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  • The Electrochemical Society  (11)
  • 1
    Online Resource
    Online Resource
    The Electrochemical Society ; 2017
    In:  ECS Meeting Abstracts Vol. MA2017-02, No. 4 ( 2017-09-01), p. 242-242
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2017-02, No. 4 ( 2017-09-01), p. 242-242
    Abstract: Alpha manganese oxide (α-MnO 2 ) is of interest as a cathode material for lithium-ion batteries and as an electrode/electrocatalyst for hybrid Li-ion/Li-O 2 systems. It has a tunnel structure with large 2x2 channels that accommodate different species such as Ba 2+ , K + , NH 4 + , or H 3 O + /H 2 O. Characterization and modeling of the insertion and removal of Li, oxygen, and H 3 O + /H 2 O species under electrochemical cycling and heating is important for understanding how MnO 2 acts as a hybrid Li-ion/Li-O 2 battery material. In this talk, we will discuss our work in using in-situ synchrotron X-ray diffraction (XRD), X-ray absorption near-edge spectroscopy (XANES), in-situ UV resonance Raman spectroscopy, and density functional theory (DFT) calculations, to unravel the changes in α-MnO 2 during electrochemical cycling as well as dehydration process. We found evidence of oxygen incorporation and partial removal during electrochemical cycling, as well as two-stage water removal during heating. Both processes involve facile oxygen diffusion through the center of 2x2 tunnels. Keywords: MnO2, in-situ XRD, DFT Reference: Z.-Z. Yang, D. Ford, J.-S. Park, Y. Ren, S. Kim, H. Kim , T. Fister, M. K. Y. Chan, # M. M. Thackeray, # “Probing the release and uptake of water in α-MnO 2 •xH 2 O,” Chemistry of Materials 29, 1507–1517 (2017). Z. Yang, L. Trahey, Y. Ren, M. K. Y. Chan, # C. Lin, J. Okasinski, and M. M. Thackeray, “In-Situ High-Energy Synchrotron X-ray Diffraction Studies and First Principles Modeling of α-MnO 2 Electrodes in Li-O 2 and Li-ion Coin Cells,” Journal of Materials Chemistry A 3, 7389-7398 (2015). Acknowledgements: This work was supported as a part of the Center for Electrochemical Energy Science, an Energy Frontier Research Center funded by the US Department of Energy, Office of Science, Basic Energy Sciences under award number DE-AC02–06CH11. Use of the Advanced Photon Source, a US DOE Office of Science User Facility operated by Argonne National Laboratory, was supported by DOE under Contract No. DE-AC02-06CH11357. Use of the Center for Nanoscale Materials, an Office of Science user facility, was supported by the U. S. Department of Energy, Office of Science, Office of Basic Energy Sciences, under Contract No. DE-AC02-06CH11357. This research used resources of the National Energy Research Scientific Computing Center, a DOE Office of Science User Facility supported by the Office of Science of the U.S. Department of Energy under Contract No. DE-AC02-05CH11231. Figure 1
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2017
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  • 2
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2016-03, No. 2 ( 2016-06-10), p. 372-372
    Abstract: Hollandite α-MnO 2 , with an open tunnel structure, is of interest as a cathode material for 3 V lithium batteries [1,2] and as an electrocatalyst for Li-O 2 cells [3]. We recently proposed [4] that α-MnO 2 belong to a class of materials that can be used as the cathode in hybrid Li-ion/Li-oxygen battery systems, which can incorporate/release both lithium and oxygen during cycling with redox reactions occurring on both the transition metal ions and oxygen ions of the electrode. In this talk, we will present in-situ and operando characterization and first principles modeling results of α-MnO 2 during electrochemical cycling in conventional lithium cells and in Li-O 2 cells [5,6]. Operando synchrotron x-ray diffraction (XRD) results, combined with first principles density functional theory (DFT) modeling, indicate insertion of lithium and oxygen into, as well as partial removal of these species from, the tunnel structure during cycling. On heating hydrated α-MnO 2 , in-situ XRD and Raman studies provide information about structural changes and diffusional properties of the oxygen species in the tunnel structure. DFT studies find low diffusion barriers for H 2 O and H 3 O + species in the tunnel. The implications of the results on other high-capacity, hybrid Li-ion/Li-oxygen materials will be discussed. Acknowledgements This work was supported as a part of the Center for Electrochemical Energy Science, an Energy Frontier Research Center funded by the US Department of Energy, Office of Science, Basic Energy Sciences under award number DE-AC02–06CH11. Use of the Advanced Photon Source, a US DOE Office of Science User Facility operated by Argonne National Laboratory, was supported by DOE under Contract No. DE-AC02-06CH11357. Use of the Center for Nanoscale Materials, an Office of Science user facility, was supported by the U. S. Department of Energy, Office of Science, Office of Basic Energy Sciences, under Contract No. DE-AC02-06CH11357. References [1] M. H. Rossouw, D. C. Liles, M. M. Thackeray, W. I. F. David and S. Hull, Mater. Res. Bull., “a-Manganese Dioxide for Lithium Batteries: A Structural and Electrochemical Study,” Mater. Res. Bull., 27 , 221 (1992). [2]  C. S. Johnson, D. W. Dees, M. F. Mansuetto, M. M. Thackeray, D. R. Vissers, D. Argyriou, C.