Dramatic effect of oxidation on lithium insertion in carbons made from epoxy resins

Carbons made by pyrolyzing epoxy novolak resins at 1,000 C are made up predominantly of single graphene sheets, having a lateral dimension of about 25 {angstrom}, which are arranged somewhat like a ``house of cards.`` This structure implies significant micro- or nanoporosity. Such carbons can revers...

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Veröffentlicht in:Journal of the Electrochemical Society 1995-11, Vol.142 (11), p.3668-3677
Hauptverfasser: XUE, J. S, DAHN, J. R
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description Carbons made by pyrolyzing epoxy novolak resins at 1,000 C are made up predominantly of single graphene sheets, having a lateral dimension of about 25 {angstrom}, which are arranged somewhat like a ``house of cards.`` This structure implies significant micro- or nanoporosity. Such carbons can reversibly react with large amounts of lithium in a mechanism thought to involve the adsorption of lithium on the internal surfaces of nanopores. The authors have studied the effect of controlled oxidation of these samples, which changes the pore structure, on the subsequent electrochemical insertion of lithium in these materials using Brunauer, Emmett, and Teller surface area measurements, methylene blue adsorption tests, powder X-ray diffraction, and small angle X-ray scattering (SAX), they are also able to correlate the changes in pore structure to the electrochemical behavior of these samples. Initially, the pores are small (of the order of 15 {angstrom}), as are their openings, and the electrolyte cannot penetrate the pores, so excellent behavior is observed. Reversible specific capacities for Li as large as 570 mAh/g have been observed, with little irreversible capacity. As the samples are oxidized, the pores do not grow significantly in volume, as measured by SAX, but the size of their openings apparently does, to the point where the electrolyte can penetrate the pores, leading to irreversible electrolyte decomposition reactions during the first electrochemical reaction of lithium with the carbon, and hence large irreversible capacity. Burnoffs as small as 5% are enough to transform the samples from excellent to poor. In addition, chemisorbed oxygen (from the oxidation treatment) appears to react with lithium, leading to increases in both irreversible and reversible capacities. However, the reversible capacity due to the chemisorbed oxygen shows large hysteresis. A pictorial model is proposed that is consistent with the results.
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The authors have studied the effect of controlled oxidation of these samples, which changes the pore structure, on the subsequent electrochemical insertion of lithium in these materials using Brunauer, Emmett, and Teller surface area measurements, methylene blue adsorption tests, powder X-ray diffraction, and small angle X-ray scattering (SAX), they are also able to correlate the changes in pore structure to the electrochemical behavior of these samples. Initially, the pores are small (of the order of 15 {angstrom}), as are their openings, and the electrolyte cannot penetrate the pores, so excellent behavior is observed. Reversible specific capacities for Li as large as 570 mAh/g have been observed, with little irreversible capacity. As the samples are oxidized, the pores do not grow significantly in volume, as measured by SAX, but the size of their openings apparently does, to the point where the electrolyte can penetrate the pores, leading to irreversible electrolyte decomposition reactions during the first electrochemical reaction of lithium with the carbon, and hence large irreversible capacity. Burnoffs as small as 5% are enough to transform the samples from excellent to poor. In addition, chemisorbed oxygen (from the oxidation treatment) appears to react with lithium, leading to increases in both irreversible and reversible capacities. However, the reversible capacity due to the chemisorbed oxygen shows large hysteresis. 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The authors have studied the effect of controlled oxidation of these samples, which changes the pore structure, on the subsequent electrochemical insertion of lithium in these materials using Brunauer, Emmett, and Teller surface area measurements, methylene blue adsorption tests, powder X-ray diffraction, and small angle X-ray scattering (SAX), they are also able to correlate the changes in pore structure to the electrochemical behavior of these samples. Initially, the pores are small (of the order of 15 {angstrom}), as are their openings, and the electrolyte cannot penetrate the pores, so excellent behavior is observed. Reversible specific capacities for Li as large as 570 mAh/g have been observed, with little irreversible capacity. As the samples are oxidized, the pores do not grow significantly in volume, as measured by SAX, but the size of their openings apparently does, to the point where the electrolyte can penetrate the pores, leading to irreversible electrolyte decomposition reactions during the first electrochemical reaction of lithium with the carbon, and hence large irreversible capacity. Burnoffs as small as 5% are enough to transform the samples from excellent to poor. In addition, chemisorbed oxygen (from the oxidation treatment) appears to react with lithium, leading to increases in both irreversible and reversible capacities. However, the reversible capacity due to the chemisorbed oxygen shows large hysteresis. A pictorial model is proposed that is consistent with the results.</abstract><cop>Pennington, NJ</cop><pub>Electrochemical Society</pub><doi>10.1149/1.2048397</doi><tpages>10</tpages></addata></record>
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subjects ANODES
Applied sciences
CARBONACEOUS MATERIALS
CLATHRATES
Direct energy conversion and energy accumulation
Electrical engineering. Electrical power engineering
Electrical power engineering
Electrochemical conversion: primary and secondary batteries, fuel cells
ELECTROCHEMISTRY
ENERGY STORAGE
Exact sciences and technology
IMPREGNATION
LITHIUM
MATERIALS SCIENCE
MEASURING METHODS
METAL-NONMETAL BATTERIES
MORPHOLOGICAL CHANGES
OXIDATION
PORE STRUCTURE
PYROLYSIS
RESINS
title Dramatic effect of oxidation on lithium insertion in carbons made from epoxy resins
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