• Title/Summary/Keyword: Disordered carbon

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Mesoporous Carbon Additives for Long Cycle Life Sulfur Cathodes of Li-S Batteries

  • Koh, Jeong Yoon;Kim, Tae Jeong;Park, Min-Sik;Kim, Eun Hee;Kim, Seok;Kim, Ki Jae;Yu, Ji-Sang;Kim, Young-Jun;Jung, Yongju
    • Bulletin of the Korean Chemical Society
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    • v.35 no.11
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    • pp.3331-3335
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    • 2014
  • We examine the potential use of disordered mesoporous carbon as a functional additive for confining dissolved Li-polysulfides and improving the cycling performance of Li-S batteries. To promote a better understanding of the correlation between the total pore volume of disordered mesoporous carbon and the cycling performance of Li-S batteries, a series of disordered mesoporous carbons with different total pore volumes are successfully synthesized using a commercial silica template. Based on the electrochemical and structural analyses, we suggest that the total pore volume of disordered mesoporous carbon is a predominant factor in determining its capability for either the absorption or adsorption of Li-polysulfides, which is primarily responsible for enhancing the cycling performance. The addition of disordered mesoporous carbon is also effective in enhancing the homogeneous distribution of active sulfur in the cathode, thereby affecting the cycling performance.

Electrochemical Properties of Carbon Composites Prepared by Using Graphite Ball-milled in Argon and Air Atmosphere

  • Lee, Kyoung-Muk;Oh, Seh-Min;Lee, Sung-Man
    • Bulletin of the Korean Chemical Society
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    • v.29 no.6
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    • pp.1121-1124
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    • 2008
  • A carbon composite was synthesized by mechanical mixing of ball-milled graphite and PVC powders, followed by pyrolysis reaction of PVC. Natural graphite ball milled under atmosphere of argon or air leads to a disordered structure. It appears that the electrochemical lithium intercalation reaction is dependent on the atmosphere in which the graphite is ball milled. The carbon composite obtained using air-milled graphite shows a high reversible capacity and high initial coulombic efficiency compared to argon-milled graphite. This is attributed to the enhanced thermal stability of a disordered structure in the air milled sample. For the one with air-milled graphite, the disordered structure is maintained during heat treatment, while argon-milled graphite is partially crystallized.

The Electrochemical Characteristics of Electrochemically Prepared Poly(p-phenylene) and PPP-based Carbon (전해중합법으로 제조한 Poly(p-phenylene)과 PPP-based Carbon의 전기 화학적 특성)

  • 김주승;조재철;정운조;구할본
    • Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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    • 1997.04a
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    • pp.70-73
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    • 1997
  • The purpose of this study is to research and develop poly(p-phenylene)(PPP)-based carbon obtained by pyrolyzing electrochemically prepared PPP as a anode of rocking chair batteries. Disordered carbon materials were obtains by heat-treating of PPP films in a nitrogen atmosphere at 4$0^{\circ}C$ to 110$0^{\circ}C$ for 1 hour. The carbon prepared by heat treatment showed a broad x-ray diffraction peak having characteristics of disordered carbon. Carbon electrodes were charged and discharged at a current density of 0.1㎃/$\textrm{cm}^2$. First discharge capacity of 267㎃h/g and 34% of charge/discharge efficiency were observed from PPP-based carbon prepared at $700^{\circ}C$.

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The Electrochemical characteristics of PPP-based Carbon as Adding with Graphite (PPP-based Carbon의 Graphite 첨가에 따른 전기화학적 특성)

  • Kim, J.S.;Sung, C.H.;Gu, H.B.
    • Proceedings of the KIEE Conference
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    • 1997.07d
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    • pp.1597-1599
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    • 1997
  • Disordered carbon materials for anode of lithium rechargeable batteries were showed much larger reversible capacity than graphite. In this paper, we studied the electrochemical characteristics of PPP-based carbon, one of the disordered carbon, as adding with different amount of graphite. PPP-based carbon with 30wt% of graphite showed large reversible capacity, ${\sim}286mAh/g$, irreversible capacity ${\sim}299mAh/g$, and small hysteresis between discharge and charge in carbon/Li cell.