-K Loong and L. Christensen, “Structural and Electrochemical Studies of a-MnO 2 ”, J. Power Sources, 68/2 , 570 (1997). [3] A. Debart, A. J. Paterson, J. Bao and P. G. Bruce, “a-MnO 2 Nanowires: A Catalyst for the O 2 Electrode in Rechargeable Lithium Batteries,” Angew. Chem. Int. Ed., 47 , 4521 (2008). [4]  M. M. Thackeray, M. K. Y. Chan, L. Trahey, S. Kirklin, and C. Wolverton, “Vision for Designing High-Energy, Hybrid Li Ion/Li-O 2 Cells,” Journal of Physical Chemistry Letters 4 , 3607 (2013). [5] L. Trahey, N. Karan, M. K. Y. Chan, J. Lu, Y. Ren, J. P. Greeley, M. Balasubramanian, A. K. Burrell, and M. M. Thackeray, “Synthesis, Characterization and Structural Modeling of High Capacity, Dual-Functioning MnO 2 Electrode/Electrocatalysts for Li-O 2 Batteries,” Advanced Energy Materials 3 , 75 (2013). [6] Yang, L. Trahey, Y. Ren, M. K. Y. Chan, C. Lin, J. Okasinski, and M. M. Thackeray, “In-Situ High-Energy Synchrotron X-ray Diffraction Studies and First Principles Modeling of α-MnO 2 Electrodes in Li-O 2 and Li-ion Coin Cells,” Journal of Materials Chemistry A 3 , 7389 (2015). The submitted manuscript has been created by UChicago Argonne, LLC, Operator of Argonne National Laboratory (“Argonne”). Argonne, a U.S. Department of Energy Office of Science laboratory, is operated under Contract No. DE-AC02-06CH11357. The U.S. Government retains for itself, and others acting on its behalf, a paid-up nonexclusive, irrevocable worldwide license in said article to reproduce, prepare derivative works, distribute copies to the public, and perform publicly and display publicly, by or on behalf of the Government.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2016
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  • 3
    Online Resource
    Online Resource
    The Electrochemical Society ; 2016
    In:  ECS Meeting Abstracts Vol. MA2016-02, No. 5 ( 2016-09-01), p. 664-664
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2016-02, No. 5 ( 2016-09-01), p. 664-664
    Abstract: Layered lithium intercalation compounds LiMeO2 (where Me is transition element) materials have been widely studied and applied as cathode materials for practical lithium ion batteries. Cost of lithium resource, however, has doubled since commercialization in 1991, and tight supply is expected due to the ever increasing demands of electric vehicles and energy storage systems. Indeed, the lithium resource is unevenly distributed in Southern America. Meanwhile, sodium resources are abundant and unlimited everywhere. Recently, layered NaMeO2 materials are being intensively studied because of reversible Na+ insertion/extraction, in particular, NaCrO2 (R-3m) in Na cell. Here, we report physical and electrochemical properties of NaCrO2. The NaCrO2 powder was synthesized by solid-state method. Stoichiometric mixture of Na2CO3 and Cr2O3 powders were pelletized, and the pellet was heated at 900 oC in Ar. All chemicals and products were handled in an Ar-filled gloved box to avoid air exposure. Phase identification of the products was made using X-ray diffraction (XRD) with Cu Kα radiation and the collected XRD data were analyzed by the Rietveld refinement. Electrochemical test were carried out in coin type sodium cells. Galvanostatic electrochemical charge and discharge tests in 1M NaClO4 in PC solution were carried out at room temperature. XRD pattern of the produced NaCrO2 demonstrated a phase-pure product and it was crystallized to O3 type layer structure with space group of R-3m. The delivered capacity was approximately 110 mAh (gNaCrO2) -1 in voltage range of 2 – 3.6 V and 97 % of the capacity was retained during 50 cycles. Also, the Na/NaCrO2 cell exhibited surprising high rate properties, namely, 84 % of capacity retention at 100 C-rates. Details will be discussed in the conference site. Figure 1
    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 ; 2022
    In:  ECS Meeting Abstracts Vol. MA2022-02, No. 3 ( 2022-10-09), p. 325-325
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2022-02, No. 3 ( 2022-10-09), p. 325-325
    Abstract: The recharging capability of Ni-rich layered cathodes deteriorates rapidly upon cycling, mainly from mechanical instability caused by removing a large amount of Li ions from the host structure. 