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941.
Open‐Structured V2O5·nH2O Nanoflakes as Highly Reversible Cathode Material for Monovalent and Multivalent Intercalation Batteries
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Huali Wang Xuanxuan Bi Ying Bai Chuan Wu Sichen Gu Shi Chen Feng Wu Khalil Amine Jun Lu 《Liver Transplantation》2017,7(14)
The high‐capacity cathode material V2O5·n H2O has attracted considerable attention for metal ion batteries due to the multielectron redox reaction during electrochemical processes. It has an expanded layer structure, which can host large ions or multivalent ions. However, structural instability and poor electronic and ionic conductivities greatly handicap its application. Here, in cell tests, self‐assembly V2O5·n H2O nanoflakes shows excellent electrochemical performance with either monovalent or multivalent cation intercalation. They are directly grown on a 3D conductive stainless steel mesh substrate via a simple and green hydrothermal method. Well‐layered nanoflakes are obtained after heat treatment at 300 °C (V2O5·0.3H2O). Nanoflakes with ultrathin flower petals deliver a stable capacity of 250 mA h g?1 in a Li‐ion cell, 110 mA h g?1 in a Na‐ion cell, and 80 mA h g?1 in an Al‐ion cell in their respective potential ranges (2.0–4.0 V for Li and Na‐ion batteries and 0.1–2.5 V for Al‐ion battery) after 100 cycles. 相似文献
942.
Flexible Composite Solid Electrolyte Facilitating Highly Stable “Soft Contacting” Li–Electrolyte Interface for Solid State Lithium‐Ion Batteries
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Luyi Yang Zijian Wang Yancong Feng Rui Tan Yunxing Zuo Rongtan Gao Yan Zhao Lei Han Ziqi Wang Feng Pan 《Liver Transplantation》2017,7(22)
A flexible composite solid electrolyte membrane consisting of inorganic solid particles (Li1.3Al0.3Ti1.7(PO4)3), polyethylene oxide (PEO), and boronized polyethylene glycol (BPEG) is prepared and investigated. This membrane exhibits good stability against lithium dendrite, which can be attributed to its well‐designed combination components: the compact inorganic lithium ion conducting layer provides the membrane with good mechanical strength and physically barricades the free growth of lithium dendrite; while the addition of planar BPEG oligomers not only disorganizes the crystallinity of the PEO domain, leading to good ionic conductivity, but also facilitates a “soft contact” between interfaces, which not only chemically enables homogeneous lithium plating/stripping on the lithium metal anode, but also reduces the polarization effects. In addition, by employing this membrane to a LiFePO4/Li cell and testing its galvanostatic cycling performances at 60 °C, capacities of 158.2 and 94.2 mA h g?1 are delivered at 0.1 C and 2 C, respectively. 相似文献
943.
Dijo Damien Kalaivanan Nagarajan Ashish Raj Mahesh Hariharan Manikoth M. Shaijumon 《Liver Transplantation》2017,7(20)
Organic rechargeable batteries gain huge scientific interest owing to the design flexibility and resource renewability of the active materials. However, the low reduction potentials still remain a challenge to compete with the inorganic cathodes. This study demonstrates a simple and efficient approach to tune the redox properties of perylene diimides (PDIs) as high voltage cathodes for organic‐based sodium‐ion batteries (SIBs). With appropriate electron‐withdrawing groups as substituents on perylene diimides, this study shows a remarkable tunability in the discharge potential from 2.1 to 2.6 V versus Na+/Na with a sodium intake of ≈1.6 ions per molecule. Further, this study explores tuning the shape of the voltage profiles by systematically tuning the dihedral angle in the perylene ring and demonstrates a single plateau discharge profile for tetrabromo‐substituted perylene diimide (dihedral angles θ1 & θ2 = 38°). Detailed structural analysis and electrochemical studies on substituted PDIs unveil the correlation between molecular structure and voltage profile. The results are promising and offer new avenues to tailor the redox properties of organic electrodes, a step closer toward the realization of greener and sustainable electrochemical storage devices. 相似文献
944.
945.
Although potassium‐ion batteries (KIBs) have been considered to be promising alternatives to conventional lithium‐ion batteries due to large abundance and low cost of potassium resources, their development still stays at the infancy stage due to the lack of appropriate cathode and anode materials with reversible potassium insertion/extraction as well as good rate and cycling performance. Herein, a novel dual‐carbon battery based on a potassium‐ion electrolyte (named as K‐DCB), utilizing expanded graphite as cathode material and mesocarbon microbead as anode material is developed. The working mechanism of the K‐DCB is investigated, which is further demonstrated to deliver a high reversible capacity of 61 mA h g‐1 at a current density of 1C over a voltage window of 3.0–5.2 V, as well as good cycling performance with negligible capacity decay after 100 cycles. Moreover, the high working voltage with medium discharge voltage of 4.5 V also enables the K‐DCB to meet the requirement of some high‐voltage devices. With the merits of environmental friendliness, low cost and high energy density, the K‐DCB shows attractive potential for future energy storage application. 相似文献
946.
Lithium‐Ion Batteries: All‐Nanomat Lithium‐Ion Batteries: A New Cell Architecture Platform for Ultrahigh Energy Density and Mechanical Flexibility (Adv. Energy Mater. 22/2017)
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947.