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Preparation and Characterization of Spherical Carbon Composite for Use as Anode Material for Lithium Ion Batteries

  • Ahn, Byoung-Hoon;Lee, Sung-Man
    • Bulletin of the Korean Chemical Society
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    • v.31 no.5
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    • pp.1331-1335
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    • 2010
  • A novel spherical carbon composite material, in which nanosized disordered carbons are dispersed in a soft carbon matrix, has been prepared and investigated for use as a potential anode material for lithium ion batteries. Disordered carbons were synthesized by ball milling natural graphite in air. The composite was prepared by mixing the ball-milled graphite with petroleum pitch powder, pelletizing the mixture, and pyrolyzing the pellets at $1200^{\circ}C$ in an argon flow. The ballmilled graphite consists of distorted nanocrystallites and amorphous phases. In the composite particle, nanosized flakes are uniformly distributed in a soft carbon matrix, as revealed by X-ray diffractometer (XRD) and transmission electron microscopy (TEM) experiments. The composite is compatible with a pure propylene carbonate (PC) electrolyte and shows high rate capability and excellent cycling performance. The electrochemical properties are comparable to those of hard carbon.

The Electrochemical Properties of Poly(p-phenylene)-based Carbon According to Pyrolyzing Time (Poly(p-phenylene)-based Carbon의 열처리 시간에 따른 전기화학적 특성)

  • Kim, C.J.;Kim, J.S.;Kim, S.H.;Ryu, H.O.;Park, H.B.;Hong, S.M.;Gu, H.B.
    • Proceedings of the KIEE Conference
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    • 1997.07d
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    • pp.1606-1608
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    • 1997
  • We have synthesized PPP from benzen by chemical reaction. And then disordered carbon materials were obtained by heating-treating PPP in a nitrogen atmosphere for 1, 4, 8 and 12 hour at $700^{\circ}C$. The carbon prepared by heat treatment showed a broad x-ray diffraction peak around $2{\theta}=20^{\circ}$ having a property of disordered carbon. Carbon electrodes were charged and discharged at a current density of $0.25mA/cm^2$. In the result, PPP-based carbon obtained at $700^{\circ}C$ for 8h showed 605mAh/g of first discharge capacity and had a small hysteresis characteristic.

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Biomass Waste, Coffee Grounds-derived Carbon for Lithium Storage

  • Um, Ji Hyun;Kim, Yunok;Ahn, Chi-Yeong;Kim, Jinsoo;Sung, Yung-Eun;Cho, Yong-Hun;Kim, Seung-Soo;Yoon, Won-Sub
    • Journal of Electrochemical Science and Technology
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    • v.9 no.3
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    • pp.163-168
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    • 2018
  • Biomass waste-derived carbon is an attractive alternative with environmental benignity to obtain carbon material. In this study, we prepare carbon from coffee grounds as a biomass precursor using a simple, inexpensive, and environmentally friendly method through physical activation using only steam. The coffee-derived carbon, having a micropore-rich structure and a low extent of graphitization of disordered carbon, is developed and directly applied to lithium-ion battery anode material. Compared with the introduction of the Ketjenblack (KB) conducting agent (i.e., coffee-derived carbon with KB), the coffee-derived carbon itself achieves a reversible capacity of ~200 mAh/g (0.54 lithium per 6 carbons) at a current density of 100 mA/g after 100 cycles, along with excellent cycle stability. The origin of highly reversible lithium storage is attributed to the consistent diffusion-controlled intercalation/de-intercalation reaction in cycle life, which suggests that the bulk diffusion of lithium is favorable in the coffee-derived carbon itself, in the absence of a conducting agent. This study presents the preparation of carbon material through physical activation without the use of chemical activation agents and demonstrates an application of coffee-derived carbon in energy storage devices.

The Impedance Properties of Poly(p-phenylene)-based Carbon/Li cell (PPP-based Carbon/Li cell의 임피던스 특성)

  • 류현옥;홍성문;김주승;구할본
    • Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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    • 1997.11a
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    • pp.283-285
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    • 1997
  • We have obtained disordered carbon by pyrolyzing PPP in a nitrogen atmosphere for 8 hour at 700$^{\circ}C$. AC impedance property was measured with the PPP-based carbon/EC-DEC/Li cell. The impedance spectra of the cell were measured during the 1st discharge proceed. As the result of measurement the cell resistance decreased in intial discharge, but increase in final discharge.