1,2 The resulting microcracks expose the cathode particle interior to electrolyte attack in addition to undermining the mechanical integrity of the cathode particle. In this study, we develop a Ni-rich layered cathode by combining precursor engineering and a new doping strategy during lithiation that generates minimal microcracking and exhibits substantially improved cycling stability. Excess Al is deliberately introduced into a concentration-gradient (CG) hydroxide precursor, which exhibits a highly oriented geometry in which elongated primary particles are aligned in the radial direction of a spherical secondary particles. The excess Al ions enable the refinement of the primary particles in a controlled manner and the precise tailoring of their morphology and orientation. It is demonstrated that the chemical and microstructural engineering of a Li[Ni x Co y Al 1–x–y ]O 2 (NCA) cathode starting from its precursor stage produces a unique structure that relieves the detrimental mechanical strain and significantly extends the battery life. Thus, the designed CG Li[Ni 0.86 Co 0.1 Al 0.04 ]O 2 retains 86.5% of the initial capacity after 2000 cycles and an unprecedented 78.0% even at a severe operation condition of 45 o C. The proposed CG Li[Ni 0.86 Co 0.1 Al 0.04 ]O 2 represents a new class of Ni-rich NCA cathodes that can meet the energy density required for next-generation electric vehicles, without compromising the battery life and safety. Reference s : [1] S. Watanabe, M. Kinoshita, T. Hosokawa, K. Morigaki, K. Nakura, J. Power Sources 258 (2014) 210–217. [2] H.-H. Ryu, K.-J. Park, C. S. Yoon, Y.-K. Sun, Chem. Mater. 30 (2018) 1155–1163.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2022
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  • 5
    Online Resource
    Online Resource
    The Electrochemical Society ; 2006
    In:  Electrochemical and Solid-State Letters Vol. 9, No. 11 ( 2006), p. G320-
    In: Electrochemical and Solid-State Letters, The Electrochemical Society, Vol. 9, No. 11 ( 2006), p. G320-
    Type of Medium: Online Resource
    ISSN: 1099-0062
    Language: English
    Publisher: The Electrochemical Society
    Publication Date: 2006
    detail.hit.zdb_id: 1483551-4
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  • 6
    Online Resource
    Online Resource
    The Electrochemical Society ; 2007
    In:  ECS Transactions Vol. 2, No. 14 ( 2007-02-07), p. 1-12
    In: ECS Transactions, The Electrochemical Society, Vol. 2, No. 14 ( 2007-02-07), p. 1-12
    Abstract: We establish a thermodynamic model of ionic conductivities model for solid polymer electrolyte/salt systems based on modified double lattice (MDL) model. The proposed model takes into account both the mobility and the charge interactions of the solid polymer electrolyte/salt systems. The interactions between Li ion and polymer molecules are described by electrostatic potential (ES) when Li ion is passing by a polymeric membrane. In comparison with experimental data, quantitative descriptions of the proposed model show better agreement for the given systems than those of existing models.
    Type of Medium: Online Resource
    ISSN: 1938-5862 , 1938-6737
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2007
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  • 7
    In: ECS Transactions, The Electrochemical Society, Vol. 33, No. 5 ( 2010-10-01), p. 143-146
    Abstract: We fabricated oxide and oxide/organic hybrid TFTs on the glass substrate using the In-Ga-Zn-O (IGZO) as an active layer, and Al2O3 and PVP-PMMA co polymer as gate insulators, respectively. The Protection Layer (PL) for the oxide active was adopted to improve and understand the hysteresis characteristics of these oxide based TFTs. By adopting the PL layer, we can obtain the improved saturation mobility (usat) and sub-threshold swing (SS) compared to the without PL device from 17.63 cm2/Vs and 0.19 V/decade to 20.43 cm2/Vs 0.13 V/decade, respectively. The hysteresis characteristics with clock-wise direction were also dramatically improved in the PL process device from 1.22 V to the 0.02 V. We believe that this phenomenon is related to the contamination or damage of back channel surface of oxide semiconductor by photo-resist, solvent, and etchant that can generate the trap sites in the oxide active layer.
    Type of Medium: Online Resource
    ISSN: 1938-5862 , 1938-6737
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2010
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  • 8
    In: Journal of The Electrochemical Society, The Electrochemical Society, Vol. 155, No. 12 ( 2008), p. A952-
    Type of Medium: Online Resource
    ISSN: 0013-4651
    RVK:
    Language: English
    Publisher: The Electrochemical Society
    Publication Date: 2008
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  • 9
    Online Resource
    Online Resource
    The Electrochemical Society ; 2005
    In:  Journal of The Electrochemical Society Vol. 152, No. 5 ( 2005), p. A864-
    In: Journal of The Electrochemical Society, The Electrochemical Society, Vol. 152, No. 5 ( 2005), p. A864-
    Type of Medium: Online Resource
    ISSN: 0013-4651
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    Language: English
    Publisher: The Electrochemical Society
    Publication Date: 2005
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  • 10
    Online Resource
    Online Resource
    The Electrochemical Society ; 2008
    In:  Journal of The Electrochemical Society Vol. 155, No. 6 ( 2008), p. A414-
    In: Journal of The Electrochemical Society, The Electrochemical Society, Vol. 155, No. 6 ( 2008), p. A414-
    Type of Medium: Online Resource
    ISSN: 0013-4651
    RVK:
    Language: English
    Publisher: The Electrochemical Society
    Publication Date: 2008
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