Conjugated dicarboxylate anodes for Li-ion batteries.
TL;DR: Two organic salts, Li(2)C(8)H(4)O(4), with carboxylate groups conjugated within the molecular core, with enhanced thermal stability over carbon electrodes in 1 M LiPF(6) ethylene carbonate-dimethyl carbonate electrolytes, which should result in safer Li-ion cells.
Abstract: Present Li-ion batteries for portable electronics are based on inorganic electrodes. For upcoming large-scale applications the notion of materials sustainability produced by materials made through eco-efficient processes, such as renewable organic electrodes, is crucial. We here report on two organic salts, Li2C8H4O4 (Li terephthalate) and Li2C6H4O4(Li trans-trans-muconate), with carboxylate groups conjugated within the molecular core, which are respectively capable of reacting with two and one extra Li per formula unit at potentials of 0.8 and 1.4 V, giving reversible capacities of 300 and 150 mA h g-1. The activity is maintained at 80 °C with polyethyleneoxide-based electrolytes. A noteworthy advantage of the Li2C8H4O4 and Li2C6H4O4 negative electrodes is their enhanced thermal stability over carbon electrodes in 1 M LiPF6 ethylene carbonate-dimethyl carbonate electrolytes, which should result in safer Li-ion cells. Moreover, as bio-inspired materials, both compounds are the metabolites of aromatic hydrocarbon oxidation, and terephthalic acid is available in abundance from the recycling of polyethylene terephthalate.
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TL;DR: The notion of sustainability is introduced through discussion of the energy and environmental costs of state-of-the-art lithium-ion batteries, considering elemental abundance, toxicity, synthetic methods and scalability.
Abstract: Energy storage using batteries offers a solution to the intermittent nature of energy production from renewable sources; however, such technology must be sustainable. This Review discusses battery development from a sustainability perspective, considering the energy and environmental costs of state-of-the-art Li-ion batteries and the design of new systems beyond Li-ion. Images: batteries, car, globe: © iStock/Thinkstock.
5,271 citations
TL;DR: In this article, the authors present the present status of lithium battery technology, then focus on its near future development and finally examine important new directions aimed at achieving quantum jumps in energy and power content.
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TL;DR: This Review introduces several typical energy storage systems, including thermal, mechanical, electromagnetic, hydrogen, and electrochemical energy storage, and the current status of high-performance hydrogen storage materials for on-board applications and electrochemicals for lithium-ion batteries and supercapacitors.
Abstract: [Liu, Chang; Li, Feng; Ma, Lai-Peng; Cheng, Hui-Ming] Chinese Acad Sci, Inst Met Res, Shenyang Natl Lab Mat Sci, Shenyang 110016, Peoples R China.;Cheng, HM (reprint author), Chinese Acad Sci, Inst Met Res, Shenyang Natl Lab Mat Sci, 72 Wenhua Rd, Shenyang 110016, Peoples R China;cheng@imr.ac.cn
4,105 citations
TL;DR: In this paper, a variety of electrode materials including cathodes and anodes as well as electrolytes for room-temperature stationary sodium-ion batteries are briefly reviewed and compared the difference in storage behavior between Na and Li in their analogous electrodes and summarize the sodium storage mechanisms in available electrode materials.
Abstract: Room-temperature stationary sodium-ion batteries have attracted great attention particularly in large-scale electric energy storage applications for renewable energy and smart grid because of the huge abundant sodium resources and low cost. In this article, a variety of electrode materials including cathodes and anodes as well as electrolytes for room-temperature stationary sodium-ion batteries are briefly reviewed. We compare the difference in storage behavior between Na and Li in their analogous electrodes and summarize the sodium storage mechanisms in the available electrode materials. This review also includes some new results from our group and our thoughts on developing new materials. Some perspectives and directions on designing better materials for practical applications are pointed out based on knowledge from the literature and our experience. Through this extensive literature review, the search for suitable electrode and electrolyte materials for stationary sodium-ion batteries is still challenging. However, after intensive research efforts, we believe that low-cost, long-life and room-temperature sodium-ion batteries would be promising for applications in large-scale energy storage system in the near future.
2,687 citations
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TL;DR: Researchers must find a sustainable way of providing the power their modern lifestyles demand to ensure the continued existence of clean energy sources.
Abstract: Researchers must find a sustainable way of providing the power our modern lifestyles demand.
