    URL: Issue
    Language: Unknown
    Publisher: Korean Academy of Addiction Psychiatry
    Publication Date: 2017
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  • 6
    Online Resource
    Online Resource
    Frontiers Media SA ; 2022
    In:  Frontiers in Immunology Vol. 12 ( 2022-1-11)
    In: Frontiers in Immunology, Frontiers Media SA, Vol. 12 ( 2022-1-11)
    Abstract: A novel coronavirus designated severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) emerged and caused an outbreak of unusual viral pneumonia. Several reports have shown that cross-reactive antibodies against SARS-CoV-2 also exist in people unexposed to this virus. However, the neutralizing activity of cross-reactive antibodies is controversial. Here, we subjected plasma samples from SARS-CoV-2-unexposed elderly Korean people (n = 119) to bead-based IgG antibody analysis. SARS-CoV-2 S1 subunit-reactive IgG antibody analysis detected positive signals in some samples (59 of 119, 49.6%). SARS-CoV-2 receptor-binding domain (RBD)-reactive antibody levels were most significantly correlated with human coronavirus-HKU1 S1 subunit-reactive antibody levels. To check the neutralizing activity of plasma samples, the SARS-CoV-2 spike pseudotype neutralizing assay was used. However, the levels of cross-reactive antibodies did not correlate with neutralizing activity. Instead, SARS-CoV-2 pseudovirus infection was neutralized by some RBD-reactive plasma samples (n = 9, neutralization ≥ 25%, P ≤ 0.05), but enhanced by other RBD-reactive plasma samples (n = 4, neutralization ≤ -25%, P ≤ 0.05). Interestingly, the blood plasma groups with enhancing and neutralizing effects had high levels of SARS-CoV-2 RBD-reactive antibodies than the plasma group that had no effect. These results suggest that some SARS-CoV-2 RBD-reactive antibodies from pre-pandemic elderly people exert two opposing functions during SARS-CoV-2 pseudovirus infection. In conclusion, preformed RBD-reactive antibodies may have two opposing functions, namely, protecting against and enhancing viral infection. Analysis of the epitopes of preformed antibodies will be useful to elucidate the underlying mechanism.
    Type of Medium: Online Resource
    ISSN: 1664-3224
    Language: Unknown
    Publisher: Frontiers Media SA
    Publication Date: 2022
    detail.hit.zdb_id: 2606827-8
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  • 7
    Online Resource
    Online Resource
    The Electrochemical Society ; 2014
    In:  ECS Meeting Abstracts Vol. MA2014-04, No. 3 ( 2014-06-10), p. 504-504
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2014-04, No. 3 ( 2014-06-10), p. 504-504
    Abstract: Lithium-oxygen chemistry offers the highest energy density for a rechargeable system; such a system is known as a “lithium-air battery”. Most studies of lithium-air batteries have focused on demonstrating battery operations in an environment of pure oxygen; such a battery should technically be described as a “lithium-dioxygen (O 2 ) battery”. Consequently, the next step for the lithium-“air” battery is to understand how the reaction chemistry is affected by the constituents of ambient air. Among the components of air, CO 2 is of particular interest because its solubility in organic solvents is about fifty times higher than that of O 2 , and it can react actively with O 2 - · , which is the key intermediate species in Li-O 2 battery reactions. In this work, we investigated the reaction mechanisms in the Li-O 2 /CO 2 cell under various electrolyte conditions using quantum mechanical simulations combined with experimental verification. Our most important finding is that the subtle balance among various reaction pathways influencing the potential energy surfaces can be modified by the electrolyte solvation effect. Thus, a low dielectric electrolyte tends to primarily form Li 2 O 2 , while a high dielectric electrolyte is effective in electrochemically activating CO 2 , yielding only Li 2 CO 3 . Most surprisingly, we further discovered that a high dielectric medium such as DMSO can result in the reversible reaction of Li 2 CO 3 within a Li-air cell (contrary to conventional belief) over multiple cycles. We believe that the current mechanistic understanding of the chemistry of CO 2 in a Li-air cell and the interplay of CO 2 with electrolyte solvation will provide an important guideline for developing Li-air batteries. Furthermore, the newly discovered possibility for a rechargeable Li-O 2 /CO 2 battery based on Li 2 CO 3 formation chemistry may have merits in enhancing cyclability by minimizing side reactions.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2014
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  • 8
    In: Cancer Biomarkers, IOS Press, Vol. 12, No. 3 ( 2013-03-07), p. 115-124
    Type of Medium: Online Resource
    ISSN: 1875-8592 , 1574-0153
    Language: Unknown
    Publisher: IOS Press
    Publication Date: 2013
    detail.hit.zdb_id: 2525487-X
    detail.hit.zdb_id: 2525475-3
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  • 9
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2019-03, No. 2 ( 2019-02-01), p. 165-165
    Abstract: Cobalt-free layered lithium-rich nickel manganese oxides, Li[Li x Ni y Mn 1−x−y ]O 2 , are promising positive electrode materials for lithium rechargeable batteries because of their high energy density and low materials cost. Utilization of the oxygen anionic redox in this series of materials enables realization of a high capacity beyond that achieved via the conventional transition metal cationic redox when charging above 4.5 V vs. Li/Li + . However, substantial voltage decay is inevitable upon electrochemical cycling, which makes this class of materials less practical. The undesirable voltage decay has been proposed to be linked to irreversible structural rearrangement involving irreversible oxygen loss and cation migration. Herein, we demonstrate that the voltage decay of the electrode is correlated to the activation of Mn 4+ /Mn 3+ redox and subsequent cation disordering, which is able to be remarkably suppressed via simple compositional tuning to induce the formation of Ni 3+ in the pristine material. By implementing our new strategy, an alternative redox reaction involving the use of this pristine Ni 3+ as a redox buffer, which has been designed to be widened from Ni 3+ /Ni 4+ to Ni 2+ /Ni 4+ , subdued the Mn 4+ /Mn 3+ reduction without compensation for the capacity in principle. Negligible change in the voltage profile of the modified lithium-rich nickel manganese oxide electrode is observed upon extended cycling, and manganese migration into the lithium layer is significantly suppressed. Based on these findings, we propose a general strategy to suppress the voltage decay of Mn-containing lithium-rich oxides to achieve long-lasting high energy density from this class of materials.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2019
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  • 10
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2012-02, No. 10 ( 2012-06-04), p. 1030-1030
    Abstract: Abstract not Available.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2012
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