Zhengyuan Tu Michael J. Zachman Snehashis Choudhury Shuya Wei Lin Ma Yuan Yang Lena F. Kourkoutis Lynden A. Archer 《Liver Transplantation》2017,7(8)
Successful strategies for stabilizing electrodeposition of reactive metals, including lithium, sodium, and aluminum are a requirement for safe, high‐energy electrochemical storage technologies that utilize these metals as anodes. Unstable deposition produces high‐surface area dendritic structures at the anode/electrolyte interface, which causes premature cell failure by complex physical and chemical processes that have presented formidable barriers to progress. Here, it is reported that hybrid electrolytes created by infusing conventional liquid electrolytes into nanoporous membranes provide exceptional ability to stabilize Li. Electrochemical cells based on γ‐Al2O3 ceramics with pore diameters below a cut‐off value above 200 nm exhibit long‐term stability even at a current density of 3 mA cm?2. The effect is not limited to ceramics; similar large enhancements in stability are observed for polypropylene membranes with less monodisperse pores below 450 nm. These findings are critically assessed using theories for ion rectification and electrodeposition reactions in porous solids and show that the source of stable electrodeposition in nanoporous electrolytes is fundamental. 相似文献
948.
High‐Temperature Treatment of Li‐Rich Cathode Materials with Ammonia: Improved Capacity and Mean Voltage Stability during Cycling
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Evan M. Erickson Hadar Sclar Florian Schipper Jing Liu Ruiyuan Tian Chandan Ghanty Larisa Burstein Nicole Leifer Judith Grinblat Michael Talianker Ji‐Yong Shin Jordan K. Lampert Boris Markovsky Anatoly I. Frenkel Doron Aurbach 《Liver Transplantation》2017,7(18)
Li‐rich electrode materials of the family x Li2MnO3·(1?x )LiNia Cob Mnc O2 (a + b + c = 1) suffer a voltage fade upon cycling that limits their utilization in commercial batteries despite their extremely high discharge capacity, ≈250 mA h g?1. Li‐rich, 0.35Li2MnO3·0.65LiNi0.35Mn0.45Co0.20O2, is exposed to NH3 at 400 °C, producing materials with improved characteristics: enhanced electrode capacity and a limited average voltage fade during 100 cycles in half cells versus Li. Three main changes caused by NH3 treatment are established. First, a general bulk reduction of Co and Mn is observed via X‐ray photoelectron spectroscopy and X‐ray absorption near edge structure. Next, a structural rearrangement lowers the coordination number of Co? O and Mn? O bonds, as well as formation of a surface spinel‐like structure. Additionally, Li+ removal from the bulk causes the formation of surface LiOH, Li2CO3, and Li2O. These structural and surface changes can enhance the voltage and capacity stability of the Li‐rich material electrodes after moderate NH3 treatment times of 1–2 h. 相似文献
949.
Rutile TiO2 Inverse Opal Anodes for Li‐Ion Batteries with Long Cycle Life,High‐Rate Capability,and High Structural Stability
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Rutile TiO2 inverse opals provide long cycle life and impressive structural stability when tested as anode materials for Li‐ion batteries. The capacity retention of TiO2 inverse opals (IOs) is greater than previously reported values for other rutile TiO2 nanomaterials, and the cycled crystalline phase and material interconnectivity is maintained over thousands of cycles. Consequently, this paper offers insight into the importance of optimizing the relationship between the structure and morphology on improving electrochemical performance of this abundant and low environmental impact material. TiO2 IOs show gradual capacity fading over 1000 and 5000 cycles, when cycled at specific currents of 75 and 450 mA g?1, respectively, while maintaining a high capacity and a stable overall cell voltage. TiO2 IOs achieve a reversible capacity of ≈170 and 140 mA h g?1 after the 100th and 1000th cycles, respectively, at a specific current of 75 mA g?1, corresponding to a capacity retention of ≈82.4%. The structural stability of the 3D IO phase from pristine rutile TiO2 to the conductive orthorhombic Li0.5TiO2 is remarkable and maintains its structural integrity. Image analysis conclusively shows that volumetric swelling is accommodated into the predefined pore space, and the IO periodicity remains constant and does not degrade over 5000 cycles. 相似文献
950.
Revealing Anisotropic Spinel Formation on Pristine Li‐ and Mn‐Rich Layered Oxide Surface and Its Impact on Cathode Performance
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Saravanan Kuppan Alpesh Khushalchand Shukla Daniel Membreno Dennis Nordlund Guoying Chen 《Liver Transplantation》2017,7(11)
Surface properties of cathode particles play important roles in the transport of ions and electrons and they may ultimately dominate cathode's performance and stability in lithium‐ion batteries. Through the use of carefully prepared Li1.2Ni0.13Mn0.54Co0.13O2 crystal samples with six distinct morphologies, surface transition‐metal redox activities and crystal structural transformation are investigated as a function of surface area and surface crystalline orientation. Complementary depth‐profiled core‐level spectroscopy, namely, X‐ray absorption spectroscopy, electron energy loss spectroscopy, and atomic‐resolution scanning transmission electron microscopy, are applied in the study, presenting a fine example of combining advanced diagnostic techniques with a well‐defined model system of battery materials. The present study reports the following findings: (1) a thin layer of defective spinel with reduced transition metals, similar to what is reported on cycled conventional secondary particles in the literature, is found on pristine oxide surface even before cycling, and (2) surface crystal structure and chemical composition of both pristine and cycled particles are facet dependent. Oxide structural and cycling stabilities improve with maximum expression of surface facets stable against transition‐metal reduction. The intricate relationships among morphology, surface reactivity and structural transformation, electrochemical performance, and stability of the cathode materials are revealed. 相似文献