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The electrochemical Characteristics on the Anode Material of Lithium Ion Secondary Batteries with Discharge Voltage (방전전압에 따른 리튬 이온 2차전지용 음극물질의 전기화학적 특성)

  • Park, Jong-Gwang;Han, Tae-Hui;Jeong, Dong-Cheol;Im, Seong-Hun;Han, Byeong-Seong
    • The Transactions of the Korean Institute of Electrical Engineers C
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    • v.49 no.6
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    • pp.328-334
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    • 2000
  • A lithium ion secondary battery using carbon as a negative electrode has been developed. Further improvements to increase the cell capacity are expected by modifying the structure of the carbonaceous material. There are hopes for the development of large capacity lithium ion secondary batteries with long cycle, high energy density, high power density, and high energy efficiency. In the present paper, needle cokes from petroleum were examined as an anode of lithium ion secondary battery. Petroleum cokes, MCL(Molten Caustic Leaching) treated in Korea Institute Energy Research, were carbonized at various temperatures of 0, 500, 700, $19700^{\circ}C$ at heating rate of $2^{\circ}C$/min for lh. The electrolyte was used lM liPF6 EC/DEC (1:1). The voltage range of charge & discharge was 0.0V(0.05V) ~ 2.0V. The treated petroleum coke at $700^{\circ}C$ had an initial capacity over 560mAh.g which beyond the theoretical maximum capacity, 372mAh/g for LiC6. This phenomena suggests that carbon materials with disordered structure had higher cell capacity than that the graphitic carbon materials.

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Electrochemical Properties of Pyrolytic Carbon and Boron-doped Carbon for Anode Materials In Li-ion Secondary Batteries (리튬 이온 이차전지 부극용 열분해 탄소 및 붕소첨가 탄소의 전기화학적 특성)

  • Kwon, Ik-Hyun;Song, Myoung-Youp;Bang, Eui-Yong;Han, Young-Soo;Kim, Ki-Tae;Lee, Jai-Young
    • Journal of the Korean Electrochemical Society
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    • v.5 no.1
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    • pp.30-38
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    • 2002
  • Disordered carbon and boron-substituted disordered carbons $C_{l-x}B_x(x=0.05,\;0.10,\;0.20)$ were synthesized by Pyrolysis of LPG(liquid Propane gas)and $BCl_3$. Their electrochemical properties as anode materials for Li-ion secondary batteries were then investigated. When PVDF is added to the sample in a weight ratio 5 : 95, the disordered carbon with x=0.00 had the first discharge capacity 374 mAh/g. Its cycling performance was relatively good from the second cycle and it had the discharge capacity 258 mAh/g at the 10th cycle. When PVDF is added to the sample in a weight ratio 5 : 95, the sample with x=0.05 among the samples $C_{l-x}B_x(x=0.05,\;0.10,\;0.20)$ exhibited the largest first discharge capacity 860 mAh/g and discharge capacity 181 mAh/g at the 10th cycle. All the samples had similar cycling performances from the second cycle. The sample $C_{0.90}B_{0.10}$ showed the best electrochemical properties as a anode materials fur Li-ion secondary battery from the view points of the first discharge capacity(853 mAh/g when $10w1.\%$ PVDF is used), cycling performance, discharge capacity(400mAh/g at the 10th cycle when $10wt.\%$ PVDF is used). All the samples showed generally larger charge and discharge capacities when $10wt.\%$ PVDF ratter than $5wt.\%$ PVDF is used. The plateau region in the range of voltage lower than 1.25V becomes larger probably since the structure becomes less disordered by the addition of boron. When boron is added, the charge and discharge capacities decreased suddenly at the second cycle. This may be become only a part of Li are reversibly deintercalated and intercalated and a part of Li which are strongly combined with B are not deintercalated. The increases in charge and discharge capacities are considered to be resulted from the increase in the potential of Li in the boron-added carbons, caused by the strengthening of the chemical bond between the intercalated Li and the boron-carbon host since the boron acts as electron acceptor.