15,980 citations
"Conjugated dicarboxylate anodes for..." refers background in this paper
...The focus is exclusively on lithium, and we shall witness a forking in technologies as the quest for ever higher energy densities for electronics is pursued at (almost) any price, but large batteries will be selected for their safety...
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TL;DR: In this paper, the application of the Rietveld refinement technique to synchrotron X-ray data collected from a capillary sample of Al2O3 in Debye-Scherrer geometry is described.
Abstract: The application of the Rietveld refinement technique to synchrotron X-ray data collected from a capillary sample of Al2O3 in Debye–Scherrer geometry is described. The data were obtained at the Cornell High Energy Synchrotron Source (CHESS) with an Si(111) double-crystal monochromator and a Ge(111) crystal analyzer. Fits to a number of well resolved individual peaks demonstrate that the peak shapes are very well described by the pseudo-Voigt function, which is a simple approximation to the convolution of Gaussian and Lorentzian functions. The variation of the Gaussian and Lorentzian half widths, ΓG and ΓL, with Bragg angle can be approximated quite closely by the functions V tan θ and X/cos θ which represent the contributions from instrumental resolution and particle-size broadening respectively. Rietveld refinement based on this model yields generally satisfactory results. The refined values of V and X are consistent with the expected vertical divergence (≃0.1 mrad) and the nominal particle size (≃ 0.3μm). In particular, the use of a capillary specimen virtually eliminates preferred orientation effects, which are highly significant in flat-plate samples of this material.
2,469 citations
TL;DR: This paper presents a meta-analyses of the chiral stationary phase of the LaSalle-Seiden–Seiden virus, which has implications for the design of vaccines and their application in the treatment of infectious disease.
Abstract: Author(s): Robert W. Kates, William C. Clark, Robert Corell, J. Michael Hall, Carlo C. Jaeger, Ian Lowe, James J. McCarthy, Hans Joachim Schellnhuber, Bert Bolin, Nancy M. Dickson, Sylvie Faucheux, Gilberto C. Gallopin, Arnulf Grübler, Brian Huntley, Jill Jäger, Narpat S. Jodha, Roger E. Kasperson, Akin Mabogunje, Pamela Matson, Harold Mooney, Berrien Moore III, Timothy O'Riordan, Uno Svedin Reviewed work(s): Source: Science, New Series, Vol. 292, No. 5517 (Apr. 27, 2001), pp. 641-642 Published by: American Association for the Advancement of Science Stable URL: http://www.jstor.org/stable/3083523 . Accessed: 28/02/2012 04:14
2,107 citations
TL;DR: In this paper, a defect spinel-framework structure was examined in nonaqueous lithium cells and it was shown that the lattice dimension did not change during the reaction since the reaction consists of lithium ion and electron insertion into/extraction from the solid matrix without a noticeable change in lattice dimensions.
Abstract: having a defect spinel‐framework structure was prepared and examined in non‐aqueous lithium cells. (white in color) was reduced to (dark blue) at a voltage of 1.55 V and the reaction was highly reversible. X‐ray diffraction measurements indicated that the lattice dimension did not change during the reactionSince the reaction consists of lithium ion and electron insertion into/extraction from the solid matrix without a noticeable change in lattice dimension, called a zero‐strain insertion reaction, capacity failure due to the damage to the solid matrix was not observed even after 100 cycles. Feasibility of zero‐strain insertion materials for advanced batteries is discussed based on the experimental results.
1,779 citations
TL;DR: The goal of the present article is to provide a survey of electroactive polymers in view of potential applications in rechargeable batteries, and reviews the preparative methods and the electrochemical performance of polymers as rechargeable battery electrodes.
Abstract: Electrochemical energy storage systems (batteries) have a tremendous role in technical applications In this review the authors examine the prospects of electroactive polymers in view of the properties required for such batteries Conducting organic polymers are considered here in the light of their rugged chemical environment: organic solvents, acids, and alkalis The goal of the present article is to provide, first of all in tabular form, a survey of electroactive polymers in view of potential applications in rechargeable batteries It reviews the preparative methods and the electrochemical performance of polymers as rechargeable battery electrodes The theoretical values of specific charge of the polymers are comparable to those of metal oxide electrodes, but are not as high as those of most of the metal electrodes normally used in batteries Therefore, it is an advantage in conventional battery designs to use the conducting polymer as a positive electrode material in combination with a negative electrode such as Li, Na, Mg, Zn, MeH{sub x}, etc 504 refs
1,481 citations